Table 1.

This is a table of the csv file with coordinates in microns the same as those used in Fig. 5(a). This table is also identical to the csv file used to specify the RoIs used in Fig. 7(a). The length column here specifies that all RoIs are square single-pixel wide RoIs. The csv includes RoIs for the anterior cingulate (AC), visual cortex (V1), secondary motor cortex (M2), barrel cortex (BC), retrosplenial cortex (RS), primary motor cortex (M1), and the hindlimb cortex (HL) for each hemisphere (left, L, and right, R). Coordinates were adapted from the Allen Mouse Brain Connectivity Atlas.^16,36 The position of seeds for BC and M1 was adjusted to maximize the remote correlation between them. Their positions are still within the general region of motor and barrel cortex.³⁶ We previously mapped functional and anatomical coordinates of transgenic mice using sensory stimulation in combination with in vivo large-scale cortical mapping using channelrhodopsin-2 stimulation to confirm the coordinates below.^12,24

(1) RoI name	(2) Length	(3) $X$ coordinate	(4) $Y$ coordinate
L-V1	1	$-2516.8$	$-4267.8$
L-BC	1	$-4300$	$-760$
L-HL	1	$-1694.2$	$-1145.7$
L-M1	1	$-1500$	2000
L-M2	1	$-870.02$	1420.5
L-RS	1	$-620.43$	$-2885.8$
L-AC	1	$-260$	270
R-V1	1	2516.8	$-4267.8$
R-BC	1	4300	$-760$
R-HL	1	1694.2	$-1145.7$
R-M1	1	1500	2000
R-M2	1	870.02	1420.5
R-RS	1	620.43	$-2885.8$
R-AC	1	260	270