| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:634066-634113 | Rare:19 | ||||
| chr1:778598-778820 | Common:4; Rare:95 | ||||
| chr1:827401-827809 | Common:3; Rare:130 | ||||
| chr1:2112583-2112753 | Common:6; Rare:44 | ||||
| chr1:2148778-2148948 | Rare:56 | ||||
| chr1:2151427-2151570 | Common:1; Rare:31 | ||||
| chr1:2229563-2229642 | Rare:26; Clinvar (benign):3 | ||||
| chr1:2305786-2306070 | Common:1; Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:2510733-2510998 | Common:1; Rare:67 | ||||
| chr1:2546103-2546407 | Common:5; Rare:98 | ||||
| chr1:2548728-2548988 | Common:6; Rare:76 | ||||
| chr1:2554113-2554299 | Common:1; Rare:60 | ||||
| chr1:2578375-2578594 | Common:2; Rare:47 | ||||
| chr1:2585520-2585628 | Common:1; Rare:23 | ||||
| chr1:6487895-6488029 | Common:1; Rare:20 |