| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:11805905-11806265 | Common:2; Rare:100; Clinvar:1 | ||||
| chr1:11934489-11934784 | Common:6; Rare:97; Clinvar:6; Clinvar (benign):1 | ||||
| chr1:13583693-13584097 | Common:2; Rare:180 | ||||
| chr1:13584714-13584921 | Common:3; Rare:45 | ||||
| chr1:15526539-15526914 | Common:2; Rare:122 | ||||
| chr1:16017948-16018245 | Common:7; Rare:103 | ||||
| chr1:16212616-16212921 | Common:1; Rare:52 | ||||
| chr1:16352410-16352680 | Common:4; Rare:128 | ||||
| chr1:19210231-19210436 | Rare:79 | ||||
| chr1:19251505-19251848 | Common:6; Rare:112 | ||||
| chr1:19312028-19312343 | Common:8; Rare:154 | ||||
| chr1:19596688-19597096 | Common:3; Rare:140 | ||||
| chr1:20185850-20186134 | Common:1; Rare:86 | ||||
| chr1:20508063-20508236 | Common:2; Rare:62 | ||||
| chr1:20661346-20661709 | Common:3; Rare:131; Clinvar:4; Clinvar (benign):6 |