| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:38094585-38094833 | Common:4; Rare:61 | ||||
| chr10:42638084-42638748 | Common:11; Rare:276 | ||||
| chr10:42782401-42783096 | Common:2; Rare:173 | ||||
| chr10:43076890-43077133 | Common:5; Rare:85; Clinvar:3; Clinvar (benign):2 | ||||
| chr10:43137981-43138090 | Common:1; Rare:13 | ||||
| chr10:43138238-43138557 | Common:3; Rare:105 | ||||
| chr10:43138714-43138957 | Common:1; Rare:52 | ||||
| chr10:43396237-43396347 | Rare:35 | ||||
| chr10:43396468-43397062 | Common:2; Rare:178 | ||||
| chr10:43397188-43397538 | Common:3; Rare:108 | ||||
| chr10:43407680-43408144 | Common:3; Rare:138 | ||||
| chr10:43408721-43408991 | Common:1; Rare:87 | ||||
| chr10:43409086-43409474 | Common:4; Rare:129 | ||||
| chr10:43436152-43436417 | Common:4; Rare:56 | ||||
| chr10:43436706-43437243 | Common:6; Rare:206 |