| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70293375-70293504 | Rare:45 | ||||
| chr2:70293645-70293917 | Common:5; Rare:153 | ||||
| chr2:70301975-70302112 | Common:3; Rare:169 | ||||
| chr2:70553776-70554420 | Common:5; Rare:249 | ||||
| chr2:70994746-70995101 | Common:8; Rare:206 | ||||
| chr2:71068050-71068370 | Rare:83 | ||||
| chr2:71068515-71068678 | Rare:150 | ||||
| chr2:71129600-71130130 | Common:1; Rare:115 | ||||
| chr2:71130220-71130674 | Common:7; Rare:177; Clinvar:2; Clinvar (benign):4 | ||||
| chr2:71130690-71130910 | Common:1; Rare:131 | ||||
| chr2:71276361-71276654 | Rare:181 | ||||
| chr2:71276680-71277350 | Common:4; Rare:234 | ||||
| chr2:71331560-71331915 | Common:5; Rare:105 | ||||
| chr2:71453497-71453737 | Common:1; Rare:49 | ||||
| chr2:72144880-72145250 | Common:2; Rare:101 |