| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:105854403-105854533 | Rare:40 | ||||
| chr14:105854535-105854754 | Rare:75 | ||||
| chr14:105854915-105855238 | Common:3; Rare:94 | ||||
| chr14:105855426-105855829 | Common:3; Rare:145 | ||||
| chr14:105855894-105856299 | Common:5; Rare:140; Clinvar (benign):2 | ||||
| chr14:105856451-105856827 | Common:5; Rare:59 | ||||
| chr14:105856969-105857082 | Rare:17 | ||||
| chr14:105858180-105858448 | Common:3; Rare:77 | ||||
| chr14:105860678-105861028 | Common:1; Rare:188 | ||||
| chr14:105861951-105862373 | Common:4; Rare:170 | ||||
| chr14:105862439-105862606 | Rare:96 | ||||
| chr14:105862759-105862834 | Rare:42 | ||||
| chr14:105863196-105863325 | Common:6; Rare:208 | ||||
| chr14:105863519-105863884 | Common:1; Rare:396 | ||||
| chr14:105864238-105864320 | Rare:113 |