| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:50081952-50082256 | Common:1; Rare:85 | ||||
| chr13:50909765-50910079 | Common:1; Rare:70; Clinvar:4; Clinvar (benign):1 | ||||
| chr13:51804097-51804208 | Common:2; Rare:39 | ||||
| chr13:52012127-52012428 | Common:2; Rare:97; Clinvar:1 | ||||
| chr13:52159558-52159698 | Common:1; Rare:25 | ||||
| chr13:52455218-52455503 | Common:3; Rare:86 | ||||
| chr13:52455943-52456017 | Common:1; Rare:26 | ||||
| chr13:52652322-52652456 | Common:2; Rare:39 | ||||
| chr13:52652625-52652916 | Common:3; Rare:89 | ||||
| chr13:52848637-52848769 | Common:1; Rare:35 | ||||
| chr13:57631647-57631915 | Common:3; Rare:62 | ||||
| chr13:60163892-60164052 | Rare:39 | ||||
| chr13:60397146-60397372 | Common:4; Rare:83 | ||||
| chr13:70108414-70108569 | Rare:39 | ||||
| chr13:72727574-72727938 | Common:7; Rare:131 |