| Tag | Content |
|---|
EnhancerAtlas ID | HS052-26216 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr3:53136560-53137960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF3 | MA0522.2 | chr3:53137085-53137095 | AGCAGGTGTT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 53136597 | 53136930 | | chr3 | 53136655 | 53137000 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH03I053102 | chr3 | 53136597 | 53137153 | | GH03I053103 | chr3 | 53137919 | 53139189 |
|
Enhancer Sequence | GAAAAAGCAA AGCAAAGCTA GGTGTGAGAA GGATTTCTAA GAAAAGCCTC TAGAACACTT 60
ACAAAGACCC TAATTAAATG CAGGGCTAAT CCCAAACAAC GGAAGAGAAG CCACACCCCT 120
ACACAAAAGC CTGTCCGTGC TGTGTCCGAG TCCCACATCT GGAGATGGCC AGTACAGCTC 180
ACAGGTAAGT AGTCCACTTC CAGGGTGAAG ACAAAGACAA GTACACAACT GGGGACAGCA 240
GTGTTGCGAG TTCCACTTTC AAAACTAAGA TGATGGGCTG AGTCATGATA ATGATGGGAC 300
AGCCCCCTCC TTGAGGCAAC GCCCTGTGAT TGTGTGACAT TAGAGGCTGC TCCTTGGTGA 360
TTGCTTTCTA AAGGGGAAGA GCTGCTACAG AATAGTCGAG TTCCCAATCT CTGCCCATAA 420
ACTTACTAAT GCCTTCCTCA TGAGGCCTCC CCACAGCTGC CAGATGGAAA TACACTTCTC 480
ACAGCACAAG CCCCAGGGAG CTGCAAACCA CTTCACTGGT TTCACAGCAG GTGTTTCTCC 540
AAACTTAATG ACCTTTGCTC TGGTATAGAA ACCTGGCCCT TCCTCCCCTA ACACCAAAAG 600
TTTGGGCCCC ATTGTAGTGG AGACTAAAAC ATGCTAGTGA ACTTGTAAAA TGGCATTTGA 660
CAAAGCCCTT TATATTGAGA TGGGGCAGCA GAAAGAAGTC CTCAGCGTTC TTGTCCAGCG 720
ACCTGAGAAA TTAAAAACAT CTTTGCTAAA CCCAAGATGA AGCACTGCAA ATGGACTGCC 780
AGCTTACAGC CCAGCACATT TTGAAATTGA TGAAGTCCCC AAGACCTAAC AAGTGCTGTG 840
AGATCCTCAG CGGCCTGGTG TTTCAAAATT AGACACATTC AATACTTTTC TTCTTCAAAA 900
ACTGAGAGTC ACTGGATTAA ATATACCATT TTATTTGCAG AGATCAATTT TATTCTCTGC 960
AAATGGCTTT GGGTTATCCT TCAGAGGCTT TTATGCACTA GGCTGGGAGA TTTATGTGGC 1020
ATTTACTATC TTCAGATGTG TTTAGTACCA AGTGGAGACT CATTACCGTC TGCCCTCTGC 1080
CTTCCTCCCT CACCCCAGAG GGAGCACAGG GAAGCGCTTG GCAAAACACA TTCTAGGCCC 1140
GAGAGGAAAG CCAACAGCAA GGAGAAGTCC TAATAACTTC TCCAAGTGAG GCTGGGGAAG 1200
CTGATTGTCC TGGCGCCAAC GCCCCTGCCT ATACCTTGAG TGTGTGTCTG GAGTTGAACG 1260
AGGGGAACAG TCCCACAGCC CCTGCCACCA GACAGTTTTC CCTACACTGA CACAGATAAC 1320
AACTGTGTGT GCACAAGTTC TTGAATTTCG TGACTCTTCT ATTTATGTTG GGAAATCAGA 1380
AAAAATCCAG AAAAACTCTT 1400
|
