| Tag | Content |
|---|
EnhancerAtlas ID | HS092-10288 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:104454220-104455640 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxo1 | MA0480.1 | chr11:104454499-104454510 | TGTAAACAGCA | - | 6.14 | | ZNF263 | MA0528.1 | chr11:104454322-104454343 | GAGGGAGAAGGAAGAAGGAAA | + | 6.16 | | ZNF263 | MA0528.1 | chr11:104454325-104454346 | GGAGAAGGAAGAAGGAAAGAG | + | 6.3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGTTTGACTC TTGGCTCTTT CCCCTTCCTT AAATAAACTG GTGATTTTGA GAAGTGGGCA 60
TATGGAGCAC GCAAAAGAAA GATAAAAAGA AAGAAAAAGA TAGAGGGAGA AGGAAGAAGG 120
AAAGAGAGCA GTTGAGGAAG AAAGTAGGAA GGTTGTATGA GGAGAGACAG AAAATTAGGA 180
AAGGGGATAC ATAGTAGGTA GTCTAGGAAG TCTAGCTTTT CTATAGGAGA AATGTGCCAG 240
TACACAAGAC TAACATCCGC TAAATGGGTC ATAGATGTGT GTAAACAGCA TACAAACATC 300
CAGGCCAGAC AGATTTCCAT GAAGTTAGGG TATAAGATAG GTCTTCCATG ATGCTGTTAC 360
AGGTAGTTAG GCATGAGCAG GGCAGGAGAG GGCTGTCCCC CACCCACTAG AAATGTCTGG 420
CAATGATTCG GCAATTACTG CATTGCCCCT CTAAAAGTGA TAAATTGGCA GCCGGCTCCA 480
GGCAGAGGCG ATTTCCTGAT GTTCCACATC TGTTTAACAT TAAAGTGTTA ACTAAATGCA 540
GATCCCAGGG AGAAAGCAAC TCCCTGGGTA TGCACATTAA GAAACAAAAA TGGCGAAGTA 600
CAATCTTACG GGTACACTCC AACAGAAAAA GGAAAAAAGC CTCAGATGGG CATGTGTACA 660
ACTTCCTAAA CACACTGAGC GTGCTCACTT CCCAAGGGTA AGGAGGGGTC TGCGCATGCG 720
GCGGCACACC CTACGGGAAG AATCATAGGA AAGAGGGGAG CTCATAAAGT CATAGGATCA 780
AGCCCTTTCT TGTTGCTGTC TTTTCTCCCT TGGAACTTCA GGTTCCTGCT TGGTCTCTTC 840
CAAGCAAATT TTCCTTTCTT TCCTTTTCTA AAGCCTTTTT AAATAAACTT CCACTCTTGC 900
TCTGAAACTT GCCTTGGTCT CTTATTCTGC TTTATGCCCT CCAGTCGAAT TATTTCTTCT 960
GGGGAGGCAA GGACTGAATT TGCTATAGAT ACACCACAGG TAACTCAGGG TAACTCGGAT 1020
CTCTTCCTCT GGTAACAATG CCAGGGTGAG CACTGACATT CAGCCTGGCC CCTTACACAT 1080
TTATTCCTGC CTCCATGGCC CTCAACAGAG CACTGTGGAG CAGCCATGCC CCCATAAATA 1140
TGGATTGTTT ATGAATGCAG CTGAAGGCTT TTGTACAGAG TCTGTGGCTT CTTCCTCACC 1200
TACCCTGCTT AACTCTCCAA GCTTTTAACA TTGTCTCTCA TCCTCCTGTT TTCTTTTGTC 1260
TTTTACTTTT TTTAATGCAG TCATGATTTC CTCCTGATTC TGACTTTCTT TTCAGGGCAA 1320
TTCTATTTCT CTATTTTGGC ATTATCTGGA GAGTGTTCTC TAACTTGCAC CCCCTCCTTA 1380
TTTGATTTGT CCCTTTCAAC CCTATTCGTG AGCAATACAT 1420
|
