| Tag | Content |
|---|
EnhancerAtlas ID | HS091-29803 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr20:3528140-3529600 |
Target genes | | Number: 19 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr20:3529524-3529539 | AGTTAATTATTTATT | - | 6.88 | | HNF1B | MA0153.2 | chr20:3529525-3529538 | GTTAATTATTTAT | + | 6 | | IRF1 | MA0050.2 | chr20:3528141-3528162 | AGCTTCTTTCATTTTTATTTT | + | 6.67 | | Stat6 | MA0520.1 | chr20:3528453-3528468 | TATTTCCTCAGAAAC | + | 6.52 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAGCTTCTTT CATTTTTATT TTTTCTTCCA TTTATAGAAC ATTCCCACTA AATAAATTAT 60
AGATTGACTT TATTCTTAGC ACCTATATAA TTTATATTAA TCAAATACGA GGTAGCATTT 120
AAGCTTGAAA CATCCCTCTA TCTAGCTGCT TATGAATTTC GGTTTCATAC ATGTGTGGTC 180
ATGGTCTTTA GAATTATGGA GGGTTGGCCA TTTTTTGCAT CCTGTGTGTG AAAGTTGGAG 240
AACTTGGACT CAGTCATAAA AGGATGTAGC AGAGAGCCAA GCTGGGAGAT GGGACAAGAG 300
CTGACAATAA TGATATTTCC TCAGAAACAC ACTCTAAGTT CAGAGAAAAT TGGTGTCAGT 360
TATACATTAG AATCTTAAAG GAGTTAGCTA ATAGTTATCT ACAGAAATAA TTAAAGAAGC 420
TTTAGGGAAT TATTTAAGGG GTGAGTGATA ATAACTGTTA TTAATTTGGT GATTTTTCTT 480
GTAAACTTAC CCCTTCCTCA GAACCTTTTT ACTTTGAAAG GAAATATGCT GGTTTAAATA 540
CCTTAGTTTG TTGGGTTTGG CTGACATTTT AGAGTTAATA ATTGAAGAAT TTCAGTATCT 600
ACCATTGTGC AAATATTGCA GCAGAAGCCA AACCTCCCAA GAATGGAGTC TGTTTCTTCA 660
ATTTGTTTAA GTTTTTTGAT TTACCAGAAG ATGGATAGTT TGTATGATTG CTCCCGGGTC 720
TAGTTATCAA ACTTATTCCT CCATATCCAC AAGTTCTGCA TCTACAAATT CAAACAACCA 780
TGTGTAGAAA ATATTCAGGA AAAAAACACA ATAAAAGATA ATACAGGCTG GGTGTGGTGG 840
CTCATGCCTG TAATCCCAGC ACTTTGGGAG GCCAAGGCAG GCGGCTCACT GAGGTCAGGA 900
GTTCGAGACC AGCTTGGCCA ACATGGTGAA ACCCTGTCTC TACTAAAAAA TACAAAAATT 960
AGGTGGGCAT GGTGGCAGGC ACCTGTAATC CCAGCTACTT GGGAGGCTGA GGCAGGAGAA 1020
TGTCTTGAAC CCTGGAGGTG GAGGTTGCAG TGAGCCGAGA TCATACCACT GCACTCCAAC 1080
ATGGATAACA GAGCCAGACT CCATCTCAAA AAAAAAAAAA AAAAAAAGAT AATACAAATA 1140
AAAGATACGC ATATGAAAAC AACCATTTAC ATAGCATTTA CATTGTGTTA AGTATTATAA 1200
GTAATCTAGA GGTGAGTTAG AGTATATGGC AGGATGTGTG TAGGTTATAT GCAAGTGTTA 1260
CATCACTAGT TTATATTAGG GACCTTGAGC ATCTGTGGAT TTTGGTACCA AGGGCATCCT 1320
GGAACCAGTC CCCTGTGGAT ATTGAGGGAT AACTGTATAT TTTATCCTTA AGATTTTTCA 1380
TGTGAGTTAA TTATTTATTT ATCTGTGCTT TCTCCTGAGA GTTGCTTAAG CAGGTATTTC 1440
ATTACCAAAA AAACCCTAAC 1460
|
