| Tag | Content |
|---|
EnhancerAtlas ID | HS091-18707 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:3544620-3546320 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE40 | MA0464.2 | chr17:3545104-3545114 | GTCACGTGAT | - | 6.02 | | MITF | MA0620.2 | chr17:3545100-3545118 | CATGGTCACGTGATCATC | + | 6.42 | | MITF | MA0620.2 | chr17:3545100-3545118 | CATGGTCACGTGATCATC | - | 6.42 | | STAT1 | MA0137.3 | chr17:3545176-3545187 | TTTCCGGGAAA | + | 6.32 | | TFEB | MA0692.1 | chr17:3545104-3545114 | GTCACGTGAT | - | 6.02 | | USF2 | MA0526.2 | chr17:3545100-3545116 | CATGGTCACGTGATCA | + | 6.67 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I003639 | chr17 | 3542896 | 3545718 |
|
Enhancer Sequence | TTGCCTCTTG GGTCAAATAC AAAAATCAGA TACATATATA TATATATATA TATATATATT 60
TTTTTTTTTT TTTTTTTTTT TTTGAGACAG AGTCTCACTC TGTCGCTGAG GCTGGTGTGC 120
AGTGGCACGA TCTCAGCCCA CTGCAACCTC CACCTCCCGG GTTCAAGCAA TTCTCCTGCC 180
TCAGCCTCCC TAGTAGCTGG GATTACAGGC ACCCGCAACT ACGCCCAGCT AGTTTTTTGT 240
ATTTTTAGTA GAGATGGGGT TTCACCATGT TGGCCAGGCT GGTTTTGAGC TCCTGACCTC 300
GTGGCTCGCC TGCCTTGGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACCGTGCCT 360
GGCCCAGATA CCTTAAATTC CCATTTCAAG TGAACCTTGA CAAACAATAC AAATCCTGCA 420
GAGGTTTCCC CAGAGCCTAG CACCATTGCC GTTATCTGGC CTCTTGCATC TCTGAGGAAA 480
CATGGTCACG TGATCATCTC TTCCAGGTTT GTTAAACAAT CAGTAATGTT TGTAGTCACA 540
CTTTGTGGAT AAGCAATTTC CGGGAAAGGC AGGTCTTTCA GACCCTGGAA CCTGGTGTTT 600
CTTAATACAG ACGTCAGAAC CCTGTCCCCA CCCTGTAGGA TCAGACTTTG TAAGACTGAG 660
GCTGGAGCAT GTGCGTGTGC CTGGGAGTGT GCGCGCGCGT GTATTTGCCT GGGCCTGTGT 720
GTGTGTGTGT ACCCGGGCGT GTGTGTGTGT GTGTGTGCCT GGGCGTGTGT GTGTGTGCCT 780
GGGTGTGTGT CTGCGTGCAT GTATGTGTGC CCGGGCGTGT GTGTGTGTGT GTGTGTGTGC 840
CCAGTCGCTC ATACATACTC TTTAAAGCCC CATTAGTAAT GCTAACACGC TCCCCTAGGA 900
GAAAAACAAA AAATCCAGCT ACCACCACTC CAGTTACCTG GAGGGGAAGC AGGCCCAGAG 960
AGGGTAGAAG GCTTCCCCAA AGTCACACAG CTAGAAAGTA ACAAAGCTGG GACCTGCATA 1020
GGATCCCTGC TGCATGAGAT CACTTTGCCT CCTTTCCTGA ATGCCATTAG AAAAGAATGG 1080
GCCAGGTGCT GTAGTTCACG CCTGTAATCC CAGCACTTTG GGAGGCCAAG GTGGGTGGAT 1140
CTCTTGAGGT CAGGAGTTCG AGACCAGCCT GGCCAACATG GTGAAACCCC GTCTCTACTA 1200
AAAATACAAA ATTAGCTGGG CATGGTGGCG AGCGCCTGTA AGCCCAGCTA CTTAGGAGGC 1260
TGAGGTAGGA GAATCGCTTG AACCCGGGAG GCAGGAGGTT GCAGTGAGCT GAGATCACGC 1320
CACTGCACTC CAGCCTGGGT GACAGAGCAA TTCCCCATCT CAAAAAGAAA AAAGGAAAGA 1380
AGAATGGAAG CCACCATAAA ATCAAGTCAC TGGAATTGAA TCTCCAACCT CATTCTGCCC 1440
TTGCTGTTTC TTTCTTCTCT TTGCTTTGGG TAGTAATTAT GAAGGACCAC AGATGAGATG 1500
ATTGGCCTTC AGACTTGTCT GTCTCTGACT TCTCTGGGTG GAATCTTGAG GCAGTGCAGC 1560
CTCATGGCAA GAACCTGGGC TTTGGACTAG ACAGGCCTAA GTTTGAATCT TGCCCTCACC 1620
ATTTTCAAGC TGTGTGGGCA AGAAACCTTT CCTCTTAGAA TGCTCAGTTT CCTGAAATGT 1680
AAAATAGGAA TAATAATGCC 1700
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