Tag | Content |
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EnhancerAtlas ID | HS091-18893 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:7943300-7945680 |
Target genes | Number: 29 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr17:7944865-7944884 | GGCCACCACCTGGTGGCAG | - | 6.35 | EWSR1-FLI1 | MA0149.1 | chr17:7943875-7943893 | AAAAGGAAGGAAGGAAAA | + | 6.4 | IRF1 | MA0050.2 | chr17:7943968-7943989 | GAAAAGAAAGAGAAAGAAACT | - | 6.9 | NFYA | MA0060.3 | chr17:7945429-7945440 | TCTGATTGGCC | - | 6.02 | NFYB | MA0502.1 | chr17:7945430-7945445 | CTGATTGGCCCAGCT | - | 6.42 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 7945234 | 7945331 | chr17 | 7943993 | 7945198 |
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Enhancer Sequence | AGTGAGGAGG GGGTTACTGA TGGGGGAGGG TGTGCCCAAA CGATGAGGGG CAGCTTGAGT 60 GTCCTGGTCA TGACAGAGAT TAAAAGCCCC TGCCTCCACC TCTCCTATCA AAGCTGCTCC 120 TGGGATCAGC AGCGTCTACA GGAACGTATT AGAAATGCAA ATTCTCAGGC CACCTCCAAC 180 CTACTACGAC ACTGAGGGTG TAGAGTGGGA ATTTTTGTTT TGACAAGCCT TCCAGATGAC 240 TCTGGTGGCC ACTGATGTTT GAAAAACACT GCTCTAGGGC CAGGTGCCGT GGTGGCTCAC 300 ACCTGTAATC TCAGCACTTT GGGAGGCTGA GGGAGGCGGA TCACTGGAGG TCGGGAGTTC 360 GAGACCAGCC TGGCCAACAG GGCGAAACCC CATCTCTACT AAAAATACAA AAATCAGCTG 420 GGTAGGGTGG CGGGCACCTG TATTCTCAGC TACATGGGAG GCTGAGGCAG AAGAATAGCT 480 TGAACCCGGG TGGTGGAGGT TGCAGTGAGC CGATCACGCC ATTGCACTCC AGCATGGGGG 540 ACAGAGCAAA ACTCCATCTC AAAAAAAGAA AAAAAAAAAG GAAGGAAGGA AAAGGAAGGA 600 AAGAGAGAAA GAAAGAGAGA GAAAGAAAGA AAGAAAGAAA GAAAGAAAGA AAGAAAGAAA 660 GAAAGAAAGA AAAGAAAGAG AAAGAAACTG CTTTAAATGC CTTACCTTTG CTGGTGTCTT 720 CCTTGCCCTG GGACTTTTTC ATGCATCGGC TTGTTGTGTC CTCCCAGAAA TCTGAGTAGA 780 GCCAGAAACA CGCCCTTCAA GCCCCAGGAA ACTCACCCTC CAGGGCTAGC AAGGGGTGAG 840 ATGGGGGCTC TCTCTGTGCT CTGGGCTCAG CATTGGAGAT CACAGGGGAA AACTGGGACT 900 TGGAGATAAC AGAGGAGTTG GGGCCGCTAG TGAGGATTCC CTTGGCACAA AGCCAGGAAC 960 TGCATTCAGA AACAGATTTT CAAAAGATCT TGATCCGGCC AACTCATCTG CTATCTAAAG 1020 CCTGGGCTGC AGGCTTTTGC TCCTGGTCTG TGGGATCAGA GCAGCCACAG GCTCATTTGG 1080 TTCCTGGTGA TTCTCCATGT GTCATGAATT CCACCCCTAA GGAAACCATT GCACCAAATC 1140 TGGCAGCAAC AGCCCCAAGA GAGGGAATAG ACATTGAGAT CTACTGTGTC CATGGAGACC 1200 CAGAGTCAGC CTAGGCCCTG CCAAAACGAG CTGTGAGATC TTAGACCAAT TTTTTCATCT 1260 CTTCAATTCT TATTTTCTTC TGTAAAAGAA ACTAAGAATA CCAATCTCGT TTGGGTTAGG 1320 AGGAACAAAT GAGAAAATGG TTAAGAATGT AGGTGGTCAG CTGCTAAGTC TTGCACAACT 1380 GTGTGCTCTT GCTGTTGTTC CTGTCTTTCA GTTCACTCTG TTCCAACACT CTAGGCTCTT 1440 ATAAAACGTA CAGTGAGGTC TCAGATCCAT TGCAACAGCA TTGCCTGGGA GCTTGTTAGA 1500 AATCAGAATC TGCATTTAAC CAAGATCTCT ATGTGAGAGG GATTCAAGTC TGAGAGGAAG 1560 GGTTTGGCCA CCACCTGGTG GCAGTGTACT TTAATTGCAA ATTTTTCTTT GAAGTTGAAA 1620 GCTCAAACCC AAAAGCAAGT TTTGAATGAA TCAAAGAATG AATGAGTGAG AGCATGACTG 1680 GCTAGGGGTC ATCAAGTTTG CAGATACATG AATTTACCAT TTCCCTGGAA GGTCTTTGGC 1740 TGTGTTGCTT GTTTGAGAAT AGAATTTAGA GATGCCTCGG GCGGCTCCCC CTAAACTATG 1800 AAGGCTGAAG TGCCTCTCTA TGGGACACCT ACCAAAGGCA ACTGAAACCT TCTGCGCAGC 1860 CCCTGTCCCA GGATAGTCTC GCCTCTACAA GATGCGTCTG TGTTAGTCGG GACTTCTATA 1920 GTTGCAAGAA CAAAAGCTAA CTCCAACTAG CAGGCAGAAA AAAAGTTTGT CGGCCAGACA 1980 CAGAGGCACT TACAGAAACA CAGGCAGGAA TTGTCCACCC AGTGGAAAAT GGCCATAACT 2040 AACAGTCTGT GTTTACTGCT ATAATCTACA TATCCAGAGA GAGACCACCT CTCTGGCTCA 2100 GCCCCAATGG CAAATTCCCT GGAAAGGACT CTGATTGGCC CAGCTCTAGT CAGGTGCTCA 2160 ACTCTGGACC AATCACCCTT GACCAGGGGA GCCATCTCAC TGTGGGAAAA TGGCAGCTCC 2220 CTTGCAGCCT CCTTGGGTAG AATGGAAGGG CAGCTCCCAG GAGGGCCCTC TTGGCTGAAG 2280 GGGTCTGGCT GTGACCAGGC CCCCCAAGGG GACTGCCACT CCATCTGCCC TAGCAAAGAG 2340 TCTCCCTGAG GCCTCTTGCT GACCACCTTC CCTCTCTACC 2380
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