Tag | Content |
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EnhancerAtlas ID | HS091-09794 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr12:48750030-48751700 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr12:48750582-48750600 | CCTTCTTTCCTACCTTCT | - | 6.47 |
| | 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 |
GH12I048356 | chr12 | 48750261 | 48750510 |
| Enhancer Sequence | GATGGTAGCA TAGTGATCAT AGGCCATGGC AGAGAACAGA CAGGCTTCCG TTCCCCCAGA 60 GAGAGTGAAA AAGAAACTTG GTGAGGCAGC CCCACATTGA GATGCTTTTC TTCTGAGAGG 120 AAATTTTGTA GCATCCTGGG CACAGTAACT AGGAGTAGCT GAGATCCAGA AAGGACAGAT 180 GTCAAAGGAA GAAGTACATG GGTCTTTGAA GGTGAGAATC AGCCCTGATC TCCAGGATCA 240 TCACCAGCTT CCCCGTCAAA GTCAGGAGAT GAATCACCAG GATTAGCACA AAGAGCATGA 300 TCTGGATCTC TGCATCACTG GAAAATCCCA CAAGGACAAA CTCAGGACTA ATATTGACAT 360 TTATTATGGT TGCTTAGAGA TTCTGTCCCT CAAAAGAAAT GAATGGTTCT CTACTTGGCA 420 GGGCATTCAT CTGAGTCATT CTCACTGAAC AGGAGTTTTC TACTTACAGA CGAGTATACC 480 TCCTTACCTA TGGCCCAAAA TGGGAAACTC GGGATAAGGA AGTGTCATCT TAAGTACAAT 540 CTCCTCACTT GCCCTTCTTT CCTACCTTCT AGTACTGTCT CTGCATGATC TTGAAGGCTT 600 TACTCTGTAC CTCCATCACT GTTTAGTAAA TGTACCAAGT GCATATGAAT CAGGTAGGTC 660 CTGGAGTCAA AATGAGACAA ACTGCCCCAG TGGCAAAGCC TAGAAAATCT TCTCTGGATA 720 AGGGTTGGGA GGCCTATCGG AAAATGATTC CTTCTCAGAA TGGTAAGATC ATAGACTCAC 780 ACTATGTGAG GACATTTACA TAATATACTT TAATCCCTTC ATTTTACAAA TGAAGAGAAT 840 GCATTGCCTA TGGTCTCATA GCAAAGTGAG GACTAGGTTG GGACTAAAAC CAGTCAAGGT 900 TGGAACTAGA ACCAGGTGTT TCAGCTAGTC TTGTATGCAT CCAAGTGCAT CATACTTGGT 960 GATTTTGAAT TGTTAGAGCT GAGTCTTGTG TGGTTAGGGG ATCATGTGCA ACTTTGCTAG 1020 TAGGGAGTTC GCTTCTTAAA AATTTTTTTC TTTCAGCTCC CCACACATCT AAATATTTTG 1080 TAAGGAGATA CTTTGAAAGG GTAAGTCTGG CTCCATGAAT GTCCCATCTG TATAGCTGCA 1140 AAGTATCCTG ATTTAGAAGG GTCCTGAGCT CTGGCCCTGT TTACTTTTTT TTTTTTTTTT 1200 TTTAGACAGG GTCTCACCAT GTTGCCCAGG CTGGAGTGCA GTGGCACAAT CACAGCTCAC 1260 TGCAGCCTCG ACCTCCTGGG CTTGAGCGAT CTTGCTGCCT CAGCCTCCTG AGTAACTGGG 1320 ACTACATGAG TAGCTGGGAC TACAGGTATG TACCACCATG CCCAGATACT TTTTTTTAAT 1380 TTTTTTTTTT TTGTAGAAAC AGGGTCTTGC TATGTTGCCC ACGGTGGTCT GAATTCTTGG 1440 GCTTAAGCCA TCCACCTGCT TTGGACTCCC AAATTGCTGG ATTTACAGGC ATGAGCCACC 1500 ATGCCTGGCT TAGTAGGAAG TTCACTTAAA TTATAATATA TTCCAGTAAT CCTTGGCTCT 1560 GACACCCAGC CAATGGTCTC TATAGTTCTG TGTCAACTGC TACTGAAGTA AAAAGAGCAC 1620 TAGTCTTAGA GTAAGGGGCT TAGTTTGTCC TGGCCCACAC ATTCTAGTGG 1670
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