Tag | Content |
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EnhancerAtlas ID | HS030-10617 | Organism | Homo sapiens | Tissue/cell | CyT49 | Coordinate | chr20:36008380-36009860 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr20:36009245-36009266 | ATTTTCTTTTATTTTTTCTTT | + | 6.16 | ZEB1 | MA0103.3 | chr20:36008717-36008728 | CCCACCTGCCC | + | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAAGAAAAAG ACCGAGAGAG CTTGGAGTGG CCTGAGAAGA TGCTCTGAAC ACACTAACAC 60 ATAAAGTGAA AAGAGGGAGG CGGCAGTGTA GAATCTCCTC TGGGTATCTC AGGGCCTCAG 120 TTTCCTCATC TGGAAAGTGG GGGCCACAGT GCTACCCGCA TGACCCTCAG TGGGCCATTC 180 TTGCTCAAGG ACGTTCTGCT CGGAGCTTTC TCAGGCTTTC TCTGGGAGTG GGGTGGGCTG 240 CTTTATCCTC TCACCCCTCT TCCAAGGCCA TCTGGCTGCT TTGTGAGAGA GATCCCTGGG 300 GGTAGGAGGT GGGGCCTGTG AGTTTCAGCC CCTGATTCCC ACCTGCCCAG TGTGGTGGCC 360 CCTTTTCACT CTCACCCATG CTGTGTGACT TCAGGCAAGT TCTTCAACCT CTCTGTGTCT 420 TAATGTCCTC AACAGTAAGA TAAAGACATG ATTAGTATTT ACCTCCTAGA TTATCATGAG 480 GAGCCGATGA GTCAATGTTT GCAAAGTACT TAGAGCAAGG TCCAATTCAA GGTCTGAGCT 540 CTGGGAGTAT TTGAATACCA CGGAATGATA TTTAGTCTTT TCAGTGTGGC ATTGCAGGAA 600 CAAAGTAGGA TGCAAATTAT ACATCCATGC CCATTTAGTC TTTTGTCTAT TCTGCAAATA 660 GTTCCAGAGC ACCTAGTGGG TGTCAGGCCC GTCCTGGTCT CTGGGGGCAT GGAGATGGAT 720 CCTGCCTGGC CCTGACAGCC GCGAGTGCAC AGTGGAGGGC ACTGGGTGGA CCCCAGTTTG 780 TTGACCGTCT TGCGTTGCTG TGACGCTGGA AGGAAACGCA CCACCACACC CAGGTGTTTG 840 TCTTCTAGGG GCAGAATTAT GGGGCATTTT CTTTTATTTT TTCTTTTCTT TTTTTTTAAT 900 CTTCTTGTAG TTCTCAAAGA GTCCACTCTG AATGATAAAA GTTACCATTT ACGGAGGCCT 960 GGTAACGTTC CGTGCCATCC TGAGCATGTT CCGTGTACTT TTCTCACGGA TTCTCCCAGC 1020 AGTCCTGACA CGGGTGTTAT TCCCGATCGA TAGAGAGGAA AACTGAGGCG AAGGGCGGCC 1080 GGCCAGGATT CAAACCAGGG AGTCTGCTCC AGCACTCCGG CTCTTAACCT CAACCGTCTG 1140 CCTCTCCACA AACACCAGGA TCAACCACCA AGACCAAAAA AACAGTCTCA CAAACCATCA 1200 AACATTGCAC TTGGTGGCTC AGGACCTTAG CTTCGTCTTA AAGGTCCCTG TTATGCTTTT 1260 TCTGAGTGCC CCAGTGTGGA GTGGTCTTCG TGTTTGTGAG TGCAGGGGTC AGGGGTTGTG 1320 TCTTTTCTTC TTGTCCCCTT CCAAGAGGTG ACATGTATCC TTGATACTGG AAGGGCCCTT 1380 AAGGTCTAGC CCTGGCTCTC TGTCTCCCTT CATGGCACAT CAGCCAAGTA CCCATTCTCC 1440 CGTCTTTGAT TACCTCCAGT GACAGGGAGC TCACTCCTCA 1480
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