Tag | Content |
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EnhancerAtlas ID | HS176-29665 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr4:114961480-114962980 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr4:114962454-114962465 | TGCTGAGATTT | - | 6.32 | IRF1 | MA0050.2 | chr4:114961710-114961731 | AACTGGAAAGTGAAACTAATA | - | 7.39 | IRF2 | MA0051.1 | chr4:114961714-114961732 | GGAAAGTGAAACTAATAA | + | 7.99 | Myog | MA0500.1 | chr4:114962508-114962519 | CTGCAGCTGTT | - | 6.02 | RUNX1 | MA0002.2 | chr4:114961944-114961955 | AAACCACAGAG | - | 6.14 | Tcf12 | MA0521.1 | chr4:114962508-114962519 | CTGCAGCTGTT | - | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 114961793 | 114962552 | chr4 | 114962639 | 114962757 |
| Enhancer Sequence | GTAACTTTTT TCTATCATAA TTTCACAGAA CTTGAGAAAC ATTGGGCCTC AAAGAGATCA 60 GCCTGGTAAC AATAACAGTA TTTTGCAGAT GTGGCGGTTG AGGGCTAACA AAATTGAGGG 120 AGCTGACCAA AGTCACTCAG TAGCAAAGCC AGAAGTAGAA ACCCTGTCTT CCAGTTGACA 180 GCTTAGCAGC ATAAAATATG CAAACTTTAT TTTTGATTTT CAGTTTTTTA AACTGGAAAG 240 TGAAACTAAT AATCATAATT TACAGTGTTG CTTTGAGTGG AAGCCATGTA AAGAGGCTAG 300 GTCCTTTTCT GGAAAGTAAT AGGTCATCCA AAACATAGAT CCCTTTCTTT CCTTCCTCAC 360 TTATCTCTAG CATCTGTAAC CACACATGGT AAAAACCACT CTGTTCAGCC TGGGAGGCCA 420 CCCTGAAACA GAAACTTCAG CCCTGGGTGA AAAGCCTCTA TCAGAAACCA CAGAGGTTAG 480 GAGGGAAGGT GGGAAAGCAC AAATACCTAA GCTCAGAAAA GAAGGCGAAA ATGTTAACAG 540 TTGGCCTTCT GTCCAGAGAG GCAATGGAGT GGACAGTGTA CAGCCAAATC CCCAAATCAG 600 GCAGCTATTA ATATATGAGC TAGACATCCC ACAAGTCACA CTTAGGACTG GGGCACTGTT 660 CTGGTTTGTC TTAGGGATCT GGATCTCTGG ATTATGAGTA GAGCAGAGCT GATGAGGTGA 720 GTGACAAATA CTGAAAGGGA ATTCATATGT AAGCACATTA AGGAGAGAAA CGAGAGGCAG 780 AGGCTAAGAT CAAGATCAGA GATCAATTTT GCCCCGATGT TTGTTTCTTA AATGCCAACT 840 AAAATAATTT TGGAATTTAA TTTATTGCCT CTTTGTTTAT GCATGAATTC TTTATGTAGA 900 TGTCAGGTAA TAGTGTAACA TCTTAGCAAT TTGTGAACAT ATGGAAACCA ATGACTCTGT 960 GTTCTTGGAA TCTCTGCTGA GATTTTTATC TTGTAGCATG GACAAAGATC CCAATCAATG 1020 GGCATTGCCT GCAGCTGTTA CATGCATGTA ACAATCTACT TTTATTCAAG CGTACTGGAA 1080 TCATTTGTCC ACTGACTTCC TTTGAAGAGT GAAATGAAAT AATAAGTTAT AGTTAATGTT 1140 TCTGTTATTA AAAACTCTGC CTTTTAATGT ATTAACTTTT TTTTCTTATT AAAGTGCTTA 1200 TTAAGTAATA ATCTCTTTGG CCTGGCTTAC ATGGTCAGAT TGTCTGATAT TATGAGCTTT 1260 GGTCACTTTC GAATTCCACA AATAAATACC ATAACATTTT TGTACAATAT CACTTAATAA 1320 ATCAAAATAA CTTAAAATCT AGCCAATTAT TGTTACTGTT TTTTTCCTTC TTAACACATG 1380 TGTGTTTTAT CAAATCTCAA ATCCTGTTAT AGATAAAGAA TGCTGGTCGG GCATGGTGGC 1440 TCACGCCTGT AATCCCAGCA CTTTGGGAAG CTGAGGTGGG CAGATCACCT GAAGTCAGGA 1500
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