Tag | Content |
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EnhancerAtlas ID | HS129-36102 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr8:121081410-121082890 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr8:121082868-121082879 | GTCTTTGTTTT | - | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_13897 | chr8:121074520-121082923 | CD34_Primary_RO01536 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I120066 | chr8 | 121079019 | 121083585 |
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Enhancer Sequence | GGGCACCTTG GGCTTTCATT GAGGAGTTGG GGAACAGAAA GGAAAGCAAG GACTCCATAG 60 AAAAACTTTA CGAAAGAGGG CAGCTAGAGG CAGACTTCCC TTCCAACCAA GATTGGCTAG 120 GCTCCCAGTT CTACCTGCCC CGGCTCCTGT TTCAGCTCCA TTGTTGGAAA GTACAACTGT 180 GATGGTTAAT ACTGAGTGTC AACTTGATTG GATTGAAGGA TGTAAAGTAT TAATCCTGGG 240 TGTGTCTGCA AGGGTGTTGC CAAAGGAGAT TAACATTTGA GTCAGTGGGC TGGGAGAGGC 300 AGACCCCCCT TAATCTGGAT GGGCACCATC CAGATCAGCT GCCAGCGAAT ATGAAGCAGG 360 CAGAAAAATG TGAAAAGGTT AGACTGGCCT AGCCTCCCAG GCTACATCTT TCTCCCATGC 420 TGCATGCTTC CTGCCCTGAA ATATCGAACT CCAAATTTCT TCAGTTTTGG ACTCGAACTA 480 GCTCTCCTTG CTCCTCAGCC TGCAGATGGC CTATTGTGGG ACCTTATGAT TGTGTTTCTG 540 AGTTAATACT TAATAATCTC TCCCTTATAT ATGTGTGTGT GTGTGTGTAT ATACACACTA 600 TATATTCTGT TCCTCTAGAG AACCCTAATT CAACAACCGT TTATGATGAA ACTTGGAACA 660 AAGAGAGGCG CTACTTTTTG CCACCGTGAT AGGATCCTCT CTACCTTGCA GAAGAGTTCT 720 TGGTGGCTAA AACTCAACAA GAATCTGCTT GTCCCCAGCC CAGACTTTCT CTGGGAGAAA 780 AGGAATGGAT AAACGTATGG AAGATTGATT GAGTGACTGT GGGCTCCCAC CCAAAGAGAT 840 GATTCAGTCC AGTGGCAGGG AGAAGAGTGA GACCCAGTGG AACGTGATTT CGCAATGGGC 900 CCGTTGCCAC GACAGGGAAC ACACTGTTTA CTAAAGAGAG CTCTTCAACC TCTCAGTCAT 960 CTTTGCCTTC CAGAAAACTG CAGCCTCAAC TCTAGTAAGT AATCCACCGG CTCAGCCCAA 1020 GCCCTGTTGG AGCGGATAGG GCTATCCTTG CCACAGTACT GAACAGCAGG AATGTTGCTC 1080 GCAAAGCCTG CCCTTTGGAA GTAGCCAGCA AGGCTGAAAG TGCTCAACCA CTCTTTGGAA 1140 TGCCACATTG TATATGGGAA GTTCCATAAT GCGCTACTAA TAAGTAAAGT TTCTCTTGCT 1200 GGGTTGTAAG TATCTGGGCA AGTCACAGGA AATTCTTCTT GGAACTAAGC AATATGGGAA 1260 TAAACACACG TATTAACATC TGCTCATGAT AACTAGCTAA TGAAATAGCC CACTTTGGCC 1320 CAGAGTTCGG GATAATGAAA CAAATGACTG GTGGTTAATA AATCGCTTCA GTGCCGGTAT 1380 ATGTTCACTG TACATCTTGT GTGTCCCGTG TGTTCATTTG TTCTTTCAAT TGATTCTTCT 1440 TTCATTGTCC AAGACACAGT CTTTGTTTTT AAACTTTTTA 1480
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