Tag | Content |
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EnhancerAtlas ID | HS129-00694 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:28201120-28202260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr1:28202191-28202204 | TAATTAATTAATT | + | 6.78 | Lhx3 | MA0135.1 | chr1:28202192-28202205 | AATTAATTAATTT | - | 6.92 | POU6F1 | MA0628.1 | chr1:28202193-28202203 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr1:28202193-28202203 | ATTAATTAAT | - | 6.02 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_09233 | chr1:28198278-28207102 | CD14 | SE_20343 | chr1:28199013-28203940 | CD56 | SE_50884 | chr1:28199013-28201650 | Sigmoid_Colon | SE_50884 | chr1:28201667-28202339 | Sigmoid_Colon | SE_53500 | chr1:28198475-28202256 | Spleen | SE_62491 | chr1:28184415-28220281 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 28201800 | 28202156 | chr1 | 28201378 | 28202229 | chr1 | 28201272 | 28202191 |
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Enhancer Sequence | TGTCTCTACA CAAAATAAAA AAATTAGTCA GGTGTGATGG TGCATGCCTG TAGTCTCAGC 60 AACTCAGGAG GCTGAGGTGG GAGGATTGCT TGAGCCTGGG AGGTTGAGGT TGCAGTGAGC 120 TATGATTGCA CCACTGCACT CCAGTCTGGG CGACAGTGAG ACTCTGTCTC GAAAAAAAGG 180 ACGAGGTCTG TGTTGCCCAG GCTGGTCTTG AATTCCTGTC CTCAAGCAGT CCTCCCACTT 240 TAGCCTCCCA AAGTGTTGGG ATTACAAGCG TGAGCCACCG CACCCAGCCA TAACTTCCAG 300 TTCTGCCTCC TATTACCTGA TCATCATGTA CAACCTACTC AGCCCCTGAG AGGCTGTTTC 360 TTTTTCTTCT TCTTCTTTTT TTTTTTTGAG ATGGAGTCTC CCTCTGTCAC CCAGGCTGGA 420 GTGCAGTAGC CTGATTTCAG CTCACTGCAA CCTCCACCTC CTGGGTTCAA GCAATTCTCC 480 TGCCTCAGCC TCCTGAGTAG CTGGGATTAC AGGTGCCAAC CTCCACACTG GGCTAATTTT 540 TGTATTTTTA GTAGAGACGG GGTTTCACCA TGTTGGCCAG GCTGATCTCG AACTCCTGAT 600 CTCAGGTGAT CCCCCTGTCT TGGCCTCCCA AAGTGCTGGG ATTACAGGCA TGAGCCACCA 660 TTCCTGGCCA GCTGTTTCAT TATTTAGGAA ATTGAAACTG CCTGTCTCCG CAAGAGCAGT 720 CATGGGTCTT AAACACAATG ACGCATCAGT AGCCCTTGGC ACAGTGCCGG GTATCTGTAG 780 TACCACAGCT GCTGTTCTCA CCAGTCTGGA AGGCCCATGC TCTGACATTG TAAACAGACT 840 GTGGTTTATG ACTGGTGGGC ATTTTCCTGG CAGTACGTGG GGAGGTTTTC ATCAGTTTCT 900 CAGGGCTGAT GTTGGAGCTG CCCTGTGGGT GGGGCTGGGT TCAGGTGGCC TCAAGGTCCT 960 GCCACGTAGT CTGTTGTCCT CCATTAGCTG GATGGAGAGA CTGTGCACTC GTGTGTGCGT 1020 GAGAGATCTT TATTGAGCAA CTTCTGTGTT CTCGACACCA CTTACACACT TTAATTAATT 1080 AATTTATTTT TATTTATTAT TTTTTTTTTG AGACGGAGTC TCACTCTGTC ACCCAGGCTG 1140
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