Tag | Content |
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EnhancerAtlas ID | HS138-03772 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:227616580-227618130 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Sox3 | MA0514.1 | chr1:227616788-227616798 | AAAACAAAGG | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_38470 | chr1:227615017-227620880 | HUVEC |
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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 |
GH01I227427 | chr1 | 227615288 | 227618816 |
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Enhancer Sequence | TGCTTTCCTC CCTTCTTCTA TTTCTGTGCG ATTTTCCCAT GGCATCCAGC CAGAGCATCT 60 ACACCAGTAA TGTCTAGAGG ATTTATGAGG CCAAGCGATC CTTTGGGTTT CTACGCAGAC 120 CTAAACAGGA AACCCACACA AGGAAATGCC CTTTCTGTTT GCAGGCCAAA TTCCCAGGAT 180 GCCTTCGCCA GAGTGCCCTG GCTGGAACAA AACAAAGGCC TGGCACAATA AATGCCCTTA 240 GCTCCAAAGG CAGAGGTGCC CTCCCCACCT CTCCCCACCT CTCCCCATCC CCTCCCTAGT 300 CCAGGAGGCC CTCTATTAGT TTAATGAGAA TGAAACTTCC TTCTCTCAGA ACTCAGCTTC 360 ACTTAATCCA ACTGGTTGAG ATGCTGGAGG GGGTCCCCCT GGATCTCCAG GTGGATTTCA 420 GGGTATTACT TCTCCTTACC TGTGCAAAGT CAACCTGGGC AAGTCCTCCA GGTTAATTAA 480 CCAGACACCC TACTCACACC CCTCTTATTC TTTCTCCATG TTTAGCCCCT AGAAGATGCC 540 TTAGAGATGA AAAAAAAAAC ACACGCATTT CCTAATGAAG AGGCAGCCAG ATGCAGCCTC 600 TGAGCCCTGA CTGCACAGTG TGACAGTCAC TCAACCCAAC ACAGCTCTCT TGCCTTTGCT 660 GCAACCTCAA CACCCTGCGT CCTGCCAAAT CTCTTCCCAT TTCATCAGTC CATCTATGCT 720 GGTGTCCAGC CATTCCAGCC CACCATGGCA TTTAAAAATC TTTCCAGCTC TCTGTGGAAG 780 ATCTGAGACT TGAGAAAGAG ACTGTTGCTC AGGGCTGGAC AGGAAGGAAG TATGCATTCC 840 TGGCTCCCAG AACAGAACAG CAATGTGGGT GACCCTTCGT CCCCTCCCCA AGGCGTCCCC 900 TTGGGCCGAC ACAAAAATAG ATTCTATCCT CCTTGGTTCG TCTCCACCTC CCTCGGGAAA 960 GAAGACACAG GCTTCGAGTG AGTCAACAGT ATTATCGGGG CTTGACTGTC TTTCAGGAAT 1020 GACCAGATGT TGGGAAGAGG ATAATGTGCC ATTTCCTTTA ACAAATAGTC CGGGCATCTG 1080 TGCATTTCCT TTTGAGCCAG CTCTTCAGGA GACTGTGCTG CTGTGACAGG GAAGGACGAA 1140 TCACCCTGGT TTCTACTCTC ACGGATACTA GGGGGCTCCT TGAACCCTTT GGATTCCAGC 1200 CCTCCATTAA GAAAATATTT CTGTCCTTTG TATGCATGAG TGACACCACG AGAAGACAGC 1260 ATAGGGAGTG GTTACAAGCA AAGAATTTAG AGACAAAATA AATGCTCTAA GGGAAAAAGA 1320 CAAGTAGCCA AGGAACGCTG GGAGAGGGCT TGGAGGAAGC AAATTGTTCA TCCATTCCCC 1380 CAAATCAGTG GTTCTCAGTA GAAAACCAAC ATGAGTAACA TTTGCCTGGG AACTTGTCTA 1440 CCACCCCAGC CCTACTGAAA CTCCAGGGGT GAAGCCCAGC AATCTCCTTT GACAAGCCTT 1500 CCAGGAGATT CTGATGTGAG CTCAAGATTG AGAACTACTG ATCCAGATAG 1550
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