Tag | Content |
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EnhancerAtlas ID | HS138-01033 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:53976550-53979260 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr1:53976947-53976962 | TGACCTCGTGACCCT | - | 6.36 | SREBF1 | MA0595.1 | chr1:53977346-53977356 | GTGGGGTGAT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33491 | chr1:53977320-53979867 | H2171 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I053511 | chr1 | 53977561 | 53978453 |
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Enhancer Sequence | ACAGAGCCTG AGGGGGATGC AGGCTCTAGA CTGTGCACTC TGGAAACTCA TGTTCTGAAA 60 CAAGACTGCA GTGGCTGAGA GCAGCACAGG TGCCCTGAGC CCAGCCCAGC CCGAGGGCCC 120 ACTACCTGGA CCACAGGATG CTGCAGGCCA GGTTCCCTTC TCATGCTACC TTCCTAAGCC 180 CCTGGGCCCC GTTCACAGGG GCTAAAATGA CTTTGGGATC AATGGCTTGG GGGCTCTGGG 240 GACAAGGCTG AAGGCTCCCA GCCTGTAAAG CATTTATGTA CATGGCAGAA AGAGGGAGAT 300 AGTGAGAGCT CGGAGTCCCC ATTTTCTTGT CTGGATTTGT GGCTTGTTGG ACCATCCACA 360 TTAAAATATA CAGCGAATTC AATGTCACAG CTCCAGGTGA CCTCGTGACC CTTGCCCACC 420 CTCTGAGACA CCAAGTATTG ACAAACAGAT CAGTGCCTCT CTGAAGGAAG CAGGGCTATC 480 TGGAAATGGG GAAAGCAGAT TTGGAGAGAG GCTGGGGTCT CCGCATCTGT GCTGTGCCAA 540 GTTCCTCTCT GCTCCCTCCA ACGTTGGCAG CCCCTCCACT GCCCCTCCAG TCTGCTGTCA 600 TCATCCACAC GTGTGGGGCC CCCGTCACTG TGAGCTCGCT GAGGACAGGG GAAGCAGGGC 660 CTCGGTGCTG GGTCCCTGGC CCGGCCACTG ATACACTGTG GGTCCCTGTC ACTGTTTTAA 720 GTTCATGAGA CGAATCCTCA TCACACCTCC AGGAATAAAT TATCATTATC ATCATCATTA 780 TTTTTAGGCC TGTCTTGTGG GGTGATCAAG TGGGACAGCG TCTTCCTCTA TGCACTAGAA 840 ACCGTGGACA GCTGTGCACG AGCTGTGTGT TCTCATGACC AGTTCTGGCT GAAGCTGGGC 900 TGGGGCCTGG CCGGAGAGTG GCTCCTCCTT CCTGCAGGCC TGCTGTGTGG TGGCTGCCTT 960 ATCCCCATCC CATCTGGGCA CCCACAACCC AGCCCTCCCC TGGTTTCCTG AAGCCCCTGT 1020 AGGGAGGGCC AGGTCTTGGC CCTTCTCGGT CACCCGGTGC CCAGCGCTGG GCATGGCACA 1080 CAGTGAAAAA CCAATGACAC TAATAAATGA GTTTCTGAAT CTCTCAGTTG CAAATCCCAG 1140 AGATTAACAG CATTGCAGGA TTAAGATGAA CCAGATATGA AGGGGAAAAA ACATGTGTTT 1200 TCAAAAGTTT GTTTTTCCTG TCTCACTCCA CCATAAATTC ACATTTGCCA CCTTCACAGC 1260 TGGTGAAATT AAACAGAACA CAACTCTCTC CACAGCAGAC ATGACGCCTG AGGCTATGCT 1320 GCTCTACCTG AACCCTTTAA AAGGCAAAAA AGATCTTCTG GAGCTCCTCC TCTGAGTCAT 1380 GCAAATGATT CCTAAATCAA ATATTTTTGC TTCAACTGGA ACCTATAAAA ATTAATATAA 1440 AACCTCACTA GCCTGGCAGA CTGAGGGCTT CATACCTCGC ACAAGGCTGG GAAAAAAAAT 1500 ACCCTATTCG GCGTCTTCTC TGAGCCAGGG TAAATAAATT TGGTCATGAA GTCAGGCCCT 1560 CTTAGCATAT TTTTGAGTGA ATCAGATAAT TCTGTCAAGC TATTTAAACG TCCCAGCAAA 1620 CCACTGGGGA GCCACGAGTG GCCGTTCCTT GTTGACTTTG GCAGGAAGTG GAGGCTGAAG 1680 GCCCTTTCCC CACTCTCTTC TCAGGGGATG AAAAAAGAAA CCCATTCACG CTGGGCCTGG 1740 GCCTGGTGTC AGGCACGAGG ACGCTTCTCT CCTGCAGCTG GACCCGAGGC TCCTACCCGC 1800 AGGCAGGGGT GGGCAGGCGG GGGTCCCGTC TTGTCATCAC TCTGCTTCTC ACTGCAGAAT 1860 TCTTGACGGG CACTTATGCA GGCGGCAGGC AGGTGATGAA TGAGGCGGAG CAGAGTGCAC 1920 GGGCCCAAGC AGCGAACGGC CTTCGTGGTT TATTTTCCTT TGGTTGGAGA TGTTTTTCGG 1980 CTGGTTGGTG GGTGAGCAGG TGGCCTGAGC AGCTATGGGT GGGGGCGGGG ACCATCGTAG 2040 TAGAGCCTGT GCCAGGTGAG GCACACAGTG TCAGGCGTGT GTACGGCCCT CACCACCTTC 2100 CTCAGGGAGG GCCTTATAAT GCCTTTCACA GAAGCAGCAG CTGAGGCTCA AGGAGGGCCC 2160 GGTTTTCTGG GTCCCCCTTT GCACCCCCTT CAGGCTGCCT CTTCATGGTT CTCTGCTCAC 2220 ACTCACAGCC ACAATCTTCC CCTGCCTGTC AGCAGCCCCT CTGGACCCCC AGCTCATCCC 2280 TGAGGCCTCC TCCTCTCCCT GCCCAGCTCG GATTTCCTAC TCCCGCTGCC TCCAGTGCCA 2340 CCACTGCCTT CCGGGCTCCC CCTCCCCAGC CTGAACCAGG CCCTGGCTTG GGATGCTGTC 2400 TGTCCAGCGC CCCACAGTCC ACCCCACCCC TGCAATGCCG CCCTGCGTCC TCATCCCCAA 2460 ACCTGACCAC ATCACTGCTC AACACTCTTC AGGTCGAGTC TCATCCCAGG CCTTGGGATC 2520 TGGACCTGGC GACATCGCTC CCAAGTTCGT CACCCCACAC AATGACTCAT GTTTCCCAGA 2580 ACACCCCAAG CTCTCACCAT GCCTACCTTC ACTCTTGCTA CTCCTTCCTC CCAGCTTCTC 2640 CACTCATCCA ACTCCAGCCT CACCTCCTCC AGGAAGCCTT CCCTGACACC CTCCTGGCAG 2700 CCACACCCCA 2710
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