Tag | Content |
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EnhancerAtlas ID | HS098-14446 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:108976180-108978610 |
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) |
FOSL1 | MA0477.1 | chr12:108978441-108978452 | GATGAGTCACT | - | 6.02 | JUND | MA0491.1 | chr12:108978441-108978452 | GATGAGTCACT | - | 6.32 | ZNF263 | MA0528.1 | chr12:108977736-108977757 | TCCTCTTCCCCCTCCAGCTCT | - | 6.3 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_37622 | chr12:108975556-108979381 | HSMMtube |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I108582 | chr12 | 108975922 | 108978721 |
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Enhancer Sequence | TCACAGCCAC CCCCCGGGGG CAGGAGCAGA GGAGATATCC AATGCCTTTG ATGCCATGCA 60 TCCCCTCTGC TCCTCATTCG AGGGCCCAGC CTTGAAAAGG GCATAGCACT CCCTTCTCAA 120 CATTTATTGA GCACCTACTG GGTGCCTAGC TCCACACTGG ACTCTAAGCA CCAGGGCTCG 180 GAGGAGGAGC CACCCAATCT CACAAATCAG AACTGCCCGA GGGAGGCAGC GTGCTCTTTA 240 GAGCTTCCTG AGGGCAAGGG CAGCAGGGAT CATTGGAACC ACCCTTATTC CATCCTGGGC 300 CCTGGGCCAT GCACCCCACC AGCGTTTTCT CCTCGGGACC CCAACAGGGC AGGACCTGTG 360 GGTTCGCAGG TGAAGCCCTG AGGCTCCAAA AGGAGGCCGA AGCTGCTCCA CATCACAGCC 420 TGGATGTGGA ATTTGAAGGC TGGGATTTGA ACCCAAGTCT TCTGGGAGGT GAGTCAGACG 480 CCTTGCGCTC TTCCCCCACT GTGCCTGGAG AACGTTGCTA CCTAGGGTCC ATGCTGACAA 540 GTTTATATAG ATGGGAACAT AACAGAGAGA AGGCGGAAGT TCCAGGTCAC CCAGTCATTA 600 GCCCAGCTGG GTCCCCCTTC TCCTTCCACC CAGAAATAGC CCTGGCGCCT GCCCCAGACC 660 AGCCCTAGCC TCTGGGCTCC CCGACGCTTG TCACCAGTTA CATCTCCAGC CACACTGGCC 720 CAGACAACAT CTAAGCCCTG GTTGTGGTCG CCGCACCCCA GAGGAAGACA GGGAACAGCT 780 GAGGCATGAC CCCTCACCTC ACTGGGTGCA CAGCCCCCGC AGAGGCATGC ATGGATTGGA 840 GGGCCTTTTT GCCACCCAGA GGGTAAAGGG AACCTGTCTC TTCTCCAGCC ACATCCTTCG 900 CCCCTCCCTG GGGTTTGCAG GTCTTCCCTG GCTCCTGGCC CTGCTCTGGC CTCTCCAACA 960 CTTCCACTGC CCTGCCCCCT ATGAAAAGAT GTTAAGACTG TAAAGTTTCA AGCATCTGAG 1020 AATACTGATC TTATGATTCT GAAGCCTCTA AACTAGACCT GGAAAGAAAA GGTGACTCTA 1080 GAACAGCTGG ATGTTTAGAG ATAGAAGTTT CCCCCTTTCC CCTTCTGCGG GCATTGCACT 1140 TCACAGTTCA CAGCTAACCA CAGCTTACAT TCCCACAGGC AGCCCATTCC AAGCACTTTA 1200 ATAAATGAAC TCAACTCTCA CCCACACTCC AAGGTAGGTA CCACCATTAT TGCCATTTCA 1260 CAGATCAGGA AACGCAGGCC TACAGGAGTT AAGTGATTTA TCCAGGGGAG ATAGTAGAAC 1320 TAGGATTCCA GCCCAGGTCA TCTGAAACCT GCACCCCTAA CCACCATACA CACTTCTGGG 1380 AACATTTGTA AAGTGCATCC ATATTTCTTA GCCTCACTGT ATTCTGGGGG AAGAGGAGAG 1440 GCAGGGCAGG GGCTGTGGCC CCAGTGCCCT TCTACCTCCC TCTGCCCTTT GCTGTCTGTA 1500 ATCTTTGACC CCTATGACCC CTGAAGGGGG AAGAAGAAGG ATGCAGTCCC CATCCCTCCT 1560 CTTCCCCCTC CAGCTCTGCC AGTTGGGCCT GACTGCCCAT ACTCTAAGGG AGAGGCTGCA 1620 GGTGGTCACC CCCAAGCCTG GACTCTCCAG CCTTCCAGGG CACCCCAGGT GTCACTACAG 1680 GGCCCCAGTG GGTGGTAGAC ATCGCAGGGG CCTCAGTGGC CAGAGTGGAT TTACCAGCAG 1740 GGCTGTTATT TGCTTTGCAG CTGCCACCAT AAACCCTGGA CGCCCCTGGG GAGAGGGAGC 1800 AGCTGCCGGG AAACCTCCCG GGCCCTGGAG CCGTCACCAA ATCCCTGCTG CTATTTCTGA 1860 GCAGCCAAAG GAATCCTGAA ATTAAAACCT TCTGAAAAAA ATGGCAATTC CCCGTCCCAC 1920 TCCAGACAGA TGAAGATACT TCTCCCAAAA TAGATGAAGA ACCAAGGAGG AAACAGCGCA 1980 GAGCTGGACA CAGCTCAAGA CTTCCCACAA GAGACCTGAT TCCTGCCCAG CTCTGCCCCA 2040 CCCAAGCCCC TGTCTGGTCC TCACCTGCCC GACTATAAAA TAAAGGGCTG GGATCCTCAA 2100 CTTTAGTACA TCAGAATCAC CTGCAGAGCT GAAACAGCAC TCAGGGGTCC CAGGTGATGC 2160 TGATGTCCTC TGAACCTTAG AAGTTTCCCT AAAGTCACTT TCAGCTCACA CATCCCCACT 2220 CTTTAAGGTT TGACACTCCA ACTACTGGCT GTGTGATGTT GGATGAGTCA CTTGACCCCT 2280 CTGAGTCTCC ATTCTTCTCA TCTGTATAAT GGAGAGAAAG AATGATCACC TCCTCTTGAA 2340 GGTTGTGAGG AAAAAATCAA ATAACATTAG TAGTTCATAG CAACTTTGTA ATATCCCAAA 2400 ACTGGAAACC ATCCAAATGT CCATTAGCAG 2430
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