Tag | Content |
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EnhancerAtlas ID | HS098-16524 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr13:106642660-106644860 |
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) |
MSC | MA0665.1 | chr13:106644268-106644278 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr13:106644268-106644278 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr13:106644268-106644278 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr13:106644268-106644278 | AACAGCTGTT | - | 6.02 | Myog | MA0500.1 | chr13:106643662-106643673 | CTGCAGCTGTT | - | 6.02 | NEUROD2 | MA0668.1 | chr13:106643391-106643401 | ACCATATGGC | - | 6.02 | NFIC | MA0161.2 | chr13:106644247-106644258 | TCTGCCAAGAA | - | 6.02 | RORA(var.2) | MA0072.1 | chr13:106642969-106642983 | TTGACCTAAATTAA | - | 6.01 | Tcf12 | MA0521.1 | chr13:106643662-106643673 | CTGCAGCTGTT | - | 6.62 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_34149 | chr13:106642640-106645099 | HCC1954 | SE_36583 | chr13:106641912-106645243 | HMEC |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I105989 | chr13 | 106642150 | 106644938 |
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Enhancer Sequence | ATTGGTGATT TCCAAAATCT CGACTGCCTT AAGTATCATT TCTGTTATTC TACTAGAAAC 60 ATCCGGCTCA GGGATTCTCC ACCTTAACCC TATTGACATT TTGGGTCAGA TGAGTCTTTG 120 TGGTTGGGGT TGCCCTGTGC CTCACAGGAT GTTTTCCCAC TAGATATCAG TAGCACTCCC 180 TGGCTCCAGA TGGGACAACC AAAGTGTTTG CAGACATTCC CAAATGTCCC TTGTGGGGTG 240 GGGTAGGGGA GTGGTAAAAT TGCCCTGCTT GAGAACTACT GAATTCTAAC TGCATGTCCT 300 GCCAGCCATT TGACCTAAAT TAAATTCTTC CCCCAAATAT CCCATTTTTC TCACTTCCTT 360 ATTTCTCTTT GTGGGTCTAA TTTTTCCTCA GTCGTTCAAG CTCAACATGT CTGTGCTATG 420 TCTGACTCAG CCCCCACCCC CCATCCTCCA CACCCAACCC ATCACTAAGA CTCATAGCAT 480 TGACTTCTAC TCCCAAGCCC CTCCTTCCCT TTCCTGTTTA TCTTTTAGAT TCTGGCCTCT 540 GTGATCTCAC ATTAACGCCA ATAGCTTTTT TCTGGTTTCC CTATCATTAA TTCATCCTAT 600 CCAGTGATGA TAGATAAGGT TTTCTCAAAG GTAGCTTGTA GTATGTTCCT TCTTTCATTA 660 GAACCTTCAG TGTTTCCCAA TGATAGACCA AATTAAGTAC AAATTGCTCA CTCTTGCATT 720 TCAGAGCCTC CACCATATGG CACCAACTCC CTTTCCAGTC TCAGTTCACA CATCTCCTCT 780 ACAAGTACCA ACAGGGTGGC TCACTGCTCA TCAAAAGTGG GCTATGCATA TGCCCTGATG 840 CCTTTTTCTC ATGCTGTTAC CTCACTTGGT GAGTTCTCCT CCACAATGTT CCCCTAAAAA 900 AGCTCACTCT TCTTTCAAAG CCAGTCTGAT ATTCCACAAT ATTCACAAAT CATTTTTTTC 960 TGGTTGACCC AACAGAATGT ATTCACTTTC CCATCTGAAT CTCTGCAGCT GTTCATACTG 1020 CCTCTTCTGT CAGGTTACAC ATCATCCCCT GGTATAGCCC GTGTAGTGTT AATAGTATCT 1080 GCTTTGCCAG ATTGTAATCT TAATGATGGC AGAACTATGG TCATATTCTT CTTCATACAC 1140 TCTAGTATTT AGCACAGCTA TATGCATTTT AGATGTTCTT AATTATTTGT CTAAATGAGT 1200 AATAACAGTG AACTTACCTG CTTACTATCT TAACACAGTT CCTCACCATT CTTTTCTTAA 1260 ATAATTGGTT TCTCAGCTGG TCTTTTGACT CATGTCTTTC CAACCCATTC TCTGCCTGGT 1320 ACAAAAGTCA CTTTCCAAAC ACAAGTCTGA TCATGCTGAC CCTGACTGAG AACTTGGAAT 1380 GGCTCCCGTT GCCTAGAGGA TGGGTGCAAA CTCCTTGGTA TGACACACAA AGCCCTCTGT 1440 ATTCTGGCTA CTGTGGTTTG TCTCAGCAGT CCTCCCTCCA ACTGCATTCT TGCGACATGC 1500 TAAGTTTCCA GTTCCAGCTG TCACGCTGCT CCTTTCCCCA CATCTCCCAT ACCTTTGTTT 1560 GTACTGCTCC TTCTGCCAGG AATGCCTTCT GCCAAGAATG CCACCTACAA CAGCTGTTTA 1620 CTTCTCACTA CTATGCAAGG AGGGCCCTGG CCTTCCACAC CATGAGCCTC CTTCCAGGGG 1680 CATCCACTGG GCTCTGCACG TACTCCTGCC ACAGCTCCTG TAATATTTTG CTGTGTTGAC 1740 TTTTCATGCC TGAATCCAGC TGCTCACAAT GAGCACATAG AGCAAAATGA ACTGTGTTTT 1800 ATAGTCCTTT GCCTTTCAGA TGCCTAGATA GTGCTGACAA TGGAGGAAGC TAATGAAAAC 1860 TATCTTGCCC AATGACTGAT GAATGGATGA ATCCAAAGCA GAAAACCAGT CTATTCTAGT 1920 CACCAACTAG AAGAGTTTGT TTCATAGATT ATGTATGTCA GTGTTTAAAA TGCCACCAAC 1980 AAACTCTGTT TATTTTGTGA GACCTGAATG TCTGACATCA TTAAGAGGAG AGATCAGCTG 2040 AGCGAGTCTA TTAGCCAGTG TATTGCCATT TTCAGTTTTA TATTTAAAAA CTTTTAAAAC 2100 CACATTAGAT ATTTCCCTGA CTTGGTCAAC AGGATATTCC GGAAATAATG TTACTCTCCT 2160 CCTATAATGG AGTTATCATT ATGAGAATAC ATTTCTATAT 2200
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