Tag | Content |
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EnhancerAtlas ID | HS116-08739 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr12:104900200-104901300 |
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) |
LBX2 | MA0699.1 | chr12:104901044-104901054 | GCCAATTAGC | + | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_25350 | chr12:104900836-104902569 | DND41 | SE_59750 | chr12:104849529-104923220 | Ly4 | SE_62327 | chr12:104849575-104918276 | Tonsil |
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| Number: 2 | ID | Chromosome | Start | End |
GH12I104506 | chr12 | 104900741 | 104900890 | GH12I104507 | chr12 | 104901021 | 104901170 |
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Enhancer Sequence | ATGATGCATG TAAATTACTG GATGACTTGA CCAGGATGGA CGGTCCTGCA CATTAGAAAG 60 GCTGTTTTCA AATGTTGGAG TGGGACAATC ACTTGGAAAC TTATTCAGAG GTCCCCCTCA 120 GATAGTCGAT TCATTAGGGC CAGGATGAGG CTTGGAATCA AACAGGCACC CTCAGGGATT 180 CTAGCTGTGC TGTGCCACTT TGAGAAACCT AGTCCAGGTG CTAAATTTAC AGTGATCACC 240 TTGGGATTCT GGTGTCCGAC AGAGATGGAA ACTTCGCAGG AAATGTTCCC CAGGCGGGAG 300 GGCTAAGAGG ACACAGTAAC TCTTGAGAGT TGCTCCGACA GACCTTTTAT TTTGGCAAGG 360 GCTTGTGCTT TCTTTGCCAA GCCATCATTC GTTACTTGGC TAGAGGAGGG ACCACAGGGA 420 GGGGAGAGGG GACATATACA GCTGGCTGTC AGAACAGTCG ACCTCTAAAT GGGATAACCT 480 CAGAGCCAGG CATAAGCAAT CTGGAAACAA GGAGGGGAGG TGATGGAAGG TGGGAGCAGA 540 GGCAGGTGCT GGAGACATTG CTGCAGACTT CCTGGAAGGG GTTGCCAAGC CGGGAAGATT 600 CAGAGGGGAA GAGCACAGCT GGGGAGAGAG CCCCTGCTGG CTCCAGGTGC TGGTCCCAGA 660 AGGCATCTTT GGAGGGAAGG GTCTGAGCTG TGACGGTTCA GTGCAGGGAC AGGTGGGGTA 720 AGCTCAGGTG TGCCGGGCTC CCTGTGCGTG TTGCAGAGCT CCCGGGGAGG GCAAGGATGT 780 GAAGTGCGAG CAGATGGTCT CCGTCACTGC CAACCTAAAT CAATGACTGG AGAGGGCGAA 840 TGCTGCCAAT TAGCAGGATA TCCAGAGCTC TTTCTCCCAG CCCAGTGGCC CCACCTGGGA 900 GCCAGGCAGC ATGCTTTGCC TCCTGCTGAG ACAGATCCTG CTTTTGCTGC TTCCTTGAGA 960 GAAGTTTTAA CACATGAAAA TGGCTAAGAG CAAAGGCTTT GGCACCGCTG CCTGCTTTCA 1020 GATTGCTGCT TTTGCTAGCC ATGTCATCTT GATCCTGTTT CTTCCCTTCT CTGGGCCTTG 1080 GTTTCCCCAT TTGTAAAATG 1100
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