Tag | Content |
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EnhancerAtlas ID | HS043-15990 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr16:12230840-12231890 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RARA(var.2) | MA0730.1 | chr16:12231234-12231251 | TGGCCTTCACTTGACCT | - | 6.54 | TCF3 | MA0522.2 | chr16:12231764-12231774 | AACACCTGCT | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_37165 | chr16:12230856-12232224 | HSMMtube | SE_58393 | chr16:12172505-12268710 | Ly1 |
|
| Number: 2 | ID | Chromosome | Start | End |
GH16I012137 | chr16 | 12230941 | 12231090 | GH16I012138 | chr16 | 12231341 | 12231490 |
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Enhancer Sequence | CCTGCTTCAG CCTCCCAAAG TGCTGGTATT ACAGGCGTGA GCCACGGTGC CCAGCCTAGG 60 AAAGACTTTT TAGCGGGCAT GTTATGGCTA AGAGTCAGCA GAGGGCCATG ATTGACAGTC 120 TTACCAGGTC CCCAAGGCAA GCAGCGGGCA GCAAAAGCAT GTCTCTTGCA TTTTTTCCTA 180 GGATTGTTGG GACGGTTACA TCAGCTGAGG CTCCTAAGCA CTCAGCATAG CTCCAGGCCC 240 TCAGTAAGCG CTCAGTGAAT GTCACCTAAT TTCTTCTTCT TGGCTGGTGT CTTGGCTGTA 300 GGTGGCTGGG GATGCTGAGG CGAGGCCAGA ATCTCTTGGG CCCTTTCCTT GTCCAAGCCT 360 CCCCTGCAGT GAGCATCTTA GAGCCCTTGG CCCCTGGCCT TCACTTGACC TTCAGCTCCT 420 CCTGGTGTTA TTTTTCCAGC CCTGCCTGCC CAGTGTGTGT CCCTTTGTTT ATTTGTCCCT 480 GCTGGGCTGC TGAGCAGTGA GAACTTCCTT GACAGTGTTG TGCATGTGAG ATTGAGAACT 540 GTACTGTACA TCCTGGAATG GCCTTGGGAG CCCTGCTCAG ATCATGCTGT CCTGCACCCC 600 AGGCGACCTT TATTGGCTTT CTATGAAGGC TTTAAATCTC ACACTCCACC CTGAGGGTCA 660 GCCTCTGCCT TCCTTTGCTT TTAAATCATT GGAGAAATAT GAAGACTATG TCCTTTGTAA 720 AAAAGGACAG TACATTTCTT CAGTGTCCAT TCAAAGGCAC TGATTATATT TTTATCACAA 780 GAGTCAAATG GTGGGAATTG AGAAGGTCAG GCATACTGAT TTGAATTATG GGGAATACTG 840 GCTTGAATTC CAGCCCAGCT TGGGCTAGGG ATGGCCTTTG GAATCAAGGG TGTGGGCCGT 900 TTCATTGCTA TCTCCCCAGT TCAGAACACC TGCTCTGGCG GGAAAAGCCA GTAGGCTTCA 960 TCCTGCTGCC AACTCTGGTA GTCGCTGCCT GGGATTCTGG CTGAGAAGGA CTGGAGTGCT 1020 GTCAGGACTC AACAGAAAAG AGTGTTGTTA 1050
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