Tag | Content |
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EnhancerAtlas ID | HS044-04976 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr15:99319630-99321130 |
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) |
Myod1 | MA0499.1 | chr15:99321035-99321048 | GGGAGCAGCTGCA | - | 6 | Nr2f6(var.2) | MA0728.1 | chr15:99319633-99319648 | TGAACTCCTGACCTC | - | 6.22 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_31674 | chr15:99319451-99321175 | Gastric | SE_43426 | chr15:99319521-99323022 | MCF-7 |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I098776 | chr15 | 99319427 | 99324455 |
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Enhancer Sequence | TCTTGAACTC CTGACCTCAG ATGATCCACG CGCCTTGGCC TCCCAAAGTG CTGGGATTAC 60 AGGTGTGAGC CACTGCGCCC AGCCAGATTT TATTTCTTTA AAAAAGAAAC TTACTAGTTA 120 TCAGGACACT TGTGTTCTTG GTACTTGATT TTGTCAGCAT TATTTTTAAG AGCCTCTTCC 180 CTCCTTCCCC CTACCTCCCT GTTGAGCCCA GGCTCTGAAA TAACATAGGT GCATGTGAAG 240 TTCCCCTACC TGCCATTACC AGACATTGGT GCTGGGCGGC CCTCACCTCC ACCTCCTCTC 300 ACCTGAGGCC ACAGCGGTGT GCAAGGATGT GGTCTGTCTT GAGTGTGTTT TCAAAGCAGC 360 TGTTTGGTCT GTGCCTTGGA TGTTTTTCCA CAGATAAGCC CAAAAGAGAA CCACATCTTA 420 AAACGCCCGT GACCTTGAAT GGTCTTTCCG GAGGGGCGGC TGGATTTGTG CTCTCATCGT 480 CTCAGGTATG TGTCAAGCCA CTGTTGTTTC AGAGCTGGAC ACAGGTGCTT AGGAAAATTC 540 CTCACTGAAG GGTTTTCAGG ATTTACAAGT TCTTGCTGTT TTTGTGACCT TGTGTGGTTT 600 CTGGTTTCAC AGAAGGCTTT GTTTCTTGGT TCTTGTTGCT GCTTTCAGCC TTGGCCTGTA 660 ATCACTGGGC GCCAGGGAGG GCTGCGGTCT GTTTCCCGGG GTGTGCTCAG ATACCGTGTC 720 AGTTCACATG TGTTGCTGCA GCGGCAGGGG GCCAGGCAGG AGGGGCGGGT GTCCTGAAGC 780 ACGCTCAATT TGCTGATCAG GGCCTTCACT TGGATTTTGC ACTTGCCGCA GTGGAGACAT 840 TCCTCGTAGC TACTCAGTGT GGTTTGTTTT AAGTGGGCCA TCCGTTAATT CATGTGACCT 900 GGAACTTGGT TAATGTACTT GCCAAGGTTA AAGTTGAGAC GCTGTTTGTT AAACCTTTCA 960 AAGAGGGAAG AAGGTTGCCT TGAATTCAGT TCCAGGGTTT GGGAGTCTGA GAGGGAGGTG 1020 GTGAGGGGCC CGGGGAGGCC CTGAGAAACA AAATGCTGGT TAAGGACACA GTCTGCTCAC 1080 CGACCTCGGA AGTCTCTAGA CGTCTAAAGA AGTCCAAGCA AGGAATGATG ACCGAAGAGG 1140 AACCTCAAGG GTGCAGGCGG CTCTGGGATC TCAGCACATC TCAGTGATGG AATGAGCTGC 1200 CGGGGAATGA CCCCTGTGGG GGCTGTCCAA AGTCAGAGCA GACACAAACG TAGCTCTCCA 1260 GGCCCCATAC CTTGGTGGGC AAGAGGGCAG CAAGTGCATC CTCACAGTTG ATGGGGAGAG 1320 CAGCATTTCA GCCTGCAGAA AAGAGAACCA CACAGATGTA AGATGAGGTC TGCACTCACT 1380 TGCCTGGTCA TGCAGAGACG GAGCTGGGAG CAGCTGCATG ACTTTTCAGA GAAGTGGCAC 1440 ACGTTTACTG TAAGGGTCCC AAATGTAGAC CACTGCAGAT CGTAAGGTCT AGATGGAGGG 1500
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