Tag | Content |
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EnhancerAtlas ID | HS061-22954 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr7:127743390-127745090 |
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) |
NR2F1 | MA0017.2 | chr7:127743944-127743957 | CAAAGGTCAGGGG | + | 6.13 | Zfx | MA0146.2 | chr7:127744997-127745011 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_58728 | chr7:127743411-127776818 | Ly1 | SE_60951 | chr7:127740843-127758458 | DHL6 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I128103 | chr7 | 127743353 | 127745052 |
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Enhancer Sequence | GTAGCTGGGA CTACAGGCGT GCGCCACCAC GCCAGGCTAA TTTTTTGTAT TTTAGTATAG 60 ACGGAGTTTC ACCACTTTGG CCAGGATGGT CTCGATCTCC TGACCTCGTG ATACTCCCGC 120 CTCGGTATCC CAAAGTGCCG GGATTACAGG CATGAGCCAC AGCGCCCGGC CCCTAGTTCT 180 TTTTAAAAAA CGCTAGATCC GTCCGCTGCG CTGAGTGGAG GCGGGGCAGG CCTCCGTTCT 240 CCAATTGGCC TTATCCACCG AGCTCTCCCC TTGTGCCGGG CTCTGTGCCA AGCACATCAC 300 ACGCTGTATC CTGCGGCCAG GTTGCTGTGG TCCAGGGTCG TACCCTGGTC CAAGGTCGCA 360 AACCGAGGTG GGACTCCGAT CCGGCAACCA CGCCCGTGGC CCGGAAACGG CGTCCCCTGA 420 GGCCCAGGAG AGGCCGGGCG GTGAGCGGCT GTGGAGCCGA GCGCGGGCAG TGCGGATGCT 480 GCCTATGGGG GAGGCAGCCA AGGACGGAGG GCGAGAGGCG GTTCTTCCAA GGTCACCCTC 540 TTCCGGGTTG CAAGCAAAGG TCAGGGGATC CCGGAATGGT TAGTGCAGGA GCTTCTCTGT 600 GCCTTCCACG TCCTAGATCC TCAGAGCCTC AGAAACGGAG ATCATCGTCC CCACCCCCAT 660 TTTACAGATG AAGAAACTGA GCCGAGGAAA GGAAGCGACT TGGCCAAGGT CGGAGAGCTC 720 ATTCTTTGCA GGGCGGGGTT TGGAACCCGG GGTCTGGCTC TCGGCAACGC GCCCTCGGCC 780 CGCAGCCTCC TGCCCCCTGT GCCCCGCTTC GGCCCCCAGC GCAGCTGCAG AGGGGCCCCC 840 CTCGACGCAT ACACTCAAGA GCCCGACCGC GCGGCTGAAA TCGCGGAGCT CGGAGCCGCG 900 GCTGGCTGAG CGATCGCGGT TCCTGGGCTG CGTGCGCGCC CCTTGGAGCT GAAAGGAGCG 960 CCAGGATCGG GGGCGCTGCA CCGGGCTGGG CCCCTCAACG CTCGCAGACC GGGCCGGGCT 1020 GCAGCTGGAG ATGGCAGCAA TCCCGGGAGG TCTCCGGGCC TCTTCAGGGT GCGTCCAGGA 1080 GGCGGGTTCC GTGCGACGCG GCGCAGCCCA CCCCCACGAG ACCGCTTAAC TTCGCGGGGG 1140 CAGCCTCGGG CGCTCGGAGA CGCGGAGGCC CAGACTGCAG CCTCCGGATG CTGGAAGCCC 1200 AGACTCCCTG GGGTCACCGG CTCTCCCGCC ACCCCAGCTG CAAAGAGTCC CATTGCTTCA 1260 CCGTCCGGAG CTTAGTCTCC TTGTTCCTCT ACCAGTCCCT CCCTCCGCAG GTCTCTGGGG 1320 ACTTCTGACC GCCTGTTCTT ACTCTCCCCC TGCCCCCATA CTTCCCGCCC TTGTCTCAGG 1380 AACGGTGATA CAGTCATCGG ATTGCTCTCC ATCTCCTGTT AGTCTACACT GCACACAACT 1440 CAATAATCCG CTCCCTTCAT CCGGGTGACA GAGACACAGA TAATCTGAGC TAGTGGTGCT 1500 CAAAGTACCG GTCCCAGAAC AGCAGCATCA GCATCTCTTG GGAACTTGTT AAAAATGAGA 1560 ATTTGGGCCG GGCGCGGTGG CTCACGCCTG TAATCCCAGC ACTTTGGGAG GCCGAGGCGG 1620 GCGGATCACG AGGTCAGGAG ATCGAGACCA TCCCGGCTAA AACGGTGAAA CCCCGTCTCT 1680 ACTAAAAATA CAAAAAATTA 1700
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