Tag | Content |
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EnhancerAtlas ID | HS139-54904 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr8:142327600-142329350 |
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) |
NR2C2 | MA0504.1 | chr8:142329285-142329300 | CAGGGTCAGGGGTCA | + | 6.63 | NR2C2 | MA0504.1 | chr8:142329309-142329324 | CAGGGTCAGGGGTCA | + | 6.63 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_32282 | chr8:142327743-142329307 | Gastric | SE_65316 | chr8:142327721-142329653 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I141318 | chr8 | 142328341 | 142328490 |
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Enhancer Sequence | AAAATTTTTA AAATTTGCCA GGCATGGTGG CACCCACCTA TAGTCCCAGC TACTCCAGAA 60 AGTGAGGAGG GAAGATCACT TGAGCTCGAG AGTTTGAGGC TGCAGTGAGC CAGTGGTAAT 120 CCCACCACTT TGGCAAGCCG AGGTGGGCAA ATCACTTGAG CCTGAAAGTT CAAGACAAGC 180 CAACATGGTG AAACCCTGTC CCTACTAAAA ATACAAAAAA TTAGCTGGGC ATAGTGGTGC 240 GCTTGTAGTC CCAGCTACTA GGGAGGCTGA GGTGGGAGAA TCACCTGAGC CTGGGAAGTT 300 GAGGCTGCAG TGAGATGAGA CTGCACCACT ACACTCCAGC CTGAGCCATG GGAGTGAAAC 360 CCTGACTCAA AAGAAAATAG AAAGAAAAAG GGAGGTGGGA GAGAGCAATG CTAAAGCCAG 420 AGGCAACTGG GGCCACAGTG ACTGGGTGCG GCAGGGCATC CTGGGTCAAG GGTGGCAGCC 480 TGTTAGACAG CTGCCCATGG CAGGGTTGCT ACTGTCTGGC CCTGTGGTGG GAGAGCCCAA 540 TAGAAGTTGC CCGGGGTGCC TGAGGTCCGG AGCCAGGAAC GCAGGCTGCA GAGAGGGCTG 600 ACCCCATTTC CCGAGGCAGT GGTGCCAGGA GGCCTGTTTT CCAGGGTGTT TACTGGGCTC 660 TCCGGCTCCA AGGAGCTCTG AGTATTTGGG CTGAGTGCCC GGGGTCAGCC CCTCGACAGC 720 ACGCTGGGAG GTGGGGGTGG CTGTGCTGAT GCCACCCTGG GCCAGTGGAG AAGGGTGGAG 780 GCAGCAGACT GCCCGGCAAC CCATGAGTGG GAGGGGAGGC TCCACCCTCC TTAACCACAG 840 CCTGAGCAGC CACTTCCCAG GCCCACCTCT GATTTGGGTG GAGCTGAGCT GGGAGCACTT 900 TTCCAGGCTA CCTAGTGAGG GAGGGGCACA GCAGATAGCA AAGGGGTCAC GATTCAGTCA 960 ACAGGGTCAG GCTCAGCCGG GAAGCGAATA GGATCAGGGC TTAGTGGGTA AAATGAGAGC 1020 CAGTGCTAAG TCGAGGGAAG GATCATGGTT TAACATATAA CCAGGGTCAG GGATTAATGT 1080 CCAAGCAAGG TCAGGGCTCA GTCTGTGACC AGGATCAGGG CTCTGTGTGT GACTAGGATC 1140 AGGGCTCAAA ATGTGACCAG GGTCGGAACT CAGTGTGTGA CCACGATCAG GACTCAAAGT 1200 ATGACCAGGA TCAGGGTTCA GTGTGTGACC AGGGCTAGGG CTCAGTGTGT GACCAGGATC 1260 AGGGCTCAGA GTGTGACTAG AATCAGGGCT CAGAATGTGA CCAGGATCAG GGCTCAGAGT 1320 GTGACCAGAA TCAGGGCTCA GAATGTGACC AGGGTCAGAA CTCAGCATGT GACCAGGATC 1380 AGGACTCAAT GTATGACCAG GATCAGGGTT CAGTGTGTGA CCAGGGCCAG GGCTCAGAAT 1440 GTGACCAGGG TCAGGGTTCA GTGTGTGACC AGGATCAGGG CTCAGAATGT GACCAGGGTC 1500 AGGGCTCAGA GTATGACCAG GATCAGGGCT CTGTGTGTGA CCAGGATCAG GGATTAGAGT 1560 GTGACCAGGG TCAGGGCTCA GCATGTGACC AGGGTCAGAG CTCAGCGTGT GACCAGGGTC 1620 AGGGCTCAGA GTATGACCAG GATCAGGACT CAGTGTGCTA CGAGGATCAG GGCTCAGAGT 1680 GTGACCAGGG TCAGGGGTCA GAGTGTGACC AGGGTCAGGG GTCAGAGTGT GACCAGGGTC 1740 AGGGCTCAGA 1750
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