Tag | Content |
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EnhancerAtlas ID | HS099-20743 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr7:76638550-76640030 |
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) |
NFE2L1 | MA0089.2 | chr7:76639672-76639687 | AGATGACTCAGCAGG | + | 6.66 | TCF7L2 | MA0523.1 | chr7:76639689-76639703 | AAACATCAAAGGAA | + | 8.12 | ZNF263 | MA0528.1 | chr7:76638607-76638628 | GAGGGAAGAAGGAGAGAGGAG | + | 6.03 | ZNF263 | MA0528.1 | chr7:76638611-76638632 | GAAGAAGGAGAGAGGAGGAGA | + | 6.23 | ZNF263 | MA0528.1 | chr7:76638614-76638635 | GAAGGAGAGAGGAGGAGAGAG | + | 6.59 | Znf423 | MA0116.1 | chr7:76638680-76638695 | GGCACCCATGGTGGC | + | 6.18 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_26739 | chr7:76638557-76640122 | Esophagus | SE_68923 | chr7:76639200-76640242 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I077009 | chr7 | 76639119 | 76640130 |
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Enhancer Sequence | TCAAGACCAG CCTGGGCAAC ACAGCAAGAC CCCATCTCTA AAAAGTTTTT TTAAAAAGAG 60 GGAAGAAGGA GAGAGGAGGA GAGAGAGCTA CTCAGAGAGA CCAGGGGTGT ATACGGTCCT 120 GTTCTGCAGT GGCACCCATG GTGGCCAAGG GGTGGTAGCA GGGATTGTGG GCTGGGAAGA 180 ACCAGATCTG AACCAGGGCA GACACAGAGG ATTGGAGAGG AAGAGTTGGA TTCCAGAAAT 240 ATGCAGGAGG TGGCCGCAGG AATTGGGAGA TAAGGCAGAG GGAAGAGGCC ATGCCCAGTT 300 TCTGATGTGG CCTGGGCGTG AATGCAAAAA TTGGGGTCTT CTGTGCTTTG CAAGTGAGTG 360 CACCACCACA GTTTGCTTTA CGGCAAGGCC CCAGGAAAAG GGGTTCTGGG GATGTCATCT 420 CAACGGCAGG TGTGTTCCAC AAGAACATTA ATACATCGTT AATATTTTTG AAAGACAAGA 480 CTGGGCATGG TGGCTCACAC CTGTAATCCC AGCCCTTTGG GTGGCTGAGG CAAGTGGATC 540 ACTTGAGCTC AGGAGTTTGA GACCAGCCTG GGCACCATGG CAAAACCCCG TGTCTACTAA 600 AAATACAAAA AATAGCCAGA TGCGGTGGCT CGTGCCTGTA GTCCCAGCTA CTCGGGAGGC 660 TGAGGCAGGA GAATCGCTTG AATCTGGGAG GCAGAAGTTG TAGTGAGCCG AGATCACACC 720 ACTGCACTCC AGCCTGGGCA ACACAGCGAG ACTCCATCTG AAGATAAAAA AAAAAAAAAA 780 AGAAGAACCC AAGGGAGGGG GCACTGCCCA GCACAGGCAC AGTCCCATCA GGCCCTGGGG 840 AGCCATGCCA GGGCGTTCTG CCCAGCACAG TCACACCTAA AAGGGTCCTC AGCCGAACCC 900 CATCCCCTTG AATACCAGCT CATGACGGCT TTGAGCAGAA CATGTCACGG GAACGGCATT 960 GTGTAGAACT TTTTATTAAA TGGCATTTAA AATATTCCCC AGGACTGTGT AGCTGGGGAA 1020 ACACCACAAA ATCCATTGGC CCGGAACATA ATGGCTCAAT GGTACGAAAC AAATGCATTG 1080 TTAAAAAGGA AAAACAGCAA CTGTTGCGGG GTAATGACTT GCAGATGACT CAGCAGGCCA 1140 AACATCAAAG GAATTCGGAT GGCAGCAGGT GGGCACAGGC AGCCAGGAAG CACCCCTCCC 1200 TCGCTCTCAC TTCCAGCGAT CGCTTTACCT CCCTGGAGTG TCTAAGCCAC CCATTTCTCT 1260 CCATCATCCC TGCAATCCCC AAGCAAGAAC CACCTTGGTC TCCCGCTGGG ATGTCCGTGG 1320 TTCCTCTCTA GCTGAACTCT CCATGTCCAC TCCTGCCCGT CGCCCATTCC CCTCTCAGTA 1380 TCCAGAGGGA CCAGGTTCTT TGTTCTTTTT TTTTTTTTTT TTTTAAGATA GAGTCTCACT 1440 CTGTTGCCTA GGCTGGAGTG CAGTGGTGTG ATCTCGGCTC 1480
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