Tag | Content |
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EnhancerAtlas ID | HS003-42008 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr7:76638590-76640510 |
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 | AAAAGTTTTT TTAAAAAGAG GGAAGAAGGA GAGAGGAGGA GAGAGAGCTA CTCAGAGAGA 60 CCAGGGGTGT ATACGGTCCT GTTCTGCAGT GGCACCCATG GTGGCCAAGG GGTGGTAGCA 120 GGGATTGTGG GCTGGGAAGA ACCAGATCTG AACCAGGGCA GACACAGAGG ATTGGAGAGG 180 AAGAGTTGGA TTCCAGAAAT ATGCAGGAGG TGGCCGCAGG AATTGGGAGA TAAGGCAGAG 240 GGAAGAGGCC ATGCCCAGTT TCTGATGTGG CCTGGGCGTG AATGCAAAAA TTGGGGTCTT 300 CTGTGCTTTG CAAGTGAGTG CACCACCACA GTTTGCTTTA CGGCAAGGCC CCAGGAAAAG 360 GGGTTCTGGG GATGTCATCT CAACGGCAGG TGTGTTCCAC AAGAACATTA ATACATCGTT 420 AATATTTTTG AAAGACAAGA CTGGGCATGG TGGCTCACAC CTGTAATCCC AGCCCTTTGG 480 GTGGCTGAGG CAAGTGGATC ACTTGAGCTC AGGAGTTTGA GACCAGCCTG GGCACCATGG 540 CAAAACCCCG TGTCTACTAA AAATACAAAA AATAGCCAGA TGCGGTGGCT CGTGCCTGTA 600 GTCCCAGCTA CTCGGGAGGC TGAGGCAGGA GAATCGCTTG AATCTGGGAG GCAGAAGTTG 660 TAGTGAGCCG AGATCACACC ACTGCACTCC AGCCTGGGCA ACACAGCGAG ACTCCATCTG 720 AAGATAAAAA AAAAAAAAAA AGAAGAACCC AAGGGAGGGG GCACTGCCCA GCACAGGCAC 780 AGTCCCATCA GGCCCTGGGG AGCCATGCCA GGGCGTTCTG CCCAGCACAG TCACACCTAA 840 AAGGGTCCTC AGCCGAACCC CATCCCCTTG AATACCAGCT CATGACGGCT TTGAGCAGAA 900 CATGTCACGG GAACGGCATT GTGTAGAACT TTTTATTAAA TGGCATTTAA AATATTCCCC 960 AGGACTGTGT AGCTGGGGAA ACACCACAAA ATCCATTGGC CCGGAACATA ATGGCTCAAT 1020 GGTACGAAAC AAATGCATTG TTAAAAAGGA AAAACAGCAA CTGTTGCGGG GTAATGACTT 1080 GCAGATGACT CAGCAGGCCA AACATCAAAG GAATTCGGAT GGCAGCAGGT GGGCACAGGC 1140 AGCCAGGAAG CACCCCTCCC TCGCTCTCAC TTCCAGCGAT CGCTTTACCT CCCTGGAGTG 1200 TCTAAGCCAC CCATTTCTCT CCATCATCCC TGCAATCCCC AAGCAAGAAC CACCTTGGTC 1260 TCCCGCTGGG ATGTCCGTGG TTCCTCTCTA GCTGAACTCT CCATGTCCAC TCCTGCCCGT 1320 CGCCCATTCC CCTCTCAGTA TCCAGAGGGA CCAGGTTCTT TGTTCTTTTT TTTTTTTTTT 1380 TTTTAAGATA GAGTCTCACT CTGTTGCCTA GGCTGGAGTG CAGTGGTGTG ATCTCGGCTC 1440 ACTGCAACCT GCAGCTTCAG GTTCAAACGA TTCTCCTGCC TCAGCCTCCC AGGTAGCTGA 1500 GACTATAAAC GTGCGCCACC GTGCCTGGCT AATTTTTTTG TATTTTTAGT AGACGGGGTT 1560 TCACCATGTT GACCAGGCTG GTCTCAAACT CCTGACCTCA GGTGATCCAC CCACCTCGGC 1620 CTCCCAAAGT GCTGGGATTA CAGGTGTGAG CCACTGCACC CAGCCAGGAC CAGGTTCTAA 1680 ACCTGATCAC ATCACACCTC TGCTCCCAAC ATTCAGGAAC TTCACACTGC AAGAACAGAA 1740 TCTAGGTTCA GACAGGTGTG GCGGCTCACA TCTGCAATCC CAGCACTTTG GGAGGCCAAG 1800 GCAGGCGGAT CACTTGAGGC CAGGAGTTCG AGACCAGCCT GGCCAGCATG GTGAAATGCC 1860 ATCTCTACTA AAAATACAAA AATTAGCCAG GCATGGTGAT GGGCGCCTGT AATTTCAGCT 1920
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