Tag | Content |
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EnhancerAtlas ID | HS003-00149 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr1:7953580-7955150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr1:7954096-7954111 | TGCTTAGTCACTCTG | - | 6.34 | ZBTB18 | MA0698.1 | chr1:7955059-7955072 | TGTCCAGATGTTT | + | 6.07 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 7953883 | 7954188 | chr1 | 7954452 | 7954667 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I007893 | chr1 | 7954001 | 7954150 |
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Enhancer Sequence | CAAACCAAAC CTGGGGATTT AAATGCTTCC AGAAATACCA ATTTTGCAAA AATAGGTGAT 60 GACACGTCAC AGACCCCCAA CAGCGTTGCC ATGTGGACGA CAAACATCTT GTGAGGACTC 120 TAAGACCATG AGCTGAATAT TGACTGGCCT GGTCACCTCT GTGCCTGGTT TTACGCTGCT 180 CCTGGAGGGC ACAGTCGCAG GGCTGGAAGT GGGTGCACCT AACACGGTAT TGCCCTCAAG 240 ACTGTCTCCA TACACTCACC CATATATTTC GTCGCACTTT TTAATATTCA CTTACAACCC 300 ACTAAAATAT GACCGTCCTT CTCTCCCTCA CCTTGAACAG AAGGAAAAAA CCCACACCAT 360 CATTCACTTT AATGCCACAA TTGGGAAATG ATAGATTCTT CTTTGTCTAA AAACCGTAGA 420 GTGAGTCAGA GGCATAGCTA GAGAGAGAAT TCGGGTCTGG CTGCCGTGCC AAGCTCTCTC 480 TGCCCAGTGG TGGGGGTGCT TGGCCCCCTT AACTGTTGCT TAGTCACTCT GCGTCTTGCC 540 AAAGTAAATG GAGATGTTTG AACTCTACCC CATCCACTGT TCTCTCTGGG TTTGCACCAC 600 TTCTCTGATT TCTTTTTTTT TTTTCTTCTT CTTTTTCTTT CTTTATCTCT CTCTTTTTTT 660 ATTTCTTTTT TCTTTTTTTT AAGATGGGCT CTTGCTCTGT CTCCCAGGCG GGAGTGCAGT 720 GGCACGATCA TAGCTCACTG CAGCCTCAAC CTCCCAGGCT CAAGTGATGC TCCTACCTCA 780 TCCTCCCAAG TAGCAGGCCC CCACCACTAC ATCCAGCTAG TTTTTGTATT TTTTGTAGAG 840 ACGGGGTCGC ATCATGTTGC CCAGGCTCGT CTCAGACTCC TGATCTCAAG TGATCCACCC 900 TCCTCGGCCT CCCAAAGTGC TGGAATTACA AGCATGAACC ACCGTGCCCG ACCTCTTCTC 960 TGATTTCTTA GCACAAGGGC TGTGGTGAAT GAAACAGAAC CCTGCCCCTC TGGCCAGTGC 1020 ACTAAGGACA AATCACATAT CACATGTGAG CCACTGCCCA ACCCCCCGGC CCTGCCCTTA 1080 GACTCTGCAT TGCTAATGAA TTCCCGTGTC ATTCCAGGGG TAGAGGCCCA TGGACCCCAC 1140 CCTGAATAAA CAGAATAACA TTTTTGCAAT AAAAAATATG GCCGGGCGCG GTGGCTCACA 1200 CCTGTGATCC CAACACTTTG GGAGGCTGAG GCGGGCAGAT CACGAGGTCA GGAGATGGAA 1260 ACCAGCCCGG CAACATGGTG AAACCCTGTC TCTACCAAAA ACACAAAAAT TAGCCGGGAG 1320 TGGTGGCACA AGTCCAGGAG TTCTAGGCTG CAATGAGCTC TGATCACACC ACCGCATTCC 1380 AGCCTGGGCG AGAGAGCAAG ACCCTGTCTC AAACAAAACC AAACCTGGAA GTTGTTTATA 1440 ATCCTTTACT TATTTTTTGC CTCTATTATT TTTTATATCT GTCCAGATGT TTAATTTGTA 1500 TCTTCTTCGT CGGCTTTGTG CATAAGGACA GCATATGACT CAATTTGTCG GTTAAAATTA 1560 GGCCTAGGCC 1570
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