Tag | Content |
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EnhancerAtlas ID | HS193-00120 | Organism | Homo sapiens | Tissue/cell | U87 | Coordinate | chr1:7953490-7955010 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr1:7954096-7954111 | TGCTTAGTCACTCTG | - | 6.34 |
| | 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 |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I007893 | chr1 | 7954001 | 7954150 |
| Enhancer Sequence | GCAGTGAACT GAGGTTGTGC CACTGCACTC CAGCCTGGAC GACAGAGCCA GACCCTGTCT 60 CTAAATAAAT AAATAAATAA ATAAATAAAA CAAACCAAAC CTGGGGATTT AAATGCTTCC 120 AGAAATACCA ATTTTGCAAA AATAGGTGAT GACACGTCAC AGACCCCCAA CAGCGTTGCC 180 ATGTGGACGA CAAACATCTT GTGAGGACTC TAAGACCATG AGCTGAATAT TGACTGGCCT 240 GGTCACCTCT GTGCCTGGTT TTACGCTGCT CCTGGAGGGC ACAGTCGCAG GGCTGGAAGT 300 GGGTGCACCT AACACGGTAT TGCCCTCAAG ACTGTCTCCA TACACTCACC CATATATTTC 360 GTCGCACTTT TTAATATTCA CTTACAACCC ACTAAAATAT GACCGTCCTT CTCTCCCTCA 420 CCTTGAACAG AAGGAAAAAA CCCACACCAT CATTCACTTT AATGCCACAA TTGGGAAATG 480 ATAGATTCTT CTTTGTCTAA AAACCGTAGA GTGAGTCAGA GGCATAGCTA GAGAGAGAAT 540 TCGGGTCTGG CTGCCGTGCC AAGCTCTCTC TGCCCAGTGG TGGGGGTGCT TGGCCCCCTT 600 AACTGTTGCT TAGTCACTCT GCGTCTTGCC AAAGTAAATG GAGATGTTTG AACTCTACCC 660 CATCCACTGT TCTCTCTGGG TTTGCACCAC TTCTCTGATT TCTTTTTTTT TTTTCTTCTT 720 CTTTTTCTTT CTTTATCTCT CTCTTTTTTT ATTTCTTTTT TCTTTTTTTT AAGATGGGCT 780 CTTGCTCTGT CTCCCAGGCG GGAGTGCAGT GGCACGATCA TAGCTCACTG CAGCCTCAAC 840 CTCCCAGGCT CAAGTGATGC TCCTACCTCA TCCTCCCAAG TAGCAGGCCC CCACCACTAC 900 ATCCAGCTAG TTTTTGTATT TTTTGTAGAG ACGGGGTCGC ATCATGTTGC CCAGGCTCGT 960 CTCAGACTCC TGATCTCAAG TGATCCACCC TCCTCGGCCT CCCAAAGTGC TGGAATTACA 1020 AGCATGAACC ACCGTGCCCG ACCTCTTCTC TGATTTCTTA GCACAAGGGC TGTGGTGAAT 1080 GAAACAGAAC CCTGCCCCTC TGGCCAGTGC ACTAAGGACA AATCACATAT CACATGTGAG 1140 CCACTGCCCA ACCCCCCGGC CCTGCCCTTA GACTCTGCAT TGCTAATGAA TTCCCGTGTC 1200 ATTCCAGGGG TAGAGGCCCA TGGACCCCAC CCTGAATAAA CAGAATAACA TTTTTGCAAT 1260 AAAAAATATG GCCGGGCGCG GTGGCTCACA CCTGTGATCC CAACACTTTG GGAGGCTGAG 1320 GCGGGCAGAT CACGAGGTCA GGAGATGGAA ACCAGCCCGG CAACATGGTG AAACCCTGTC 1380 TCTACCAAAA ACACAAAAAT TAGCCGGGAG TGGTGGCACA AGTCCAGGAG TTCTAGGCTG 1440 CAATGAGCTC TGATCACACC ACCGCATTCC AGCCTGGGCG AGAGAGCAAG ACCCTGTCTC 1500 AAACAAAACC AAACCTGGAA 1520
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