Tag | Content |
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EnhancerAtlas ID | HS003-10044 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr12:40404780-40406020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr12:40405135-40405154 | TGCCCACTAGGGGGCAAAA | + | 6.23 | Crx | MA0467.1 | chr12:40405671-40405682 | AAGAGGATTAA | + | 6.14 | EWSR1-FLI1 | MA0149.1 | chr12:40405437-40405455 | CTTTCCTTCCTCCCTCCC | - | 7.57 | ZNF263 | MA0528.1 | chr12:40405441-40405462 | CCTTCCTCCCTCCCCGTCTCC | - | 6.05 | ZNF263 | MA0528.1 | chr12:40405447-40405468 | TCCCTCCCCGTCTCCTCCCTC | - | 6.07 | ZNF263 | MA0528.1 | chr12:40405444-40405465 | TCCTCCCTCCCCGTCTCCTCC | - | 7.35 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I040011 | chr12 | 40404963 | 40405802 |
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Enhancer Sequence | CTGTGTAGTG TATCTCGTGC AAATGTTAAG TTACACTTCC TACTCACCAG CTTCGTTCTT 60 CAGTCTTCAT GTGGTAAAAA ATACAACAAC CTACGATCCA GGCTACAGCC AGAGGCTCAA 120 CTAACTTTTG AGTAACCTCC CACGCCCGGT ACCAAGAGTT GGAGACACAA ATAATAACGG 180 TAGGCAGGGT TTATCAACAT CACCTGTGTT GAGTGTTGAC TTTTTGGGCC AAAAAGTTCT 240 ATGTTGCAGG GGCTGTTCTG TGTATTTGTA GCATTAAACA TCCTACTACC CACTAGATGT 300 CAACATCACA TTCCCTGAGC TGTGACAATC AAAAATGCCT CCAGACATTG CTAAATGCCC 360 ACTAGGGGGC AAAATTCCTC CTGACTGAGA ACAAGTGAGG GTGGATCAGG AGCTTTCAGT 420 TTCTAATAAA CTTTCTTGGG TCCTTCCCTT TGTTGGGACT CACAGAATTT CATACTCTTA 480 GATCTATCAA GAATCTTTTC CTTCAAGTTT TATTTTAGAT TCAGGGGATA CATGTGCAGG 540 TTTGTTACAC AGATATATTG TGTGATGCTA AGGTTTGATC CTTAACATCA TAAACATGCA 600 TAAATGATCC TGTCACCCAA ATAGTGAGCA CAGGACCCAA TAGGTCGTTT TTCAACCCTT 660 TCCTTCCTCC CTCCCCGTCT CCTCCCTCTA GTAGTCCTCG GCGTCTACTG TTCCCATCTT 720 TATGTCCATG TATACCCGAT GCCTAGCTCC AGAATCTTTT GGTTGCCTTC TCTGAAATTC 780 AGAGAAGTAA GCTGTGAACA GCCAGTTGTG GTTGCCTAAT TTGTAGGGCT GAGGGCAAAA 840 TGAAAATGTG AGTCCCGTGC TCAAAAATTA CAACTCTGAA GACAGTGACA GAAGAGGATT 900 AAACCAAGGG CAGGACCCTT CTGAGTGCAG GGCTCTGGGC AGCTGCAGAG GTCGCGTGTC 960 CATGAAGCCA GCCCTGCAAT AGCCACCTAG TGATAGGCAG AGCAGGAGTT ACAACCTGGG 1020 ATTCCTGTCA CTCTTTCCAC TAAACTGACA GTCACATAAA GATCTGCTGC ATCTCAATAA 1080 GCCAAGAGGT ATTAATAGTT CAACTTCCTA ATTTTTACTA CAGTTTTTGC TAATATTCCT 1140 TATACTTAGC AAGAAATATT GTACATAATA GTGAATTAGT TTCTCATCTC AACTTTTTGA 1200 AATCAAATTT ATCAACAGAA ACCTACTAAA TTAGATTGAC 1240
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