Tag | Content |
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EnhancerAtlas ID | HS197-00621 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr1:40455670-40457040 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mecom | MA0029.1 | chr1:40456874-40456888 | CCTTATCTTGTCTC | - | 6.17 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_34178 | chr1:40455345-40456907 | HCC1954 | SE_64654 | chr1:40456040-40456884 | NHEK |
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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 |
GH01I039989 | chr1 | 40455446 | 40456909 |
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Enhancer Sequence | AATCACTGCC ATCATTATCA CTACCACCCT GGTCCCAGCT ATTGTCATCT CTCCCCAAAT 60 GGTTACAACA GCCTCCAAAA TGGTCTCTAT GCTTCGACTC TGGTCTCTAC TTTCTATTTG 120 CAACATGCCA GCCAGTGTGA CTTTTTTTTT TTTTTTAAAA AGACTGGATC TCGGCCAGGC 180 AGGGTGGCTC ACGCCTGTAA TCCCAGCACT TTGGGAGGCT GAGCAGGGGT GGATCACGTG 240 AGGTAAGGAG TTCGAGAACA GCCTGGCCAA CATGGTGAAA CCCCATCTCT ACTAAAAATA 300 CAAAAAATTA GTCAGGTGTG GTGGCAAGCG CCTGTAATCT CAGCTACTTG AGGGGCTGAG 360 GCAAGGAGAA TTGCTTGAAC CTGGGAGGCA GAGGTTGCAG TGAGCCCAAG ATCACGCCAC 420 TGCACTCCAG CCTGGGTGAC AGAGCGAGAC TCTGTCTCAA AAACAAACAA AAATACCACA 480 GACTGGGTGG TTTAAACAAC AGAAATTTAT TTCCTCACAG TTCTGGAAAC TGGAGGTCTA 540 GGATCCAGGT GTCAGCAGGT TTGGTTTGCT CCCGAGGCCT CTCCTCTTGG TCTCAACTTC 600 CTCACCTCAA GTGATCCGCC CTCTTTGGCC TCCCAAAGTG CTGTGACTAC AGGTGTGAGT 660 CACTGCACCA AGCCCAAATT TCCTCTCATA AGGACACCAG TTAGATTGGG TTAGGGCCCA 720 TCATAATGGG CTCATTTTAA CGTAATTACC TCTTTAAACA TCCTGTCTCC AAATATAGTC 780 TTAATCTGAG GAACTGGGGA ACTGGGGGTT AGGATTTCAA CATAGAAATT TTGAGGGAAT 840 GCAGTTCAGC CATAACCACC TTTATTTATA TAAGGAATAG GTGTTCACGG GTCAAACCAA 900 GGGAAGGGCT GCTTATTCTC ACGGCCCAAT AACGAGATGC AGATGAATTG GGAAAGGAGG 960 GAGTTTATTT CTGTAACTGG GTACAGGGAG AAGGCCTGGA AAATATCAAC AGACGAACTC 1020 AAAATTACAG AGTTTCCAGA GCTTATGCAC CTTCTAAGCT ATATGTCTAC GTGTAAGTGT 1080 GCATTCATCT AAAGACGTGA GTGATTAACT TCTCCTGTAA CTGAGATCTG AGTCCTGAAG 1140 ACCTTCCTCT GGAGCCTCAG TAAATTTATT TAATCTAAAT GGCTCCCGGT GCTGGGGTGA 1200 TTACCCTTAT CTTGTCTCCT GCTAAATCAT GGAGGTTTGG GGAGTTCCTT CAGACTCTCA 1260 GTAAACTTAT TCGTGGAGGT CTGGGGAGTT TCTTCAGACC CCTAATGAAA CTTATTTAAT 1320 CCTAAATAAG TCCTGTTAAG AATTGCTTCA TTGGCCGGGT GGTGGCTCAC 1370
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