Tag | Content |
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EnhancerAtlas ID | HS117-00209 |
Organism | Homo sapiens |
Tissue/cell | LHCN-M2 |
Coordinate | chr1:46378960-46380400 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DUX4 | MA0468.1 | chr1:46380373-46380384 | TGATTGAATTA | - | 6.14 | ESRRB | MA0141.3 | chr1:46379690-46379701 | TCAAGGTCAAA | + | 6.14 | Esrra | MA0592.2 | chr1:46379689-46379700 | TTCAAGGTCAA | + | 6.14 | MSC | MA0665.1 | chr1:46379009-46379019 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr1:46379009-46379019 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr1:46379009-46379019 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr1:46379009-46379019 | AACAGCTGTT | - | 6.02 |
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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 |
GH01I045912 | chr1 | 46377794 | 46381008 |
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Enhancer Sequence | AGTCTTCGCT CATTATTTTA CCAGTTTCTT CCAGTCCCTT GCCCACTGCA ACAGCTGTTT 60 AGCCTGGCCC ATGCCTTCTG GGTTAATAGT ATTTCTGACA CAGTGTGAGT TTTCAAGTTG 120 CTATGTATAA TTTCTGCCAG AGTTTTTACT GCCGCCAGGC CTCAGGGTTG GAGGTTGCAA 180 CTGATTTGTG GGGGAGGGAG TTTGGTGCTT GTCACTGACG CAGGAACAAG GTGCTTTCTG 240 TAGCTCTGAT TTGTTGCTGG CTGAGTGTGA ATGATGTCAG GCAGATCAGA GGACAGCTGA 300 TTCATTTGGG ATCTGGAACT TGTCACTGTC CCACTGCTGC CTCGTGGGCT CTTAGGTCTT 360 TTGTGGGGGG ATGGGAGGGG TGTTCTGAAG ATCATGTTTT TGAAGAAAAG TACTTTAATT 420 TTTGCCGTAA GTTTGGGAAG CTTTTATAAT TTCCTTTGGC TGACAGAACT GCATACCCCT 480 TGTGTGAGAG AACTTCCTAC CAAGACTCCA GTGTGAGGGC AAAACTTGAG TAGCCAGGAG 540 AATGATGAAA CGGAGGCAAG AGAGACTGGG AGCACCATGT CTGCGGATTC AGTAAGGAGG 600 TTGGGGTCTC TATGGAAACT GGCAGATGTC AGGAAAAAAA ACTAATGCCA ACTAACACAG 660 CTTCGTTCAT TTGGATGAAG ACTGTTTTGG AGATGCCTGT CAGGAAGAGG GCTGAGCTGG 720 CTTGATTAAT TCAAGGTCAA AACAGTGGTC CTTGGCAGGG GCATATGAGG TTTCCAATTC 780 CAGAAACTGA ATTAGATGTC ATTTTAGGGG TTCCTGAATA CTTGGAGAAC TGGGTAAAAA 840 AATGAAGACA ATTATTTTCT TCCCTTGAAA GCAAATGTTT ATTTAAAGTT AGTGTCAAGG 900 CTGCAAATAC AAACCCCGTG AATGTGAGAA ACCAATGGAA ACAAAAAGTA CCTCCTCCTT 960 TGACTAGAGA GGGTATTGTA TTTCTGCCCA TGGCCTGTCA GCTCAGGACC TCAGATCTGC 1020 CCTTGCAGAT TCAAGCATGG GTCCTTTAGG GTGTGACCTC TATTTTATTT CTATATTGGC 1080 CAATATAGAA ATAAACTTTA TTAGGTGAGA ATATCAAAGC TGGGAGTGGA AGAAGGCTTC 1140 CTCTTCAGGG TGACTTTTCC AAGAGCAGCT CAGGCTTATT TAATGAAGAA GTGCCAAGTG 1200 AATTCATCAG TAAATTAGAG AACCAGTGAA AGAAGAGACC TAGAATTCAT TTCACCTCAA 1260 TTATCTGTCT TGAACTGCCT TTGTTTAACC CACAGGGCTA AGGGAGTGTA CTTCAGATTT 1320 TCTTCCTGAG TCAAACTGCT TGCCCTGAGA CAGACAGGCT TCTTCAGTGG GCTTCCTTTG 1380 TGATGTTGCC CTTCAGTGTC TGTGGATGCT TATTGATTGA ATTAATGATT CTATTAGACC 1440
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