Tag | Content |
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EnhancerAtlas ID | HS139-15881 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr13:113768640-113769970 |
Target genes | Number: 11 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF2 | MA0051.1 | chr13:113769636-113769654 | ATTGGACTTTCACTTTCC | - | 6.03 | ZNF263 | MA0528.1 | chr13:113769291-113769312 | GGAGGAGGCTGAAGAGAGAGG | + | 6.62 |
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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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Enhancer Sequence | GGTTTGTTTT TTTTTTAACC ATCTGAATAT TAAATTATCA CAAAGTTTGA GGCCCCCAAC 60 CTCCCTTGGG TTCAGTAATT CACTAGAAGG ACTCATAGAA TCCACTGAAG TGGATACACT 120 CACAGGTACC GTTTATTACA GCAAAGGATG CAGGCTTAAG TCTGCAGAGG GACCAGGCAC 180 AAGCTTCCCC TTGTCCTCTC CCTGTGGGGT CATGTGGACA GTCCTTAATT CTCCCAGAAT 240 GACGTGTGAC GAGACGTGGG AAGTACTGCC AACTTGGGAA GCTCTACGAG CCCCGGTGTC 300 CAGAGGTTTT ATCAGGGCTC AATCACATAG ACCCAGCTGA CCACCCGCAT GGCTGACCTC 360 AGTCTCAGCC CCTCCAGAGG CTACGCCGAT AGTGCGGCCC AAGGCCCCAC CATACATCAC 420 ATTGTCAGCT AGACCATCCA GCATGGCTCA AGGCCCAGGT AAACACCAAC ATTCCCTCAG 480 GCAAGACCTT CCAAGGGCTT AGCGGTCATT TCCCAGGAGC CAAGGCAAAG GCTACCCTTT 540 CTCTGGCACA GCAGTTCATC CTTGACCACC CAAGACCACA TTCTTACACT GAATGAGCTC 600 TCCTGTGCAG CAGCCATTTT CTTCTCTAAG CAGAAGAGAG CCCAGCAAGC TGGAGGAGGC 660 TGAAGAGAGA GGCTTCCTGC TGGTCATCTG GGTCCAGAAT GCCTGGAGAT CTCTGCTCAG 720 CCCTGGTGCC CAGCAGCCCT GGTGTGCATC CTGCAGGGCA GGCCTTCCCG CCGGAGTCCT 780 GGACTTGCTC AGGGCCACTC CCCTTGCCCA TGTCAACCAA AGTCAGGCTG CCGGTTCTGC 840 TTCTTCTGTC TGAGCCCATG ACCAGTGCTG GGACTAACTG TCCCCAGGCG GGCTCACGGT 900 GGTACGAGGC CAGCTTGGAG AACTGTCTCA GCTCTCTGGT CCTCTCGTCA GTTGGGTCTC 960 TGATTGGAAA GTCCCTTGGA CACTTTTACC ATCCCCATTG GACTTTCACT TTCCCCCAGG 1020 CTCCCATCAG CTGCTCGGAA GAGTGGTCAC CCTGGAGGCC ACTGCCCACC AGCCAGGCAC 1080 CCCCCAAATG CAACCGCAGC CAGCACTGCC AGCCACTGGC AAGGCTGTTC AGACATGTGG 1140 CTCCTCTGAT CCACGCCTTG TCCTTTGGAT CAGTCCACGG AGCAGGTGGT GCCAAGCTCA 1200 GGCTCTGTCA CCCACAGCTC AGTGCCACCT TCCAGGCAGA ACACCACTGC TGACCCAGGG 1260 CATGGCCACC CCGGGGGCTG GCTCTCGCTG ACCCCCAGAA GCCCCTCTCA GGGTGTCCCC 1320 TTCCTGTCCC 1330
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