Tag | Content |
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EnhancerAtlas ID | HS095-13442 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr18:3816470-3817930 |
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) |
Myod1 | MA0499.1 | chr18:3817872-3817885 | TGCAGCTGTCTCT | + | 6.36 | Stat6 | MA0520.1 | chr18:3816979-3816994 | ATTTCTCAGGAAATT | - | 7.11 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr18 | 3816534 | 3817464 | chr18 | 3816827 | 3817202 |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I003816 | chr18 | 3816094 | 3818425 |
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Enhancer Sequence | CTTCAGATTG AAGAGATGCT ACTATTCATG GTCTTGAAAA CAGTGGTTTG TAGGTTCTAA 60 TTCTGAAAAG TACTAACCAA GATGAAGCAT CACCCTGCAG CATGTTCATT TTATTTAATA 120 AATTCTTATA TTGTGCTCCT GTGTGCAGGC ACTGTTCTAA GTGCTTTTTA AATGTCAGCT 180 CATTTGATCC ACACAGCGGA GGGGTGGTAT TATTATTATT CCCATTTTAC AAATGAGGAC 240 ACTAAAGTTA TGTAGCTCAC TCAGAGTTAC AGCTAAGAAG GGGCTGAGTT TCAATGAGGC 300 AGTTCCTAGG GCCATATCTT GACCACTGTT TAATGCTCCT TGTCTTTCTA GGCTGTGCTT 360 TGTGGCACCT GCAGAACTGA GCAATTATAG TCCCGGACAC CTTTGTGCTC ATCACATTTG 420 ATACACTTGT CATTTATTAA TTATGCTAGT AACAATGTAA TGTTTTTACT TTTGTAGGTA 480 AAAGCATCAA AATCACCACA GCAACAAAGA TTTCTCAGGA AATTATAAAT GCTGAGAACA 540 GTCTTGTTTT CCTTGCATTG GCAGGTGACT CACTGCATAG ATATGATCAT CTTCAGAGCC 600 TCATTATAGG TTTAGCAATT ACATTTTAAA AATTAACTTG GTACAGCTGA GGGTCATAGA 660 TGACGCACAC CACACTTGCT ATTTCTCAAT CCTGATGTGA AGTTCATAAG CATTGCTCTC 720 TGGAGTATGT CAGAGACTAA TGACAAACTG ATTAGCTCAT ATGGCTTATG CAACAAAACA 780 TGGCAAATTT TGTTCAGATA TTTTTTTCAA AGTTAGTTTA TGGTAGAAAT TTGGGCTCAT 840 ACTAGAAACA GTCTGTAACT GTTGTTTAGG GAACCAGCTG AGAAGTATTT AACCTGTGTA 900 TCTTTCAATT AATCTTACTT TTCAAATGAT AGCAGCTAAG AAGTTATGTG GAAGTGACTT 960 CCATTGGAGT GGAATTTGAA TAGTAATACA TTATTTATAT ACCTAAAGGT AGCATACAAC 1020 AAGATTACAC ATAAAATAAT ACAGTAATCC GTTCTAGGGA AAGTGTAAAG ACAGAAAATC 1080 GAGACCTTGG AGAAGAAAAA CACAACTGCT GAACTGTAAG GGCCATTAAC ATCGATATAA 1140 TCGAGTCAGT TTTTAGTTTT TGTTTCTTAA ACCCTAAAGC AAAAGGGAGA CATTGCTTAG 1200 GTAGATAGTT TTAGAAGAAA GCATATAAAG TGATAAGCAT ACCAGGCCCA AAGAGTGAAA 1260 TGTTACTGCC TTTTGATTGT AAAGAAAGGG AGAATTACAT GGCTGCAGCT GCTATTGTGA 1320 GCTGGGCAGA GGTTGCTGTG TCTTTCCATT TCAGCTGCAC AGAGAGAAAA GATTTAGGAA 1380 AATCCAAAGA AAAAGATAAC CTTGCAGCTG TCTCTGAAAA GCCTGCGTTA TTACTGTGGT 1440 GGCAGTTTCA GGAGCTGGAA 1460
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