Tag | Content |
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EnhancerAtlas ID | HS105-36517 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr18:3816110-3817500 |
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) |
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 | TCTCATTTCA TCAATACAAC AACCTGTGCA TATTTTTCTG TTTTTCTCAG GTGAGAAGCA 60 GGAGGTCAGA GAAGGTGAGT AACTTGCCAA AGGACACACA GCTAAAACGG CAGCACTAGG 120 GTTCGAGGTG TTTAACTCCT AAGATCAAAA TTATATTAAT CAAAATTTTA TGATTTATGT 180 CACTTTGAAA CCTAAAGTGT TAAGAAAATT GTCCACAATA GCACACACAC ATATCAGACA 240 CAGATTTCTA AATATTATAG GTTCTAAGGA AGTGAGAATA GATGTTCTAC TAAAAGAGCA 300 TAATTCTTTC CTTTTTAATT GTTAATTCAC CTGTATAACT GGAAAGTTTA GATCTAAGAA 360 CTTCAGATTG AAGAGATGCT ACTATTCATG GTCTTGAAAA CAGTGGTTTG TAGGTTCTAA 420 TTCTGAAAAG TACTAACCAA GATGAAGCAT CACCCTGCAG CATGTTCATT TTATTTAATA 480 AATTCTTATA TTGTGCTCCT GTGTGCAGGC ACTGTTCTAA GTGCTTTTTA AATGTCAGCT 540 CATTTGATCC ACACAGCGGA GGGGTGGTAT TATTATTATT CCCATTTTAC AAATGAGGAC 600 ACTAAAGTTA TGTAGCTCAC TCAGAGTTAC AGCTAAGAAG GGGCTGAGTT TCAATGAGGC 660 AGTTCCTAGG GCCATATCTT GACCACTGTT TAATGCTCCT TGTCTTTCTA GGCTGTGCTT 720 TGTGGCACCT GCAGAACTGA GCAATTATAG TCCCGGACAC CTTTGTGCTC ATCACATTTG 780 ATACACTTGT CATTTATTAA TTATGCTAGT AACAATGTAA TGTTTTTACT TTTGTAGGTA 840 AAAGCATCAA AATCACCACA GCAACAAAGA TTTCTCAGGA AATTATAAAT GCTGAGAACA 900 GTCTTGTTTT CCTTGCATTG GCAGGTGACT CACTGCATAG ATATGATCAT CTTCAGAGCC 960 TCATTATAGG TTTAGCAATT ACATTTTAAA AATTAACTTG GTACAGCTGA GGGTCATAGA 1020 TGACGCACAC CACACTTGCT ATTTCTCAAT CCTGATGTGA AGTTCATAAG CATTGCTCTC 1080 TGGAGTATGT CAGAGACTAA TGACAAACTG ATTAGCTCAT ATGGCTTATG CAACAAAACA 1140 TGGCAAATTT TGTTCAGATA TTTTTTTCAA AGTTAGTTTA TGGTAGAAAT TTGGGCTCAT 1200 ACTAGAAACA GTCTGTAACT GTTGTTTAGG GAACCAGCTG AGAAGTATTT AACCTGTGTA 1260 TCTTTCAATT AATCTTACTT TTCAAATGAT AGCAGCTAAG AAGTTATGTG GAAGTGACTT 1320 CCATTGGAGT GGAATTTGAA TAGTAATACA TTATTTATAT ACCTAAAGGT AGCATACAAC 1380 AAGATTACAC 1390
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