Tag | Content |
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EnhancerAtlas ID | HS141-13238 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr3:122379820-122381400 |
Target genes | |
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) |
JUN(var.2) | MA0489.1 | chr3:122380707-122380721 | AGGAAGTGAGTCAT | + | 6.69 |
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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: 2 | ID | Chromosome | Start | End |
GH03I122660 | chr3 | 122379671 | 122379962 | GH03I122662 | chr3 | 122380848 | 122381047 |
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Enhancer Sequence | GCAGTGTGTT TACCACGTGA ACCCAGCAAT CCAGAGAGGT TGAAAGGTTT TGGTTATGCT 60 GAATTTGACG ACCTGGATTC CCTGTTCAGT GCCCTGAGTC TCAATAAAGA ATCTCTAGGT 120 AACAGGAGAA TTCGAGTGGA CGTTGCTGAC CGAGCACAGG ATAAAGACAG GGACGATCGT 180 TCTTTTGGCC ATGAGAGAAA TCGGGATTTT GACAAAACAA ATACAGACTG GAGGGCTCGT 240 CCTGTCACAG ACAGCTTGGA TGACTACTCG CCTAGAAGAG GTGATGATTG CTTTGGAGAC 300 AAGTATCAAG ATCGTTATGA TTCAGACCGG TATCGCGGTG GGTATCGGGA GGGGTATCAG 360 GATGGCCCAC GCTGGGATAT GGATCGATAT GGCGGCCAGG ATTGCTATGA TGACCCAGGC 420 AGCAGACACT ATGATAGAGG CTATGATTCC CAGATAGGCA ATGGCAGAAG AGCATTTGGT 480 AGTGGGTACC GCAGGGATAA TGACTACAGA GGAGGCAGGG ACCGCTCTGA AGACCGATAC 540 AACAGACGGG ATGATCGGTC GTGGAGCTCC AGAGATGATT ACACTTGGGA TGATTATAGG 600 TGTGATGATA GAGGTCCCCG CAAAGACCCA AACTGAATCT AAAGCTTTGG AGTACTCCCA 660 AGGAAGATGA TTCCTCTGCT AGTACCTCCC AGTCCAGTCG AGCTGCTTCT ATCTTTGGAG 720 GGGCAAAGCC GGTTGACACA GCTGGTAGAG AAAGAGAAGT AGAAGAAATG CTACAGAACA 780 AGAGAAGTTG CAGCGTCAGC TGGATGAGCC ATAACTAGAA CGACGGCCTC GGGAGAGACA 840 CCCAAGCTGG CAAAGTGAAG AAACTCAAGA ATGGAACGGT CGCGGACAGG AAGTGAGTCA 900 TCGCAGACTG AGACCTCCGC CATACCCAGC AGAAATGCAC GAAGGAGAGA GAGTGAGAAG 960 TCTCTAGAAA ATGAAACACT CAATAAGGAG GAAGATTGTC ACTCTCCAAC TTCTAAACGT 1020 CTCAAACCTG ATCCTACCAG ACCCAAAGGT AATGCCAGCC CCTCCACCAA AGGAGAATGC 1080 TTCGGTGAAG TGAAGTTCTA ACGCTCCTGC TCCATCTCAG AGCTCAGACA CAGAGCAGCA 1140 ATCCCCTACA AGTGGTGGGG GAAAAGTAGC TCCAGCTCGA TCATCTGAGG AAGGACCAGC 1200 AAAGAAAGAT GAAAATAAAG TGGATGGGAT GAAAGTCCCA AAAGGTCAAA CTGGGAACTC 1260 TAGCTGTGGT CCAGGAGATG GAGGGAACAA AGACCACTGA AAGGAGTCAG ATAGGAAAGA 1320 TGGCAAAAAG GATCAAGACT CCAGATCTGC ACCTGAGCCA AAGAAACCTG AGGAAAATCC 1380 AGCTTCCAAG TTCAGTTCTG CAAGCAAGTA TGCTGCTGTC TCCGTTTCTG GTGAAGATGA 1440 AAACAAGGGA GAAGATTATG CCGAGTGGAC CTAGACATCC TGTGCTTTCT CCTAGTTTCT 1500 CTCCACCCTG GAACGTTCGA GAGCAAATCA AACTTCTATC CAGACAAGAC AAAATAAAAC 1560 TCACCATCTC CTGGAGACTT 1580
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