Tag | Content |
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EnhancerAtlas ID | HS098-41369 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:195170940-195172140 |
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) |
Sox3 | MA0514.1 | chr3:195171426-195171436 | AAAACAAAGG | - | 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 |
GH03I195450 | chr3 | 195170804 | 195172762 |
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Enhancer Sequence | AGGCGTGAGC CACCGCGCCT CATCTCAACT GTCTTTGTAT TATTTATCTG TGACCAGTTC 60 CCTGGCCCAC TGGCACAATG GCTGTTCTCA AACCTTGCTG CTCTCCTCAA GCCTCCCAGC 120 AAATGTGCCC CACCCCACTC ATGATTTGCA AACAACATTG GGTCCTCAAA AAGAAAATAA 180 GAGTCATTAG GAACACTCTT CTACCCCCAG CCCACATACT CATCTATGTT CGCACTTTTC 240 TTACTTCTTA CCCACCTATC TCAGAGGAAG GTGGCATCTC TTTCTGCCAC TCCTGATCTG 300 TGCTCTAGGG AATCCACCCC TTCTGTTCTC TTTGGAGAAT GGCTCTATCA ATTATCCCCT 360 CCTTCTCTGT ACCTTCAAAC TCTCAACTGA CCATTCTTCT GTCTTTGGAA GAAAGAGAAG 420 AAAATCATAC ACCGTCTGTA TCAGAAAGGA TTATTTTTGT TGTAAGAGAA ACTATGTGAG 480 TTAATGAAAA CAAAGGGTTC ATGATGGGTT AGTTTCACCC AGAACCAGAT GGCTGGCTTT 540 CCTTGAAACT TGAGAAGGAT TTAGAACGAG GGCCTGTAAA GCCGGCAGCT CCTTCCTGTC 600 TGCCCATTTC CACATCTGCA GCTTACTTCA TCTGACTCTC CAGGCAGCAG CTCCCAACAC 660 TACCCAACCA ACCGGAGAGG ATGGGCTTTC TCTCTAGGCC CCAAATCTAA ATTTCTTGGA 720 GGAAGTATTG GCCCACCTTG GATGCTGTAC CCCGCACAGA GGCCAATCAA CTACAGTCAA 780 GGAGGCAGCT GTGTACAAAC ATGGCTCCTG AGAGTCTGCC CCTGTGACCT TGTAGTTGGG 840 AAATCTCTTA GCCAAGAAGG GGGACATGTG AGTTGGAAAA ATTCCCCTCT GACTATTGCC 900 AAATCTCCTT CCGTTGCTTT ATATCTAAGA CTCTTTAACA GCACAGTCTC CACTCCCTAC 960 TCCACAGTTT CTCCTCCCAT TCATTCCAAT ATCCTCTGCA TTCTGTTCTC CACTCTCTCC 1020 AACACCCCTG CTCCCTACCA ACTGTTTCAG GAAGGTCACT TTCCAACGGC CAAACCCAAA 1080 GCACACTTTC AGTACTTGTT TTCCTGACGT CTCCTCAGCA TTTGCCACTG TTTCCAAGTC 1140 TTTCCACCTG GGAAACTCAT GCCACTTTCC TGCTTAAGAT TCTTCAAGGG TTGGTCATTG 1200
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