Tag | Content |
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EnhancerAtlas ID | HS099-12275 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr2:100279020-100280540 |
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) |
POU4F2 | MA0683.1 | chr2:100279905-100279921 | ATGCATTATAAATAAG | + | 6.03 |
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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 |
GH02I099662 | chr2 | 100278761 | 100280614 |
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Enhancer Sequence | ATGTCTAATT CATTAAGACC AACAAGCCAG CATCTTACAT GATGTTTGGT ACTTAGTAGG 60 TATTTGAGAC TATACTCAGT TTTTTGCAAA AACTGTCTAG CTCTTGTTTG CCTACAAATA 120 ACATTGACAA TACAGTTCAT TTCTAATGTA GGAGAAACTT CATTTTGGAG CCTTGCCCCT 180 CAAACCTGGT CCTGATTACT GCTTCAACTC CTGTTTATAT AATTCTACAC AATTTTGGCA 240 GGATTCAAGA GCACATACCA GGGTGTTGGC TTTTATGAAT CTCCTGGGAT GTGAATGTCA 300 CGCTGACTGG ATGAACCCTG GCCACAAATC CCAGACAAGC ACAATGATTC TATTTATTCA 360 GACTTGGCTG CCTGAATGCA GATTGACTCT GTGGGTAATA AATTTTCACA GGCCAAGAGC 420 GTCAGGATCA ACCAAGCTGA TCCTGAGAAG AAAAATGCAA CTAAGGAAGT AGAGTTGGGC 480 TGCAAAAACC TCCTATGTTT TTATTCCATG TCTGCATATC ATTCAGCTAA TTCATTTAGT 540 TACTGATTGA CATGTACTGT CAATGCTTTC AGACATTTTA AAAGCTCTGC TTTGTGTTAT 600 GCAATTGTCA TATTAAAAAG AAACAAGGGA AAAAATGAAG AGCTTCCATT ACAATTGGCA 660 ATCTGCTTTT AAGAGTACAC CCAAAACTGA TGTGAGTCAT CCAGTAATCT CTGTGGTAAA 720 GAGCACAGAA TTGAGATGGG AATGTTTCTT GTGCTGCTCC ATAGGAAACC AAAGGAAACA 780 GCAATAAGAA CTGCAATTTT GTGCTCAGAG CAACCTCACC TACAATCTTG GTATCTTGAT 840 GAAGCAAGGC TTTACATTAT TTCTAAGAGA CACGACTATT ACTCTATGCA TTATAAATAA 900 GAAAATAATT GGCTCTTTAA TTTGCAGATT TATGTTAATG ATCTAGATAT CTATTAAATT 960 AATTGCATGC TCTCCAAATA TTGATTGGGG ATTAAAAGGC AGCTTTTCAT TGTGCAAGAA 1020 GTAAATTAAC GCCAATGGGG AAATTTCCCT CTACAGATTA GATCCAATGA TTGTTGTCTG 1080 TAAAATTAAA ATAGTCAGTT AAAGGGGATA AACCATGTTC ATTTAAAGAG AAAAATGTGG 1140 CAACAGAGTT AAAATAAAAA GACTGCCCAA TATGTTTGGA TAACGTAATT ACTGGAAGCT 1200 GCAGGCATGT ACATAGCCAT TCAATTTAGA TCCCTGGTCC CTTCCTCTCC CTAAGCTATG 1260 TATTTGTCAT CTCCGAAACA CTTGTCTGCA GTTGACACTA TCTCAGCTGC TCCTTGCTGA 1320 AAGTCTTAAT CATGTGTCCC TGTCCTCATG CCTTAGCTAT AGTAATGCCA TCTACTTATT 1380 TGCTTGTGTC CAACCTCCCA AGCTTACCCT GACTTGAGAG GCAGAGCTCA TCTTTTTGCC 1440 AAATGGGAAG ACATGCAATA TAATTAATCA GTCCCTTCCT AATCTATTAA ATTTTTTTAA 1500 TACTTACTGT CTTAAGTCTT 1520
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