Tag | Content |
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EnhancerAtlas ID | HS145-22889 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr6:122101400-122102470 |
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) |
FOSL2 | MA0478.1 | chr6:122102245-122102256 | GGATGACTCAG | + | 6.32 | JUNB | MA0490.1 | chr6:122102245-122102256 | GGATGACTCAG | + | 6.14 |
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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 |
GH06I121779 | chr6 | 122100734 | 122102691 |
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Enhancer Sequence | GCAGGTTCTG GAGTACAGAG GAAGTTTCCA GATAGTGCTC TGGTTACCTA CTGCCACATA 60 ACACTCCCGC TCCAATGAAG CTTAGTGGCT TAAAATGACA GCAACATTTA TTTTTCTTGC 120 AAACCTGTAA TTTGAGTAGG GCTTAATGGG GACGTGTTTC TGCTTCATTT GGCATCAGCT 180 GGGGCAACTT GAAGGCTGGA AGCTGGAATG ATCTGCAGCC TGTCTTACTC ACTTGTCTGG 240 TGGTTGGGGA TGGCCATCAG CCATCTGCTG GGGCTGGGCC AGCACTCCCA CACATGGCCT 300 GTCCATGTGG CTGCCTGGTT TCCTCATACA TGGTTGTGTT CCAAGGGTGC ACATGCCAAG 360 AGAGACAGAA CCAGGGTGAA GCTGTATTAC CTTTCCCAGT CTAGCCTCAG GAGTCCCACA 420 GCGTCACTTT TGCTTCTTTC TACTTACTAG AAGTAAGTCA ATTACTAAGC CTGGCCCCTA 480 TTCAAAGGGA GGGGAATCAG ACTCCACCTT TGGTAAGAGG TGTGTCAAAA CATTTATGGA 540 CTTGTTTTAA AACTATTACA GCTTAAAAAA ACAGATTTGG AAATCACTGG CATATTGCTG 600 ACATTTATAC CCATTAGAAG AGATGAAATT GCTTAGGGAG AGAGTAAAGC CAGAAGAGAC 660 AGAAGGCCAA GGACTATACC CTGGAAGATC ACTGACATGT AGTTTCTCAG AGTTAGAGGA 720 ACCAGAAAAG AAGACTCAGA AGGGGAAGCC ATTGAAAAAG GGAGAAAACC AGAACAATGT 780 GGTGTCCTGA AAGCCAAGAG ATGAAAGGTG CTTCACCAAG GAGAGACAGC GGTGTCTGAT 840 ACTGTGGATG ACTCAGACAG ATTAAGCAAG GTGCAGACAA TGAACTGGTG ACTGGGTGTT 900 GTGAGGTGGA GGTTGCTGGG ACTTTGACAA GACAAGAGCA GTTTGGTTGT GTAATGACAA 960 CACAAACCTG GTTGGGGGGA TTTCAAGATA TAACTGGGAG GTGAAAAAGC AAAGACCACT 1020 TTTCAGTCTT CTTCCATATG TTCTGTGATG CACAAGGCCC CATGGAGTCA 1070
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