Tag | Content |
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EnhancerAtlas ID | HS148-15999 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr6:122101460-122102370 |
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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH06I121779 | chr6 | 122100734 | 122102691 |
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Enhancer Sequence | ACACTCCCGC TCCAATGAAG CTTAGTGGCT TAAAATGACA GCAACATTTA TTTTTCTTGC 60 AAACCTGTAA TTTGAGTAGG GCTTAATGGG GACGTGTTTC TGCTTCATTT GGCATCAGCT 120 GGGGCAACTT GAAGGCTGGA AGCTGGAATG ATCTGCAGCC TGTCTTACTC ACTTGTCTGG 180 TGGTTGGGGA TGGCCATCAG CCATCTGCTG GGGCTGGGCC AGCACTCCCA CACATGGCCT 240 GTCCATGTGG CTGCCTGGTT TCCTCATACA TGGTTGTGTT CCAAGGGTGC ACATGCCAAG 300 AGAGACAGAA CCAGGGTGAA GCTGTATTAC CTTTCCCAGT CTAGCCTCAG GAGTCCCACA 360 GCGTCACTTT TGCTTCTTTC TACTTACTAG AAGTAAGTCA ATTACTAAGC CTGGCCCCTA 420 TTCAAAGGGA GGGGAATCAG ACTCCACCTT TGGTAAGAGG TGTGTCAAAA CATTTATGGA 480 CTTGTTTTAA AACTATTACA GCTTAAAAAA ACAGATTTGG AAATCACTGG CATATTGCTG 540 ACATTTATAC CCATTAGAAG AGATGAAATT GCTTAGGGAG AGAGTAAAGC CAGAAGAGAC 600 AGAAGGCCAA GGACTATACC CTGGAAGATC ACTGACATGT AGTTTCTCAG AGTTAGAGGA 660 ACCAGAAAAG AAGACTCAGA AGGGGAAGCC ATTGAAAAAG GGAGAAAACC AGAACAATGT 720 GGTGTCCTGA AAGCCAAGAG ATGAAAGGTG CTTCACCAAG GAGAGACAGC GGTGTCTGAT 780 ACTGTGGATG ACTCAGACAG ATTAAGCAAG GTGCAGACAA TGAACTGGTG ACTGGGTGTT 840 GTGAGGTGGA GGTTGCTGGG ACTTTGACAA GACAAGAGCA GTTTGGTTGT GTAATGACAA 900 CACAAACCTG 910
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