Tag | Content |
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EnhancerAtlas ID | HS118-12071 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr22:29524460-29526620 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PRDM1 | MA0508.2 | chr22:29526277-29526287 | GTGAAAGTGA | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 29525346 | 29525741 | chr22 | 29525298 | 29526023 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I029128 | chr22 | 29524881 | 29526218 |
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Enhancer Sequence | AAAGTATGTT TTCTTTAGTA TAGTGCCTTT ACTGGAGGTG TCAAGCAGAA ATAATCTGGA 60 TTAAATTGTA AATGCAGCAC TATGGAAATA GTCTCTAAAG TGCACACCAA GTAGCATCTT 120 TGGTACTACT AGGAAAGAGT ACTGGCCCTC ACATAAAGGT GCACTGAAGT GAATTAATTA 180 TAACAACAAT TATTGCTATT TACTGAGTGC TTGTCATGTG CTAGACTTGA TGCCAAGTGC 240 TTTTGTGAAT TTTATGTTAT TTAATCCTTG TAGCAATCCT GTTGATAAGA AAACTGTGGA 300 TCAAAAGATG AAGTAATTTG TCTATGCTAG TAAGTGCCAG AGCCAGGATT CAAACCCTGG 360 TTTGCCACAT TTGAAATTTT TCTATTTTCA GCAGCTAGAA TCCCTTTTAT TAACAATAGT 420 AAAAATAGAT CATAATAACG GATCCAGTTT TATGCTTTAA AGTTATATGA ACAAAGTATG 480 CCCAGTTCTG ATTATTCCCA CATTGGCCCC TTGTGCAGCT CTCCAGAAGC TGCCCTTCCT 540 GGCTTGCATT TGCTCAAGGA CTAAGAAGGC TGGCATTCTG AGAGGCTGCT CACGCCATCC 600 TCCAGAGGCC CAGATGCCTG TGGTCTACAG GACCCCTGAC AGCAGCCAGT TCTGTAACTC 660 ACACCCCATT GCTCTGCTGA GAAAGGTACA AAATGCAGCA CTGTATAAAT AATCTCTAAA 720 GGTGCATCTA GAGGCCGGCA CAGGGGTGCA CACCTGTAAT TCTAGGCTGG AGGCTGAGGC 780 AGGAGAATCG CTTCAACCCG GGAGGTGGAG GTTGCAGTGA GCCGAGATCA CACCACTGTA 840 CTCCAGCCTG GGCGACAGAG TGAGACTCCA TCTAAAAAAA AAAAGGTCCA TCTAGTAGAG 900 AGTAAAATAG TTTGAACAGC TCAAGTACCG CCTCATGGAA ATCCTTATGA CTCATTGAAC 960 AAGGCTGAGC ACTTTGGAAA TGGTGACCAC AGACTGTCCC ATGATTTAGG AGGGTGAAGA 1020 TGTCTCCCTA AAGATATTGG AGAAGTTAGA TGGTGAGAAA CGACCAGGTT ACAGTCTGTC 1080 TCCCAGAACA TGAGGCCCTG CTACCAGTGT GGCTCGCATG TGGGTCTCAG TCAGAGTGTC 1140 AGCGACATCT TCCTGTCCTC TGCTGATTAG AGGAACACCC AGGCTCCTCT GCAGTAGAAG 1200 TACTCAGGCT GTGTTTGCTC TTTGGCAGAC AGACGACGGG GCTAGTGGGG GTGGAGGGTG 1260 AGGGGCAGCT GGCAGAAGCT GTCTGCTCAG TCATCACTGC CACATCAAGT AATTTGTCAC 1320 AGACTCTCTG GCTGATTTTT CAGCAAGCTC ATGGACTTGG AGAGGTCACA GAGGTGAGCT 1380 GTGTACTGTG GGCAAGCACA ACACTGACGG GGGCTTCATA GCCTCTGCTA CCCCTAGGGA 1440 TTATAATTTA TTGAATTAAC ATAACCAAAC AGAAGAACAT GTAGGCCAGA GTCAACAGTG 1500 GGTTACAGGA ACTACCCAGG CTAGCCTGTT GGGACTCCCT TGGCTTCTAG GCCCTGAAGG 1560 GAGGGGTCAG TCATCTGGAT TGGACCTTAT TTTGTAGCAT TAGTTGAACA TTTATCATTG 1620 ACAGGAGCCT GTGCTATTCA CTTTACATGC GTTGTCTCCC TTAATTCTCA CAGTACTGTG 1680 AAGCAGGTAC TGTTATGCTT ATTTTACAGA TGAGAAAACT GAGGCTCATA AAAGTTCAGT 1740 AATCTGCCCA AGGTCCCACA GATAAAGATC CTGCCTTCAT GGAACCTTTA TTTTAGTGGG 1800 AAGGGAAGAG ATTAATTGTG AAAGTGATTG GTCTAAGGAT GGGTAGGATC TGGCTCCTGG 1860 GACTGTGTTA GCAATTGCAT TTCATAGACT CTAAGATGCC TCAATTCTGA GGTGCAACAT 1920 TATTTTATAC ACCATTAAGG GAAAAAGTAT TTCCAGTTTA ACAATGACAT GCATTGACTA 1980 AAAGATACAT CCCAGTTTAA AAGATTAAAG TGTATCCCTT AGAGTTGATG AAATATGGTA 2040 CCAGCCTTCT TTCTTGGGTG CCAAGAAAGA GTAGAATCTT TCCATCCTGA GTGGAATCTG 2100 ATTCATGGCT GGGACCCATT TGGCTAAGGT TTGTTTCCTG AGACATGCCC ATTATCATTC 2160
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