Tag | Content |
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EnhancerAtlas ID | HS026-00447 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr1:19120220-19122340 |
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) |
IRF9 | MA0653.1 | chr1:19120720-19120735 | AAAGAAACTGAAACA | + | 6.12 | Klf1 | MA0493.1 | chr1:19122286-19122297 | GGCCACACCCT | + | 6.32 | PHOX2A | MA0713.1 | chr1:19121352-19121363 | TAATTCAATTA | + | 6.14 | Phox2b | MA0681.1 | chr1:19121352-19121363 | TAATTCAATTA | + | 6.14 | ZNF263 | MA0528.1 | chr1:19121923-19121944 | CCCTCCTTCTCATCCTTCCCT | - | 6.04 | ZNF263 | MA0528.1 | chr1:19121920-19121941 | GCCCCCTCCTTCTCATCCTTC | - | 6.83 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr1 | 19120562 | 19120930 | chr1 | 19121141 | 19121402 | chr1 | 19120665 | 19121099 | chr1 | 19121850 | 19122247 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I018794 | chr1 | 19121121 | 19121310 |
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Enhancer Sequence | CCTCACGCCA ATTCCTTCCT CTTTTCATCT TCAACTTAAC AAGTGTTGTC TGATCACAGC 60 CTATGGGCCA AGGGCTGGGG ATGCTACAGG GAATAAGATA CGGTTCCCGG CTGTAGATAG 120 TCAGTGTTCT CTGGGCCTCA GTTTCTCATC TGCAGAACGG GGCACCAATC CCTCCCTGGA 180 TGGCTTCATG GAGCGACTGT GAGGATCCTG GAGGGTCGTT AATGTGGGCA TAGTGGGAAA 240 GCAGTTGGTG CAGAGAATAG ATCACCCAAC ACAGAGTCAG GGTGCCTGGG TTCAAGTCCC 300 GGTATAGCCA CCGGCAAGCT GAGGGGCTGC AGGCAAATTA CTGCTTCTCC CTGAGCCTGT 360 CTTCTCGCTG CAAAGTGGGG AGAGCAGACA TAACCTAAAT AATATCTATT TGTCAAGCAC 420 TTACATGTGC CGGGCACTGT TCCAAGCTCT TCGGAAGACA TGAGTTAATT TAAGCTCCAC 480 AACCTCCCGT TTCGTAGATG AAAGAAACTG AAACACAAGA GGTCAAATAA CAGGCCCAAG 540 GCCACACAGC CAGGCAGTCT GGCTCCAGTA CCTGCTCTCC TAAGCCCCTT GCTCCGGCAT 600 CTCTCACCAC CCATCCATGA GCACCTCGGC CCAATCAGGC ATCTCTCCGC CTCCCCAGAG 660 TTCACGCAAA ACAAATGCCT CTATAATGCT CTCTCAGAGT CCACGGCAAC CAGGTCTCAT 720 TTTATTTTTA CCTTTCTTGG TATGTGTTTC TGTCTTTTGG TTTGGTTTTA AGCATCAGAC 780 AGGAAACTCT ATCAGGGCAA TTGCTATGCC TCCCCCATCC GGTAGCTCCC TCAAACAGGG 840 GCTGATCTCC CCATCATTCT GGGGGTTCCC CAGAGTGAGG ACAGGAGGGG AGCTCTGGGT 900 CTCATGGCAG TTTTTCCACC GGCCTGTTCT TAACCTCCCC AGTTCCCATC GGAGGCCCAG 960 CCCTTCCTGG AGCCATCTGG TCTACCTCCT CAGGGGCACC ACCTGCAGGA TGATTCTCTC 1020 CAGCCGCCTT GGGGAAATGA ATATGGTAAT ACCCTTTCCT AAATTACTGT CGTAGTTGGC 1080 TGAATGTGAG AAACCTAGAG CTGGGGGCAT TGGCAGCTCA AGTGCTAAGA GTTAATTCAA 1140 TTAGCCAGAG CACAGAAAGC TTGGGCCTGC TGTCTGCCTG CAGCACAGAC CAGCAGGCTT 1200 CCGGGGCACT TTCCACACCT CTGAAATCTC AGCTCCCCTT CCACACCCCA TGTGGCTTTC 1260 CCAGTCTTCC CTTATCCAAA ACTAAGGCTT AGATTAGGAC AAATACCTAA TGCATGCAGG 1320 GTTTAAAACC TAGATGATGG GTCGATAGGT GAGCAAGCCA CCGTGGCACG TGTATACCTA 1380 TGTAACAAAC CTGCACATTC TGCACATGTA TGCCAGAACT TAAAGTAAAA TACATAAAAT 1440 AAAATAAAAT AAAATAAAAT AAAATAAAAT AAAATAAAAT AAAATAAAAT AAAATAAAAT 1500 AAAATAAAAT AAAACTAAGG CTTGGAAGCA TGAGCGAGTC CAACTCCAAC AGGCGACCTG 1560 ACATGAAAGG GCCCTGACCC GAGGCCCCTC AGCACGTCGT GGCAGCCTCA GGCTTTGAAC 1620 CCAGGACTTC CGGTTCAAAG TTCTGCTTTT GCATTTGCTG CTCCCCCTGC CTAGAATGCT 1680 CTCCCCTAGA TCTTTGCCCA GCCCCCTCCT TCTCATCCTT CCCTAATCCC ATCATCTAAA 1740 GCCCAGGCAC ACTCCCTCCA GGGCAGCACC CATCCCCCTC CCTGCCTTGC TTTCCAAGCG 1800 TGTTGTCTTC CACGGAGAGG GCCCTGTCTA CCTGATCCCC ACCTCCCCCC ATGTTTAGGC 1860 TGCCAGCCCC ATGAAGCCAG CGCCACGGCC GTCTGCCTCA CATCAGTCTA GGTCACAGCT 1920 GTGTTGCCAG AACCTGGCAT GTGGTTGTCT TCAGTAAATC TTTGTGGAAT GAACAAATGG 1980 GGGTCCATGA AGACCCCATA GCCTGGAACT TGGGCCTCTT GTTCTGTGGC CATGGCAGGA 2040 GGGATGCCAG GGGGACCAGC ACTATGGGCC ACACCCTTCC CAAAGCCTAG CTGTGGCTGC 2100 AGCCGCCTCT GATTAGGCCC 2120
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