Tag | Content |
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EnhancerAtlas ID | HS031-01387 |
Organism | Homo sapiens |
Tissue/cell | Denditric_cell |
Coordinate | chr1:151893780-151895290 |
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) |
ESR2 | MA0258.2 | chr1:151894819-151894834 | AGGTCAGCCTGCTCT | + | 6.04 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 151894048 | 151894438 | chr1 | 151894842 | 151894943 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I151919 | chr1 | 151892234 | 151895202 |
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Enhancer Sequence | CGCCAGCCTC GGCCTCCCAC AGGCAAGATC ATAAATCAAT ACATGAAGGC TACACATTGG 60 TTTTGGCCTA AAGTGGCAGG ATAACTTGAA GGGGATGGCT TACAGGGTCA TAGGTAGACT 120 CAAATATTTT CTGATTTGCA ATTGGTTAAG AAAGACAAGC TTTGTTTAAA ATTTGGGGTC 180 AGCAGAAAAT GTTAGATTTG CTTTGTGGTT GTGACTCCAT CCAGGTTCCT CAGGAAGAAA 240 TTTAGAACAA AGAATTGAGG CAGGAGCATA GCAGAGGGAA CTGGAGGTTG GATAAAGGGT 300 GGAATGAGTA GGAGCAGAAG AAAGATAAAG AGGCAGGTGA GCAAAAGCAG AAGCAAGACA 360 AGAAGCAGAA GTTGAGCAAA ACCAGAAGTA AGATACAGAA GTGAGTAAGG AGCCCCATGG 420 TTGGCTAGAT CTGGACTAAA CCAGTAAGGG GCAGCTCCTA AGAGATGGGC ATGCCCGCTA 480 GAGAGAAAAT ATATCCTTAA AATGACCCCA CAATTACCCA TGGTGATTAG CTACTTAAGG 540 CTCATGCATA TGGGCTGTAT ATCATGCATG TACTTAAAAT TATGGAATGG AAGTGTCACG 600 CAAATGCACA GAGGCCAAGA AACTGAGCAA CCCACCTGTC AATCAAAAGG CACATGCTGG 660 CTAGAGATTA GGTAGTTTGG GGAAGAGAAG AAAAAAACAG GCTGGGCTCA GAGGCTCACA 720 CCTGTAATCC CAGCACTTTG GGAGGCCGAG GTGGGTGGAT CACTTAAGGT CAGGAGTTGA 780 AGACCAGCCT GGCCAATGTC GTGAAACCCT GTCTCTACTG AAAATACAAA AAAAAAAAAA 840 AATTAGCTGG GCATGGCAGC GCACACCTGT AGTCCCAGCT ACTCGGGAGG CTGAGGCAGG 900 AGGATCTCTT GAACCTGGGA GGTAGAGGTT GCAGTGAGAC GAGATTGTGC CACTGCACTC 960 CAGCCTGGGC GACAGAGCAA GATTCTGTCT AAAAAAAAAA AAATGACCCA AAATACACCA 1020 AACTGATCTC ATTTTTCAGA GGTCAGCCTG CTCTTCCCTC TCCGAGAGTG TGTTATTGTG 1080 CTTGATAAAC TTTTTGCTGC TTTGCTGTTT GTGCGTGTCA CTTCCACTTC TTTGTTCAGG 1140 ACACCAACGG CCTGGAACTG TGCAGGACTA TCCAGTAACA GAATGGGTGG TCAGAGTTCA 1200 GTCTTCAGTG CTCCTGTAAC CACCCAGTGG GTTCTCCTTG CCTGCTGCCT AGACAGAGAC 1260 AGTTTATCAA GACAGGAATT CCAATAGAGA AAGGCTTTAA TTTGTGTAGA GCCTCCGTAT 1320 GGTAGACTGG AGTTTTATTA TTACTCAAAT CAGTCTCCCC CAAAATTTGG GGATTGCATT 1380 TTTTAGGGAT AATTTGGTGG GTAGAGGGTT GGGAAGCAGG AATGCTGATT GTTTGGGTGG 1440 GAGATGAAAC AGGGAATTGA AGCTATCCTC TTGTGCTGAG TCAGTTTCTG GGTTGGGGCC 1500 ACAAGACCAA 1510
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