Tag | Content |
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EnhancerAtlas ID | HS104-12046 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr11:113384480-113387050 |
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) |
ZNF263 | MA0528.1 | chr11:113386415-113386436 | TCTCTCTTCTCTCCTTCCACC | - | 6.1 |
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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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Enhancer Sequence | TGCAGGTGGT AAAATCCATC ACCTTCTTTG ATTGTCATAC TGATCCTTAA GTGAGGCAAG 60 ACAGGAGATA TTGTTCAGAT TTTGCAGAGG TAGAAATTGA AGCTTGAAGA TGGGGAAGTT 120 CCAGGGTTGA GACCTGAGAC CAGGTCTTCT GATGCTCTTA TTCTGAAGCC TTTCAAGGAA 180 GGACAACTGG TCCTCATCTG TTGGCTGGAG CTGGAAGGAG TGACCTTTGG CAGGTCCTGT 240 TGACCAGGTG TCCAATGGCC TTTACCTCTG GACAGGGCAG CATCTCCTCC AGTCCTCCTG 300 GTCCTAGGAG ATTAACCGAT CAGCAAATAA TCATGGATTG AAACATAATT TGCTGAAGGT 360 ATCATGGAAG TTACAAAGAA GGATGATTCC TGCTCTGACT TACGGAGCTC ATGGCCTAAA 420 TGGGGAGCCA AGACCGACAG ACATTTATGA TGAGTAGCGA TAGTATCACA TTCAGTTTAT 480 CTGAGAGTTT GTCCAATGTC AAAGCACGTT ATTACTTGGG ATTATAATCT CCTCTGTATC 540 TGTCTGTATG TAAAGTATTT GGCTTGATAT GCCCTGGAAA GCAAAAATGT GAAGCTTTTA 600 TTATTATTAT TACTTAGATT ATTTTTCACT GGACTGCACA CTACTTGAGG GTGAAGCTAT 660 GTTTTCTTCA TCATTGTGGC CTCTGCACAT CATTTTGCGT GTTTTGAAGG AAATACAGAA 720 TTAATGTTTG CAAATGTTGA ATGAATGAAG GTCATTTAAA CTTCACAAGA AGTCTGTGGA 780 GTGATTTTTT TTCCTGTAAA GACAAGGAAT CTGAGACACA AGTAGGGAAA GTGATACGCA 840 GTTAGTGACA GAGCTCCTGG GGCAAGAAGA CATCCTATGC CAAGTGTAAA AGGAAGACAT 900 GGGAATTCTG CACTGGGAAG GTCAGGGAAG ACTTCATGGA GGAGGTGTCA CTTTTATAGG 960 CTCTTTCATG AGTGAGTTTC AGAAAGGCAT AAAAGAAAGA GGTATCAATG AGGGGGAACT 1020 GCATGAACAA ACTCCTGAAG AGGCAGGAAT GCACCGCACA GAGAAGGTTC AGTGACAAAG 1080 GGTCCAACCA GGTAGACAGG GACCAGGTCT GGGAGGGCCT TGAACATCAA GCTGAAGGTT 1140 GAGGCTAGGA CTGGGGCACT ACCTGGACCA CTGTCCACCT GAGGACACCA ACTTTGGGCC 1200 TACATCCATC CAATGTGGGG GCTCTGTGTC AGTGCTAGTG AGTGTCAGAT CCGGGAAGCA 1260 TGGGAGCACT TTCACCCAGG ACAGGACAGG GCCGTGTGCT GGGCAAGGTG AGTCATTCAT 1320 CATCACCAGG AAAAGGTGAG CAATCTGCCC AGGCTCTAAT GAGAAAGATT GGAGCCCACA 1380 AGCACATGTT TATTACTGAA GGTGCCACAT TAATTATGGA CTCTGAAAGG GGAGGGAGAA 1440 GTCATGGGCT CACACTGGGA AGCAGAGGAC TGCCATCCAT CTGGAAGAAG TGGCCAGAGT 1500 GATGTGCATG CTACTCTGAG CCTGGCCCAG ATATTGCTCA GTGCCCTGAG AAATATCCAC 1560 ACAGCTCGCA TTCATTCATT TGCTCAGCAA ATATTCCTTA AACACCAACT GGTCACAAGG 1620 CACCTGTGTA AAGGCCTGGG CTCGGTGCCC TGGAGGACCT CAGAATCCAG TGACTGTTGG 1680 AGACAGATGC ACAATCAGAT ATTTGGGATA AAGTCTGCTG GGATGGAGTC GAAGTGTGGG 1740 CACATCACCT GGCCTGGAGG TGACCAGGAT GGGTAGGAGT TAGCTACAGC ACCCTTGTAA 1800 GGCACTTAAG GGGCTGATTC TTCAGCCTGT CAGCAATGAG AGCCACTGAA AGAATGGAGA 1860 GGGATGTCAC ATGGTCAGAT ATGCTCTATT GCACTGCACA TCACCCCTGG CCACCCCTGC 1920 CTCCTGATGG GGCCTTCTCT CTTCTCTCCT TCCACCTTGC CTGTCCTGGA CTCCATCTCT 1980 TCAGGGACAA GGGGTGCCAG AGTGCTATGC TATGGGGCTT CTGGAATTGG TTTGTCCACA 2040 CCTGGGCATA TGTTTGAGGG CAGGACGACC ACAGGTGGGA TTCATACCAC ATGGACTAAG 2100 TGCTCATTTT GTTGCCTCCA TCCAGCCCCA AAGGGCTACG GAGGCTCCCC TTGGCCTAAG 2160 GTATAAGGCA GCTATAACAG ACCAAGAGCC ATCATGGGAC CTTAGGATCA GAATGAGGGG 2220 GCTGGAGCCT CCTAGAGACC ACCTGGTGAG AAATAGTGCA ACAGCACTGA GCAGGACTCT 2280 GAAAGACCCC AGGTCCCCAG CACAGGAGCT CTGTCATCCT GATTCACCTC TCAGGCCTTA 2340 GCAAGCTCTC TTCTCTCTAC CTGGTCCTCT TCTCCACTCT GCCCTCCCTC CTGCTCTCTC 2400 TTCTCATTTC CACTGCCCAT TCACCTGGGC AAGGTAATCA TTCCTCTTCC CCAAATCCTT 2460 GGAAACCAGA GCCCTGATCC TAGTGAGAGG TGGGAGCAGG ATTAGGGAAA GAAGGATCCC 2520 AGACCAGAAT TCAGAAAGCA TGTGTCCAAG GTTCAGTTCA GTATTGAGTG 2570
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