Tag | Content |
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EnhancerAtlas ID | HS052-00264 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:11340160-11342610 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RELA | MA0107.1 | chr1:11342410-11342420 | GGAAATTCCC | - | 6.02 |
| | 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 |
GH01I011280 | chr1 | 11340140 | 11343382 |
| Enhancer Sequence | AAAGTGACGT TCAAACTAGG ACTTGAAGAC GGAAGGATAA GGAGCTGGCC ACGGGGTGGA 60 ATTGGAGTCT GATTGTGATG CTGAGTCCTC CAGGGCTGAA GGACCACTAA GTGCAAATGT 120 GGTGGGTGAG AGAGAGTGTG ACATTGGCTA GGATCTACTG AAAGGTCTGT GTGAGCCAGA 180 GGGGGCATGA GACACAGTTG GTGAGTTAGG CAGGGTCTCT GTCATGGCGA TCTTAACCAG 240 TCCTACTCCC CAACCTCCAG GGCTCAGTCC TTGGGCCTCT TTTCTCTATC TCCATGTACT 300 CCCTTGGTGA TGTAGCTCAT GGCTTCAGAT GCCATCTGTT AAGCTAGTGA CTCTTAAACT 360 CCAGACTCAT ATCCAACTTC TTGCTCAGCA ACTTCTCCTA GAACTGTCTC ATAAACATCT 420 CAAGCTTAAC ATGTCTGAGA CCAAATTCTG ATCTTCTCCC CAAGGAAACC TGCTTCGCCC 480 ACAGCTTTTT CCCCATTTTG CTCAATGGCA GCTTCATCCT AGTTCTTCAG GCCAAAAGCT 540 GTGGGCATCG TCCTTGACTC CCACGTCTCA CATCCAGTTC ATCAGCAAAT TCTGTTGACT 600 CTCCTTTCAA AATGCATGTA GGATCTGACC ACTTCTTACC GTGTCCAGCC ACCACTGTGA 660 TCATCTGTCC CTGGATTTTT GCGGCAGGCT CCCAACTGGT CTCTTTACCT CTGTTCTGGT 720 CCCATTCAGG CTGTTCCCAC TCAGCCACCA GAGTAATTCT GTTAAAATAT AGGGCAGCCC 780 TGTCAGTCCT GCTTAGAACT CTTCAGTGGC TCCCATCTTG CTCAGAGTAA AGGCCAGGGT 840 CTTTACAGTG ACTCCCTAGG GCCCTACATT CTTTGCCCAC CTTTTGCCCT CCCCCCAGTT 900 CTCTGACCCA CCCTCCTCCT TTCTTCCTGC TCATCCTGGG CCAGCCACAC TGCCCTTTCT 960 AGTCCAGGAG CATGCACAAC CCCTCCTGCC CCTCCCTCAG GTCCTTTGTA GATGCAGCTT 1020 CCTCTGTTTG AAATGCTTTT CCTGCTTCTA ACCATGTGGT TCACTTTCTC ACTTCCTTCA 1080 CCTATTTGCC CAAATGTCAG CTGCTCAGTG AGGCCTTGCT TTCTACCTTG CTTAAAATTA 1140 CACACCCACT CCGTGCCCCC ACCTGATACT TCCCCTGCTG CTCTTCTCTG CATTAGTTTT 1200 CCTCATAGCA CATGTTACCT TCTAATGTGC CATATAAAGT ACTTAATTGG TTAATTATCT 1260 TCCCCCTTCG ACTGCGAGCT CCCTCCCTGC AGTCAGGGAT TTCTGTCTCT GGTATTAGCT 1320 GAACCCCTAG CACCCAGAGC ACTGCCTGGC ATGTAATATT ACTTAGTAAA TATCCAGTGA 1380 ACAAATGGGA AGGCATTGAA ATATACTGAG CAGAGTAGTG ACATAATCTG GTTTAAGATT 1440 TTTTAAACAT TGTCTTTTAT TGACATATAA TTGACACACA GTGAAATGCA CAGGTTTTTA 1500 GTGTTGCAGC TTGATGAATT TTGATAAATG TATACAGTTG CATAACCCAC ACCCCGTCAT 1560 CATCCAGAAC ACTTCCATCA CCCCCAAAAG CTTCCCAGTG CTTCTTGCCT GTCAATCCCA 1620 CACTCCCTGC CCCCATCCAG AGACAGGAAA AGAACCACTG TTCTGATTCC TCTCACAGAG 1680 ATTAGTTTTG CCTGTCATAT AAATGGAACC TTTCACTATG AACTATGTAT GTATGTATGT 1740 ATGTGTATTT ATTTCAGTCT GAGCTCTCGT CTGGCTTCTT TTGCTCAGCG TGATGTTTTT 1800 GAGATTCATT GTTTTATTGC GTGTATCAGT AGTTCCTTTT TTTGCTGACT AGCATTCCAT 1860 TGTAACATAC CACAACTTCT TTTTATCCAT TCTCCTTTTC AGGGACATTT GGATTGCTTC 1920 CATATTTTGG CTATTACGTC TGAACATTCA TGTTCAAGTC TTTTTGTGGA TATTTGTTTT 1980 CATTTTTCTT GGGTAAATGC CCAGGAGTAG AATTGCTGGG TCACAGGGCA GATGATGTTT 2040 AATTTTATGA GAAACTGCCA AACTGTTTTC TGAAGTGGTT GTACTTCTTT ACACTCCCCC 2100 CAGCAAGTGT TCCAGTTGCT CTGCGTCTTG CCAACTTTTT GACTTAAGTC TTAACAGATT 2160 CATTCTGGCT GCCGTGTGGA GAACCGGCCC AGTATTTCAC TGTGTAAGCT CATTCAGAAA 2220 ATGGGGTTGG GAGAGGAGGA ATGCCTAAAA GGAAATTCCC AGATGGGCCA CGTCTCTGAA 2280 TCAGGTAGAG CACATGAAGC CTTGGGCCAT GTATCAAATG CTAGGAAACA GCTTTCTCCC 2340 CAAGGGCTCT ACTGTTTTCT TGTGTCAGAT AACCAGATCT TTTTCCTCCC CAGAGTGGGT 2400 TGCTCTTGGT TTTGGGGTGG GGACAGAGAT CTCTGCTCAA CCTTGCTTAC 2450
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