Tag | Content |
---|
EnhancerAtlas ID | HS052-00071 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:2312430-2314770 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:2313353-2313372 | GGCTGCCCCCTGGTGGATG | - | 6.92 | MAX | MA0058.3 | chr1:2314106-2314116 | AGCACGTGGT | - | 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 |
GH01I002381 | chr1 | 2313039 | 2313840 |
| Enhancer Sequence | GCCGTTTTCT CTCCAGGTTG AAGGTGGAGG AGAGGCACTG TGACCGGAGG GCCCAGCGCT 60 AAGATGCAGA GCAGAGAACT GAGCAGCTGA GCCAAGAGAG CCTCGCTTCT CCTCATTATC 120 CAGAGTCCAA GGGACAGACC TGGTAATGTC TTCTTGCACA AACAGCCATG TGAAAACCTC 180 CTGCCTCTGA AGCGTGGTCT GGCAGCCACG GCTGTGCTGC GTGGGAGGCG GCCCCGGCCC 240 AGTCCTGACC TGAGGGGATG GGAGCCCAGC CTGTCCTTTT GGCCTCGGGC GCCCTTCTCA 300 GCGTCTACAT CGGTCTGGGC AGGAGGAATG CCTGGAGAAG GCGCTGGAGG AGCAGGCAGC 360 TCACTGGCCA TGGTCTGCCC GTGCCTGCAG GTGTCAGCAG CGTGGACGAG GCCAGGGGAC 420 TGCTGCCACC AGTGACACTG CCCAGAGCAC CCCGTGGGGC AGCAAGCACC AGCACACAGC 480 AGTGTCCCCA GGGAGCTCAA GCCACGGGCC TGCCTGGGGA GGGTGTGCGG GCCTCGGTTG 540 GCAGGCGGTC CCAGGGCCTG CCCAGGTCTC CCAGTCCTCT GGGCCTGGAC GGCAGAGGAG 600 TGGGGAGGTC ATGTTATAAC CCCAGGGAAT GTAGGTCACG CGAAGGGTTT GGCACCAAGA 660 CTCTCGCAGA AATCCTCTGC AAAACCCTCT GCAGAATTCA AGGTTTTACC ACCAAGGGGA 720 GAAACCATCC CAAGCAGAAA GGCCTGGGGG GCCGCTTGGG GGCCCGGCTC TCAGGAGTAC 780 CCAGCCAGCC CTTGGGCCCA GTGGCCATCC CAGGCCATCC TCCCCCGTCC AAACTCATGG 840 CTTGGGAATA AGCTCTGGGC TCCCGGGGAG GAGCTGCCTC CCTCCAGCAA GGCCCGGGCC 900 AGTGTGGTGC CGGGACAGGG CTGGGCTGCC CCCTGGTGGA TGCGCTGAGC ACCCTGGTGC 960 TGTCAGCCCA GGAGGGAGGG CGCCGTCCCT TGCCTGGTCC TCTCTCTTGG CCCAGGGCGC 1020 TGGTGACCAG CAAGCAGTGT GGACCCGAGT TGGCGCCTGG GTAGTAGCCA GGGGACCTGT 1080 GGGACAGAAC AGCCTCTGGG GACAGGGCTA GGCTGGGAGT GGGGGTGGGG AGGACAAAGC 1140 TGTCCATGGT CCTCTGGAAG AACAGGAGCT GCTTCTCGCC CGGCCCAGGC CGGAGGGGAT 1200 GGCCCTGTCT GGCAGCAGGC GGCACCTCTG TGTCCCTGGG CCATGAGACA GGCCCTGACC 1260 AGGTCCTCCT GAATCTCAGG GAACATGAGG ATTGGGTGAG TGGCTGGGGG CCCCCAGGGC 1320 TGTGTTGCCC TGGTGAGGGA GCCTGCCATC CTAGCACCTC AGCTTCCTCA CCTATGCCCT 1380 GCTCGGACTG GTGGGGATCA TGAGCCAATG CACCGAAAGG CTGACAGCAG CGCCTGGCAC 1440 CCAGGAAGTG AAACCACACA CCCGAGCCCA AGCTCCAGAG CTGTGCACCA GCGCCGGCCC 1500 CAGCTTTGCC CTAGCCCTGC AAGGCGAGGG AATCGTCATG GTGGCAGTGG GGTGGGGGCC 1560 CGGGTGTGCT CGGGTGGGAA GGGGCGGGCA GAAGAGAATT CTGCCCAGGG ACTCCCTTAG 1620 GCGCACTCTC CCACTGCCAC TCTGGACAGT GAAGACAAGG GAGCAGTGGC TGCCCCAGCA 1680 CGTGGTGAAG TCTGGTCCTG TAGGATGGAC ACAAGTCCCC AGGGGAGAAG AGGCTACAGC 1740 ATCTCCTGCA TATGGCTCAG GTGAGAACCC GCAGCACCAG CCCAGGCCAG CAGGGGCAGC 1800 AACGACGCTG ACATGGGCTC CCGTGGTCCA GCAAGGACAC TGCCAATGGT CAACTGCCCT 1860 GAGCAGGGCT GGCAGACCCC GGAGTGGGTA TGGGTGGCAC TTTTACCCAA GCAGGATGCT 1920 GTTTCAAGAG CAGGGAGGGT GGACATGCAT GCGGAGGGGA GCCACACTGC ACCTCCCGCC 1980 TGACCACCCC TCCAGGGGCC CCACATCTGA CCACCTCTGA GGCCCTGCTG CGGGCAGCTG 2040 TGCCAGCCAG GATGAGTCTC CCATCCCCAC CCCCAACTCC TCCATCCCCA TGTGGCCCCA 2100 TGCCAACTGC CAACCCATCA CCTCTCAGTT CCCAGCACCC CCCTTCCTTG CCCACTTTTG 2160 CCTGACGGGA ACTGGACCCT GTCAACGTTT CTCCTTTGCC AACAAGTGCA ATGCCAGGCT 2220 TTGTCAACAG AGAACAAGGC GGGACTGTGG GAGGTAGTGT TTCTACTTTA ACTCCTATGG 2280 CCAGGGCCAG TGGCCTGTGG AACACCCCAG AGTCTGGTCT CTGGCAAGCG TCTCCTGCAC 2340
|
| |
|
|
|