Tag | Content |
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EnhancerAtlas ID | HS187-14932 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr2:242382680-242384140 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr2 | 242382742 | 242382880 | chr2 | 242383219 | 242383586 | chr2 | 242383200 | 242383800 |
| | Number: 1 | ID | Chromosome | Start | End |
GH02I241443 | chr2 | 242383361 | 242383530 |
| Enhancer Sequence | AAAGGTGTCA AAGGGCCACT GCCTCATTAT TGACTTGAGA CCCAGAAATA GTGCTGTGTG 60 TAGATAGTGG TCTTGGAGAG GCGTTGGTTT AAAATGCACT TATGTAAGTT TGAGCTGTTT 120 TCTTTTCTTC AGCTTAATTG GGAACTAGAA GATACGTGGT TGCAAAAAAA GCAGAACCAG 180 ACACACCATG GGCATCATTC TGTCCCAGGA CAATGGGAAG GGTCCCAGGG GCAGGTGTGC 240 CAAGGTGGCC CTGCCCACCC ATCCAGCGTA CCCGTAAACA CATACCAGGT GCCATGGGCC 300 CTGCTGGGTA CCACATGGAG AGCTTCTCAG TCTAAACCAC CATAAAAGTC AAGGCTGATG 360 TTTGTGGCAC AGAGTGGGTA GGTCCATCCA GGGACGTCAT GGGGAAACCA CTGCCATGCA 420 GCTCAGCACC CACAAGTGCC GGTCTCAGGC CAGCCCTAGA TGACACTGTT CAATTTGTCA 480 AGTCCACAGA TAGGGTTGGG GTTTTTGTTG TTTTTCTTTT CTGATCTTAC CTAGTAGTGC 540 AATACCACAT TTAAAGTTTA ATTCTCTTCC CAGAATGTCT TGTGGAAACT TTACATTTCA 600 TTCCTGTTCA CATTGTAAGA TCTCTGATGT TTTGCCTGGA TGGATTTACT GTGATTGCAC 660 AGGGACCACG TGGCTCAGGT GTCTGAGCCA TTGAGGGCAT CTTGCAAGGG CTGGTTTTCC 720 TTTTCTCATC AGTGTTGGCT GGATGCCAGC AGGGGTTTTG TGGCTAACCA CATCAGGCAG 780 TTTCCCATTT TTGTAGCTTT GTTATACCTA AACCGCAGTC TCATCATTTT GCTTATGCAG 840 CTAGAAGTTT CAGTCTGTAT AGTTGTTATT CATTCTGTCC CTGGTAATTT AGACCTGCCT 900 TCTTGATGCT TTAGGGGCCA TTGGGCACAG CTTTCTACAT TGGCTAACAA ATACCTGTGA 960 AAATGTTAAC AGACAGAAGC GCAGCAGTGA ACCTGAGGTC AGGACAGGAC TGTTTGGGAG 1020 GTTCTTCTTT TCTTACTGTC ACTCCAAAAA TAAACCTTGG ATTTGTGTGC TGGGGAGAAA 1080 TGAGTATAGA TAACATTTAA AACGTTTTCC TAAACCTTAG TATTCATATG GTAGCTGATG 1140 GTTCCTCTCC CCTTCATTAC TGTTGCCTGA CGACGGTCCT TGCTGATGCT GTGAACTAAC 1200 AAAGTTGTCT TTTTGTTTTT AAGGGAACCC ACCCTGGCGT CTGGACAGCA GGTTAGGTTT 1260 GGGTGGTTTT GAGCTAGCAC TGCTGTGGGG CAGGGGTGGC CGCTCCCTGG TGAAGCTAAT 1320 GCTGTGGAAG CTGGAATGTT CCTTCCTAAG GAGTGGGATC ATGCCCCTAC CCCAGCAGAG 1380 GTATCTCATC ACTCGCTCAT GTGCGAGATT CTAAATAAAT TTTGTTCTTG GGCATCTTCT 1440 ACTAGGCCTC CTATAAAATA 1460
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