Tag | Content |
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EnhancerAtlas ID | HS176-38520 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr7:127540100-127541520 | 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 |
chr7 | 127540800 | 127541000 | chr7 | 127540400 | 127540659 | chr7 | 127540360 | 127540800 |
| | Number: 1 | ID | Chromosome | Start | End |
GH07I127900 | chr7 | 127540369 | 127541599 |
| Enhancer Sequence | GTCATTTTAT TTTCTTTAGA TCTCTTTCAT GTATGAAAGT AGTTCTTTTT GTAAAACTCT 60 GTTGAAAGCT CCTGCTCCCT CAGAAAATTC ACAGATACTT TAGGGTGGAT CAGAGATATT 120 TCTAGCATCT GAGCTGACGT GCACTATGTC CCCAGGTTAA GAATTCCTGA TGTGATAACT 180 ATTTTATGAT TGTGATAAGG TTGGATCTAG CCATAAATCC TTTGAATTTC TTTGTAAGCT 240 CACAAAAATA TTTGTTCAGA ATAACAATCT ACTGTCGTTG AATTGGCAGT AAGATGGAGG 300 CCTGTTTGTT GGCACGGGAG GGACTGTGAC TGCGGTGCTC AGACATCCAG CTTGGAGAGC 360 ATTGGTCTTG AGATTTTCTG GATGAACTAG AGACTGCAAA CCTAAGAGCA GACTCTTCCT 420 TGGCATGAAA TGTGTGCAGA TTCTAATCTT GTGCTGAGGC CATGGAGATG ATCTCCCTGC 480 AAAAATGTTG TCTGCCTTTG CAAAGTTGTA GGTTTTTTCT TCTAGAGGAA AAGCAGCAGC 540 TAATATGTGA GAGTTTCGAG CTTTGCTGTT TAAAGAAAGC AGAGTTTTCC AGTGGTCTGA 600 ATAGAGTTCA TCTTCCCACA CTGTAGTACC ATACAGCCCT GTGGCTCCTA GAAACAACCT 660 AGAAAGCTGT GTTTTCATCT TTCTGTTGCC CTGCCACTCC TTGGCATGTG TGTGGATATA 720 TACTTTCTTT CCCTGACTGG TGATGATGTT TGTCAGTTAT TGACACTGGT AGTCTTTGCT 780 GTCTTTGTAC TGCTGCATCT TGGAGAAGAA AGCTGCTGAG AGGAGTAGGC TATGTTCTGC 840 CCCACTGTTT CCTTTCTGCT GGCTGGCCTG CACACTAGCC TGCCTTTGTG AGGAAGCGGC 900 TGTTAAGCAG ACACAGCAGG AGAAGTTTAG AAGTCAGGAG TTTCATTCCT TGCCTAATGA 960 AAAGGGATGC AGACTTGTGG CTGAGGCCAA CAGGGAAAGG CAGTATGGGG AGCAGGAATT 1020 AGTGTTTGCT CTGTGGAGCA GATAAGGTGG AAGCCAGCCT GCGGTCTGCC TACCTTCCCA 1080 TGTCTCAAAG ACAGAGCTCC ACAAATCTAT CCCAGAGAAA CTGGGTTATG TGAGATGCAG 1140 AGGAGAACCC CACTGAGAAG TGGTAGCAAG GCAGTACACC TTGTTTTCAG CAGAGCCTGG 1200 GTCTCCATGT CATGTATCCT CATAGCCTGG AATAAAGATG GTACTCTCCC TTTGCAGATA 1260 GTGGTGGCAG GCCTCCCCTC TTGGAATTTG CTCCTCTCCT CTGTGAGATT CATTCCTGAA 1320 TTCCTACTTC CCCCAGATAC TCTTTCGTGG AGAATCTCTT GCTGTGGCAT CAGACTTGTG 1380 ACAAGCAGAG GGAGGTTTTC TGGAAATGGC TCACTCAGCA 1420
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