Tag | Content |
---|
EnhancerAtlas ID | HS148-18536 | Organism | Homo sapiens | Tissue/cell | NHLF | Coordinate | chr8:142374530-142377300 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_68690 | chr8:142376088-142378743 | H9 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 142375764 | 142376252 | chr8 | 142376716 | 142377281 |
| Enhancer Sequence | TGCTTGCTGA GCTCTCCAAA TGGGGTCAGA CTCACCCCAG GTCACCTAGC AAGTCCCAGG 60 TGACCCTGGC CAGAAGCCAA GTCTTTCTCC CTGTCCCCCA CGCCCACAGG CCAGGGCTCC 120 CTCCACCCCA GTGCAGAGAG AGACGTCACT GGTGGGCACA GACTGAGCTC TGTGGGGAAG 180 GACACCTGGG CCCCATCTGA CCCGACTCTG CCTCAGTTCC ACCAGCTAAG AGCCCTCTTG 240 CTGAGACTGC GGCTCTAACG GAAACACCAG TGTCTCTGGG AGGGGCATAG CCAGTTGGAG 300 GTCCTGCATG TCACCTGCCA GCCCCTCCCT GCCTCCCCAT CATTGGGTTC ATTGCTCACC 360 TCTAGCTGGG TGTCTCTGGG AGGGGCATGG CCAGTTGGAG GTCCTGCGTG TCACCCACCA 420 GCCCCTCCTT TCCTCCCCAT CACCGAGTTC ATTGCTCACC TCTAGCTGGG ATAGCCGTAG 480 CTGCAGCAGC TCCTGAAACC CCTCCCCAAC CTCAGCCTCT CCAGGAGCTG CTGGGACAGG 540 CATTCTGTCA TGTGCACCTG CCTGGCCTCA GCCTGGTCCT TCCGCCTGAA GCTCCTCAGC 600 CTGGTCCTCT CAGCCTCTTC CCTCTGCATG TGCTGTTCCT TCTGCCCGGA ATGCTGTTTC 660 TCTCCCTGTG CCACCTGGTG AAGGCTCCGG GCACCCACAG TCATTGTTCC ACAGAGCTCT 720 CCCTGAGCCC CTCTGATGCC CTAGTGCCCT GGATGCCCCT GCCCCAGGGG GAGAGCTATG 780 ATCCCACAAT CTGAAGGGCA CCCGCTGGGC TCATCCTTCC CAGGGTCTTA TTGACTTCCC 840 TCAAGATGCC CCTGGGTGGG TGTTTCTGGC CCCACTGTGC CTGTGGGGAA CCAATACAGA 900 GGGGCTAAGT CATGTGTCCG GGCTCACCCA GCTGGGGTGC AGGAGGGGCT GAGCTCTGCC 960 TCAATCTGCC TGCTGGCACT TTGTCCCAGT GCCTGGGATC AGCCTTCTGC GGCACCCAGC 1020 CCTGTGTGTG GAGGGAATCA GAGGCCCCAG GCCACACAGC CCCGTGCAGT TTGGAGGTGT 1080 CAGACCAGGA CTTAGACCCC AGCACTGCGG GCACAAATGG GTCCCAGGCA GACCTGGCCC 1140 CACCTTTCCG AGCTGACAGC TCAGGGTAGG GTGGGAGGTG GCTGGTCACG GCCGGGATGG 1200 GCCTCAGGAC AATCAGAGGG AAGAGCGCTC CCGGCAGCAG GAAGGGCACA GTGAGCATGA 1260 AGGGCCAGAG GTGGGAAGGA GAGTCTGTGT TCAGGGCTCT GTGAGACACC GGGGGCGTGG 1320 GGAGGGCTTT GGGACGTATG GTGAGGGGAT CAACTTAAGG TTCTTTGGGC CCTGACGCCC 1380 CTCCTCAGGG AGGCCCTCCA GAGCCCACAG CCCCGCACGC CTGCACCGCC TGGCTTCCTT 1440 CGCAGTGCCC TGCCACGCGC AGTTCCCTAT GTCCCTGCTT TCCTGTTCGC TGTGCTTCCC 1500 TCACTGAACT GGAGTGCCTC AGGGGCCCTG GCCTTGGCTG GCCCCTCTGA GTCACTGAGT 1560 CACTGCTGAG TGATGGAGTG GATGATTTTA GAATACCCCT CTGATCTCCT TGAGCCTCAG 1620 TTTCCTCATC TATAAAGAGG AGATGCTAAT ACCACTTAAC AAGAAGACAA TGAAGCCACC 1680 CCGTGGGCTC CAGGAGCTGC TCAGAAATGG TCCAAACTGC ATGGCCCCCA CGCCCGGCTC 1740 TCCAGCCGCA GACCCCGCCT TTGCTGATGG GCCCACACCG TGTGGCTCAG AGAGGGGCAG 1800 CGACTTGCCA CGGCCACTCA GCAGACCGCC CTGGAGCCCA GCGACTGGAT GAGTCCTGGG 1860 GGGAGAGGGG AGGGAAGACC CAGGATGACC AGCTGTTGAA GGAAGAAGAC AGGGCAAGTG 1920 GACAGGCCCA GCCTCCTGCG GGGTGCATTC CCCGTCCTGC GAGGTCGCCA GCTGCTCCAC 1980 GTCTGCCCCG CCAGCACCCT GGCTGCTGGC CAGTTCCCAG CCCGCTGCCC CCTCGGGACC 2040 CTGTCCTGCC GCCTTCTCAC AGCGCAGTCC CAGTGCGAGC TTCGCGGGGC TGGAGCCAGC 2100 TTCTAGGTCC ACACTGAGGG CTGGCAAGCA AGCCTTCCCT GGGACTCAGT TTCCCCACCC 2160 CTAAGGGGTA GAGACAGCAC CAAGGCTACT GCAGAGGGCC TGAGCTGTGG GATGGCAGGA 2220 CGGGCACTCT GAAGAGGGAG CATGGCGCTT GGAGCCCATG CCCACAAAGC CCTCACCATG 2280 GCCCTGCCCC AGCTGCGGGG TGGTGGTGGC TGAGGCCCCA GAGCCTGCCA AGTGCCTCTG 2340 GGGTCCCCCA ACTCTGTCCC TGGCTTGGCC TGTGGGCCAC CCTGCTGCCT TGCCAGGTGG 2400 GGAAACCAAG ACCCAGCTCT GGGCACCCAG CAGATGCTCG GTGAGTGTTG AACGGAGGGA 2460 TGAATGAGTG AATGAATGAA ATCCAGAGTT GGGTGGGCAC CTAGCAGCGC AGCTCCCCCT 2520 TATGCAGCCA GCCCAACTCA CGCCCATGTT CTCCCTCAGG TCTCTGTTTT CTCATCTGAG 2580 AAATGGCTCC CTGTCCAGCA GGACCTGCTC TGAGCTCTCC CCAGCCCGGA TCTGGAGGCA 2640 GTTTCTCTGC CCTGCCCTTC CCACTCCTGC TTGGCTGGGG GTGAGAACCC CTGCAGGGAG 2700 CAGCTCAGGA GCCTCCTATC TAGGGAAGCT GGGGAGAGGG AGGCTGGGGC CAGCCCACAG 2760 GGGAACTTAC 2770
|
| |
|
|
|