Tag | Content |
---|
EnhancerAtlas ID | HS050-10958 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr11:3155410-3158070 | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 3156864 | 3156988 | chr11 | 3157477 | 3157742 |
| | Number: 1 | ID | Chromosome | Start | End |
GH11I003136 | chr11 | 3157481 | 3157730 |
| Enhancer Sequence | CTTCCAATGT CACATCAGAT GCTGGGTCGC CTCGTGGGCC TCCTGCTGTC ACCAGACAGG 60 ACAGGAAGGG CCTCCTGCTC TCCTCCAGGG GCCCTGTGTT TGCCACTGTA GCCATCCGCT 120 GGCCACCCAG CAGGCACGAC TTCCATTGTT GGGGGTTGCC TGTGTCCCCA GGAACCAATT 180 CTCCAAGTGC CCCTTGCCTG GGGGAGCGCC AGGTTTTGTT CAGCTGTTGG GCAGACCTAG 240 TGACTAGGGT GGGGGCCACT CTTCCTAGTC CAGAGTGAGC CAGGCCCACT CCCCAGCCTG 300 TGAAGGCTCA AGGTGAGCAG GGCTGGCCCC CCAGCCCCTC CTCCTGCTGC TGGTCCCTAG 360 CCCATCCCAG GTGGGTGCCC TGCCCAGCCG CTCTTCTCAG TCATGACTTT GTGCCTCTTT 420 GGGCCTTTTG GAAAGGAGGG AGGGAGGCAC CAAAAGGGAA CACTTTGGAC TTGGGTTGGG 480 GTGGAGACCC GCTGTCCACC GAAAGAATGT GCTCTGAGCA GAGCCTCCTC TGCCATGTGG 540 CGGGATGGGC CGGGGAGCCC ACAGGGGCTG GGCTTCAGCT GCGTGAGTGG GTCTCCTCAG 600 AGGTCTGCTG GGACTTGGGG GTGGGGTGGG GGTGATCCTG TGACCCAGAG AGGGGCTGAG 660 GGTGGGGGAG GGGCAAGTGT GGGTGCCGGG TGCAGGCCCG TGGGCAGGGC CAACCACCAG 720 CCTGGGAGAG CTGACAATCC CACTTGTGGT CCCACTAGGC TGGAGAGGGG ACGCGGGAGA 780 AGCTCGGCCC ATGGAAGGCC CCCCTTTCTC TGCACCCCAG CCCCCGAGCT GGGCCTTTGC 840 TTCTGCCTGG CCCTCTGCAG GGGGCTCCTC CTTCTTCCTC GGAGACCCAG CCCCTTTGTC 900 CAAGAACGTT TCCCCAGCTG TCAGTCCTCA GGAGCAGCTG ACCGCCCCCG TGCGTCTCTT 960 TGGACCTGAA GTGCGCCCTG GCGGTGCTTC GCTTTGGCCT GGGTGGGTTC CCCTGAACTG 1020 AGCTGTGCTG GGCTGGGCAG GGCCGTGCTT CCGCCAAGGG GACACTGGCC CAGCTGACTT 1080 CCTTGACTAC TCAAGCACCT CTGGACCCAG TTGGGCGGGG CACACACAGG GGCCAACTCT 1140 GCATCTCTAG AATGAATTCG CTCATGGCTG GAAGGGGGCT TGAGAGACGC TGGAGCTGCT 1200 AAGGGCCGGG GAACGTTCTG GAGGGCCAGA GAGTAAGGGG GACAGAGAGC CAGAACCGTG 1260 GCAGCCAGGC AGAGGCCACT CCTGAGGCCC TCCTCTGGGC AAGGAGGTGG ATGCCCAGGC 1320 AGGCAGGGAT GGGTGCCCCT TCCAGGTCCT CTCCTGAGAC CCCAGCACCC TCCTCCAGGC 1380 TAGCCCCAGA CTCCCACCCC TGCCTGTGCC CAAAGCTGCA GAATGCCCAG GCCAGATGGA 1440 CATGTGGGGC TCTCGGGGAC TGCAGGTGGC CGTGATGGTG TCGTGCAGCT GCTGCACTCC 1500 TGAGACCACA GCTAAGACAC CGCCCCGTGG TGGCAGCGCC TGGGGGCCGC CTTGCCTGCG 1560 GCAGGGTCCC ACCCACACCC AGAGCCACTG CTTGACCCCC CTTCCTGTTA ACCACAGGCA 1620 CCTCCTGGTC CCCTCCTCAT GGCTCCCACT TCCTCCTGCC CTGCTGAGTT TCCTGGGCCA 1680 CCTAGGAGTT GCGGAGGGGA CAGAGGCGAG GGCACAGGAA GGGAGTGAGC TCTGACTCTG 1740 GGCTGACCAC CCCTCCCCAA CCCCCACTGC ATAGGCTGGA GCAGGCTCTT CCTTCCATTT 1800 CTCATGTGGG GCATGAAAGA CCCCTTCCAC CACTGGGAGA CAAGAGGTCC CATGTGGTGC 1860 CAGCCCAGAG CAGATGGGGA GGGACAGGTC AGGTTCTGCC TCTGCCTGGC CAGCCCTGTG 1920 TCCCTGAGGA TGCTTGCCTC TGGACACCTG GGGAGGGGCC ATGCTCTCTG ACCCCACGCC 1980 AAGGCCAGCT GTTTGGCAGC ATGGGGCCCA GGCCCAATGG GGGCCCCACC CAGAGCCAGT 2040 GCACATGGCC CCCCTGCCTC CGCCAGCTGC CTTCCCAGCA GTAATCCAGC CTCCAAAGTG 2100 CTCCTTACCC CCTGCCTCCC AGACGCTCGC CTTCAGGCTA GGATAAAGGG ATTCTTGTAA 2160 AGAAAGGTCA CTGGCGCCTC CTCAGGCCAC ATAGAGCCAT CAGCTGGGGC CACACTTAGC 2220 TGAACCTTGG CCAGGGGCAG ACACTGCCTC AGCTCTGGGA AAGGCTGAAG CTCTGAGAAG 2280 GAATCCAGCT GAGTCCTGGA CTCATTCCGC ATCCTTCCTG TGCCCAATTC CTCCTCTGTC 2340 CTCCTGCAGA GGCCTGGGGA CCGCAGAGCT GGGGAAAAGG GCCCAGCCAT GACTCCAGTG 2400 GTTGTGTGGC CTCAGCTGGC CACCTTCATC TCTCAGGCCC TGTTTGTAAA TCAGGACTTG 2460 CTCTGAGTCA GGGAGATGAT GTCCCAGGCC CACAGGAGGC CCTGGGGAAG GCGCCTGCAG 2520 AGGTGAGTGT GAGCCCAGAC CCAGCCCCCT CCACGCCTAT GTGGCTTCCT CACCCACAGC 2580 CCAGAGTGAC AGGGCTGGGC CGCGCTGCAT GGGGGCAGAG AGGAGGCTCT GGCCACTGGG 2640 GTGCTCCATC AATTGGCAGG 2660
|
| |
|
|
|