| Tag | Content |
|---|
EnhancerAtlas ID | HS055-08115 | Organism | Homo sapiens | Tissue/cell | FT33 | Coordinate | chr8:21540470-21543110 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| | | 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 |
| GH08I021683 | chr8 | 21541041 | 21542695 |
| Enhancer Sequence | GCTGGCTCCA AGGGTGGAAG TCAGGGGGCT TGCAGAGGGC AAAGAGAATC CTTAGGGATC 60
CCCCGAGAGA GACTCCTGTT CAGGGGGATC CCTGGGAGCA CTCATCTTGC TGCCAGAAAT 120
CAATCACTCC ATCAGTCATG TTGGTTGCCG AATGAGTAGT ACCCTCCTTG CGTCCCCCCA 180
CTGTCCTGCC ACTGTCTAAT TTAATTCTGT GGATGCTCCC AGGGCCTGGC CCTAAACAGA 240
GCCCTCCCCA GGAGGGCTTT ATCTCTGATG GGATCCTTTG CAAGGTGCAG ACTCAGCGAA 300
GCAGATCCTG GGTGGTGTGG ACTTCCTAGT CCTGCCAACC AATGCCCAAA AAGGAAGGAG 360
GCTCACGGGG CCAGCTCAGC CCAACTTCCC ACTCACAGCA GGGACCCAAC AGTGTGGCTG 420
CTTCCACAAA CACTTCTCAG ACTGCCCGGT GCTTTTTCTA GACCTGTCCT CTCCAAGGCT 480
GCCCTGGGAC TTCATATCAA GATGCAGGAG GGGGAGTTTG AGGGGTCGGG CTAGGTCATC 540
ACTGTCATCA CCTGGGACCA CAGCACCCCT GGACCATTTC CAGTTGTGAA GAAGATCAAG 600
TTTCCTCCAT TTGAAAGAAA AGGTTATTCC AGCAGCCCCC ATCACCACCA CGCACTCCAG 660
GTAGAAATAC CAGAAATACA TTTCCCAGAA TAAGATATTT TAGTACAGAT CCCTCATGTC 720
ACTGCAGCCT CCCACTCAGC CAGCTTTCTA GCAAAACGAG AATTAAGAGT AATTTCAGGT 780
TGCTGGGGCC CCTGAAAAAG GCTTATCTTC CACTGAGGAT AAAAGTGAAG GATAGACTGG 840
GCCAGGCGGG GTCATTCCAC AAGGATTTGT TTGACCAACC AGGCTGGACC CTGACTATTA 900
AATGGAGTAG GATGAGAGCA GCGACCTCAT CTTACATTGT GAGCCTCCTG TGTGTTGGTG 960
GGCAGGGAAG GAGAGGGGCG GGGTCAGTCC ACTGTGCTGG GCTGGAAAAA ATCAAAGAGT 1020
TTTTCCTGGA AGACTCTCTT CTGGCTGTAA GAGCTTCAAC ACACGCAGTC ACGCTCACCA 1080
CGGTGGTTGT GCAAACCTCC CACAGAGATG TTTGATGAGA TTAGTCACTT TCTGCCAGGG 1140
TGGTTGGTCC ATGCGTAGGA GACTTCATGA CCTCTGATGC TGGGCAGTGT CTAGGTCAAG 1200
GTGGTGACTC AAGTGTGCCC TCCTCCAGGG AGGGAGGCCA GGCGGGGGCT GAGTCATTGC 1260
TTCACATGGC CCCAGAGGTT GGCTTCCCAA GAAATGCTGT CTTGAAGGAG TGGGAACAGG 1320
CCAGCGTGTA AGGTGCCACG CACAGAGCAA GCTCTAAGGT GGCAGTCCAC AGCTCTGGAC 1380
TAGAGGCTCA GAGAAAAATT GAAGCAACCA AGCATGTGGC GGTGTTTGCT GAAAGGGAGA 1440
TGAATTCTGC CTCCTTTCAA GTCATTTTTC CCCAGGCCGG TGAGTTCAGG AATGGCTGCC 1500
AGTCACAGAA TCACAGAATC CCATTGCCGA GGGAAGGTTG GGGAGCAGCC CCTCTGACCT 1560
CTCCCTCTGA AGATGAGGGC AGGAGAGTCC AGGGAGGGTA AGTGACTTGC CCACAGCCAT 1620
GCAGCGCTCT CAGGGGCTTC TCTGTGCACT CAGGACCCTT GTCCCCTCCC CAGCCACTGG 1680
GGTGGCAGCT CCATTTGCTC TTGGCCACAA GTTCTCCGCA AGCACACAGA GAAACCTTGG 1740
TGCAAATTAG AGAATGATGC CCCCTCCTCG GGGCTGAGGC CCAGGTTGGG TGCACAGATG 1800
GGTGAGTTGA GGGTGGCTGG CTTTCAGCCC CATTCGCCCT GCTTACCAGA TGCCCCTGAT 1860
CAGAGTACAA TCTCACAGTG GCAAGCAAAG TCCCCACATT CCAGCCCACA CCTATGTGTG 1920
CCTGGTCCAC AGGCTACCTG CCTTCTCTCC TTGCACCTCT GGACCGCATG CAGGACGGTT 1980
CCTCCCAGCT TTCTCCTCCA CCAACTCCCA TGTGAGTTCA CCTCCCTTTG CACAATGGGC 2040
CAGTGTGCCC TCTCTCTTCC TCCAACTTAA GGATGATTTC AGCCCTGTCA CCCATCAGTC 2100
ACTCCCCGCT GCAAACCCTC AGAGTTCCAA CTGCCTGGGG TGGACAGCTT GGTCTCAGAG 2160
GTCATCTAGA GCAGGGGTTG GCAAACTACA GCCCATGAGC CAAATCTGGC CTGTGCCTGT 2220
TTCTGTAAAT AAAGTTTTGT TGGAACACAG CCATGCCTAG TCATTGACAT TGCCTATGAC 2280
TGCTTTGGAA CTACAGCAGA ACAGTTGCTA GTTGCAATGG AAATGGCATA GCACACAAGG 2340
CCTGTCATTT TCACCATCTG GCCCTTTACA GAGAAAGTGT GCCCATCCCT GACCTAGAGC 2400
AAACTTTCCA AGGCTCAGAG AAGTTCAGTG ACCTAGCTGA TGTCACCAGC TGCTGGATGG 2460
CAAAGCCAGC ATTTGAACCT GGATCCCCTG ATACTCCTTC TGGTATATTC CAGACTCCTT 2520
GAGAAAAGAA ATGACTTTAC TATGTCATCA GACTCTCACC CCGTTGCCAA ACTTTTTGTT 2580
GTTGTTGTTG TTTTGAGACG GAGTCCCACT CTTTTGCCCA GGCTGGAGTG CAGTGGCGTG 2640
|
| |
|
|
|
