| Tag | Content |
|---|
EnhancerAtlas ID | HS188-06493 | Organism | Homo sapiens | Tissue/cell | Th2 | Coordinate | chr19:35660790-35661980 | 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 |
| GH19I035170 | chr19 | 35661278 | 35661320 |
| Enhancer Sequence | ATCTCTGATC ATTTGGGACA GGGGAGTGGA AAGAGGAGGC AGGGGCTGCC TCAGGGCCCT 60
CAAGGAATAA AGCAAAGGCC GGACGTGGTG GCCCACACCT ATAACCCCAG CACTTTGGGA 120
GGCTAAGGCG GGAGGATCAC TTGAGGCCAG TAGTTCAAGA CTAGTCTGGG CAACATAGTG 180
AGACCTTGAC TCTACAAAAA ATAAAAATAT TAGCTGGGCA TGGTGGTGCG TGCCTAGAGT 240
CCCAGCTACT CAGGAGGCTG AGGCAGGAGA ACTGCTTGAG CCCAGGAGGT CGAGACTGTA 300
GTGAGCTGTG ATTGCACCAC TATATTCCTG CCTGGGTGAC AGAGTGAGAT CCTGTTTCTA 360
AAAAAGAAAA ATATAACAAG CCAAGGCAGG GAATAAAGTT AGGGAAGCCA GTCTAGTGTG 420
TGGCAGACAG GATGGCGGTG GGCGGTTGCA GGTGAGTCTG TGTGCTGGGT GACTGGCCAG 480
AGAGAGAGTC AGGGCTGGCT TCTGCCTGCA GTCAGTTTGA GAACACTGGC GTGGTCCCCA 540
TAAGGGAGCA GGTACCCAGT GTCAGCTCAC CCCTAACATT TTTAAGGGTT TGGAGGTCCC 600
AGATCACAGG GATCCCCTCT CCTTCCTACT TCTAGTCCCT TCCCACACCG GGAGGGGCCT 660
TGCACACATG AGTGTGGATG CCACAGCCTG CACCTCCAAG CTCTATCCAC AGCCCCCAAT 720
ACACAAATGG CCACCCTCCA GGGCACTTCT TGGCTTAGGA ATGTGTCCAC CAAGAAGGCC 780
CTGCAGGCCC CAGCATGGGC GCAGAGCAAT TTGGGAGAGG AATTCAGGGG TCCTAGGGAT 840
CTAGAACATG GTCGAGAAGA GCATAGGTGC TGGTGGGCAC TTCCTGAAGG CCCTTGGGCT 900
CGACCAGATT AGGCCAGAGC AGGTCCCCTG AAGTGCAGGA CTTAGACCAG AGCTCTACTC 960
AGGCTTAAGG GTCGTGCCAA AATCAAGAGA CAAGGTCCCG GTCACAGGGC TTACATAACA 1020
GTGTTTCACA ACTTCAGGTC ATAGCCCATT CATGGGTTAC TAAATCAGTT TAGTGGGCTC 1080
TGAGTAGCAT AAGAAAAAAG AGAGAAAGAA AGAATAATTT TTAAAAGACA TTAGTATATC 1140
ACTAATAAAT GTAAGATTGT ATATATATAA TATACATAGC ATGTCATATA 1190
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