| Tag | Content |
|---|
EnhancerAtlas ID | HS076-30878 | Organism | Homo sapiens | Tissue/cell | H1 | Coordinate | chr2:308990-310440 | 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 |
| GH02I000308 | chr2 | 308988 | 309816 |
| Enhancer Sequence | GTGTCTGCTG CTGTTCCCAT GGCCCCGCTG TGCTGCGGAA CAGTCCCTCG AGGTAACAGG 60
TTGGCTGCCT CACACTTGAG GTTTTGTTTT TCCAGCCCTC AGGTGGAGTC TTCATTATTC 120
TTCTGTAGTT GGACCTGATC TGGCCACAGC TGGCATCCCC AGAACGTCCC TACACCGATT 180
CTCCCGCTCA GGACTGGACA TGTAGCGTGT GGCACTTCCA ATCAAGGCCT CCACCAAGGC 240
AGGTGTGACT TGCTGAAGGG CAGTTGGCTT CCCTTGAGGC TTGCAGGGCA GTGGACTGGC 300
ATAACCATGC CTGGTCCCCA TGAGAGCACT TCACTTCATC TGAATTCCTG GAATGTGAGC 360
TAAAAGCAGT AGGTGGGTGA GAGTTTTGTG AGGCGTTGAG GTCTGGCAGT AGGTGGTCTG 420
TGGAAGAGAA GCGGTTTGTC TGCTGGCTCC TTTGTTGCCA GAATACTCAG GGGAGGGGCT 480
GGTGATGTCG TCGTCTACAG AGTGGAGGGA CAGGCTATAG GGAAACAGAG CTGTTGTAAC 540
ACCCAGGGGC CCCACCCACT TCCAGACCAG AAGGGGTGAG GGAGGGAATG GCCAGGAGGG 600
GTGATCTCCA GTGTGGAGAC AGTGTGCTGG GGTGGCTCTC CAGGGAGCAG TGAGAACAGG 660
CGGCAAGGTT TGGGGACCTG TTTAGCCCAC AGGAGCGCCC CAGGGGATGT GGGCCTGACT 720
GTGGTCACAC AGCTGTTCAG CACACCTGCC TGCAGGTAGC CCTTGCCTCC TTACTCACCG 780
AAGCCTAATT GTGAGGGTGG TCTTTGGGCA GCTGCACACA CGATCTCTTA TCACACAAAT 840
CAGAGCCACT TTAAAACCAT TAAGACAAAA GCTAAACCCA GGGTGTATGA AGCAGAAAAA 900
CGTTGGGACT TGAATGAATT GTGGAGCTGC TGTTTCAGTC TGCCTTGCCT AATTGTGGGC 960
TGCTGATTTT ATGCAAAAGA TAATTATTGA TTTGGTCAAG CCACTGCAAG TTGGTTTTCT 1020
GGTACATATT ACCAAACTCA ACCCTAATAT ACACGAATTT AACCCATCAG TGAACCCACC 1080
GACTGCTCAA TCAATTCATG TGACTTAGCG CTGCTGCTGC AAGTATGAAT CTGGGTTACT 1140
GCCTGTGAAA ATGACAACTT ACTCTTATCT TTTCCATGAA TATGAATCTG GGTTACTGCT 1200
TATGAAAATG ACAACTACTC TTACATTTTC TGTCGTTCAT CAAGGGCTGA GGCAGCTCCG 1260
CTTTACAGGC AGCAGGATTT CTTTGTGCTT GAAAGTCTTT GTGTAGGAAT CTCCATTTGT 1320
TTCTCTTGTT GTCGAGTGAA TTGATCTGAT CCTAGAACTG CACCGGAACT AATGCCTGGG 1380
GTTGCAGGAG CTCCAGGAAG CCCCTGTCGG AACAGGGAGA TGGCTCATTG GAACCAGGTC 1440
GCCAACCCTC 1450
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