| Tag | Content |
|---|
EnhancerAtlas ID | HS061-00441 | Organism | Homo sapiens | Tissue/cell | GM12892 | Coordinate | chr1:25327120-25328210 | 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 |
| GH01I025000 | chr1 | 25327370 | 25328214 |
| Enhancer Sequence | CACCGTGCCT GGCCGGAGAA GTTTTCTTGA CTAGAAATGC ACTTTGGCTC TCGAGGGCAG 60
AGGGGACAGC CTGTCATTGT CCTCTACCAC TTCCTTGCTG TGTAATGTTG AGCAAGTTTC 120
TTAATTTCTC TGGGCCTCAG TTTCCATGTA AATGGCAGTA TAACCATACC TCCTTCCCAG 180
GGCTTTCGGG GAGGATCTGG TGAAAAGATG CTGCAGGGAG ACTACGTGGT CAGTGGTCAG 240
CGGGTGTCAG CCACTCCAGT CATGAACACT CCAGGAGACG CTCAGTCCGC GTGAATTCCT 300
CTCCCTTTCC TTTTTCATCC TGCCTCTTGT TCCTCCCTCC AGGTCCCTCA TCCCAGGCCC 360
TCCCCAGTGA TAGAGAGCCT CCAGAGACCC AGCTTGGAGC ACTTGTGGTC CCTGGAACAG 420
GCCAGGGCCT GTGGGCTTGT CCTTGGGCAC CTGGAAGACA TCACACCATG GCCTCACTAC 480
CATCTGCCTG GGCTCCCCCA AGCCGCCCCT CCTGTGCCCT CTGCTCTGGC TACTGCCAGC 540
CATGCCCCCA GGAGACAAGC TTGGGCTGGG CAGGGCTGGA TGTATTTACT CTTTGCCGAG 600
GCTGGTTTCT CTGTTGCTGA CGTGAAGGCC TGCTGGGTGC CCATGTTTCC TGCCTGGGTT 660
TTCCCTGGCC GGTGCTGGGT TGCCATGTCT TCCAGCCACC CAACCCGGGG CCCCTCCACC 720
TTGGCCACAA GCTCTCCCGC TACGTACCCT CCCTGGCCAC CGGAAATCAG ACTCAGAAGC 780
CTCCAGGGGC CCTCGGGTTC TCCCTCAGCA GGAAGTTGGC ACCCAAGGGC AACTGGCCTG 840
GGCCAGGTCG TTCTTTGGTC CAACTAGGAA GGCCGCAGAC TACACACTGG TCAGCTGTTC 900
CGGAACACAG GGAGCCACTG CCTTGCAGCC CCGGGTCTAC AAAGAGGTGC TTTCTGCCTC 960
AGGCGCTTCT GACCATTGTT AGAGACCAGC ATCCTGGATT GGGCTGGGGA GTTGGGGCTG 1020
GGGGCGGTGA CCCATCTTAA AGACCCGTTT TAAACTCCTG CCTGTTGGCT TGATGACTCA 1080
GGAAGAAACA 1090
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