| Tag | Content |
|---|
EnhancerAtlas ID | HS007-17732 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr9:135707800-135709620 | 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 |
| GH09I132833 | chr9 | 135709141 | 135709290 |
| Enhancer Sequence | GGAGACGCAG CGTCTGACAG CTCCCTCACA GTTCTGGAAG CCGAACCAAC ATTTTCTGAA 60
CTTTAGCTAA ATTCATACCC CCTTATTTTT CCTTCATTTG GACGGGGAGG GATTGTGAGC 120
CCATTGATTG CTGCTTCTAG TACAAGGGCT GGCAATTCTG TTTTAGTCCC TTTTTGAAGC 180
TGGAAGGTTG GAACTCCATC TTTGCTCAGC ACTGAAAAAG GCCTCTGCTT TTAATATTGC 240
ATTACTGAGC AATCATTATA ATCTCACCCA TAAATTTGCA GCAGATATCA GTATGTGGTC 300
CAAGGCTTTT AGAACTATTC AGGGGAACAG CTCTCACTGA CTTTTCACCA GAGAAAGCGG 360
GACTTCCAAT TACACAGGAA AAGTGCAGCA AAATGAGGAA CATCTCCCTA ATTAGCCTGG 420
CCTCACTGGA GTGTCATTCT GGTGCAGATG TGAAAATCTA AAAGGAAGAA GGTGGGGGGC 480
TCTGGAGTGA GCCCTAGGCC ACCAGCTCTC CAGGTCTGCT CTGAGCTGGG GAAATGGTAC 540
GATCACCTGG GGACTAAGAA ACAAGGTCCC CGAGGAAGCC CTCGAGCAGC ACCCAGGCCC 600
CATTAGAGCC ACCCCCCACT GTATGGAGAA GGCAGCCATG GAGGCTCTTC CTCTCTGCGC 660
CAGCCCACGC TGGTCCACAC TGGTCCACCT GGAAGGGAGG GCGCCTTGAC CAAACCTCTG 720
TTGAAGGCGG GTCTGTCCTA CGGCATTCTC AAGATGAAAG CTGCAGGCTT GGGGCTCAGA 780
AAAGATCTTC TTTCCCAGAG CTCTTGCATT TAAAGGGGTT ATTTGCCCAG CTGCAAAATG 840
GGCTGCACGT TCACAGGGAA GCAGCAATTT TGGCTGGGAG GACTTTAATG GCTACAAATT 900
CTGGCAAAGC AAGAAGTCAT AAATCAGTAA ATAGCACCCG ACAACTGCCA TGATGGGACA 960
TTAAGACATT CCCAACAAGC CTGTGTTGCG AGGTTCGCGG GTCTCACGTC CAGGAGTGGC 1020
TGGATGTGGA GGTATCAGTC AATCCCTAAT TAGAATACAT TATCCATCTT CCTGACACTT 1080
CAGTGAAATG TCTATTCCAC TCTGAGCTGC AGCTTTGTTC AGAGCAGGTT AATTGATATT 1140
CTGATGCCTT CGCTCACCGT ACCCCCGTGG CTCGGTTCTG TTTTATCACA CATCAAAAAG 1200
GCCGTATGCT CAGGGCACTC CAGGCACCAG TGCAGAGCTG GAGGTCTGCA CAGCTGCGAG 1260
GGGTATGGTA TCACAGGAGG GACAAGCACT GAGCAGATGT CACAGATGAA AAAAAAGCAA 1320
AGAAAAGACG CCAGTCAGCC TGGGGAACTT GGCGAGGCCC AGCAGAGCAC GGCCTGATGC 1380
GGCACGAGCC GTCCGGCTTT GTGCGAACAC TGGCCTCTTT TGCCCTCCTG ACTATTATTA 1440
AAGCGCAATT AGCAACTTCA CATGGGAAGG CTCTGTTGCC CTCTGGGCCT CTGCCTTTTT 1500
GATGCGTTGC CTTTCCGCTC CTCCCCTCTC CTCCCAGGAC CAGAGCGTGG GGCTCCCTGG 1560
GTGTTTTCCC CAGTCCTGCC TCTGATCTGG CTCGCAGCTC CGACTGCAGA CTCCACCGGA 1620
GGCATTCCCT GGAGCTGCAT GCTCAATCTC TGCAGTCCCA ACGAGGCAAG CTGAGGCTGA 1680
AGACTTGGAC TCGATAAATC AGTTTCGCTC AGTTCCAAGT CTGAACCAGG GCAAGCCTCA 1740
CAAGAGGCAC TGCAGGCTGA ACGCGGCCTA ATGTGGTTTC CCAACATAGA GGAGAGAGAT 1800
TCTGTCAGCC AGGAAGGAAA 1820
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