| Tag | Content |
|---|
EnhancerAtlas ID | HS041-08319 | Organism | Homo sapiens | Tissue/cell | EWS502 | Coordinate | chr16:89733960-89735180 | SNPs | | Number: 2 | 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 |
| GH16I089668 | chr16 | 89735009 | 89735208 |
| Enhancer Sequence | CTTGGAAGGC TGAAGTGGGA GGATCATTTG AGCCCAGGAA GTTGAGGCTT CAGTGAGCCA 60
TGATCATGCC ACAGCATTTC AGCCTGGGCC ACAGACCTTC AAGATCCTGT CTCAAAAAGA 120
AAAAGGGATA TCGCTCAGTG CTTAGTGCAG CTGTGGGTCA TTCGGCAGCT GACACAGATG 180
AGGCTATGTA ACGCAGCACT GCAGGCAGAG GGGGAGGCCA AGGCCTGAAT ACCCCGTCTG 240
ACTAGCCTTA GGCAGGCGAC TTGGCCTCTC TGCCTCCCCC ATCTGGTTAG CCTTGGGCAG 300
TCGAGTTGGC CTCTGTGTCT CCCCTGTTTG ACTAGCCTTG GGCAGATGGC TTGGCTTGTC 360
TGTACCTCAG TTTTGTCTGA AATATGGGTT GTCAGAGACC TATAGCAGAA GCTGCTGTGT 420
GTCATTATTC ACTGTTCTAG GGCTCAGAAC AGGCACGCGA TAAAAGCCAG CACCGTTGGC 480
CGGGCGCATT GGCTCACGCC TGTAATCCCA GCACTTTGGG AGGCCAAGGC AGGTAGATCA 540
CCTGAGGTCG GGAGTTCAAG ACCAGCCTGG CCAACATGGA GAAACCCTGT CTCTACTAAT 600
AATACAAAAA TTCCCCAGGT GTGGTGGCAG GAGCCTGTAG TCCCAGTTGC TCAGGAGGCT 660
GAGGCAGGAG AATCACTTGA ACTCAGGAGG TGGAGGTTGC AGTGAGCCGA GATCACACCA 720
CTGCACTCCA GCCTGGGTGA CAGAGCGAGA CTCCGTCTCA AAAACTAAGA AGAAGATTAA 780
TAATAAACCA GCACTGCCAT TGCCAGCAGT CCATCCTACC TCGCATCCAG GTTCGTGAGC 840
TACCAAGTGT CCCCACAAAG CTGTAAAACA ACATGACCAC TGTAGTTACG TTTCTGTAAA 900
AAGGTGACTG AGTCTTCTAA CCCTGACCAC ACATATGTGT GCAGAGAGAG CCAGCTCCAT 960
CCTGCTCTCC CAGAAGCCTG AACAGCTGTG CCCTAGCTCG TAGCAGTGGC ACTCCAGGAA 1020
GGGGGCGGGC GGCTGTGCCC GAGCTCGTAG CAGTGGCACT CCAGGAAGGG GGCGGGCGGC 1080
TGTGTCTGAG CTCGTAGCAG TGGCACTCCA CGAAGGGGGT GGGCGGCTGT GCCCGAGCTT 1140
GTAGCAGTGG CACTCCAGGA AGGGGCGGCC GGCCAGCCAG GAGAGCAGCC GGTGAAGGAG 1200
CACTTTTGCT TTGTACGTGG 1220
|
| |
|
|
|
