| Tag | Content |
|---|
EnhancerAtlas ID | HS101-09003 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr11:116577680-116578810 |
Target genes | |
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 |
| GH11I116707 | chr11 | 116578117 | 116578516 |
|
Enhancer Sequence | CCTCTTTTCC CAACGCTGGT GATTAGAAAC TTCTTGCTTC TCTGCCATGG TGGTGGGCAT 60
GGTGATGTGG GGTACAGCTG GGAGCCTCAG GTCCACACGG GAGATTTAAG ATTGCACCCT 120
CTCAGGAACA AAGCCAGAGC CCCCGTCCAA ACCCCTACAC CTAGCTCAGG CCCTGACCCG 180
TAGAAGGTTC TCCATAAATG TCTGCTGAAC TGCCCTGCGT TGCTGGGTCA CGCGAGGAAA 240
ATGGAATTAA GAGTCCGCTG ACCCGGAGGG CTGGTTCCGG CGCACTATTG ACTGGCTCCA 300
GGGCCTTGAG CCGGGGATTT AACCTCTCGG CTTCTCGATT TCCTCGCTGG CAAAATGAAT 360
CTGATACCGC CCTGACCGCC CTTGCTTAGC AGGGGTGAGT CTCACTAGAG GCTGAAGGCG 420
TGAGAAAGGC ACAGAGCGCT GTCCAGGCAG GGAGCCACTC GGGCTGCCAC CTCCCGCGCC 480
CGCTGGAGAC CGTAAGCCAG GAGAGCTGGC TCAGCCGTCA GCAATTACCT GCGCCCCGAA 540
CACAACACCT GCGCTCCACT TCCGCACAGG CAGATGGTGC AATCTGGCCG CGCCGCACCC 600
TCCCGCACCC CACCCGCGGC GGCCTTGCCG TGACAGCGCT CGCGCCAGGT GTCGGTGTGC 660
AGGCTGGTCC GGGACGCTGC GACTGCAGCC GGCAGGAACC CGCGCGAGGG GAAAGGGGCG 720
CTGGGACCAG GCCATGGGAT GCCCAAGGCA CCCCTCTCAA GTCCAAGGGA ATAAGGCCAG 780
CTTCTCCTGG ATTCTTAAAA CCCCTCTGAA AGGAGAGCAG GGAGCAGGTA TCAGCTCCCT 840
GCGTTCCACG TGGAGAGACT GGGGCTCAGA GAGACGAGGT GGCCTGAGGA TGGACACACA 900
CATATTAAGT GATGGGGGCG GAGGGAAGCC CAAGTCTCTA ACTCCGGGTC CACCATTCCT 960
CCCCGGGCTG GCACTGCTCT GACTGCACAG ACCAGCTGAC TCGTCTTGGG CAAGGGTGGA 1020
ATTCTTCCTT TTGCCCAGGG CTGGCTTTGC CTCCTTCCAC CCCGTGGCCT TGCCACTCCT 1080
GTGCCACCCA GCCTCCTCCC AAACACCACG CCCATCTCAC ATACCCTAAG 1130
|
