| Tag | Content |
|---|
EnhancerAtlas ID | HS098-39933 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:127997490-127998660 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr3:127998593-127998604 | TTCTGTGGTTT | + | 6.32 |
|
| | 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 |
| GH03I128277 | chr3 | 127996830 | 128000288 |
|
Enhancer Sequence | GCTTCAGCTG TTTCATCTAA AGTTATAATT CCGATGCTTT AAAGGCTCCC AACCCTCTTC 60
TTGTTCATGG TGGGGGAGCC TTCCTAGTTG TGAAAGGGTC TGAGTGGCTC CAGCTTTGGC 120
ATATTAGGGT GCAGGGGAGG GTATTTCTAG GGACACTCTG GGAGAAGCTG CCCAGCCTGC 180
ATGGTGCTAG TGCCAGTCTG CAAAATCTCC AGGTAATAGA GAGGGCAGGC CCCTGCCCAC 240
CCCCTTGCAG CCTCCAATGC TGCTGCTGTG GCAGCTGCTG CTGCGAAACA AACCAGGGTG 300
ACTGGGCGGA AGGTCAGGAG TTTAAGAGCT TGTTTGATTC AAAACTAGGC TAAAAGACAG 360
GAGGGGAGTG AGCTGGTTTT CTGTGTGGAT CCTGGTATTT TCCTTTGAGT TGGGGAGGAG 420
AATGGTGGGG CAGGGAGGGA AGGCCGGCCG CCAGAGGGAA CGCTGCCAAG CAGAGCGCAG 480
CTAATGTGAA CCATACGGCG GCGGCGTTGG GCAGTGGCGG CCATCTCCCG CCCAGCTTAG 540
TACAGCCCTT ACTGCGGGCA GGGGTGCAGA CAGGCAGGAA GGCAGCTCGG GCTGTGCGGC 600
CACTTAACCC TTCCAGTGCT GAACTACAAG CAGGGCTCCT TCACCTCAGC ACATTGATGT 660
TTCAGCCAAT AATCCTCTGT CCTGGGCACT GTAGATGTCT AGCAGCATCC CTGGCCTCTA 720
CCCACTAGAT GCCAATAGCA CCCTCTCCCA GCTGTGATGA CCACAAGTGT CTGCAGACAT 780
TCTAAATGCC TCCTGGGGGG AAATTATCCC TGGCGGAGAA CCAGTGGCCT AGAACAGGCG 840
GCCCCCTCAG CTGCTGGGCC TGCCTGGACT CTGATGGGCC TGCACCCTTC AGGGGCCCTG 900
CCCCAGACAC ACCACATCCA TGTTTGGAGT GCTGCCTGGG GCTGAGCATG TGGGGGTCGT 960
TTTCCCATGA AGCAGGCAGC CATAGGGTCA GAGGGGAGAC GAGACCTACC CAGAGTTGTA 1020
TGCCAGTAGG AGCCAGGGTC CAGGATTGGT GTTGCTCCAC ACATTCCCTG TCCCCCTGCT 1080
CCCAGGCATG GCCCCCATTC AGTTTCTGTG GTTTTAAGTG GGAGGTGTGC AGCCTGCCCC 1140
TGACTGGCTT CCTGGGGGGA CTAATTCCTA 1170
|
