| Tag | Content |
|---|
EnhancerAtlas ID | HS082-24376 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr3:127997020-127998770 |
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 | GAGGGGAGCC AGGACCTTTC TGGGGACTAG TGGGGAGGCT GTTGCCATAG TCCAGGCAGA 60
TTGAGGTGGC TTGGATCAAG CTGGCAGCAA TCCAATGGGC ATTAAAGGCA TTCAGGAGAT 120
GGAATTAACA AGGCTTTGTG ATGGACTAGA TATAGGGACA GTGAAGGGGA GAGGCATATT 180
ACCGATGGAC CCCAGATCTC TGGCTTCAGT GACAGGCCAG GTGGAGGAGC CGTTGGTGAG 240
AGAGAATCCA GAACAATCTG GAGGGGAGAG TGAACAGAGC CAGGAGTATG GCTTGGGCTT 300
CACTAAGTTG GGGACGTTTG GGGAACCCAC TTGGAAAGGT CTAGGAAGCA AGCTGACATA 360
AGTGTCTGAA GCTCAGAGAA GTTTGGGATA GGACATATAT TTATGTGCTG TTGGTGGCTC 420
CAACCTTGGT AGTTGGGGCC TCTGGCTAGA AAAGAAAAGT TAAAAAGCAA GCTTCAGCTG 480
TTTCATCTAA AGTTATAATT CCGATGCTTT AAAGGCTCCC AACCCTCTTC TTGTTCATGG 540
TGGGGGAGCC TTCCTAGTTG TGAAAGGGTC TGAGTGGCTC CAGCTTTGGC ATATTAGGGT 600
GCAGGGGAGG GTATTTCTAG GGACACTCTG GGAGAAGCTG CCCAGCCTGC ATGGTGCTAG 660
TGCCAGTCTG CAAAATCTCC AGGTAATAGA GAGGGCAGGC CCCTGCCCAC CCCCTTGCAG 720
CCTCCAATGC TGCTGCTGTG GCAGCTGCTG CTGCGAAACA AACCAGGGTG ACTGGGCGGA 780
AGGTCAGGAG TTTAAGAGCT TGTTTGATTC AAAACTAGGC TAAAAGACAG GAGGGGAGTG 840
AGCTGGTTTT CTGTGTGGAT CCTGGTATTT TCCTTTGAGT TGGGGAGGAG AATGGTGGGG 900
CAGGGAGGGA AGGCCGGCCG CCAGAGGGAA CGCTGCCAAG CAGAGCGCAG CTAATGTGAA 960
CCATACGGCG GCGGCGTTGG GCAGTGGCGG CCATCTCCCG CCCAGCTTAG TACAGCCCTT 1020
ACTGCGGGCA GGGGTGCAGA CAGGCAGGAA GGCAGCTCGG GCTGTGCGGC CACTTAACCC 1080
TTCCAGTGCT GAACTACAAG CAGGGCTCCT TCACCTCAGC ACATTGATGT TTCAGCCAAT 1140
AATCCTCTGT CCTGGGCACT GTAGATGTCT AGCAGCATCC CTGGCCTCTA CCCACTAGAT 1200
GCCAATAGCA CCCTCTCCCA GCTGTGATGA CCACAAGTGT CTGCAGACAT TCTAAATGCC 1260
TCCTGGGGGG AAATTATCCC TGGCGGAGAA CCAGTGGCCT AGAACAGGCG GCCCCCTCAG 1320
CTGCTGGGCC TGCCTGGACT CTGATGGGCC TGCACCCTTC AGGGGCCCTG CCCCAGACAC 1380
ACCACATCCA TGTTTGGAGT GCTGCCTGGG GCTGAGCATG TGGGGGTCGT TTTCCCATGA 1440
AGCAGGCAGC CATAGGGTCA GAGGGGAGAC GAGACCTACC CAGAGTTGTA TGCCAGTAGG 1500
AGCCAGGGTC CAGGATTGGT GTTGCTCCAC ACATTCCCTG TCCCCCTGCT CCCAGGCATG 1560
GCCCCCATTC AGTTTCTGTG GTTTTAAGTG GGAGGTGTGC AGCCTGCCCC TGACTGGCTT 1620
CCTGGGGGGA CTAATTCCTA TGCCAGCCTT CTCTGCCTAT TCAACATGCA GTTGCCCAAG 1680
GGAACATGGC ACGGGTGTTT ACCACACTGT TCTTATACCA AGAGTCAGTG CACACGAGCT 1740
CAGTGTCCAG 1750
|
