| Tag | Content |
|---|
EnhancerAtlas ID | HS044-09243 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr3:127996820-127998640 |
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 | CATTTGGCAT CTGGACTGGA GCCCAGAGAC AAATGTGGGG TGAGAGGTGC TGTAGAGGTA 60
AGTGGCACCA GACCATGCAA GGCCAGTTCA AGTTCTGTCT ATTCTTATGA CGCAGCTGGT 120
TTTGCAGGGT GGGTGATGTA GTGTGTGTGC AATTTATTTG TGTGTTTGAG GGAAAGACAG 180
ATGGTTTGGA GAACAGATTT GAGGGGAGCC AGGACCTTTC TGGGGACTAG TGGGGAGGCT 240
GTTGCCATAG TCCAGGCAGA TTGAGGTGGC TTGGATCAAG CTGGCAGCAA TCCAATGGGC 300
ATTAAAGGCA TTCAGGAGAT GGAATTAACA AGGCTTTGTG ATGGACTAGA TATAGGGACA 360
GTGAAGGGGA GAGGCATATT ACCGATGGAC CCCAGATCTC TGGCTTCAGT GACAGGCCAG 420
GTGGAGGAGC CGTTGGTGAG AGAGAATCCA GAACAATCTG GAGGGGAGAG TGAACAGAGC 480
CAGGAGTATG GCTTGGGCTT CACTAAGTTG GGGACGTTTG GGGAACCCAC TTGGAAAGGT 540
CTAGGAAGCA AGCTGACATA AGTGTCTGAA GCTCAGAGAA GTTTGGGATA GGACATATAT 600
TTATGTGCTG TTGGTGGCTC CAACCTTGGT AGTTGGGGCC TCTGGCTAGA AAAGAAAAGT 660
TAAAAAGCAA GCTTCAGCTG TTTCATCTAA AGTTATAATT CCGATGCTTT AAAGGCTCCC 720
AACCCTCTTC TTGTTCATGG TGGGGGAGCC TTCCTAGTTG TGAAAGGGTC TGAGTGGCTC 780
CAGCTTTGGC ATATTAGGGT GCAGGGGAGG GTATTTCTAG GGACACTCTG GGAGAAGCTG 840
CCCAGCCTGC ATGGTGCTAG TGCCAGTCTG CAAAATCTCC AGGTAATAGA GAGGGCAGGC 900
CCCTGCCCAC CCCCTTGCAG CCTCCAATGC TGCTGCTGTG GCAGCTGCTG CTGCGAAACA 960
AACCAGGGTG ACTGGGCGGA AGGTCAGGAG TTTAAGAGCT TGTTTGATTC AAAACTAGGC 1020
TAAAAGACAG GAGGGGAGTG AGCTGGTTTT CTGTGTGGAT CCTGGTATTT TCCTTTGAGT 1080
TGGGGAGGAG AATGGTGGGG CAGGGAGGGA AGGCCGGCCG CCAGAGGGAA CGCTGCCAAG 1140
CAGAGCGCAG CTAATGTGAA CCATACGGCG GCGGCGTTGG GCAGTGGCGG CCATCTCCCG 1200
CCCAGCTTAG TACAGCCCTT ACTGCGGGCA GGGGTGCAGA CAGGCAGGAA GGCAGCTCGG 1260
GCTGTGCGGC CACTTAACCC TTCCAGTGCT GAACTACAAG CAGGGCTCCT TCACCTCAGC 1320
ACATTGATGT TTCAGCCAAT AATCCTCTGT CCTGGGCACT GTAGATGTCT AGCAGCATCC 1380
CTGGCCTCTA CCCACTAGAT GCCAATAGCA CCCTCTCCCA GCTGTGATGA CCACAAGTGT 1440
CTGCAGACAT TCTAAATGCC TCCTGGGGGG AAATTATCCC TGGCGGAGAA CCAGTGGCCT 1500
AGAACAGGCG GCCCCCTCAG CTGCTGGGCC TGCCTGGACT CTGATGGGCC TGCACCCTTC 1560
AGGGGCCCTG CCCCAGACAC ACCACATCCA TGTTTGGAGT GCTGCCTGGG GCTGAGCATG 1620
TGGGGGTCGT TTTCCCATGA AGCAGGCAGC CATAGGGTCA GAGGGGAGAC GAGACCTACC 1680
CAGAGTTGTA TGCCAGTAGG AGCCAGGGTC CAGGATTGGT GTTGCTCCAC ACATTCCCTG 1740
TCCCCCTGCT CCCAGGCATG GCCCCCATTC AGTTTCTGTG GTTTTAAGTG GGAGGTGTGC 1800
AGCCTGCCCC TGACTGGCTT 1820
|
