| Tag | Content |
|---|
EnhancerAtlas ID | HS092-28961 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr3:127996720-127998990 |
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 | AGGAGAAGAT GAGCAAGGTG TGGGTAGAGA GGATTCTGGG CAAATGCAAA GGCCCCATGG 60
TGGGAGAGAG CCTAATGTGT TTGAAAACCT AAAAGGAAGG CATTTGGCAT CTGGACTGGA 120
GCCCAGAGAC AAATGTGGGG TGAGAGGTGC TGTAGAGGTA AGTGGCACCA GACCATGCAA 180
GGCCAGTTCA AGTTCTGTCT ATTCTTATGA CGCAGCTGGT TTTGCAGGGT GGGTGATGTA 240
GTGTGTGTGC AATTTATTTG TGTGTTTGAG GGAAAGACAG ATGGTTTGGA GAACAGATTT 300
GAGGGGAGCC AGGACCTTTC TGGGGACTAG TGGGGAGGCT GTTGCCATAG TCCAGGCAGA 360
TTGAGGTGGC TTGGATCAAG CTGGCAGCAA TCCAATGGGC ATTAAAGGCA TTCAGGAGAT 420
GGAATTAACA AGGCTTTGTG ATGGACTAGA TATAGGGACA GTGAAGGGGA GAGGCATATT 480
ACCGATGGAC CCCAGATCTC TGGCTTCAGT GACAGGCCAG GTGGAGGAGC CGTTGGTGAG 540
AGAGAATCCA GAACAATCTG GAGGGGAGAG TGAACAGAGC CAGGAGTATG GCTTGGGCTT 600
CACTAAGTTG GGGACGTTTG GGGAACCCAC TTGGAAAGGT CTAGGAAGCA AGCTGACATA 660
AGTGTCTGAA GCTCAGAGAA GTTTGGGATA GGACATATAT TTATGTGCTG TTGGTGGCTC 720
CAACCTTGGT AGTTGGGGCC TCTGGCTAGA AAAGAAAAGT TAAAAAGCAA GCTTCAGCTG 780
TTTCATCTAA AGTTATAATT CCGATGCTTT AAAGGCTCCC AACCCTCTTC TTGTTCATGG 840
TGGGGGAGCC TTCCTAGTTG TGAAAGGGTC TGAGTGGCTC CAGCTTTGGC ATATTAGGGT 900
GCAGGGGAGG GTATTTCTAG GGACACTCTG GGAGAAGCTG CCCAGCCTGC ATGGTGCTAG 960
TGCCAGTCTG CAAAATCTCC AGGTAATAGA GAGGGCAGGC CCCTGCCCAC CCCCTTGCAG 1020
CCTCCAATGC TGCTGCTGTG GCAGCTGCTG CTGCGAAACA AACCAGGGTG ACTGGGCGGA 1080
AGGTCAGGAG TTTAAGAGCT TGTTTGATTC AAAACTAGGC TAAAAGACAG GAGGGGAGTG 1140
AGCTGGTTTT CTGTGTGGAT CCTGGTATTT TCCTTTGAGT TGGGGAGGAG AATGGTGGGG 1200
CAGGGAGGGA AGGCCGGCCG CCAGAGGGAA CGCTGCCAAG CAGAGCGCAG CTAATGTGAA 1260
CCATACGGCG GCGGCGTTGG GCAGTGGCGG CCATCTCCCG CCCAGCTTAG TACAGCCCTT 1320
ACTGCGGGCA GGGGTGCAGA CAGGCAGGAA GGCAGCTCGG GCTGTGCGGC CACTTAACCC 1380
TTCCAGTGCT GAACTACAAG CAGGGCTCCT TCACCTCAGC ACATTGATGT TTCAGCCAAT 1440
AATCCTCTGT CCTGGGCACT GTAGATGTCT AGCAGCATCC CTGGCCTCTA CCCACTAGAT 1500
GCCAATAGCA CCCTCTCCCA GCTGTGATGA CCACAAGTGT CTGCAGACAT TCTAAATGCC 1560
TCCTGGGGGG AAATTATCCC TGGCGGAGAA CCAGTGGCCT AGAACAGGCG GCCCCCTCAG 1620
CTGCTGGGCC TGCCTGGACT CTGATGGGCC TGCACCCTTC AGGGGCCCTG CCCCAGACAC 1680
ACCACATCCA TGTTTGGAGT GCTGCCTGGG GCTGAGCATG TGGGGGTCGT TTTCCCATGA 1740
AGCAGGCAGC CATAGGGTCA GAGGGGAGAC GAGACCTACC CAGAGTTGTA TGCCAGTAGG 1800
AGCCAGGGTC CAGGATTGGT GTTGCTCCAC ACATTCCCTG TCCCCCTGCT CCCAGGCATG 1860
GCCCCCATTC AGTTTCTGTG GTTTTAAGTG GGAGGTGTGC AGCCTGCCCC TGACTGGCTT 1920
CCTGGGGGGA CTAATTCCTA TGCCAGCCTT CTCTGCCTAT TCAACATGCA GTTGCCCAAG 1980
GGAACATGGC ACGGGTGTTT ACCACACTGT TCTTATACCA AGAGTCAGTG CACACGAGCT 2040
CAGTGTCCAG CGGTGGGTCT GGTTCTCTAA ACCGTGCGAT ACCACGTGCC CATCGAACAC 2100
GATGGTGCAG ATCTATGTGG AAAGACCACC ATTAGAATCA TCAGATCCGC GAGGACAGAG 2160
ACTTTTGTCA GTCATGTTCC TGGGCCCTTA ATAAATGTCC TGTGAATAAA TAAAATGCTA 2220
ATTGCAAAAC CAAATCTCAA TATGTATGAT TTGGTCCCAT TATGTAGGAA 2270
|
