Tag | Content |
---|
EnhancerAtlas ID | HS112-02717 | Organism | Homo sapiens | Tissue/cell | KELLY | Coordinate | chr11:2866680-2868100 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr11:2866740-2866751 | AAACCACAGAA | - | 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 |
GH11I002846 | chr11 | 2867481 | 2867630 |
| Enhancer Sequence | GCTGGCGGGT CCTTGGGTGT GAGAGACCCC GGTGGATGGC CCTGGGCCCC TGCCCCTGCC 60 AAACCACAGA AGTCCTGCAC CCCTTTCCTC CATAGTCTGG GCCTCACATC AGGTTTATCT 120 GGGAAAAATA AAACATGGGG CTCCCTCTGG CCTGGACCGT CAGACCTCGG ATGTACACCT 180 GCCCTTGTGT TCAGGACAGT TGGGTCTCAG ACTCACCCCA TACCTGCAAG GCAGAACCAC 240 AGGGGAGCCA GGGAGCCTCC ACACTGCAGC CCCCACCACC CAGGGCTGGA AGTGGGTCCC 300 CTGGGCTCCT GCTCTGGGCA GGGCACAGTC CCACCCTCCC AGGTGGAGGC TGCCCACCTA 360 GCCCTCTAGA CAGACGCTCG GCCCCACTCA GGCAGGCGCC CCCCTCTCAT CTCAGCCTCT 420 CACAGCACCC TGTTGGCCGC CTCTTCCTTA GCCTGCTCAG CCTCCGTGGT AGGTGCTGTG 480 GGTGACGACC ACAGCACCCA GCCTTTGAAG CTGGCCCGGG TCCACCCAGA CCCTAGCAAA 540 CTGGTTGCTC CCTCTCTGGC CATCCCGGGG CTTGTGCCCA CGTCACCCAG CAGCATCTTC 600 CCTGGGGTTG TCTCACCCGC ACAGAACCCA GCCCTGGCCC ACACCTCACC CCAAGCCTAT 660 CCGGCTGGAT CAGCAGTGGG GCCGGGCGCA TGAGGGACCA GGCCCGCCCG GCGCAGCCTA 720 GGGTGCAGAC CCCTGGAGTG CACGGCCAGG TGGACCGGGC CAGCTCCCGC CTGCTGCCTG 780 TGCTTAGGGC CAGTGGTTGA CGTTGCTGTG GCTGAGTCAT CTTCGTGCCT CTCTCTGGAG 840 CCATACGTTT CCCTGAAGCA GCTCTGCTGT TCAGCCCTTA TCGCGTGCTG ATCTGTTTGC 900 CCCTCCCCCA CCACTTCTAG GTCTTTCCAG GCCTCCAGGT ACCCACGGTG GGGGAGGGTC 960 TACTTCATTC TCCACAGAGC ACGCTGAGGG GCTCTCCTGC AAGAACACCG CAGGCTGAAG 1020 GACCAGCCCT GTCTCCTGTG GCCACCAACA GAGCTGTGCG CCCTCCCCGA ACCCTCACTC 1080 ATGCTAGGGC CCCCAGGTCC AACCTCCTAG GGAGAGGGGT CCCCAACCTG GACTCCCTCA 1140 CCTGCCCTAG TCTGCCCCTG GGGTTGGCCC TGCTCCACCC AGCACCTGCT CTGAGGGTGC 1200 CAGGGTGCCG GCCTGCCGGC CAGGGCCTTC CAGTCTCCCC ATCAAGGCTG GATGGCCACT 1260 TCCCACCCGG GGCGGGCTCC AGCCTCATTC CCCAGCGGTG CTGTCCTTCC AAGGAGCTCT 1320 CAGATCACCT GGCTGTCCAC TCGTTTGGGG CTTCTCTGCT GCCTCCGCAG CACTGCGAGG 1380 CCTCTGATCA CCTACTCTCT GTGCTGGGTG CATTTCGGGT 1420
|
| |
|
|
|