Tag | Content |
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EnhancerAtlas ID | HS051-20626 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr4:1309390-1310810 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF740 | MA0753.2 | chr4:1309661-1309674 | CCCCCCCCCCCCC | + | 6.03 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGTGCCCGC CAGACGCAGG CACAGCGCCC CAGCTGGCCC CAGGCCTATG GCCAGCCGCC 60 CTGTGGCATG TCCCCCGGCA TGCCTGTGTC CCTACATGCT TGTGTTCCCC TCCCCCCACC 120 CCCGTATGCT TGTGTTCCCC TCCCCCCACC CCCGTGTGCG TGTGTCCCCC CTCCAGTGTG 180 TGTGTGTGTC CCCCTCCCCG TGTGCGTGTC CCCCTCCCCC CATGTGCATG TCCCCACCCC 240 TGTGTGCGTG TGTCCCCTTC CCGTGTGTGT GCCCCCCCCC CCCCAATGTG CGTGTTTCTC 300 CCCCACCCCG TGTGTGTGTC TGCGCTGTGG TGAGGGCCTC CTCCCCAGCT GAGAGGCCCT 360 GACCCTTTGT GGAAACGCAC CTGGGACTTA GCCTTCTGAA GGCAGGAAGT CAGTGTCTAA 420 GCGGCTCTCC AGGTTCTTCT CATTTCCCTG TGGTGTCTGC ACACATCCTG CTTAGGATTT 480 TCCCGCCCGA TACCTGTACC CCGGGTTTTG CGCTGACACA TGCTCCATTG CTTCCTCGTG 540 AGAGCTTTGC CTTTATCTCA GGCGGGGTGC GTTTTCCGTG TTTTCTGTGG CACCCTGTAG 600 AAACACGTGG CACCCTTGCC CTCTGTGGCT ACAGCTGAGC AGACGCTGGG CGGTGCTGCC 660 CTCTGGCACC TTTGGGCCAG GTTAGCTGGG GCGGCCTCTC TGCCATCGGG CAGTTGTCCA 720 CTGCTGTGGG GGCCCATGGC AGTTGGAGCC TCCCAGACCA GCACTTGGGC CCGTCGCCCT 780 TGCCCCTGTC CAGATCCTGC TGTGGGAGCA CAGCCTCACC TGACTCGGGT TAAGGTGGCG 840 TCCGTGTTCC ATTTGACTGA GATGACAACA CTTGAGAACC TCTCAGGCAG GACTTGTGCG 900 AGAGGATTGT GCCCCATGGC CCTGTCCCGG GCCCAGCCTC CCCATGCCCA GCCATGCGCC 960 TGGCCCCACA GGCCTCCCTC CCATGCTGCT CCCTGCCACG GCTCCTCAGC CCACCTCCTC 1020 CCTGCTTCTG TCTAACCAGG GGTCTTCTCT CTTTCCACGG CTTAAATCCC ACCCACATGT 1080 GTGTGGCTCC CACCTGGGGC ATCATGGGCC TCAGCCCTGG CTGAATTCAA CCCCAGCACA 1140 AGGCTCCCTT CCCAGCCTTG GAGGCGGCCT CACATTGTGC AGTCCAAGGC CTCGGGTGCC 1200 CATGGGGCCA CACTCACGCC CCCATGCAGC CATCTGCACG CCCTGCTGGC TTGCAGCCTC 1260 CCCCACACTC CTGTCACGCT CCTGCCCAGC TCCCCAGCCT TGCGGCACTC CAGACTCACC 1320 CCCAGGCCCA CCCGGCCCCA CACTCCAGAC TCACCTGCAG GCCCACCACG GCCCCACACT 1380 CTAGACTCAC CCCCAGGCCC ACCCCGGCCC CCACACTCCA 1420
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