| Tag | Content |
|---|
EnhancerAtlas ID | HS105-59373 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr4:1309390-1311770 | 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 GACTCACCTG CAGGCCCACC 1440
CGGTCCCACA CTCCAGACTC ACCCCCAGGC CCACCCCGGC CCCCACACTC CACACTCACC 1500
TGCAGGCCCA CCCGGTCCCA CACTCCAGAC TCACCCGCAG GCCCACCCCA GCCCCCACAC 1560
TCCAGACTCA CCTGCAGGCC CACCCCAGCC CCCACACTCC AGACTCACCC GCAGGCTCAC 1620
CCCAGCCCCC ACACTCCAGA CTCACCCGCA GGCCCACCCC AGCCCCCACA CTCCAGACTC 1680
ACCTGCAGGC CCACCCGGCC CCACACTCCA GACTCACCCG CAGGCCCCAC ACTCTGGACT 1740
CATCTGCAGG CCCCACACTC CGGACTCATC TGCAGGCCCC ACACTCCGGA CTCACCCGCA 1800
GACCCACCTG GCCCCACCCT CTTGCTGGCT CTTGTCCTCG GCATTTGTCC CGCACCTCGT 1860
TCACCTTCTC TCAGATGCTG CCCTGGGTGG AGCGGCACCC TCCCACCCAT GCCTTCTCCC 1920
CACTGCTGCA CAGCCTCCCT GCTTGTGTGT GTGTGTGGTG TCCGTCCTGC CCTCCAGGAG 1980
GGGAGTGGCG AGCAGCTGCC CAGTGGGCAG GGTGAGCGAG TGAGTCCTCG TGTCCTGGAG 2040
GCCCTCATCT GCCCAGACCT GCACAGCACT GTTGCTCTCG GCACCGCTGG GGTATGGCGT 2100
CTCGGTTCAC AAGCGTGAAT GTGATGTGTC ACAGCTGTGC CATGAGTTGA TCTGCCAGAT 2160
GGCAAAGTGC ACTGATCCTC TGCGGTGACC GGGGCTGGTG CCCCTGGGTG CCCTGCAGTC 2220
TTGTTGAGTT TCCGAAGTCT CCAGGTCATG ACTCGCAGCC ACTCCAGTGT GCACCCAACA 2280
TTCTCATCGC TGGACGGGGT CGTCTGTGAT GCCTCTGCCG TGCTGCCCAC TGGGCTGCTG 2340
TGGCCCCCAT CTGGTGCCAT TTTTCCTCCA CCTGGGTGTC 2380
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