| Tag | Content |
|---|
EnhancerAtlas ID | HS059-26140 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr2:111799840-111801530 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF740 | MA0753.2 | chr2:111800813-111800826 | CCACACCCCCCAC | + | 6.03 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 111800784 | 111801000 | | chr2 | 111801000 | 111801430 |
| Enhancer Sequence | TTCAGTACCT CCTATTTGCC AGACTTAGGA CTCAGATTAT CAGAACAATG TGACGCTTTT 60
CAATCCAGCA GAGGGAATAG GATGTGAACA CAGCGCCCAC ACACACATGG AGCAGGAGAG 120
CCTGTGAGAG GTGCAGGCTC CCTGCACGGC CACAGGCTCC CACGTGGTGT CACAGAAGAC 180
CCATTGGTGC TGGGTCTTGA AACATGCATA GGTTCCCGAA GGTGGGGACG TGGCTCTGCA 240
GGATGGGAAG AAGCCATAGA GTGGACAGAA GTGGAGGTGG CAGAGTGAAG GGCTTGAACA 300
GGGAATGACA AGGGGCCTGC CTTATCAGGA GGAAGGTGTT TGGGAGAAAG GCCAAGAAAC 360
AATATTGAGA GAATGAGCCT GGAAAAGTGG GCCAGGGTGG GTCGTGAGGT GTGCTGGATG 420
CTACATCATG GAGCTTAGCC TCTGCTGGGC AGCAGTAGCT GGCCAAGGAA GGGAAGGAGT 480
TGGAGAGTGA CCATCACACC AGGACTCCCT GGAGGGAAAG TTTCCTGGCT TCGGGGGATG 540
CGGTGCTTTG GAGAAAGAGA CCCCAGAGTG GAGCTGGATG GAGGATGGAG ACCAAAACAA 600
GTGGATGTGA CCAGCAAGCC AGAGGACAAA GATCTGCAAA GAGGTCGTGG CAGTGGGGGT 660
CGAAAGGAGG GTTGGCATTG GAGGAGCAGT GGCCCATTGC CATCCTGGAG GAAGCTGTCC 720
CTTGGGAAGT GCTGAGATCC CAGTGTTCGG AGCAGAAAAC ATGTTGAGAC TTAGTTGTAG 780
ACCAAGAGCT TGTCTGCCAG AGAAGAGATG CATGCTGGCT CCTGTGGGCT TTCAGTTGTG 840
GGGCCAGAGA AAAGGAGGGC CACATGTGTC ATGCTCTGCC GCTCTCTGGA ACAGAGGTGC 900
TTTCTGACAG GGCAGGCTGG GGGACAGTGA GCAGGGCCCT CACCCTCTCG TGGAGGTCCC 960
CCGAGGGCCA GCTCCACACC CCCCACCACA TCTCAACGTG CAGGAGACTG GCTGCACCAT 1020
GACTGCTGGT TGCGAAGAAG TTAAAGGCCC CTGTCAACCC TCCGTGTTGA TTCTGAAAAC 1080
AAAGCCAGAG TTCTTTCTGC AAAACGAAGC CTTTTTGTTT CTCTCTCTCT CTTTCAACAT 1140
TTCCCTGTTG TGTTATGAAA AAGAGGTGGG TGGGGGACTT CAGAAGCTGT CTGGAGTGGC 1200
AGACAGCTCT GCAGGATGAG CTGAGAGCGC CGCAGTCACA CACAGGTGGG AGGAGAGGGC 1260
TGAGGGACAG TGGGCGCAGT GTCCCACCTC GTGGTGCGGT CAGTGGAGAA GGAGTCATCG 1320
ATAAGGGGCC CCTGGCCAGG AGCCTCAGAT ATGGCTGCTG GGGAGCTTGA CCCTCAAGGC 1380
TCTCAAGGAG AGGCTGGTGA GGAGACGTGG GGCCCTCTAC TTCTGGTGCC AGGGAAGCCT 1440
CAGTAAGGGA GGTCGCTGCC TCTAGAGAAG GCTGCCTGGT TCCCAGCAAT GCTCAGCCAT 1500
CAAACTCCTC CAGAGGAGCT GTCCATGGAG GGGTAGGTGT CAGCCCCCAT ATTTCTGCCA 1560
CAACTAAGAG GAAGCTGGCT TCCTCATCTT CACTGTAGGT ATCTGAGATG AGAGCCACAT 1620
TTCCCTACCA GACTGAAGCT CAGCTGGTGC AATCTCCTCT TTCCAGGGAC CTGGTATTTT 1680
AGTGCCAGGT 1690
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