| Tag | Content |
|---|
EnhancerAtlas ID | HS023-14744 | Organism | Homo sapiens | Tissue/cell | CD8+ | Coordinate | chr2:111800140-111802020 | 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 | GGGAATGACA AGGGGCCTGC CTTATCAGGA GGAAGGTGTT TGGGAGAAAG GCCAAGAAAC 60
AATATTGAGA GAATGAGCCT GGAAAAGTGG GCCAGGGTGG GTCGTGAGGT GTGCTGGATG 120
CTACATCATG GAGCTTAGCC TCTGCTGGGC AGCAGTAGCT GGCCAAGGAA GGGAAGGAGT 180
TGGAGAGTGA CCATCACACC AGGACTCCCT GGAGGGAAAG TTTCCTGGCT TCGGGGGATG 240
CGGTGCTTTG GAGAAAGAGA CCCCAGAGTG GAGCTGGATG GAGGATGGAG ACCAAAACAA 300
GTGGATGTGA CCAGCAAGCC AGAGGACAAA GATCTGCAAA GAGGTCGTGG CAGTGGGGGT 360
CGAAAGGAGG GTTGGCATTG GAGGAGCAGT GGCCCATTGC CATCCTGGAG GAAGCTGTCC 420
CTTGGGAAGT GCTGAGATCC CAGTGTTCGG AGCAGAAAAC ATGTTGAGAC TTAGTTGTAG 480
ACCAAGAGCT TGTCTGCCAG AGAAGAGATG CATGCTGGCT CCTGTGGGCT TTCAGTTGTG 540
GGGCCAGAGA AAAGGAGGGC CACATGTGTC ATGCTCTGCC GCTCTCTGGA ACAGAGGTGC 600
TTTCTGACAG GGCAGGCTGG GGGACAGTGA GCAGGGCCCT CACCCTCTCG TGGAGGTCCC 660
CCGAGGGCCA GCTCCACACC CCCCACCACA TCTCAACGTG CAGGAGACTG GCTGCACCAT 720
GACTGCTGGT TGCGAAGAAG TTAAAGGCCC CTGTCAACCC TCCGTGTTGA TTCTGAAAAC 780
AAAGCCAGAG TTCTTTCTGC AAAACGAAGC CTTTTTGTTT CTCTCTCTCT CTTTCAACAT 840
TTCCCTGTTG TGTTATGAAA AAGAGGTGGG TGGGGGACTT CAGAAGCTGT CTGGAGTGGC 900
AGACAGCTCT GCAGGATGAG CTGAGAGCGC CGCAGTCACA CACAGGTGGG AGGAGAGGGC 960
TGAGGGACAG TGGGCGCAGT GTCCCACCTC GTGGTGCGGT CAGTGGAGAA GGAGTCATCG 1020
ATAAGGGGCC CCTGGCCAGG AGCCTCAGAT ATGGCTGCTG GGGAGCTTGA CCCTCAAGGC 1080
TCTCAAGGAG AGGCTGGTGA GGAGACGTGG GGCCCTCTAC TTCTGGTGCC AGGGAAGCCT 1140
CAGTAAGGGA GGTCGCTGCC TCTAGAGAAG GCTGCCTGGT TCCCAGCAAT GCTCAGCCAT 1200
CAAACTCCTC CAGAGGAGCT GTCCATGGAG GGGTAGGTGT CAGCCCCCAT ATTTCTGCCA 1260
CAACTAAGAG GAAGCTGGCT TCCTCATCTT CACTGTAGGT ATCTGAGATG AGAGCCACAT 1320
TTCCCTACCA GACTGAAGCT CAGCTGGTGC AATCTCCTCT TTCCAGGGAC CTGGTATTTT 1380
AGTGCCAGGT CTTCCTTCCC TACCAGGAAG GAGCCTGCCC CTCCTATGTG GGGCCCAGGG 1440
CAGAATTACA AAGCAAGCTT ACAACATGTT GAAGAAAATC TACTCTGCCC TCCTGCCCTG 1500
ACAAATGTAG CTTTGTTCAT CCAGAAGGCC AGATTCGAAT TTAGAATGCC CAGGCTCCTA 1560
GCAGTTATGT GAACTCTGCA GCATGGTGAG AAGCAGCCCT TTGGCCCACC TCTCTCTCAT 1620
TGCACCTCCA GGTCTACCCT ACACTGTGCA GATCATCTGG TCTAGACACT CAAGGTCTGT 1680
CCACATCCCT GCAATCAGCT GCCCCTTGGC TACCCCATGG GTCTAGAGTG GACACGGCAG 1740
TGGTGTGGTT CCCCAGTAGC AACACATCGC AGAAAAGAGG CTTAAGGTAT TTGGGTCAGG 1800
AAACAAGAGA ACTGGTCCCT GGAGGAGTGG GTGCAAGTTC CAGGTGGGCA GTACCCATAG 1860
CCCCATGGGC AGGGCCCTCT 1880
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