| Tag | Content |
|---|
EnhancerAtlas ID | HS082-20770 | Organism | Homo sapiens | Tissue/cell | HCASMC | Coordinate | chr2:242446210-242447420 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr2:242447038-242447052 | CAGGCCGAGGCCGC | - | 6.99 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGGTGGCAGA TTTTTCTCCC AGCACCTTAG TCATGTAAGT TACCAGATAC AGAATGCCAA 60
AAGCAAACCA AAAATCTGTT AGCTTAATTC AGCAACAGTC AGCAAGCCCC AGTCTCATCT 120
GTGACCACGC AGGTCCAGGT TGCCTGGCCC AACAGCTGCA CATGGTGTTC CGGGTCTCTA 180
GGCTGGTCCG GTTTCCTCCA AAGCAGCCCT GACTCCAGTT CCTGCCCCTA CGCGAACAGA 240
CGCCCTTCCT GTTCCACTGC AGGCCCAACT CTCCATTCAG CACATAGGAG TGAACAAGGA 300
GGGCCACACA TTTTAGCGGC GATTCCAACG CCTTAGGTAG AGCCAAGGCA TCAAGGAGAA 360
TAAAACCGAA CAGCTAAGAT GTAAGAAAAC CCAGCGGCCA GAGTCAAAAA AGTGGGGAGG 420
GGTAGAGAAT GCAAGTCCCC AGGCCCCAGG TTGGCTGACC CCACCCTCCT TCCCCGGCAA 480
GCCCTTTGGC ACCAGCAGCT GGTCCTCATT CCAGGCTAAG GGCTCGCCGT AGTGGCTCCC 540
TCCGAGGCTG TCCCACCAGA CGCTTAAAGG TGGCTCCATA GTGGAAACGA CTTCTTTAAA 600
GAAGAAAGAT GAGTCTCATG TTCGGGCAAC CGCCCGTCGC AGGGGTTAAA CGGTCCTGAC 660
AGAGCAGCCT TTTCACCCTC CCCTGGGCCA AAGCACACAC GTGTTCTCTG CTTTCCCTGC 720
ACACCGGCCA CTCAGATCTG CTTCTCCACA ATCTCAGCCC CTCAGCGCCC GCCAGGGTCT 780
CCCCTACAGC CCCTGCCCAG CCCAACACGG CCAGAATGAC CCGCGGCCCA GGCCGAGGCC 840
GCAGGGTGGC CCCCGACCTT CCACTGCCTT CGGATGCTGA CATGAGGTTC CCGCCCCGCG 900
CTGGGGGCAG CGCCCCGTCC CTGCGCCGGT GTCTCTTCAC GCACCTCCAC CGCCCTCGCA 960
CAGGCGGAGC CACCAGGGGC TCGGTTTCTA GAGGCCTGCG AGCTTCTGCC ACGCAAAACG 1020
CCACAGGCAC ACGGCAGAGC CCCGGGGCCG CCCTGCGCCC ACCTCAGGAC GGCTCCGCTG 1080
GTCGCACGAC GCGCGCTCCT TCCCTCACCC CACTGCCCGC TCCGGCGTGG CGCTCCCCTC 1140
TGAACCCCCA GGAGACTCTG GAGCCCCTCG GTGAGAGGCC GCTAGTCTTC CTGACCTGCA 1200
CCCTTCTCAC 1210
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