Tag | Content |
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EnhancerAtlas ID | HS038-13807 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr22:39941470-39942340 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr22:39941963-39941984 | TTCAGCACCACGGACAGCAGC | + | 10.52 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH22I039545 | chr22 | 39941881 | 39942070 |
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Enhancer Sequence | CTGGGAAACG GAAGTCACAG CTCTGTTTGT TCTGTGACAG TGTGAAAACT CACAACCTTT 60 TCATCGAGAT GGGTAACGAA AACATGAGAA AACTGGAAGT GCTTTGGTTT GGCTCAGCTG 120 AGGACATTAC TCCAAGCCCG CCCAGGCTCT CCCCTCCGGC CTGGATTCGT TTCTGTGTCA 180 ACACTCGCCC AGCCTTGCAC AGCCGGGCAC ACGGGCGTCT CCCTCTGCAG TGGTTCCCCG 240 ACTTGTCGGC CATCTTCGCT GGTGGTGTTT TCCTTGGTCA CTGTGGTTAT TTGAAAGCGA 300 TGTCAAAGCA AACACTGCTC TCTCTCCCTG AAAACCCCTG GCAGGAGCTG CCTTTCTCAC 360 CGTCCCTGTC CTTCGTCTCC TCCTGTCCCT TCCTTCCTGC CGCAGCCTCT TCCCTCAATC 420 CTACTGAACT CCTTCCTGGG AGAGGTTAGG GCGGGAATCG CCACCTTCCA GGGCACGGAG 480 AGGCGAAGCG GAATTCAGCA CCACGGACAG CAGCCCGGCG CGCAGTTGGC GTGCGGTTGG 540 CTCAGGAAGT TATTCTGTAG GTTTTGTAGG TTTATGACCC GCTGTTGGGT AGCAAAAGGC 600 CTTGAACGCT GACTCAGGAG GTCGGGGTGC AGGGAGCTGG ATCGGGGGTG CTGATGATGT 660 CGGAGGAGCT CCTTGTGGAT CTGGAGATAA TTTTCCTATA AAATTCCCTC TCTCCTTTGT 720 TTCCAAGACC CTTGACCACA CTTGCACCTT CCCCTACCAC CTCTCCCTCC ACAGTTAATA 780 ATAACATACA TGTGTCTGTG TGTACTCGAC AGGGAATGCG AACGTATTTG CGTGAATCTG 840 TACCTTGGTG TAATAGTGTA TTTAATACAA 870
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