| Tag | Content |
|---|
EnhancerAtlas ID | HS187-16378 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr22:39941370-39942430 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr22:39941963-39941984 | TTCAGCACCACGGACAGCAGC | + | 10.52 |
|
| | 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 |
|
Enhancer Sequence | GAAGGTTAGT GCTCCTCTCC CTCCCCAGAG GAAAACAAAA TTTTAGAGAC TGTCAGAAAT 60
GTGATGGAGC TGTCAGGAGA ACATGAAACA GCCACGTACC CTGGGAAACG GAAGTCACAG 120
CTCTGTTTGT TCTGTGACAG TGTGAAAACT CACAACCTTT TCATCGAGAT GGGTAACGAA 180
AACATGAGAA AACTGGAAGT GCTTTGGTTT GGCTCAGCTG AGGACATTAC TCCAAGCCCG 240
CCCAGGCTCT CCCCTCCGGC CTGGATTCGT TTCTGTGTCA ACACTCGCCC AGCCTTGCAC 300
AGCCGGGCAC ACGGGCGTCT CCCTCTGCAG TGGTTCCCCG ACTTGTCGGC CATCTTCGCT 360
GGTGGTGTTT TCCTTGGTCA CTGTGGTTAT TTGAAAGCGA TGTCAAAGCA AACACTGCTC 420
TCTCTCCCTG AAAACCCCTG GCAGGAGCTG CCTTTCTCAC CGTCCCTGTC CTTCGTCTCC 480
TCCTGTCCCT TCCTTCCTGC CGCAGCCTCT TCCCTCAATC CTACTGAACT CCTTCCTGGG 540
AGAGGTTAGG GCGGGAATCG CCACCTTCCA GGGCACGGAG AGGCGAAGCG GAATTCAGCA 600
CCACGGACAG CAGCCCGGCG CGCAGTTGGC GTGCGGTTGG CTCAGGAAGT TATTCTGTAG 660
GTTTTGTAGG TTTATGACCC GCTGTTGGGT AGCAAAAGGC CTTGAACGCT GACTCAGGAG 720
GTCGGGGTGC AGGGAGCTGG ATCGGGGGTG CTGATGATGT CGGAGGAGCT CCTTGTGGAT 780
CTGGAGATAA TTTTCCTATA AAATTCCCTC TCTCCTTTGT TTCCAAGACC CTTGACCACA 840
CTTGCACCTT CCCCTACCAC CTCTCCCTCC ACAGTTAATA ATAACATACA TGTGTCTGTG 900
TGTACTCGAC AGGGAATGCG AACGTATTTG CGTGAATCTG TACCTTGGTG TAATAGTGTA 960
TTTAATACAA GTAGTATCTG GGTGTACGTG TGAGGATGTT TGTGGGATTT GTGGGTCTGT 1020
GTGAACGTGT CAGTCTCTGT GTCTGTGTGT GTGTGCACAT 1060
|
