| Tag | Content |
|---|
EnhancerAtlas ID | HS190-06198 | Organism | Homo sapiens | Tissue/cell | Treg_cell | Coordinate | chr19:6362550-6363710 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr19:6362600-6362611 | GGGTGACTCAG | + | 6.02 | | JUNB | MA0490.1 | chr19:6362600-6362611 | GGGTGACTCAG | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr19:6363352-6363367 | TGAACTCCTGACCTC | - | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGGTGAGCA GGGTCTTTCC TGGGTGCCAG GGGCACTCGT CAGGGCACAC GGGTGACTCA 60
GGGGACCAGA ATCCCGGGTC AGGGATGTTC TCTCTCTGGG AAAGGGTGCA GAGCGTCAGA 120
GTTCCAGAAG TGGCTTTAAA CCACCAAAAG GTGCCTGTTG CTGGCTTTTG AGCCTCGGTT 180
CACAAGTCAG GATGTGGCCT CTTTGATCCT GCACATACTG TTCTGCCAAC CTGACCCGGC 240
TGACATTTAA AAATTGGTAG ATTTTAGGCC GGGCACAGTG GCTCACACCG GTAATCCCAA 300
CACTTTGGGA GGCTGAGGCG GGCGGATTGC TCGAGCTCAG GAGTTCAAGA CCAGCCTGGG 360
TAACGTAGTG AGACCCCATC TCTACAAAAA AAGTACAAAG ATTAGCCGGG CAATGTGGCG 420
TGTGCCTGTA GTCCCAGCAA CTCGGAAGGC TGAGGGAGAA GGATCACTTG AGCCCAGGAG 480
GTCGAGGCTG TAGTGAGCCC ATCTCAAAAA TAATCATAAT TGGTAGATTT TTTCCCCCTC 540
CCCAAAAAAA GTAGTCAATT TTGATTGAGC ACTTATGATG GAGGCATTTT TTTTTTTTTT 600
TATTGAGATG GAGTCTCGTT CTGTCACCCA GGCTGGAGTG CAGTGTTGCA ATCTCAGCTC 660
ACTGCAACCT CTGCCTCCTT GGGTTCAAGC GATTCTCCAG CTTCAGCCTC TCAAGTAGCT 720
GGGGATTACA GGCATGTGCC ACCATGCCTG TCTAATTTTT TGTATTTCGT AGAGATGATG 780
TTTCACCATG TTAGGCTGGT CTTGAACTCC TGACCTCAAG TGATCCACCC GCCTCAGCCT 840
CCCAAAGTGC TGGGATTACA GGCATGAGCC ACCACGCCTG GCCTGATTTC TAGTTTCTCT 900
TGGAAATTTA GTAGATCTGA TCCCATGGTC CACTGGCACA TCTGGCAAGA GTCAGCTGAC 960
TGTAAAGCAA GCGCTCTGCC TTTTGCCTGC ACCTGGGCCG TGTCACTTGT TTTTGTCACC 1020
TCCCAACCCC TGGAAGCATT TGTGTTTGTG AACCCTGCTT TAAAGAGCTG CTTCTAGACC 1080
GGACGCAGTG GCTTACGCTT GTCATTCCAG CACTTTGGGA GGCTGAAGTG GGCTGATCAC 1140
TTGAGGTCAG GAGTTTGAGA 1160
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