| Tag | Content |
|---|
EnhancerAtlas ID | HS187-12043 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr19:15666590-15667760 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:15666824-15666843 | GGGCGCCCCCCGGTGGCCT | - | 6.19 |
| | | 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 |
| GH19I015555 | chr19 | 15666212 | 15667930 |
| Enhancer Sequence | TAGAAACTGA GCCCCCGAAT GAAGTGACTT ACCCAAGATC ATTCGGTGCG GCCTCAGCGC 60
TGGCGCTGAG TCCTCTTCTG CCCCACCCCT CAGGCTCCCA GTCCTGGTCT AGATCCCTAG 120
CCACGTAGCG TAGAAGGGGG CGTCGACGGG GGTTGGGCTA GAGTTGGAGC GGGGAGGAGA 180
TGAGCTAAAG CGGGGCTGGC TGTGCGAGAG GCAGTAGCAG CGGCGTGTGT CCTGGGGCGC 240
CCCCCGGTGG CCTGTGCTGG GGTCGTCGGC CGGGATCCCC TGTTCGACGT ACTCCGGGGC 300
TGAATGGGAA ACAGACAGTC CCAGACCCTA CGTGAGCCAC CCGGATCTTG CAGGTGCTGC 360
CTCTCCTACA CCCCCCTCCC AACCGAGGGT CTCCAAGAGC GCATCCTTTG CCAAACATCT 420
CCTGGGCCCT TTTCGGCGCA ACCTCGCCAT CCACTAGCAA ACGAAGTTAG CCTTGAGATC 480
CGACATATGT GGGCTCAATC TAGGCTCTTC CTTCCTAGGG GCGGCCTTGG GCACGTGACT 540
GTCCCTCTCT GCACCTCGGC TTTTTCTTGT CATGCGAATA GTCCGGTATC ATCATGCTTG 600
TAATGCACAC TGAGTTTCCG CCAAGGGCCA CGAGGGTGAA TAAATGAGAA TGAGAAGGGG 660
AGGAGTAAGG TCCCTGGGTC CCCGGAGCCC TGTTACACGT ACTGCAAGTG TAATTCTCAA 720
AACACCGAAG TCTGGTCCTG TCGCTGGCGG CTGTGGGACC TCCTTCCTCC TGAGTGTGAA 780
GAACGCTCCC TCTGCTGGAC AATTTGGAGA TCCATTCTCT ATTCGTTCAA TTTTGTGTCC 840
GTGCACGTTT GAGCGTGCAT GTGTGACCGC GTATGTGTTT GGGTGCATTT GGGTAACAGT 900
GTGTGCATGT GTTGTAGTGT GCACACGAGT GTGTGTAAAC GTGTATGTGT CGGTGTGACT 960
GTGTGTGCGC ATATGGATGG GTGTGTTGGA AGGAGAGGAG AGGAGAACTC CACTCACTGA 1020
GTCACTGTAA CTATCCACAC ACACCAGGCT GTGTTCCTGC TCATGGCTGG AGCCACTGTC 1080
AGAGCCCTTG CCTCTGTCCC CAGGTCTGAC CTGTGCGGTG CAGGCAGGAC ATTCTGGAGA 1140
AATCATGCCC TTGGAGGAAG CTGTCAGTAA 1170
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