| Tag | Content |
|---|
EnhancerAtlas ID | HS187-11088 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:78400390-78401360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:78400847-78400866 | TGGCCTCCAGGGGGCAGCA | + | 7.66 | | EWSR1-FLI1 | MA0149.1 | chr17:78401020-78401038 | CCTTTCTTCCTCCATTCC | - | 6.64 | | TFAP2C | MA0524.2 | chr17:78400763-78400775 | TGCCCTGGGGCA | + | 6.44 | | TFAP2C | MA0524.2 | chr17:78400763-78400775 | TGCCCTGGGGCA | - | 7.22 |
|
| | 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 |
| GH17I080426 | chr17 | 78400600 | 78401201 |
|
Enhancer Sequence | TAGTGTGCCC TGATTGGGCC ACTGCACTCC AGCCTGGGTG ACAGAGCAAG ACCTTATCTC 60
AAAAAAACTT TAAAAAACAA AAACTCAGCA GGAAGGTGTG GCCGGAGCCA GATGGCAGTG 120
AAGTACAGAG TGGGTGGGAG CCCGTGAGCA TCTTGGGGTG CGCCAGGGTT TCAGACGTCA 180
CCCACAGGGA CTTGGATGGC TGTGAGTTGG CAGCGGGGCG CCCGCAGATT GGCCTTTTTA 240
GGTGGCCGCT GTGCGTGCTG TGGAGGCTGT GGACGCAGGT CTGCACAAGC CATGCTGCTT 300
CCAGCAGCCC AGCCCCTGAG CCTCCCTGGT GTCTGCCCCT TCCCCATCTT ACCCCACCGC 360
TTGCCCTGCA GCCTGCCCTG GGGCAGCCGC AGCACCGGTG GAAAACCCCC AGGCCACCAC 420
CTTCGGGCCG GGGCCTTCCG GCTGCTGGCG CGCAGTGTGG CCTCCAGGGG GCAGCAGCAG 480
CCCACATACC ACAATGGCCC TCGCCCTGGG GAGCTGTGCT CAGTGGTGGC GTCTGAGAGC 540
GGGCTCCACA GCCTTGCAGG GCTTTGCTCA GGGCACAGGT GTGTGGACTC TCAAGCCTGT 600
GAGCTGTGTC CCCAGCCCCC AGGAAAGAGG CCTTTCTTCC TCCATTCCAA CTCAGCCGTG 660
TGGTCTTCCG AGAGAGAACC CAAGAAACTG TCCCCCAGGC CTTCAGCCAC AGGAACTTTA 720
GGTCGTGCTG CTGCTGCAGA CAGCACAGTT CCTGGAGCTC CTGTACCTTT TTCTGCCTCA 780
GCGCGCCCCA GAGTAGGACA GTGGCCCATC CTTGCAAGGG AGGGGACACC TGGCCTGTGA 840
GTACCTTAAG CATCTAGAAA TAGAGCAAGG ATCTGTGCCT AGCACCAGCA AAGAGCCTGC 900
CAAATCCTGG GCCCACCCTC CAGAGGAAGG AAAGCCGCAA CCAGTTGGGA TATGCAGCCA 960
CCCCGTACCA 970
|
