| Tag | Content |
|---|
EnhancerAtlas ID | HS187-09987 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:4316120-4316850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:4316664-4316683 | CAGCGCCACCTGGTGGCCA | - | 9.86 | | EWSR1-FLI1 | MA0149.1 | chr17:4316831-4316849 | TCCTTCTTCCTTCCTTCC | - | 7.2 | | IRF1 | MA0050.2 | chr17:4316817-4316838 | GCTTGCTTTCTCTTTCCTTCT | + | 6.71 | | ZNF263 | MA0528.1 | chr17:4316823-4316844 | TTTCTCTTTCCTTCTTCCTTC | - | 6.13 | | ZNF263 | MA0528.1 | chr17:4316361-4316382 | TCTTCCCCTTTTCCGTCCTCC | - | 6.89 | | ZNF263 | MA0528.1 | chr17:4316364-4316385 | TCCCCTTTTCCGTCCTCCTTC | - | 7.49 |
|
| | 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 |
| GH17I004412 | chr17 | 4316139 | 4317190 |
|
Enhancer Sequence | AAGAAAAAAA AAAGATTGAT TTCCCCACCT CCCCACCTCT TCCACGAGTT CCCCAAGCCC 60
TGCAAGATGA CTTCGATGGG ATACAATTGT TTCCACCTCA TCACAGCAGA ATGATAATGC 120
CTATAGCCTG TCAATGGCAA GTTCTCGAAT GTGTGGGCAC CAGGAACACA CCCCGGAAGC 180
CACATGTCCT TGCCCCAAGG GAAGGGCCCT GGAGAGCAGA AGAGAGGAGG AAAGTTGAGC 240
CTCTTCCCCT TTTCCGTCCT CCTTCCTCCT GCCCTGATTC TGCCCACAGA GGAAGGGTCT 300
GAGCTAGAGG AACCTGGACA GTGAATCCAC ACCCTATGGA CAGATGAGAA GACCGAGGCC 360
AGAGACAACG CAGGGTCCGG CCCCTGGTCC TATGCCTGAT GCCTCTCACT GGAGACCCCT 420
CCCCCACTTC AAGGTCGCCC CTAGAAGGCA AACGCTGAAG CCAAGTGTTC TTGGAGCGTC 480
TCTTGGTGGA CGCTTCGGCC CTGCCACGGA ACGGCCCCTT AGTGAAGGTT CTCAGCTTAG 540
ACTTCAGCGC CACCTGGTGG CCACCGGGCA TCAGACCTGG GACTTGCCTC GAGGGCTGCC 600
AGAAACTTGA GTTTGTCCAC TCACATCACT GCATCCCGTG GAGAAGTCCC AGTGCCGACC 660
TGCTTGCTTG CTTGCTTGCT TGCTTGCTTG CTTGCTTGCT TGCTTTCTCT TTCCTTCTTC 720
CTTCCTTCCT 730
|
