| Tag | Content |
|---|
EnhancerAtlas ID | HS187-26047 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chrX:152996090-152997200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chrX:152997100-152997112 | TTCTGTTTACTG | - | 6.02 | | Foxd3 | MA0041.1 | chrX:152996342-152996354 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chrX:152996498-152996510 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chrX:152996502-152996514 | GTTTGTTTGTTT | + | 6.32 | | HSF1 | MA0486.2 | chrX:152996979-152996992 | TTCTGGAAGATTC | + | 6.09 | | IRF1 | MA0050.2 | chrX:152997087-152997108 | TGTGTCTTTCGGTTTCTGTTT | + | 6.34 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chrX | 152997036 | 152997174 | | chrX | 152996642 | 152996817 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH0XI153730 | chrX | 152995693 | 152998536 |
|
Enhancer Sequence | GTTAGGTTAA TCAATAGCTC CGCCTTCTCC TGGACCTTAG AACGCAGAAG CAGCCCCGTG 60
GGGCATGGCA TCATAGCCCA GCCAAGAGTT GGATTTGTAC CTAGTTTTTC CTCTTTGCTA 120
TCGCCTTATC CACACGTGTT GAAACTCACT CGCATGTTTG CTGAGTTCTG TGCTCACCAT 180
TTCGTTCCTA CATCTCAATT TCTCTTCTAT GTTCTGTTAT CTTCCTCCAG ATAGACATGT 240
TTTTAGTTTT TTGTTTGTTT GTTTTTTAAC TCACAACTAT GCTCAGGACA AACAGTCATC 300
AGTGCTTCTA GTTGTGGTTG GTTTTTAAAA AAGGTTCTTT CAGCAAGGGT TTTGTCATGG 360
GAAATTCTTG ATTATTTTAT TGTAATTCTT TGTGTTGTTT AGTTTTTTGT TTGTTTGTTT 420
GTTTTTTGTA GAGGCAGGTT CTCGCTGTGT TGCCCAGGCT AGTGTGGAAC TCCTGGGCTC 480
AAGCGGTCCT CCCGCATTAG CCTCTCAAAG TGCTGGGATT ACAGACGTGA GCCACCACAC 540
CCAGGCTGTT GTCATTCTTG ATTATTTTTG TTGAAAATGT TTCTATTTCA CCCTTATTCC 600
CAAGCTAAAG TTGAGTTGCG CAATGGAGTC TAGGTGGACT GTTCTTTTCT CTCAGCCCTT 660
TCACAATGTC TCATTGTCTC CCTGCTTCTT CTGTAGCTGC TGACAAATCT GTAGCTGCTA 720
ACAAATTGTC CTCCCTGAGT ACCCTGTGTT TCTTTTTTTC TGGGTACTTT GATCACTTTC 780
TTTCTTTTTG GCATTCTGCA GTTTCACTAT GACATGTTTA GGTGTCAGTT TTTGTTGATT 840
CTGCTTGAGA CTTGTTATAT GTCCTTTGAA TATTTGAGTT TTTCAATCAT TCTGGAAGAT 900
TCTCAGCTAT TAGCTTTTCA GATATTGCCT GACTCTCATT CTTTTTTCCT GTTCTTCTAG 960
AACTGGCAGC CAGTGCTGGA CTTCTGACTC TCTTCGTTGT GTCTTTCGGT TTCTGTTTAC 1020
TGTTTCCCAT CTCACACTGT CTGTGCTGAA TTCTGGGGAT GCCCTGAGGC CTTCCTGTTT 1080
GCTCATTTTC CAGTTCACCA GTTTTCTCTT 1110
|
