| Tag | Content |
|---|
EnhancerAtlas ID | HS191-40191 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chrX:18894900-18895960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MLX | MA0663.1 | chrX:18895812-18895822 | ATCACGTGAT | + | 6.02 | | MLX | MA0663.1 | chrX:18895812-18895822 | ATCACGTGAT | - | 6.02 | | MLXIPL | MA0664.1 | chrX:18895812-18895822 | ATCACGTGAT | + | 6.02 | | MLXIPL | MA0664.1 | chrX:18895812-18895822 | ATCACGTGAT | - | 6.02 |
|
| | 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 |
| GH0XI018877 | chrX | 18895701 | 18895850 |
|
Enhancer Sequence | GGACTAAGGG TGCGTGCCAC CACACCCAAC TAATTCTTAA ATTTTTGGTA GAGATGAGGT 60
CTCACTATGT TGCTCAAGCT GGTCTCAAAC TCCTGGGCTC ACGTGATCTT CCTGCCTCAG 120
CTTCCCAGAT TGCTGGGATT GCAGGCATGA GCCACGGTGC CAGGTCAATT GCTTACATTT 180
TAATGGCCAA AGGGAAGAAG TTGTTCTCTA ACTTCTGAAA GTGTTCGGAA AAACTGCAGA 240
GCTTAAATGA CTGCTGAGAG ATTTGGGATT CTGAACAGAC ACTGCGAGGA GCCAGAGTTT 300
GGGGGTTGGT GACCTGGACA CAGCTGCCGC CACTTTCTGA TGGAGAGAGG GTCCTCTGAG 360
TGGAGCTAGT GGCAGAGGTT GTAGAGCCCA GCACCACTAG GAGGGATGGG AGGTCCCTGA 420
GGAGGGAGAA CAGGCAGGGT CCCACTTGGA AGTACCGCAA TGGCTGTGTC TTCCTTGGTC 480
CTTCCAGGGC GTTGCTGCTT GTGATTCTTT GCTTTCCCAG GGTCCATGTG GGAGGAAACA 540
GCTCACAGGT CATCAATGAG ACATCGGAGA GAGCCGCTAG GTGTTGTGGC AGATGAGGCA 600
GTGCCTCCAC GTGTGCTCAT GGGCACTCCC GGTCATGAAG AGTGACCCAC CTTGGCAAGG 660
CTCTGGAGCT TGGTGGCCTT TGACATCCCG ACCCAGAGCC TATTCAGGAT CCCAGTGTCT 720
CCTTGGATTT GGAGACACTC ATTCATTCCC AGCAATGAAC ACCAAGCTTT TCTCATTCCT 780
TTGGCTTGTA CAGTACAGAC CCCTCAGCAA CTGCGCTCCA TGCACGCAGC ACTGTGTGGA 840
CTTGTTCCCC TGGTAACCAC CTTCTATTCC CTATTACTGT GAGCTGGACT TTAGATTCCA 900
CATAGAAGAA GGATCACGTG ATATTTGTCT GTGTCTGGCT TATTTCACTT AGCATAATGC 960
CCTCCAGGTG CATTCGTGTG GAGGCAGGAC TTCCTCCTCC ATTTTTTTTT TTTTTTTTAA 1020
GGCAGAGTCT CGCTCGGTCA CCTAGGCTGG AGTGCAGTGG 1060
|
