| Tag | Content |
|---|
EnhancerAtlas ID | HS059-49665 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chrX:154285190-154286190 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chrX:154285799-154285818 | CATCGCCCCCTTGTGGCGG | - | 6.55 |
| | | 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 |
| GH0XI155056 | chrX | 154284937 | 154286370 |
| Enhancer Sequence | AGACTGTATT CTGATTGTCT GAATTAAGAT CTGTAGGTAG GTCCCTCCTG AAGTTTTTTC 60
CCAGCTGGCT GCCTCTACGA CTGTGAGGGT CATGGTTGAG GTCAGTATTG CAGGTTGGCC 120
TCATCCTGCT AGTATGAGAA CGGCTGTGAG TTCTGCCCAC GGTGTGAGGC CACTGTGACC 180
ACTTGGGATT GTGCAGAGCT GGCATGGAGG TTGAACACGC ACAGCTGCAC ACCTTGTTTT 240
CAGTTTAGCT GAACCATCGG TGAAGGAGGC TCAGGCATTT GGGGTTACCT GTGAATCAAG 300
GCCCTATTGT GCCAGCAGTT TTGTTTCAGG TGGTGAAGTG GGAGTTAAGG TTTCCCCCAA 360
AAGAACAGCT GCCACTCCTC CATGCAAAAC CGAGATGATT CAAGGACCAG GCAGCTCCAC 420
CTTTCAGTGC ACTACTTTCA TTTGACTGGA GAGGCCTGCT TAGCTAGGCA CGTATTTTCT 480
CCAGTAGCAG AGTCCAATGA CGCTCTGGAC TTCCTAATTA GTGGTGGTGG GGCGGAAGTT 540
TTTCCTTGGG AAGAGCGTTG TCGCTGTATA TGGTCCGCAG AAACTTGACT TGGAATGTGT 600
TCGGGGTTTC ATCGCCCCCT TGTGGCGGCG ACGTGGTAAC ACCGCACTCA AGGCTTCCAA 660
CTTGTCAACC AATAGGATGG CATCTACGTA GTGAAGGCTT CCCTTCCCTT GTCCTGCAGC 720
GTGCTGGACA GTGTCCCGGC TCAGGGACCC CTTCTGTCCC CTTCCTGGCT ACTATGGGTC 780
GGCCCTGCGT CCTCACCACT TTGAGCCACC CTTTGACCCA GCGTCTCTCC CGCAATGGGA 840
CCTGGTGGGA TGGGGACTTG GAGCATGCTA CAGGAGAGGT AGAACTTTTG AGTCTCTTCT 900
TCCCAAGGTT CTCCCCAGAG TCGGAGAGCA GAGACGGATC CAGGGGCACT TTCTGGCCGC 960
TGCCTGCTCG GGCTCAACAG ATGGAGTCCA ATGTTTCAGT 1000
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