| Tag | Content |
|---|
EnhancerAtlas ID | HS047-35339 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chrX:2242770-2243870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| YY1 | MA0095.2 | chrX:2243252-2243264 | CAAGATGGCGGC | + | 7.22 | | YY1 | MA0095.2 | chrX:2243301-2243313 | CAAGATGGCGGC | + | 7.22 | | YY1 | MA0095.2 | chrX:2243350-2243362 | CAAGATGGCGGC | + | 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 |
| GH0XI002324 | chrX | 2242842 | 2243935 |
|
Enhancer Sequence | GTAAGGGTAT GGGAGTCCTC GGCAAGGCTT TTTTCTTTTC TTTTTTTTTT TTTTTTTGAG 60
ATGGAGTCCC GCTCTGTCGC CCAGGCTGGA GTGTAGTGGC GTGATGTTCG CTCATTGCAA 120
CCTCCGCCTC CCGGGTTCAA GCAATTCGCC TGCCTCAGCC TCCTAAGTAG CTGGCATTAT 180
AGGTACGCAC CACCAAGCCC GGCTAATTTT TGTTTTGTTT TTTTTTTTTT TAGTAGAGAC 240
GCGGTTTCAC TGGTCAGGCT CGTCTCGAAC CCCTGACCTA ATGATCCACC CGCCTCAGCC 300
TCCAAAAGTG CTGGGATGAC AGGTGTGAGC CACTGCGCCC GGCAGCTTTT CTCTTTAACG 360
AAAAGCAGCC CCAAGTCATT TTCTAACAAT GAACAGCCTG TCAAGTCGAG CTGCAGACAT 420
ACACAAGCCA GCTGGGAGCT TGTACGGGTG AATGTCGGGA GGACCTAGGG ACTAGACACG 480
TTCAAGATGG CGGCTCCATC TTCCCGGGAG GAACTAACGA CTAGACACGT TCAAGATGGC 540
GGCTCCATCT TCCGGGCAGG AACTAGGGAC TAGACACGTT CAAGATGGCG GCTCCATCTT 600
CCCGGCAGGA ACTAGGGACT AGACACGTTC AAGATGGCGG TTCCATCTTC CCGGCAGGAA 660
CTAGGGACTA GACACATTCA AAACGGCGGC TCCATCTTCC CAGCAGGAAC TAGAGACTAG 720
ACACGTTCAA GACAGTGGCT CCATCTTCCC TCCTCTTTGT CAGCCACATG TAAAGTAAGA 780
AAAACAGGAC CGAGAGCCCC GACCAACTAC AAAGCCCATT TGCATAACCG ATTAGGGTGG 840
GCAACCAGCC TTTCCTGTGG GCTATGTAAA TGTCATGCTT GATGGAACCA ATCTCTCGGA 900
GAGCCCCGAC CAACTACAAA GCCCATTTGC ATAAACGATT AGGGTGGGCA ACCAGCCTTT 960
CCTGTGGGCT ATGTAAATGC CATGCTTGAT GGAACCAATC TCTGAGCTCT ATGTAAATGA 1020
GACACCGCCT CCTCAAACTG GACTATAAAA TCCATCACAT TTGGTGCCAG CTGGTCCTTT 1080
CCGCTCGGAG ACCCCTTTCT 1100
|
