| Tag | Content |
|---|
EnhancerAtlas ID | HS184-15168 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr19:8749420-8750170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:8749595-8749610 | TGAACTCTTGCCCTC | - | 6 | | SCRT1 | MA0743.1 | chr19:8749863-8749878 | ACACACTTGTTGCAT | - | 6.01 | | TCF7L2 | MA0523.1 | chr19:8749983-8749997 | TGCCTTTGATGTCA | - | 6.22 |
|
| | 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 |
| GH19I008637 | chr19 | 8747255 | 8750711 |
|
Enhancer Sequence | CTCTTTTGTA TAACAGATGT TACCCAGATG TCAGCTGGGG TCAATAGAGC CTCAGAGATT 60
TGGCGTCTGC CTCTCTCCCA CGACCTGTGG GAAGCCTGGT GCCCTCTGTG AGATGCTTGT 120
GAATTCCCAG GGCCTCTGTT CTCATGGTTG CGTCTTGGCC TGAGTTCCTG CCCGCTGAAC 180
TCTTGCCCTC ACCCACCTTC CTGGGGCCAG TGCTTTGCAG GTGAACCGGT CCTGTGTTCT 240
TGATTTTCCC CCAGATCACT CTTGCACATG GACTGCCTGC AGGTTGCCTC TCAAGATACT 300
GTGCTCTCCC AGTCTGGCCA ATGTAGCAAG AACCTATTGT TCCTGCTGTA GTTTTTTTTT 360
TTTTTTTTTT TTTTTTACCA TTGCTTGAGC TTCTGCATAA GATGTTGCTT GACAAAGCAT 420
TCCACCACCA ACAGGAAAAG TTTACACACT TGTTGCATAA CACAGCATAG AGCGTGATGA 480
CCGGCTTGGA GTTTACCAGG CTGTCCTGTG AAGGGGAAGT TCACTTAGGA CACCCGGGGC 540
CAATGGCTGT GAGCAGCAGA AGGTGCCTTT GATGTCAAGC TGTCTTGAAC GCTGCTGCTC 600
CCGGGTGGGT AAGAGCTGGC ACAGTCCAGA AAAATTGAGG CGGCGACACG ATGAGAGACA 660
GCAACCCATC CCCAGACAAA CCTCAAGAGA CCAGAAGCAG CCACATTGCA CCAGACTTCT 720
GGAAAATTAG GCAAGCGTTG GCAACAGAAT 750
|
