| Tag | Content |
|---|
EnhancerAtlas ID | HS184-14374 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:78102820-78103540 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZBTB18 | MA0698.1 | chr17:78103173-78103186 | GAACATCTGGCTT | - | 6.19 | | ZNF263 | MA0528.1 | chr17:78102921-78102942 | TTTCACCCATCCCCCTCCTCC | - | 6.36 | | ZNF263 | MA0528.1 | chr17:78102924-78102945 | CACCCATCCCCCTCCTCCCCC | - | 6.91 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 78102927 | 78103224 | | chr17 | 78103252 | 78103414 |
|
Enhancer Sequence | TCAGTTGTTA GTACACTTGT ACAACCATCA CGATTATCTA ATTCCAGAAC ATTAGAATCA 60
CCTTCAAAAG AAACCCTATA CTCATTTTCA GCCACTCCTT GTTTCACCCA TCCCCCTCCT 120
CCCCCCTCAA GCTCCTGAAA CCACTGTGAA TGGTTTCCTG CTAATCTCTC TATGGATCTA 180
CCTGTTCAGG ACGTTTCATG TAAATGGAAT CACACCACGT GTGGCCTTTT GTGTCTGCCT 240
TCTTCCACCT AGCATATTGC CGAGGTTCAT CCAGGTTGTA GTGTGTCAGC ACTTCATGCC 300
TTTTTATTGC CAAGTAATAT TGTGTGGATT CACCAGTTTT GCTTACAGCT GATGAACATC 360
TGGCTTGTGT CCACTTTTTG GCTCTTATGA ACAATGCTAT GAACACATTA GGTTTATGTG 420
TGCAGATTTT TTAATTCTCT TGAGTATAGA CCTAGGAGGA GAATTGCTAG GTCAACTCCT 480
ATGTTCAACA TTTTGAGGAA CTGCCAAGCT GTTTTCCATA AAGGCTGTGC CTGTTTACAA 540
TCCCACTAGC AATGTATGGG GGTTCCAGTT TCTCCACATT CTCCTAAACA CTGCAGAGCA 600
GTATATTAGT CCATTTTCAT ATTGCTATAA AGAACTGCCT GAGCCCGGGT GCTTTAAAAA 660
GGAAAGAAGT TTAATTGACT CACAGTTCAG TGTGGCTGGG GAGACCTCAG GAAACTTACA 720
|
