| Tag | Content |
|---|
EnhancerAtlas ID | HS184-23651 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr5:20109170-20110070 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxq1 | MA0040.1 | chr5:20109247-20109258 | AATAAACAATG | - | 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 |
| GH05I020109 | chr5 | 20109561 | 20109710 |
|
Enhancer Sequence | GAAGCTTTGC TGTGCTTAAT ACTGTATCTC TGATGCCAAA GGTAACATAT TAAGATGCAT 60
CCCATACATT TAGTTGGAAT AAACAATGTG ACAGACAAGG AAAAATCTAA TCTTTTATGA 120
TTGAAATGGG GATAGCAATT GAGACTGCCC CTATAAACAA CACAAGAAAG AGCTTAGGGA 180
CACAGTTTAG AAGTAGACAT CCTTTTACGA AAGAGGGTTC CTTCTGAGAA AATGCTCTGA 240
CGAGAGACAC AGTCTCCAAG TTTAAAAGAA CATTTCATTA TCGGCAACAT GCAGAGGGCA 300
TGAAAGACAG AAATCTCAGC TCTAGCAGGC ACACTGACGA GAACAGCAAA GACTGAAGGA 360
TAAAAATGAT CTGAGTTGAT AAGGGCTTTG CAGTTAAAAC AACAGACTTA TACGGCAACA 420
CTCTATGCCC CAGAGGAACG TGGCTCCGGG AAGGGAATGA GGGCCAGTGC TGAACCAGCA 480
GCCAGTGTCT AACTGACTTG CAAATACCTG TTCAGCAGGT AGTTTTCCTT CAGACCTTCC 540
CAAGCCAGGT TCCCCTAAGG CTGTGTTTAT GGTTTTTGAA GTATGGAATG TATAGCCTTT 600
TTCCTTTTCT TGGTGCTTTA ATTTAGGAAA CAGCACAGTC ATTTTTTGCT TATTTAATTG 660
TTTTTGTTTG TTTTGCTTTT GCAACAACAA AGGATTGTTT TCTGGAAGAC GTGATTATCT 720
TTCTCCTGCT TTGTTCCTTT CTAACTTCAA AGAGGTTTTT GAATAATGAA GACATTTCTT 780
TAGAATTAAA AAAAATACTT TTGGATGTCT TCTAGGCATT CAGGAATTTG AAGTAAAGTC 840
ACTTGAAACT AAATACTTGT GTTAGAATGT AAAGCAATGT TTTGGTATTG TTCTTTAATG 900
|
