| Tag | Content |
|---|
EnhancerAtlas ID | HS184-04988 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:6658780-6659780 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr11:6659387-6659402 | GAGGACAAGAGGTCA | + | 6.81 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 6659229 | 6659458 | | chr11 | 6659189 | 6659513 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I006637 | chr11 | 6658721 | 6658927 | | GH11I006638 | chr11 | 6659163 | 6659930 |
|
Enhancer Sequence | CCAGAGATCC TGAGCCCCTA GTAGGCCCTT GAACAAACTG GGCCCTCCCA CACCTCTGTG 60
CACCTCACCT CTGCTTGGAA GCCTTCCCCC ATCTGATACT CTCATAAATT GCTCATTCTT 120
TAAGTCTCAA CTCAGGGATC CCTTCCTTCA GGAAAGCACT CATACTGCCT ATCTGTACCT 180
CATATATATC CCCAAATGGA AATGTTCTTA TTGGAATGAA ACTATTTCTT TGCACATGAA 240
TCTCCCCTCT ATAAACTCCT TAAGATGAGG GGAGTGACGC ATTCATGACT GTATTCCGTG 300
TCTCTAATAC AGTGACTAGC ACATGGTAGA CATTCAATAC ATGTATATTG AATAAATCAA 360
ACATTAAGAC TTCTTGTGAC AGTTGTAAAC CCCAAATGGT CATTTTTACC CCGATTCTCT 420
ATGGTTACTA ATAGTAAAAA CTCCAGGAAA CCACCTGGAG AGTTGCCCTC TTGCTTCAGG 480
CACTAGTGAG GAGAGAAGTC TGGAAGCCAT AGCCCATTGG TCCTGGACAA GAAGGAGAGT 540
AAACACGTGG AAGAGTGGGT GGTGGAGCTG CACAGCAGCA GGCGAGCAAA TATGCAGAGT 600
CTGGCCAGAG GACAAGAGGT CAGCCAGGCC CAGAGCTAGC CTGGAAGTCT ATGCCCTGAG 660
GAGATGTTCA AGAGTCTGGT GGAGTTTGGA GACATAAGGA CACTAAGCAC CAGCCTCCTA 720
AGAGGACTCC CTGCCCACTG TCCTCTCTCC TGCTGCCATT CTCCACAGTG CAGCCAAAGC 780
AATCTTTCTT AAAGACATAT CAGATTTGCT TAGAGTCCTT CACTTGCTCC CTATGATTTT 840
CAAGATAAAG TTGAATTTGT GACCTGGCTC CTGTCTACTG TCTTTTCTCA TCTCCCCCGA 900
CTCTTTCTCA TTAGTACAGC TGATGCCAGC CTGAACAATA CAGTCTCCTG AACACGTCCT 960
GGTATTTGTT CAGCAGCTCT TTCCTTAGGC CTGGAGTCTC 1000
|
