| Tag | Content |
|---|
EnhancerAtlas ID | HS184-19255 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr22:27159580-27160420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr22:27160063-27160075 | GTTTGTTTGTTT | + | 6.32 | | KLF4 | MA0039.3 | chr22:27159820-27159831 | GCAGGGTGTGG | - | 6.62 | | MYCN | MA0104.4 | chr22:27160177-27160189 | GGCCACGTGGCC | + | 7.22 | | MYCN | MA0104.4 | chr22:27160177-27160189 | GGCCACGTGGCC | - | 7.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH22I026764 | chr22 | 27159661 | 27159850 | | GH22I026763 | chr22 | 27159905 | 27160573 |
|
Enhancer Sequence | CAAGGTCCCG TTCACAGTTC CTGGGGATTA GGACTTTAAC ATTGTTTTGG GTGACACAAC 60
CTAACCCATG ATAGGCCCAT AATGAAATAA ACATGATACA GTGGTTTCTG AGCATCAGTT 120
GTATACCTGG CATGGTGCCA GGCCCTGGGC ATTCCAAGAT GCTGAGGCGA CATTCCTGCC 180
CTCATGGTGC CCTGAGCACA TTGAAGGAGA CGAATCATTG CTGGGGGAGA GGACCACAGC 240
GCAGGGTGTG GACTGAGGGT GGCGGCACGT GAGCTACATC TCTGGCTTGC AGGAGGCACA 300
TGGGGATGCT CCTTTGCTAT GTTTCTGGCT TGCAAGGGGC ACCCCGGGAT GTTCCTAGAA 360
AGGAAGGTGG CATGATGGTG ACAGCCTTGA TGCCAGGAGA GGAGCTAGCA ACTGAACCAC 420
AGAGACATTC CCAGCAGTCA ACAGGAGCCA CAGATTGATG AGCTAAAGAG TTGTGCAAAC 480
AGTGTTTGTT TGTTTTGTTT GGAGAGGGAA GTCCGTGTGT TTAGAGCTCA GCTTGTCTCC 540
CTCCCTCATG TTACAGGGGA AGAATCGGAG GTTCCGAGTG GGGAGTGACT CTCGCAAGGC 600
CACGTGGCCA GCCACGGCCA AGAGCGACAC CAGAAGGTGA TAGTTCTACT TGCTTCTGAG 660
TCCTTAGAGC GCATAGCCTA GTCTGCAGTT ACAAACATGC TTGTTCAAAA CACAACAGCC 720
GTTGCTGATG ACAATAGAAG TCGTTTGCCT GGTTTCGTTC ATCTGCATCT CTAGGGGTTA 780
GTAAATTTGC AGCCAATTTT CAAGGATTTC AAATTGAATT TCTAGGTAGC TTCTACTGAA 840
|
