| Tag | Content |
|---|
EnhancerAtlas ID | HS184-13781 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:48704940-48706210 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TBX20 | MA0689.1 | chr17:48705754-48705765 | GAGGTGTGAAG | + | 6.02 | | ZNF263 | MA0528.1 | chr17:48705746-48705767 | GGAGGAGGGAGGTGTGAAGGT | + | 6.29 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_24488 | chr17:48705345-48705863 | Colon_Crypt_2 | | SE_24488 | chr17:48705903-48706227 | Colon_Crypt_2 | | SE_31702 | chr17:48705315-48706265 | Gastric | | SE_47221 | chr17:48704801-48721750 | Panc1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 48705400 | 48705800 | | chr17 | 48705800 | 48706075 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I050627 | chr17 | 48704961 | 48708888 |
|
Enhancer Sequence | GGAAGCTTCA GGGCTGCCTC TTTGTGTGTG TATGAGTGTG TATGTGTTTG TGTATATGAG 60
TGCGTGTGTG TATATGAGTG TGAGAGTGTG TGTGTCTGAG AGTGAGAGAA CCTGAACCCC 120
TTGCTGTGGA AGGCTGCACC TCTAGCCTGC CCTCCCCAGC CGTGAAGGAG AGGAGGAGCC 180
CCTCCGCCTG GTGCAGGCTG GGGAGGCAGG GTCTCTTCTG CTGCTATCAA AGCTTTACAG 240
CTTCCTCTAG CTAGGCAGCT CAGTGAATGG GAGTAATTCC AGATTAACTC TTATTTCTGC 300
TGACAGCTAT CAGCCGCACA TTGAAAGCTG GAAATTGGCA TAATGAAGCT GTTTTGGTTA 360
ATGGGGCCGA CTGAGGCTGG GGGAGGTTGC CTCAGAGGCT GCAGATCTGG ATCTGTGGGT 420
TGGTGGGGGA GGGGGGAAGT GTTTCTGGGT TTTCCTTCCT GAAGCTTCAG CACGGATTTG 480
CCACACTTCT GGCTGGATGC GTGACCTGAG CTGTCTGGAC TTCAGCCTCC TGCCTTGGGG 540
GCGGGCTTAG CTGACTGGCA TTACAGGCAC TGTCCGATGG GGACCTCGTC CACCTGCCCG 600
CAATGGAATT AAACCGTGTC AACGGAGTGG GCTGTGCTTC CTGAGGATGA GAGTCCAGGG 660
CTGGGCGTCC AGAGGCAACC TCCTGGTGGA GGTGGTAGGG TCAGAGGCCA GGTGCTGAGT 720
GGGGAGCTGG CCCCCTGGGC GGTGATGAGC GAGCGCTCAA GATGTTTACA TGCACTGCTG 780
CTGCTGCCTG CCTAGCGGGA GCCAGTGGAG GAGGGAGGTG TGAAGGTGGC CAGGGGCAGG 840
CAGACAGGAA GAGGGGGAGT GGCGTGGCCC AGGCCACCTG TCTGGTGCTA CTGCAGACAA 900
TATTCTCTTG TCTGAAATCT TGGTGCCAAG AGGTGGTGAC CATGGGTCCA GCCAGCCTGT 960
CACCTAGCCA CCTCCCAAAC ATCTGTCCCA ATCCCACTCC CTTGAACAGC CCCCTCCCCT 1020
CGCCCCCAGG GCCTTCAAAC CCCAGGATTG GATTGGGTTT TTGAAACCTC AGTGGCAACG 1080
CTCGCTCACA AACCGTCTGA TCCGGTCAAC TGGGAGCTGG GGGCACCAGG CTGCCGGGCG 1140
AGTGGACCTG GAGGCGTTGT CCAGCATTGT TTTCTAAGCT GGGTGAGAGC TTTTCTCATT 1200
GCTCTTTTGG ACAGAACTCA TACCGCTCCT TGAAGCCAAA GCCTGGTTTT ATCCTTTTAG 1260
GGTGTGCAAT 1270
|
