| Tag | Content |
|---|
EnhancerAtlas ID | HS184-19285 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr22:29189050-29189610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr22:29189196-29189211 | TGAACTCCTGACCTC | - | 6.22 | | RARA | MA0729.1 | chr22:29189193-29189211 | CCATGAACTCCTGACCTC | - | 6.39 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_25378 | chr22:29186430-29189597 | DND41 | | SE_31638 | chr22:29188459-29189369 | Gastric | | SE_43527 | chr22:29183276-29200009 | MM1S | | SE_54242 | chr22:29188403-29189110 | Spleen | | SE_59596 | chr22:29187211-29199229 | Ly3 | | SE_62966 | chr22:29186510-29220159 | Tonsil | | SE_67157 | chr22:29183276-29200009 | MM1S |
|
| | 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 |
| GH22I028791 | chr22 | 29187501 | 29189479 |
|
Enhancer Sequence | GCTGCATCCT CTGCCTCCCG GGTTCAAGTG ATTCTGCCGC CTCAGCCTCC TGAGTAGCTG 60
GGATTACAGG CATATGCGCC ACCACACCCA GCTAATTTTG TATTTTTACT AGAGATGGGG 120
TTTCACTATG TTGGTCAGGC TGGCCATGAA CTCCTGACCT CAGGTGATCC GCCCACCTCA 180
GCCTCCCAAA GTGTTGGGAT TACAAGCGTG AGCCACTACA CCTGGCCTAC ACCAAAGGTA 240
TTCTATAATC CACTTTGCCT TGCTGCTTGG GATTCTCTGA ATCCTGCCTT TTTTCTACTC 300
ATTCACTTTG ACCTCCCCAG AGTTAGTCTT TGTAAGTTGG GAACATAGCA TTTAAATGCT 360
AAATTGGCAT AGAATGATTT CATCTACTGG CATAGGTGAA ATTTTTATAA ATAAGTAAAG 420
TCCTGTAAAA CCTTGTAAGA TTTCCAAGGA AAAGATGCTA TGAAGGATGA GGAGGTTATC 480
AAGTCTTTGG GAGTTGTATT AATATCACTA GGATTTTTTC TTGAAGAGGT TTATTTATTT 540
ATTTATTTAT TTATTTATTT 560
|
