| Tag | Content |
|---|
EnhancerAtlas ID | HS184-19084 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr21:44465400-44466390 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIC | MA0161.2 | chr21:44465728-44465739 | TCTGCCAAGAA | - | 6.02 | | Stat4 | MA0518.1 | chr21:44465704-44465718 | CCGTTTCCTGGAAG | - | 7.58 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_41747 | chr21:44464351-44466950 | LNCaP | | SE_68804 | chr21:44464232-44466970 | H9 |
|
| | 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 |
| GH21I043044 | chr21 | 44464553 | 44470895 |
|
Enhancer Sequence | CCTGCCTCCC TGATCAGCAA GTTCCTAGGG GCTCCCCGAA TATCATCACT CCCTGGAGCC 60
ACAGAGACCC TCACAGCTCC CTGCTTGGGG CTCCTCCGCA TCCCGCACAA GCTCCCCCTT 120
CAGTTCCTGA CGTGTACCCC TGCCCTCTGC AGGTGCTATG TAGGGGCCCC GCCAGCCTCC 180
GAGGCCCACA AGGGCTTCTG GTTCAGGAAG GCTCTGTGGT TACCTCAACT CCAAACCCTC 240
TCCACCCCCA CCCCCAGGCA GCATGCTGGC ACCCTAGCCC CGGGCACCCT GAGAACACCA 300
AGTGCCGTTT CCTGGAAGAG GAAATGTTTC TGCCAAGAAG TTTCCACGCC TCTGGCCTAT 360
GATTGACTGA CTTGCTTTTG AAACCCGTTC AGGAGAGGTC ATGCCTATCC CCTTCCTCTA 420
CCCGCTGGCC TGCCCTGGCT CACTTGGCTG CATAGTGGGA AACAGGAACT TTTCCACTGG 480
CCCTAAGCAA AGCCTACTCT CCAGAGACTG GCAGAAAACC AAGTGCCTGA GGAGAGTTGG 540
GTGCGGGGAA AGCCGGAGGC TCCCGTGGGG CCCTGTAGCG GGAGTGCCTT CCCAGTCGCT 600
CTGGGAAGCC CTGCCCTCTC CTCCTCCCAC CTGCCTCCCT GCCAGTGTCC TCCCCCAGCA 660
GACCTGCAGG AACAACACCG TCATGGGGGC CCGAGAGTCG GGGACCTCCC AAGCCAGCAC 720
TACAGCCCAG CACAGATGCC ACCAACCTGT GGAGAAAAGC CTTTGTTCGT GTCCACAGCG 780
GCTCTGTCTC CATCCTTTAG GTAGCTTGAT ACCAGGGCAT AATTCAAGCC ATTGCTGAGA 840
TGCCCAGAGA CCAAGAACAT GAAGCTGGCC AGGCTTGGTC ATTAGGAAAG CCCTGGGCAC 900
CAAGACCTGC CCCCTCACAG CTGCTACAGC TGGCTGGCTG GCTGGCTGGA TCCTTCAGGG 960
TGGGGCTGCA GTCATCGTTT CATGAGCCAC 990
|
