| Tag | Content |
|---|
EnhancerAtlas ID | HS095-19246 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr21:44465320-44466570 |
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 | GCCACCCCAC ACTGGGGTGG ATGGGGCCGT GCCCTGCCCT CCCTGAGGCT CACTCACTGT 60
GCCCCTCTCC TGGCTTCTCT CCTGCCTCCC TGATCAGCAA GTTCCTAGGG GCTCCCCGAA 120
TATCATCACT CCCTGGAGCC ACAGAGACCC TCACAGCTCC CTGCTTGGGG CTCCTCCGCA 180
TCCCGCACAA GCTCCCCCTT CAGTTCCTGA CGTGTACCCC TGCCCTCTGC AGGTGCTATG 240
TAGGGGCCCC GCCAGCCTCC GAGGCCCACA AGGGCTTCTG GTTCAGGAAG GCTCTGTGGT 300
TACCTCAACT CCAAACCCTC TCCACCCCCA CCCCCAGGCA GCATGCTGGC ACCCTAGCCC 360
CGGGCACCCT GAGAACACCA AGTGCCGTTT CCTGGAAGAG GAAATGTTTC TGCCAAGAAG 420
TTTCCACGCC TCTGGCCTAT GATTGACTGA CTTGCTTTTG AAACCCGTTC AGGAGAGGTC 480
ATGCCTATCC CCTTCCTCTA CCCGCTGGCC TGCCCTGGCT CACTTGGCTG CATAGTGGGA 540
AACAGGAACT TTTCCACTGG CCCTAAGCAA AGCCTACTCT CCAGAGACTG GCAGAAAACC 600
AAGTGCCTGA GGAGAGTTGG GTGCGGGGAA AGCCGGAGGC TCCCGTGGGG CCCTGTAGCG 660
GGAGTGCCTT CCCAGTCGCT CTGGGAAGCC CTGCCCTCTC CTCCTCCCAC CTGCCTCCCT 720
GCCAGTGTCC TCCCCCAGCA GACCTGCAGG AACAACACCG TCATGGGGGC CCGAGAGTCG 780
GGGACCTCCC AAGCCAGCAC TACAGCCCAG CACAGATGCC ACCAACCTGT GGAGAAAAGC 840
CTTTGTTCGT GTCCACAGCG GCTCTGTCTC CATCCTTTAG GTAGCTTGAT ACCAGGGCAT 900
AATTCAAGCC ATTGCTGAGA TGCCCAGAGA CCAAGAACAT GAAGCTGGCC AGGCTTGGTC 960
ATTAGGAAAG CCCTGGGCAC CAAGACCTGC CCCCTCACAG CTGCTACAGC TGGCTGGCTG 1020
GCTGGCTGGA TCCTTCAGGG TGGGGCTGCA GTCATCGTTT CATGAGCCAC AGCCAAGAGG 1080
TGTCATAAGC AGCTGCAGAG GTTTGTGGAG GACATATGAA CAGCCACCCA TCTGCAGTCG 1140
GGGCTGCTGT GGACAGGTGT GCAGGTTGTG AACGGCACAA CTCCATGCCT CCATGCCCTC 1200
AGAGTCTACG CCTGGATGGG CACGTGCAGC ACCCCGTGTG GACTTCTCAG 1250
|
