| Tag | Content |
|---|
EnhancerAtlas ID | HS098-36065 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr21:44816320-44817390 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr21:44816870-44816881 | GATGAGTCACT | - | 6.02 | | JUND | MA0491.1 | chr21:44816870-44816881 | GATGAGTCACT | - | 6.32 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_10405 | chr21:44817042-44821699 | CD19_Primary | | SE_11196 | chr21:44815919-44822475 | CD20 | | SE_20443 | chr21:44816879-44822492 | CD56 | | SE_31895 | chr21:44816274-44817372 | Gastric | | SE_34640 | chr21:44815394-44818758 | HeLa | | SE_52671 | chr21:44816087-44820368 | Small_Intestine | | SE_58455 | chr21:44763901-44850830 | Ly1 | | SE_59568 | chr21:44816711-44859975 | Ly3 | | SE_62541 | chr21:44767678-44851140 | Tonsil | | SE_65619 | chr21:44815998-44817928 | Pancreatic_islets |
|
| | 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 |
| GH21I043395 | chr21 | 44815753 | 44822219 | | GH21I006140 | chr21 | 44816315 | 44817952 |
|
Enhancer Sequence | CCTCCCGCTG GCTGGCCCTG AGCAGCAAAG AGGACACCTG CGCGGCCTTC CTCTCCCGGC 60
CCCTAACTGA GCCACGGCTA CATCCCGCTC CTCCCACCAA AGCTCTTCGG CCAGTCAGCC 120
CTCAGGCTCC AGCGCGGCTC GGAGGGGCCT GCCCCTGGTA TAGCGCCCAT GGTCACTGTC 180
GGACACTCTT AAAACAACGG CCGTGTTTCT GTTCTGCGCT GGGCCCTGAA GCTCATGTCA 240
TCAGCCCTGC CGGCTGTGGG GCTCCCGGAT TCTCTGACCT TGACCCATGC TGCAGCCACT 300
CCGCCTGTTT CCTGGGGCTG GTTTACACCC CGAGATGCAG GGAAGGCCCA GCTGCGGAGC 360
CCCAGGGAGG CCAGGAGCTG TTCACAACTC CAGGAAGCCA CACTGGGCCT CAGTTGACGA 420
AGAAGGCGAC ACCTTCGTGT GGGCCTTGCC TGCTAATCGG TGTCCTCAAC CCAAGGGCAC 480
AGGCGCCGCT CCCAGGCCGC GCAGGCAGAG TAGAGCTGGG GTGGATGGCA GGCTTCAGGG 540
ACCCAGCCCC GATGAGTCAC TTGGAAGGCA TTTGCCCCAG AGCTTCCCTG GCCACTGCGC 600
CTCCTCCCGC CCCAATCCAG CCCCATCTGG GTCCGAGCCT CTGGAGAGGA GCTGGCAGGT 660
CAGGATGCGG TTCCCGTGCT CTTGCCTGTG TGTGGGGACC CGAAAGCCAG GCTGGTGGCC 720
GAGGATGGCG AGCACAGCCC CAGCCCCTCG GCCTAGCGGG AGCTTCACGG GACGGTGCTC 780
CCCCCACACC GTGGTGTTGC TTCTGTGGCC CCCTTCAGGG CCCACAGAGG GAAGGGGCCT 840
GGCTCTCCCA CGGGGCCTCT GTAATATTTA ACCATAAACC AAGGCTGCGG GGAACCCCCA 900
GTTTGCAGTA AACTTCCATT TCTCTCCACT GGATGCGCAG GACTCCACTC AGCCAGGTAG 960
GAGAATCTGC ACTCACCTGG TTTCCGGAGC AAGGAGGCTG ATGGCATCAG GGACTACCTC 1020
CCCTCAGCTT CCTCGGGCCA CGCAGGAGTC CCCGGCCCGC CTCCTCCAAG 1070
|
