| Tag | Content |
|---|
EnhancerAtlas ID | HS098-36066 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr21:44817560-44818780 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxo1 | MA0480.1 | chr21:44818598-44818609 | AGTAAACAGGA | - | 6.32 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_10405 | chr21:44817042-44821699 | CD19_Primary | | SE_11196 | chr21:44815919-44822475 | CD20 | | SE_20443 | chr21:44816879-44822492 | CD56 | | 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 |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH21I043395 | chr21 | 44815753 | 44822219 | | GH21I006140 | chr21 | 44816315 | 44817952 | | GH21I006137 | chr21 | 44818153 | 44820751 |
|
Enhancer Sequence | GCAGCAGGTC ACACCAGCAG CTTGGGCTCC CAAGAGCCTC GGGACCCCAG AACCACAGGT 60
GGCCTGGCCT CTGGGGATGG TCGGGGGCTG AGCGTGAGAC CCCAGCTGGG TGGCAGAGGC 120
TCCAGTACTG AGGATTCCAG GCTGTGGTAG CACTCCACTG CAGGCCGACC TGCAGGCCAG 180
GAGGAAGGGG CCCGCCGCCC AGGGTGTCTG TTCTAAGGAG CGCAGGGACA GGGCCTCCCC 240
TGCAGGCGAG GCCACAGAGT GGGCCACCTC CTCCTCCCTG ACCCCTCCTC CCAAGGGGCT 300
TATCCTCCTC TGCAGGGCTG GTGTTACTCC CCCAAAGCCA TCACCCCCCT GTGTCACCTC 360
CTCCCGTGGC CACTTGGAGA AGTGGTCATT GTGGTCACTC CCCACTGTGG TCACCTCCCC 420
CCAGGTGACC TCCCCACCAG GTCAATTCCC CACCAGGTCA CCACCCTACT ATGGCCTCCT 480
CCCCCAGAAG TCACTTCCTC CTGTGGCCAG CTCCCCACTG TGGTCATCTG CCCCCACATA 540
ACCTGACACT GTCAGGTCAT CTCCCCGCTG TGATCACCTC CCCCAGAAGC CACCCCTTCC 600
CGTGGTCACC TCCCACCAGG GTGTCTCCCC CCAGGTCACC TCCCCACCAG GTCACCTCCT 660
CCTGTGGCCA GGTCCCTGTT GTGGTCATCT GCCCCAGGTA TCTCCTCATC AGGTCATCCT 720
CCCCTGTGGT CACCTCCCCC AGAGGCCACC TCTCCCTGTG GTCACCTCCC TCCCAGGTCA 780
CCTTTCCCCC AGGTCACCTC TACCCCACAC TCATGCTGAC CAACATGAGG TGCCCTTCTC 840
CTGCCGGGAG CCCGCCCGGT CACCAACACT CCCCCTGGGG CTCTCTGGCT CCTGACCTGG 900
AGTCACTAGG GCCAACCCCA TCAGACATGC TGGACAACTT TATGTGGGTC ACTTAATGCC 960
TCTGAACCTC AGCTTCCTCT TCTGCACGAT GGAGACAAAA ACATTTGCTC TTCAAGCCTG 1020
TGGTAGGGAC CAGGTCAGAG TAAACAGGAA GACAGCTTTC GGCCAGGCGG TGCACCTCGG 1080
TGCCGGTGAG TGTGAGCGTG TGTGCGTGTG CACGTGTGCA GATGTGTGTG GACGCTCCCT 1140
TCTCCGCAGC AGCTCCTGAC CCCCTGCAGG TGACCCTCAG CCAGCCCCAG GGCTGCCCCC 1200
ACTCTCCCCT GTGGACACCT 1220
|
