Tag | Content |
---|
EnhancerAtlas ID | HS098-37430 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr22:50345480-50346680 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RELA | MA0107.1 | chr22:50346115-50346125 | GGGAATTTCC | + | 6.02 | RREB1 | MA0073.1 | chr22:50346028-50346048 | ACCCCAACCACCCCGACACC | + | 6.95 | ZNF263 | MA0528.1 | chr22:50346362-50346383 | GCCTCATCCCCCCCTTCCCCC | - | 6.25 |
|
| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00426 | chr22:50345544-50354348 | Adipose_Nuclei | SE_03028 | chr22:50345319-50346038 | Bladder | SE_23129 | chr22:50340142-50347336 | Colon_Crypt_1 | SE_23738 | chr22:50340192-50347293 | Colon_Crypt_2 | SE_24687 | chr22:50340156-50348528 | Colon_Crypt_3 | SE_26808 | chr22:50341423-50346477 | Esophagus | SE_28169 | chr22:50340100-50347261 | Fetal_Intestine | SE_29459 | chr22:50340194-50347426 | Fetal_Intestine_Large | SE_31381 | chr22:50340030-50364844 | Gastric | SE_34375 | chr22:50344227-50346963 | HCT-116 | SE_35007 | chr22:50344121-50348457 | HeLa | SE_41142 | chr22:50346484-50349918 | Left_Ventricle | SE_41617 | chr22:50344224-50349802 | LNCaP | SE_42159 | chr22:50339996-50364887 | Lung | SE_47471 | chr22:50340157-50349301 | Pancreas | SE_49074 | chr22:50346485-50350496 | Right_Atrium | SE_50117 | chr22:50339205-50347666 | Sigmoid_Colon | SE_52469 | chr22:50340730-50346981 | Small_Intestine | SE_53398 | chr22:50346200-50348926 | Spleen | SE_56937 | chr22:50340142-50346911 | VACO_400 | SE_57421 | chr22:50344221-50347177 | VACO_503 | SE_58096 | chr22:50342032-50347148 | VACO_9m | SE_61206 | chr22:50315437-50364432 | HBL1 | SE_61985 | chr22:50315627-50364432 | Toledo | SE_62450 | chr22:50318672-50364388 | Tonsil | SE_65335 | chr22:50344193-50351013 | Pancreatic_islets | SE_68380 | chr22:50327316-50364640 | TC32 | SE_68381 | chr22:50327316-50364640 | TC32 | SE_68382 | chr22:50327316-50364640 | TC32 | SE_69071 | chr22:50344309-50347260 | H9 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH22I049942 | chr22 | 50336159 | 50349619 |
|
Enhancer Sequence | GGGCCAGTTG GAAGGGCCAC CAACTCCCGC ACACCTGTGG CTGGTTTCTG CCCAGATCTC 60 ACTGGAGGGA TCCACGCCCA GGCAGGCTGC TGAGTCGCCT CTGCTGGGAG CTCAGGACCC 120 AGGTGGGATT TCAGGACCGC AGGCCCTCCA CTGAGGCCCG TGTGCCCCCA CTCAGCCCAG 180 CCCACCTCCC TCCCACCCAC ATCCTTCCAA GACTCAGCTC CTCCCAGTGC CCTAGGCCTG 240 GCCAGTGGTA ATGCTGAGGT GTGACCACAA GGCCCATTTC ACAGCTAGGA AGGTGGGCTC 300 AGGGTGGAGG CCCCACCGGG CCACAGACTC CATCGAGGTG CCTCTGATCT TGGGGCTAAG 360 TCAGTGACCA GGAAAGAGAG GCCGCCCGAC TGAGGTGTAA GGAGTGCCTG GGCCCCAGCA 420 ACTGTAGCCC TCACTCCTGC CACCGGCAGC CCGGCCTCAG CAGAGCTGAC ACAGAAGAGT 480 GGGTTGCAGG CTGAGCTGGT CCTCCGGGGC CCAAACCAGG CCTGGCACCC ACGACCCTGA 540 AGAGTGGGAC CCCAACCACC CCGACACCTA GTCGGGGCAG GGCAGCAGGG ACGGGAGGGA 600 GCTCTGGGCC ACCGAAGGGG CCAGGGCGCT GGATGGGGAA TTTCCTGGAG GTGGAGGAGC 660 CCAGCAAGGG TAAAAGTGCA GAATTCTTTC CATTCTTTGC ATTTCTCTGA GATGATTCTG 720 CAGAGTGTGT TGCCTGGAAG ACCCGTGGTG TCTGTGTGTG TGTGTGTGTG TGCACGCGTG 780 TGGTGCGTGT GCATGTGTGA ACATGTGTGT GGTGTGTGTG CACGTGTGTG GTGTGTACTT 840 GTGTGTGGTT GTGTGTGTGT GTGCACGCAG CCTGCCCCTG GTGCCTCATC CCCCCCTTCC 900 CCCTGGGAGC GGCCCCGCTG TGCTGGCAGT TCGGCCCCCA CAGGTCTGCA CTGGTGAACC 960 CTCATGGTCC CTCAGGGAGC CCGGGAGAGG TGAGGAGGAC CTGGATAGGG CCCAGGCCCA 1020 GATGCCTGCA GGGGAGAAAG CTCCACACAA GGGGTTTGTG AGGCCTTGCC CCAGCCCCAA 1080 CGAGATTCAG GTGCCCAGCT GTGGGATATG GGGACAGGCA GGTGACGGCC CGGCTCTCAG 1140 GCTCCCCATC TGGACGATGG ATGGACACGC GTAAGCAAGA CCCTGAGGCC CTGTCCCTCA 1200
|