| Tag | Content |
|---|
EnhancerAtlas ID | HS109-10808 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr19:4108550-4109590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr19:4109571-4109586 | TGCTATTTTTATCCC | - | 6.34 | | ZNF263 | MA0528.1 | chr19:4108835-4108856 | CGAGGAAGACGAGGAGGAGGA | + | 6.46 | | ZNF263 | MA0528.1 | chr19:4108820-4108841 | GGAGGAGGGGGAAGACGAGGA | + | 6.53 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_19502 | chr19:4108550-4109785 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20194 | chr19:4108131-4110745 | CD56 | | SE_22707 | chr19:4108432-4110877 | CD8_primiary | | SE_26575 | chr19:4108511-4109673 | Esophagus | | SE_31428 | chr19:4108584-4109590 | Gastric | | SE_50061 | chr19:4108477-4110110 | Sigmoid_Colon | | SE_53358 | chr19:4108433-4110130 | Spleen |
|
| | 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 |
| GH19I004107 | chr19 | 4107951 | 4110634 |
|
Enhancer Sequence | ACCTCGGAAC TTTTAAAGGG TGCACTCCAT AACACAGACA GCACGGCCTG TGTCTCCCTC 60
CTGCAGCCTG GTGGTCTGTG TGGTGTCCCC TGGGGTGCCA GCACCCACTC TGGGAACCCC 120
CATTTTAAAT TCACCAAGAA TAGAGGTTGG GGGCGGGTTG CCACACTGTC CCCTTTCTGC 180
ATGGGAGGAA GGGGGCTCGA GAACTGAGTC AGCCACACAA AACGAGGATG GACAGAACTC 240
CTGAGTAGCG AGGGTGCCTG CCGGGCGCGA GGAGGAGGGG GAAGACGAGG AAGACGAGGA 300
GGAGGAATAG GGAGCACCAC ATGACAGAGG GGCTGCCTCA GACCACAAAG CGCTTCCTCA 360
TCCTTTCCTC GCCCTTTGAT GCCGCCGGCA ACGTGACTCT GCGAGCAGCG GGGCAGACGC 420
CAGGTCTCCC TCGCAGGCGG GAAAGGGGCT CCAAGGCGGG TGCTGCCTTG CTCGGGTCAC 480
ATGGCTACGT GGGGGCCTTG CTCAAATTCA CTTCCTGCCT TCATTACAAA ACTGTCAAAG 540
GGGATCGCAC GTTTGCAGGG TGTCACCCAA GCATTCTGGT TTTGCAAACG ACGCTGTGCG 600
GCAGGCGGTC TGATACCTGA TGAGCTCGGT GTGGCGGGGT CGGCAGCATT TCCTCCGGGG 660
TTTTGAGCTC TGGCCACTTC TCCTTTTGTT CCACCCAATC TCACCCACTT CTGGGCTTCG 720
AGGCCAGAGT GTCTTAACAA GGGGGCACGT CAGAGTCAAT GAAGGGGGTG CCTGTACCCC 780
ACCCTAGAGA CTGTGGTCCC ACAGATCTGA GCTGGGGGAG GCACAGGCCT GCCTTGACAA 840
GCTCAGACTG CCACACTTTC CTGAGAAGGC CATTTAAAAA CAGTCATCAG CTTTGTTATG 900
TTTTGAGACA GCATCTCGCT CTGCTGCCCG GGCTGGAGTG CAGTGGCGTG ACCAAAGCTC 960
ACTGTAGCCT CAACCTCCTG GGCTCAAGTG ATCTTCCCAC CTCAGCCTCT CATGTAGCTG 1020
GTGCTATTTT TATCCCCATT 1040
|
