| Tag | Content |
|---|
EnhancerAtlas ID | HS182-11669 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr19:55609050-55610150 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr19:55609622-55609633 | ACAGATAAGGA | - | 6.14 | | TBX20 | MA0689.1 | chr19:55609064-55609075 | CTTCACACCTT | - | 6.32 | | TBX21 | MA0690.1 | chr19:55609065-55609075 | TTCACACCTT | - | 6.02 | | ZNF263 | MA0528.1 | chr19:55610074-55610095 | TCCCCCTCTGCACCCTCCTCT | - | 6.51 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_41403 | chr19:55609387-55611930 | Left_Ventricle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 55610040 | 55610094 | | chr19 | 55609378 | 55609687 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I055098 | chr19 | 55609569 | 55610862 |
|
Enhancer Sequence | CAGTTCACCA CCGTCTTCAC ACCTTTGTAC TGGGAGGGCC CTTCATTCCT GCCCTTCTAG 60
CAAACTCTTA GTGCTGTAGT ACTCACGTCT TCCAGAAAGT GTCCCCAGAT GCTCCCAGGC 120
TGGTCTCCCC CCATATCTGG GCCCCCTGAG CTGACCCTGC CCCACCTATT AAACCCCTCA 180
TGGCCGTATC ACCCTCAGGA TGGAAGCCAC CATGCTCCTC GCCTGGCACT CGTGGCCCTC 240
CCGGGTCTGC CCTGCCTTAC GCTCCCCTCC CTGGGCACCT CAGGGCACCC ACACTTGCCC 300
CCCAGCCTGT GTGAGATCTT CTCCTACATC CATCAGCCTC CACTTCGCTC CTGCCAACCT 360
TTCAAAAGAG GAAGCTGTCT CCGCTCCCCT GCCCACGCAC CAGAAGCCCT AGGCCTGGCC 420
TTGGGAGCTT CCTGTCACCT CACAGAGCTC ACTGAACGCT GGCATGGCTC TAGTGCTTTC 480
CAGGGGCACG TACTCCCCCG AGCTCCTGAC AGCACAATCC ACGTGTCACG CATGACCCCT 540
CATACAGTTG CGCACCATAC CATTCCCATT TGACAGATAA GGAAACTGAG GCCCGGAAAG 600
GAAAGTGGCT GGCTGAGACT CACGGCAGAT CCATGGCAGA GCCGGGATTC CAACCCAGGC 660
AGTCTGGCCA AGGCTCACGC CCTTCACTCC TTCACTCTAA GTTTTCCCAG CAAGGCTGCC 720
CCGGGGATGG CTGGGGGACA CCTTGTGGGT GACCAGCCCA GCCTGAGTCT AGGACAATCC 780
TGCACATGGC TGCTGCCAAG GGCCACCCTG AGGTGATGAG GTGTGCTAAG CAACCTCATC 840
AGGGTGTCAG ACAACCCTGT CCAAATCCTT CTGCCGCCCC CACCACCAGG CAGGCAGGAA 900
GCTCTGCAGC CCCATCTCTG TCCTGCCCCG GCTGGGGGTC TCTCCTGAGG CTGGGGCTGG 960
GGCTGGGTCA CCAAGAGGGA AATAGCAGGT CGCTGGGGTG GTGGGTGTCA GAAGTCGGGG 1020
GGGTTCCCCC TCTGCACCCT CCTCTGAGGA GCTGAGGGGA CATGGGGAGT CTGGGGTAAG 1080
CCCCTCAGCC CTGACACTCA 1100
|
