Variant report
Variant | rs10127459 |
---|---|
Chromosome Location | chr1:213116929-213116930 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:213107800-213119400 | Weak transcription | H9 Cell Line | embryonic stem cell |
2 | chr1:213115600-213117000 | Enhancers | HepG2 | liver |
3 | chr1:213116000-213121200 | Enhancers | GM12878-XiMat | blood |
4 | chr1:213116400-213123400 | Weak transcription | Right Atrium | heart |
5 | chr1:213116600-213117000 | Bivalent Enhancer | IMR90 fetal lung fibroblasts Cell Line | lung |
6 | chr1:213116600-213118600 | Enhancers | Primary B cells from peripheral blood | blood |
7 | chr1:213116800-213117000 | Enhancers | Fetal Intestine Small | intestine |
8 | chr1:213116800-213118000 | Enhancers | Primary B cells from cord blood | blood |