Variant report
Variant | rs2456815 |
---|---|
Chromosome Location | chr1:212870103-212870104 |
allele | C/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:212857200-212871600 | Weak transcription | Dnd41 | blood |
2 | chr1:212858600-212872200 | Weak transcription | Gastric | stomach |
3 | chr1:212858800-212872200 | Weak transcription | Aorta | Aorta |
4 | chr1:212862600-212871600 | Weak transcription | NHLF | lung |
5 | chr1:212863400-212872200 | Weak transcription | Spleen | Spleen |
6 | chr1:212865600-212871000 | Weak transcription | Primary T regulatory cells fromperipheralblood | blood |
7 | chr1:212866800-212871800 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
8 | chr1:212867000-212872200 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
9 | chr1:212867200-212871800 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
10 | chr1:212869400-212872000 | Weak transcription | Right Atrium | heart |
11 | chr1:212869600-212870400 | Bivalent Enhancer | Primary neutrophils fromperipheralblood | blood |
12 | chr1:212869600-212870600 | Transcr. at gene 5' and 3' | Primary T helper 17 cells PMA-I stimulated | -- |
13 | chr1:212869800-212871000 | Active TSS | Primary T helper cells PMA-I stimulated | -- |
14 | chr1:212869800-212871000 | Bivalent Enhancer | K562 | blood |
15 | chr1:212870000-212870200 | Bivalent Enhancer | Monocytes-CD14+_RO01746 | blood |
16 | chr1:212870000-212870400 | Bivalent Enhancer | Primary monocytes fromperipheralblood | blood |
17 | chr1:212870000-212872600 | Flanking Active TSS | GM12878-XiMat | blood |