Variant report

Variant rs2456815
Chromosome Location chr1:212870103-212870104
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
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

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