Variant report

Variant rs2817476
Chromosome Location chr1:245961606-245961607
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:245932000-245966200 Weak transcription Primary T cells from cord blood blood
2 chr1:245949200-245999600 Weak transcription Gastric stomach
3 chr1:245952000-245970400 Weak transcription Aorta Aorta
4 chr1:245955000-245964000 Weak transcription Osteobl bone
5 chr1:245955200-245964200 Weak transcription Placenta Amnion Placenta Amnion
6 chr1:245955200-245970800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr1:245955600-245964000 Weak transcription Fetal Stomach stomach
8 chr1:245957000-245970400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr1:245960400-245965200 Weak transcription K562 blood
10 chr1:245961400-245962000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr1:245961400-245964600 Enhancers Fetal Heart heart
12 chr1:245961400-245965000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr1:245961400-245968000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
14 chr1:245961600-245961800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr1:245961600-245961800 Enhancers Fetal Brain Male brain

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