Variant report

Variant rs2817474
Chromosome Location chr1:245963214-245963215
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr1:245961400-245964600 Enhancers Fetal Heart heart
11 chr1:245961400-245965000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
12 chr1:245961400-245968000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
13 chr1:245961800-245980000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr1:245962000-245972600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
15 chr1:245962600-245970400 Weak transcription HepG2 liver
16 chr1:245963000-245963400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
17 chr1:245963000-245963400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
18 chr1:245963000-245963600 Enhancers Left Ventricle heart

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