Variant report

Variant rs2791397
Chromosome Location chr1:245965170-245965171
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr1:245955200-245970800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr1:245957000-245970400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr1:245960400-245965200 Weak transcription K562 blood
7 chr1:245961400-245968000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr1:245961800-245980000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr1:245962000-245972600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr1:245962600-245970400 Weak transcription HepG2 liver
11 chr1:245963400-245970400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
12 chr1:245964600-245968400 Enhancers Placenta Placenta
13 chr1:245964600-245971200 Weak transcription Fetal Heart heart
14 chr1:245964800-245965600 Weak transcription Placenta Amnion Placenta Amnion
15 chr1:245964800-245970400 Weak transcription NH-A brain
16 chr1:245964800-245973800 Weak transcription Fetal Stomach stomach
17 chr1:245965000-245965400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung

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