Variant report

Variant rs2163628
Chromosome Location chr1:174752938-174752939
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174745000-174756800 Weak transcription HSMMtube muscle
2 chr1:174747000-174768400 Weak transcription Primary B cells from cord blood blood
3 chr1:174749200-174753200 Weak transcription Fetal Kidney kidney
4 chr1:174751000-174753800 Weak transcription Ovary ovary
5 chr1:174752000-174757800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:174752400-174760800 Weak transcription H1 Cell Line embryonic stem cell
7 chr1:174752400-174764000 Weak transcription Fetal Intestine Small intestine
8 chr1:174752400-174764200 Weak transcription HUES48 Cell Line embryonic stem cell
9 chr1:174752600-174754800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr1:174752600-174757000 Weak transcription K562 blood

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