Variant report

Variant rs232892
Chromosome Location chr1:59110018-59110019
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:59093200-59115400 Weak transcription NHEK skin
2 chr1:59096000-59121600 Weak transcription HUVEC blood vessel
3 chr1:59096600-59121600 Weak transcription Gastric stomach
4 chr1:59102000-59130400 Weak transcription Aorta Aorta
5 chr1:59103600-59115200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:59104600-59115600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr1:59104600-59115600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr1:59107200-59110200 Weak transcription Primary T cells from cord blood blood
9 chr1:59108000-59115600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
10 chr1:59108200-59130400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
11 chr1:59108400-59115600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
12 chr1:59108600-59121600 Weak transcription Duodenum Mucosa Duodenum
13 chr1:59108800-59114400 Weak transcription Primary T cells fromperipheralblood blood
14 chr1:59109000-59121600 Weak transcription HepG2 liver
15 chr1:59109400-59110800 Strong transcription Breast Myoepithelial Primary Cells Breast
16 chr1:59109400-59121600 Weak transcription Rectal Mucosa Donor 29 rectum
17 chr1:59109600-59117800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
18 chr1:59109800-59115400 Weak transcription Primary B cells from cord blood blood
19 chr1:59109800-59115800 Weak transcription H9 Cell Line embryonic stem cell

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