Variant report

Variant rs10919120
Chromosome Location chr1:169240084-169240085
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:169227600-169257400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr1:169228400-169257400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:169234600-169240800 Weak transcription Primary T cells from cord blood blood
4 chr1:169235200-169240200 Weak transcription Rectal Mucosa Donor 31 rectum
5 chr1:169235400-169240200 Weak transcription HepG2 liver
6 chr1:169239600-169241000 Enhancers Rectal Smooth Muscle rectum
7 chr1:169239600-169241000 Enhancers Stomach Mucosa stomach
8 chr1:169240000-169240200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr1:169240000-169240800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr1:169240000-169240800 Enhancers Colon Smooth Muscle Colon
11 chr1:169240000-169241000 Enhancers Primary hematopoietic stem cells short term culture blood
12 chr1:169240000-169241000 Enhancers Fetal Intestine Large intestine
13 chr1:169240000-169241000 Enhancers Fetal Intestine Small intestine

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