Variant report

Variant rs12027835
Chromosome Location chr1:246363094-246363095
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:246314200-246369000 Weak transcription Aorta Aorta
2 chr1:246338400-246371400 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr1:246340200-246384600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:246342600-246369400 Weak transcription Fetal Stomach stomach
5 chr1:246343200-246378400 Weak transcription Primary T cells from cord blood blood
6 chr1:246349400-246373000 Weak transcription Primary hematopoietic stem cells blood
7 chr1:246350200-246369200 Weak transcription Primary hematopoietic stem cells short term culture blood
8 chr1:246361200-246363200 Enhancers Brain Germinal Matrix brain
9 chr1:246361800-246363200 Enhancers Cortex derived primary cultured neurospheres brain
10 chr1:246362000-246363800 Enhancers Ovary ovary
11 chr1:246362200-246363200 Enhancers Brain Cingulate Gyrus brain
12 chr1:246362400-246364800 Enhancers K562 blood
13 chr1:246362600-246363200 Enhancers Brain Hippocampus Middle brain
14 chr1:246362600-246363200 Enhancers Brain Inferior Temporal Lobe brain
15 chr1:246362800-246363200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr1:246362800-246363200 Enhancers Fetal Lung lung
17 chr1:246362800-246363600 Enhancers Brain Substantia Nigra brain
18 chr1:246363000-246363200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
19 chr1:246363000-246363200 Enhancers Fetal Kidney kidney
20 chr1:246363000-246363600 Active TSS Brain Angular Gyrus brain
21 chr1:246363000-246376800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
22 chr1:246363000-246377400 Weak transcription Osteobl bone

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