Variant report

Variant rs10476601
Chromosome Location chr5:93402522-93402523
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:93380400-93403800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr5:93380600-93402600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr5:93380600-93403200 Weak transcription Sigmoid Colon Sigmoid Colon
4 chr5:93393600-93413000 Weak transcription Stomach Smooth Muscle stomach
5 chr5:93398600-93402600 Weak transcription H1 Cell Line embryonic stem cell
6 chr5:93398800-93404200 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr5:93398800-93430800 Weak transcription Pancreas Pancrea
8 chr5:93399400-93403800 Weak transcription Esophagus oesophagus
9 chr5:93400800-93403600 ZNF genes & repeats Primary T regulatory cells fromperipheralblood blood
10 chr5:93401200-93402800 ZNF genes & repeats Primary T helper memory cells from peripheral blood 1 blood
11 chr5:93401200-93403400 Weak transcription Fetal Thymus thymus
12 chr5:93401200-93403600 Weak transcription Fetal Stomach stomach
13 chr5:93401200-93403800 Weak transcription Aorta Aorta
14 chr5:93401200-93409400 Weak transcription Ovary ovary
15 chr5:93401400-93403600 Weak transcription Fetal Intestine Small intestine
16 chr5:93401600-93402800 Weak transcription Primary Natural Killer cells fromperipheralblood blood
17 chr5:93402400-93403600 ZNF genes & repeats Primary B cells from cord blood blood

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