Variant report

Variant rs13183291
Chromosome Location chr5:16497839-16497840
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:16488400-16499800 Weak transcription Gastric stomach
2 chr5:16492200-16499600 Weak transcription Right Ventricle heart
3 chr5:16495800-16504400 Weak transcription Rectal Mucosa Donor 29 rectum
4 chr5:16495800-16509000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr5:16496200-16509000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr5:16496400-16501400 Weak transcription Primary T helper naive cells from peripheral blood blood
7 chr5:16496600-16498200 Enhancers Skeletal Muscle Male skeletal muscle
8 chr5:16496800-16498200 Weak transcription Sigmoid Colon Sigmoid Colon
9 chr5:16497000-16505800 Weak transcription Duodenum Mucosa Duodenum
10 chr5:16497000-16506200 Weak transcription Thymus Thymus
11 chr5:16497200-16498400 Enhancers Fetal Heart heart
12 chr5:16497200-16498400 Weak transcription Psoas Muscle Psoas
13 chr5:16497200-16504600 Weak transcription Fetal Intestine Small intestine
14 chr5:16497200-16506800 Weak transcription Rectal Mucosa Donor 31 rectum
15 chr5:16497600-16499800 Weak transcription Left Ventricle heart
16 chr5:16497600-16500000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr5:16497600-16501400 Strong transcription Primary T cells from cord blood blood
18 chr5:16497800-16498000 Enhancers Pancreas Pancrea
19 chr5:16497800-16498000 Flanking Active TSS Skeletal Muscle Female skeletal muscle
20 chr5:16497800-16498400 ZNF genes & repeats Primary T helper naive cells fromperipheralblood blood

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