Variant report

Variant rs58510967
Chromosome Location chr3:291139-291140
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:285400-307400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
2 chr3:286200-315400 Weak transcription Ovary ovary
3 chr3:288800-291400 Enhancers Fetal Brain Female brain
4 chr3:289200-291200 Enhancers Fetal Brain Male brain
5 chr3:289400-291400 Enhancers Fetal Lung lung
6 chr3:289400-291800 Enhancers Brain Germinal Matrix brain
7 chr3:289600-291600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr3:289800-296400 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
9 chr3:290400-291400 Enhancers Fetal Kidney kidney
10 chr3:290600-291400 Enhancers HUES48 Cell Line embryonic stem cell
11 chr3:290600-291600 Enhancers HepG2 liver
12 chr3:290600-291800 Enhancers Breast Myoepithelial Primary Cells Breast
13 chr3:290600-292800 Enhancers Primary B cells from peripheral blood blood
14 chr3:290800-291200 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
15 chr3:290800-291200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr3:290800-291400 Enhancers Pancreatic Islets Pancreatic Islet
17 chr3:290800-291800 Enhancers iPS-20b Cell Line embryonic stem cell
18 chr3:290800-292400 Enhancers Primary B cells from cord blood blood
19 chr3:291000-291600 Enhancers iPS-18 Cell Line embryonic stem cell

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