Variant report

Variant rs4563642
Chromosome Location chr5:177799777-177799778
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:177797800-177800600 Enhancers Cortex derived primary cultured neurospheres brain
2 chr5:177798200-177799800 Enhancers Placenta Placenta
3 chr5:177798200-177800400 Bivalent Enhancer Fetal Muscle Trunk muscle
4 chr5:177798400-177799800 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
5 chr5:177798400-177799800 Enhancers Ovary ovary
6 chr5:177798600-177800400 Bivalent Enhancer Fetal Stomach stomach
7 chr5:177798600-177804800 Weak transcription Gastric stomach
8 chr5:177798800-177800200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr5:177798800-177800800 Weak transcription Thymus Thymus
10 chr5:177798800-177802400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
11 chr5:177798800-177803400 Weak transcription Spleen Spleen
12 chr5:177798800-177816400 Weak transcription Right Atrium heart
13 chr5:177799200-177799800 Flanking Active TSS Stomach Smooth Muscle stomach
14 chr5:177799200-177803800 Weak transcription Fetal Thymus thymus
15 chr5:177799600-177799800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr5:177799600-177799800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
17 chr5:177799600-177799800 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
18 chr5:177799600-177799800 Enhancers Fetal Lung lung
19 chr5:177799600-177799800 Bivalent Enhancer Fetal Muscle Leg muscle
20 chr5:177799600-177803600 Weak transcription Fetal Intestine Large intestine

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