Variant report

Variant rs4650607
Chromosome Location chr1:78621340-78621341
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:78584200-78630600 Weak transcription Fetal Adrenal Gland Adrenal Gland
2 chr1:78609200-78624600 Weak transcription Pancreas Pancrea
3 chr1:78609200-78624800 Weak transcription Sigmoid Colon Sigmoid Colon
4 chr1:78611600-78631400 Weak transcription Liver Liver
5 chr1:78619200-78622400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr1:78619800-78622800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr1:78619800-78624400 Weak transcription Duodenum Mucosa Duodenum
8 chr1:78619800-78624600 Weak transcription Spleen Spleen
9 chr1:78620200-78621400 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr1:78620400-78621400 Enhancers HUES64 Cell Line embryonic stem cell
11 chr1:78620400-78621400 Enhancers iPS-15b Cell Line embryonic stem cell
12 chr1:78620600-78621400 Enhancers ES-I3 Cell Line embryonic stem cell
13 chr1:78620600-78621400 Enhancers HUES48 Cell Line embryonic stem cell
14 chr1:78620600-78624200 Weak transcription Fetal Intestine Small intestine
15 chr1:78621000-78621400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
16 chr1:78621200-78622000 Weak transcription HSMMtube muscle
17 chr1:78621200-78622600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
18 chr1:78621200-78624600 Weak transcription Fetal Intestine Large intestine
19 chr1:78621200-78626800 Weak transcription Right Ventricle heart

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