Variant report

Variant rs10218788
Chromosome Location chr1:151563069-151563070
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:151554800-151566200 Weak transcription Ovary ovary
2 chr1:151555000-151568800 Weak transcription Liver Liver
3 chr1:151555400-151580800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr1:151555600-151566600 Weak transcription Stomach Smooth Muscle stomach
5 chr1:151556400-151569200 Weak transcription Pancreas Pancrea
6 chr1:151556600-151566600 Weak transcription Rectal Mucosa Donor 29 rectum
7 chr1:151557000-151566400 Weak transcription Colon Smooth Muscle Colon
8 chr1:151558200-151566600 Weak transcription Fetal Stomach stomach
9 chr1:151558600-151566600 Weak transcription Fetal Kidney kidney
10 chr1:151558800-151563400 Weak transcription K562 blood
11 chr1:151559600-151568800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr1:151560000-151564600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr1:151560000-151566200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
14 chr1:151560000-151568400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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