Variant report

Variant rs10799432
Chromosome Location chr1:227819760-227819761
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:227770000-227853800 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
2 chr1:227790400-227834800 Weak transcription Placenta Amnion Placenta Amnion
3 chr1:227800200-227820600 Weak transcription Skeletal Muscle Male skeletal muscle
4 chr1:227801200-227821800 Weak transcription Stomach Smooth Muscle stomach
5 chr1:227805800-227823600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:227811800-227830600 ZNF genes & repeats Liver Liver
7 chr1:227815200-227828800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr1:227815400-227820800 Weak transcription Ovary ovary
9 chr1:227817400-227821200 ZNF genes & repeats Sigmoid Colon Sigmoid Colon
10 chr1:227818600-227822200 ZNF genes & repeats Cortex derived primary cultured neurospheres brain
11 chr1:227818600-227822600 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
12 chr1:227818600-227830600 ZNF genes & repeats Duodenum Mucosa Duodenum
13 chr1:227818600-227834200 ZNF genes & repeats Fetal Brain Female brain
14 chr1:227818800-227822800 ZNF genes & repeats Primary B cells from cord blood blood
15 chr1:227819000-227822400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
16 chr1:227819400-227823800 ZNF genes & repeats Fetal Muscle Leg muscle

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