Variant report

Variant rs7602918
Chromosome Location chr2:187191206-187191207
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:187173200-187192200 Weak transcription Placenta Amnion Placenta Amnion
2 chr2:187188600-187216200 Weak transcription Primary hematopoietic stem cells blood
3 chr2:187189200-187193000 Weak transcription Fetal Intestine Small intestine
4 chr2:187190000-187191800 Enhancers HMEC breast
5 chr2:187190000-187192400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr2:187190400-187191800 Enhancers Placenta Placenta
7 chr2:187190400-187192800 Enhancers NHEK skin
8 chr2:187190600-187192800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr2:187190800-187192800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr2:187191000-187192200 Weak transcription HUES48 Cell Line embryonic stem cell
11 chr2:187191000-187192600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
12 chr2:187191000-187194400 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr2:187191200-187191400 Enhancers GM12878-XiMat blood

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