Variant report

Variant rs6704957
Chromosome Location chr2:187192676-187192677
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:187188600-187216200 Weak transcription Primary hematopoietic stem cells blood
2 chr2:187189200-187193000 Weak transcription Fetal Intestine Small intestine
3 chr2:187190400-187192800 Enhancers NHEK skin
4 chr2:187190600-187192800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr2:187190800-187192800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr2:187191000-187194400 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr2:187192000-187193000 Flanking Active TSS GM12878-XiMat blood
8 chr2:187192000-187193400 Enhancers HUES6 Cell Line embryonic stem cell
9 chr2:187192200-187193000 Enhancers HUES48 Cell Line embryonic stem cell
10 chr2:187192200-187193200 Enhancers Placenta Amnion Placenta Amnion
11 chr2:187192400-187211600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr2:187192600-187192800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
13 chr2:187192600-187193200 Enhancers H9 Cell Line embryonic stem cell
14 chr2:187192600-187193400 Enhancers Ovary ovary

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