The 2.0 version of rSNPBase

Variant report

Variant rs6928341
Chromosome Location chr6:33345813-33345814
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:33341000-33352400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr6:33341200-33358600 Weak transcription H9 Cell Line embryonic stem cell
3 chr6:33342400-33347200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr6:33343800-33350200 Weak transcription Colon Smooth Muscle Colon
5 chr6:33343800-33359200 Weak transcription Right Atrium heart
6 chr6:33344000-33348000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr6:33344000-33348000 Weak transcription HMEC breast
8 chr6:33344000-33348200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr6:33344000-33350200 Weak transcription Stomach Smooth Muscle stomach
10 chr6:33344000-33351800 Weak transcription Esophagus oesophagus
11 chr6:33344200-33347400 Enhancers K562 blood
12 chr6:33344200-33348000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr6:33344400-33348000 Weak transcription NHEK skin
14 chr6:33344400-33350000 Weak transcription Placenta Placenta
15 chr6:33345600-33358800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr6:33345800-33348000 Weak transcription Fetal Adrenal Gland Adrenal Gland

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Last update: Aug 31, 2015