The 2.0 version of rSNPBase

Variant report

Variant rs4699926
Chromosome Location chr5:57741777-57741778
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:57735200-57751400 Weak transcription Psoas Muscle Psoas
2 chr5:57737000-57747400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr5:57737400-57747000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr5:57737800-57748600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr5:57737800-57749000 Weak transcription Fetal Lung lung
6 chr5:57740400-57742400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr5:57740400-57743000 Weak transcription HSMM muscle
8 chr5:57741000-57742200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr5:57741200-57742200 Weak transcription A549 lung
10 chr5:57741200-57744800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr5:57741200-57745200 Weak transcription NHEK skin
12 chr5:57741200-57747000 Weak transcription Fetal Adrenal Gland Adrenal Gland
13 chr5:57741400-57742200 Weak transcription HMEC breast
14 chr5:57741400-57746000 Weak transcription Fetal Muscle Trunk muscle
15 chr5:57741400-57750200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
16 chr5:57741600-57745800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr5:57741600-57747200 Weak transcription Esophagus oesophagus

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Last update: Aug 31, 2015