Variant report

Variant rs321649
Chromosome Location chr4:48011339-48011340
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:48005400-48017400 Weak transcription Placenta Amnion Placenta Amnion
2 chr4:48006400-48013000 ZNF genes & repeats HUES64 Cell Line embryonic stem cell
3 chr4:48007400-48013200 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell
4 chr4:48007600-48013000 ZNF genes & repeats HUES48 Cell Line embryonic stem cell
5 chr4:48008000-48017600 Weak transcription Psoas Muscle Psoas
6 chr4:48008600-48013800 ZNF genes & repeats H1 Cell Line embryonic stem cell
7 chr4:48009200-48012800 ZNF genes & repeats iPS-15b Cell Line embryonic stem cell
8 chr4:48010200-48017200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr4:48010200-48017600 Weak transcription Rectal Mucosa Donor 31 rectum
10 chr4:48010600-48012600 ZNF genes & repeats Fetal Intestine Large intestine
11 chr4:48010600-48014400 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr4:48011000-48017400 Weak transcription Colonic Mucosa Colon
13 chr4:48011000-48017600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr4:48011000-48017600 Weak transcription Skeletal Muscle Female skeletal muscle
15 chr4:48011200-48011400 ZNF genes & repeats Esophagus oesophagus
16 chr4:48011200-48013000 ZNF genes & repeats Fetal Intestine Small intestine
17 chr4:48011200-48013200 Strong transcription Liver Liver
18 chr4:48011200-48017600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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