Variant report

Variant rs4731012
Chromosome Location chr7:121076726-121076727
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:121069200-121077600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr7:121069800-121078000 Weak transcription Fetal Kidney kidney
3 chr7:121072200-121077600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:121073800-121076800 Weak transcription Primary B cells from peripheral blood blood
5 chr7:121074400-121077400 Enhancers Placenta Amnion Placenta Amnion
6 chr7:121074400-121078000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr7:121074400-121080800 Weak transcription Pancreas Pancrea
8 chr7:121074600-121077400 Weak transcription Fetal Intestine Small intestine
9 chr7:121074600-121077800 Weak transcription GM12878-XiMat blood
10 chr7:121076000-121078200 Enhancers Fetal Intestine Large intestine
11 chr7:121076000-121079000 Enhancers Placenta Placenta
12 chr7:121076200-121076800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr7:121076200-121077800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr7:121076400-121076800 Enhancers ES-I3 Cell Line embryonic stem cell
15 chr7:121076400-121077200 Enhancers H1 Cell Line embryonic stem cell
16 chr7:121076400-121077200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
17 chr7:121076400-121077800 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
18 chr7:121076400-121078400 Enhancers Primary T helper cells PMA-I stimulated --
19 chr7:121076600-121077600 Weak transcription iPS-15b Cell Line embryonic stem cell
20 chr7:121076600-121077600 Weak transcription Esophagus oesophagus
21 chr7:121076600-121077600 Weak transcription NHEK skin
22 chr7:121076600-121078000 Weak transcription HUVEC blood vessel
23 chr7:121076600-121078200 Enhancers HUES6 Cell Line embryonic stem cell

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