Variant report

Variant rs7519967
Chromosome Location chr1:217065312-217065313
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:217058200-217067600 Weak transcription iPS-20b Cell Line embryonic stem cell
2 chr1:217058400-217067800 Weak transcription Small Intestine intestine
3 chr1:217058600-217067800 Weak transcription Fetal Kidney kidney
4 chr1:217058800-217066000 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr1:217062600-217067600 Weak transcription HUES64 Cell Line embryonic stem cell
6 chr1:217062600-217078000 Weak transcription Pancreas Pancrea
7 chr1:217062800-217066000 Weak transcription Psoas Muscle Psoas
8 chr1:217062800-217067400 Weak transcription Skeletal Muscle Female skeletal muscle
9 chr1:217062800-217068000 Weak transcription H1 Cell Line embryonic stem cell
10 chr1:217062800-217068000 Weak transcription Left Ventricle heart
11 chr1:217062800-217076000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr1:217062800-217076200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr1:217062800-217087800 Weak transcription Fetal Muscle Leg muscle
14 chr1:217063000-217065600 Weak transcription Fetal Intestine Large intestine
15 chr1:217063000-217066200 Weak transcription Fetal Heart heart
16 chr1:217064000-217065600 Weak transcription Duodenum Mucosa Duodenum
17 chr1:217065200-217065800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
18 chr1:217065200-217066000 Enhancers Fetal Intestine Small intestine

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