Variant report

Variant	rs11838301
Chromosome Location	chr12:103953401-103953402
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:103950200-103955600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr12:103951200-103956600	Enhancers	Placenta	Placenta
3	chr12:103951600-103953600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr12:103951600-103954000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr12:103951600-103954600	Weak transcription	Fetal Muscle Leg	muscle
6	chr12:103952400-103956000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr12:103952600-103954000	Enhancers	A549	lung
8	chr12:103952800-103954200	Enhancers	NHEK	skin
9	chr12:103952800-103956800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr12:103952800-103958200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr12:103953200-103954000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr12:103953200-103954000	Weak transcription	Fetal Intestine Large	intestine
13	chr12:103953200-103956400	Enhancers	HMEC	breast
14	chr12:103953400-103953800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr12:103953400-103955600	Enhancers	NHDF-Ad	bronchial

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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