Variant report

Variant	rs12306150
Chromosome Location	chr12:116877693-116877694
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:116872600-116878400	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr12:116872800-116881600	Weak transcription	Esophagus	oesophagus
3	chr12:116873000-116879000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr12:116873400-116878800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr12:116873600-116878800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr12:116873600-116879000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr12:116874400-116882200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr12:116874600-116886200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr12:116874600-116891000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr12:116874800-116878600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr12:116874800-116878600	Weak transcription	Thymus	Thymus
12	chr12:116875600-116880800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr12:116876000-116886000	Weak transcription	Fetal Intestine Small	intestine
14	chr12:116877000-116879000	Weak transcription	Fetal Muscle Trunk	muscle
15	chr12:116877000-116880800	Weak transcription	Fetal Muscle Leg	muscle
16	chr12:116877200-116878400	Weak transcription	Fetal Thymus	thymus

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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