Variant report

Variant	rs11614374
Chromosome Location	chr12:4959178-4959179
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11831080	0.88[ASN][1000 genomes]
rs16931738	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16931772	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16931774	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17177689	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17784177	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2302355	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55936059	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73048603	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74056145	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7956904	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7960689	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:4929200-4966600	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr12:4929400-4966600	Weak transcription	Brain Angular Gyrus	brain
3	chr12:4935800-4965000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr12:4938600-4960200	Weak transcription	Fetal Brain Female	brain
5	chr12:4939200-4959400	Weak transcription	Brain Germinal Matrix	brain
6	chr12:4939600-4966600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr12:4943000-4966800	Weak transcription	Fetal Brain Male	brain
8	chr12:4948200-4960200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr12:4948400-4960000	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr12:4948400-4966800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr12:4957400-4961400	Weak transcription	Fetal Muscle Leg	muscle
12	chr12:4958600-4963200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:4958800-4962200	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr12:4958800-4963400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr12:4959000-4959200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr12:4959000-4961800	Strong transcription	Fetal Stomach	stomach
17	chr12:4959000-4963800	Weak transcription	Fetal Intestine Small	intestine

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

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