Variant report

Variant	rs10845850
Chromosome Location	chr12:14023364-14023365
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10845847	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10845851	0.93[ASN][1000 genomes]
rs1120905	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12582848	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2193512	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2284426	0.80[EUR][1000 genomes]
rs7959821	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:14019400-14033200	Weak transcription	Fetal Kidney	kidney
2	chr12:14022400-14024000	Enhancers	Fetal Heart	heart
3	chr12:14022800-14023400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr12:14022800-14023600	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr12:14022800-14023800	Enhancers	Stomach Mucosa	stomach
6	chr12:14023000-14023400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:14023000-14023400	Genic enhancers	A549	lung
8	chr12:14023000-14023600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr12:14023000-14023600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr12:14023200-14028600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr12:14023200-14033200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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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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