Variant report

Variant	rs12237102
Chromosome Location	chr9:110850958-110850959
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10979189	0.98[EUR][1000 genomes]
rs10979190	0.84[AMR][1000 genomes]
rs10979191	0.84[AMR][1000 genomes]
rs10979192	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10979195	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10979197	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10979198	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10979199	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10979202	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10979204	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10979206	0.89[CEU][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes]
rs12235917	0.95[AMR][1000 genomes]
rs12236285	0.89[CEU][hapmap];0.86[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes]
rs1412437	1.00[CEU][hapmap];0.82[JPT][hapmap];0.98[EUR][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110847000-110851200	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr9:110847000-110851400	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr9:110847200-110855800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr9:110848200-110856200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr9:110848400-110851400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr9:110848800-110854200	Weak transcription	K562	blood
7	chr9:110849800-110851200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr9:110850200-110851000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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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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