Variant report

Variant	rs2264767
Chromosome Location	chr12:104816325-104816326
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs2248343	0.94[EUR][1000 genomes]
rs2248939	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2249041	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2249045	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2251917	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2252144	0.91[EUR][1000 genomes]
rs2252514	0.88[EUR][1000 genomes]
rs2252543	0.88[EUR][1000 genomes]
rs2254984	0.94[EUR][1000 genomes]
rs2264770	0.91[EUR][1000 genomes]
rs2464677	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2464679	0.97[EUR][1000 genomes]
rs2468910	0.94[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104808800-104824200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr12:104811000-104817200	Weak transcription	Fetal Thymus	thymus
3	chr12:104814800-104816600	Enhancers	Hela-S3	cervix
4	chr12:104815200-104816600	Weak transcription	NHEK	skin
5	chr12:104815200-104817400	Weak transcription	Thymus	Thymus
6	chr12:104815400-104820200	Weak transcription	HMEC	breast
7	chr12:104816000-104817000	Enhancers	HSMMtube	muscle
8	chr12:104816000-104818000	Weak transcription	Gastric	stomach
9	chr12:104816200-104817000	Enhancers	HSMM	muscle
10	chr12:104816200-104817200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:104816200-104824000	Weak transcription	Aorta	Aorta

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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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