Variant report

Variant	rs1347135
Chromosome Location	chr5:167484417-167484418
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10866620	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10866621	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11952245	0.95[CHB][hapmap]
rs1347136	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17069705	0.82[CHB][hapmap]
rs247990	0.82[CHB][hapmap]
rs3860782	0.94[ASW][hapmap];0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.94[JPT][hapmap];0.98[LWK][hapmap];0.95[MEX][hapmap];0.92[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6897683	0.91[CHB][hapmap]
rs918527	0.91[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:167468000-167500800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:167474400-167485000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr5:167474600-167491400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:167475000-167484800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr5:167475000-167491800	Weak transcription	NH-A	brain
6	chr5:167475400-167489200	Weak transcription	HSMM	muscle
7	chr5:167477800-167489200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr5:167478000-167489000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr5:167479200-167484800	Weak transcription	NHEK	skin
10	chr5:167483200-167486200	Weak transcription	Fetal Lung	lung
11	chr5:167483200-167489400	Weak transcription	Left Ventricle	heart
12	chr5:167483200-167502400	Weak transcription	Fetal Heart	heart
13	chr5:167484200-167485600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr5:167484200-167485600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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