Variant report

Variant	rs1504446
Chromosome Location	chr12:60789212-60789213
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 115 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:110)

rs_ID	r²[population]
rs1021886	1.00[EUR][1000 genomes]
rs10784049	1.00[EUR][1000 genomes]
rs11173425	0.81[YRI][hapmap]
rs1119985	1.00[EUR][1000 genomes]
rs1119986	1.00[EUR][1000 genomes]
rs1119987	1.00[EUR][1000 genomes]
rs12312951	1.00[EUR][1000 genomes]
rs12313027	1.00[EUR][1000 genomes]
rs1394325	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1394329	0.92[YRI][hapmap];0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1466939	1.00[EUR][1000 genomes]
rs1472738	1.00[EUR][1000 genomes]
rs1504445	1.00[EUR][1000 genomes]
rs1504447	1.00[EUR][1000 genomes]
rs1504448	1.00[EUR][1000 genomes]
rs1504461	1.00[EUR][1000 genomes]
rs1580917	0.92[EUR][1000 genomes]
rs1587822	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1587823	1.00[EUR][1000 genomes]
rs1604863	1.00[EUR][1000 genomes]
rs1604864	1.00[EUR][1000 genomes]
rs17123529	0.85[EUR][1000 genomes]
rs1827639	1.00[EUR][1000 genomes]
rs1827640	1.00[EUR][1000 genomes]
rs1910676	1.00[EUR][1000 genomes]
rs1960370	1.00[EUR][1000 genomes]
rs1961693	1.00[EUR][1000 genomes]
rs1967225	1.00[EUR][1000 genomes]
rs1995517	1.00[EUR][1000 genomes]
rs2047909	1.00[EUR][1000 genomes]
rs2047910	1.00[EUR][1000 genomes]
rs2047911	1.00[EUR][1000 genomes]
rs2089152	1.00[EUR][1000 genomes]
rs2089153	1.00[EUR][1000 genomes]
rs2102256	1.00[EUR][1000 genomes]
rs2134884	1.00[EUR][1000 genomes]
rs2134885	1.00[EUR][1000 genomes]
rs2134886	1.00[EUR][1000 genomes]
rs2202361	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2202362	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2202363	1.00[EUR][1000 genomes]
rs2202364	1.00[EUR][1000 genomes]
rs2262938	1.00[EUR][1000 genomes]
rs2262940	1.00[EUR][1000 genomes]
rs2363586	1.00[EUR][1000 genomes]
rs2363588	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2455997	1.00[EUR][1000 genomes]
rs2468380	1.00[EUR][1000 genomes]
rs2468381	1.00[EUR][1000 genomes]
rs2655849	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2655850	1.00[EUR][1000 genomes]
rs2655851	1.00[EUR][1000 genomes]
rs2655854	1.00[EUR][1000 genomes]
rs2655855	1.00[EUR][1000 genomes]
rs2655862	1.00[EUR][1000 genomes]
rs2655863	1.00[EUR][1000 genomes]
rs2655864	1.00[EUR][1000 genomes]
rs2655865	1.00[EUR][1000 genomes]
rs2655866	1.00[EUR][1000 genomes]
rs2655867	1.00[EUR][1000 genomes]
rs2655870	1.00[EUR][1000 genomes]
rs2655872	1.00[EUR][1000 genomes]
rs2655874	1.00[EUR][1000 genomes]
rs2655876	1.00[EUR][1000 genomes]
rs2655881	1.00[EUR][1000 genomes]
rs2655882	1.00[EUR][1000 genomes]
rs2655883	1.00[EUR][1000 genomes]
rs2731450	1.00[EUR][1000 genomes]
rs2731452	1.00[EUR][1000 genomes]
rs2731453	1.00[EUR][1000 genomes]
rs2731454	1.00[EUR][1000 genomes]
rs2731460	1.00[EUR][1000 genomes]
rs2731461	1.00[EUR][1000 genomes]
rs2731463	1.00[EUR][1000 genomes]
rs2731464	1.00[EUR][1000 genomes]
rs2731466	1.00[EUR][1000 genomes]
rs2731478	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2731479	1.00[EUR][1000 genomes]
rs2731480	1.00[EUR][1000 genomes]
rs2731481	0.83[EUR][1000 genomes]
rs2731483	1.00[EUR][1000 genomes]
rs2731486	1.00[EUR][1000 genomes]
rs2731489	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2731493	1.00[EUR][1000 genomes]
rs2731496	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2938648	1.00[EUR][1000 genomes]
rs2938649	1.00[EUR][1000 genomes]
rs2956516	1.00[EUR][1000 genomes]
rs4500518	1.00[EUR][1000 genomes]
rs55897976	0.85[EUR][1000 genomes]
rs59465291	0.85[EUR][1000 genomes]
rs60106464	0.85[EUR][1000 genomes]
rs6581317	1.00[EUR][1000 genomes]
rs7307145	1.00[EUR][1000 genomes]
rs74093673	0.85[EUR][1000 genomes]
rs74093676	0.85[EUR][1000 genomes]
rs74096730	0.85[EUR][1000 genomes]
rs74096924	0.85[EUR][1000 genomes]
rs74096934	0.85[EUR][1000 genomes]
rs74096935	0.85[EUR][1000 genomes]
rs74096939	0.85[EUR][1000 genomes]
rs74096943	0.85[EUR][1000 genomes]
rs74096947	0.85[EUR][1000 genomes]
rs74096948	0.85[EUR][1000 genomes]
rs74096953	0.85[EUR][1000 genomes]
rs74096958	0.85[EUR][1000 genomes]
rs7968422	1.00[EUR][1000 genomes]
rs7974290	1.00[EUR][1000 genomes]
rs905724	1.00[EUR][1000 genomes]
rs905725	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899137	chr12:60568891-60797083	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv1054287	chr12:60601870-60861866	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv832431	chr12:60626292-60809233	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1047466	chr12:60702221-61521156	Active TSS Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	esv3351746	chr12:60788685-60793483	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:60787800-60789400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr12:60787800-60789800	Enhancers	Hela-S3	cervix
3	chr12:60788000-60789600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:60788000-60789600	Enhancers	HMEC	breast
5	chr12:60788000-60789800	Enhancers	NHEK	skin
6	chr12:60788200-60789800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr12:60788400-60789400	Enhancers	HUVEC	blood vessel
8	chr12:60788400-60789600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links