Variant report

Variant	rs12037055
Chromosome Location	chr1:193316688-193316689
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:193312128..193314773-chr1:193315936..193317775,2	K562	blood:
2	chr1:193248975..193251649-chr1:193316395..193319289,2	K562	blood:
3	chr1:193312128..193313756-chr1:193315786..193317436,2	K562	blood:

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs10754048	0.90[CEU][hapmap]
rs10754049	0.90[CEU][hapmap]
rs10754052	0.90[CEU][hapmap]
rs10754054	0.84[EUR][1000 genomes]
rs10754055	0.86[EUR][1000 genomes]
rs10801179	0.90[CEU][hapmap]
rs10801183	0.91[CEU][hapmap]
rs10801194	0.86[EUR][1000 genomes]
rs10921325	0.90[CEU][hapmap]
rs10921336	0.83[EUR][1000 genomes]
rs10921343	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12025186	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12025393	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12032958	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12034095	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12040365	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12040832	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12041558	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12041893	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12047390	0.95[CEU][hapmap];0.86[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12048579	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12124282	0.96[ASN][1000 genomes]
rs1221502	0.89[EUR][1000 genomes]
rs1325197	0.86[CEU][hapmap]
rs1339961	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1361404	0.86[CHB][hapmap];0.91[JPT][hapmap]
rs1361405	0.95[CEU][hapmap];0.86[CHB][hapmap];0.91[JPT][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1616234	0.86[EUR][1000 genomes]
rs1632444	0.86[EUR][1000 genomes]
rs16835282	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16835304	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16835319	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs16835320	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs16835338	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1749429	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1749430	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1749431	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1749432	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1769999	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1770000	0.96[ASN][1000 genomes]
rs1972344	0.83[EUR][1000 genomes]
rs1972345	0.89[EUR][1000 genomes]
rs2050799	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2182106	0.90[CEU][hapmap]
rs2254646	0.86[EUR][1000 genomes]
rs2275506	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2370029	0.90[CEU][hapmap]
rs2477549	0.87[EUR][1000 genomes]
rs2486842	0.82[EUR][1000 genomes]
rs2486843	0.96[ASN][1000 genomes]
rs4379660	0.90[CEU][hapmap]
rs4428863	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4657848	0.90[CEU][hapmap]
rs4657854	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4657855	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4657856	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4657858	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs475163	0.81[EUR][1000 genomes]
rs497362	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs503265	0.86[EUR][1000 genomes]
rs515964	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs523402	0.83[EUR][1000 genomes]
rs524701	0.83[EUR][1000 genomes]
rs531327	0.84[ASN][1000 genomes]
rs543788	0.86[EUR][1000 genomes]
rs560900	0.89[EUR][1000 genomes]
rs569656	0.95[CEU][hapmap];0.87[EUR][1000 genomes]
rs571029	0.84[EUR][1000 genomes]
rs578639	0.89[EUR][1000 genomes]
rs59264807	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6428152	0.82[CEU][hapmap]
rs6428154	0.91[CEU][hapmap]
rs6428159	0.90[CEU][hapmap];0.83[EUR][1000 genomes]
rs6428163	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6428166	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6662104	0.96[ASN][1000 genomes]
rs6665666	0.90[CEU][hapmap]
rs6671476	0.86[EUR][1000 genomes]
rs6673271	0.90[CEU][hapmap]
rs6675833	0.90[CEU][hapmap]
rs6676878	0.90[CEU][hapmap]
rs6680224	0.91[CEU][hapmap]
rs6693734	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6697195	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6702762	0.96[ASN][1000 genomes]
rs693519	0.86[CEU][hapmap];0.81[EUR][1000 genomes]
rs7518792	0.82[CEU][hapmap]
rs7528595	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7543029	0.95[ASN][1000 genomes]
rs7550521	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs817136	0.83[EUR][1000 genomes]
rs817138	0.81[EUR][1000 genomes]
rs817140	0.86[CEU][hapmap];0.81[EUR][1000 genomes]
rs817142	0.83[EUR][1000 genomes]
rs817143	0.83[EUR][1000 genomes]
rs843844	0.86[CEU][hapmap];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872831	chr1:193152317-193322087	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv1001174	chr1:193186758-193363372	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv997891	chr1:193271839-193566441	Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:193305800-193317200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr1:193308000-193317400	Weak transcription	HSMM	muscle
3	chr1:193311000-193324000	Weak transcription	Duodenum Mucosa	Duodenum
4	chr1:193312200-193317600	Weak transcription	Ovary	ovary
5	chr1:193315600-193317200	Weak transcription	HSMMtube	muscle
6	chr1:193316000-193317800	Weak transcription	Fetal Intestine Small	intestine
7	chr1:193316200-193317600	Weak transcription	Fetal Intestine Large	intestine
8	chr1:193316400-193323400	Weak transcription	Stomach Mucosa	stomach
9	chr1:193316600-193317800	Weak transcription	Fetal Kidney	kidney

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