Variant report

Variant	rs4511111
Chromosome Location	chr1:152211624-152211625
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 91 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs10749669	0.93[CEU][hapmap]
rs10749670	0.93[CEU][hapmap];0.91[CHB][hapmap];0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs10788824	0.93[CEU][hapmap];0.87[CHB][hapmap]
rs10888470	0.93[CEU][hapmap];0.91[CHB][hapmap];0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs10888471	0.93[CEU][hapmap];0.91[CHB][hapmap];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10888473	0.93[CEU][hapmap];0.91[CHB][hapmap];0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10888475	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11204939	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11204944	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11204947	0.93[CEU][hapmap];0.91[CHB][hapmap];0.90[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11204948	0.93[CEU][hapmap];0.91[CHB][hapmap];0.93[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11204949	0.85[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11204951	0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11204952	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11204978	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11204980	0.93[CEU][hapmap];0.91[CHB][hapmap]
rs11204981	0.93[CEU][hapmap];0.90[CHB][hapmap]
rs11583524	0.93[CEU][hapmap];0.87[CHB][hapmap]
rs11584340	0.93[CEU][hapmap];0.91[CHB][hapmap]
rs11584427	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11586114	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11587676	1.00[CEU][hapmap];0.82[CHB][hapmap];0.81[JPT][hapmap]
rs11588174	0.93[CEU][hapmap]
rs11589532	0.82[AMR][1000 genomes]
rs11589587	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11590365	0.86[EUR][1000 genomes]
rs12405278	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs12405678	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12406105	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12408581	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12409762	0.80[AMR][1000 genomes]
rs12566867	0.83[ASN][1000 genomes]
rs12748016	0.84[AMR][1000 genomes]
rs1390485	0.85[AMR][1000 genomes]
rs1390488	0.93[CEU][hapmap];0.91[CHB][hapmap];0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1390490	0.93[CEU][hapmap];0.87[CHB][hapmap]
rs1466757	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1496045	0.93[CEU][hapmap]
rs1845791	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1858480	0.93[CEU][hapmap];0.91[CHB][hapmap]
rs1858482	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1969019	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2065955	1.00[CEU][hapmap]
rs2132418	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2184953	0.81[CEU][hapmap];0.91[CHB][hapmap]
rs2338430	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2338555	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2879174	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs3120659	0.93[CEU][hapmap];0.91[CHB][hapmap]
rs3126066	0.93[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap]
rs3126085	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3126088	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3126091	0.92[CEU][hapmap];0.91[CHB][hapmap]
rs36033453	0.90[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs41266134	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4326625	0.87[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4511113	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4582793	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4845423	0.93[CEU][hapmap]
rs4845428	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4845430	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4845431	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4845736	1.00[CEU][hapmap]
rs4845745	0.93[CEU][hapmap];0.81[CHB][hapmap]
rs4845750	0.93[CEU][hapmap];0.91[CHB][hapmap];0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4845751	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4845752	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs55654502	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55957623	0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55982921	0.89[EUR][1000 genomes]
rs56013982	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6587666	0.93[CEU][hapmap];0.91[CHB][hapmap]
rs6666382	0.93[CEU][hapmap];0.91[CHB][hapmap];0.90[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6668499	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6675889	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6676012	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6678951	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs72696952	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72696963	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72696969	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs74127901	0.88[AMR][1000 genomes]
rs7534716	0.81[ASN][1000 genomes]
rs7535078	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7537637	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7550106	0.93[CEU][hapmap];0.91[CHB][hapmap]
rs877776	0.93[CEU][hapmap]
rs991231	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007097	chr1:151832796-152227977	Strong transcription Genic enhancers Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
2	nsv547853	chr1:152008671-152236760	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
3	nsv1014095	chr1:152104486-152454591	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv947506	chr1:152203216-152223222	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4511111	FLG	cis	Thyroid	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152207600-152215400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links