Variant report

Variant	rs35079003
Chromosome Location	chr1:216799913-216799914
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10495031	1.00[AFR][1000 genomes]
rs10863254	0.91[AFR][1000 genomes]
rs10863255	1.00[AFR][1000 genomes]
rs10863257	1.00[AFR][1000 genomes]
rs11117619	1.00[AFR][1000 genomes]
rs11117622	1.00[AFR][1000 genomes]
rs11117623	1.00[AFR][1000 genomes]
rs11117625	1.00[AFR][1000 genomes]
rs11117632	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11117633	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11117637	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11117638	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11117639	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11572727	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11572731	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11577409	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs11581434	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11585397	1.00[AFR][1000 genomes]
rs11587086	1.00[AFR][1000 genomes]
rs11590373	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12122051	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12123789	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs12128352	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12129039	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12131827	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12132004	0.91[AFR][1000 genomes]
rs12133226	1.00[AFR][1000 genomes]
rs12134503	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12136640	0.80[AMR][1000 genomes]
rs12138981	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12140540	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs12141843	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12145447	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs1532501	0.98[ASN][1000 genomes]
rs17669502	1.00[AFR][1000 genomes]
rs17670802	0.93[ASN][1000 genomes]
rs17671012	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2173371	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72737319	0.80[AMR][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	nsv549199	chr1:216384908-216814702	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv1003815	chr1:216504235-216836498	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv535289	chr1:216504235-216836498	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv873178	chr1:216714314-216813244	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:216775200-216835400	Weak transcription	Fetal Intestine Small	intestine
2	chr1:216787400-216853800	Weak transcription	Pancreas	Pancrea
3	chr1:216792400-216809000	Weak transcription	Gastric	stomach
4	chr1:216795800-216801400	Enhancers	Fetal Heart	heart
5	chr1:216799400-216800000	Enhancers	Right Ventricle	heart
6	chr1:216799600-216800000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
7	chr1:216799600-216800800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr1:216799600-216801000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr1:216799800-216800000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:216799800-216800000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
11	chr1:216799800-216800200	Enhancers	Left Ventricle	heart
12	chr1:216799800-216800200	Enhancers	Psoas Muscle	Psoas
13	chr1:216799800-216800800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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