Variant report

Variant	rs13151051
Chromosome Location	chr4:30924444-30924445
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10000401	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10013694	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10027633	0.83[EUR][1000 genomes]
rs10805300	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10939317	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10939318	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10939325	0.80[CEU][hapmap]
rs11722640	0.82[EUR][1000 genomes]
rs11727594	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11735048	0.90[CEU][hapmap];0.81[YRI][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12512796	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12651441	0.80[AFR][1000 genomes]
rs13120686	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13127450	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28670870	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2871476	0.87[CEU][hapmap];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4075130	0.87[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4235012	0.82[ASN][1000 genomes]
rs4235013	0.86[CEU][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4235014	0.87[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4235015	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4259023	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4260492	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4261943	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4266255	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4337695	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4358358	0.90[CEU][hapmap];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4361347	0.87[CEU][hapmap];0.85[EUR][1000 genomes]
rs4374588	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4380481	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4441719	0.84[EUR][1000 genomes]
rs4469028	0.90[CEU][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4487300	0.87[CEU][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4491979	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4536889	0.83[EUR][1000 genomes]
rs4557225	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4585258	0.87[CEU][hapmap];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4586889	0.80[EUR][1000 genomes]
rs4692107	0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4692483	0.81[EUR][1000 genomes]
rs4692485	0.83[EUR][1000 genomes]
rs4692487	0.83[EUR][1000 genomes]
rs4692488	0.83[EUR][1000 genomes]
rs4692489	0.92[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs4692490	0.87[CEU][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs5001866	0.87[CEU][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6448726	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6448727	0.81[EUR][1000 genomes]
rs6819406	0.86[EUR][1000 genomes]
rs6821487	0.94[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs6839087	0.82[EUR][1000 genomes]
rs6840698	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6856017	0.85[AFR][1000 genomes]
rs7658077	0.90[CEU][hapmap];0.81[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7661924	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7662881	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7665348	0.81[EUR][1000 genomes]
rs7669015	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7673048	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7678386	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7679853	0.85[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs7683848	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7683968	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7696462	0.90[CEU][hapmap];0.81[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9685207	0.90[CEU][hapmap];0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9990832	0.83[EUR][1000 genomes]
rs9996030	0.94[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs9997116	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9997529	0.80[EUR][1000 genomes]
rs9998569	0.94[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs9999771	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv878810	chr4:30823157-30987395	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv998450	chr4:30823631-31628179	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30914200-30947200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr4:30914400-30928200	Weak transcription	Fetal Lung	lung
3	chr4:30914400-30940600	Weak transcription	Colon Smooth Muscle	Colon
4	chr4:30918600-30925800	Weak transcription	Fetal Intestine Small	intestine
5	chr4:30919400-30926200	Weak transcription	Left Ventricle	heart
6	chr4:30920600-30947400	Weak transcription	Fetal Stomach	stomach
7	chr4:30922000-30935800	Weak transcription	Aorta	Aorta
8	chr4:30922400-30926800	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr4:30922400-30929400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr4:30922400-30929600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr4:30922400-30931400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr4:30922400-30933800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr4:30922600-30927000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr4:30922600-30934200	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr4:30923400-30928200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr4:30923800-30930200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr4:30924200-30924800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr4:30924200-30931400	Weak transcription	Fetal Muscle Leg	muscle

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