Variant report

Variant	rs7074652
Chromosome Location	chr10:54770299-54770300
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:54769210..54771714-chr10:54777628..54779140,2	K562	blood:
2	chr10:54767534..54770532-chr10:54779157..54781249,2	K562	blood:

Extended variants
information (count: 120 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:109)

rs_ID	r²[population]
rs10508979	0.93[EUR][1000 genomes]
rs10508980	0.93[EUR][1000 genomes]
rs10824851	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11003297	0.84[AMR][1000 genomes]
rs11003298	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11003300	0.85[EUR][1000 genomes]
rs11003301	0.83[EUR][1000 genomes]
rs11003305	0.93[EUR][1000 genomes]
rs11003306	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11003307	0.93[EUR][1000 genomes]
rs11003308	0.93[EUR][1000 genomes]
rs11003309	0.93[EUR][1000 genomes]
rs11003311	0.93[EUR][1000 genomes]
rs11003313	0.93[EUR][1000 genomes]
rs11003314	0.93[EUR][1000 genomes]
rs11003316	0.93[EUR][1000 genomes]
rs11003317	0.93[EUR][1000 genomes]
rs11003318	0.93[EUR][1000 genomes]
rs11003319	0.93[EUR][1000 genomes]
rs11003320	0.91[EUR][1000 genomes]
rs11003321	0.93[EUR][1000 genomes]
rs11003322	0.93[EUR][1000 genomes]
rs11003323	0.91[EUR][1000 genomes]
rs11003324	0.91[EUR][1000 genomes]
rs11003325	0.91[EUR][1000 genomes]
rs11003326	0.91[EUR][1000 genomes]
rs11003327	0.92[EUR][1000 genomes]
rs11003328	0.93[EUR][1000 genomes]
rs11592153	0.93[EUR][1000 genomes]
rs11594477	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11594875	0.94[EUR][1000 genomes]
rs11594930	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11596013	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11596708	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11598902	0.93[EUR][1000 genomes]
rs12354890	0.80[CEU][hapmap];0.85[YRI][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12355649	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12356355	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12358058	0.83[YRI][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12359301	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1343049	0.80[CEU][hapmap];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1343050	0.80[CEU][hapmap];0.85[YRI][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1573146	0.93[EUR][1000 genomes]
rs1573148	0.93[EUR][1000 genomes]
rs16936072	0.93[EUR][1000 genomes]
rs16936083	0.93[EUR][1000 genomes]
rs16936094	0.93[EUR][1000 genomes]
rs16936097	0.93[EUR][1000 genomes]
rs16936108	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs16936179	0.93[EUR][1000 genomes]
rs16936282	0.94[EUR][1000 genomes]
rs16936283	0.94[EUR][1000 genomes]
rs2091176	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2384102	0.84[AMR][1000 genomes]
rs2891424	0.84[AMR][1000 genomes]
rs35747583	0.93[EUR][1000 genomes]
rs4083148	0.80[CEU][hapmap];0.89[YRI][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4258288	0.84[AMR][1000 genomes]
rs4294491	0.93[EUR][1000 genomes]
rs4403716	0.93[EUR][1000 genomes]
rs4564234	0.80[CEU][hapmap];0.84[YRI][hapmap];0.85[EUR][1000 genomes]
rs4589197	0.80[CEU][hapmap];0.85[EUR][1000 genomes]
rs4611108	0.85[EUR][1000 genomes]
rs4622164	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4636566	0.85[EUR][1000 genomes]
rs56667843	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs56999418	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs59171053	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs59605539	0.93[EUR][1000 genomes]
rs59993736	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs60635951	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs61134451	0.93[EUR][1000 genomes]
rs61387465	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs61844531	0.83[EUR][1000 genomes]
rs7084055	0.97[EUR][1000 genomes]
rs7086840	0.87[EUR][1000 genomes]
rs7475455	0.93[EUR][1000 genomes]
rs7893356	0.84[AMR][1000 genomes]
rs7893527	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7894017	0.93[EUR][1000 genomes]
rs7894623	0.84[AMR][1000 genomes]
rs7894718	0.93[EUR][1000 genomes]
rs7896118	0.84[EUR][1000 genomes]
rs7899425	0.93[EUR][1000 genomes]
rs7899454	0.93[EUR][1000 genomes]
rs7899582	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7900326	0.93[EUR][1000 genomes]
rs7903815	0.94[EUR][1000 genomes]
rs7905190	0.93[EUR][1000 genomes]
rs7905634	0.93[EUR][1000 genomes]
rs7906006	0.93[EUR][1000 genomes]
rs7906107	0.93[EUR][1000 genomes]
rs7907039	0.86[EUR][1000 genomes]
rs7910673	0.84[AMR][1000 genomes]
rs7912023	0.93[EUR][1000 genomes]
rs7912367	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7912728	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7914381	0.84[EUR][1000 genomes]
rs7914999	0.93[EUR][1000 genomes]
rs7915183	0.93[EUR][1000 genomes]
rs7915769	0.93[EUR][1000 genomes]
rs7917355	0.93[EUR][1000 genomes]
rs7918032	0.93[EUR][1000 genomes]
rs7918282	0.93[EUR][1000 genomes]
rs7921542	0.93[EUR][1000 genomes]
rs7923744	0.93[EUR][1000 genomes]
rs9787467	0.84[EUR][1000 genomes]
rs9787531	0.93[EUR][1000 genomes]
rs9787652	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895404	chr10:54545590-54850707	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1043809	chr10:54645158-54860817	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv540627	chr10:54645158-54860817	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv467201	chr10:54697623-54929003	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv550906	chr10:54697623-54929003	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv470939	chr10:54700783-54917339	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv467202	chr10:54735164-54830687	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv550907	chr10:54735164-54830687	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	esv1826571	chr10:54765608-54788821	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv895405	chr10:54765608-54824741	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv508585	chr10:54769376-54796804	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54764400-54771200	Enhancers	HepG2	liver
2	chr10:54765200-54782600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr10:54767600-54782200	Weak transcription	Fetal Kidney	kidney
4	chr10:54769200-54772600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr10:54769800-54770800	Enhancers	Fetal Brain Female	brain
6	chr10:54770000-54770600	Enhancers	Stomach Mucosa	stomach
7	chr10:54770000-54770800	Enhancers	Fetal Lung	lung

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