Variant report

Variant	rs10832601
Chromosome Location	chr11:16418549-16418550
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:16399981..16401703-chr11:16417138..16418693,2	K562	blood:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1004283	0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs10741698	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10766324	0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs10766325	0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs10832602	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10832603	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10832604	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10832607	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10832609	0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10832610	0.87[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11023932	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11023934	0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11023940	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11023942	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11023943	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11023947	0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12221729	0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12221945	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12221946	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12222249	0.94[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1393924	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1393926	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1503440	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16933105	0.92[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs16933117	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1948824	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2134610	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2174164	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs297332	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs297335	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs297337	0.92[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs297338	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4756850	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4756851	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4757397	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4757398	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4757399	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4757402	0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4757403	0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs61883215	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7926068	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7935820	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7951243	0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7951760	0.81[AMR][1000 genomes];0.98[ASN][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	nsv529731	chr11:16122782-16468170	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv553566	chr11:16329009-16799044	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv832075	chr11:16391700-16490934	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:16409000-16419200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr11:16410000-16418800	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr11:16415200-16419400	Weak transcription	Small Intestine	intestine
4	chr11:16415400-16424400	Weak transcription	Fetal Heart	heart
5	chr11:16416000-16419200	Active TSS	Fetal Intestine Large	intestine
6	chr11:16416200-16419200	Active TSS	Pancreatic Islets	Pancreatic Islet
7	chr11:16416400-16418800	Enhancers	Liver	Liver
8	chr11:16416400-16419200	Active TSS	Fetal Intestine Small	intestine
9	chr11:16416600-16419400	Active TSS	Duodenum Mucosa	Duodenum
10	chr11:16417200-16434200	Weak transcription	Psoas Muscle	Psoas
11	chr11:16417400-16419400	Active TSS	Duodenum Smooth Muscle	Duodenum
12	chr11:16417600-16418600	Active TSS	HepG2	liver
13	chr11:16417800-16419200	Active TSS	Fetal Kidney	kidney
14	chr11:16418000-16425200	Weak transcription	Brain Germinal Matrix	brain
15	chr11:16418200-16419000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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