Variant report

Variant	rs3026781
Chromosome Location	chr10:43620134-43620135
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:43616569..43618189-chr10:43619172..43621560,2	MCF-7	breast:
2	chr10:43620062..43622835-chr10:43632716..43635230,3	MCF-7	breast:
3	chr10:43614895..43617172-chr10:43618877..43621238,2	K562	blood:

Variant related genes	Relation type
ENSG00000273008	Chromatin interaction
ENSG00000169826	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10159558	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11238441	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11238465	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12258585	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12260994	0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12262152	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12765436	0.82[ASN][1000 genomes]
rs12765715	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12765838	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12766298	0.82[ASN][1000 genomes]
rs12775330	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12775743	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12779732	0.82[ASN][1000 genomes]
rs17363630	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1799939	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1800863	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1864393	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2075911	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28401552	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2900627	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3026776	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3026779	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3026782	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34817887	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4987091	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7074319	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7086299	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7092548	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7096367	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs71505665	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71505667	0.82[ASN][1000 genomes]
rs71505668	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72783237	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72783242	0.82[ASN][1000 genomes]
rs7893332	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7903283	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7910648	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7910805	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7921281	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7923256	0.83[AMR][1000 genomes]
rs9804209	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534548	chr10:42890664-43729688	Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv430159	chr10:43291894-43946294	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	nsv1038102	chr10:43441601-43642908	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv895082	chr10:43530071-43755506	Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv895083	chr10:43549708-43765485	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	nsv1051701	chr10:43555542-43642895	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
7	nsv1046892	chr10:43609488-43636278	Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
8	esv275022	chr10:43613026-43620551	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43601400-43632800	Weak transcription	Gastric	stomach
2	chr10:43601600-43624800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr10:43606400-43632600	Weak transcription	Right Atrium	heart
4	chr10:43606600-43626000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr10:43609800-43626800	Weak transcription	Fetal Intestine Small	intestine
6	chr10:43611800-43621200	Weak transcription	Fetal Intestine Large	intestine
7	chr10:43614800-43626800	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr10:43615600-43621400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr10:43617200-43620400	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr10:43617200-43624600	Weak transcription	Fetal Lung	lung
11	chr10:43617200-43632000	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr10:43617400-43620200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr10:43617400-43622000	Weak transcription	HUVEC	blood vessel
14	chr10:43617400-43632200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr10:43617600-43621800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr10:43617600-43623200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr10:43617600-43624400	Weak transcription	Fetal Thymus	thymus
18	chr10:43617800-43621200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr10:43618000-43621800	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr10:43618000-43622000	Weak transcription	Primary B cells from cord blood	blood
21	chr10:43618000-43622000	Weak transcription	GM12878-XiMat	blood
22	chr10:43618000-43622200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr10:43618000-43632600	Weak transcription	Spleen	Spleen
24	chr10:43618400-43621600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr10:43618600-43622000	Weak transcription	Primary hematopoietic stem cells	blood
26	chr10:43618800-43622600	Weak transcription	Colonic Mucosa	Colon
27	chr10:43619400-43622200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr10:43619600-43625800	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr10:43619800-43622600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr10:43620000-43620200	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
31	chr10:43620000-43621800	Weak transcription	Primary B cells from peripheral blood	blood

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