Variant report

Variant	rs73529608
Chromosome Location	chr8:10656486-10656487
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:10654838..10657527-chr8:10667570..10669417,2	K562	blood:
2	chr8:10655273..10657441-chr8:10673003..10675779,2	MCF-7	breast:
3	chr8:10444773..10445405-chr8:10656129..10656744,2	MCF-7	breast:
4	chr8:10447773..10448295-chr8:10656037..10656649,2	MCF-7	breast:
5	chr8:10447404..10448576-chr8:10655982..10656998,11	MCF-7	breast:

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs1052523	0.88[EUR][1000 genomes]
rs11997941	0.93[EUR][1000 genomes]
rs13256603	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13256636	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13258593	0.80[EUR][1000 genomes]
rs13259278	0.80[EUR][1000 genomes]
rs13270447	0.80[EUR][1000 genomes]
rs13270498	0.80[EUR][1000 genomes]
rs13271456	0.80[EUR][1000 genomes]
rs13273767	0.85[EUR][1000 genomes]
rs13275368	0.93[EUR][1000 genomes]
rs13277664	0.98[EUR][1000 genomes]
rs13279753	0.85[EUR][1000 genomes]
rs13280573	0.98[EUR][1000 genomes]
rs13281048	0.80[EUR][1000 genomes]
rs17152289	0.80[EUR][1000 genomes]
rs17152398	0.85[EUR][1000 genomes]
rs17152442	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17152492	0.98[EUR][1000 genomes]
rs17721019	0.80[EUR][1000 genomes]
rs17773567	0.80[EUR][1000 genomes]
rs17773826	0.80[EUR][1000 genomes]
rs2409653	0.95[EUR][1000 genomes]
rs2898244	0.95[EUR][1000 genomes]
rs2898246	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34349857	0.93[EUR][1000 genomes]
rs34380949	0.80[EUR][1000 genomes]
rs34535545	0.93[EUR][1000 genomes]
rs35039898	0.85[EUR][1000 genomes]
rs35660623	0.93[EUR][1000 genomes]
rs35873156	0.88[EUR][1000 genomes]
rs61064518	0.80[EUR][1000 genomes]
rs6601531	0.86[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs6601532	0.86[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs6982062	0.91[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs6983180	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6989930	0.95[EUR][1000 genomes]
rs6990041	0.95[EUR][1000 genomes]
rs6992312	0.93[EUR][1000 genomes]
rs6993463	0.95[EUR][1000 genomes]
rs6993632	0.95[EUR][1000 genomes]
rs6993753	0.93[EUR][1000 genomes]
rs7005389	0.88[EUR][1000 genomes]
rs7006707	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7009841	0.91[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs7015820	0.91[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs71516594	0.80[EUR][1000 genomes]
rs71516595	0.85[EUR][1000 genomes]
rs73531562	0.88[EUR][1000 genomes]
rs7814489	0.95[EUR][1000 genomes]
rs9969476	0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022994	chr8:10190618-10660122	Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking 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	32 gene(s)	inside rSNPs	diseases
2	nsv539466	chr8:10190618-10660122	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv917085	chr8:10237508-10828204	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv1026802	chr8:10576444-10754489	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
5	nsv539469	chr8:10576444-10754489	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
6	nsv1017836	chr8:10591801-10803617	Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
7	nsv1034988	chr8:10591801-10804243	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer 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	14 gene(s)	inside rSNPs	diseases
8	nsv519768	chr8:10600254-10691993	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1024806	chr8:10605438-10662555	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv831232	chr8:10606053-10774948	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
11	nsv1031709	chr8:10610545-10657726	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	esv2764105	chr8:10610557-10657726	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv519376	chr8:10611708-10691993	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
14	nsv429860	chr8:10615990-10685890	Strong transcription Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
15	nsv1023085	chr8:10617908-10657584	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
16	nsv539470	chr8:10617908-10657584	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
17	nsv1019754	chr8:10617908-10700140	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
18	nsv539471	chr8:10617908-10700140	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
19	nsv1031726	chr8:10627742-10749369	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10610800-10662000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr8:10618800-10665200	Weak transcription	Fetal Brain Female	brain
3	chr8:10619400-10661600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr8:10620000-10669800	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr8:10621200-10662000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr8:10623400-10656800	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr8:10623400-10662600	Weak transcription	Fetal Thymus	thymus
8	chr8:10623400-10662800	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr8:10623400-10665000	Weak transcription	Fetal Intestine Large	intestine
10	chr8:10623600-10667000	Weak transcription	Thymus	Thymus
11	chr8:10623800-10656800	Weak transcription	Gastric	stomach
12	chr8:10635400-10664400	Weak transcription	Primary hematopoietic stem cells	blood
13	chr8:10635600-10656800	Weak transcription	Ovary	ovary
14	chr8:10640200-10669800	Weak transcription	Aorta	Aorta
15	chr8:10640600-10662800	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr8:10641200-10657000	Weak transcription	Psoas Muscle	Psoas
17	chr8:10641200-10665000	Weak transcription	Dnd41	blood
18	chr8:10641400-10662000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr8:10644200-10661400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr8:10644400-10656800	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr8:10645000-10670000	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr8:10646800-10662800	Weak transcription	GM12878-XiMat	blood
23	chr8:10647000-10674400	Weak transcription	Right Ventricle	heart
24	chr8:10647000-10681200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr8:10647200-10656800	Weak transcription	Primary B cells from cord blood	blood
26	chr8:10647200-10656800	Weak transcription	NHLF	lung
27	chr8:10647200-10657000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:10647200-10657000	Weak transcription	Colon Smooth Muscle	Colon
29	chr8:10647200-10659400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr8:10647200-10661800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr8:10647200-10673600	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr8:10647800-10657000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
33	chr8:10647800-10661600	Weak transcription	Brain Anterior Caudate	brain
34	chr8:10647800-10669800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr8:10648000-10656800	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr8:10648000-10656800	Weak transcription	Placenta	Placenta
37	chr8:10648000-10656800	Weak transcription	Left Ventricle	heart
38	chr8:10648000-10657000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr8:10648200-10656800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr8:10648200-10656800	Weak transcription	Lung	lung
41	chr8:10648200-10656800	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr8:10648200-10656800	Weak transcription	HSMMtube	muscle
43	chr8:10648200-10661000	Weak transcription	Brain Cingulate Gyrus	brain
44	chr8:10648200-10661400	Weak transcription	Brain Hippocampus Middle	brain
45	chr8:10648200-10661600	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr8:10648200-10663600	Weak transcription	Fetal Muscle Trunk	muscle
47	chr8:10648200-10669800	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr8:10648200-10683400	Weak transcription	Brain Angular Gyrus	brain
49	chr8:10648400-10656800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr8:10650000-10656800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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