Variant report

Variant	rs9864231
Chromosome Location	chr3:50158410-50158411
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:50157801..50161419-chr3:50224013..50228566,6	MCF-7	breast:
2	chr3:50157579..50160318-chr3:50233509..50235124,2	MCF-7	breast:
3	chr3:50157617..50159229-chr3:50261958..50264421,2	MCF-7	breast:
4	chr3:50157890..50164898-chr3:50186493..50191745,15	MCF-7	breast:
5	chr3:50157879..50160528-chr3:50162974..50166130,4	K562	blood:
6	chr3:50153410..50155870-chr3:50157177..50159023,3	K562	blood:
7	chr3:50156913..50158492-chr3:50221059..50222752,2	K562	blood:
8	chr3:50158102..50159885-chr3:50296008..50298288,2	MCF-7	breast:
9	chr3:50157983..50159948-chr3:50231806..50233770,3	K562	blood:
10	chr3:50157123..50160509-chr3:50182287..50185771,3	MCF-7	breast:
11	chr3:50157840..50167526-chr3:50182100..50196634,43	MCF-7	breast:
12	chr3:50157403..50159553-chr3:50273403..50275024,2	K562	blood:
13	chr3:50131320..50133089-chr3:50157321..50159844,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000003756	Chromatin interaction
ENSG00000001617	Chromatin interaction
ENSG00000235016	Chromatin interaction
ENSG00000230454	Chromatin interaction
ENSG00000114353	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs12330297	1.00[AFR][1000 genomes]
rs13316958	0.87[AFR][1000 genomes]
rs13318943	1.00[AFR][1000 genomes]
rs13321551	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs13323932	0.87[AFR][1000 genomes]
rs13324545	1.00[AFR][1000 genomes]
rs13327678	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs55968312	1.00[AFR][1000 genomes]
rs7629425	1.00[YRI][hapmap]
rs9811223	0.87[AFR][1000 genomes]
rs9819888	1.00[AFR][1000 genomes]
rs9820116	0.87[AFR][1000 genomes]
rs9825506	0.87[AFR][1000 genomes]
rs9825944	1.00[AFR][1000 genomes]
rs9826259	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs9828683	1.00[AFR][1000 genomes]
rs9829573	0.87[AFR][1000 genomes]
rs9835029	1.00[AFR][1000 genomes]
rs9835838	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs9847587	0.86[AFR][1000 genomes]
rs9849605	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs9850145	0.87[AFR][1000 genomes]
rs9852055	0.86[AFR][1000 genomes]
rs9860546	0.87[AFR][1000 genomes]
rs9862830	1.00[AFR][1000 genomes]
rs9863339	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs9866016	1.00[AFR][1000 genomes]
rs9875038	1.00[AFR][1000 genomes]
rs9883977	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834690	chr3:50101835-50267584	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv515986	chr3:50104307-50267584	Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv432418	chr3:50114496-50224196	Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv1001775	chr3:50129479-50311666	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
5	nsv818139	chr3:50144951-50174572	Weak transcription Strong transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv876768	chr3:50144951-50267584	Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
7	nsv523662	chr3:50144951-50584999	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
8	nsv1013949	chr3:50151712-50339163	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
9	nsv590250	chr3:50153356-50332697	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
10	nsv876769	chr3:50155468-50408398	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
11	esv1821728	chr3:50156142-50657253	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
12	esv3386929	chr3:50156348-50161346	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
13	esv1793751	chr3:50157364-50476363	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
14	esv1828162	chr3:50157364-50506151	Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50128200-50158800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:50128400-50159000	Strong transcription	Lung	lung
3	chr3:50128600-50158600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr3:50128600-50158600	Strong transcription	Colonic Mucosa	Colon
5	chr3:50128600-50158800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr3:50128600-50158800	Strong transcription	Brain Germinal Matrix	brain
7	chr3:50128600-50158800	Strong transcription	Placenta Amnion	Placenta Amnion
8	chr3:50128600-50159000	Strong transcription	Brain Angular Gyrus	brain
9	chr3:50128600-50159000	Strong transcription	Placenta	Placenta
10	chr3:50128600-50159000	Strong transcription	Sigmoid Colon	Sigmoid Colon
11	chr3:50128600-50159200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr3:50128600-50159200	Strong transcription	Liver	Liver
13	chr3:50128600-50159200	Strong transcription	NHEK	skin
14	chr3:50128600-50160400	Strong transcription	Fetal Thymus	thymus
15	chr3:50128800-50158600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr3:50128800-50158600	Strong transcription	HMEC	breast
17	chr3:50128800-50159000	Strong transcription	Brain Anterior Caudate	brain
18	chr3:50129000-50158600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr3:50129000-50158600	Strong transcription	Duodenum Mucosa	Duodenum
20	chr3:50129000-50158800	Strong transcription	Fetal Intestine Large	intestine
21	chr3:50129000-50159000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr3:50129000-50159200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr3:50129000-50159200	Strong transcription	Primary B cells from peripheral blood	blood
24	chr3:50129000-50159400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr3:50129000-50159400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr3:50129000-50160000	Strong transcription	Fetal Stomach	stomach
27	chr3:50129000-50160000	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr3:50129000-50160800	Strong transcription	Primary neutrophils fromperipheralblood	blood
29	chr3:50129200-50158600	Strong transcription	Rectal Mucosa Donor 29	rectum
30	chr3:50129200-50158800	Strong transcription	Primary B cells from cord blood	blood
31	chr3:50129200-50158800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr3:50129200-50158800	Strong transcription	Brain Hippocampus Middle	brain
33	chr3:50129200-50159000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr3:50129200-50159600	Strong transcription	Stomach Smooth Muscle	stomach
35	chr3:50129200-50160000	Strong transcription	Primary monocytes fromperipheralblood	blood
36	chr3:50129200-50160200	Strong transcription	Fetal Brain Female	brain
37	chr3:50129400-50158800	Strong transcription	Pancreas	Pancrea
38	chr3:50129400-50159400	Strong transcription	Spleen	Spleen
39	chr3:50129600-50159200	Strong transcription	Primary T cells from cord blood	blood
40	chr3:50129600-50161600	Strong transcription	Thymus	Thymus
41	chr3:50129800-50158600	Strong transcription	Duodenum Smooth Muscle	Duodenum
42	chr3:50130000-50159200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr3:50130400-50159800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr3:50131400-50159600	Strong transcription	Dnd41	blood
45	chr3:50132400-50159000	Strong transcription	Primary T helper cells fromperipheralblood	blood
46	chr3:50133000-50158600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr3:50133200-50159200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr3:50133200-50159200	Strong transcription	Rectal Mucosa Donor 31	rectum
49	chr3:50133800-50161200	Strong transcription	Right Ventricle	heart
50	chr3:50134000-50159400	Strong transcription	Muscle Satellite Cultured Cells	--

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