Variant report

Variant	rs16963995
Chromosome Location	chr15:51269382-51269383
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:51269282..51271249-chr15:51274355..51276243,2	MCF-7	breast:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10519288	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11631783	1.00[JPT][hapmap]
rs16963993	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16964012	0.92[AFR][1000 genomes]
rs16964061	0.86[EUR][1000 genomes]
rs17522120	1.00[JPT][hapmap]
rs17600241	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2063290	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2063291	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28412002	0.84[EUR][1000 genomes]
rs28504625	0.86[EUR][1000 genomes]
rs28668174	0.86[EUR][1000 genomes]
rs4312259	0.86[EUR][1000 genomes]
rs58355375	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58753046	0.86[EUR][1000 genomes]
rs60008926	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61064093	0.81[AFR][1000 genomes]
rs7178693	1.00[CEU][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes]
rs7181613	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72742341	0.81[ASN][1000 genomes]
rs74013150	0.84[EUR][1000 genomes]
rs882299	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047443	chr15:50744781-51647023	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	nsv457136	chr15:50789125-51294995	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	nsv569398	chr15:50789125-51294995	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
4	nsv569399	chr15:50874964-51562198	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
5	nsv569400	chr15:50874964-51767265	ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers 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	80 gene(s)	inside rSNPs	diseases
6	nsv529339	chr15:51048579-51270372	Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
7	nsv428636	chr15:51154834-51298044	Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
8	nsv569403	chr15:51191421-51304373	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
9	nsv1038778	chr15:51196641-51356728	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
10	nsv904214	chr15:51204364-51535192	Strong transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
11	nsv569404	chr15:51234595-51294995	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv1049644	chr15:51265447-51560445	Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51201800-51271600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr15:51210600-51298400	Weak transcription	Stomach Mucosa	stomach
3	chr15:51243800-51283000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr15:51252400-51283800	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr15:51257600-51272800	Weak transcription	Pancreas	Pancrea
6	chr15:51261600-51272800	Weak transcription	Colonic Mucosa	Colon
7	chr15:51261600-51295600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr15:51261600-51298200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr15:51263000-51304800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr15:51263200-51276000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr15:51263400-51281000	Weak transcription	Fetal Heart	heart
12	chr15:51263600-51287200	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr15:51263600-51293600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr15:51263600-51296400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr15:51263600-51297800	Weak transcription	NHLF	lung
16	chr15:51263600-51299200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr15:51263600-51300200	Weak transcription	Small Intestine	intestine
18	chr15:51263600-51301200	Weak transcription	HepG2	liver
19	chr15:51263600-51303000	Weak transcription	HUVEC	blood vessel
20	chr15:51263800-51269400	Weak transcription	Psoas Muscle	Psoas
21	chr15:51263800-51272600	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr15:51263800-51275400	Weak transcription	NH-A	brain
23	chr15:51263800-51296200	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr15:51263800-51296600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr15:51263800-51300400	Weak transcription	Right Ventricle	heart
26	chr15:51264400-51269400	Weak transcription	Colon Smooth Muscle	Colon
27	chr15:51264400-51271000	Weak transcription	Osteobl	bone
28	chr15:51264400-51283200	Weak transcription	Brain Substantia Nigra	brain
29	chr15:51264400-51294200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr15:51264600-51296600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr15:51265000-51270800	Weak transcription	Brain Anterior Caudate	brain
32	chr15:51265000-51272800	Weak transcription	Thymus	Thymus
33	chr15:51265000-51275800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr15:51265200-51270600	Weak transcription	Left Ventricle	heart
35	chr15:51265200-51272600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr15:51265200-51272600	Weak transcription	NHEK	skin
37	chr15:51265200-51272800	Weak transcription	Aorta	Aorta
38	chr15:51265200-51272800	Weak transcription	Esophagus	oesophagus
39	chr15:51265200-51272800	Weak transcription	Lung	lung
40	chr15:51265200-51272800	Weak transcription	Ovary	ovary
41	chr15:51265200-51272800	Weak transcription	Spleen	Spleen
42	chr15:51265200-51273000	Weak transcription	Fetal Thymus	thymus
43	chr15:51265200-51274000	Strong transcription	Primary B cells from cord blood	blood
44	chr15:51265200-51275400	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr15:51265200-51276200	Weak transcription	A549	lung
46	chr15:51265200-51292600	Weak transcription	Brain Angular Gyrus	brain
47	chr15:51265200-51296400	Weak transcription	Brain Germinal Matrix	brain
48	chr15:51265200-51302400	Weak transcription	Brain Hippocampus Middle	brain
49	chr15:51265200-51315600	Weak transcription	Gastric	stomach
50	chr15:51265400-51271200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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