Variant report

Variant	rs7183226
Chromosome Location	chr15:99752610-99752611
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:99643948..99646697-chr15:99752022..99754887,3	MCF-7	breast:
2	chr15:99643946..99646615-chr15:99751647..99755247,3	MCF-7	breast:
3	chr15:99640796..99641313-chr15:99752001..99752808,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000182253	Chromatin interaction
ENSG00000259475	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10152912	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs1223950	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs1223951	0.81[CHB][hapmap];0.81[JPT][hapmap]
rs1238348	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12907394	0.91[CHB][hapmap];0.84[CHD][hapmap];0.82[JPT][hapmap];0.81[MEX][hapmap]
rs12911768	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs12915090	1.00[ASW][hapmap]
rs1567416	0.80[CHD][hapmap];0.81[JPT][hapmap]
rs1703761	0.83[CHD][hapmap]
rs1976589	0.82[CHB][hapmap];0.80[CHD][hapmap];0.82[JPT][hapmap]
rs2048301	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs260114	1.00[ASW][hapmap]
rs2602018	1.00[ASW][hapmap];0.82[CHB][hapmap];0.87[CHD][hapmap]
rs2602021	1.00[ASW][hapmap]
rs2602026	1.00[ASW][hapmap];0.82[CHB][hapmap];0.87[CHD][hapmap]
rs2602030	0.82[CHB][hapmap];0.87[CHD][hapmap];0.82[JPT][hapmap]
rs2602036	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.92[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2623184	0.89[ASW][hapmap];1.00[YRI][hapmap]
rs2623190	1.00[ASW][hapmap]
rs2623191	1.00[ASW][hapmap]
rs2623199	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2862139	0.82[CHB][hapmap];0.80[CHD][hapmap];0.82[JPT][hapmap]
rs4965217	0.87[CHD][hapmap]
rs4965221	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4965224	0.82[CHB][hapmap];0.82[JPT][hapmap];0.81[MEX][hapmap]
rs7164003	0.82[CHB][hapmap];0.80[CHD][hapmap];0.82[JPT][hapmap]
rs8042021	0.89[CHB][hapmap];0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531079	chr15:98907913-99878547	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	97 gene(s)	inside rSNPs	diseases
2	nsv1039575	chr15:98982045-99924685	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
3	nsv869529	chr15:99416774-99903351	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS 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	60 gene(s)	inside rSNPs	diseases
4	nsv1055008	chr15:99477144-100019861	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
5	nsv1045124	chr15:99504843-99847210	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
6	nsv1038870	chr15:99510479-99768374	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	nsv904543	chr15:99513231-99991506	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
8	nsv533926	chr15:99519820-99997114	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
9	nsv915926	chr15:99519820-100138705	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
10	nsv1051782	chr15:99621061-99792967	Enhancers Active TSS Weak transcription Strong transcription 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	26 gene(s)	inside rSNPs	diseases
11	nsv916822	chr15:99621061-99878564	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS 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	30 gene(s)	inside rSNPs	diseases
12	nsv949203	chr15:99621061-99932797	Strong transcription Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS 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	31 gene(s)	inside rSNPs	diseases
13	nsv817289	chr15:99621061-100138705	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
14	nsv431411	chr15:99621061-100143999	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
15	nsv570716	chr15:99629901-99916332	Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
16	nsv904546	chr15:99696046-100166300	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
17	nsv1052528	chr15:99736977-99874210	Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
18	esv2760374	chr15:99739048-99754071	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
19	nsv1036346	chr15:99752391-100365458	Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
20	nsv542520	chr15:99752391-100365458	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription 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 target site	47 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs7183226	TTC23	cis	cerebellum	SCAN
rs7183226	SYNM	cis	cerebellum	SCAN
rs7183226	SYNM	cis	parietal	SCAN
rs7183226	TTC23	cis	parietal	SCAN
rs7183226	NR2F2	cis	parietal	SCAN

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:99673200-99789400	Weak transcription	Small Intestine	intestine
2	chr15:99697000-99756400	Weak transcription	Stomach Mucosa	stomach
3	chr15:99717400-99761000	Weak transcription	Gastric	stomach
4	chr15:99717800-99758000	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr15:99721200-99758400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr15:99722000-99758400	Weak transcription	Right Ventricle	heart
7	chr15:99722600-99757600	Weak transcription	Psoas Muscle	Psoas
8	chr15:99724400-99769600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr15:99726600-99758200	Weak transcription	HMEC	breast
10	chr15:99728400-99760000	Weak transcription	NHDF-Ad	bronchial
11	chr15:99732800-99758000	Weak transcription	Spleen	Spleen
12	chr15:99732800-99761000	Weak transcription	Lung	lung
13	chr15:99733000-99758400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr15:99733000-99760400	Weak transcription	Esophagus	oesophagus
15	chr15:99733200-99756800	Weak transcription	Aorta	Aorta
16	chr15:99733200-99758200	Weak transcription	Colonic Mucosa	Colon
17	chr15:99733400-99752800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr15:99733400-99787400	Weak transcription	NHEK	skin
19	chr15:99734200-99758200	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr15:99734400-99758000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr15:99734600-99757800	Weak transcription	Primary hematopoietic stem cells	blood
22	chr15:99735200-99758200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr15:99737200-99755200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr15:99737200-99758000	Weak transcription	Duodenum Mucosa	Duodenum
25	chr15:99737400-99758000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr15:99739400-99759200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr15:99739800-99757600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr15:99740000-99758400	Weak transcription	Hela-S3	cervix
29	chr15:99740200-99754800	Weak transcription	Adipose Nuclei	Adipose
30	chr15:99740200-99754800	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr15:99740200-99755400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr15:99740200-99755400	Weak transcription	HSMM	muscle
33	chr15:99740200-99756800	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr15:99740200-99757000	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr15:99740200-99757600	Weak transcription	Dnd41	blood
36	chr15:99740200-99758000	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr15:99740200-99758000	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr15:99740200-99758000	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr15:99740200-99758000	Weak transcription	HSMMtube	muscle
40	chr15:99740200-99760800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr15:99740200-99761000	Weak transcription	Fetal Kidney	kidney
42	chr15:99740200-99763800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr15:99740400-99756800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr15:99740400-99757600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr15:99740400-99757600	Weak transcription	Placenta	Placenta
46	chr15:99740600-99755600	Weak transcription	Liver	Liver
47	chr15:99740600-99756800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr15:99740600-99758000	Weak transcription	Pancreas	Pancrea
49	chr15:99743000-99758000	Weak transcription	Brain Anterior Caudate	brain
50	chr15:99743200-99755400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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