Variant report

Variant	rs10067900
Chromosome Location	chr5:74706661-74706662
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:74704826..74707671-chr5:74805831..74807766,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000122008	Chromatin interaction
ENSG00000113163	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10036682	0.89[EUR][1000 genomes]
rs10038945	0.89[EUR][1000 genomes]
rs10041470	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10055011	1.00[CEU][hapmap];0.81[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10059022	1.00[CEU][hapmap];0.84[JPT][hapmap];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10061689	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10074747	0.83[EUR][1000 genomes]
rs10076819	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10077427	1.00[CEU][hapmap];0.81[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.93[EUR][1000 genomes]
rs10078671	1.00[CEU][hapmap];0.81[CHB][hapmap];0.93[JPT][hapmap];0.89[EUR][1000 genomes]
rs10474437	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12173076	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13360099	1.00[CEU][hapmap];0.81[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13361353	0.93[EUR][1000 genomes]
rs1422702	0.82[CEU][hapmap]
rs1469051	0.85[EUR][1000 genomes]
rs1553234	0.93[EUR][1000 genomes]
rs1820049	0.88[EUR][1000 genomes]
rs1909719	0.93[EUR][1000 genomes]
rs2287710	0.88[EUR][1000 genomes]
rs28408106	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28612248	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28668361	0.89[EUR][1000 genomes]
rs28874007	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3804231	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4703671	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4703675	0.89[EUR][1000 genomes]
rs4704213	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4704229	1.00[CEU][hapmap];0.81[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.87[EUR][1000 genomes]
rs56859362	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs5744544	0.88[EUR][1000 genomes]
rs5744545	0.86[EUR][1000 genomes]
rs5744636	1.00[CEU][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.93[EUR][1000 genomes]
rs5744667	0.90[CEU][hapmap];0.87[EUR][1000 genomes]
rs5744704	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs5744709	0.88[EUR][1000 genomes]
rs5744712	1.00[CEU][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.88[EUR][1000 genomes]
rs57907925	0.85[EUR][1000 genomes]
rs58519566	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs58841453	0.89[EUR][1000 genomes]
rs61303403	0.81[EUR][1000 genomes]
rs6891560	1.00[CEU][hapmap];0.81[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72633963	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72633964	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72633965	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72633966	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72633967	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72633968	0.90[EUR][1000 genomes]
rs72633969	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72633970	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72633971	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72633972	0.91[EUR][1000 genomes]
rs72633973	0.93[EUR][1000 genomes]
rs72633974	0.93[EUR][1000 genomes]
rs72633975	0.89[EUR][1000 genomes]
rs72633976	0.87[EUR][1000 genomes]
rs72633977	0.81[EUR][1000 genomes]
rs7356633	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7726478	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs904743	0.85[EUR][1000 genomes]
rs9293652	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9293654	0.88[EUR][1000 genomes]
rs9293655	1.00[CEU][hapmap];0.81[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.91[EUR][1000 genomes]
rs979182	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882192	chr5:74641707-74707762	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv882193	chr5:74656175-74917862	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers 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	15 gene(s)	inside rSNPs	diseases
3	nsv882194	chr5:74656175-74946455	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats 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	15 gene(s)	inside rSNPs	diseases
4	nsv882195	chr5:74678937-74896798	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS 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	nsv882196	chr5:74678937-74917862	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS 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	nsv882197	chr5:74692776-74946455	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer 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

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74656400-74725600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr5:74656800-74731400	Weak transcription	Rectal Smooth Muscle	rectum
3	chr5:74657800-74708000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr5:74659800-74720600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr5:74660000-74722800	Weak transcription	Fetal Heart	heart
6	chr5:74660200-74707800	Weak transcription	Stomach Mucosa	stomach
7	chr5:74667000-74723200	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr5:74670800-74709400	Weak transcription	Pancreas	Pancrea
9	chr5:74670800-74720600	Weak transcription	Right Ventricle	heart
10	chr5:74670800-74731400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr5:74671000-74722800	Weak transcription	Hela-S3	cervix
12	chr5:74674400-74761400	Weak transcription	Esophagus	oesophagus
13	chr5:74675400-74720800	Weak transcription	Small Intestine	intestine
14	chr5:74676200-74721000	Weak transcription	Brain Hippocampus Middle	brain
15	chr5:74677400-74722800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr5:74677600-74709200	Weak transcription	Gastric	stomach
17	chr5:74677600-74734200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr5:74677800-74721000	Weak transcription	NH-A	brain
19	chr5:74677800-74725000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr5:74677800-74731400	Weak transcription	Aorta	Aorta
21	chr5:74678000-74708000	Weak transcription	NHLF	lung
22	chr5:74678000-74720600	Weak transcription	Colonic Mucosa	Colon
23	chr5:74678000-74730800	Weak transcription	Psoas Muscle	Psoas
24	chr5:74680600-74721000	Weak transcription	HMEC	breast
25	chr5:74680800-74722600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr5:74681000-74723200	Weak transcription	HUVEC	blood vessel
27	chr5:74681400-74718400	Weak transcription	Brain Germinal Matrix	brain
28	chr5:74681800-74720600	Weak transcription	Fetal Brain Male	brain
29	chr5:74682000-74708000	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr5:74684000-74709000	Weak transcription	Spleen	Spleen
31	chr5:74684000-74720400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr5:74684000-74720800	Weak transcription	Thymus	Thymus
33	chr5:74684000-74731200	Weak transcription	HSMMtube	muscle
34	chr5:74685200-74707200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr5:74685200-74708400	Weak transcription	Osteobl	bone
36	chr5:74685800-74709200	Weak transcription	Dnd41	blood
37	chr5:74685800-74711800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr5:74686000-74707800	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr5:74690000-74707000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr5:74692000-74708400	Weak transcription	K562	blood
41	chr5:74692000-74709000	Weak transcription	HepG2	liver
42	chr5:74695200-74707600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr5:74695200-74718200	Weak transcription	Colon Smooth Muscle	Colon
44	chr5:74695400-74721000	Weak transcription	Brain Anterior Caudate	brain
45	chr5:74695400-74721000	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr5:74695400-74723200	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr5:74695600-74721000	Weak transcription	Brain Angular Gyrus	brain
48	chr5:74696000-74715800	Weak transcription	Ovary	ovary
49	chr5:74696200-74713800	Weak transcription	Fetal Brain Female	brain
50	chr5:74696400-74706800	Weak transcription	HUES64 Cell Line	embryonic stem cell

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