Variant report

Variant	rs1504368
Chromosome Location	chr6:80320660-80320661
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:80319015..80321979-chr6:80327268..80328969,2	MCF-7	breast:
2	chr6:80309921..80312950-chr6:80318776..80321900,3	MCF-7	breast:
3	chr6:80314692..80316652-chr6:80320135..80321870,2	K562	blood:
4	chr6:80318365..80321776-chr6:80322794..80325239,3	K562	blood:

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs10498921	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1158770	0.86[JPT][hapmap];0.93[ASN][1000 genomes]
rs1158771	0.93[ASN][1000 genomes]
rs11965020	0.86[JPT][hapmap];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11966497	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1385536	0.86[JPT][hapmap]
rs1385537	0.86[JPT][hapmap];0.93[TSI][hapmap]
rs1485370	0.86[JPT][hapmap]
rs1485372	0.93[ASN][1000 genomes]
rs1485377	0.86[TSI][hapmap]
rs16890774	0.86[JPT][hapmap];0.93[ASN][1000 genomes]
rs16890835	0.86[JPT][hapmap];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16890850	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16890862	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16890875	0.92[CEU][hapmap];0.86[JPT][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17335231	0.92[CEU][hapmap];0.86[JPT][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17727505	0.86[JPT][hapmap];1.00[TSI][hapmap];0.93[ASN][1000 genomes]
rs1883878	0.86[JPT][hapmap]
rs2575204	0.93[ASN][1000 genomes]
rs2575208	0.86[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2655666	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2655677	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2655679	0.80[ASN][1000 genomes]
rs2655680	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2655703	0.83[CEU][hapmap];0.86[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2746314	0.86[JPT][hapmap]
rs2746317	0.86[JPT][hapmap]
rs2803188	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2803189	0.93[ASN][1000 genomes]
rs2803197	0.86[JPT][hapmap];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2812712	0.86[JPT][hapmap]
rs2812713	0.86[JPT][hapmap]
rs41269343	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55830218	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55873641	0.95[AFR][1000 genomes]
rs55989614	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56087572	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56745436	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61152095	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62411332	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62411348	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62413360	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62413362	0.80[ASN][1000 genomes]
rs62413366	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62413368	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62413370	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62413371	0.87[EUR][1000 genomes]
rs62413372	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62413377	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62413380	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62413382	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62413385	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62413387	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62413388	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62413389	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62413390	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62413391	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62413395	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62413396	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62413399	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62413401	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62413414	0.95[AFR][1000 genomes]
rs62413416	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62413421	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6454124	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6454125	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6907133	0.86[JPT][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6917186	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6920332	0.95[AFR][1000 genomes]
rs6920635	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6921102	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6925212	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6926534	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6934060	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6939569	0.95[AFR][1000 genomes]
rs73747413	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73750727	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7745158	0.92[CEU][hapmap];0.86[JPT][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7745429	0.92[CEU][hapmap];0.86[JPT][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7749776	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7760677	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7761245	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7763266	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7763268	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7768651	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7768724	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7769778	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7772722	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7775232	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs992872	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028607	chr6:79853272-80767716	Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv886301	chr6:80111104-80339088	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv886302	chr6:80111104-80355973	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv1027388	chr6:80113449-80355973	ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv830707	chr6:80134625-80325171	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
6	nsv1029259	chr6:80142754-80340332	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
7	nsv1018318	chr6:80241029-80465282	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
8	nsv1032347	chr6:80284809-80694778	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
9	nsv886304	chr6:80294265-80355973	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:80298600-80324200	Weak transcription	Right Ventricle	heart
2	chr6:80311000-80324400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr6:80311200-80324400	Weak transcription	Pancreas	Pancrea
4	chr6:80313400-80321800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr6:80313600-80321600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:80315000-80340600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:80315200-80320800	Enhancers	K562	blood
8	chr6:80316800-80321000	Enhancers	Fetal Intestine Small	intestine
9	chr6:80317000-80323200	Weak transcription	Liver	Liver
10	chr6:80317400-80324400	Weak transcription	Left Ventricle	heart
11	chr6:80318000-80340200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr6:80318600-80322600	Weak transcription	Gastric	stomach
13	chr6:80319000-80321400	Weak transcription	HSMMtube	muscle
14	chr6:80319200-80324400	Weak transcription	Fetal Heart	heart
15	chr6:80319400-80322600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr6:80319400-80328000	Weak transcription	Esophagus	oesophagus
17	chr6:80319600-80320800	Enhancers	HepG2	liver
18	chr6:80320400-80320800	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr6:80320600-80321800	Weak transcription	Placenta	Placenta
20	chr6:80320600-80322200	Weak transcription	Stomach Mucosa	stomach
21	chr6:80320600-80324000	Weak transcription	Duodenum Mucosa	Duodenum
22	chr6:80320600-80324200	Weak transcription	Fetal Intestine Large	intestine
23	chr6:80320600-80324200	Weak transcription	Lung	lung

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