Variant report

Variant	rs11765215
Chromosome Location	chr7:51022160-51022161
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:51020833..51022713-chr7:51029451..51032212,2	MCF-7	breast:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1016431	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1016432	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1018941	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1018942	1.00[AMR][1000 genomes]
rs1018979	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1018980	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1024472	0.90[AMR][1000 genomes]
rs10262964	0.90[AMR][1000 genomes]
rs1074570	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1074571	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12534954	0.90[AMR][1000 genomes]
rs13310888	0.90[AMR][1000 genomes]
rs1859264	0.90[AMR][1000 genomes]
rs1859265	0.81[AMR][1000 genomes]
rs1859477	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1989265	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2023879	0.82[AMR][1000 genomes]
rs2189428	0.81[AMR][1000 genomes]
rs2189429	0.81[AMR][1000 genomes]
rs2189822	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2214494	0.90[AMR][1000 genomes]
rs2214495	0.85[AMR][1000 genomes]
rs2214497	0.81[AMR][1000 genomes]
rs2329566	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2329568	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2329569	0.90[AMR][1000 genomes]
rs2876901	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4947464	1.00[AFR][1000 genomes]
rs4947530	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4947902	1.00[AFR][1000 genomes]
rs4948086	1.00[AMR][1000 genomes]
rs4948088	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4948146	0.81[AMR][1000 genomes]
rs6943902	0.90[AMR][1000 genomes]
rs6971609	0.86[AMR][1000 genomes]
rs6979183	0.90[AMR][1000 genomes]
rs720068	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7776597	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7780389	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7790800	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7800611	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7803628	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs886437	0.81[AMR][1000 genomes]
rs917072	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs917073	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs976088	0.90[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016665	chr7:50452552-51404524	Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv606907	chr7:50899168-51195380	Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv888022	chr7:50933678-51046674	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv508453	chr7:50963780-51030439	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv2761146	chr7:50975457-51957019	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
6	nsv1027122	chr7:50984824-51376078	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv538836	chr7:50984824-51376078	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv830999	chr7:51020735-51164809	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:51020000-51022800	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr7:51020000-51023200	Enhancers	Adipose Nuclei	Adipose
3	chr7:51020000-51024000	Enhancers	Pancreas	Pancrea
4	chr7:51020200-51022400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr7:51020200-51023000	Enhancers	Left Ventricle	heart
6	chr7:51020200-51028400	Enhancers	HUVEC	blood vessel
7	chr7:51020400-51022200	Enhancers	Psoas Muscle	Psoas
8	chr7:51020400-51022400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr7:51020600-51022800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr7:51020600-51030000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr7:51020800-51022200	Enhancers	Hela-S3	cervix
12	chr7:51020800-51022800	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr7:51021000-51022200	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr7:51021000-51022200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr7:51021000-51022400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr7:51021000-51022400	Enhancers	Muscle Satellite Cultured Cells	--
17	chr7:51021000-51022600	Enhancers	Osteobl	bone
18	chr7:51021000-51023000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr7:51021000-51023000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr7:51021000-51023800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr7:51021000-51030600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr7:51021200-51022200	Enhancers	HSMM	muscle
23	chr7:51021200-51022400	Enhancers	Right Atrium	heart
24	chr7:51021200-51022600	Enhancers	NHDF-Ad	bronchial
25	chr7:51021200-51022800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr7:51021200-51022800	Enhancers	NH-A	brain
27	chr7:51021200-51023000	Enhancers	Spleen	Spleen
28	chr7:51021400-51022200	Enhancers	A549	lung
29	chr7:51021400-51022600	Weak transcription	Fetal Muscle Leg	muscle
30	chr7:51021800-51022600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr7:51021800-51022800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:51021800-51030000	Weak transcription	Esophagus	oesophagus
33	chr7:51022000-51022400	Weak transcription	Lung	lung
34	chr7:51022000-51029800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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