Variant report

Variant	rs827550
Chromosome Location	chr8:104336672-104336673
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:104333812..104335583-chr8:104335809..104337466,2	MCF-7	breast:
2	chr8:104309902..104312898-chr8:104334770..104339269,4	MCF-7	breast:
3	chr8:104332978..104337328-chr8:104338203..104342176,5	K562	blood:

Variant related genes	Relation type
ENSG00000164930	Chromatin interaction
ENSG00000247081	Chromatin interaction

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs1004468	0.94[ASN][1000 genomes]
rs10505042	0.97[ASN][1000 genomes]
rs1053917	0.95[ASN][1000 genomes]
rs1095713	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1095714	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs11781252	0.94[ASN][1000 genomes]
rs11987172	0.92[ASN][1000 genomes]
rs12164188	0.97[ASN][1000 genomes]
rs12546491	0.95[ASN][1000 genomes]
rs12550097	1.00[ASN][1000 genomes]
rs1357354	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1370008	0.92[ASN][1000 genomes]
rs1370009	0.92[ASN][1000 genomes]
rs1464550	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1464552	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1522708	0.98[ASN][1000 genomes]
rs1522710	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1522711	0.95[ASN][1000 genomes]
rs1522712	0.97[ASN][1000 genomes]
rs16870346	0.94[ASN][1000 genomes]
rs1851483	0.97[ASN][1000 genomes]
rs1916117	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2010308	0.94[ASN][1000 genomes]
rs2388532	0.95[ASN][1000 genomes]
rs2642363	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2642364	0.95[ASN][1000 genomes]
rs2642366	0.95[ASN][1000 genomes]
rs2642368	0.95[ASN][1000 genomes]
rs2687351	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28392906	0.96[ASN][1000 genomes]
rs2917550	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2934719	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2948447	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3133827	0.96[ASN][1000 genomes]
rs35019987	0.92[ASN][1000 genomes]
rs35935697	0.98[ASN][1000 genomes]
rs3736047	0.97[ASN][1000 genomes]
rs3808553	1.00[ASN][1000 genomes]
rs3808554	1.00[ASN][1000 genomes]
rs3808556	1.00[ASN][1000 genomes]
rs3808559	0.97[ASN][1000 genomes]
rs4734698	0.92[ASN][1000 genomes]
rs62525498	0.81[ASN][1000 genomes]
rs62525511	1.00[ASN][1000 genomes]
rs7008838	0.94[ASN][1000 genomes]
rs7012843	0.91[ASN][1000 genomes]
rs827530	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs827534	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs827535	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs827536	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs827539	0.84[EUR][1000 genomes]
rs827547	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs827552	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827554	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs827578	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs827579	0.92[ASN][1000 genomes]
rs827580	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs827581	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs827582	0.92[ASN][1000 genomes]
rs827583	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs827584	0.92[ASN][1000 genomes]
rs827585	0.83[ASN][1000 genomes]
rs827586	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs827587	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs827588	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs844136	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs865461	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs865462	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][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	nsv429931	chr8:104097396-104878014	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	esv1848810	chr8:104128496-104369288	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active 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	45 gene(s)	inside rSNPs	diseases
3	esv1844303	chr8:104128696-104369090	Genic enhancers Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	nsv1015965	chr8:104192086-104361108	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv1023181	chr8:104298542-104366365	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv1020476	chr8:104312212-104924482	Genic enhancers Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
7	nsv539704	chr8:104312212-104924482	Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
8	nsv1016395	chr8:104327541-104473005	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104311600-104343600	Weak transcription	Spleen	Spleen
2	chr8:104311800-104343600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:104312000-104337200	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr8:104312000-104337200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr8:104312000-104343800	Weak transcription	Small Intestine	intestine
6	chr8:104312000-104348400	Weak transcription	Thymus	Thymus
7	chr8:104312000-104350200	Weak transcription	Esophagus	oesophagus
8	chr8:104312200-104337200	Weak transcription	Brain Anterior Caudate	brain
9	chr8:104312200-104337800	Weak transcription	Primary T cells from cord blood	blood
10	chr8:104312200-104339000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr8:104312400-104345000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr8:104312400-104345000	Weak transcription	Right Ventricle	heart
13	chr8:104312400-104350000	Weak transcription	Lung	lung
14	chr8:104312600-104337200	Weak transcription	Brain Angular Gyrus	brain
15	chr8:104312600-104342400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr8:104312600-104344800	Weak transcription	Fetal Intestine Small	intestine
17	chr8:104312600-104350000	Weak transcription	Colon Smooth Muscle	Colon
18	chr8:104313200-104336800	Weak transcription	Duodenum Mucosa	Duodenum
19	chr8:104317400-104354000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr8:104317600-104345800	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr8:104318000-104345200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr8:104318200-104342600	Weak transcription	Brain Substantia Nigra	brain
23	chr8:104318600-104343400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr8:104319400-104347200	Weak transcription	Hela-S3	cervix
25	chr8:104320400-104343600	Weak transcription	Fetal Intestine Large	intestine
26	chr8:104320600-104337200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr8:104320800-104337000	Weak transcription	HSMMtube	muscle
28	chr8:104321400-104337200	Weak transcription	NHLF	lung
29	chr8:104321400-104342000	Weak transcription	Placenta	Placenta
30	chr8:104321400-104358800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr8:104321600-104350200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr8:104322000-104337000	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr8:104322400-104337000	Weak transcription	Aorta	Aorta
34	chr8:104322400-104337000	Weak transcription	HUVEC	blood vessel
35	chr8:104322800-104336800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr8:104322800-104350200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr8:104324800-104348200	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr8:104325800-104342000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr8:104327800-104342000	Weak transcription	HSMM	muscle
40	chr8:104327800-104344800	Weak transcription	A549	lung
41	chr8:104328000-104337000	Weak transcription	HMEC	breast
42	chr8:104328200-104344600	Weak transcription	HepG2	liver
43	chr8:104328200-104355800	Weak transcription	Gastric	stomach
44	chr8:104328200-104361200	Weak transcription	Pancreas	Pancrea
45	chr8:104328800-104345600	Weak transcription	Fetal Heart	heart
46	chr8:104329400-104338000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr8:104330400-104350200	Weak transcription	Psoas Muscle	Psoas
48	chr8:104330800-104339600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr8:104331400-104339000	Weak transcription	Colonic Mucosa	Colon
50	chr8:104331800-104336800	Weak transcription	Duodenum Smooth Muscle	Duodenum

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