Variant report

Variant	rs6511030
Chromosome Location	chr19:19471446-19471447
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:19470787..19473518-chr19:19582679..19585409,2	K562	blood:
2	chr19:19469546..19472054-chr19:19474284..19475951,2	MCF-7	breast:
3	chr19:19463250..19466094-chr19:19470613..19472204,2	MCF-7	breast:
4	chr19:19469711..19473651-chr19:19475756..19478808,4	K562	blood:
5	chr19:19469138..19472356-chr19:19472972..19475692,3	K562	blood:
6	chr19:19464266..19466426-chr19:19469770..19472098,2	K562	blood:

Variant related genes	Relation type
ENSG00000129933	Chromatin interaction
ENSG00000167491	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs1009136	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1010207	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10409234	0.80[AMR][1000 genomes]
rs10419672	0.86[ASN][1000 genomes]
rs10421505	0.85[ASN][1000 genomes]
rs12460764	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs12977937	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs12982276	0.85[ASN][1000 genomes]
rs12985655	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13964	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs15622	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2023882	0.82[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs2074088	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2074089	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2074090	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2074091	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2269873	0.80[AMR][1000 genomes]
rs2285627	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2301669	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2301784	0.80[AMR][1000 genomes]
rs2301786	0.81[AMR][1000 genomes]
rs2315022	0.81[AMR][1000 genomes]
rs2315025	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs2315279	0.83[AMR][1000 genomes]
rs2315281	0.83[AMR][1000 genomes]
rs2315283	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2905421	0.88[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs2905423	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2905424	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2905425	0.84[EUR][1000 genomes]
rs2905427	0.80[EUR][1000 genomes]
rs2905430	0.81[AMR][1000 genomes]
rs2905431	0.81[AMR][1000 genomes]
rs2965175	0.84[AMR][1000 genomes]
rs2965191	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2965193	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2965198	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2965199	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2965200	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34538000	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3934667	0.82[AFR][1000 genomes]
rs4808937	0.82[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs4808938	0.82[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs62135552	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6511026	0.80[AMR][1000 genomes]
rs6511028	0.81[AFR][1000 genomes]
rs6511032	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs67720221	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7246748	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7247309	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7254230	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7254927	0.80[AMR][1000 genomes]
rs769267	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8101499	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs8101938	0.80[AMR][1000 genomes]
rs8103197	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv911303	chr19:19256870-19505087	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS 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	39 gene(s)	inside rSNPs	diseases
2	nsv911305	chr19:19303802-19663850	Genic enhancers Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	nsv1056419	chr19:19421218-19510611	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:19435600-19477600	Weak transcription	Fetal Heart	heart
2	chr19:19440400-19475400	Weak transcription	Right Atrium	heart
3	chr19:19454400-19475600	Weak transcription	Fetal Kidney	kidney
4	chr19:19458200-19471800	Weak transcription	Hela-S3	cervix
5	chr19:19458400-19471800	Weak transcription	K562	blood
6	chr19:19459200-19475400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr19:19460800-19475600	Weak transcription	Psoas Muscle	Psoas
8	chr19:19465200-19483600	Weak transcription	NH-A	brain
9	chr19:19465400-19471800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr19:19466600-19475600	Weak transcription	NHDF-Ad	bronchial
11	chr19:19466800-19475600	Weak transcription	HMEC	breast
12	chr19:19467000-19471800	Weak transcription	Stomach Mucosa	stomach
13	chr19:19467000-19472000	Weak transcription	HepG2	liver
14	chr19:19467200-19471800	Weak transcription	GM12878-XiMat	blood
15	chr19:19467200-19472000	Weak transcription	A549	lung
16	chr19:19467200-19475400	Weak transcription	Small Intestine	intestine
17	chr19:19467200-19475600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr19:19467200-19477600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr19:19467400-19471600	Weak transcription	Primary B cells from cord blood	blood
20	chr19:19467400-19473000	Weak transcription	HUVEC	blood vessel
21	chr19:19467400-19475400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr19:19467400-19475600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr19:19467400-19475600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr19:19467400-19475600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr19:19467600-19475600	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr19:19467600-19475600	Weak transcription	HSMM	muscle
27	chr19:19468000-19471600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr19:19468000-19475400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr19:19468000-19475600	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr19:19468200-19471600	Weak transcription	Colon Smooth Muscle	Colon
31	chr19:19468200-19472200	Weak transcription	Ovary	ovary
32	chr19:19468200-19475400	Weak transcription	NHEK	skin
33	chr19:19468200-19477600	Weak transcription	Brain Substantia Nigra	brain
34	chr19:19468400-19472800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr19:19468400-19475400	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr19:19468400-19475400	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr19:19468400-19475400	Weak transcription	Rectal Smooth Muscle	rectum
38	chr19:19468400-19476000	Weak transcription	Left Ventricle	heart
39	chr19:19468400-19477600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr19:19468400-19478000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr19:19468600-19471600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr19:19468600-19471800	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr19:19468600-19471800	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr19:19468600-19472000	Weak transcription	Dnd41	blood
45	chr19:19468600-19477600	Weak transcription	Fetal Lung	lung
46	chr19:19468800-19471800	Weak transcription	Primary T cells from cord blood	blood
47	chr19:19468800-19471800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr19:19468800-19472000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr19:19468800-19472200	Weak transcription	Right Ventricle	heart
50	chr19:19468800-19475600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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