Variant report

Variant	rs67969809
Chromosome Location	chr5:74913796-74913797
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:74907136..74909579-chr5:74911861..74913808,3	K562	blood:
2	chr5:74912024..74914449-chr5:74921744..74924749,4	K562	blood:
3	chr5:74913060..74915078-chr5:74915803..74919443,3	K562	blood:
4	chr5:74912024..74914449-chr5:74922011..74924010,2	K562	blood:
5	chr5:74912858..74914560-chr5:74917246..74919606,2	K562	blood:

Variant related genes	Relation type
ENSG00000189045	Chromatin interaction

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10038723	0.89[EUR][1000 genomes]
rs10043621	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10044053	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10060260	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10067641	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10075139	0.93[EUR][1000 genomes]
rs10434644	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10474436	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1051795	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10942739	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13354407	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1427924	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17739580	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1863934	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1863935	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1995267	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2287711	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs253392	0.83[ASN][1000 genomes]
rs253393	0.95[ASN][1000 genomes]
rs253407	0.93[ASN][1000 genomes]
rs253408	0.88[ASN][1000 genomes]
rs253409	0.95[ASN][1000 genomes]
rs2878519	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2878520	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3213801	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34340	0.95[ASN][1000 genomes]
rs34344	0.87[ASN][1000 genomes]
rs34345	0.87[ASN][1000 genomes]
rs34350	0.82[ASN][1000 genomes]
rs4045166	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4385188	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4440336	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4703674	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4704224	0.83[EUR][1000 genomes]
rs4704228	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57149337	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs57312935	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs5744533	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs5744555	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs5744575	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5744595	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs5744598	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs5744601	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs5744621	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs5744663	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs5744703	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59506842	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61430233	0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6453134	0.80[EUR][1000 genomes]
rs6861279	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6863398	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6872314	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6874781	0.93[EUR][1000 genomes]
rs6886841	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6891949	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73120833	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7445415	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs767676	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7706857	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7709282	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7717505	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7723531	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs924452	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9293656	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9332464	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9885386	0.83[EUR][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	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
2	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
3	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
4	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
5	nsv882199	chr5:74757758-74946455	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription 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	13 gene(s)	inside rSNPs	diseases
6	nsv1027368	chr5:74759999-75663712	Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
7	nsv882202	chr5:74808417-74946455	Strong transcription Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
8	nsv518475	chr5:74863041-75411804	Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
9	esv1850196	chr5:74890618-75138443	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74907800-74921400	Weak transcription	Aorta	Aorta
2	chr5:74907800-74921400	Weak transcription	Lung	lung
3	chr5:74908000-74916000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr5:74908200-74918800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr5:74908200-74919600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr5:74908200-74923600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr5:74908600-74918000	Weak transcription	Small Intestine	intestine
8	chr5:74908600-74920400	Enhancers	Fetal Intestine Small	intestine
9	chr5:74909000-74916000	Weak transcription	A549	lung
10	chr5:74911200-74914000	Enhancers	Fetal Stomach	stomach
11	chr5:74911600-74914000	Enhancers	Fetal Kidney	kidney
12	chr5:74911800-74913800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr5:74911800-74913800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr5:74911800-74913800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr5:74911800-74914000	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr5:74912000-74913800	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr5:74912000-74914000	Enhancers	Stomach Mucosa	stomach
18	chr5:74912200-74913800	Enhancers	Fetal Muscle Leg	muscle
19	chr5:74912200-74914000	Enhancers	HSMMtube	muscle
20	chr5:74912200-74914000	Enhancers	K562	blood
21	chr5:74912200-74914000	Enhancers	NH-A	brain
22	chr5:74912200-74914400	Enhancers	Fetal Intestine Large	intestine
23	chr5:74912400-74913800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr5:74912400-74913800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr5:74912400-74914000	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr5:74912600-74914000	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr5:74912600-74914000	Enhancers	NHEK	skin
28	chr5:74912600-74914200	Enhancers	Muscle Satellite Cultured Cells	--
29	chr5:74912600-74914200	Enhancers	Duodenum Mucosa	Duodenum
30	chr5:74912600-74914400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr5:74912600-74917200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr5:74912800-74913800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr5:74912800-74913800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr5:74912800-74913800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr5:74912800-74913800	Enhancers	Esophagus	oesophagus
36	chr5:74912800-74913800	Enhancers	Placenta	Placenta
37	chr5:74912800-74914200	Enhancers	HMEC	breast
38	chr5:74913000-74913800	Enhancers	Ovary	ovary
39	chr5:74913000-74914000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr5:74913000-74914000	Enhancers	Fetal Brain Male	brain
41	chr5:74913200-74913800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr5:74913200-74913800	Enhancers	Osteobl	bone
43	chr5:74913200-74914000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr5:74913200-74914600	Weak transcription	Fetal Muscle Trunk	muscle
45	chr5:74913400-74913800	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr5:74913400-74913800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr5:74913400-74913800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr5:74913400-74914000	Enhancers	NHLF	lung
49	chr5:74913400-74916600	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr5:74913600-74913800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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