Variant report

Variant	rs10060260
Chromosome Location	chr5:74923581-74923582
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:74912024..74914449-chr5:74921744..74924749,4	K562	blood:
2	chr5:74912024..74914449-chr5:74922011..74924010,2	K562	blood:

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10038723	0.85[EUR][1000 genomes]
rs10043621	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10044053	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10067641	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10075139	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10434644	0.81[EUR][1000 genomes]
rs10474436	0.81[EUR][1000 genomes]
rs1051795	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10942739	0.83[EUR][1000 genomes]
rs13354407	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1427924	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17739580	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1863934	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1863935	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1995267	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2287711	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs253392	0.96[ASN][1000 genomes]
rs253393	0.85[ASN][1000 genomes]
rs253407	0.83[ASN][1000 genomes]
rs253409	0.85[ASN][1000 genomes]
rs2878519	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2878520	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3213801	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34340	0.85[ASN][1000 genomes]
rs4045166	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4385188	0.81[EUR][1000 genomes]
rs4440336	0.83[EUR][1000 genomes]
rs4703674	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4704224	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4704228	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs57312935	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs5744533	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs5744555	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs5744575	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs5744595	0.81[EUR][1000 genomes]
rs5744598	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs5744601	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs5744621	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs5744663	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs5744703	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59506842	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61430233	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs67969809	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6861279	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6863398	0.82[EUR][1000 genomes]
rs6872314	0.81[EUR][1000 genomes]
rs6874781	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6886841	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6891949	0.82[EUR][1000 genomes]
rs73120833	0.82[EUR][1000 genomes]
rs7445415	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs767676	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7706857	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7709282	0.80[EUR][1000 genomes]
rs7717505	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7723531	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs924452	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9293656	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9332464	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74908200-74923600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr5:74913800-74923600	Weak transcription	Esophagus	oesophagus
3	chr5:74913800-74923600	Weak transcription	Fetal Muscle Leg	muscle
4	chr5:74913800-74933600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:74914000-74930800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr5:74915000-74925800	Weak transcription	Fetal Muscle Trunk	muscle
7	chr5:74916600-74931800	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr5:74918400-74944200	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr5:74918800-74934000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr5:74920000-74923600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr5:74920200-74926000	Weak transcription	NHEK	skin
12	chr5:74920200-74936600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr5:74920400-74929000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr5:74920400-74944200	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr5:74920600-74933400	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr5:74921800-74964400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr5:74922000-74931600	Weak transcription	Lung	lung
18	chr5:74922000-74932000	Weak transcription	Aorta	Aorta
19	chr5:74922000-74932400	Weak transcription	Fetal Intestine Small	intestine
20	chr5:74922800-74923600	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr5:74923400-74923800	Enhancers	Gastric	stomach
22	chr5:74923400-74924600	Enhancers	Stomach Mucosa	stomach

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