Variant report

Variant	rs2860472
Chromosome Location	chr10:52309380-52309381
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:52308145..52313390-chr10:52380498..52385309,7	K562	blood:
2	chr10:52305141..52307249-chr10:52308669..52310332,3	K562	blood:
3	chr10:52308481..52311283-chr10:52312051..52314747,2	MCF-7	breast:
4	chr10:52308954..52311040-chr10:52345342..52347602,2	K562	blood:
5	chr10:52309255..52311683-chr10:52321787..52323365,2	K562	blood:

Variant related genes	Relation type
ENSG00000198964	Chromatin interaction
ENSG00000251950	Chromatin interaction
ENSG00000226200	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10763584	0.89[JPT][hapmap]
rs10763585	0.88[JPT][hapmap]
rs10826234	0.88[JPT][hapmap]
rs11006102	0.87[ASN][1000 genomes]
rs11006119	0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs11006155	0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs12358162	0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs1884571	0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs2208036	0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs2983360	0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs2983364	0.88[JPT][hapmap]
rs3011707	0.88[JPT][hapmap]
rs3011710	0.88[JPT][hapmap]
rs3920545	0.88[JPT][hapmap]
rs4935731	0.87[ASN][1000 genomes]
rs4935732	0.87[ASN][1000 genomes]
rs55669848	0.87[ASN][1000 genomes]
rs55735989	0.85[ASN][1000 genomes]
rs56403030	0.87[ASN][1000 genomes]
rs61858108	0.87[ASN][1000 genomes]
rs6481433	0.88[JPT][hapmap]
rs7074405	0.86[ASN][1000 genomes]
rs7075104	0.88[JPT][hapmap]
rs7088807	0.88[JPT][hapmap];0.81[ASN][1000 genomes]
rs7898315	0.88[JPT][hapmap]

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	nsv1054775	chr10:51595893-52392361	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv1051087	chr10:51886486-52447295	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv916214	chr10:51886486-52458983	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv918212	chr10:51886486-52465482	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
5	nsv817412	chr10:51911034-52432990	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
6	nsv469522	chr10:52276564-52447589	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
7	nsv482564	chr10:52276564-52447589	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52280200-52328000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr10:52299000-52310200	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr10:52299200-52310200	Weak transcription	Pancreas	Pancrea
4	chr10:52299600-52320600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr10:52300600-52310200	Weak transcription	Placenta	Placenta
6	chr10:52300800-52310800	Weak transcription	Gastric	stomach
7	chr10:52300800-52322800	Weak transcription	Primary B cells from cord blood	blood
8	chr10:52301600-52310200	Weak transcription	Left Ventricle	heart
9	chr10:52301600-52327200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr10:52303200-52310200	Weak transcription	Fetal Lung	lung
11	chr10:52303200-52310200	Weak transcription	Stomach Mucosa	stomach
12	chr10:52303200-52312200	Weak transcription	Rectal Smooth Muscle	rectum
13	chr10:52303400-52309400	Weak transcription	Liver	Liver
14	chr10:52303400-52310200	Weak transcription	Spleen	Spleen
15	chr10:52303400-52310800	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr10:52303400-52312200	Weak transcription	Adipose Nuclei	Adipose
17	chr10:52303400-52314000	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr10:52304000-52312000	Weak transcription	Colon Smooth Muscle	Colon
19	chr10:52304400-52312000	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr10:52305000-52309800	Weak transcription	Brain Anterior Caudate	brain
21	chr10:52305000-52310000	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr10:52305000-52310200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr10:52305000-52310200	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr10:52305200-52309800	Weak transcription	Brain Angular Gyrus	brain
25	chr10:52305200-52310000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr10:52305200-52310000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr10:52305200-52310200	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr10:52305200-52310200	Weak transcription	Right Ventricle	heart
29	chr10:52305400-52329600	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr10:52305600-52309600	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr10:52305600-52309600	Weak transcription	Brain Hippocampus Middle	brain
32	chr10:52305800-52309600	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr10:52305800-52309600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr10:52305800-52309600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr10:52305800-52310400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr10:52306000-52309600	Weak transcription	Brain Cingulate Gyrus	brain
37	chr10:52306000-52309600	Weak transcription	Duodenum Mucosa	Duodenum
38	chr10:52306000-52310000	Weak transcription	Psoas Muscle	Psoas
39	chr10:52306000-52312600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr10:52306000-52312800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr10:52306000-52312800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr10:52306000-52314200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr10:52306000-52316000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr10:52306000-52319000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr10:52306000-52321400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr10:52306000-52322000	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr10:52306000-52331800	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr10:52306200-52310000	Weak transcription	HepG2	liver
49	chr10:52308000-52337200	Weak transcription	Primary T cells from cord blood	blood
50	chr10:52308400-52309400	Enhancers	K562	blood

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