Variant report

Variant	rs10763584
Chromosome Location	chr10:52352418-52352419
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MYC	chr10:52352406-52353405	K562	blood:	n/a	n/a
2	MYC	chr10:52352240-52353137	K562	blood:	n/a	n/a
3	MYC	chr10:52352415-52353632	K562	blood:	n/a	n/a
4	MYC	chr10:52352359-52353082	K562	blood:	n/a	n/a
5	E2F6	chr10:52352250-52353454	K562	blood:	n/a	chr10:52352411-52352423 chr10:52352412-52352419 chr10:52352888-52352899 chr10:52352412-52352419 chr10:52352412-52352419
6	EGR1	chr10:52352271-52352502	K562	blood:	n/a	chr10:52352415-52352428 chr10:52352414-52352429 chr10:52352416-52352427

No.	Distal block	Cell Line	Cell type
1	chr10:52342133..52345402-chr10:52352257..52355042,3	MCF-7	breast:
2	chr10:52350667..52353261-chr10:52381881..52384796,3	K562	blood:
3	chr10:52346124..52348507-chr10:52350618..52352666,3	K562	blood:
4	chr10:52351092..52355625-chr10:52355822..52361152,8	K562	blood:

Variant related genes	Relation type
RNU7-107P	TF binding region
ENSG00000198964	Chromatin interaction
ENSG00000226200	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10763585	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10826234	0.85[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11006119	0.89[CHB][hapmap];0.94[JPT][hapmap]
rs11006155	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs12358162	0.89[CHB][hapmap];0.94[JPT][hapmap]
rs1884571	0.90[CHB][hapmap];0.94[JPT][hapmap]
rs2208036	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2860472	0.89[JPT][hapmap]
rs2983360	0.95[CHB][hapmap];0.94[JPT][hapmap];0.83[YRI][hapmap];0.85[ASN][1000 genomes]
rs2983364	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs3011707	0.89[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs3011710	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs3011802	0.87[ASN][1000 genomes]
rs3920545	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55735989	0.80[ASN][1000 genomes]
rs6481433	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7074405	0.92[ASN][1000 genomes]
rs7075104	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7088807	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7898315	0.85[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.93[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	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:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52336800-52363000	Weak transcription	Rectal Smooth Muscle	rectum
2	chr10:52337800-52352800	Weak transcription	Fetal Brain Male	brain
3	chr10:52338000-52356400	Weak transcription	Fetal Brain Female	brain
4	chr10:52338000-52363800	Weak transcription	Fetal Kidney	kidney
5	chr10:52338000-52367000	Weak transcription	Aorta	Aorta
6	chr10:52338200-52353600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr10:52338200-52353800	Weak transcription	Stomach Smooth Muscle	stomach
8	chr10:52338600-52353400	Weak transcription	Brain Germinal Matrix	brain
9	chr10:52338600-52353600	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr10:52340400-52360200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr10:52341200-52373000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr10:52341400-52355400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr10:52341400-52360200	Weak transcription	GM12878-XiMat	blood
14	chr10:52341800-52352800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr10:52341800-52355000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr10:52341800-52362000	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr10:52342400-52353000	Weak transcription	Brain Cingulate Gyrus	brain
18	chr10:52342600-52356400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr10:52342800-52360200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr10:52343000-52353000	Weak transcription	Fetal Heart	heart
21	chr10:52343400-52360600	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr10:52343600-52356200	Weak transcription	Stomach Mucosa	stomach
23	chr10:52343600-52362200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr10:52343800-52360000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr10:52345000-52353000	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr10:52346000-52355400	Weak transcription	Colon Smooth Muscle	Colon
27	chr10:52346400-52358600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr10:52346600-52352600	Weak transcription	HSMMtube	muscle
29	chr10:52346600-52352600	Weak transcription	NHDF-Ad	bronchial
30	chr10:52346600-52352800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr10:52346600-52355400	Weak transcription	Psoas Muscle	Psoas
32	chr10:52346600-52363400	Weak transcription	Adipose Nuclei	Adipose
33	chr10:52346600-52363800	Weak transcription	Spleen	Spleen
34	chr10:52346800-52352600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr10:52346800-52352800	Weak transcription	NHLF	lung
36	chr10:52346800-52353200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr10:52346800-52360600	Weak transcription	HUVEC	blood vessel
38	chr10:52347000-52352800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr10:52347000-52352800	Weak transcription	HMEC	breast
40	chr10:52347000-52353000	Weak transcription	NHEK	skin
41	chr10:52347000-52353600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr10:52347000-52359600	Weak transcription	A549	lung
43	chr10:52347200-52352800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr10:52348000-52363400	Weak transcription	Primary hematopoietic stem cells	blood
45	chr10:52348200-52358400	Weak transcription	HepG2	liver
46	chr10:52348200-52360000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr10:52348400-52363000	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr10:52349000-52354000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr10:52349000-52363200	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr10:52349200-52360400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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