Variant report

Variant	rs1005907
Chromosome Location	chr10:4873106-4873107
allele	C/T
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	POLR2A	chr10:4873031-4873704	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:4861761..4864684-chr10:4870409..4873110,2	K562	blood:
2	chr10:4866089..4871671-chr10:4873094..4876081,6	MCF-7	breast:
3	chr10:4869313..4873235-chr10:4874956..4878368,5	K562	blood:
4	chr10:4872071..4873648-chr10:4875186..4877993,2	MCF-7	breast:

Variant related genes	Relation type
AKR1E2	TF binding region
ENSG00000165568	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10508287	1.00[CHB][hapmap]
rs10904348	1.00[JPT][hapmap]
rs11252729	1.00[JPT][hapmap]
rs11252867	1.00[CHB][hapmap]
rs11595166	1.00[JPT][hapmap]
rs12761692	1.00[JPT][hapmap]
rs12764114	0.93[ASN][1000 genomes]
rs12769532	0.93[ASN][1000 genomes]
rs17370636	1.00[CHB][hapmap]
rs2123351	0.85[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2895005	1.00[LWK][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894792	chr10:4832920-5498724	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription 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	47 gene(s)	inside rSNPs	diseases
2	nsv948794	chr10:4863093-5227382	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv1045155	chr10:4872239-5211318	Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv1040343	chr10:4872814-5196815	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv540462	chr10:4872814-5196815	Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4868800-4874600	Weak transcription	Spleen	Spleen
2	chr10:4868800-4879800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr10:4869000-4875000	Weak transcription	Primary hematopoietic stem cells	blood
4	chr10:4869000-4881000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr10:4869200-4873400	Weak transcription	Fetal Stomach	stomach
6	chr10:4869200-4874000	Weak transcription	Lung	lung
7	chr10:4869200-4875400	Weak transcription	Ovary	ovary
8	chr10:4869200-4875600	Weak transcription	Gastric	stomach
9	chr10:4869200-4876600	Weak transcription	Fetal Brain Female	brain
10	chr10:4869200-4877600	Weak transcription	Pancreas	Pancrea
11	chr10:4869200-4877800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr10:4869200-4883600	Weak transcription	Thymus	Thymus
13	chr10:4869200-4884800	Weak transcription	Esophagus	oesophagus
14	chr10:4869200-4889200	Weak transcription	NHLF	lung
15	chr10:4869200-4889600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr10:4869200-4890400	Weak transcription	Right Atrium	heart
17	chr10:4869200-4891600	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr10:4869200-4892200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr10:4869400-4873200	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr10:4869400-4873400	Weak transcription	Fetal Muscle Trunk	muscle
21	chr10:4869400-4876000	Weak transcription	Brain Germinal Matrix	brain
22	chr10:4869400-4877200	Weak transcription	Rectal Smooth Muscle	rectum
23	chr10:4869400-4877600	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr10:4869400-4878400	Weak transcription	Placenta	Placenta
25	chr10:4869400-4879000	Weak transcription	Fetal Lung	lung
26	chr10:4869400-4883400	Weak transcription	Colonic Mucosa	Colon
27	chr10:4869400-4886800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr10:4869400-4889600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr10:4869400-4889600	Weak transcription	HSMM	muscle
30	chr10:4869400-4891600	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr10:4869600-4873200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr10:4869600-4875000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr10:4869600-4875600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr10:4869600-4877000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr10:4869600-4877200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr10:4869600-4877200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr10:4869600-4877600	Weak transcription	Osteobl	bone
38	chr10:4869600-4878600	Weak transcription	Colon Smooth Muscle	Colon
39	chr10:4869600-4883400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr10:4869600-4885000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr10:4869600-4889200	Weak transcription	HUVEC	blood vessel
42	chr10:4869600-4889600	Weak transcription	NHEK	skin
43	chr10:4869800-4873200	Weak transcription	Duodenum Mucosa	Duodenum
44	chr10:4869800-4880600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr10:4869800-4884800	Weak transcription	Right Ventricle	heart
46	chr10:4869800-4885800	Weak transcription	Stomach Mucosa	stomach
47	chr10:4870200-4877000	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr10:4870200-4879600	Weak transcription	Fetal Heart	heart
49	chr10:4870400-4873400	Weak transcription	Primary T cells from cord blood	blood
50	chr10:4870400-4875600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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