Variant report

Variant	rs7918711
Chromosome Location	chr10:43696769-43696770
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:43696369..43700743-chr10:43891529..43894634,3	K562	blood:
2	chr10:43696064..43699246-chr10:43901638..43904576,3	K562	blood:
3	chr10:43682496..43684417-chr10:43696461..43698091,2	K562	blood:

Variant related genes	Relation type
ENSG00000169813	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs1879317	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3026742	0.87[AFR][1000 genomes]
rs3026766	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61744904	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7898242	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7919610	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534548	chr10:42890664-43729688	Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv430159	chr10:43291894-43946294	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	nsv895082	chr10:43530071-43755506	Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS 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	12 gene(s)	inside rSNPs	diseases
4	nsv895083	chr10:43549708-43765485	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats 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	nsv916378	chr10:43622151-43868356	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
6	nsv1043661	chr10:43626619-43890162	Bivalent Enhancer Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
7	nsv540574	chr10:43626619-43890162	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
8	esv1831010	chr10:43674916-43759185	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
9	nsv895084	chr10:43688505-43765485	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	esv3424466	chr10:43694496-43697294	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
11	nsv466881	chr10:43695049-43799588	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv550696	chr10:43695049-43799588	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv895085	chr10:43695049-43804617	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43652600-43697200	Weak transcription	Pancreas	Pancrea
2	chr10:43662200-43697600	Weak transcription	NHEK	skin
3	chr10:43674400-43697800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr10:43675600-43700600	Weak transcription	A549	lung
5	chr10:43675800-43697000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr10:43678800-43696800	Weak transcription	Primary B cells from peripheral blood	blood
7	chr10:43679400-43697400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr10:43680000-43697600	Weak transcription	NH-A	brain
9	chr10:43682000-43697400	Weak transcription	Liver	Liver
10	chr10:43682600-43697400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr10:43682600-43697400	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr10:43683000-43697000	Weak transcription	Primary hematopoietic stem cells	blood
13	chr10:43683000-43697200	Weak transcription	Primary B cells from cord blood	blood
14	chr10:43683000-43697400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr10:43683000-43697400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr10:43683000-43697400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr10:43683200-43697000	Weak transcription	Fetal Brain Male	brain
18	chr10:43683200-43697200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr10:43683200-43697200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr10:43683400-43697000	Weak transcription	Fetal Intestine Small	intestine
21	chr10:43683800-43697000	Weak transcription	Fetal Lung	lung
22	chr10:43684400-43697200	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr10:43684400-43697200	Weak transcription	Ovary	ovary
24	chr10:43684400-43697400	Weak transcription	Primary T cells from cord blood	blood
25	chr10:43686800-43697000	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr10:43688600-43697000	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr10:43688600-43697800	Weak transcription	Aorta	Aorta
28	chr10:43688800-43697600	Weak transcription	NHLF	lung
29	chr10:43689000-43696800	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr10:43689000-43697800	Weak transcription	HSMM	muscle
31	chr10:43689200-43697200	Weak transcription	Thymus	Thymus
32	chr10:43689200-43697400	Weak transcription	Esophagus	oesophagus
33	chr10:43690000-43696800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr10:43690000-43697000	Strong transcription	H9 Cell Line	embryonic stem cell
35	chr10:43690000-43697400	Weak transcription	Fetal Brain Female	brain
36	chr10:43690600-43696800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
37	chr10:43690600-43697400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr10:43690800-43696800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr10:43692000-43697200	Strong transcription	Brain Anterior Caudate	brain
40	chr10:43692800-43696800	Strong transcription	K562	blood
41	chr10:43693400-43697400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr10:43693800-43697200	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr10:43694000-43697400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr10:43694600-43697400	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr10:43695200-43697600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr10:43695600-43696800	Genic enhancers	Brain Cingulate Gyrus	brain
47	chr10:43695800-43697200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr10:43696000-43697000	Weak transcription	Spleen	Spleen
49	chr10:43696000-43697200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr10:43696000-43697200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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