Variant report

Variant	rs8036094
Chromosome Location	chr15:34564171-34564172
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:34561845..34564455-chr15:34565020..34567882,2	K562	blood:
2	chr15:34553058..34555521-chr15:34561938..34565007,3	K562	blood:
3	chr15:34558780..34560972-chr15:34563410..34565603,2	K562	blood:

Variant related genes	Relation type
ENSG00000140199	Chromatin interaction

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10152189	0.88[AFR][1000 genomes]
rs10152222	0.92[AFR][1000 genomes]
rs10152351	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10152407	0.92[AFR][1000 genomes]
rs10162625	0.92[AFR][1000 genomes]
rs10467958	0.88[AFR][1000 genomes]
rs10467959	0.88[AFR][1000 genomes]
rs10468070	0.88[AFR][1000 genomes]
rs12324422	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12324469	0.92[AFR][1000 genomes]
rs13379654	0.92[AFR][1000 genomes]
rs13380356	0.84[AFR][1000 genomes]
rs13380366	0.84[AFR][1000 genomes]
rs16958911	0.92[AFR][1000 genomes]
rs16958950	0.90[AFR][1000 genomes]
rs28442188	0.92[AFR][1000 genomes]
rs28543997	0.84[AFR][1000 genomes]
rs28608058	0.88[AFR][1000 genomes]
rs28664278	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28762482	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28807170	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28857572	0.82[AFR][1000 genomes]
rs28871951	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56964418	0.88[AFR][1000 genomes]
rs57044113	0.92[AFR][1000 genomes]
rs57573060	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58198195	0.88[AFR][1000 genomes]
rs60708162	0.88[AFR][1000 genomes]
rs61659679	0.92[AFR][1000 genomes]
rs6495649	0.88[AFR][1000 genomes]
rs6495650	0.88[AFR][1000 genomes]
rs6495651	0.90[AFR][1000 genomes]
rs6495652	0.88[AFR][1000 genomes]
rs6495654	0.84[AFR][1000 genomes]
rs6495655	0.84[AFR][1000 genomes]
rs6495656	0.84[AFR][1000 genomes]
rs6495657	0.84[AFR][1000 genomes]
rs6495658	0.84[AFR][1000 genomes]
rs6495659	0.80[AFR][1000 genomes]
rs7165738	0.92[AFR][1000 genomes]
rs7165973	0.92[AFR][1000 genomes]
rs7166559	0.84[AFR][1000 genomes]
rs7167363	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7167379	0.80[AFR][1000 genomes]
rs7168029	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7168168	0.88[AFR][1000 genomes]
rs7168361	0.90[AFR][1000 genomes]
rs7168606	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7168707	0.88[AFR][1000 genomes]
rs7169731	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7169802	0.88[AFR][1000 genomes]
rs7170829	0.88[AFR][1000 genomes]
rs7175327	0.88[AFR][1000 genomes]
rs7175736	0.88[AFR][1000 genomes]
rs7176138	0.88[AFR][1000 genomes]
rs7183736	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8023999	0.92[AFR][1000 genomes]
rs8024424	0.85[AFR][1000 genomes]
rs8024443	0.84[AFR][1000 genomes]
rs8025075	0.84[AFR][1000 genomes]
rs8026499	0.88[AFR][1000 genomes]
rs8029788	0.84[AFR][1000 genomes]
rs8030737	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8032579	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8033545	0.84[AFR][1000 genomes]
rs8035044	0.88[AFR][1000 genomes]
rs8035650	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8038493	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8039233	0.92[AFR][1000 genomes]
rs8039356	0.88[AFR][1000 genomes]
rs8042422	0.83[AFR][1000 genomes]
rs8042605	0.84[AFR][1000 genomes]
rs9806767	0.85[AFR][1000 genomes]
rs9806778	0.84[AFR][1000 genomes]
rs9989297	0.88[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052804	chr15:34498529-34841447	Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv542341	chr15:34498529-34841447	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv1045173	chr15:34501055-34596995	Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	esv1798578	chr15:34543021-34988247	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
5	esv1804312	chr15:34543021-34988247	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
6	esv1821622	chr15:34543021-34988247	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
7	esv1850950	chr15:34543021-34988247	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
8	esv2758376	chr15:34543021-34988247	Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
9	esv2760024	chr15:34543021-34988247	Flanking Active TSS Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
10	nsv428303	chr15:34543021-34988247	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
11	nsv1036475	chr15:34552879-34841587	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
12	nsv542342	chr15:34552879-34841587	Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
13	nsv1048550	chr15:34553078-34841447	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
14	nsv542343	chr15:34553078-34841447	Active TSS Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
15	nsv471682	chr15:34560451-34882630	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34518000-34571800	Weak transcription	Stomach Mucosa	stomach
2	chr15:34543000-34568200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr15:34546800-34567400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr15:34546800-34568000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr15:34546800-34569400	Weak transcription	Ovary	ovary
6	chr15:34546800-34571800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr15:34546800-34573800	Weak transcription	HUVEC	blood vessel
8	chr15:34547400-34564200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr15:34547600-34591200	Weak transcription	Aorta	Aorta
10	chr15:34548200-34592600	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr15:34548600-34565400	Weak transcription	Fetal Intestine Large	intestine
12	chr15:34549200-34567400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr15:34549200-34571200	Weak transcription	Left Ventricle	heart
14	chr15:34550000-34587400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr15:34551000-34565600	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr15:34551000-34567400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr15:34551200-34565600	Weak transcription	Liver	Liver
18	chr15:34551200-34567400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr15:34551200-34569400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr15:34551200-34577000	Weak transcription	Duodenum Mucosa	Duodenum
21	chr15:34551200-34608800	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr15:34551400-34577200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr15:34552200-34566000	Weak transcription	Adipose Nuclei	Adipose
24	chr15:34552200-34566000	Weak transcription	Stomach Smooth Muscle	stomach
25	chr15:34552200-34567200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr15:34552200-34570800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr15:34553600-34567200	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr15:34555200-34584200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr15:34555200-34584600	Weak transcription	Esophagus	oesophagus
30	chr15:34555200-34606600	Weak transcription	Thymus	Thymus
31	chr15:34555600-34564200	Weak transcription	Primary T cells from cord blood	blood
32	chr15:34555600-34565800	Weak transcription	Fetal Intestine Small	intestine
33	chr15:34559800-34567400	Weak transcription	A549	lung
34	chr15:34560200-34568000	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr15:34561000-34564200	Weak transcription	Primary hematopoietic stem cells	blood
36	chr15:34561600-34565200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr15:34561600-34565200	Strong transcription	GM12878-XiMat	blood
38	chr15:34561600-34565600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr15:34562200-34565200	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr15:34562400-34584000	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr15:34562600-34566200	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr15:34563000-34565200	Strong transcription	Primary B cells from cord blood	blood
43	chr15:34563000-34569400	Weak transcription	Primary T cells fromperipheralblood	blood
44	chr15:34563400-34564200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr15:34563400-34564800	Enhancers	Hela-S3	cervix
46	chr15:34563600-34564400	Enhancers	Muscle Satellite Cultured Cells	--
47	chr15:34563600-34564600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr15:34563800-34564200	Enhancers	Osteobl	bone
49	chr15:34563800-34566200	Strong transcription	Primary B cells from peripheral blood	blood
50	chr15:34563800-34566400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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