Variant report

Variant	rs7181859
Chromosome Location	chr15:43158239-43158240
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10518779	0.96[EUR][1000 genomes]
rs16957168	0.86[EUR][1000 genomes]
rs2412748	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28374998	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28494835	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28609797	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs28613047	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28620320	0.86[EUR][1000 genomes]
rs28633493	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28796057	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28810091	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28871732	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3759792	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4274403	0.81[AMR][1000 genomes]
rs66947001	0.93[EUR][1000 genomes]
rs7166705	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7170376	0.81[AMR][1000 genomes]
rs7176957	0.85[AMR][1000 genomes]
rs7178248	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7182650	0.81[AMR][1000 genomes]
rs8028785	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs8036674	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9920061	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9920182	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9920202	0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427959	chr15:42931181-43207353	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv977054	chr15:43015821-43171355	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1050128	chr15:43056145-43262736	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv542368	chr15:43056145-43262736	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv525461	chr15:43062548-43482127	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
6	nsv904134	chr15:43097652-43357406	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv1044522	chr15:43115348-43658417	Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	nsv515876	chr15:43116906-43445305	Strong transcription Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
9	esv3400306	chr15:43135709-43164903	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv904135	chr15:43143998-43392075	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	esv3490431	chr15:43148709-43190630	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3490432	chr15:43148709-43190630	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43075800-43159200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr15:43089800-43165200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr15:43094400-43163800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr15:43095000-43165000	Weak transcription	Spleen	Spleen
5	chr15:43103000-43165400	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr15:43103400-43173200	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr15:43114800-43172000	Weak transcription	Pancreas	Pancrea
8	chr15:43119600-43168200	Weak transcription	Stomach Smooth Muscle	stomach
9	chr15:43119600-43172600	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr15:43119800-43163200	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr15:43119800-43170200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr15:43125400-43173600	Weak transcription	Hela-S3	cervix
13	chr15:43131000-43165200	Weak transcription	Thymus	Thymus
14	chr15:43131600-43171800	Weak transcription	Brain Anterior Caudate	brain
15	chr15:43132000-43186800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr15:43132200-43162400	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr15:43132200-43166200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr15:43132400-43165400	Weak transcription	Fetal Muscle Trunk	muscle
19	chr15:43132400-43172800	Weak transcription	Ovary	ovary
20	chr15:43132600-43171200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr15:43136600-43159400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr15:43136600-43167200	Weak transcription	Dnd41	blood
23	chr15:43136800-43165200	Weak transcription	Brain Germinal Matrix	brain
24	chr15:43136800-43169200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr15:43136800-43169200	Weak transcription	Fetal Intestine Small	intestine
26	chr15:43136800-43182400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr15:43137000-43164000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr15:43140000-43164600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr15:43142200-43162400	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr15:43142400-43182400	Weak transcription	Lung	lung
31	chr15:43142600-43159600	Weak transcription	Fetal Thymus	thymus
32	chr15:43142600-43160800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr15:43142600-43169400	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr15:43142600-43170200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr15:43142800-43159800	Weak transcription	Primary hematopoietic stem cells	blood
36	chr15:43142800-43172000	Weak transcription	Fetal Intestine Large	intestine
37	chr15:43145400-43169200	Weak transcription	Primary B cells from peripheral blood	blood
38	chr15:43148800-43162200	Weak transcription	Fetal Lung	lung
39	chr15:43149200-43163000	Weak transcription	Fetal Stomach	stomach
40	chr15:43151000-43169400	Weak transcription	Rectal Smooth Muscle	rectum
41	chr15:43151600-43182400	Weak transcription	Aorta	Aorta
42	chr15:43151800-43163000	Weak transcription	Left Ventricle	heart
43	chr15:43151800-43163600	Weak transcription	Esophagus	oesophagus
44	chr15:43151800-43169200	Weak transcription	Fetal Muscle Leg	muscle
45	chr15:43151800-43173000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr15:43151800-43178600	Weak transcription	Placenta	Placenta
47	chr15:43152200-43162000	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr15:43152200-43167400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr15:43152200-43170000	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr15:43152800-43159600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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