Variant report

Variant	rs10412236
Chromosome Location	chr19:37608044-37608045
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10401380	0.91[EUR][1000 genomes]
rs10401525	0.81[EUR][1000 genomes]
rs10401561	0.91[EUR][1000 genomes]
rs10404069	0.86[EUR][1000 genomes]
rs10404973	0.91[EUR][1000 genomes]
rs10405372	0.81[EUR][1000 genomes]
rs10406612	0.82[EUR][1000 genomes]
rs10407014	0.91[EUR][1000 genomes]
rs10407224	0.86[EUR][1000 genomes]
rs10407265	0.91[EUR][1000 genomes]
rs10408199	0.91[EUR][1000 genomes]
rs10410905	0.94[EUR][1000 genomes]
rs10411037	0.88[EUR][1000 genomes]
rs10413101	0.91[EUR][1000 genomes]
rs10413304	0.81[EUR][1000 genomes]
rs10414107	0.91[EUR][1000 genomes]
rs10414227	0.91[EUR][1000 genomes]
rs10417545	0.81[EUR][1000 genomes]
rs10418314	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10419174	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10419845	0.81[EUR][1000 genomes]
rs10422428	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10424841	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10425441	0.81[EUR][1000 genomes]
rs10426093	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11084873	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12972146	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12975706	0.89[EUR][1000 genomes]
rs12978093	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12983153	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13346284	0.91[EUR][1000 genomes]
rs1617883	0.88[EUR][1000 genomes]
rs1628959	0.83[EUR][1000 genomes]
rs1644702	0.84[EUR][1000 genomes]
rs1644704	0.84[EUR][1000 genomes]
rs2385412	0.91[EUR][1000 genomes]
rs28462002	0.90[EUR][1000 genomes]
rs28631881	0.90[EUR][1000 genomes]
rs28660259	0.81[EUR][1000 genomes]
rs34193103	0.91[EUR][1000 genomes]
rs34915391	0.85[EUR][1000 genomes]
rs35522655	0.91[EUR][1000 genomes]
rs35655645	0.91[EUR][1000 genomes]
rs4473303	0.84[EUR][1000 genomes]
rs4805198	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4805207	0.81[EUR][1000 genomes]
rs4805208	0.81[EUR][1000 genomes]
rs4806406	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4806414	0.86[EUR][1000 genomes]
rs62108899	0.91[EUR][1000 genomes]
rs62109879	0.88[EUR][1000 genomes]
rs6510583	0.81[EUR][1000 genomes]
rs7246473	0.91[EUR][1000 genomes]
rs7247758	0.91[EUR][1000 genomes]
rs7249696	0.81[EUR][1000 genomes]
rs7259878	0.91[EUR][1000 genomes]
rs8101338	0.86[AMR][1000 genomes];0.95[EUR][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	nsv1064851	chr19:36910259-37689721	Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
2	nsv1065698	chr19:36916796-37690124	Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	nsv543999	chr19:36916796-37690124	Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
4	nsv529817	chr19:36930549-37654062	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
5	nsv918028	chr19:37020645-38014526	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
6	esv3507199	chr19:37284708-37805639	Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
7	esv3507200	chr19:37284708-37805639	ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers 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	27 gene(s)	inside rSNPs	diseases
8	esv3497360	chr19:37290273-37745365	ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers 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	25 gene(s)	inside rSNPs	diseases
9	esv3497361	chr19:37290273-37745365	Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers 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	25 gene(s)	inside rSNPs	diseases
10	nsv458568	chr19:37325826-37747108	Strong transcription ZNF genes & repeats Genic enhancers Active TSS Weak transcription Enhancers Flanking Active TSS 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	22 gene(s)	inside rSNPs	diseases
11	nsv579461	chr19:37325826-37747108	Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
12	nsv911652	chr19:37437106-37774299	Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers 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	17 gene(s)	inside rSNPs	diseases
13	nsv911654	chr19:37487632-37758082	Strong transcription Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Genic enhancers 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	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:37597200-37608200	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
2	chr19:37597200-37608400	ZNF genes & repeats	Adipose Nuclei	Adipose
3	chr19:37597200-37608600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
4	chr19:37597200-37608800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr19:37597400-37608200	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
6	chr19:37599200-37618000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr19:37602600-37608400	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr19:37602600-37608400	ZNF genes & repeats	Fetal Lung	lung
9	chr19:37602800-37608200	ZNF genes & repeats	Brain Germinal Matrix	brain
10	chr19:37602800-37608200	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
11	chr19:37602800-37608400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
12	chr19:37602800-37608400	ZNF genes & repeats	Brain Anterior Caudate	brain
13	chr19:37602800-37608400	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
14	chr19:37603000-37608200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr19:37603600-37608200	ZNF genes & repeats	Spleen	Spleen
16	chr19:37606800-37609800	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr19:37608000-37608400	Weak transcription	Pancreas	Pancrea
18	chr19:37608000-37608600	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr19:37608000-37608800	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr19:37608000-37608800	Weak transcription	Right Ventricle	heart
21	chr19:37608000-37609800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr19:37608000-37610400	Weak transcription	Colon Smooth Muscle	Colon
23	chr19:37608000-37613600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr19:37608000-37613600	Weak transcription	Duodenum Mucosa	Duodenum

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