Variant report

Variant	rs35966728
Chromosome Location	chr19:21916981-21916982
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12972019	0.81[AMR][1000 genomes]
rs12972529	0.81[AMR][1000 genomes]
rs12972582	0.81[AMR][1000 genomes]
rs12972656	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs12973310	0.81[AMR][1000 genomes]
rs12973798	0.81[AMR][1000 genomes]
rs12975386	0.86[AFR][1000 genomes]
rs12975387	0.81[AMR][1000 genomes]
rs12977947	0.81[AMR][1000 genomes]
rs12978145	0.81[AMR][1000 genomes]
rs12981854	0.81[AMR][1000 genomes]
rs12982134	0.81[AMR][1000 genomes]
rs12982588	0.81[AMR][1000 genomes]
rs12982621	0.81[AMR][1000 genomes]
rs12983229	0.81[AMR][1000 genomes]
rs12985617	0.81[AMR][1000 genomes]
rs16998300	0.81[AMR][1000 genomes]
rs28492771	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs34063259	0.81[AMR][1000 genomes]
rs34387769	0.81[AMR][1000 genomes]
rs34569334	0.81[AMR][1000 genomes]
rs34617884	0.81[AMR][1000 genomes]
rs34652503	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs34906160	0.81[AMR][1000 genomes]
rs34908429	0.93[AFR][1000 genomes]
rs35161629	0.81[AMR][1000 genomes]
rs35251105	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs35407033	0.81[AMR][1000 genomes]
rs35409731	0.81[AMR][1000 genomes]
rs35441629	0.81[AMR][1000 genomes]
rs35447051	0.81[AMR][1000 genomes]
rs35587380	0.81[AMR][1000 genomes]
rs35588095	0.81[AMR][1000 genomes]
rs35590941	0.81[AMR][1000 genomes]
rs35621425	0.81[AMR][1000 genomes]
rs35646356	0.81[AMR][1000 genomes]
rs35715827	0.81[AMR][1000 genomes]
rs35725943	0.81[AMR][1000 genomes]
rs35923238	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs55694447	0.81[AMR][1000 genomes]
rs55799773	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs55817748	0.81[AMR][1000 genomes]
rs57394342	0.81[AMR][1000 genomes]
rs57450176	0.81[AMR][1000 genomes]
rs58873883	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs59556202	0.81[AMR][1000 genomes]
rs59825581	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs60086097	0.86[AFR][1000 genomes]
rs61182414	0.81[AMR][1000 genomes]
rs61196724	0.81[AMR][1000 genomes]
rs73928595	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs74167876	0.89[AFR][1000 genomes]
rs74167877	0.81[AMR][1000 genomes]
rs74167878	0.81[AMR][1000 genomes]
rs74167879	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs74167880	0.81[AMR][1000 genomes]
rs8107583	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv911422	chr19:21752009-21973929	ZNF genes & repeats Strong transcription Active TSS Genic enhancers Weak transcription Flanking Active TSS 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	13 gene(s)	inside rSNPs	diseases
2	esv3441368	chr19:21781459-22182822	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	esv3339694	chr19:21781479-22182792	Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv1063115	chr19:21782104-22528039	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
5	nsv458525	chr19:21796943-22019697	Weak transcription ZNF genes & repeats Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv578969	chr19:21796943-22019697	ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS 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	13 gene(s)	inside rSNPs	diseases
7	esv3392559	chr19:21798396-21965956	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv911424	chr19:21798441-22471156	Strong transcription Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS 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	36 gene(s)	inside rSNPs	diseases
9	nsv833783	chr19:21821406-21991838	ZNF genes & repeats Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	esv1815274	chr19:21825750-21981855	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	nsv911425	chr19:21841379-22338142	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
12	nsv911426	chr19:21892040-21973929	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv911427	chr19:21900898-21960407	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv833784	chr19:21902647-22037153	ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS 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	9 gene(s)	inside rSNPs	diseases
15	nsv578970	chr19:21906655-21973929	Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
16	nsv961193	chr19:21911308-21950500	Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
17	esv3342879	chr19:21913482-21968857	Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21905600-21947200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr19:21906200-21919400	ZNF genes & repeats	Dnd41	blood
3	chr19:21906200-21927600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr19:21906200-21949200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr19:21908000-21920400	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr19:21908200-21920400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr19:21908800-21948800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
8	chr19:21909200-21919600	ZNF genes & repeats	Liver	Liver
9	chr19:21909200-21946000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr19:21910800-21920800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr19:21910800-21922000	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr19:21911000-21917000	Weak transcription	Stomach Smooth Muscle	stomach
13	chr19:21911200-21917000	Weak transcription	Colon Smooth Muscle	Colon
14	chr19:21911200-21917400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr19:21911200-21917400	Weak transcription	Fetal Brain Male	brain
16	chr19:21911200-21924600	Weak transcription	Osteobl	bone
17	chr19:21911200-21935600	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr19:21911400-21917400	Weak transcription	Brain Angular Gyrus	brain
19	chr19:21911400-21918400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr19:21911400-21922000	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr19:21911400-21930000	Weak transcription	Right Ventricle	heart
22	chr19:21912800-21922800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
23	chr19:21913000-21919800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr19:21913000-21920600	ZNF genes & repeats	Primary B cells from cord blood	blood
25	chr19:21913000-21925000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr19:21913000-21925400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
27	chr19:21913400-21925600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
28	chr19:21913400-21941200	Weak transcription	NHDF-Ad	bronchial
29	chr19:21913600-21918000	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr19:21913600-21918400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr19:21914000-21922400	Weak transcription	HSMM	muscle
32	chr19:21914000-21934600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
33	chr19:21914200-21922600	ZNF genes & repeats	Brain Germinal Matrix	brain
34	chr19:21914800-21917800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr19:21915000-21918400	Weak transcription	Placenta	Placenta
36	chr19:21915000-21918600	Weak transcription	Fetal Stomach	stomach
37	chr19:21915000-21919000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr19:21915000-21919600	ZNF genes & repeats	Primary B cells from peripheral blood	blood
39	chr19:21915000-21920000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
40	chr19:21915000-21920800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr19:21915000-21921800	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr19:21915200-21918400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr19:21915400-21918600	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr19:21915600-21917200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr19:21915600-21917600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr19:21915800-21922000	Weak transcription	Fetal Kidney	kidney
47	chr19:21916000-21921600	Weak transcription	Stomach Mucosa	stomach
48	chr19:21916200-21917200	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr19:21916200-21917200	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
50	chr19:21916200-21917600	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood

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