Variant report

Variant	rs10403231
Chromosome Location	chr19:18765290-18765291
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:18756524..18758579-chr19:18764245..18767050,2	K562	blood:
2	chr19:18763880..18765742-chr19:18767245..18768815,2	K562	blood:
3	chr19:18570477..18573833-chr19:18762488..18765349,3	K562	blood:
4	chr19:18747224..18749100-chr19:18763072..18765971,2	K562	blood:

Variant related genes	Relation type
ENSG00000167487	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10402536	0.96[CEU][hapmap];0.92[CHB][hapmap];0.95[JPT][hapmap];0.83[YRI][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10423102	0.85[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10423271	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10423676	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[YRI][hapmap];0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10423852	1.00[ASN][1000 genomes]
rs1076234	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1076235	1.00[CEU][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11085237	1.00[CEU][hapmap];0.88[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11085239	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11668617	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12052075	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12610845	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12974161	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12974777	1.00[ASN][1000 genomes]
rs12976741	0.97[ASN][1000 genomes]
rs12980154	0.82[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs12983476	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1473115	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2014914	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34143665	1.00[ASN][1000 genomes]
rs34190814	0.96[ASN][1000 genomes]
rs3795026	0.96[CEU][hapmap];0.81[JPT][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4808146	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4808841	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4808842	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs71332133	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs889362	1.00[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs889363	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:36 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1057795	chr19:18453362-18883844	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
2	nsv543925	chr19:18453362-18883844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS 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	nsv532615	chr19:18534867-18796031	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
4	nsv911282	chr19:18624964-18928480	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
5	nsv833776	chr19:18638028-18782264	Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
6	nsv911286	chr19:18652844-18811112	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
7	nsv911289	chr19:18700047-18811112	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
8	esv1849639	chr19:18747006-18780799	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	esv3401944	chr19:18763177-18765925	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	esv3433649	chr19:18763427-18765750	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
11	nsv578760	chr19:18763596-18765572	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	esv18322	chr19:18763872-18765637	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
13	nsv578762	chr19:18764152-18765290	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
14	nsv578763	chr19:18764152-18765411	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
15	nsv578764	chr19:18764152-18765465	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
16	nsv578765	chr19:18764152-18765572	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
17	nsv578768	chr19:18764218-18765290	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
18	nsv578769	chr19:18764218-18765411	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
19	nsv578770	chr19:18764218-18765465	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
20	nsv578771	chr19:18764218-18765572	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
21	nsv578772	chr19:18764218-18768955	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
22	nsv578777	chr19:18764320-18765290	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
23	nsv578778	chr19:18764320-18765411	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
24	nsv578779	chr19:18764320-18765465	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
25	esv1827771	chr19:18764320-18765572	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
26	esv1842496	chr19:18764320-18765572	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
27	esv1846277	chr19:18764320-18765572	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
28	nsv578780	chr19:18764320-18765572	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
29	esv1811733	chr19:18764320-18780799	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
30	esv1845237	chr19:18764320-18780799	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
31	nsv578781	chr19:18764376-18765411	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
32	nsv578782	chr19:18764376-18765572	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
33	nsv578783	chr19:18764537-18765411	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
34	nsv578784	chr19:18764537-18765465	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
35	nsv578785	chr19:18764642-18765572	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
36	nsv578786	chr19:18764751-18765572	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18748600-18774400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr19:18749200-18768200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr19:18749200-18778400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr19:18749400-18774000	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr19:18755800-18766600	Weak transcription	HepG2	liver
6	chr19:18756400-18778400	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr19:18759400-18776200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr19:18759800-18778400	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr19:18760000-18770000	Weak transcription	Gastric	stomach
10	chr19:18760000-18770000	Weak transcription	Stomach Mucosa	stomach
11	chr19:18760200-18775000	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr19:18760400-18774000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr19:18760400-18794800	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr19:18760600-18774800	Weak transcription	Thymus	Thymus
15	chr19:18760800-18776200	Weak transcription	Liver	Liver
16	chr19:18760800-18778400	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr19:18761000-18767200	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr19:18761000-18767800	Weak transcription	GM12878-XiMat	blood
19	chr19:18761200-18768000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr19:18761200-18768000	Weak transcription	Brain Cingulate Gyrus	brain
21	chr19:18761200-18769600	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr19:18761400-18766200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr19:18761600-18769600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr19:18761800-18768000	Weak transcription	Fetal Intestine Large	intestine
25	chr19:18762000-18765400	Weak transcription	Fetal Kidney	kidney
26	chr19:18762000-18766800	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr19:18762000-18767400	Weak transcription	Brain Substantia Nigra	brain
28	chr19:18762000-18768600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr19:18762000-18770200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr19:18762200-18767800	Weak transcription	Brain Germinal Matrix	brain
31	chr19:18762200-18771200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr19:18762400-18768400	Weak transcription	Colonic Mucosa	Colon
33	chr19:18762600-18766800	Weak transcription	Fetal Heart	heart
34	chr19:18762600-18767800	Weak transcription	Brain Angular Gyrus	brain
35	chr19:18762600-18767800	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr19:18762600-18768000	Weak transcription	Rectal Smooth Muscle	rectum
37	chr19:18762600-18768200	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr19:18762600-18774600	Weak transcription	Primary T cells from cord blood	blood
39	chr19:18762600-18775600	Weak transcription	Dnd41	blood
40	chr19:18762800-18765600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr19:18762800-18765600	Weak transcription	Fetal Stomach	stomach
42	chr19:18762800-18766600	Weak transcription	Brain Hippocampus Middle	brain
43	chr19:18762800-18766600	Weak transcription	Lung	lung
44	chr19:18762800-18767200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr19:18762800-18767200	Weak transcription	Brain Anterior Caudate	brain
46	chr19:18762800-18767200	Weak transcription	Right Atrium	heart
47	chr19:18762800-18767600	Weak transcription	HSMMtube	muscle
48	chr19:18762800-18767800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr19:18762800-18768000	Weak transcription	Colon Smooth Muscle	Colon
50	chr19:18762800-18770600	Weak transcription	Psoas Muscle	Psoas

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