Variant report

Variant	rs10424769
Chromosome Location	chr19:53144284-53144285
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:9 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SIN3A	chr19:53144202-53144335	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr19:53144198-53144751	SK-N-MC	brain:	n/a	n/a
3	POLR2A	chr19:53144281-53144306	HUVEC	blood vessel:	n/a	n/a
4	POLR2A	chr19:53144217-53144303	K562	blood:	n/a	n/a
5	POLR2A	chr19:53144236-53144637	PANC-1	pancreas:	n/a	n/a
6	NFYB	chr19:53144046-53144428	K562	blood:	n/a	chr19:53144190-53144205 chr19:53144190-53144205 chr19:53144190-53144204 chr19:53144192-53144202
7	POLR2A	chr19:53144107-53144501	K562	blood:	n/a	n/a
8	POLR2A	chr19:53144017-53144648	K562	blood:	n/a	n/a
9	EGR1	chr19:53144281-53144558	K562	blood:	n/a	chr19:53144432-53144454

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53144247-53144297	HCM	heart:	n/a
2	chr19:53144247-53144297	CMK	blood:	n/a
3	chr19:53144247-53144297	NHDF-neo	bronchial:	n/a
4	chr19:53144247-53144297	AG04449	skin:	fetal
5	chr19:53144247-53144297	A549	lung:	n/a
6	chr19:53144247-53144297	AG09319	gingival:	n/a
7	chr19:53144247-53144297	ovcar-3	ovarian:	n/a
8	chr19:53144247-53144297	HAEpiC	amniotic membrane:	n/a
9	chr19:53144247-53144297	MCF-7	breast:	n/a
10	chr19:53144247-53144297	K562	blood:	n/a
11	chr19:53144247-53144297	HUVEC	blood vessel:	n/a
12	chr19:53144247-53144297	HCT-116	colon:	n/a
13	chr19:53144247-53144297	GM19239	blood:	n/a
14	chr19:53144247-53144297	AG10803	skin:	n/a
15	chr19:53144247-53144297	BE2_C	brain:	n/a
16	chr19:53144247-53144297	SK-N-SH_RA	brain:	n/a
17	chr19:53144247-53144297	NT2-D1	testis:	n/a
18	chr19:53144247-53144297	HRCEpiC	kidney:	n/a
19	chr19:53144247-53144297	MCF10A-Er-Src	breast:	n/a
20	chr19:53144247-53144297	HIPEpiC	eye:	n/a
21	chr19:53144247-53144297	H1-hESC	embryonic stem cell:	embryo
22	chr19:53144247-53144297	HNPCEpiC	eye:	n/a
23	chr19:53144247-53144297	PFSK-1	brain:	n/a
24	chr19:53144247-53144297	HCF	heart:	n/a
25	chr19:53144247-53144297	AG04450	lung:	fetal
26	chr19:53144247-53144297	U87	brain:	n/a
27	chr19:53144247-53144297	SKMC	muscle:	n/a
28	chr19:53144247-53144297	PrEC	prostate:	n/a
29	chr19:53144247-53144297	Caco-2	colon:	n/a
30	chr19:53144247-53144297	HMEC	breast:	n/a
31	chr19:53144247-53144297	ProgFib	skin:	n/a
32	chr19:53144247-53144297	GM12892	blood:	n/a
33	chr19:53144247-53144297	BJ	skin:	n/a
34	chr19:53144247-53144297	HEK293	kidney:	embryo
35	chr19:53144247-53144297	HepG2	liver:	n/a
36	chr19:53144247-53144297	SK-N-MC	brain:	n/a
37	chr19:53144247-53144297	NB4	blood:	n/a
38	chr19:53144247-53144297	NHBE	bronchial:	n/a
39	chr19:53144247-53144297	GM06990	blood:	n/a
40	chr19:53144247-53144297	HRE	kidney:	n/a
41	chr19:53144247-53144297	SK-N-SH	brain:	n/a
42	chr19:53144247-53144297	Jurkat	blood:	n/a
43	chr19:53144247-53144297	HEEpiC	esophagus:	n/a
44	chr19:53144247-53144297	HL-60	blood:	n/a
45	chr19:53144247-53144297	AG09309	skin:	n/a
46	chr19:53144247-53144297	SAEC	small airway:	n/a
47	chr19:53144247-53144297	Hepatocyte	liver:	n/a
48	chr19:53144247-53144297	NH-A	brain:	n/a
49	chr19:53144247-53144297	HPAEpiC	pulmonary alveolar:	n/a
50	chr19:53144247-53144297	T-47D	breast:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53141360..53143345-chr19:53143350..53145363,3	K562	blood:
2	chr19:53139623..53144311-chr19:53192220..53194807,4	MCF-7	breast:
3	chr19:53143960..53145524-chr19:53164055..53166816,2	K562	blood:

No data

Variant related genes	Relation type
ZNF83	TF binding region
ZNF83	CpG island
ENSG00000167766	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10406117	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10411742	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10412842	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10418303	0.85[ASN][1000 genomes]
rs10423447	0.80[AFR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10423500	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10424979	0.85[ASN][1000 genomes]
rs10426781	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11672421	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12980672	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12982142	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12985319	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12986098	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13345810	0.85[ASN][1000 genomes]
rs13345824	0.85[ASN][1000 genomes]
rs13345832	0.85[ASN][1000 genomes]
rs4287691	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1057296	chr19:52950339-53396986	Weak transcription Active TSS ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv833874	chr19:53058014-53257875	Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv912305	chr19:53092465-53349850	Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv912306	chr19:53092465-53400760	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	nsv912307	chr19:53092465-53433054	Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv912308	chr19:53092465-53436337	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
7	nsv912309	chr19:53092465-53440653	Weak transcription Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS 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	32 gene(s)	inside rSNPs	diseases
8	nsv912310	chr19:53092465-53451291	Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv912311	chr19:53103875-53212361	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
10	nsv912312	chr19:53103875-53296371	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
11	nsv912313	chr19:53103875-53436337	ZNF genes & repeats Weak transcription Strong transcription Active TSS 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	30 gene(s)	inside rSNPs	diseases
12	nsv912315	chr19:53105547-53149967	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	9 gene(s)	inside rSNPs	diseases
13	nsv912316	chr19:53105547-53158023	Flanking Active TSS Active TSS Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
14	nsv912317	chr19:53105547-53440653	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
15	nsv1066762	chr19:53112568-53552217	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
16	nsv912318	chr19:53118278-53451291	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
17	nsv458744	chr19:53120559-53236331	Genic enhancers Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
18	nsv580028	chr19:53120559-53236331	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
19	esv3489404	chr19:53121944-53391394	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
20	esv3489405	chr19:53121944-53391394	Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
21	nsv1066876	chr19:53123577-53157096	Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
22	nsv580029	chr19:53137583-53164172	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
23	esv1184159	chr19:53144284-53144285	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53141800-53160000	Weak transcription	Hela-S3	cervix
2	chr19:53142200-53147200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr19:53142200-53147400	Weak transcription	Ovary	ovary
4	chr19:53142200-53147800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr19:53142200-53149200	Weak transcription	Pancreas	Pancrea
6	chr19:53142200-53149600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr19:53142200-53149600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr19:53142200-53151200	Weak transcription	Aorta	Aorta
9	chr19:53142200-53151800	Weak transcription	NHDF-Ad	bronchial
10	chr19:53142200-53155800	Weak transcription	Brain Anterior Caudate	brain
11	chr19:53142400-53144400	Weak transcription	Placenta	Placenta
12	chr19:53142400-53145000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr19:53142400-53148000	Weak transcription	Fetal Stomach	stomach
14	chr19:53142400-53149400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr19:53142400-53149800	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr19:53142400-53150200	Weak transcription	NH-A	brain
17	chr19:53142400-53150600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr19:53142400-53151000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr19:53142400-53151000	Weak transcription	HSMM	muscle
20	chr19:53142400-53151000	Weak transcription	Osteobl	bone
21	chr19:53142400-53151200	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr19:53142400-53151200	Weak transcription	HSMMtube	muscle
23	chr19:53142400-53152000	Weak transcription	Stomach Smooth Muscle	stomach
24	chr19:53142400-53154000	Weak transcription	Brain Angular Gyrus	brain
25	chr19:53142400-53154000	Weak transcription	Brain Hippocampus Middle	brain
26	chr19:53142400-53154200	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr19:53142400-53156000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr19:53142400-53156400	Weak transcription	Brain Substantia Nigra	brain
29	chr19:53142600-53146800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr19:53142600-53147200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr19:53142600-53147200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr19:53142600-53148800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr19:53142600-53149200	Weak transcription	Primary hematopoietic stem cells	blood
34	chr19:53142600-53149200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr19:53142600-53149400	Weak transcription	Fetal Muscle Leg	muscle
36	chr19:53142600-53149600	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr19:53142600-53149600	Weak transcription	Brain Germinal Matrix	brain
38	chr19:53142600-53149600	Weak transcription	Fetal Lung	lung
39	chr19:53142600-53150000	Weak transcription	Dnd41	blood
40	chr19:53142600-53150200	Weak transcription	Left Ventricle	heart
41	chr19:53142600-53150600	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr19:53142600-53152600	Weak transcription	Fetal Brain Female	brain
43	chr19:53142600-53156400	Weak transcription	Fetal Brain Male	brain
44	chr19:53142800-53149600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr19:53143000-53154200	Weak transcription	Primary T cells from cord blood	blood
46	chr19:53143000-53154400	Weak transcription	Colon Smooth Muscle	Colon
47	chr19:53143600-53144400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr19:53144000-53144400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr19:53144000-53144600	Enhancers	K562	blood
50	chr19:53144200-53144400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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