Variant report

Variant	rs188656423
Chromosome Location	chr19:55894223-55894224
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6)
CpG islands
(count:0)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:6 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TCF12	chr19:55893884-55895026	A549	lung:	n/a	n/a
2	SIX5	chr19:55893790-55894933	A549	lung:	n/a	n/a
3	CBX3	chr19:55893861-55894812	K562	blood:	n/a	n/a
4	MAX	chr19:55893890-55894231	K562	blood:	n/a	n/a
5	BCL3	chr19:55894055-55895108	A549	lung:	n/a	n/a
6	RCOR1	chr19:55894065-55894448	K562	blood:	n/a	n/a

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:55892436..55894364-chr19:55964923..55967093,2	MCF-7	breast:
2	chr19:55787879..55795650-chr19:55893762..55898931,9	MCF-7	breast:
3	chr19:55764902..55773441-chr19:55891413..55900303,21	K562	blood:
4	chr19:55724006..55730191-chr19:55893749..55903961,17	K562	blood:
5	chr19:55774813..55777090-chr19:55892887..55895596,2	MCF-7	breast:
6	chr19:55767441..55773483-chr19:55893952..55900251,14	MCF-7	breast:
7	chr19:55848515..55857343-chr19:55894079..55900232,19	MCF-7	breast:
8	chr19:55660000..55662027-chr19:55893629..55896601,2	MCF-7	breast:
9	chr19:55854922..55862011-chr19:55892906..55898744,13	MCF-7	breast:
10	chr19:55763551..55774813-chr19:55891413..55900376,23	K562	blood:
11	chr19:55893657..55895479-chr19:55950087..55951998,2	MCF-7	breast:
12	chr19:55790016..55797764-chr19:55893451..55899813,15	MCF-7	breast:
13	chr19:55848915..55854876-chr19:55892600..55899757,13	MCF-7	breast:
14	chr19:55669654..55671920-chr19:55893818..55896729,2	MCF-7	breast:
15	chr19:55723904..55730206-chr19:55894141..55899052,9	MCF-7	breast:
16	chr19:55863669..55866367-chr19:55893657..55895581,3	MCF-7	breast:
17	chr19:55808885..55818962-chr19:55893792..55900928,16	MCF-7	breast:
18	chr19:55847613..55856135-chr19:55893756..55900268,15	K562	blood:

No data

Variant related genes	Relation type
ENSG00000269275	TF binding region
RPL28	TF binding region
ENSG00000267577	Chromatin interaction
ENSG00000267649	Chromatin interaction
ENSG00000133265	Chromatin interaction
ENSG00000160471	Chromatin interaction
ENSG00000063241	Chromatin interaction
ENSG00000133247	Chromatin interaction
ENSG00000160469	Chromatin interaction
ENSG00000105048	Chromatin interaction
ENSG00000267531	Chromatin interaction
ENSG00000105063	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1816335	chr19:55683977-55901099	Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
2	nsv1065760	chr19:55721521-55929740	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
3	nsv912456	chr19:55725410-55925500	Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
4	nsv912457	chr19:55725410-56019597	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer 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	228 gene(s)	inside rSNPs	diseases
5	nsv432086	chr19:55807586-56050844	Weak transcription Bivalent Enhancer Genic enhancers Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking 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 miRNA target site	220 gene(s)	inside rSNPs	diseases
6	nsv912460	chr19:55814881-55897327	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
7	nsv912461	chr19:55845386-55897327	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
8	nsv470162	chr19:55845386-55902257	Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
9	nsv912462	chr19:55845386-55925500	Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	203 gene(s)	inside rSNPs	diseases
10	nsv912463	chr19:55845386-56004901	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	219 gene(s)	inside rSNPs	diseases
11	nsv912464	chr19:55850269-55921164	Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	203 gene(s)	inside rSNPs	diseases
12	nsv516199	chr19:55854313-55901099	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	95 gene(s)	inside rSNPs	diseases
13	nsv912465	chr19:55854313-55935184	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
14	nsv912470	chr19:55872591-55897170	Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	79 gene(s)	inside rSNPs	diseases
15	nsv912473	chr19:55874642-56145428	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
16	nsv544085	chr19:55875808-55911275	Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	97 gene(s)	inside rSNPs	diseases
17	nsv912476	chr19:55876747-55897327	Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	91 gene(s)	inside rSNPs	diseases
18	esv3354937	chr19:55894165-55896713	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	48 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:55881400-55894800	Weak transcription	Right Atrium	heart
2	chr19:55888800-55894600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr19:55889600-55894400	Weak transcription	Lung	lung
4	chr19:55889600-55894600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr19:55889600-55894600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr19:55889600-55894800	Weak transcription	Ovary	ovary
7	chr19:55889600-55894800	Weak transcription	Right Ventricle	heart
8	chr19:55889600-55894800	Weak transcription	NH-A	brain
9	chr19:55890600-55894600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr19:55891000-55894800	Weak transcription	HSMMtube	muscle
11	chr19:55891400-55894800	Weak transcription	Brain Angular Gyrus	brain
12	chr19:55892000-55894800	Weak transcription	HSMM	muscle
13	chr19:55893000-55894800	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr19:55893200-55894400	Enhancers	Pancreas	Pancrea
15	chr19:55893400-55894400	Enhancers	Stomach Mucosa	stomach
16	chr19:55893400-55894800	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr19:55893400-55894800	Enhancers	Gastric	stomach
18	chr19:55893600-55894400	ZNF genes & repeats	A549	lung
19	chr19:55893600-55894600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr19:55893600-55894600	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr19:55893600-55894600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr19:55893600-55894800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
23	chr19:55893600-55894800	Enhancers	Stomach Smooth Muscle	stomach
24	chr19:55893600-55894800	Flanking Active TSS	Hela-S3	cervix
25	chr19:55893600-55895000	Flanking Active TSS	Dnd41	blood
26	chr19:55893600-55895200	Enhancers	Fetal Brain Male	brain
27	chr19:55893600-55895200	Enhancers	Spleen	Spleen
28	chr19:55893800-55894400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr19:55893800-55894400	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr19:55893800-55894400	Enhancers	Fetal Brain Female	brain
31	chr19:55893800-55894600	Enhancers	Primary T cells fromperipheralblood	blood
32	chr19:55893800-55894600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr19:55893800-55894600	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr19:55893800-55894600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
35	chr19:55893800-55894600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr19:55893800-55894600	ZNF genes & repeats	Fetal Intestine Small	intestine
37	chr19:55894000-55894600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr19:55894000-55894600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr19:55894000-55894600	Enhancers	Brain Germinal Matrix	brain
40	chr19:55894000-55894600	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr19:55894000-55894800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr19:55894000-55894800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr19:55894000-55894800	Enhancers	Placenta	Placenta
44	chr19:55894200-55894400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
45	chr19:55894200-55894400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
46	chr19:55894200-55894400	Enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr19:55894200-55894400	Flanking Active TSS	Esophagus	oesophagus
48	chr19:55894200-55894400	Enhancers	Fetal Thymus	thymus
49	chr19:55894200-55894400	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr19:55894200-55894600	Enhancers	Primary neutrophils fromperipheralblood	blood

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