Variant report

Variant	rs9677031
Chromosome Location	chr19:42755605-42755606
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:42754694-42755612	HL-60	blood:	n/a	n/a
2	POLR2A	chr19:42749868-42759399	HepG2	liver:	n/a	n/a
3	MAZ	chr19:42754805-42760905	IMR90	lung:	n/a	chr19:42759369-42759378 chr19:42755056-42755065 chr19:42756308-42756319 chr19:42758228-42758238 chr19:42759385-42759395 chr19:42758595-42758605 chr19:42757003-42757010 chr19:42757000-42757013 chr19:42757002-42757011 chr19:42760033-42760042 chr19:42757284-42757293 chr19:42757002-42757012 chr19:42759330-42759339 chr19:42759102-42759117 chr19:42758566-42758576 chr19:42758254-42758264 chr19:42757001-42757012 chr19:42759119-42759129 chr19:42759365-42759374
4	MXI1	chr19:42754690-42755757	IMR90	lung:	n/a	n/a
5	POLR2A	chr19:42746451-42758038	PFSK-1	brain:	n/a	n/a
6	POLR2A	chr19:42748210-42757941	K562	blood:	n/a	n/a
7	POLR2A	chr19:42745727-42755683	PFSK-1	brain:	n/a	n/a
8	POLR2A	chr19:42754993-42759794	K562	blood:	n/a	n/a
9	POLR2A	chr19:42749752-42759489	K562	blood:	n/a	n/a
10	POLR2A	chr19:42748038-42760873	SK-N-MC	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:42754219..42757685-chr19:42805206..42807524,5	MCF-7	breast:
2	chr19:42747132..42763787-chr19:42768368..42776785,67	MCF-7	breast:
3	chr19:42722598..42724600-chr19:42754486..42756039,2	MCF-7	breast:
4	chr19:42719999..42721511-chr19:42755568..42757404,2	MCF-7	breast:
5	chr19:42754290..42756701-chr19:42804402..42806386,2	K562	blood:
6	chr19:42744297..42761073-chr19:42776978..42802286,113	MCF-7	breast:
7	chr19:42755150..42756670-chr19:42837239..42839468,2	K562	blood:
8	chr19:42743599..42762610-chr19:42780302..42801550,102	MCF-7	breast:

Variant related genes	Relation type
ERF	TF binding region
ENSG00000079432	Chromatin interaction
ENSG00000167625	Chromatin interaction
ENSG00000079462	Chromatin interaction
ENSG00000188368	Chromatin interaction
ENSG00000160570	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs11673599	1.00[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv522854	chr19:42120283-42931004	Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv520239	chr19:42357455-42931004	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats 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
3	esv1805469	chr19:42367635-42798851	Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
4	nsv911782	chr19:42514712-42931004	Bivalent/Poised TSS Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
5	esv1794508	chr19:42580026-42791462	Strong transcription Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
6	nsv1055554	chr19:42619671-42821642	Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
7	nsv833833	chr19:42657276-42783122	Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
8	nsv526186	chr19:42676481-43203507	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
9	esv2422471	chr19:42733141-43669485	Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Strong transcription 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	70 gene(s)	inside rSNPs	diseases
10	nsv833834	chr19:42736444-42835027	Genic enhancers Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	42 gene(s)	inside rSNPs	diseases
11	nsv911784	chr19:42741124-42787664	Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	36 gene(s)	inside rSNPs	diseases
12	nsv911785	chr19:42741124-42917545	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
13	nsv911786	chr19:42744234-42797959	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	39 gene(s)	inside rSNPs	diseases
14	esv1802977	chr19:42754437-42789945	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42749000-42757000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr19:42749400-42755800	Enhancers	Fetal Heart	heart
3	chr19:42749400-42756200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr19:42751000-42756200	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr19:42752600-42757400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr19:42753600-42756400	Genic enhancers	Spleen	Spleen
7	chr19:42753800-42756000	Genic enhancers	HepG2	liver
8	chr19:42753800-42757000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr19:42753800-42757800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr19:42754000-42755800	Genic enhancers	Fetal Intestine Small	intestine
11	chr19:42754000-42755800	Genic enhancers	Fetal Stomach	stomach
12	chr19:42754000-42756000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr19:42754000-42756600	Enhancers	Left Ventricle	heart
14	chr19:42754200-42756200	Enhancers	Primary hematopoietic stem cells	blood
15	chr19:42754200-42756200	Enhancers	Fetal Brain Male	brain
16	chr19:42754200-42756800	Enhancers	Esophagus	oesophagus
17	chr19:42754200-42757200	Flanking Active TSS	Brain Hippocampus Middle	brain
18	chr19:42754200-42757400	Flanking Active TSS	Brain Germinal Matrix	brain
19	chr19:42754200-42757800	Transcr. at gene 5' and 3'	A549	lung
20	chr19:42754400-42755800	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr19:42754400-42755800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr19:42754400-42755800	Weak transcription	Fetal Kidney	kidney
23	chr19:42754400-42755800	Weak transcription	K562	blood
24	chr19:42754400-42755800	Enhancers	NHDF-Ad	bronchial
25	chr19:42754400-42756000	Enhancers	Ovary	ovary
26	chr19:42754400-42756200	Enhancers	Duodenum Mucosa	Duodenum
27	chr19:42754400-42756400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
28	chr19:42754400-42756600	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr19:42754400-42757000	Enhancers	Stomach Mucosa	stomach
30	chr19:42754400-42757200	Enhancers	Small Intestine	intestine
31	chr19:42754400-42757600	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr19:42754400-42757800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr19:42754400-42757800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr19:42754600-42755800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr19:42754600-42756200	Enhancers	Fetal Lung	lung
36	chr19:42754600-42756400	Flanking Active TSS	Stomach Smooth Muscle	stomach
37	chr19:42754600-42756400	Flanking Active TSS	HSMM	muscle
38	chr19:42754600-42756400	Transcr. at gene 5' and 3'	NHEK	skin
39	chr19:42754600-42756800	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr19:42754600-42756800	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr19:42754600-42757000	Enhancers	Placenta Amnion	Placenta Amnion
42	chr19:42754600-42757200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr19:42754600-42757200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr19:42754600-42757400	Flanking Active TSS	HMEC	breast
45	chr19:42754600-42757400	Flanking Active TSS	HUVEC	blood vessel
46	chr19:42754600-42757400	Flanking Active TSS	Osteobl	bone
47	chr19:42754600-42757800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr19:42754800-42755800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr19:42754800-42755800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr19:42754800-42755800	Enhancers	Duodenum Smooth Muscle	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links