Variant report

Variant	rs4590193
Chromosome Location	chr5:177564346-177564347
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:13)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:13 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr5:177563924-177564377	GM12878	blood:	n/a	n/a
2	POLR2A	chr5:177563344-177564761	Hela-S3	cervix:	n/a	n/a
3	POLR2A	chr5:177563701-177564361	K562	blood:	n/a	n/a
4	POLR2A	chr5:177563930-177577112	K562	blood:	n/a	n/a
5	POLR2A	chr5:177564112-177564357	GM12892	blood:	n/a	n/a
6	POLR2A	chr5:177563796-177564372	GM12892	blood:	n/a	n/a
7	POLR2A	chr5:177564022-177564365	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr5:177562825-177564484	K562	blood:	n/a	n/a
9	POLR2A	chr5:177563501-177564568	K562	blood:	n/a	n/a
10	POLR2A	chr5:177563771-177564971	MCF10A-Er-Src	breast:	n/a	n/a
11	POLR2A	chr5:177563836-177564347	GM12892	blood:	n/a	n/a
12	POLR2A	chr5:177561918-177566392	K562	blood:	n/a	n/a
13	POLR2A	chr5:177563275-177565346	SK-N-MC	brain:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr5:177560352..177564718-chr5:177565737..177570754,8	K562	blood:
2	chr5:177541179..177543567-chr5:177562431..177564513,2	K562	blood:
3	chr5:177554586..177557949-chr5:177561501..177564806,6	K562	blood:

No data

Variant related genes	Relation type
RMND5B	TF binding region
ENSG00000145916	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10036388	0.88[CHB][hapmap]
rs10903275	0.81[CHB][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs11743865	0.81[AFR][1000 genomes]
rs17080239	0.80[CHB][hapmap];1.00[JPT][hapmap];0.94[MKK][hapmap]
rs3812082	0.93[ASN][1000 genomes]
rs6601211	0.81[CHB][hapmap]
rs7380422	0.84[ASN][1000 genomes]
rs7446073	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030383	chr5:177310325-177571254	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
2	nsv948342	chr5:177384542-178168737	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	141 gene(s)	inside rSNPs	diseases
3	nsv1021198	chr5:177386267-177611648	Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv1029398	chr5:177502106-178070654	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	136 gene(s)	inside rSNPs	diseases
5	nsv462567	chr5:177505021-177572927	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
6	nsv471058	chr5:177505021-177572927	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	nsv600392	chr5:177505021-177572927	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	nsv1019404	chr5:177507080-177859089	Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	126 gene(s)	inside rSNPs	diseases
9	nsv883190	chr5:177532201-177620189	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
10	nsv883192	chr5:177535370-177564346	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
11	nsv600394	chr5:177549491-177608195	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 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	chr5:177558800-177569600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr5:177558800-177576800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr5:177559000-177565000	Weak transcription	Brain Angular Gyrus	brain
4	chr5:177559000-177569000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr5:177559000-177569200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr5:177559000-177569200	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr5:177559000-177569200	Weak transcription	Gastric	stomach
8	chr5:177559000-177569200	Weak transcription	HSMM	muscle
9	chr5:177559000-177569400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr5:177559000-177569600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr5:177559000-177569800	Weak transcription	HUVEC	blood vessel
12	chr5:177559000-177569800	Weak transcription	NHDF-Ad	bronchial
13	chr5:177559000-177570600	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr5:177559000-177572800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr5:177559000-177572800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr5:177559000-177574000	Weak transcription	Small Intestine	intestine
17	chr5:177559000-177580000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr5:177559000-177580000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr5:177559200-177565000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr5:177559200-177565000	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr5:177559200-177568800	Weak transcription	HSMMtube	muscle
22	chr5:177559200-177569600	Weak transcription	HMEC	breast
23	chr5:177559200-177569800	Weak transcription	Colon Smooth Muscle	Colon
24	chr5:177559200-177570400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr5:177559200-177573000	Weak transcription	Psoas Muscle	Psoas
26	chr5:177559200-177573200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr5:177559200-177579800	Weak transcription	Right Atrium	heart
28	chr5:177559400-177570400	Weak transcription	Fetal Heart	heart
29	chr5:177559600-177567000	Weak transcription	Fetal Kidney	kidney
30	chr5:177559600-177569000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr5:177559600-177569400	Weak transcription	Hela-S3	cervix
32	chr5:177559600-177569800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr5:177559800-177577600	Weak transcription	Fetal Brain Male	brain
34	chr5:177560200-177566000	Strong transcription	Brain Germinal Matrix	brain
35	chr5:177560200-177568800	Strong transcription	Fetal Muscle Leg	muscle
36	chr5:177560200-177579400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr5:177560200-177579600	Strong transcription	HUES64 Cell Line	embryonic stem cell
38	chr5:177560200-177579800	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr5:177560400-177566000	Strong transcription	H9 Cell Line	embryonic stem cell
40	chr5:177560400-177578400	Strong transcription	Primary monocytes fromperipheralblood	blood
41	chr5:177560400-177578400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr5:177560400-177578600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr5:177560600-177569200	Strong transcription	Fetal Stomach	stomach
44	chr5:177560600-177579400	Strong transcription	Fetal Intestine Small	intestine
45	chr5:177560800-177564400	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr5:177560800-177565000	Strong transcription	K562	blood
47	chr5:177560800-177565400	Strong transcription	Fetal Brain Female	brain
48	chr5:177560800-177565800	Strong transcription	Skeletal Muscle Male	skeletal muscle
49	chr5:177560800-177566000	Strong transcription	Dnd41	blood
50	chr5:177560800-177567800	Strong transcription	Stomach Smooth Muscle	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links