Variant report

Variant	rs337387
Chromosome Location	chr5:176947404-176947405
allele	A/C/G/T
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:5)
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	POLR2A	chr5:176947170-176947656	HepG2	liver:	n/a	n/a
2	POLR2A	chr5:176947366-176947755	K562	blood:	n/a	n/a
3	POLR2A	chr5:176946017-176949426	K562	blood:	n/a	n/a
4	POLR2A	chr5:176947283-176947682	U87	brain:	n/a	n/a
5	POLR2A	chr5:176946338-176947749	SK-N-MC	brain:	n/a	n/a
6	POLR2A	chr5:176947304-176947557	Hela-S3	cervix:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:176946975..176948535-chr5:177025631..177027200,2	MCF-7	breast:
2	chr5:176943414..176949809-chr5:177018256..177021226,8	MCF-7	breast:
3	chr5:176940745..176945959-chr5:176946691..176949947,5	MCF-7	breast:
4	chr5:176946421..176948274-chr5:176956521..176958507,2	MCF-7	breast:
5	chr5:176946312..176949197-chr5:177018379..177020484,2	K562	blood:

No data

Variant related genes	Relation type
DDX41	TF binding region
ENSG00000027847	Chromatin interaction
ENSG00000184840	Chromatin interaction
ENSG00000183258	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs28379386	1.00[AMR][1000 genomes]
rs28392715	1.00[AMR][1000 genomes]
rs28396982	1.00[AMR][1000 genomes]
rs28464438	1.00[AMR][1000 genomes]
rs28483466	1.00[AMR][1000 genomes]
rs28491669	1.00[AMR][1000 genomes]
rs28494836	1.00[AMR][1000 genomes]
rs28587302	1.00[AMR][1000 genomes]
rs28613023	1.00[AMR][1000 genomes]
rs28615269	1.00[AMR][1000 genomes]
rs28688891	1.00[AMR][1000 genomes]
rs28723606	1.00[AMR][1000 genomes]
rs335430	1.00[MKK][hapmap]
rs337369	1.00[MKK][hapmap]
rs337399	1.00[AMR][1000 genomes]
rs388783	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4976650	1.00[AMR][1000 genomes]
rs5013573	1.00[AMR][1000 genomes]
rs58021881	1.00[AMR][1000 genomes]
rs6600953	1.00[AMR][1000 genomes]
rs7444245	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916108	chr5:176688459-177078723	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
2	nsv883160	chr5:176740996-176952919	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Flanking Active TSS 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 miRNA target site	116 gene(s)	inside rSNPs	diseases
3	nsv1024444	chr5:176751921-177427715	Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	142 gene(s)	inside rSNPs	diseases
4	nsv883161	chr5:176754722-176958397	Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
5	nsv1020334	chr5:176779108-176954933	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
6	nsv883164	chr5:176780545-177003616	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
7	esv1816147	chr5:176787037-176966509	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
8	nsv883170	chr5:176824137-176952919	Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
9	nsv883175	chr5:176842474-176952919	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking 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 target site	103 gene(s)	inside rSNPs	diseases
10	nsv1028123	chr5:176861503-176949149	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer 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 target site	83 gene(s)	inside rSNPs	diseases
11	nsv537965	chr5:176861503-176949149	Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
12	nsv883177	chr5:176868358-177003616	Genic enhancers Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS 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 target site	84 gene(s)	inside rSNPs	diseases
13	esv2752795	chr5:176898619-177488281	Active TSS Strong transcription Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
14	nsv984570	chr5:176923414-176956300	Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
15	nsv5147	chr5:176938196-176983018	Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
16	esv1002656	chr5:176942755-176950441	Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	16 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	chr5:176944600-176948200	Weak transcription	Stomach Mucosa	stomach
2	chr5:176944800-176947600	Weak transcription	Small Intestine	intestine
3	chr5:176944800-176948200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr5:176944800-176951400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr5:176944800-176951600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr5:176944800-176952000	Weak transcription	Psoas Muscle	Psoas
7	chr5:176944800-176953000	Weak transcription	Fetal Brain Male	brain
8	chr5:176944800-176955000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr5:176944800-176963400	Weak transcription	Right Atrium	heart
10	chr5:176944800-176972800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr5:176945800-176948000	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr5:176946000-176948400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr5:176946000-176949000	Genic enhancers	Fetal Muscle Trunk	muscle
14	chr5:176946000-176949200	Genic enhancers	Primary T cells fromperipheralblood	blood
15	chr5:176946000-176949200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr5:176946000-176949200	Genic enhancers	Fetal Muscle Leg	muscle
17	chr5:176946000-176949400	Genic enhancers	HSMM	muscle
18	chr5:176946000-176949400	Genic enhancers	HSMMtube	muscle
19	chr5:176946000-176966200	Strong transcription	Primary neutrophils fromperipheralblood	blood
20	chr5:176946000-176968000	Strong transcription	Fetal Thymus	thymus
21	chr5:176946000-176970000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr5:176946200-176947800	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr5:176946200-176948000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr5:176946200-176948800	Genic enhancers	Skeletal Muscle Female	skeletal muscle
25	chr5:176946200-176949200	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr5:176946200-176949200	Strong transcription	NH-A	brain
27	chr5:176946200-176966200	Strong transcription	Fetal Brain Female	brain
28	chr5:176946200-176966200	Strong transcription	Fetal Intestine Small	intestine
29	chr5:176946200-176966800	Strong transcription	Fetal Stomach	stomach
30	chr5:176946200-176968000	Strong transcription	HUES6 Cell Line	embryonic stem cell
31	chr5:176946200-176969800	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr5:176946200-176970200	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chr5:176946200-176971000	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr5:176946400-176947600	Genic enhancers	Primary T helper cells fromperipheralblood	blood
35	chr5:176946400-176947600	Strong transcription	Brain Angular Gyrus	brain
36	chr5:176946400-176947600	Strong transcription	Brain Cingulate Gyrus	brain
37	chr5:176946400-176947600	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr5:176946400-176947800	Strong transcription	Brain Germinal Matrix	brain
39	chr5:176946400-176947800	Genic enhancers	Pancreas	Pancrea
40	chr5:176946400-176948400	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr5:176946400-176949000	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:176946400-176949200	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
43	chr5:176946400-176949200	Strong transcription	HepG2	liver
44	chr5:176946400-176949400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
45	chr5:176946400-176949400	Strong transcription	Duodenum Mucosa	Duodenum
46	chr5:176946400-176949600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr5:176946400-176949600	Strong transcription	Adipose Nuclei	Adipose
48	chr5:176946400-176957200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr5:176946400-176957800	Weak transcription	Fetal Heart	heart
50	chr5:176946400-176960200	Strong transcription	Aorta	Aorta

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