Variant report

Variant	rs11734153
Chromosome Location	chr4:119512158-119512159
allele	C/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	ATF1	chr4:119512070-119513121	K562	blood:	n/a	n/a
2	RFX5	chr4:119511877-119513411	SK-N-SH	brain:	n/a	chr4:119512788-119512803 chr4:119512551-119512560
3	ZNF384	chr4:119512107-119513049	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:119505891..119507633-chr4:119509359..119512309,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000260404	TF binding region

Extended variants
information (count: 22 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10004322	1.00[ASN][1000 genomes]
rs10022024	1.00[ASN][1000 genomes]
rs10031029	0.87[ASN][1000 genomes]
rs10857060	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12331454	0.97[ASN][1000 genomes]
rs13137401	1.00[ASN][1000 genomes]
rs2389780	1.00[ASN][1000 genomes]
rs35890030	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4001330	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs71610209	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs71610221	0.82[EUR][1000 genomes]
rs72676188	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7656990	1.00[ASN][1000 genomes]
rs7669896	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7689541	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519017	chr4:118828807-119771481	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv1002771	chr4:119125361-119571237	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	esv3355840	chr4:119296640-119774737	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv427693	chr4:119493919-119674742	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv980150	chr4:119499004-119514502	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv964088	chr4:119510579-119514502	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv980251	chr4:119510579-119563981	Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs11734153	RP11-384K6.6	cis	Esophagus Mucosa	GTEx
rs11734153	RP11-384K6.2	cis	Thyroid	GTEx
rs11734153	RP11-384K6.6	cis	Artery Tibial	GTEx
rs11734153	RP11-384K6.2	cis	Nerve Tibial	GTEx
rs11734153	RP11-384K6.6	cis	Adipose Subcutaneous	GTEx
rs11734153	RP11-384K6.2	cis	Artery Tibial	GTEx
rs11734153	RP11-384K6.2	cis	Whole Blood	GTEx
rs11734153	RP11-384K6.6	cis	Nerve Tibial	GTEx
rs11734153	RP11-384K6.2	cis	Skin Sun Exposed Lower leg	GTEx
rs11734153	RP11-384K6.6	cis	Thyroid	GTEx

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119506600-119512800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:119507200-119512400	Weak transcription	Hela-S3	cervix
3	chr4:119507200-119512600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:119507400-119512200	Weak transcription	Stomach Mucosa	stomach
5	chr4:119507400-119512400	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr4:119507800-119513200	Weak transcription	Spleen	Spleen
7	chr4:119508000-119512200	Weak transcription	K562	blood
8	chr4:119508000-119512400	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr4:119508000-119512400	Weak transcription	Fetal Muscle Trunk	muscle
10	chr4:119508000-119512400	Weak transcription	Ovary	ovary
11	chr4:119508000-119512600	Weak transcription	HSMM	muscle
12	chr4:119508200-119512400	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr4:119508800-119512400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr4:119509000-119512400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr4:119509400-119512200	Weak transcription	Liver	Liver
16	chr4:119510400-119512400	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr4:119511000-119512800	Weak transcription	Gastric	stomach
18	chr4:119511400-119512400	Enhancers	Brain Substantia Nigra	brain
19	chr4:119511600-119512400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr4:119511800-119512200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr4:119511800-119512400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr4:119512000-119512200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr4:119512000-119512200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr4:119512000-119512200	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr4:119512000-119512200	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr4:119512000-119512200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr4:119512000-119512200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr4:119512000-119512200	Enhancers	Adipose Nuclei	Adipose
29	chr4:119512000-119512200	Enhancers	Dnd41	blood
30	chr4:119512000-119512400	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr4:119512000-119512400	Enhancers	Primary B cells from peripheral blood	blood
32	chr4:119512000-119512400	Enhancers	Primary T cells fromperipheralblood	blood
33	chr4:119512000-119512400	Enhancers	Primary hematopoietic stem cells	blood
34	chr4:119512000-119512400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr4:119512000-119512400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr4:119512000-119512400	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr4:119512000-119512400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr4:119512000-119512400	Enhancers	Fetal Intestine Large	intestine
39	chr4:119512000-119512400	Enhancers	Left Ventricle	heart
40	chr4:119512000-119512400	Enhancers	Pancreas	Pancrea
41	chr4:119512000-119512400	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr4:119512000-119512600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr4:119512000-119513400	Active TSS	Fetal Brain Male	brain
44	chr4:119512000-119513600	Active TSS	HepG2	liver

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