Variant report

Variant	rs6449161
Chromosome Location	chr4:15692954-15692955
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:15682774..15685413-chr4:15691736..15693825,4	K562	blood:
2	chr4:15681921..15686275-chr4:15691863..15696153,5	MCF-7	breast:
3	chr4:15656248..15659090-chr4:15690576..15694462,3	MCF-7	breast:
4	chr4:15690253..15693117-chr4:15724608..15727161,2	MCF-7	breast:
5	chr4:15690443..15693747-chr4:15694264..15697002,4	MCF-7	breast:
6	chr4:15691991..15693828-chr4:15939773..15942027,2	MCF-7	breast:
7	chr4:15682706..15688918-chr4:15689234..15693729,6	K562	blood:
8	chr4:15685927..15688320-chr4:15691706..15694352,2	K562	blood:
9	chr4:15680881..15687102-chr4:15687861..15693031,11	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000118564	Chromatin interaction
ENSG00000237765	Chromatin interaction
ENSG00000137440	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10008376	0.93[ASW][hapmap];0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.86[MEX][hapmap];0.90[MKK][hapmap];0.85[YRI][hapmap];0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10008975	1.00[ASW][hapmap];0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.86[MEX][hapmap];0.92[MKK][hapmap];0.80[TSI][hapmap];0.85[YRI][hapmap];0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10214	1.00[ASW][hapmap];0.82[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.81[MEX][hapmap];0.92[MKK][hapmap];0.82[TSI][hapmap];0.81[YRI][hapmap];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10939621	0.85[JPT][hapmap]
rs12499412	0.84[AFR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12500587	0.82[CEU][hapmap]
rs12500770	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs12644655	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12649803	0.86[JPT][hapmap]
rs12651550	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13120905	0.84[AFR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13147590	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1789	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4270584	1.00[ASW][hapmap];0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.86[MEX][hapmap];0.92[MKK][hapmap];0.85[YRI][hapmap];0.86[AFR][1000 genomes];0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4333182	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4358397	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4453929	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4470622	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4557256	0.86[CHB][hapmap];0.95[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.90[MKK][hapmap];0.87[AFR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4616746	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4631041	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4698402	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4698404	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4698407	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4698409	0.80[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6414765	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6414767	0.86[AFR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6414768	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6449146	0.86[JPT][hapmap]
rs6449147	0.86[JPT][hapmap]
rs6850422	1.00[ASW][hapmap];0.81[CEU][hapmap];0.90[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];1.00[LWK][hapmap];0.86[MEX][hapmap];0.93[MKK][hapmap];0.88[YRI][hapmap];0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7438356	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.80[TSI][hapmap];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs759212	0.86[JPT][hapmap]
rs7662032	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7685083	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.86[MEX][hapmap];0.90[MKK][hapmap];0.80[TSI][hapmap];0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7687003	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7690362	0.81[EUR][1000 genomes]
rs7696127	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7696938	0.84[CEU][hapmap]
rs7697314	0.86[JPT][hapmap]
rs8180240	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9996452	0.86[JPT][hapmap]
rs9997068	0.86[AFR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3448986	chr4:14928802-15805558	Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	esv2757923	chr4:15444617-15749520	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	esv2759227	chr4:15444617-15749520	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers 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 target site	23 gene(s)	inside rSNPs	diseases
4	nsv428439	chr4:15556961-15749520	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer 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	22 gene(s)	inside rSNPs	diseases
5	nsv1012988	chr4:15597510-16091527	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs6449161	C1QTNF7	cis	parietal	SCAN
rs6449161	LOC285550	cis	multi-tissue	Pritchard
rs6449161	FBXL5	cis	multi-tissue	Pritchard
rs6449161	CC2D2A	cis	parietal	SCAN
rs6449161	FAM200B	cis	parietal	SCAN

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:15684000-15697000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:15684000-15704400	Weak transcription	Left Ventricle	heart
3	chr4:15684800-15693600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr4:15684800-15694200	Weak transcription	Fetal Brain Male	brain
5	chr4:15684800-15704400	Weak transcription	Aorta	Aorta
6	chr4:15685000-15693000	Weak transcription	Psoas Muscle	Psoas
7	chr4:15685000-15695800	Weak transcription	Stomach Mucosa	stomach
8	chr4:15686600-15704400	Weak transcription	Thymus	Thymus
9	chr4:15687200-15701200	Weak transcription	Fetal Intestine Small	intestine
10	chr4:15687600-15696800	Weak transcription	Fetal Stomach	stomach
11	chr4:15687600-15697000	Weak transcription	Esophagus	oesophagus
12	chr4:15688400-15697200	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr4:15688400-15703800	Weak transcription	Fetal Kidney	kidney
14	chr4:15688600-15695600	Weak transcription	Fetal Lung	lung
15	chr4:15689400-15693000	Weak transcription	K562	blood
16	chr4:15689400-15693600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr4:15689600-15697200	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr4:15690000-15693000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr4:15690000-15693400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr4:15690200-15695000	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr4:15690400-15694200	Enhancers	Adipose Nuclei	Adipose
22	chr4:15690600-15693600	Weak transcription	Primary B cells from peripheral blood	blood
23	chr4:15690600-15694600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:15690600-15697800	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr4:15690800-15693200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr4:15690800-15693600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
27	chr4:15690800-15693800	Enhancers	HSMMtube	muscle
28	chr4:15690800-15694000	Enhancers	HMEC	breast
29	chr4:15690800-15694000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
30	chr4:15691000-15693200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr4:15691000-15693800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr4:15691000-15694400	Enhancers	Muscle Satellite Cultured Cells	--
33	chr4:15691000-15697000	Weak transcription	Duodenum Mucosa	Duodenum
34	chr4:15691000-15698600	Weak transcription	Dnd41	blood
35	chr4:15691200-15693000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr4:15691200-15693000	Weak transcription	Fetal Muscle Trunk	muscle
37	chr4:15691200-15693200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:15691200-15693200	Enhancers	Hela-S3	cervix
39	chr4:15691200-15694000	Enhancers	HUVEC	blood vessel
40	chr4:15691400-15693200	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr4:15691400-15693200	Enhancers	Brain Substantia Nigra	brain
42	chr4:15691400-15693400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr4:15691400-15693600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:15691400-15694200	Weak transcription	Fetal Thymus	thymus
45	chr4:15691400-15694600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr4:15691400-15694800	Enhancers	Osteobl	bone
47	chr4:15691400-15696000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr4:15691400-15697200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr4:15691400-15698400	Weak transcription	Primary T cells from cord blood	blood
50	chr4:15691400-15698400	Weak transcription	Liver	Liver

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