Variant report

Variant	rs6298
Chromosome Location	chr6:78172992-78172993
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10806098	0.96[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.94[TSI][hapmap];0.81[YRI][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12662392	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13192352	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2000292	0.84[EUR][1000 genomes]
rs4142329	0.91[CEU][hapmap];0.86[CHD][hapmap];0.86[GIH][hapmap];0.86[JPT][hapmap];0.89[MEX][hapmap];0.88[TSI][hapmap]
rs62416459	0.82[EUR][1000 genomes]
rs6296	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6916063	0.91[CEU][hapmap];0.86[CHB][hapmap];0.91[JPT][hapmap]
rs6920728	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017082	chr6:77585310-78258237	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv534282	chr6:77764575-78351994	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1034979	chr6:77781244-78426249	Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv538324	chr6:77781244-78426249	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1015307	chr6:77902559-78352291	Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1028259	chr6:78059491-78709871	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv538325	chr6:78059491-78709871	Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	esv2758062	chr6:78100020-78283042	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	esv2759445	chr6:78100020-78283042	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6298	IRAK1BP1	cis	parietal	SCAN

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:78169400-78174600	Active TSS	Aorta	Aorta
2	chr6:78171400-78173600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
3	chr6:78171400-78174400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr6:78171400-78174600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
5	chr6:78171400-78174600	Bivalent/Poised TSS	Brain Anterior Caudate	brain
6	chr6:78171600-78173000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr6:78171600-78174400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr6:78171600-78174600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
9	chr6:78171800-78173800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
10	chr6:78171800-78174200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
11	chr6:78171800-78174400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
12	chr6:78171800-78174400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
13	chr6:78171800-78174800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
14	chr6:78171800-78174800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
15	chr6:78172000-78173000	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr6:78172000-78173000	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr6:78172000-78174200	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr6:78172000-78174200	Active TSS	HUVEC	blood vessel
19	chr6:78172000-78174400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
20	chr6:78172200-78173000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
21	chr6:78172200-78173000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr6:78172200-78173000	Bivalent/Poised TSS	Monocytes-CD14+_RO01746	blood
23	chr6:78172200-78173200	Active TSS	A549	lung
24	chr6:78172200-78173400	Bivalent/Poised TSS	Colonic Mucosa	Colon
25	chr6:78172200-78173400	Bivalent/Poised TSS	NHDF-Ad	bronchial
26	chr6:78172200-78173600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
27	chr6:78172200-78173800	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr6:78172200-78173800	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
29	chr6:78172200-78174000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr6:78172200-78174200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
31	chr6:78172200-78174200	Bivalent Enhancer	Liver	Liver
32	chr6:78172200-78174200	Bivalent/Poised TSS	Left Ventricle	heart
33	chr6:78172200-78174200	Flanking Active TSS	Pancreas	Pancrea
34	chr6:78172200-78174200	Active TSS	NH-A	brain
35	chr6:78172200-78174400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr6:78172200-78174400	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
37	chr6:78172200-78174400	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr6:78172200-78174400	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
39	chr6:78172200-78174400	Bivalent/Poised TSS	Osteobl	bone
40	chr6:78172200-78174600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
41	chr6:78172400-78173000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
42	chr6:78172400-78173000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
43	chr6:78172400-78173000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr6:78172400-78173000	Flanking Active TSS	Gastric	stomach
45	chr6:78172400-78173200	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr6:78172400-78173200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
47	chr6:78172400-78173200	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr6:78172400-78173200	Flanking Bivalent TSS/Enh	Brain Substantia Nigra	brain
49	chr6:78172400-78173200	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
50	chr6:78172400-78173200	Bivalent/Poised TSS	HSMM	muscle

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