Variant report

Variant	rs9380013
Chromosome Location	chr6:27688111-27688112
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	chr6:27686786..27690624-chr6:27717358..27721129,5	K562	blood:
2	chr6:27683083..27685640-chr6:27686917..27688772,2	MCF-7	breast:
3	chr6:27687163..27689366-chr6:27693364..27696456,4	K562	blood:
4	chr6:27687897..27691780-chr6:27691811..27694513,3	MCF-7	breast:
5	chr6:27665264..27666796-chr6:27688059..27690362,2	K562	blood:
6	chr6:27660493..27662208-chr6:27687324..27689056,2	MCF-7	breast:
7	chr6:27658926..27663446-chr6:27685398..27690588,6	K562	blood:
8	chr6:27684698..27689044-chr6:27689656..27693289,4	K562	blood:
9	chr6:27659151..27662876-chr6:27687364..27691190,4	K562	blood:

No data

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs1010261	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs12174918	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16867962	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs175597	1.00[CHB][hapmap]
rs17693877	1.00[CHB][hapmap];0.85[JPT][hapmap];0.83[YRI][hapmap];0.93[ASN][1000 genomes]
rs200481	0.80[ASN][1000 genomes]
rs200482	1.00[CHB][hapmap];0.80[ASN][1000 genomes]
rs200483	1.00[CHB][hapmap];0.82[ASN][1000 genomes]
rs200484	1.00[CHB][hapmap]
rs200485	1.00[CHB][hapmap];0.80[ASN][1000 genomes]
rs200490	1.00[CHB][hapmap]
rs200501	1.00[CHB][hapmap]
rs200948	1.00[CHB][hapmap]
rs200949	1.00[CHB][hapmap]
rs200953	1.00[CHB][hapmap]
rs200954	1.00[CHB][hapmap]
rs200965	1.00[CHB][hapmap]
rs200968	1.00[CHB][hapmap]
rs200973	1.00[CHB][hapmap]
rs200974	1.00[CHB][hapmap]
rs200975	1.00[CHB][hapmap]
rs200977	1.00[CHB][hapmap]
rs200981	1.00[CHB][hapmap]
rs200989	1.00[CHB][hapmap]
rs200990	1.00[CHB][hapmap]
rs200995	1.00[CHB][hapmap]
rs201002	1.00[CHB][hapmap]
rs2277104	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2394001	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2747054	1.00[CHB][hapmap]
rs36108923	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs370155	1.00[CHB][hapmap]
rs401763	1.00[CHB][hapmap]
rs4236045	1.00[ASN][1000 genomes]
rs4711158	0.88[AMR][1000 genomes]
rs4711161	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4713116	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4713117	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4713122	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4713124	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56870390	1.00[EUR][1000 genomes]
rs56911191	0.81[AMR][1000 genomes]
rs58322250	0.82[ASN][1000 genomes]
rs58727692	0.88[AMR][1000 genomes]
rs59015666	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7742887	0.82[ASN][1000 genomes]
rs7773905	0.82[ASN][1000 genomes]
rs9295738	0.86[ASN][1000 genomes]
rs9348779	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs9357041	1.00[CEU][hapmap];0.88[AMR][1000 genomes]
rs9357052	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs9368515	0.88[AMR][1000 genomes]
rs9368516	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes]
rs9368534	1.00[EUR][1000 genomes]
rs9368535	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs9368536	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[EUR][1000 genomes]
rs9379987	0.81[AMR][1000 genomes]
rs9379988	1.00[CEU][hapmap];0.88[AMR][1000 genomes]
rs9379989	1.00[CEU][hapmap];0.88[AMR][1000 genomes]
rs9379991	0.88[AMR][1000 genomes]
rs9379993	0.80[AMR][1000 genomes]
rs9379997	0.80[AMR][1000 genomes]
rs9380009	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9380014	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9380015	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9380018	0.80[ASN][1000 genomes]
rs9380026	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs9393825	0.88[AMR][1000 genomes]
rs9393829	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap]
rs9393845	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes]
rs9393854	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs9393855	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9393858	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9393862	1.00[EUR][1000 genomes]
rs9468183	0.88[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022797	chr6:27396961-27864277	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	390 gene(s)	inside rSNPs	diseases
2	nsv883510	chr6:27550712-27730064	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
3	nsv1023673	chr6:27570731-27688782	Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv830618	chr6:27593274-27789605	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
5	nsv1031337	chr6:27596676-27734884	Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
6	nsv601204	chr6:27655564-27689502	Strong transcription Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	nsv601205	chr6:27656255-27730064	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
8	esv3327708	chr6:27683503-27692934	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:27662800-27688400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr6:27662800-27688600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr6:27662800-27689000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr6:27663000-27688600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr6:27663200-27688400	Weak transcription	HMEC	breast
6	chr6:27671600-27688600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr6:27678800-27689000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:27679400-27688400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr6:27681200-27688200	Weak transcription	A549	lung
10	chr6:27681200-27688600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr6:27681200-27688600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr6:27681200-27688600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr6:27681200-27688800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:27681200-27688800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr6:27681600-27692200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr6:27681800-27688600	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr6:27682000-27688600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr6:27682400-27688400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr6:27682400-27688600	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr6:27682800-27688600	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr6:27687200-27688600	Enhancers	GM12878-XiMat	blood
22	chr6:27687200-27688600	Enhancers	HepG2	liver
23	chr6:27687400-27688400	Weak transcription	K562	blood
24	chr6:27687800-27688400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr6:27687800-27688400	Enhancers	NHEK	skin
26	chr6:27687800-27689800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links