Variant report

Variant	rs7164674
Chromosome Location	chr15:51176716-51176717
allele	C/G
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:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:50977345..50980340-chr15:51175475..51179077,6	MCF-7	breast:
2	chr15:51173960..51175662-chr15:51175864..51177753,2	K562	blood:
3	chr15:51169436..51172227-chr15:51174524..51176801,3	MCF-7	breast:
4	chr15:51176099..51177660-chr15:51207519..51209221,2	K562	blood:
5	chr15:51169182..51171979-chr15:51176658..51178721,2	K562	blood:
6	chr15:51056324..51059354-chr15:51172484..51179110,10	MCF-7	breast:
7	chr15:51176297..51178705-chr15:51190226..51192825,2	MCF-7	breast:
8	chr15:50977263..50981217-chr15:51174338..51179159,10	MCF-7	breast:
9	chr15:50854287..50856205-chr15:51176623..51178248,2	MCF-7	breast:
10	chr15:51147815..51150812-chr15:51176681..51178652,2	MCF-7	breast:
11	chr15:51175847..51180099-chr15:51197260..51201772,6	K562	blood:
12	chr15:51166538..51169087-chr15:51176701..51178224,2	MCF-7	breast:
13	chr15:50976848..50980229-chr15:51173151..51177604,4	K562	blood:
14	chr15:51171742..51173328-chr15:51175943..51178564,2	MCF-7	breast:
15	chr15:50840397..50843164-chr15:51176115..51178210,2	MCF-7	breast:
16	chr15:51176620..51178151-chr15:51189371..51192335,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000243027	Chromatin interaction
ENSG00000138600	Chromatin interaction
ENSG00000092439	Chromatin interaction
ENSG00000081014	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs28384292	1.00[AMR][1000 genomes]
rs28469428	1.00[AMR][1000 genomes]
rs28485299	1.00[AMR][1000 genomes]
rs28535266	1.00[AMR][1000 genomes]
rs28538716	1.00[AMR][1000 genomes]
rs28564149	1.00[AMR][1000 genomes]
rs28763343	1.00[AMR][1000 genomes]
rs28817052	1.00[AMR][1000 genomes]
rs6493468	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7163999	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7166742	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7168505	1.00[AMR][1000 genomes]
rs7169184	1.00[AMR][1000 genomes]
rs7169696	1.00[AMR][1000 genomes]
rs7169746	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7170963	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7176764	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7177527	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7179077	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7179759	1.00[AMR][1000 genomes]
rs7183508	1.00[AMR][1000 genomes]
rs72740488	1.00[AMR][1000 genomes]
rs8026659	1.00[AMR][1000 genomes]
rs8029061	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8029899	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8033812	1.00[AMR][1000 genomes]
rs8038031	1.00[AMR][1000 genomes]
rs8038307	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043805	chr15:50715572-51208891	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	nsv542384	chr15:50715572-51208891	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers 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	82 gene(s)	inside rSNPs	diseases
3	nsv1047443	chr15:50744781-51647023	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
4	nsv457134	chr15:50770868-51184583	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
5	nsv471242	chr15:50770868-51184583	Genic enhancers ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
6	nsv569396	chr15:50770868-51184583	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
7	nsv457135	chr15:50770868-51189707	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
8	nsv569397	chr15:50770868-51189707	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers 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	54 gene(s)	inside rSNPs	diseases
9	nsv1047039	chr15:50782070-51187804	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
10	nsv542385	chr15:50782070-51187804	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
11	nsv457136	chr15:50789125-51294995	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
12	nsv569398	chr15:50789125-51294995	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
13	nsv1042372	chr15:50846461-51208891	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
14	nsv542386	chr15:50846461-51208891	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
15	nsv569399	chr15:50874964-51562198	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
16	nsv569400	chr15:50874964-51767265	ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
17	nsv529339	chr15:51048579-51270372	Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
18	nsv516168	chr15:51114437-51217361	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
19	nsv428636	chr15:51154834-51298044	Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51151200-51177400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr15:51169200-51178200	Weak transcription	Right Ventricle	heart
3	chr15:51169200-51180000	Weak transcription	Right Atrium	heart
4	chr15:51169400-51177400	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr15:51169600-51177400	Weak transcription	Brain Anterior Caudate	brain
6	chr15:51169600-51177400	Weak transcription	Fetal Muscle Leg	muscle
7	chr15:51169600-51177600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr15:51171000-51177800	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr15:51171600-51177400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr15:51171800-51177000	Weak transcription	Small Intestine	intestine
11	chr15:51172600-51177400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr15:51173000-51177400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr15:51173600-51177600	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr15:51173600-51177800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr15:51173800-51177400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr15:51174800-51176800	Weak transcription	HepG2	liver
17	chr15:51175800-51176800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr15:51175800-51177200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr15:51175800-51177400	Enhancers	Primary B cells from cord blood	blood
20	chr15:51175800-51177600	Enhancers	Primary hematopoietic stem cells	blood
21	chr15:51175800-51177600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr15:51175800-51177600	Enhancers	Liver	Liver
23	chr15:51175800-51177600	Enhancers	Placenta	Placenta
24	chr15:51175800-51177800	Enhancers	Dnd41	blood
25	chr15:51175800-51178200	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr15:51175800-51178200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr15:51175800-51178200	Flanking Active TSS	GM12878-XiMat	blood
28	chr15:51176000-51177400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr15:51176000-51177600	Enhancers	NHDF-Ad	bronchial
30	chr15:51176000-51177600	Enhancers	NHLF	lung
31	chr15:51176000-51178200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr15:51176000-51178200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr15:51176000-51178200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr15:51176000-51178600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
35	chr15:51176000-51179400	Enhancers	HUVEC	blood vessel
36	chr15:51176200-51176800	Flanking Active TSS	NHEK	skin
37	chr15:51176200-51177400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr15:51176200-51177400	Enhancers	Hela-S3	cervix
39	chr15:51176200-51177600	Enhancers	Adipose Nuclei	Adipose
40	chr15:51176200-51177600	Weak transcription	Spleen	Spleen
41	chr15:51176200-51177600	Flanking Active TSS	A549	lung
42	chr15:51176200-51178000	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr15:51176200-51178000	Enhancers	HSMMtube	muscle
44	chr15:51176200-51178200	Enhancers	Duodenum Mucosa	Duodenum
45	chr15:51176400-51176800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr15:51176400-51176800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr15:51176400-51177000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
48	chr15:51176400-51177400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr15:51176400-51177400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr15:51176400-51177400	Weak transcription	Primary B cells from peripheral blood	blood

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