Variant report

Variant	rs2955787
Chromosome Location	chr15:31255167-31255168
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:31252830..31256274-chr15:31263661..31267030,3	K562	blood:
2	chr15:31242525..31245070-chr15:31253686..31255271,2	K562	blood:
3	chr15:31253352..31256135-chr15:31282312..31285268,3	K562	blood:
4	chr15:31253352..31256135-chr15:31282609..31285268,3	K562	blood:

Variant related genes	Relation type
ENSG00000166912	Chromatin interaction

Extended variants
information (count: 114 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:98)

rs_ID	r²[population]
rs10047979	0.85[CEU][hapmap];0.86[YRI][hapmap]
rs10163148	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1043251	0.85[CEU][hapmap]
rs10519726	0.83[CHB][hapmap]
rs11070678	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11070718	0.92[CHB][hapmap]
rs1133642	0.91[CHB][hapmap];0.85[ASN][1000 genomes]
rs11638295	0.92[CHB][hapmap]
rs11852466	0.83[CHB][hapmap]
rs12437580	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12439664	0.85[ASN][1000 genomes]
rs12441318	0.85[CHB][hapmap]
rs12442333	0.82[CHB][hapmap]
rs12443369	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12901022	0.92[CHB][hapmap]
rs12906480	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12914207	0.87[ASN][1000 genomes]
rs12914438	0.85[ASN][1000 genomes]
rs1404467	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1404468	0.92[CHB][hapmap];0.82[ASN][1000 genomes]
rs1404469	0.92[CHB][hapmap];0.85[ASN][1000 genomes]
rs1404470	0.85[ASN][1000 genomes]
rs1425291	0.85[ASN][1000 genomes]
rs1474381	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1474382	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1524876	0.92[CHB][hapmap];0.85[ASN][1000 genomes]
rs1524877	0.85[CEU][hapmap];0.86[YRI][hapmap]
rs16956341	0.83[CHB][hapmap]
rs16956362	0.83[CHB][hapmap]
rs16956366	0.83[CHB][hapmap]
rs16956414	0.83[CHB][hapmap]
rs16956422	0.83[CHB][hapmap]
rs1880499	0.92[CHB][hapmap];0.85[ASN][1000 genomes]
rs2042613	0.92[CHB][hapmap]
rs2113945	1.00[CHB][hapmap]
rs2113946	0.92[CHB][hapmap]
rs2140735	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2272218	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2272219	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2293319	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2293320	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2339048	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28564430	0.82[ASN][1000 genomes]
rs2860452	0.85[CEU][hapmap];0.82[YRI][hapmap]
rs28693590	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2873	0.92[CHB][hapmap]
rs2949569	0.92[CHB][hapmap]
rs2949570	0.92[CHB][hapmap]
rs2949572	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2949573	0.92[CHB][hapmap];0.82[ASN][1000 genomes]
rs2949575	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2949576	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2949577	0.92[CHB][hapmap];0.85[ASN][1000 genomes]
rs2949578	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2955778	0.86[CEU][hapmap];0.86[YRI][hapmap]
rs2955781	0.86[CEU][hapmap];0.87[YRI][hapmap]
rs2955783	0.92[CHB][hapmap];0.85[ASN][1000 genomes]
rs2955788	0.85[CEU][hapmap]
rs2955789	0.85[CEU][hapmap];0.82[YRI][hapmap]
rs2955790	0.92[CHB][hapmap]
rs2955791	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2955792	0.85[CEU][hapmap]
rs2955796	0.85[CHB][hapmap]
rs2959039	0.85[CHB][hapmap]
rs2959047	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2959049	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs2959050	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2959051	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3743231	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3743233	0.82[ASN][1000 genomes]
rs3784588	0.83[CHB][hapmap]
rs4344701	0.83[ASN][1000 genomes]
rs4779796	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4779797	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs565	0.85[CEU][hapmap]
rs6493352	0.85[CEU][hapmap]
rs6493358	0.83[CHB][hapmap]
rs71474640	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7161812	1.00[CHB][hapmap]
rs7164530	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7164939	0.83[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs7165798	0.92[CHB][hapmap]
rs7169064	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7170710	0.92[CHB][hapmap];0.85[ASN][1000 genomes]
rs7170772	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7175256	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7175951	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7176351	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7178375	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7178533	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7182143	0.92[CHB][hapmap]
rs7183880	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs798101	0.85[CHB][hapmap]
rs8040989	0.92[CHB][hapmap];0.80[ASN][1000 genomes]
rs8041717	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs871312	0.83[CHB][hapmap]
rs872843	0.83[CHB][hapmap]
rs9806159	1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427955	chr15:30467980-31273174	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv531138	chr15:30653877-31609679	Active TSS Weak transcription Enhancers Strong transcription 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 miRNA target site	96 gene(s)	inside rSNPs	diseases
3	nsv916936	chr15:30921917-31337510	Active TSS Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv525795	chr15:30936285-31324531	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS 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	35 gene(s)	inside rSNPs	diseases
5	nsv903831	chr15:30986051-31723279	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
6	nsv1046874	chr15:31008133-31294654	Enhancers Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
7	nsv1054147	chr15:31014507-31972706	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
8	nsv542306	chr15:31014507-31972706	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
9	nsv832951	chr15:31131239-31304469	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer 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	28 gene(s)	inside rSNPs	diseases
10	nsv1039037	chr15:31140415-31277268	Strong transcription ZNF genes & repeats Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
11	nsv542309	chr15:31140415-31277268	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
12	nsv1036018	chr15:31140415-31544888	Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
13	nsv521842	chr15:31140700-31272670	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
14	nsv903834	chr15:31179534-31293774	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
15	esv33507	chr15:31183324-31471023	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
16	nsv832952	chr15:31204426-31333998	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2955787	RP11-932O9.7	cis	Muscle Skeletal	GTEx

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31225400-31255800	Strong transcription	Fetal Intestine Large	intestine
2	chr15:31225800-31256000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr15:31226000-31255800	Strong transcription	Fetal Stomach	stomach
4	chr15:31226000-31258800	Strong transcription	Duodenum Mucosa	Duodenum
5	chr15:31226200-31269200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr15:31226400-31260800	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr15:31226600-31255200	Strong transcription	Duodenum Smooth Muscle	Duodenum
8	chr15:31227000-31269600	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr15:31227200-31255800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr15:31227200-31258800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
11	chr15:31228600-31258800	Strong transcription	Rectal Mucosa Donor 29	rectum
12	chr15:31229200-31261000	Strong transcription	Primary B cells from peripheral blood	blood
13	chr15:31230400-31258800	Strong transcription	Sigmoid Colon	Sigmoid Colon
14	chr15:31233400-31269200	Strong transcription	Liver	Liver
15	chr15:31237200-31269600	Strong transcription	Primary B cells from cord blood	blood
16	chr15:31238600-31255200	Strong transcription	Fetal Kidney	kidney
17	chr15:31242000-31282800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr15:31242400-31255800	Strong transcription	Fetal Intestine Small	intestine
19	chr15:31243200-31267600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr15:31245000-31276400	Weak transcription	Brain Germinal Matrix	brain
21	chr15:31247000-31270200	Weak transcription	K562	blood
22	chr15:31247400-31260600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr15:31247600-31261000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr15:31247800-31258800	Strong transcription	Stomach Smooth Muscle	stomach
25	chr15:31248200-31255200	Strong transcription	Rectal Mucosa Donor 31	rectum
26	chr15:31248800-31259800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr15:31248800-31283000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr15:31249000-31269600	Strong transcription	HUVEC	blood vessel
29	chr15:31249000-31270200	Weak transcription	Stomach Mucosa	stomach
30	chr15:31249000-31276000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr15:31250200-31282200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr15:31250800-31257800	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr15:31250800-31257800	Weak transcription	NHDF-Ad	bronchial
34	chr15:31250800-31261400	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr15:31250800-31270600	Weak transcription	Small Intestine	intestine
36	chr15:31250800-31282400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr15:31251200-31258000	Weak transcription	NHLF	lung
38	chr15:31251200-31272400	Weak transcription	Aorta	Aorta
39	chr15:31251200-31277200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr15:31251200-31282400	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr15:31251400-31256200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr15:31251400-31257200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr15:31251400-31257800	Weak transcription	Gastric	stomach
44	chr15:31251400-31258000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr15:31251400-31265800	Weak transcription	A549	lung
46	chr15:31251600-31282200	Weak transcription	Hela-S3	cervix
47	chr15:31252000-31256000	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr15:31252000-31257000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
49	chr15:31252000-31272200	Weak transcription	Spleen	Spleen
50	chr15:31252400-31255600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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