Variant report

Variant	rs7170742
Chromosome Location	chr15:57239070-57239071
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:57210198..57214861-chr15:57238728..57241582,5	K562	blood:
2	chr15:57222920..57225645-chr15:57236445..57240161,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000137871	Chromatin interaction
ENSG00000140262	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1430821	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1542508	1.00[AMR][1000 genomes]
rs1642932	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1642938	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1652734	0.94[ASN][1000 genomes]
rs1652735	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1652736	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1657925	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2116064	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs213145	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs213146	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs213147	0.91[EUR][1000 genomes]
rs213157	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs213158	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs213159	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs213161	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs213169	0.80[AFR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2566843	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2576928	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2585084	1.00[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs2585117	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2585118	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4494480	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs56235870	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56683633	1.00[AMR][1000 genomes]
rs56804967	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57344548	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57452003	1.00[ASN][1000 genomes]
rs57813422	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57849686	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57968080	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58388376	1.00[AMR][1000 genomes]
rs59313491	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60268394	1.00[ASN][1000 genomes]
rs604191	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7161894	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7162421	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7175983	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7180911	1.00[AMR][1000 genomes]
rs73411246	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73413325	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73413333	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73413352	1.00[AMR][1000 genomes]
rs73413365	1.00[AMR][1000 genomes]
rs74018446	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74018485	1.00[AMR][1000 genomes]
rs8025829	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8037469	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8040423	1.00[ASN][1000 genomes]
rs8043301	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3422474	chr15:56867190-57244330	Strong transcription ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv1042486	chr15:57094598-57505992	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv542393	chr15:57115116-57341363	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription 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	21 gene(s)	inside rSNPs	diseases
4	nsv904250	chr15:57225766-57294085	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv1052052	chr15:57232111-57344561	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv542394	chr15:57232111-57344561	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:57212400-57256000	Weak transcription	Pancreas	Pancrea
2	chr15:57212600-57241000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr15:57213200-57256000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr15:57216400-57241800	Weak transcription	Fetal Brain Male	brain
5	chr15:57222600-57250200	Weak transcription	NH-A	brain
6	chr15:57222800-57240800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr15:57222800-57255000	Weak transcription	HMEC	breast
8	chr15:57223200-57240400	Weak transcription	Aorta	Aorta
9	chr15:57224600-57248600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr15:57225000-57239400	Weak transcription	Left Ventricle	heart
11	chr15:57225000-57244200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr15:57225000-57249000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr15:57226400-57242000	Weak transcription	HUVEC	blood vessel
14	chr15:57227000-57249800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr15:57227600-57260600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr15:57228000-57242400	Weak transcription	Fetal Intestine Small	intestine
17	chr15:57228200-57260600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr15:57229400-57255800	Weak transcription	Fetal Stomach	stomach
19	chr15:57231200-57240800	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr15:57232000-57256000	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr15:57232200-57240000	Weak transcription	NHLF	lung
22	chr15:57232600-57239200	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr15:57233000-57250200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr15:57233800-57239400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr15:57233800-57242000	Weak transcription	Ovary	ovary
26	chr15:57234200-57240800	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr15:57234400-57239200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr15:57234400-57249000	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr15:57235200-57239400	Weak transcription	Thymus	Thymus
30	chr15:57236000-57239800	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr15:57236200-57239200	Strong transcription	Fetal Thymus	thymus
32	chr15:57236200-57239800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr15:57236200-57240400	Weak transcription	Osteobl	bone
34	chr15:57236800-57249800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr15:57237000-57239400	Weak transcription	Brain Angular Gyrus	brain
36	chr15:57237000-57242000	Weak transcription	Brain Anterior Caudate	brain
37	chr15:57237200-57240400	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr15:57237200-57241800	Weak transcription	Fetal Heart	heart
39	chr15:57237600-57239600	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
40	chr15:57238200-57239600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr15:57238200-57240400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr15:57238200-57240600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr15:57238200-57240600	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr15:57238200-57240800	Weak transcription	Fetal Lung	lung
45	chr15:57238200-57240800	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr15:57238200-57249000	Weak transcription	HSMM	muscle
47	chr15:57238400-57239200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr15:57238400-57239600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr15:57238400-57239800	Weak transcription	Dnd41	blood
50	chr15:57238400-57240600	Weak transcription	Duodenum Smooth Muscle	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links