Variant report

Variant	rs1796029
Chromosome Location	chr2:97629250-97629251
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:97533938..97536745-chr2:97629223..97631782,3	MCF-7	breast:
2	chr2:97623151..97625255-chr2:97629201..97631510,2	MCF-7	breast:
3	chr2:97523891..97526324-chr2:97628583..97631770,4	MCF-7	breast:
4	chr2:97621466..97624037-chr2:97629014..97631871,2	K562	blood:
5	chr2:97498723..97500486-chr2:97628918..97630567,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000168758	Chromatin interaction
ENSG00000252845	Chromatin interaction

Extended variants
information (count: 80 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10202644	0.95[CHB][hapmap];0.85[JPT][hapmap];0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1257000	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1257008	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1257009	1.00[CEU][hapmap];0.94[CHB][hapmap];0.85[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1257011	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1257012	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1257015	1.00[CEU][hapmap];0.95[CHB][hapmap];0.85[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1257016	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1257017	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1257018	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1257019	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1257020	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1257027	1.00[CEU][hapmap];0.95[CHB][hapmap];0.85[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1257028	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1257029	0.91[CEU][hapmap];0.87[CHB][hapmap];0.85[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1257114	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1268682	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12717787	0.92[CEU][hapmap];0.96[CHB][hapmap];0.86[JPT][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13016654	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs13021723	0.96[CHB][hapmap];0.86[JPT][hapmap];0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1623881	0.95[CHB][hapmap];0.85[JPT][hapmap];0.90[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1624844	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1730106	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1730111	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1730119	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1730120	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1730122	1.00[CEU][hapmap];0.95[CHB][hapmap];0.85[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1730123	0.92[CEU][hapmap];0.88[CHB][hapmap];0.86[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1730124	0.92[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1730126	0.96[CHB][hapmap];0.86[JPT][hapmap];0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1730128	0.96[CHB][hapmap];0.86[JPT][hapmap];0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1730129	0.95[CHB][hapmap];0.84[JPT][hapmap];0.87[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1730130	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1730131	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1796027	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1796028	0.95[CHB][hapmap];0.85[JPT][hapmap];0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1796032	0.91[CEU][hapmap];0.87[CHB][hapmap];0.85[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1796038	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1796041	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1796044	0.96[CHB][hapmap];0.86[JPT][hapmap];0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1796045	0.95[CHB][hapmap];0.85[JPT][hapmap];0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1796046	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1796047	0.96[CHB][hapmap];0.86[JPT][hapmap];0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1796049	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2678385	0.83[YRI][hapmap]
rs2707304	0.92[CEU][hapmap];0.96[CHB][hapmap];0.86[JPT][hapmap]
rs34434950	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4263148	0.92[CEU][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4366944	0.92[CEU][hapmap];0.90[CHB][hapmap];0.84[JPT][hapmap];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4586672	0.91[CEU][hapmap];0.87[CHB][hapmap];0.85[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4907251	1.00[YRI][hapmap]
rs6576992	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6576993	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6576994	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6576995	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6576997	0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6576999	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6707255	1.00[YRI][hapmap];0.90[AMR][1000 genomes]
rs6714860	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6715329	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6725927	0.83[CHB][hapmap];0.81[AMR][1000 genomes]
rs6757916	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7569434	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7584318	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7584335	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7593493	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7597743	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933671	chr2:96739308-97652262	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
2	nsv1000780	chr2:96740430-97671395	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
3	nsv535826	chr2:96740430-97671395	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
4	nsv874677	chr2:96756547-97717345	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
5	nsv1001204	chr2:96766559-97728507	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
6	nsv535827	chr2:96766559-97728507	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh 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	162 gene(s)	inside rSNPs	diseases
7	nsv874680	chr2:97309574-97678319	Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
8	nsv526313	chr2:97333492-97660619	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
9	nsv582497	chr2:97569305-97715154	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
10	esv2757819	chr2:97571109-98336507	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	64 gene(s)	inside rSNPs	diseases
11	esv2759077	chr2:97571109-98336507	Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	64 gene(s)	inside rSNPs	diseases
12	nsv1001432	chr2:97591069-97671395	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
13	esv32727	chr2:97616488-97643975	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:97620400-97629400	Weak transcription	Fetal Intestine Large	intestine
2	chr2:97620800-97629600	Weak transcription	Fetal Intestine Small	intestine
3	chr2:97620800-97643600	Weak transcription	Right Atrium	heart
4	chr2:97624200-97629800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr2:97625400-97629600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:97625600-97630600	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr2:97625600-97631200	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr2:97625600-97634200	Enhancers	Primary T cells fromperipheralblood	blood
9	chr2:97626000-97629800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr2:97626000-97631000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr2:97626200-97630400	Enhancers	Dnd41	blood
12	chr2:97626200-97635800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr2:97626400-97629600	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr2:97626400-97629600	Enhancers	GM12878-XiMat	blood
15	chr2:97626400-97630200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr2:97626600-97629800	Enhancers	Fetal Thymus	thymus
17	chr2:97626600-97631800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr2:97626600-97631800	Weak transcription	Brain Substantia Nigra	brain
19	chr2:97626800-97629400	Enhancers	Primary B cells from cord blood	blood
20	chr2:97626800-97633000	Weak transcription	Stomach Smooth Muscle	stomach
21	chr2:97627200-97630000	Enhancers	Thymus	Thymus
22	chr2:97627400-97629400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
23	chr2:97627400-97629400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
24	chr2:97627600-97630000	Weak transcription	Colonic Mucosa	Colon
25	chr2:97627800-97629400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr2:97628200-97629400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr2:97628400-97629400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
28	chr2:97628400-97629400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
29	chr2:97628400-97629600	Enhancers	HMEC	breast
30	chr2:97628800-97629600	Enhancers	Fetal Stomach	stomach
31	chr2:97628800-97630600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr2:97628800-97631200	Enhancers	Primary T cells from cord blood	blood
33	chr2:97628800-97632200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr2:97629000-97630600	Enhancers	Duodenum Mucosa	Duodenum
35	chr2:97629000-97631400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr2:97629200-97629400	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr2:97629200-97629400	Enhancers	Spleen	Spleen
38	chr2:97629200-97629400	Flanking Bivalent TSS/Enh	HepG2	liver
39	chr2:97629200-97629400	Flanking Active TSS	NHEK	skin
40	chr2:97629200-97629600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
41	chr2:97629200-97629600	Enhancers	Esophagus	oesophagus
42	chr2:97629200-97630200	Weak transcription	Primary hematopoietic stem cells	blood
43	chr2:97629200-97630400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
44	chr2:97629200-97630800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr2:97629200-97630800	Enhancers	Rectal Mucosa Donor 29	rectum
46	chr2:97629200-97633400	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr2:97629200-97634200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links