Variant report

Variant	rs61398276
Chromosome Location	chr2:110367769-110367770
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SRF	chr2:110367018-110367870	HCT-116	colon:	n/a	chr2:110367562-110367575 chr2:110367562-110367575 chr2:110367560-110367578 chr2:110367564-110367573 chr2:110367564-110367578
2	CEBPB	chr2:110367067-110367894	HCT-116	colon:	n/a	chr2:110367552-110367563 chr2:110367551-110367562
3	TEAD4	chr2:110367021-110367773	SK-N-SH	brain:	n/a	n/a
4	GATA3	chr2:110366999-110367849	SK-N-SH	brain:	n/a	chr2:110367350-110367360 chr2:110367498-110367506
5	CEBPB	chr2:110367195-110367837	A549	lung:	n/a	chr2:110367552-110367563 chr2:110367551-110367562
6	ZNF384	chr2:110366677-110367799	GM12878	blood:	n/a	n/a
7	KAP1	chr2:110366989-110367780	U2OS	brain:	n/a	n/a
8	TCF12	chr2:110366851-110367779	SK-N-SH	brain:	n/a	n/a
9	SETDB1	chr2:110367031-110367876	U2OS	brain:	n/a	n/a
10	KAP1	chr2:110367116-110367785	HEK293	kidney:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:110365749..110368166-chr2:110372173..110374120,2	MCF-7	breast:

Variant related genes	Relation type
SOWAHC	TF binding region
ENSG00000230696	TF binding region

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10211151	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10211233	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10496431	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11265637	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12612457	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12619004	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12622443	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13385504	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2903696	0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs3886070	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56840594	0.92[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs58360057	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs58602175	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58958362	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs59185208	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs59328146	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60524887	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61354480	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61449947	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs717188	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72936489	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72938233	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72938234	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72938241	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72938253	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72938256	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72938267	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72938273	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72938290	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72940203	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs72940214	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs72940230	0.97[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72940234	0.97[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs72949195	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72949197	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72949199	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72949201	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs730988	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874777	chr2:109825516-110693317	Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv874780	chr2:110078080-110432886	Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking 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 miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1011456	chr2:110290958-110980402	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
4	nsv535861	chr2:110290958-110980402	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
5	nsv482469	chr2:110302488-110452580	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
6	nsv1009367	chr2:110349178-110863354	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
7	nsv829617	chr2:110359857-110380012	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:110324000-110370400	Weak transcription	Esophagus	oesophagus
2	chr2:110329000-110369000	Weak transcription	Ovary	ovary
3	chr2:110329200-110369400	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr2:110350400-110369200	Weak transcription	Fetal Stomach	stomach
5	chr2:110352600-110369200	Weak transcription	Fetal Brain Female	brain
6	chr2:110352800-110369400	Weak transcription	Brain Germinal Matrix	brain
7	chr2:110358800-110370200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr2:110359600-110369400	Weak transcription	Fetal Kidney	kidney
9	chr2:110359800-110369200	Weak transcription	Duodenum Mucosa	Duodenum
10	chr2:110359800-110370200	Weak transcription	Brain Cingulate Gyrus	brain
11	chr2:110359800-110370600	Weak transcription	Brain Angular Gyrus	brain
12	chr2:110360800-110369200	Weak transcription	Brain Hippocampus Middle	brain
13	chr2:110362400-110369200	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr2:110362400-110370200	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr2:110362600-110369000	Weak transcription	Psoas Muscle	Psoas
16	chr2:110362600-110370400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr2:110363800-110369000	Weak transcription	Placenta	Placenta
18	chr2:110363800-110369200	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr2:110363800-110369800	Weak transcription	Right Ventricle	heart
20	chr2:110364000-110369200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr2:110364400-110368000	Enhancers	Fetal Intestine Small	intestine
22	chr2:110364600-110369000	Weak transcription	Fetal Muscle Trunk	muscle
23	chr2:110364600-110369200	Weak transcription	Lung	lung
24	chr2:110364800-110367800	Active TSS	GM12878-XiMat	blood
25	chr2:110365200-110367800	Enhancers	Rectal Smooth Muscle	rectum
26	chr2:110365400-110367800	Enhancers	Fetal Intestine Large	intestine
27	chr2:110365600-110369400	Weak transcription	Stomach Smooth Muscle	stomach
28	chr2:110366000-110370400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr2:110366600-110367800	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr2:110366600-110367800	Flanking Active TSS	HUVEC	blood vessel
31	chr2:110366800-110367800	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr2:110366800-110367800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr2:110366800-110367800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr2:110366800-110368000	Enhancers	Liver	Liver
35	chr2:110367000-110369000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr2:110367000-110369400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr2:110367200-110368000	Genic enhancers	Fetal Lung	lung
38	chr2:110367200-110368400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr2:110367200-110369000	Weak transcription	Fetal Muscle Leg	muscle
40	chr2:110367200-110369200	Weak transcription	Left Ventricle	heart
41	chr2:110367200-110369200	Enhancers	HepG2	liver
42	chr2:110367200-110369400	Weak transcription	Brain Substantia Nigra	brain
43	chr2:110367200-110370000	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr2:110367400-110368600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr2:110367400-110369200	Weak transcription	Adipose Nuclei	Adipose
46	chr2:110367400-110369200	Weak transcription	Right Atrium	heart
47	chr2:110367600-110367800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr2:110367600-110367800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr2:110367600-110367800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr2:110367600-110367800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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