Variant report

Variant	rs56696262
Chromosome Location	chr12:56437917-56437918
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:16)
CpG islands
(count:0)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr12:56437517-56437955	GM12891	blood:	n/a	n/a
2	POLR2A	chr12:56437212-56438027	GM12892	blood:	n/a	n/a
3	POLR2A	chr12:56437127-56437921	PANC-1	pancreas:	n/a	n/a
4	POLR2A	chr12:56434834-56437950	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr12:56437183-56438215	GM12878	blood:	n/a	n/a
6	POLR2A	chr12:56437543-56437951	GM12891	blood:	n/a	n/a
7	POLR2A	chr12:56437240-56437974	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr12:56435527-56438039	PFSK-1	brain:	n/a	n/a
9	POLR2A	chr12:56437313-56437937	GM12892	blood:	n/a	n/a
10	POLR2A	chr12:56437633-56437917	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr12:56437114-56437980	PFSK-1	brain:	n/a	n/a
12	POLR2A	chr12:56437258-56437982	GM12892	blood:	n/a	n/a
13	POLR2A	chr12:56437092-56438132	GM12892	blood:	n/a	n/a
14	POLR2A	chr12:56435217-56438062	GM12878	blood:	n/a	n/a
15	POLR2A	chr12:56434982-56438055	SK-N-MC	brain:	n/a	n/a
16	HEY1	chr12:56437258-56437969	K562	blood:	n/a	n/a

No data

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:56435284..56441183-chr12:56476886..56481327,8	MCF-7	breast:
2	chr12:56221098..56224816-chr12:56434415..56439287,4	MCF-7	breast:
3	chr12:56433777..56443620-chr12:56502225..56514736,38	MCF-7	breast:
4	chr12:56320043..56321671-chr12:56437761..56440177,2	K562	blood:
5	chr12:56361700..56363713-chr12:56435997..56439581,3	MCF-7	breast:
6	chr12:56434034..56442629-chr12:56495467..56501430,16	MCF-7	breast:
7	chr12:56398217..56408038-chr12:56433794..56439966,15	K562	blood:
8	chr12:56119294..56126638-chr12:56434111..56441706,13	K562	blood:
9	chr12:56399898..56405642-chr12:56433175..56438589,7	K562	blood:
10	chr12:56363397..56371565-chr12:56432514..56437993,13	K562	blood:
11	chr12:56434164..56442518-chr12:56471459..56476251,24	MCF-7	breast:
12	chr12:56433873..56442113-chr12:56515349..56524351,14	K562	blood:
13	chr12:56431889..56443161-chr12:56494616..56500426,22	MCF-7	breast:
14	chr12:56434006..56443603-chr12:56507645..56514884,44	K562	blood:
15	chr12:56364726..56370308-chr12:56432734..56438629,15	K562	blood:
16	chr12:56434525..56442579-chr12:56469196..56475242,12	K562	blood:
17	chr12:56398950..56401873-chr12:56435306..56438317,7	MCF-7	breast:
18	chr12:56387772..56393921-chr12:56435042..56439277,13	MCF-7	breast:
19	chr12:56212308..56214556-chr12:56437662..56439315,2	MCF-7	breast:
20	chr12:56387084..56388858-chr12:56435939..56438743,3	K562	blood:
21	chr12:56364085..56366217-chr12:56434598..56438715,3	MCF-7	breast:
22	chr12:56434544..56443137-chr12:56494029..56505252,21	K562	blood:
23	chr12:56222083..56225232-chr12:56434095..56438071,8	MCF-7	breast:
24	chr12:56435618..56442072-chr12:56498381..56502676,10	K562	blood:
25	chr12:56320184..56328034-chr12:56431937..56442233,20	MCF-7	breast:
26	chr12:56410866..56413481-chr12:56435830..56438234,2	K562	blood:
27	chr12:56324080..56326028-chr12:56437410..56439658,2	K562	blood:
28	chr12:56433331..56443603-chr12:56506173..56514581,35	K562	blood:
29	chr12:56437312..56439402-chr12:56550075..56552742,2	MCF-7	breast:
30	chr12:56328007..56330555-chr12:56437110..56439690,2	MCF-7	breast:
31	chr12:56364512..56372057-chr12:56434108..56438254,11	MCF-7	breast:
32	chr12:56434525..56442579-chr12:56471686..56475431,10	K562	blood:
33	chr12:56388988..56394527-chr12:56433794..56442585,20	K562	blood:
34	chr12:56320016..56322694-chr12:56437432..56439265,2	K562	blood:
35	chr12:56386022..56392601-chr12:56434180..56439537,11	MCF-7	breast:
36	chr12:56389319..56393039-chr12:56433877..56439169,10	K562	blood:
37	chr12:56424810..56427622-chr12:56435520..56438792,3	K562	blood:
38	chr12:56437402..56439705-chr12:56691985..56693629,2	K562	blood:
39	chr12:56433908..56446518-chr12:56506026..56517165,55	MCF-7	breast:
40	chr12:56435851..56438826-chr5:118405352..118408278,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000257449	TF binding region
ENSG00000185664	Chromatin interaction
ENSG00000258345	Chromatin interaction
ENSG00000172869	Chromatin interaction
ENSG00000257553	Chromatin interaction
ENSG00000257390	Chromatin interaction
ENSG00000139531	Chromatin interaction
ENSG00000092841	Chromatin interaction
ENSG00000257411	Chromatin interaction
ENSG00000258317	Chromatin interaction
ENSG00000229117	Chromatin interaction
ENSG00000196465	Chromatin interaction
ENSG00000135404	Chromatin interaction
ENSG00000111540	Chromatin interaction
ENSG00000182796	Chromatin interaction
ENSG00000123374	Chromatin interaction
ENSG00000065357	Chromatin interaction
ENSG00000257384	Chromatin interaction
ENSG00000139641	Chromatin interaction
ENSG00000170515	Chromatin interaction
ENSG00000135392	Chromatin interaction
ENSG00000249494	Chromatin interaction
ENSG00000170473	Chromatin interaction
ENSG00000258056	Chromatin interaction
ENSG00000065361	Chromatin interaction
ENSG00000135482	Chromatin interaction
ENSG00000123411	Chromatin interaction
ENSG00000257809	Chromatin interaction

Extended variants
information (count: 81 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs1066130	1.00[EUR][1000 genomes]
rs1068188	1.00[EUR][1000 genomes]
rs1068189	1.00[EUR][1000 genomes]
rs1088050	1.00[EUR][1000 genomes]
rs1091527	1.00[EUR][1000 genomes]
rs11833164	1.00[EUR][1000 genomes]
rs11834873	1.00[EUR][1000 genomes]
rs11835018	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11835310	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11837075	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11837183	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1626158	1.00[EUR][1000 genomes]
rs1681071	1.00[EUR][1000 genomes]
rs1681079	1.00[EUR][1000 genomes]
rs1681080	1.00[EUR][1000 genomes]
rs1681088	1.00[EUR][1000 genomes]
rs1689508	1.00[EUR][1000 genomes]
rs1689509	1.00[EUR][1000 genomes]
rs1689517	1.00[EUR][1000 genomes]
rs1689518	1.00[EUR][1000 genomes]
rs1701701	1.00[EUR][1000 genomes]
rs1701702	1.00[EUR][1000 genomes]
rs1702872	1.00[EUR][1000 genomes]
rs17118461	1.00[EUR][1000 genomes]
rs2035948	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2625137	1.00[EUR][1000 genomes]
rs2625146	1.00[EUR][1000 genomes]
rs2629445	1.00[EUR][1000 genomes]
rs2640566	1.00[EUR][1000 genomes]
rs2640568	1.00[EUR][1000 genomes]
rs2658478	1.00[EUR][1000 genomes]
rs2661728	1.00[EUR][1000 genomes]
rs2661729	1.00[EUR][1000 genomes]
rs2934152	1.00[EUR][1000 genomes]
rs34323718	1.00[EUR][1000 genomes]
rs4417324	1.00[EUR][1000 genomes]
rs57237559	1.00[EUR][1000 genomes]
rs57785224	1.00[EUR][1000 genomes]
rs57990974	1.00[EUR][1000 genomes]
rs58349500	1.00[EUR][1000 genomes]
rs59794023	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60740107	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61733171	1.00[EUR][1000 genomes]
rs705697	1.00[EUR][1000 genomes]
rs705710	1.00[EUR][1000 genomes]
rs705712	1.00[EUR][1000 genomes]
rs705713	1.00[EUR][1000 genomes]
rs705714	1.00[EUR][1000 genomes]
rs705716	1.00[EUR][1000 genomes]
rs7298109	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7300292	1.00[EUR][1000 genomes]
rs7304690	1.00[EUR][1000 genomes]
rs7305481	1.00[AMR][1000 genomes]
rs7309327	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7310292	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73338377	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73338385	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs772459	1.00[EUR][1000 genomes]
rs772463	1.00[EUR][1000 genomes]
rs772464	1.00[EUR][1000 genomes]
rs772470	1.00[EUR][1000 genomes]
rs772474	1.00[EUR][1000 genomes]
rs772697	1.00[EUR][1000 genomes]
rs772698	1.00[EUR][1000 genomes]
rs772699	1.00[EUR][1000 genomes]
rs772701	1.00[EUR][1000 genomes]
rs772705	1.00[EUR][1000 genomes]
rs7954155	1.00[EUR][1000 genomes]
rs7957187	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7958958	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7962107	1.00[EUR][1000 genomes]
rs7970035	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs7975405	1.00[EUR][1000 genomes]
rs7980782	1.00[EUR][1000 genomes]
rs9738143	0.94[AFR][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	nsv1051961	chr12:56262220-56629427	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	284 gene(s)	inside rSNPs	diseases
2	nsv832424	chr12:56275226-56466917	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
3	nsv1043988	chr12:56348185-56534900	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	189 gene(s)	inside rSNPs	diseases
4	nsv832427	chr12:56392545-56512774	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
5	nsv1067906	chr12:56424828-56445284	Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
6	nsv973074	chr12:56435853-56437993	Active TSS Genic enhancers Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	56 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56436400-56438000	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
2	chr12:56436400-56438000	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
3	chr12:56436400-56438000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr12:56436600-56439400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr12:56437000-56438000	Strong transcription	Fetal Kidney	kidney
6	chr12:56437000-56438200	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:56437000-56439400	Strong transcription	Lung	lung
8	chr12:56437000-56439600	Strong transcription	Left Ventricle	heart
9	chr12:56437000-56440000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr12:56437000-56447200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr12:56437000-56472800	Weak transcription	Right Atrium	heart
12	chr12:56437200-56438200	Strong transcription	Ovary	ovary
13	chr12:56437200-56439400	Strong transcription	H9 Cell Line	embryonic stem cell
14	chr12:56437200-56439400	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr12:56437200-56439400	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr12:56437200-56439400	Strong transcription	Sigmoid Colon	Sigmoid Colon
17	chr12:56437200-56439600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr12:56437200-56439600	Strong transcription	Aorta	Aorta
19	chr12:56437200-56439600	Strong transcription	Colon Smooth Muscle	Colon
20	chr12:56437200-56439600	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr12:56437200-56439600	Strong transcription	Placenta Amnion	Placenta Amnion
22	chr12:56437200-56439800	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr12:56437200-56440800	Weak transcription	Fetal Heart	heart
24	chr12:56437400-56438000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
25	chr12:56437400-56438000	Genic enhancers	Rectal Mucosa Donor 31	rectum
26	chr12:56437400-56438000	Genic enhancers	HSMM	muscle
27	chr12:56437400-56438400	Weak transcription	Primary hematopoietic stem cells	blood
28	chr12:56437400-56438800	Strong transcription	Colonic Mucosa	Colon
29	chr12:56437400-56439200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr12:56437400-56439400	Strong transcription	Esophagus	oesophagus
31	chr12:56437400-56439600	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr12:56437400-56439800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr12:56437400-56439800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr12:56437400-56439800	Strong transcription	Brain Substantia Nigra	brain
35	chr12:56437400-56440400	Strong transcription	Primary B cells from cord blood	blood
36	chr12:56437400-56440600	Strong transcription	Brain Angular Gyrus	brain
37	chr12:56437400-56440800	Strong transcription	Fetal Stomach	stomach
38	chr12:56437600-56438000	Strong transcription	Fetal Brain Male	brain
39	chr12:56437600-56438000	Genic enhancers	Fetal Intestine Small	intestine
40	chr12:56437600-56438400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr12:56437600-56438600	Genic enhancers	Primary T helper cells PMA-I stimulated	--
42	chr12:56437600-56439200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr12:56437600-56439200	Strong transcription	Right Ventricle	heart
44	chr12:56437600-56439400	Strong transcription	Cortex derived primary cultured neurospheres	brain
45	chr12:56437600-56439400	Strong transcription	Duodenum Smooth Muscle	Duodenum
46	chr12:56437600-56439400	Strong transcription	Rectal Smooth Muscle	rectum
47	chr12:56437600-56439400	Strong transcription	Stomach Mucosa	stomach
48	chr12:56437600-56439600	Strong transcription	H1 Cell Line	embryonic stem cell
49	chr12:56437600-56439600	Strong transcription	Primary T cells fromperipheralblood	blood
50	chr12:56437600-56439600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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