Variant report

Variant	rs57237559
Chromosome Location	chr12:56476567-56476568
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:7 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr12:56476347-56476595	HepG2	liver:	n/a	n/a
2	POLR2A	chr12:56474287-56477511	HepG2	liver:	n/a	n/a
3	HEY1	chr12:56473273-56476974	HepG2	liver:	n/a	chr12:56475908-56475917 chr12:56473338-56473353 chr12:56474557-56474572
4	MYBL2	chr12:56476373-56476867	HepG2	liver:	n/a	n/a
5	POLR2A	chr12:56472840-56476753	HepG2	liver:	n/a	n/a
6	POLR2A	chr12:56473297-56476833	HepG2	liver:	n/a	n/a
7	POLR2A	chr12:56472708-56476783	HepG2	liver:	n/a	n/a

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:56471198..56482935-chr12:56506922..56516262,73	MCF-7	breast:
2	chr12:56475818..56478694-chr12:56550865..56553540,2	MCF-7	breast:
3	chr12:56471261..56483436-chr12:56494778..56506435,58	MCF-7	breast:
4	chr12:56473891..56477008-chr12:56583227..56585798,3	MCF-7	breast:
5	chr12:56401139..56403498-chr12:56475848..56478502,3	K562	blood:
6	chr12:56470948..56480058-chr12:56507665..56513741,17	K562	blood:
7	chr12:56475587..56477681-chr12:56479959..56483381,3	K562	blood:
8	chr12:56391052..56392634-chr12:56475715..56477967,2	MCF-7	breast:
9	chr12:56472197..56476808-chr12:56477200..56483474,8	K562	blood:

No data

Variant related genes	Relation type
ERBB3	TF binding region
ENSG00000196465	Chromatin interaction
ENSG00000092841	Chromatin interaction
ENSG00000135482	Chromatin interaction
ENSG00000123411	Chromatin interaction
ENSG00000257553	Chromatin interaction
ENSG00000229117	Chromatin interaction
ENSG00000065361	Chromatin interaction
ENSG00000139531	Chromatin interaction
ENSG00000258345	Chromatin interaction
ENSG00000257809	Chromatin interaction
ENSG00000258199	Chromatin interaction
ENSG00000139641	Chromatin interaction
ENSG00000139613	Chromatin interaction
ENSG00000170515	Chromatin interaction
ENSG00000257411	Chromatin interaction

Extended variants
information (count: 78 )
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]
rs11575221	1.00[EUR][1000 genomes]
rs11575236	1.00[EUR][1000 genomes]
rs11833164	1.00[EUR][1000 genomes]
rs11834873	1.00[EUR][1000 genomes]
rs11835018	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11835310	1.00[EUR][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]
rs1918496	1.00[EUR][1000 genomes]
rs2035948	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]
rs4301822	1.00[EUR][1000 genomes]
rs4417324	1.00[EUR][1000 genomes]
rs56696262	1.00[EUR][1000 genomes]
rs57785224	1.00[EUR][1000 genomes]
rs57990974	1.00[EUR][1000 genomes]
rs58349500	1.00[EUR][1000 genomes]
rs59398518	0.87[AFR][1000 genomes]
rs59794023	1.00[EUR][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	1.00[EUR][1000 genomes]
rs7300292	1.00[EUR][1000 genomes]
rs7304690	1.00[EUR][1000 genomes]
rs7309327	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7310292	1.00[EUR][1000 genomes]
rs73338377	1.00[EUR][1000 genomes]
rs73338385	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	1.00[EUR][1000 genomes]
rs7958958	1.00[EUR][1000 genomes]
rs7962107	1.00[EUR][1000 genomes]
rs7975405	1.00[EUR][1000 genomes]
rs7977692	1.00[EUR][1000 genomes]
rs7980782	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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	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
3	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

No data

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56472600-56477400	Active TSS	Brain Cingulate Gyrus	brain
2	chr12:56472800-56477400	Active TSS	Brain Substantia Nigra	brain
3	chr12:56473000-56477400	Active TSS	Brain Angular Gyrus	brain
4	chr12:56473200-56476800	Active TSS	Rectal Smooth Muscle	rectum
5	chr12:56474200-56477200	Active TSS	Brain Inferior Temporal Lobe	brain
6	chr12:56474400-56497200	Weak transcription	Right Atrium	heart
7	chr12:56474600-56477600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr12:56474600-56478800	Weak transcription	Left Ventricle	heart
9	chr12:56474800-56477600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr12:56474800-56477800	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
11	chr12:56474800-56479800	Weak transcription	HMEC	breast
12	chr12:56475000-56477200	Enhancers	K562	blood
13	chr12:56475000-56485600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr12:56475200-56476800	Active TSS	Duodenum Smooth Muscle	Duodenum
15	chr12:56475200-56478800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr12:56475400-56476600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr12:56475400-56477000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr12:56475600-56476600	Enhancers	A549	lung
19	chr12:56475600-56476800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr12:56475800-56476800	Active TSS	Fetal Muscle Trunk	muscle
21	chr12:56475800-56479200	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr12:56475800-56482400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr12:56476000-56476600	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr12:56476000-56476600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr12:56476000-56476800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr12:56476000-56476800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr12:56476000-56476800	Flanking Active TSS	Liver	Liver
28	chr12:56476000-56476800	Flanking Active TSS	Stomach Mucosa	stomach
29	chr12:56476000-56477000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
30	chr12:56476000-56477200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr12:56476000-56477400	Active TSS	Brain Anterior Caudate	brain
32	chr12:56476000-56477400	Weak transcription	NHEK	skin
33	chr12:56476000-56477600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr12:56476000-56477600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr12:56476000-56477800	Enhancers	Placenta	Placenta
36	chr12:56476000-56480000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr12:56476000-56481000	Weak transcription	Spleen	Spleen
38	chr12:56476000-56481800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr12:56476200-56476600	Enhancers	Lung	lung
40	chr12:56476200-56476600	Enhancers	Small Intestine	intestine
41	chr12:56476200-56476800	Transcr. at gene 5' and 3'	Rectal Mucosa Donor 29	rectum
42	chr12:56476200-56477400	Active TSS	Brain Hippocampus Middle	brain
43	chr12:56476200-56477400	Enhancers	Gastric	stomach
44	chr12:56476200-56477800	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr12:56476200-56478000	Transcr. at gene 5' and 3'	HepG2	liver
46	chr12:56476200-56497200	Weak transcription	Fetal Kidney	kidney
47	chr12:56476400-56476600	Flanking Active TSS	Colonic Mucosa	Colon
48	chr12:56476400-56476600	Transcr. at gene 5' and 3'	Fetal Muscle Leg	muscle
49	chr12:56476400-56476600	Flanking Active TSS	HSMMtube	muscle
50	chr12:56476400-56476800	Genic enhancers	HUES48 Cell Line	embryonic stem cell

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