Variant report

Variant	rs12318057
Chromosome Location	chr12:7791428-7791429
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:7737260..7737767-chr12:7791332..7791965,2	K562	blood:
2	chr12:7371937..7372879-chr12:7790988..7791868,4	MCF-7	breast:
3	chr12:7052361..7055203-chr12:7790062..7793106,4	MCF-7	breast:
4	chr12:7368777..7371276-chr12:7789054..7791793,2	MCF-7	breast:
5	chr12:7770562..7771464-chr12:7790685..7791995,3	MCF-7	breast:
6	chr12:7741041..7741545-chr12:7790979..7791656,2	MCF-7	breast:
7	chr12:7294785..7295337-chr12:7791387..7791900,2	K562	blood:
8	chr12:7770501..7771317-chr12:7790977..7791858,2	MCF-7	breast:
9	chr12:7527269..7527851-chr12:7790980..7791613,2	MCF-7	breast:
10	chr12:7052745..7054804-chr12:7789999..7792539,2	K562	blood:
11	chr12:7371612..7372892-chr12:7790964..7791617,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000272173	Chromatin interaction
ENSG00000111678	Chromatin interaction
ENSG00000238923	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs12321726	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1041155	chr12:7655137-7821891	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv1045650	chr12:7655137-7824995	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv557270	chr12:7727544-7801532	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv468990	chr12:7729433-7801532	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv557271	chr12:7729433-7801532	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv826213	chr12:7730932-7830644	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv468991	chr12:7756706-7821692	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv468992	chr12:7756706-7821692	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv557272	chr12:7756706-7821692	Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv521149	chr12:7756706-7836988	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv898643	chr12:7760124-7794736	Bivalent Enhancer Active TSS Weak transcription Enhancers 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	4 gene(s)	inside rSNPs	diseases
12	nsv826214	chr12:7760127-7803262	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
13	nsv826215	chr12:7768336-7805060	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
14	nsv826216	chr12:7768554-7818506	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
15	nsv468993	chr12:7774028-7884351	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
16	nsv557273	chr12:7774028-7884351	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
17	esv2422373	chr12:7774520-8070089	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
18	nsv1048545	chr12:7778760-8608231	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	97 gene(s)	inside rSNPs	diseases
19	nsv541368	chr12:7778760-8608231	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	97 gene(s)	inside rSNPs	diseases
20	nsv1036408	chr12:7782625-7812010	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
21	nsv1041213	chr12:7790477-7874346	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:7775600-7791600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr12:7787800-7791800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr12:7790400-7792400	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr12:7790400-7792400	Active TSS	H9 Cell Line	embryonic stem cell
5	chr12:7790400-7792400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr12:7790600-7791600	Active TSS	Brain Anterior Caudate	brain
7	chr12:7790600-7792200	Enhancers	Primary B cells from cord blood	blood
8	chr12:7790800-7791600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr12:7790800-7791800	Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr12:7790800-7792000	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr12:7790800-7792000	Active TSS	Brain Inferior Temporal Lobe	brain
12	chr12:7790800-7792200	Enhancers	Fetal Stomach	stomach
13	chr12:7790800-7792400	Active TSS	HUES6 Cell Line	embryonic stem cell
14	chr12:7790800-7792400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
15	chr12:7790800-7793000	Active TSS	Fetal Kidney	kidney
16	chr12:7791000-7791600	Enhancers	Primary T cells fromperipheralblood	blood
17	chr12:7791000-7791600	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr12:7791000-7791600	Enhancers	Stomach Mucosa	stomach
19	chr12:7791000-7791800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr12:7791000-7791800	Enhancers	Primary T helper naive cells from peripheral blood	blood
21	chr12:7791000-7792000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr12:7791000-7792000	Enhancers	Fetal Lung	lung
23	chr12:7791000-7792200	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr12:7791000-7792400	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr12:7791000-7792400	Enhancers	Placenta	Placenta
26	chr12:7791000-7792400	Flanking Active TSS	Dnd41	blood
27	chr12:7791000-7792400	Active TSS	Osteobl	bone
28	chr12:7791200-7791600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr12:7791200-7791600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr12:7791200-7791600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr12:7791200-7791600	Enhancers	Duodenum Mucosa	Duodenum
32	chr12:7791200-7791600	Active TSS	Rectal Mucosa Donor 29	rectum
33	chr12:7791200-7791800	Active TSS	Adipose Nuclei	Adipose
34	chr12:7791200-7791800	Enhancers	HepG2	liver
35	chr12:7791200-7792000	Enhancers	Primary T cells from cord blood	blood
36	chr12:7791200-7792000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr12:7791200-7792000	Active TSS	Colon Smooth Muscle	Colon
38	chr12:7791200-7792000	Weak transcription	Fetal Brain Male	brain
39	chr12:7791200-7792400	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr12:7791200-7792400	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
41	chr12:7791200-7794600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr12:7791200-7798400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr12:7791400-7791600	Active TSS	Brain Hippocampus Middle	brain
44	chr12:7791400-7791800	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr12:7791400-7791800	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr12:7791400-7792000	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr12:7791400-7792000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr12:7791400-7792000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr12:7791400-7792000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr12:7791400-7792000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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