Variant report

Variant	rs74380742
Chromosome Location	chr12:4759609-4759610
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	JUND	chr12:4759421-4759624	HepG2	liver:	n/a	n/a
2	CEBPB	chr12:4759436-4759663	HepG2	liver:	n/a	n/a
3	JUN	chr12:4759443-4759617	HepG2	liver:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr12:4757018..4762059-chr12:4764285..4767290,6	K562	blood:
2	chr12:4756861..4759668-chr12:4760395..4765208,7	MCF-7	breast:
3	chr12:4751073..4755821-chr12:4757118..4761577,5	MCF-7	breast:
4	chr12:4757063..4759938-chr12:4760465..4764038,5	K562	blood:
5	chr12:4754845..4760714-chr12:4761830..4765057,7	MCF-7	breast:
6	chr12:4757573..4759938-chr12:4760465..4764276,3	K562	blood:
7	chr12:4758381..4761405-chr12:4778974..4782071,3	K562	blood:

No data

Variant related genes	Relation type
NDUFA9	TF binding region
AKAP3	TF binding region
ENSG00000111254	Chromatin interaction
ENSG00000139180	Chromatin interaction
ENSG00000255639	Chromatin interaction
ENSG00000256381	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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	nsv832318	chr12:4655799-4875837	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv898617	chr12:4715082-4768619	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv898618	chr12:4726068-4764137	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv898619	chr12:4737715-4771456	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv898620	chr12:4745313-4771456	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv557125	chr12:4748410-4764137	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1036308	chr12:4748657-4804156	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv898621	chr12:4751798-4768193	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv898622	chr12:4751798-4768619	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv898623	chr12:4751798-4771456	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv898624	chr12:4757474-4769876	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv557126	chr12:4757809-4768619	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv898625	chr12:4759380-4771682	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 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	chr12:4757200-4760200	Active TSS	Right Atrium	heart
2	chr12:4757400-4759800	Active TSS	Psoas Muscle	Psoas
3	chr12:4757400-4759800	Active TSS	Right Ventricle	heart
4	chr12:4757600-4760000	Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr12:4757600-4760200	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr12:4758800-4759800	Flanking Active TSS	Primary T cells from cord blood	blood
7	chr12:4758800-4759800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
8	chr12:4758800-4759800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
9	chr12:4758800-4759800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr12:4758800-4759800	Flanking Active TSS	HUVEC	blood vessel
11	chr12:4758800-4760000	Flanking Active TSS	Brain Angular Gyrus	brain
12	chr12:4758800-4760000	Flanking Active TSS	Brain Germinal Matrix	brain
13	chr12:4758800-4760000	Flanking Active TSS	Duodenum Mucosa	Duodenum
14	chr12:4758800-4760000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
15	chr12:4758800-4760000	Flanking Active TSS	Stomach Smooth Muscle	stomach
16	chr12:4758800-4763400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr12:4759000-4760000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr12:4759000-4760000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr12:4759000-4760000	Flanking Active TSS	Fetal Heart	heart
20	chr12:4759000-4760000	Enhancers	Small Intestine	intestine
21	chr12:4759000-4760200	Enhancers	Primary B cells from peripheral blood	blood
22	chr12:4759000-4760200	Flanking Active TSS	Dnd41	blood
23	chr12:4759000-4763000	Weak transcription	Placenta	Placenta
24	chr12:4759000-4763400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr12:4759000-4763400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr12:4759000-4763400	Weak transcription	Spleen	Spleen
27	chr12:4759000-4764000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:4759000-4764000	Weak transcription	Lung	lung
29	chr12:4759000-4764200	Weak transcription	Esophagus	oesophagus
30	chr12:4759000-4764400	Weak transcription	Aorta	Aorta
31	chr12:4759000-4764400	Weak transcription	Pancreas	Pancrea
32	chr12:4759000-4772600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr12:4759000-4799400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr12:4759200-4759800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
35	chr12:4759200-4759800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
36	chr12:4759200-4759800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr12:4759200-4759800	Flanking Active TSS	A549	lung
38	chr12:4759200-4760000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr12:4759200-4760000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr12:4759200-4760000	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr12:4759200-4760000	Enhancers	Primary hematopoietic stem cells	blood
42	chr12:4759200-4760000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
43	chr12:4759200-4760000	Enhancers	Brain Substantia Nigra	brain
44	chr12:4759200-4760000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr12:4759200-4760000	Enhancers	Gastric	stomach
46	chr12:4759200-4760000	Flanking Active TSS	GM12878-XiMat	blood
47	chr12:4759200-4760000	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr12:4759200-4760200	Enhancers	Fetal Intestine Large	intestine
49	chr12:4759200-4760400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr12:4759200-4763400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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