Variant report

Variant	rs10771308
Chromosome Location	chr12:9218573-9218574
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:18)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:18 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr12:9216895-9230988	HepG2	liver:	n/a	n/a
2	MBD4	chr12:9218319-9219866	HepG2	liver:	n/a	n/a
3	POLR2A	chr12:9216806-9219983	HepG2	liver:	n/a	n/a
4	CHD2	chr12:9217996-9219810	HepG2	liver:	n/a	n/a
5	POLR2A	chr12:9216389-9221070	HepG2	liver:	n/a	n/a
6	MYBL2	chr12:9218472-9220191	HepG2	liver:	n/a	n/a
7	POLR2A	chr12:9217415-9220251	HepG2	liver:	n/a	n/a
8	POLR2A	chr12:9216589-9220417	HepG2	liver:	n/a	n/a
9	MBD4	chr12:9218464-9220244	HepG2	liver:	n/a	n/a
10	JUND	chr12:9218573-9219550	HepG2	liver:	n/a	n/a
11	MYBL2	chr12:9218164-9218777	HepG2	liver:	n/a	n/a
12	MAFK	chr12:9218323-9218614	HepG2	liver:	n/a	n/a
13	POLR2A	chr12:9218510-9218685	MCF10A-Er-Src	breast:	n/a	n/a
14	SETDB1	chr12:9218231-9218813	U2OS	brain:	n/a	n/a
15	POLR2A	chr12:9216161-9220988	HepG2	liver:	n/a	n/a
16	ZNF263	chr12:9216574-9218618	HEK293-T-REx	kidney:	n/a	chr12:9217478-9217487
17	FOSL2	chr12:9217444-9219607	HepG2	liver:	n/a	n/a
18	CREB1	chr12:9216657-9219423	HepG2	liver:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr12:9218102..9220634-chr12:9230847..9232385,2	MCF-7	breast:
2	chr12:9064962..9066827-chr12:9216213..9218614,2	MCF-7	breast:
3	chr12:9218454..9221005-chr12:9232709..9234704,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLRG1-1	chr12:9218422-9219303	NONHSAT026384

No data

Variant related genes	Relation type
LINC00612	TF binding region
ENSG00000175899	Chromatin interaction
ENSG00000111752	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10743598	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10842839	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10842849	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11048839	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs113973	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1805682	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2193006	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2216143	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs226380	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs226381	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs226382	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs226386	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs226387	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs226388	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs226389	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs226390	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs226391	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs226392	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs226394	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs226400	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs226401	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs226403	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs226408	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs226415	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3759277	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4882977	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6487584	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs71453666	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7295733	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7964085	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7965790	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7976808	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832327	chr12:9081779-9246220	Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv1045317	chr12:9113216-9544655	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
3	nsv898738	chr12:9205030-9274394	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer 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
4	nsv1048491	chr12:9208806-9544655	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9216600-9218600	Active TSS	Brain Angular Gyrus	brain
2	chr12:9216600-9218600	Active TSS	NHLF	lung
3	chr12:9216800-9218600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr12:9216800-9218800	Active TSS	Fetal Lung	lung
5	chr12:9217400-9223400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr12:9217600-9223200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr12:9217800-9218600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
8	chr12:9217800-9218600	Flanking Active TSS	Adipose Nuclei	Adipose
9	chr12:9217800-9218600	Flanking Active TSS	Liver	Liver
10	chr12:9217800-9218600	ZNF genes & repeats	Thymus	Thymus
11	chr12:9217800-9218800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
12	chr12:9217800-9218800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
13	chr12:9217800-9218800	Flanking Active TSS	Stomach Smooth Muscle	stomach
14	chr12:9217800-9219200	Enhancers	Gastric	stomach
15	chr12:9217800-9220400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr12:9217800-9225000	Weak transcription	Small Intestine	intestine
17	chr12:9217800-9234200	Weak transcription	Primary T cells from cord blood	blood
18	chr12:9218000-9218600	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr12:9218000-9218600	ZNF genes & repeats	Brain Germinal Matrix	brain
20	chr12:9218000-9218600	Flanking Active TSS	Rectal Smooth Muscle	rectum
21	chr12:9218000-9218600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
22	chr12:9218000-9218800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr12:9218000-9218800	Flanking Active TSS	Colon Smooth Muscle	Colon
24	chr12:9218000-9218800	ZNF genes & repeats	Fetal Intestine Small	intestine
25	chr12:9218000-9219000	ZNF genes & repeats	Spleen	Spleen
26	chr12:9218000-9219200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr12:9218000-9220000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr12:9218000-9226800	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr12:9218000-9234000	Weak transcription	Primary hematopoietic stem cells	blood
30	chr12:9218200-9218600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr12:9218200-9218600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr12:9218200-9218600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
33	chr12:9218200-9218600	Enhancers	Lung	lung
34	chr12:9218200-9219000	ZNF genes & repeats	Placenta	Placenta
35	chr12:9218200-9219000	Flanking Active TSS	HepG2	liver
36	chr12:9218200-9219200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr12:9218200-9219200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr12:9218200-9219200	ZNF genes & repeats	Fetal Stomach	stomach
39	chr12:9218200-9219600	Enhancers	Fetal Intestine Large	intestine
40	chr12:9218200-9220000	Enhancers	Hela-S3	cervix
41	chr12:9218200-9220000	Enhancers	HMEC	breast
42	chr12:9218200-9223000	Weak transcription	Aorta	Aorta
43	chr12:9218200-9223200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr12:9218200-9224200	Weak transcription	Ovary	ovary
45	chr12:9218200-9232200	Weak transcription	Fetal Muscle Leg	muscle
46	chr12:9218200-9236200	Weak transcription	Psoas Muscle	Psoas
47	chr12:9218200-9266200	Weak transcription	Fetal Kidney	kidney
48	chr12:9218400-9218600	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr12:9218400-9218600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr12:9218400-9218600	Active TSS	HUES6 Cell Line	embryonic stem cell

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