Variant report

Variant	rs2111903
Chromosome Location	chr12:47608135-47608136
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:47603840..47605770-chr12:47607322..47609128,2	K562	blood:

Variant related genes	Relation type
ENSG00000247774	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10881077	0.88[CEU][hapmap];0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10881079	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11183779	1.00[CHB][hapmap]
rs11183783	1.00[CHB][hapmap];0.83[ASN][1000 genomes]
rs11183795	0.87[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11183796	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11183799	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12370622	0.88[CEU][hapmap];1.00[CHB][hapmap];0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1554693	0.84[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17821774	0.83[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17822189	0.88[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2004683	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2004684	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2408718	0.87[CEU][hapmap];1.00[CHB][hapmap];0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4768144	0.92[CEU][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4768782	0.84[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55711758	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55849521	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs712100	1.00[CHB][hapmap]
rs73110240	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs732523	0.87[CEU][hapmap];0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7974410	0.88[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs855146	1.00[CHB][hapmap]
rs855147	1.00[CHB][hapmap]
rs873935	1.00[CHB][hapmap]

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	nsv469368	chr12:47374908-47675680	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv558784	chr12:47374908-47675680	Genic enhancers Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv832399	chr12:47502910-47689601	Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	esv2751100	chr12:47541390-47746157	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:47583200-47628600	Weak transcription	Aorta	Aorta
2	chr12:47600000-47614600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
3	chr12:47600800-47614400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr12:47600800-47616400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr12:47601400-47610000	Weak transcription	HSMM	muscle
6	chr12:47601400-47610200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr12:47601400-47612000	Weak transcription	Gastric	stomach
8	chr12:47601400-47616200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr12:47601600-47610400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:47601600-47617400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr12:47601800-47628400	Weak transcription	Esophagus	oesophagus
12	chr12:47602000-47608600	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr12:47602000-47615200	Weak transcription	Fetal Intestine Small	intestine
14	chr12:47602200-47616600	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr12:47602600-47616400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr12:47603000-47608600	Weak transcription	Thymus	Thymus
17	chr12:47603000-47608800	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr12:47603000-47609600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr12:47603200-47608200	Weak transcription	Fetal Thymus	thymus
20	chr12:47603200-47611800	Weak transcription	Spleen	Spleen
21	chr12:47603200-47615600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr12:47603200-47616400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr12:47603800-47608200	Weak transcription	Primary hematopoietic stem cells	blood
24	chr12:47603800-47608200	Weak transcription	K562	blood
25	chr12:47604000-47608200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr12:47604200-47608600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr12:47604200-47608800	Weak transcription	GM12878-XiMat	blood
28	chr12:47604800-47612000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr12:47605200-47613000	Active TSS	Primary T helper naive cells from peripheral blood	blood
30	chr12:47605200-47613000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
31	chr12:47605200-47613600	Active TSS	Primary T killer memory cells from peripheral blood	blood
32	chr12:47605800-47608600	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr12:47606000-47608400	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
34	chr12:47606000-47608400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
35	chr12:47606200-47613400	Active TSS	Rectal Mucosa Donor 29	rectum
36	chr12:47606400-47610000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr12:47606600-47611800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
38	chr12:47606600-47616800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr12:47606800-47608200	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr12:47606800-47608200	Enhancers	Primary B cells from peripheral blood	blood
41	chr12:47606800-47608600	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
42	chr12:47606800-47608800	Weak transcription	Liver	Liver
43	chr12:47606800-47610200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:47606800-47610200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
45	chr12:47606800-47611800	Active TSS	Primary T cells fromperipheralblood	blood
46	chr12:47606800-47612600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
47	chr12:47606800-47614000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
48	chr12:47606800-47614200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr12:47606800-47616600	Weak transcription	Adipose Nuclei	Adipose
50	chr12:47607000-47609000	Enhancers	A549	lung

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