Variant report

Variant	rs11051900
Chromosome Location	chr12:32437726-32437727
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:32429617..32432029-chr12:32437705..32440529,2	K562	blood:

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10844166	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10844167	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11051897	0.83[LWK][hapmap];0.93[MKK][hapmap];0.83[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs11051901	1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs11051907	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2046588	1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2046589	1.00[ASW][hapmap];0.94[LWK][hapmap];0.93[MKK][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2121823	1.00[ASW][hapmap];0.97[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57559050	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60842376	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61346278	1.00[EUR][1000 genomes]
rs9651804	0.99[AFR][1000 genomes];1.00[AMR][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	nsv531960	chr12:32257285-32775277	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription 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	19 gene(s)	inside rSNPs	diseases
2	esv2751096	chr12:32280340-32702784	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv558171	chr12:32287259-32559693	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv832366	chr12:32328559-32511360	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32424600-32438000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:32425000-32437800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr12:32426600-32443400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr12:32426800-32442800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr12:32426800-32443200	Weak transcription	NH-A	brain
6	chr12:32426800-32446800	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr12:32427000-32437800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr12:32427000-32438000	Weak transcription	Fetal Brain Female	brain
9	chr12:32427000-32443400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr12:32427000-32458600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr12:32427000-32459400	Weak transcription	Aorta	Aorta
12	chr12:32427000-32463000	Weak transcription	NHLF	lung
13	chr12:32427200-32463000	Weak transcription	Fetal Intestine Small	intestine
14	chr12:32427400-32445200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr12:32427600-32454400	Weak transcription	Primary B cells from cord blood	blood
16	chr12:32427800-32438200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr12:32434400-32438000	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr12:32434800-32443000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr12:32435200-32448200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr12:32436200-32440200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr12:32436400-32438600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr12:32436400-32439800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr12:32436400-32440600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr12:32437000-32438200	Enhancers	H9 Cell Line	embryonic stem cell
25	chr12:32437000-32439000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr12:32437200-32438200	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr12:32437200-32439800	Enhancers	H1 Cell Line	embryonic stem cell
28	chr12:32437200-32440000	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr12:32437400-32438000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr12:32437400-32438000	Enhancers	Osteobl	bone
31	chr12:32437400-32438200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr12:32437400-32438400	Weak transcription	Ovary	ovary
33	chr12:32437400-32439000	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr12:32437400-32440000	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr12:32437600-32437800	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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