Variant report

Variant	rs9544049
Chromosome Location	chr13:76401042-76401043
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs12427729	1.00[ASW][hapmap];0.92[CEU][hapmap];0.83[CHB][hapmap];0.84[CHD][hapmap];1.00[LWK][hapmap];0.90[MEX][hapmap];0.84[TSI][hapmap];0.81[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs12428617	0.92[JPT][hapmap]
rs12428746	0.92[CHB][hapmap]
rs12430940	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17065074	0.85[ASN][1000 genomes]
rs17065145	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.95[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2120060	0.91[CEU][hapmap];0.92[CHB][hapmap];0.96[CHD][hapmap];0.92[JPT][hapmap];0.92[MKK][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2120061	1.00[ASW][hapmap];0.85[CEU][hapmap];0.85[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];0.92[TSI][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2165774	0.92[CEU][hapmap];0.92[CHB][hapmap];0.81[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs2241913	0.85[ASN][1000 genomes]
rs2296093	0.95[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs3736858	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3759445	1.00[ASW][hapmap];0.85[CEU][hapmap];0.85[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];0.92[TSI][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3783025	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3825439	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs41287008	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4885357	0.92[CHB][hapmap];0.80[AMR][1000 genomes]
rs61959583	0.95[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs629443	0.83[ASN][1000 genomes]
rs9318380	0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9530471	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9544047	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9544050	0.92[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9544051	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9544053	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9544056	0.84[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs9544059	1.00[ASW][hapmap];0.92[CEU][hapmap];0.92[CHB][hapmap];0.88[CHD][hapmap];1.00[LWK][hapmap];0.85[MEX][hapmap];0.84[TSI][hapmap];0.81[AFR][1000 genomes];0.80[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832646	chr13:76300428-76483102	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	esv2758333	chr13:76321610-76542003	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	esv2759950	chr13:76321610-76542003	Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76370400-76415600	Weak transcription	Primary B cells from cord blood	blood
2	chr13:76373000-76414600	Weak transcription	HMEC	breast
3	chr13:76376800-76415400	Weak transcription	Stomach Smooth Muscle	stomach
4	chr13:76377600-76415800	Weak transcription	Dnd41	blood
5	chr13:76377600-76416200	Weak transcription	A549	lung
6	chr13:76378200-76415800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr13:76378400-76415600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr13:76380600-76405600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr13:76387400-76402000	Weak transcription	HUVEC	blood vessel
10	chr13:76387400-76403400	Strong transcription	Muscle Satellite Cultured Cells	--
11	chr13:76387400-76404200	Strong transcription	HSMMtube	muscle
12	chr13:76387800-76402200	Strong transcription	HSMM	muscle
13	chr13:76387800-76415800	Weak transcription	Brain Germinal Matrix	brain
14	chr13:76387800-76427200	Weak transcription	Ovary	ovary
15	chr13:76388000-76415200	Weak transcription	Fetal Brain Female	brain
16	chr13:76388800-76415400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr13:76389400-76414800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr13:76390000-76402800	Weak transcription	Stomach Mucosa	stomach
19	chr13:76390400-76403600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr13:76390400-76405600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr13:76391000-76405600	Strong transcription	Liver	Liver
22	chr13:76391200-76401600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr13:76391200-76418600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr13:76391200-76431600	Strong transcription	Hela-S3	cervix
25	chr13:76391400-76402600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr13:76391400-76402800	Strong transcription	NH-A	brain
27	chr13:76391600-76415200	Weak transcription	Brain Hippocampus Middle	brain
28	chr13:76392400-76401200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr13:76392400-76403400	Strong transcription	Duodenum Mucosa	Duodenum
30	chr13:76392400-76415600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr13:76393000-76416000	Weak transcription	Brain Angular Gyrus	brain
32	chr13:76393200-76405600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr13:76393200-76405600	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr13:76393400-76415800	Weak transcription	Psoas Muscle	Psoas
35	chr13:76393600-76414400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr13:76393600-76416000	Weak transcription	Fetal Lung	lung
37	chr13:76393800-76405600	Weak transcription	Primary hematopoietic stem cells	blood
38	chr13:76394200-76415400	Weak transcription	Brain Cingulate Gyrus	brain
39	chr13:76394400-76435800	Weak transcription	Colon Smooth Muscle	Colon
40	chr13:76394800-76415800	Weak transcription	Adipose Nuclei	Adipose
41	chr13:76395600-76414400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr13:76396400-76432000	Weak transcription	Brain Substantia Nigra	brain
43	chr13:76396400-76436800	Weak transcription	Fetal Brain Male	brain
44	chr13:76396800-76415600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr13:76396800-76416200	Weak transcription	Fetal Kidney	kidney
46	chr13:76397200-76405400	Strong transcription	Fetal Intestine Large	intestine
47	chr13:76397400-76401200	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr13:76397400-76401400	Strong transcription	Left Ventricle	heart
49	chr13:76397800-76402200	Strong transcription	Primary T cells from cord blood	blood
50	chr13:76397800-76402200	Strong transcription	Sigmoid Colon	Sigmoid Colon

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