Variant report

Variant	rs2749783
Chromosome Location	chr4:3326098-3326099
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10155132	0.95[CEU][hapmap];0.82[JPT][hapmap];0.84[EUR][1000 genomes]
rs10937924	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11943298	1.00[YRI][hapmap]
rs13104157	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13150241	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16843151	0.88[YRI][hapmap]
rs2051558	0.90[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs2071666	0.88[ASN][1000 genomes]
rs2157090	0.81[CHB][hapmap]
rs2236052	1.00[CEU][hapmap];0.88[JPT][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2239725	1.00[CEU][hapmap];0.81[JPT][hapmap];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2530601	0.81[CHB][hapmap]
rs2748447	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2749778	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2749780	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2749781	0.95[CEU][hapmap];0.84[CHB][hapmap];0.88[JPT][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2749782	1.00[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2749785	1.00[CEU][hapmap];0.89[CHB][hapmap];0.93[JPT][hapmap]
rs2857861	0.90[CHB][hapmap];0.83[ASN][1000 genomes]
rs2857982	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3129308	1.00[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3129310	1.00[CEU][hapmap];0.85[CHB][hapmap];0.94[JPT][hapmap];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3129314	0.85[ASN][1000 genomes]
rs3129316	0.87[ASN][1000 genomes]
rs3129327	1.00[CEU][hapmap]
rs3129328	1.00[CEU][hapmap];0.90[CHB][hapmap];0.88[JPT][hapmap];0.82[EUR][1000 genomes]
rs3129334	1.00[CEU][hapmap];0.82[JPT][hapmap];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3135145	0.95[CEU][hapmap];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3135146	1.00[CEU][hapmap];0.81[JPT][hapmap];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs60181496	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs60208975	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6446727	0.81[CHB][hapmap]
rs6446731	0.89[CHB][hapmap]
rs6819202	1.00[CEU][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7435601	1.00[CEU][hapmap];0.81[JPT][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7661630	0.81[CHB][hapmap]
rs881816	1.00[CEU][hapmap];0.80[CHB][hapmap];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs881817	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs910568	1.00[CEU][hapmap];0.82[JPT][hapmap];0.87[EUR][1000 genomes]
rs9996868	0.84[CHB][hapmap]

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	esv3418626	chr4:2741174-3461492	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
2	esv3397632	chr4:2741239-3460583	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
3	nsv998290	chr4:3176454-3355758	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv878455	chr4:3215835-3344891	Strong transcription Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv878456	chr4:3215835-3467519	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	nsv428106	chr4:3226182-3752322	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv878461	chr4:3270488-3339038	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
8	nsv593440	chr4:3283422-3339038	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
9	nsv461165	chr4:3283422-3342137	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
10	nsv593441	chr4:3283422-3342137	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
11	nsv878462	chr4:3311548-3505448	Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
12	nsv1007847	chr4:3317904-3527357	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
13	nsv537001	chr4:3317904-3527357	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3301200-3350000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:3307200-3327000	Weak transcription	Fetal Kidney	kidney
3	chr4:3307400-3326800	Weak transcription	A549	lung
4	chr4:3308000-3327000	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr4:3309000-3327200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr4:3314200-3326600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:3314400-3327400	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr4:3314400-3328000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:3314400-3348200	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr4:3315400-3326600	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr4:3319200-3332600	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr4:3319800-3332000	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr4:3320000-3344000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr4:3320200-3328400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr4:3320400-3326400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr4:3320400-3326400	Weak transcription	Colon Smooth Muscle	Colon
17	chr4:3320400-3327400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr4:3320400-3351800	Weak transcription	Aorta	Aorta
19	chr4:3320600-3332200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr4:3320800-3327000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:3321000-3347000	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr4:3322000-3326400	Enhancers	HepG2	liver
23	chr4:3322400-3326200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:3322600-3326200	Strong transcription	Primary T cells from cord blood	blood
25	chr4:3323600-3332000	Weak transcription	Spleen	Spleen
26	chr4:3323600-3333400	Weak transcription	Gastric	stomach
27	chr4:3323600-3344000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr4:3323600-3344800	Weak transcription	Fetal Intestine Large	intestine
29	chr4:3324000-3326400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:3324000-3326400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr4:3324000-3326400	Weak transcription	Colonic Mucosa	Colon
32	chr4:3324000-3326600	Strong transcription	Fetal Stomach	stomach
33	chr4:3324000-3332600	Weak transcription	Right Atrium	heart
34	chr4:3324000-3341400	Weak transcription	Esophagus	oesophagus
35	chr4:3324000-3343600	Weak transcription	HSMM	muscle
36	chr4:3324200-3327000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr4:3324200-3327000	Weak transcription	Fetal Brain Female	brain
38	chr4:3324200-3329200	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr4:3324200-3331600	Weak transcription	HSMMtube	muscle
40	chr4:3324200-3332000	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr4:3324200-3333600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr4:3324200-3340200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr4:3324200-3342600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr4:3324200-3343600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr4:3324400-3326200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr4:3324600-3326200	Strong transcription	Fetal Muscle Leg	muscle
47	chr4:3324800-3326400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr4:3324800-3327400	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr4:3325000-3326400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr4:3325000-3326400	Enhancers	Adipose Nuclei	Adipose

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