Variant report

Variant	rs35514738
Chromosome Location	chr4:142652893-142652894
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1021446	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10519612	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10519613	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10519614	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13106911	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13107813	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13150149	0.88[ASN][1000 genomes]
rs1389102	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17007636	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17007642	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17461899	0.88[EUR][1000 genomes]
rs1907949	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2131412	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2222277	0.88[EUR][1000 genomes]
rs33979009	0.90[ASN][1000 genomes]
rs34376144	0.87[ASN][1000 genomes]
rs34468566	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35636124	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35964658	0.90[ASN][1000 genomes]
rs3775596	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3775597	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58934440	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62325678	0.89[ASN][1000 genomes]
rs62327424	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs67013870	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs68003574	0.88[ASN][1000 genomes]
rs71608457	0.83[ASN][1000 genomes]
rs957077	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880173	chr4:142355535-142666106	Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv3401979	chr4:142434442-142803321	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1018949	chr4:142451823-142732365	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1030822	chr4:142487721-142706053	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1027004	chr4:142487721-143007320	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv498005	chr4:142515689-143502988	Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	esv3448093	chr4:142612197-142704695	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:142608800-142655000	Weak transcription	Gastric	stomach
2	chr4:142629400-142654600	Weak transcription	Esophagus	oesophagus
3	chr4:142629400-142655000	Weak transcription	Spleen	Spleen
4	chr4:142629600-142657600	Weak transcription	Right Ventricle	heart
5	chr4:142634600-142653600	Weak transcription	Colon Smooth Muscle	Colon
6	chr4:142634800-142656200	Weak transcription	Pancreas	Pancrea
7	chr4:142635800-142653600	Weak transcription	HSMMtube	muscle
8	chr4:142639600-142655000	Weak transcription	Primary B cells from cord blood	blood
9	chr4:142639600-142657400	Weak transcription	Primary hematopoietic stem cells	blood
10	chr4:142640800-142653000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr4:142641400-142655000	Weak transcription	Lung	lung
12	chr4:142641800-142654200	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr4:142644800-142654400	Weak transcription	GM12878-XiMat	blood
14	chr4:142644800-142655800	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr4:142646600-142655800	Weak transcription	Small Intestine	intestine
16	chr4:142649800-142655400	Weak transcription	Fetal Intestine Large	intestine
17	chr4:142650600-142653000	Strong transcription	Liver	Liver
18	chr4:142651000-142653000	Strong transcription	Left Ventricle	heart
19	chr4:142651000-142653800	Strong transcription	Stomach Smooth Muscle	stomach
20	chr4:142651000-142654600	Strong transcription	Duodenum Smooth Muscle	Duodenum
21	chr4:142651000-142654600	Strong transcription	Skeletal Muscle Female	skeletal muscle
22	chr4:142651000-142654800	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr4:142651200-142653000	Weak transcription	Psoas Muscle	Psoas
24	chr4:142651200-142654000	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr4:142651400-142654200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr4:142651400-142655000	Weak transcription	Rectal Smooth Muscle	rectum
27	chr4:142651600-142653600	Weak transcription	Primary B cells from peripheral blood	blood
28	chr4:142651600-142655600	Weak transcription	A549	lung
29	chr4:142651800-142653400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr4:142651800-142653600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr4:142651800-142654800	Strong transcription	Aorta	Aorta
32	chr4:142652000-142653600	Strong transcription	Skeletal Muscle Male	skeletal muscle
33	chr4:142652000-142654000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:142652000-142656800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr4:142652200-142656200	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr4:142652400-142654000	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr4:142652400-142656000	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr4:142652400-142656400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr4:142652400-142656400	Weak transcription	HSMM	muscle
40	chr4:142652800-142653200	Weak transcription	Duodenum Mucosa	Duodenum
41	chr4:142652800-142655600	Weak transcription	Adipose Nuclei	Adipose
42	chr4:142652800-142656600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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