Variant report

Variant	rs35263368
Chromosome Location	chr3:112341957-112341958
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:112338141..112343361-chr3:112351475..112354709,4	MCF-7	breast:
2	chr3:112340519..112345126-chr3:112357206..112361448,6	MCF-7	breast:
3	chr3:112340785..112342316-chr3:112345669..112347185,2	K562	blood:

Variant related genes	Relation type
ENSG00000091986	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10511317	1.00[AFR][1000 genomes]
rs1072896	1.00[AFR][1000 genomes]
rs12630906	1.00[AFR][1000 genomes]
rs12634199	1.00[AFR][1000 genomes]
rs12637057	1.00[AFR][1000 genomes]
rs12637953	1.00[AFR][1000 genomes]
rs13059364	1.00[AFR][1000 genomes]
rs13063173	1.00[AFR][1000 genomes]
rs13078401	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13079599	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13081265	1.00[AFR][1000 genomes]
rs13086960	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13096943	1.00[AFR][1000 genomes]
rs16845068	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16845073	1.00[AFR][1000 genomes]
rs16859758	1.00[AFR][1000 genomes]
rs16859849	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16859890	1.00[AFR][1000 genomes]
rs16859897	1.00[AFR][1000 genomes]
rs16859930	1.00[AFR][1000 genomes]
rs16859961	1.00[AFR][1000 genomes]
rs28364588	1.00[AFR][1000 genomes]
rs28364589	1.00[AFR][1000 genomes]
rs34080815	1.00[AFR][1000 genomes]
rs34541731	1.00[AFR][1000 genomes]
rs34694961	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34829517	1.00[AFR][1000 genomes]
rs34889961	1.00[AFR][1000 genomes]
rs34949685	1.00[AFR][1000 genomes]
rs34962178	1.00[AFR][1000 genomes]
rs35526995	1.00[AFR][1000 genomes]
rs35931975	1.00[AFR][1000 genomes]
rs36045008	1.00[AFR][1000 genomes]
rs36153507	1.00[AFR][1000 genomes]
rs3736269	1.00[AFR][1000 genomes]
rs3773701	1.00[AFR][1000 genomes]
rs3773704	1.00[AFR][1000 genomes]
rs56952692	1.00[AFR][1000 genomes]
rs57224143	1.00[AFR][1000 genomes]
rs59191788	1.00[AFR][1000 genomes]
rs59650289	1.00[AFR][1000 genomes]
rs60340975	1.00[AFR][1000 genomes]
rs60646325	1.00[AFR][1000 genomes]
rs60733172	1.00[AFR][1000 genomes]
rs66546764	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66791711	1.00[AFR][1000 genomes]
rs67021100	1.00[AFR][1000 genomes]
rs71317506	1.00[AFR][1000 genomes]
rs71317507	1.00[AFR][1000 genomes]
rs71317508	1.00[AFR][1000 genomes]
rs73229350	1.00[AFR][1000 genomes]
rs73229353	1.00[AFR][1000 genomes]
rs963541	1.00[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3329419	chr3:112236688-112620544	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112312600-112346200	Weak transcription	Rectal Smooth Muscle	rectum
2	chr3:112312600-112347200	Weak transcription	Fetal Intestine Large	intestine
3	chr3:112316200-112342800	Weak transcription	Fetal Muscle Trunk	muscle
4	chr3:112330400-112346800	Strong transcription	NHLF	lung
5	chr3:112331200-112351600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr3:112331400-112354800	Weak transcription	Psoas Muscle	Psoas
7	chr3:112335200-112342200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr3:112335200-112345400	Weak transcription	Fetal Muscle Leg	muscle
9	chr3:112336000-112342000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr3:112336200-112342000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr3:112336200-112347400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr3:112336200-112351600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr3:112336400-112342000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr3:112336400-112346800	Weak transcription	Fetal Stomach	stomach
15	chr3:112336600-112351400	Weak transcription	Fetal Lung	lung
16	chr3:112336600-112355800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr3:112337000-112346800	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr3:112338000-112349400	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr3:112338400-112346200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr3:112338600-112342000	Strong transcription	NH-A	brain
21	chr3:112338600-112342200	Weak transcription	HUVEC	blood vessel
22	chr3:112338800-112343600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr3:112340000-112342200	Enhancers	Ovary	ovary
24	chr3:112340000-112342600	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr3:112340000-112342800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr3:112340000-112343400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr3:112340200-112342000	Strong transcription	Muscle Satellite Cultured Cells	--
28	chr3:112340200-112342600	Strong transcription	Stomach Smooth Muscle	stomach
29	chr3:112340200-112342800	Strong transcription	HSMMtube	muscle
30	chr3:112340800-112342000	Strong transcription	NHDF-Ad	bronchial
31	chr3:112340800-112348200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr3:112341000-112342000	Strong transcription	A549	lung
33	chr3:112341000-112342600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr3:112341000-112346200	Weak transcription	Aorta	Aorta
35	chr3:112341000-112348400	Weak transcription	Fetal Kidney	kidney
36	chr3:112341200-112342200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr3:112341200-112343400	Enhancers	Hela-S3	cervix
38	chr3:112341200-112344000	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr3:112341400-112342200	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr3:112341400-112342200	Weak transcription	Adipose Nuclei	Adipose
41	chr3:112341400-112344200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr3:112341400-112351400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr3:112341800-112342400	Enhancers	Colon Smooth Muscle	Colon
44	chr3:112341800-112342400	Genic enhancers	HSMM	muscle
45	chr3:112341800-112342400	Enhancers	K562	blood
46	chr3:112341800-112342800	Enhancers	H9 Cell Line	embryonic stem cell
47	chr3:112341800-112343200	Enhancers	HMEC	breast
48	chr3:112341800-112343400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr3:112341800-112343600	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr3:112341800-112344200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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