Variant report

Variant	rs10023440
Chromosome Location	chr4:53714178-53714179
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:53712700..53715179-chr4:53718213..53720143,2	MCF-7	breast:
2	chr4:53705671..53708824-chr4:53710798..53715308,4	MCF-7	breast:
3	chr4:53713812..53716438-chr4:53719850..53722220,2	K562	blood:
4	chr4:53713264..53715113-chr4:53726769..53729713,2	MCF-7	breast:
5	chr4:53708530..53710089-chr4:53712453..53715419,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000128045	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10003908	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10016904	0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10026162	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10026175	0.83[JPT][hapmap]
rs10032190	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11940896	0.83[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.97[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11941841	0.83[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11947787	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4864676	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4864678	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4864680	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4864685	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs62336790	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6554056	0.83[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6844680	0.83[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.97[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs730246	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs730247	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs731073	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7663943	0.83[CEU][hapmap];0.95[CHB][hapmap];0.88[JPT][hapmap];0.97[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7692692	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8287	0.95[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs881743	0.83[CEU][hapmap];0.94[JPT][hapmap];0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs936690	0.95[CHB][hapmap];0.89[JPT][hapmap];0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs962416	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9995861	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv594201	chr4:52798624-53732445	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv1004889	chr4:53436500-54106281	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv537094	chr4:53436500-54106281	Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv1004086	chr4:53698581-53773183	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr4:53708400-53719000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:53708600-53718000	Weak transcription	Lung	lung
3	chr4:53709000-53718200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:53709200-53718000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr4:53709200-53718600	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr4:53709200-53718800	Weak transcription	Colon Smooth Muscle	Colon
7	chr4:53709200-53718800	Weak transcription	Stomach Smooth Muscle	stomach
8	chr4:53709400-53716000	Weak transcription	Fetal Heart	heart
9	chr4:53709400-53718400	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr4:53709400-53721000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:53709600-53718800	Weak transcription	Right Ventricle	heart
12	chr4:53710000-53718600	Weak transcription	Fetal Muscle Leg	muscle
13	chr4:53710400-53718600	Weak transcription	Placenta	Placenta
14	chr4:53710600-53715200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:53710800-53718400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr4:53713200-53718200	Weak transcription	Right Atrium	heart
17	chr4:53713200-53718600	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr4:53713400-53719000	Enhancers	Stomach Mucosa	stomach
19	chr4:53713800-53714600	Enhancers	Fetal Kidney	kidney
20	chr4:53713800-53715200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr4:53714000-53714200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr4:53714000-53714600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr4:53714000-53714600	Enhancers	Duodenum Mucosa	Duodenum
24	chr4:53714000-53714600	Enhancers	Esophagus	oesophagus
25	chr4:53714000-53714600	Enhancers	Fetal Lung	lung
26	chr4:53714000-53715000	Enhancers	Fetal Intestine Large	intestine
27	chr4:53714000-53715000	Enhancers	Left Ventricle	heart
28	chr4:53714000-53715200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr4:53714000-53715200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr4:53714000-53715200	Enhancers	Psoas Muscle	Psoas
31	chr4:53714000-53715200	Enhancers	NHEK	skin
32	chr4:53714000-53715400	Enhancers	Fetal Intestine Small	intestine
33	chr4:53714000-53715400	Enhancers	HepG2	liver
34	chr4:53714000-53715600	Enhancers	Gastric	stomach
35	chr4:53714000-53715600	Enhancers	Pancreas	Pancrea

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