Variant report

Variant	rs8034113
Chromosome Location	chr15:55955864-55955865
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:55955042..55958046-chr15:56034053..56035749,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000166450	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10518817	0.92[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10851589	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11852298	0.84[ASN][1000 genomes]
rs11854213	0.82[ASN][1000 genomes]
rs12373006	0.91[ASN][1000 genomes]
rs12438177	0.89[ASN][1000 genomes]
rs12592192	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs12594642	0.80[AMR][1000 genomes]
rs12903822	0.90[ASN][1000 genomes]
rs1371056	0.80[AMR][1000 genomes]
rs1438918	0.82[ASN][1000 genomes]
rs1530087	0.85[AMR][1000 genomes]
rs16976450	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16976472	0.82[ASN][1000 genomes]
rs2118781	0.82[ASN][1000 genomes]
rs2414426	0.83[AMR][1000 genomes]
rs28556884	0.87[ASN][1000 genomes]
rs4392003	0.88[ASN][1000 genomes]
rs4774220	0.90[ASN][1000 genomes]
rs4774799	0.88[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4774800	0.96[ASN][1000 genomes]
rs572531	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs62043869	0.92[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs62043871	0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs62043872	0.80[AMR][1000 genomes]
rs6493805	0.96[AMR][1000 genomes];0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs715321	0.83[AMR][1000 genomes]
rs7162879	0.82[ASN][1000 genomes]
rs7165778	0.94[ASN][1000 genomes]
rs7166952	0.97[ASN][1000 genomes]
rs7171318	0.97[ASN][1000 genomes]
rs7171522	0.96[ASN][1000 genomes]
rs7171834	0.96[ASN][1000 genomes]
rs7178379	0.96[ASN][1000 genomes]
rs7180112	0.83[AMR][1000 genomes]
rs8025445	0.87[ASN][1000 genomes]
rs9920076	0.92[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs9920246	0.94[ASN][1000 genomes]
rs9920262	0.93[AMR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917323	chr15:55290499-56041334	Genic enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	nsv1043789	chr15:55400872-56092454	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv948522	chr15:55639867-56032099	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent Enhancer 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 miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv457157	chr15:55722213-56255774	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Genic enhancers 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	22 gene(s)	inside rSNPs	diseases
5	nsv569539	chr15:55722213-56255774	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer 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	22 gene(s)	inside rSNPs	diseases
6	nsv1049774	chr15:55759573-56044600	Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
7	nsv457158	chr15:55930542-55982257	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv569541	chr15:55930542-55982257	Strong transcription ZNF genes & repeats Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55911800-55977000	Weak transcription	Fetal Intestine Small	intestine
2	chr15:55920800-55987600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:55932600-55987000	Weak transcription	Ovary	ovary
4	chr15:55932800-55973400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr15:55942800-55974400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr15:55947400-55960200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr15:55951200-55956000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr15:55952200-55960000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr15:55952400-55957000	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr15:55952800-55972000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr15:55953800-55964800	Weak transcription	Right Ventricle	heart
12	chr15:55954000-55968600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr15:55954000-55971600	Weak transcription	Fetal Kidney	kidney
14	chr15:55954000-55975400	Weak transcription	HSMM	muscle
15	chr15:55954000-55977400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr15:55954200-55964400	Weak transcription	Fetal Lung	lung
17	chr15:55954200-55970000	Weak transcription	Fetal Intestine Large	intestine
18	chr15:55954400-55964400	Weak transcription	HepG2	liver
19	chr15:55954400-55987000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr15:55954600-55975000	Weak transcription	A549	lung
21	chr15:55955200-55956200	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr15:55955200-55968400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr15:55955400-55956000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr15:55955400-55957000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr15:55955400-55961400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr15:55955400-55963800	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr15:55955400-55980000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr15:55955600-55961600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr15:55955600-55961600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr15:55955600-55963000	Weak transcription	HUES64 Cell Line	embryonic stem cell

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