Variant report

Variant	rs10913730
Chromosome Location	chr1:171787717-171787718
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:171787129..171789980-chr1:171790659..171793277,3	MCF-7	breast:

Extended variants
information (count: 102 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs10158220	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10158235	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10158943	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10159080	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10489253	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10753190	0.81[ASN][1000 genomes]
rs10753195	0.81[ASN][1000 genomes]
rs10753196	0.81[ASN][1000 genomes]
rs10753197	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10753198	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1079820	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10798657	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10798658	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10798661	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10798679	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10913651	0.82[ASN][1000 genomes]
rs10913743	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10913799	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10913803	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11579138	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11580187	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11588649	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11589200	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11589823	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11590059	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11590829	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12022693	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12022753	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12031686	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12057976	0.84[AMR][1000 genomes]
rs12063769	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12562644	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12723938	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1555101	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1555102	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17597528	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17597542	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2206541	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2206542	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2232804	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2232811	0.81[ASN][1000 genomes]
rs2294719	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2294720	0.81[ASN][1000 genomes]
rs2294721	0.81[ASN][1000 genomes]
rs2294722	0.81[ASN][1000 genomes]
rs2421912	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2421913	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4292987	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6425416	0.83[ASN][1000 genomes]
rs6425417	0.83[ASN][1000 genomes]
rs6425422	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6425428	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6425435	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6425436	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6425437	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6425440	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6425441	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6657803	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6658116	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6658730	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6658980	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6659621	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6665727	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6668165	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6674810	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6675011	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6678230	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6682147	0.81[ASN][1000 genomes]
rs6685030	0.82[ASN][1000 genomes]
rs6689108	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6689213	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6690544	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6695736	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6698366	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6698467	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6698892	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6700184	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6700384	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs732304	0.81[ASN][1000 genomes]
rs732305	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7517546	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7517555	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7520688	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs752514	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7525313	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7537173	0.81[ASN][1000 genomes]
rs7537770	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7537931	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7537935	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7539505	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7541128	0.81[ASN][1000 genomes]
rs7545100	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7549347	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7550603	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7552369	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7556602	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs764179	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs764180	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs909959	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3512995	chr1:171329123-171994470	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	esv3512997	chr1:171329123-171994470	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
3	nsv872545	chr1:171735198-171805448	Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:171770200-171794600	Weak transcription	Primary T cells from cord blood	blood
2	chr1:171773000-171796000	Weak transcription	Pancreas	Pancrea
3	chr1:171785400-171787800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr1:171786000-171787800	Enhancers	Hela-S3	cervix
5	chr1:171786200-171787800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr1:171786200-171787800	Enhancers	Brain Substantia Nigra	brain
7	chr1:171786200-171788000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr1:171786400-171787800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr1:171786400-171787800	Enhancers	Brain Hippocampus Middle	brain
10	chr1:171786400-171787800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr1:171786400-171787800	Enhancers	HSMMtube	muscle
12	chr1:171786400-171787800	Enhancers	K562	blood
13	chr1:171786600-171787800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:171786600-171787800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr1:171787200-171787800	Enhancers	H9 Cell Line	embryonic stem cell
16	chr1:171787200-171787800	Enhancers	Brain Angular Gyrus	brain
17	chr1:171787400-171787800	Enhancers	NHDF-Ad	bronchial
18	chr1:171787400-171788200	Enhancers	Brain Cingulate Gyrus	brain
19	chr1:171787400-171788400	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr1:171787600-171787800	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr1:171787600-171788000	Enhancers	A549	lung
22	chr1:171787600-171788800	Weak transcription	Brain Anterior Caudate	brain
23	chr1:171787600-171789000	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr1:171787600-171789400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:171787600-171795800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr1:171787600-171796000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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