Variant report

Variant	rs10515385
Chromosome Location	chr5:107528267-107528268
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:107526145..107528996-chr5:107531733..107533472,2	MCF-7	breast:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10036675	0.94[CEU][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs10061044	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs10515388	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.80[EUR][1000 genomes]
rs11242664	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12652675	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12652687	0.87[CHD][hapmap];0.87[GIH][hapmap]
rs12653027	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12654140	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12657542	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12659437	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs17161193	1.00[CEU][hapmap];0.94[TSI][hapmap]
rs17384285	0.82[ASW][hapmap];0.87[CHD][hapmap];0.81[GIH][hapmap];0.83[JPT][hapmap]
rs17385914	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17386492	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17386875	1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs17387645	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs17388244	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs17449654	0.83[JPT][hapmap]
rs17449723	0.83[JPT][hapmap]
rs17450705	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17451397	0.94[CEU][hapmap];0.82[EUR][1000 genomes]
rs17452357	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs17452992	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2052463	0.80[EUR][1000 genomes]
rs2416528	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4129424	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4364376	1.00[CEU][hapmap];0.83[GIH][hapmap];0.94[TSI][hapmap];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55755463	0.80[EUR][1000 genomes]
rs56044682	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56855707	0.80[EUR][1000 genomes]
rs58131807	0.80[ASN][1000 genomes]
rs58212758	0.80[EUR][1000 genomes]
rs58844678	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61603913	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6870480	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6880005	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6888190	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72791270	0.80[EUR][1000 genomes]
rs73214528	0.92[ASN][1000 genomes]
rs73214536	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7711717	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7724245	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs7724860	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7724884	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7733036	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs888792	0.98[EUR][1000 genomes];0.97[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	nsv534281	chr5:107357579-107674981	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv830441	chr5:107450392-107614557	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv882683	chr5:107476501-107769095	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	nsv882684	chr5:107521677-107695558	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:107476000-107535600	Weak transcription	Left Ventricle	heart
2	chr5:107495400-107548800	Weak transcription	Pancreas	Pancrea
3	chr5:107496800-107528800	Weak transcription	Aorta	Aorta
4	chr5:107505400-107536800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:107506200-107529400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr5:107510600-107532000	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr5:107511400-107548400	Weak transcription	Primary B cells from cord blood	blood
8	chr5:107516200-107584800	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr5:107516800-107551400	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr5:107517000-107529000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr5:107517000-107571800	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr5:107518000-107532000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr5:107521400-107528800	Weak transcription	Ovary	ovary
14	chr5:107521400-107528800	Weak transcription	HSMM	muscle
15	chr5:107521400-107529000	Weak transcription	Fetal Stomach	stomach
16	chr5:107521400-107529400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr5:107521600-107528600	Weak transcription	Primary hematopoietic stem cells	blood
18	chr5:107521800-107536400	Weak transcription	Primary B cells from peripheral blood	blood
19	chr5:107522400-107535400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr5:107525200-107528800	Weak transcription	HSMMtube	muscle
21	chr5:107526000-107550800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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