Variant report

Variant	rs6861614
Chromosome Location	chr5:90346339-90346340
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:90344675..90347461-chr5:90349774..90351830,2	MCF-7	breast:
2	chr5:90343546..90347472-chr5:90675277..90677935,4	MCF-7	breast:
3	chr5:90345196..90346808-chr5:90676912..90679322,2	MCF-7	breast:
4	chr5:90343505..90346725-chr5:90355686..90358630,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000113369	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10514342	0.92[CEU][hapmap]
rs10514343	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs11744033	0.91[CEU][hapmap]
rs11949884	0.95[CEU][hapmap]
rs11951675	0.91[CEU][hapmap]
rs11952993	1.00[CEU][hapmap];0.89[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11955946	1.00[CEU][hapmap];0.94[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12188068	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12188249	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12189005	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12658697	0.95[YRI][hapmap]
rs13152882	0.95[YRI][hapmap]
rs17571029	0.91[CEU][hapmap]
rs17572843	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs3850657	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55792004	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56106025	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs56258383	0.87[EUR][1000 genomes]
rs62376462	0.86[EUR][1000 genomes]
rs62376463	0.86[EUR][1000 genomes]
rs62376490	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62376491	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6452927	0.91[CEU][hapmap]
rs6880626	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6886773	0.92[CEU][hapmap]
rs6888979	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6889138	1.00[CEU][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73771166	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs951948	0.95[YRI][hapmap]

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	nsv529544	chr5:89523963-90412409	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv1024813	chr5:90321535-90870739	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers 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	84 gene(s)	inside rSNPs	diseases
3	nsv537806	chr5:90321535-90870739	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:90324600-90350400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:90341200-90376600	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr5:90344400-90348400	Weak transcription	Adipose Nuclei	Adipose
4	chr5:90344400-90353800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr5:90344600-90348800	Weak transcription	Colon Smooth Muscle	Colon
6	chr5:90344800-90368000	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr5:90346000-90348800	Weak transcription	HUVEC	blood vessel
8	chr5:90346200-90347000	Enhancers	A549	lung
9	chr5:90346200-90348400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr5:90346200-90348400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr5:90346200-90348600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr5:90346200-90348600	Weak transcription	Hela-S3	cervix
13	chr5:90346200-90348800	Weak transcription	Rectal Smooth Muscle	rectum

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