Variant report

Variant	rs605928
Chromosome Location	chr15:59046163-59046164
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	chr15:59038409..59043803-chr15:59043836..59048384,6	MCF-7	breast:
2	chr15:59042046..59047020-chr15:59050998..59056418,7	K562	blood:

Variant related genes	Relation type
ENSG00000137845	Chromatin interaction
ENSG00000200318	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10152558	0.91[CHB][hapmap]
rs11854073	0.82[ASW][hapmap];0.92[CHB][hapmap];0.86[CHD][hapmap];0.96[GIH][hapmap];0.90[JPT][hapmap];0.96[MEX][hapmap];0.80[MKK][hapmap]
rs12911961	0.80[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs12912003	0.86[AMR][1000 genomes]
rs1427281	0.92[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap]
rs1427282	0.81[GIH][hapmap];0.80[MKK][hapmap]
rs1469343	1.00[YRI][hapmap]
rs1648532	0.89[CHB][hapmap]
rs17269397	0.91[CHB][hapmap]
rs2250583	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2555356	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs28864995	0.82[ASW][hapmap];0.84[CHB][hapmap];0.95[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap]
rs347115	0.92[CHB][hapmap];0.89[CHD][hapmap];0.91[GIH][hapmap];0.82[MKK][hapmap]
rs347117	0.91[ASW][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.80[MKK][hapmap]
rs383902	0.91[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.82[MKK][hapmap];0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs387812	0.82[MKK][hapmap]
rs442495	0.92[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs474875	0.92[CHB][hapmap];0.85[CHD][hapmap];0.98[GIH][hapmap];0.82[MKK][hapmap]
rs4774310	0.88[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes]
rs4775086	0.83[ASW][hapmap];0.87[LWK][hapmap];0.98[MKK][hapmap];0.95[YRI][hapmap]
rs4775087	0.91[ASW][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.80[MKK][hapmap]
rs4775094	0.92[CHB][hapmap];0.98[GIH][hapmap]
rs507801	0.92[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs514049	0.83[GIH][hapmap]
rs572107	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs585192	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs593742	0.96[CEU][hapmap];0.98[GIH][hapmap];0.92[MEX][hapmap];0.97[TSI][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs596379	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs602602	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs610877	0.92[CHB][hapmap];0.84[CHD][hapmap];1.00[GIH][hapmap];0.82[MKK][hapmap]
rs640704	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6494029	0.80[MKK][hapmap]
rs6494035	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6494036	1.00[ASW][hapmap];0.92[CEU][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.95[MKK][hapmap];0.94[TSI][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6494037	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs650366	0.85[ASN][1000 genomes]
rs653765	1.00[ASW][hapmap];0.92[CEU][hapmap];0.92[CHB][hapmap];0.95[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs673813	0.89[CHB][hapmap]
rs682619	0.84[CEU][hapmap]
rs714696	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs7161889	0.91[ASW][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.80[MKK][hapmap]
rs7166356	1.00[YRI][hapmap]
rs7171818	0.90[CHB][hapmap]
rs7183336	0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs8043406	0.81[GIH][hapmap];1.00[LWK][hapmap];0.98[MKK][hapmap];1.00[YRI][hapmap]
rs972801	0.82[ASW][hapmap];0.84[CHB][hapmap];0.95[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.80[MKK][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051058	chr15:58519922-59092530	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv542401	chr15:58519922-59092530	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	esv34110	chr15:58949991-59381634	Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
4	esv1843037	chr15:59005922-59115159	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
5	esv1826703	chr15:59005922-59213678	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
6	esv1798487	chr15:59027139-59213678	Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
7	nsv428638	chr15:59032300-59126567	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59042600-59062600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:59043000-59062400	Weak transcription	Psoas Muscle	Psoas
3	chr15:59043200-59046200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr15:59043200-59046200	Weak transcription	Brain Hippocampus Middle	brain
5	chr15:59043200-59046200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr15:59043200-59046600	Weak transcription	Brain Angular Gyrus	brain
7	chr15:59043200-59047000	Weak transcription	Brain Substantia Nigra	brain
8	chr15:59043200-59047800	Weak transcription	Brain Anterior Caudate	brain
9	chr15:59043200-59048400	Weak transcription	A549	lung
10	chr15:59044000-59046400	Enhancers	Placenta	Placenta
11	chr15:59044800-59048600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr15:59045400-59047200	Weak transcription	Fetal Thymus	thymus
13	chr15:59045600-59046400	Enhancers	Liver	Liver
14	chr15:59045800-59046800	Enhancers	K562	blood
15	chr15:59046000-59048600	Enhancers	Brain Cingulate Gyrus	brain

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