Variant report

Variant	rs10254104
Chromosome Location	chr7:98769288-98769289
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:98765362..98767556-chr7:98768550..98771320,2	K562	blood:
2	chr7:98766950..98769641-chr7:98774133..98776807,2	MCF-7	breast:
3	chr7:98746993..98748569-chr7:98768043..98771030,2	MCF-7	breast:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10248890	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10266364	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11764542	0.91[EUR][1000 genomes]
rs1918019	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1918020	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1918021	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2395022	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2395048	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2395049	0.93[EUR][1000 genomes]
rs2395050	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2395051	0.95[EUR][1000 genomes]
rs2894224	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4454228	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs60083526	0.91[EUR][1000 genomes]
rs62473047	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6465739	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6956645	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6961749	0.85[EUR][1000 genomes]
rs6962075	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6969313	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6975245	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73147619	0.91[EUR][1000 genomes]
rs73147622	0.91[EUR][1000 genomes]
rs73147625	0.91[EUR][1000 genomes]
rs73147628	0.91[EUR][1000 genomes]
rs73147630	0.91[EUR][1000 genomes]
rs73147632	0.91[EUR][1000 genomes]
rs73147639	0.95[EUR][1000 genomes]
rs73147651	0.91[EUR][1000 genomes]
rs73147652	0.89[EUR][1000 genomes]
rs73147654	0.89[EUR][1000 genomes]
rs73147655	0.89[EUR][1000 genomes]
rs7788750	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024529	chr7:98194830-98793518	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv539036	chr7:98194830-98793518	Bivalent/Poised TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	esv2755119	chr7:98721885-98800145	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
4	nsv464645	chr7:98755272-98788589	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv464646	chr7:98755272-98788589	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv607925	chr7:98755272-98788589	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:98767000-98770000	Enhancers	HepG2	liver
2	chr7:98767200-98769600	Enhancers	Liver	Liver
3	chr7:98768200-98769600	Enhancers	Fetal Intestine Large	intestine
4	chr7:98768800-98769400	Weak transcription	Pancreas	Pancrea
5	chr7:98768800-98769600	Enhancers	Fetal Intestine Small	intestine
6	chr7:98769200-98769600	Enhancers	Small Intestine	intestine
7	chr7:98769200-98770000	Enhancers	Stomach Mucosa	stomach

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