Variant report

Variant	rs7908102
Chromosome Location	chr10:6430913-6430914
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:6242556..6245849-chr10:6429136..6431371,4	MCF-7	breast:
2	chr10:6242870..6245619-chr10:6428211..6431866,3	MCF-7	breast:
3	chr10:6421837..6423700-chr10:6429679..6431560,2	MCF-7	breast:
4	chr10:6339981..6341771-chr10:6430124..6433037,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000213994	Chromatin interaction
ENSG00000170525	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10796089	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11258372	1.00[EUR][1000 genomes]
rs11258441	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11258935	1.00[EUR][1000 genomes]
rs11258970	1.00[EUR][1000 genomes]
rs34169455	1.00[EUR][1000 genomes]
rs584413	1.00[EUR][1000 genomes]
rs585932	1.00[EUR][1000 genomes]
rs586439	1.00[EUR][1000 genomes]
rs587378	1.00[EUR][1000 genomes]
rs599922	1.00[EUR][1000 genomes]
rs601150	1.00[EUR][1000 genomes]
rs601622	1.00[EUR][1000 genomes]
rs605806	1.00[EUR][1000 genomes]
rs611505	1.00[EUR][1000 genomes]
rs612497	1.00[EUR][1000 genomes]
rs615546	1.00[EUR][1000 genomes]
rs617197	1.00[EUR][1000 genomes]
rs630027	1.00[EUR][1000 genomes]
rs631508	1.00[EUR][1000 genomes]
rs644180	1.00[EUR][1000 genomes]
rs646830	1.00[EUR][1000 genomes]
rs647063	1.00[EUR][1000 genomes]
rs647279	1.00[EUR][1000 genomes]
rs650471	1.00[EUR][1000 genomes]
rs681023	1.00[EUR][1000 genomes]
rs682560	1.00[EUR][1000 genomes]
rs7076482	0.86[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs806394	1.00[EUR][1000 genomes]
rs806395	1.00[EUR][1000 genomes]
rs806412	1.00[EUR][1000 genomes]

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	nsv1042286	chr10:5795129-6578445	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv1054044	chr10:6155144-6487217	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv894836	chr10:6246678-6435374	Flanking Active TSS Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv430123	chr10:6309402-6448384	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv430125	chr10:6322167-6477267	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv1053440	chr10:6354798-6669469	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
7	esv3391799	chr10:6426846-6431244	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:6425600-6432800	Weak transcription	Ovary	ovary
2	chr10:6425600-6443600	Weak transcription	Aorta	Aorta
3	chr10:6429200-6432600	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr10:6430200-6431000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr10:6430800-6431400	ZNF genes & repeats	Thymus	Thymus

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