Variant report

Variant	rs7172280
Chromosome Location	chr15:41177617-41177618
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:41156581..41159555-chr15:41176856..41179338,2	MCF-7	breast:
2	chr15:41042798..41045443-chr15:41176819..41178417,2	K562	blood:
3	chr15:41154418..41156417-chr15:41177527..41179502,2	K562	blood:

Variant related genes	Relation type
ENSG00000137824	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11070301	0.82[ASN][1000 genomes]
rs11070304	0.87[EUR][1000 genomes]
rs11635602	0.88[ASN][1000 genomes]
rs11856227	1.00[CEU][hapmap]
rs12101494	0.81[EUR][1000 genomes]
rs12148523	0.82[EUR][1000 genomes]
rs12916961	1.00[CEU][hapmap]
rs16971157	1.00[CEU][hapmap];0.87[YRI][hapmap];0.86[EUR][1000 genomes]
rs16971177	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs16971186	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs16971188	0.88[CHB][hapmap]
rs1814568	0.86[CHB][hapmap]
rs1814692	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2279578	1.00[CEU][hapmap]
rs2445490	0.82[ASN][1000 genomes]
rs3100810	0.88[ASN][1000 genomes]
rs3743036	0.89[CHB][hapmap]
rs4384588	1.00[CEU][hapmap]
rs4923886	1.00[CEU][hapmap]
rs4923887	0.87[ASN][1000 genomes]
rs4924509	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs595559	0.89[CHB][hapmap]
rs601436	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs601696	0.88[ASN][1000 genomes]
rs615987	0.88[ASN][1000 genomes]
rs616606	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs617377	0.87[EUR][1000 genomes]
rs618892	0.92[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs618916	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs625058	1.00[CEU][hapmap]
rs675262	0.86[CHB][hapmap]
rs677273	1.00[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs682130	0.84[ASN][1000 genomes]
rs687949	0.88[ASN][1000 genomes]
rs690365	0.86[CHB][hapmap]
rs694213	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs8024861	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8024961	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8025867	0.88[CHB][hapmap]
rs8028660	0.88[CEU][hapmap]
rs8042095	0.85[EUR][1000 genomes]
rs880428	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv904101	chr15:40979651-41275014	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	esv1819092	chr15:41017682-41255750	Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
3	nsv904102	chr15:41046883-41201699	Strong transcription Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
4	nsv1054764	chr15:41068625-41196410	Active TSS Strong transcription Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv569228	chr15:41106485-41194151	Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
6	nsv904103	chr15:41123172-41275014	Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
7	nsv904104	chr15:41149824-41234932	Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
8	nsv904105	chr15:41149824-41275014	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 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	chr15:41172000-41184000	Weak transcription	Duodenum Mucosa	Duodenum
2	chr15:41175800-41177800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr15:41177200-41184000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr15:41177400-41186000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr15:41177600-41181600	Weak transcription	GM12878-XiMat	blood

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