Variant report

Variant	rs9393670
Chromosome Location	chr6:25789061-25789062
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:25787767..25791136-chr6:25887624..25890567,3	K562	blood:
2	chr6:25788519..25789097-chrX:98135948..98136448,2	MCF-7	breast:
3	chr6:25788140..25789474-chr6:25890294..25891442,10	MCF-7	breast:
4	chr6:25788477..25789236-chr6:25890713..25891324,2	MCF-7	breast:
5	chr6:25782886..25784532-chr6:25787589..25789523,2	MCF-7	breast:
6	chr6:25788309..25789452-chr6:26002965..26003984,3	MCF-7	breast:
7	chr6:25787936..25790848-chr6:25942188..25944677,2	K562	blood:
8	chr6:25788525..25789371-chr6:25992441..25993378,2	K562	blood:
9	chr6:25787422..25789346-chr6:25991873..25993679,2	K562	blood:
10	chr6:25788441..25789483-chr6:25942366..25943406,8	MCF-7	breast:
11	chr6:25788516..25789431-chr6:25890332..25891380,4	K562	blood:
12	chr6:25788385..25789459-chr6:25942332..25943408,5	K562	blood:
13	chr6:25786996..25789369-chr6:26029136..26033037,3	K562	blood:
14	chr6:25787874..25789586-chr6:25991513..25994332,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000272462	Chromatin interaction
ENSG00000124693	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10946798	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1165150	0.82[ASN][1000 genomes]
rs1165151	1.00[JPT][hapmap];0.83[YRI][hapmap];0.84[ASN][1000 genomes]
rs1165153	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs1165154	0.86[ASN][1000 genomes]
rs1165160	0.92[JPT][hapmap]
rs1165176	0.92[JPT][hapmap];0.82[ASN][1000 genomes]
rs1165177	0.92[JPT][hapmap];0.83[YRI][hapmap];0.82[ASN][1000 genomes]
rs1165178	0.92[JPT][hapmap];0.83[YRI][hapmap];0.82[ASN][1000 genomes]
rs1165179	0.82[ASN][1000 genomes]
rs1165180	0.82[ASN][1000 genomes]
rs1165182	0.92[JPT][hapmap];0.83[YRI][hapmap];0.82[ASN][1000 genomes]
rs1165195	0.88[ASN][1000 genomes]
rs1165196	1.00[JPT][hapmap];0.82[YRI][hapmap];0.87[ASN][1000 genomes]
rs1165199	0.88[ASN][1000 genomes]
rs1165205	0.92[JPT][hapmap];0.82[YRI][hapmap]
rs1165206	0.96[CEU][hapmap];0.92[CHB][hapmap];0.92[JPT][hapmap];0.82[YRI][hapmap];0.81[EUR][1000 genomes]
rs1165207	0.92[JPT][hapmap];0.82[YRI][hapmap]
rs1165209	1.00[JPT][hapmap];0.82[YRI][hapmap];0.88[ASN][1000 genomes]
rs1165213	1.00[JPT][hapmap];0.82[YRI][hapmap];0.88[ASN][1000 genomes]
rs1165215	1.00[JPT][hapmap];0.82[YRI][hapmap];0.88[ASN][1000 genomes]
rs1177442	0.88[ASN][1000 genomes]
rs1183200	1.00[JPT][hapmap];0.83[YRI][hapmap];0.86[ASN][1000 genomes]
rs1183201	0.92[JPT][hapmap];0.83[YRI][hapmap];0.82[ASN][1000 genomes]
rs1184803	0.92[JPT][hapmap];1.00[YRI][hapmap];0.82[ASN][1000 genomes]
rs1184804	0.92[JPT][hapmap];0.83[YRI][hapmap]
rs1185153	0.82[ASN][1000 genomes]
rs1185567	1.00[JPT][hapmap];0.83[YRI][hapmap];0.86[ASN][1000 genomes]
rs1185568	0.92[JPT][hapmap];0.83[YRI][hapmap];0.82[ASN][1000 genomes]
rs1185569	0.92[JPT][hapmap];0.82[YRI][hapmap];0.82[ASN][1000 genomes]
rs1185978	0.82[ASN][1000 genomes]
rs12201071	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12662869	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs13197514	0.80[ASN][1000 genomes]
rs13197601	1.00[JPT][hapmap]
rs1359232	0.88[ASN][1000 genomes]
rs1747522	1.00[JPT][hapmap];0.83[YRI][hapmap];0.84[ASN][1000 genomes]
rs2000351	0.81[CHB][hapmap]
rs2096386	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs2328895	0.88[ASN][1000 genomes]
rs2762353	1.00[JPT][hapmap];0.82[YRI][hapmap];0.87[ASN][1000 genomes]
rs2817188	0.88[ASN][1000 genomes]
rs35720558	0.80[ASN][1000 genomes]
rs3757131	1.00[JPT][hapmap]
rs3799352	1.00[JPT][hapmap];0.83[YRI][hapmap];0.84[ASN][1000 genomes]
rs3923	0.96[CEU][hapmap]
rs4145221	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6456693	1.00[JPT][hapmap]
rs765285	0.90[JPT][hapmap];1.00[YRI][hapmap];0.82[ASN][1000 genomes]
rs7746502	0.81[CHB][hapmap]
rs7749149	0.86[CHB][hapmap]
rs7770037	0.81[CHB][hapmap]
rs942379	0.92[JPT][hapmap];0.83[YRI][hapmap]
rs9467596	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv427747	chr6:25641380-25908218	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv883489	chr6:25789061-25821770	Strong transcription Enhancers Weak transcription	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25780400-25798800	Weak transcription	Liver	Liver
2	chr6:25787600-25790600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:25789000-25789400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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