Variant report

Variant	rs6745134
Chromosome Location	chr2:234256520-234256521
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:234255807..234258253-chr2:234261320..234263742,3	MCF-7	breast:
2	chr2:234253774..234256883-chr2:234262038..234267744,5	K562	blood:

Variant related genes	Relation type
ENSG00000259793	Chromatin interaction
ENSG00000243637	Chromatin interaction
ENSG00000077044	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10168794	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10185174	1.00[ASN][1000 genomes]
rs10193542	1.00[CEU][hapmap]
rs10929208	1.00[CHB][hapmap]
rs11892545	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs13384932	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13391864	0.87[CEU][hapmap]
rs13400563	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs13403169	0.88[CEU][hapmap]
rs13414407	1.00[CEU][hapmap]
rs13420976	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13425849	0.88[CEU][hapmap]
rs13427703	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs1901812	1.00[CHB][hapmap]
rs2124045	1.00[CHB][hapmap]
rs2289473	1.00[CHB][hapmap]
rs28437319	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28605452	0.84[ASN][1000 genomes]
rs28657808	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2971865	1.00[CHB][hapmap]
rs3762586	0.84[ASN][1000 genomes]
rs3792095	0.84[ASN][1000 genomes]
rs3792104	1.00[CHB][hapmap]
rs3792105	1.00[CHB][hapmap]
rs56871749	1.00[ASN][1000 genomes]
rs57712949	1.00[ASN][1000 genomes]
rs58222850	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73106630	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7422734	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs7572257	0.88[CEU][hapmap]
rs7588509	1.00[CHB][hapmap]
rs838557	1.00[CHB][hapmap]
rs838558	1.00[CHB][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	nsv584700	chr2:234199401-234364426	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv1002075	chr2:234225979-234277508	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv529419	chr2:234229606-234670426	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
4	nsv460135	chr2:234242347-234288048	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv584701	chr2:234242347-234288048	ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv460136	chr2:234244395-234288048	Weak transcription Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv584702	chr2:234244395-234288048	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234244600-234257800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr2:234247600-234257400	Weak transcription	Spleen	Spleen
3	chr2:234248400-234256600	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr2:234249400-234257000	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr2:234249600-234256600	Weak transcription	Primary B cells from cord blood	blood
6	chr2:234255000-234257800	Enhancers	Brain Cingulate Gyrus	brain
7	chr2:234255000-234260000	Enhancers	Liver	Liver
8	chr2:234255400-234257600	Enhancers	Brain Anterior Caudate	brain
9	chr2:234255600-234256800	Weak transcription	Brain Hippocampus Middle	brain
10	chr2:234255600-234258600	Enhancers	Brain Substantia Nigra	brain
11	chr2:234255800-234258600	Flanking Active TSS	HepG2	liver
12	chr2:234255800-234262400	Weak transcription	Right Atrium	heart
13	chr2:234256000-234256800	Weak transcription	Brain Angular Gyrus	brain
14	chr2:234256000-234257600	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr2:234256000-234257800	Weak transcription	K562	blood
16	chr2:234256200-234260800	Enhancers	Primary B cells from peripheral blood	blood
17	chr2:234256400-234256800	Enhancers	Duodenum Mucosa	Duodenum
18	chr2:234256400-234260400	Enhancers	Fetal Intestine Small	intestine
19	chr2:234256400-234262400	Enhancers	Sigmoid Colon	Sigmoid Colon

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