Variant report

Variant	rs760606
Chromosome Location	chr22:27614498-27614499
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:27614255..27616554-chr22:27616988..27619608,2	MCF-7	breast:

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1401527	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs471216	0.82[EUR][1000 genomes]
rs492416	0.87[CHB][hapmap]
rs499733	0.82[CHB][hapmap]
rs559631	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs715601	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs849449	0.82[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	nsv917333	chr22:26931825-27692024	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	142 gene(s)	inside rSNPs	diseases
2	esv34168	chr22:27289097-27678031	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	esv3413125	chr22:27404463-28121577	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
4	nsv459860	chr22:27527005-28181436	Strong transcription Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
5	nsv588872	chr22:27527005-28181436	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
6	nsv1064910	chr22:27609597-27648408	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv526167	chr22:27613130-27616264	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:27606800-27620000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr22:27609200-27615800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr22:27610200-27616000	Weak transcription	Fetal Intestine Small	intestine
4	chr22:27611000-27615800	Weak transcription	NH-A	brain
5	chr22:27611400-27614800	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr22:27611400-27616000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr22:27611600-27615800	Weak transcription	Osteobl	bone
8	chr22:27611800-27616000	Weak transcription	Colon Smooth Muscle	Colon
9	chr22:27612200-27615800	Weak transcription	Rectal Smooth Muscle	rectum
10	chr22:27613000-27615200	Enhancers	A549	lung
11	chr22:27613200-27615200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr22:27613400-27615200	Enhancers	Ovary	ovary
13	chr22:27613400-27617000	Enhancers	Adipose Nuclei	Adipose
14	chr22:27613600-27615400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr22:27613800-27615400	Enhancers	Stomach Smooth Muscle	stomach
16	chr22:27614000-27614600	Enhancers	Right Atrium	heart
17	chr22:27614200-27614600	Genic enhancers	Placenta Amnion	Placenta Amnion
18	chr22:27614200-27614800	Enhancers	Fetal Stomach	stomach
19	chr22:27614200-27615000	Enhancers	Fetal Muscle Trunk	muscle
20	chr22:27614200-27615000	Enhancers	Lung	lung
21	chr22:27614400-27614800	Enhancers	Brain Germinal Matrix	brain
22	chr22:27614400-27615000	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr22:27614400-27615400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr22:27614400-27615600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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