Variant report

Variant	rs7959670
Chromosome Location	chr12:119612484-119612485
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11064705	0.83[AMR][1000 genomes]
rs12298452	0.89[ASW][hapmap];0.94[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12304226	1.00[AMR][1000 genomes]
rs13378054	0.89[ASW][hapmap];0.94[YRI][hapmap];1.00[AMR][1000 genomes]
rs4628742	0.83[AMR][1000 genomes]
rs55845457	1.00[AMR][1000 genomes]
rs56134777	1.00[AMR][1000 genomes]
rs56249836	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59338565	0.83[AMR][1000 genomes]
rs60038524	0.83[AMR][1000 genomes]
rs7959112	0.94[YRI][hapmap];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047036	chr12:119477583-119992640	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv902	chr12:119576112-119621140	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv899550	chr12:119581131-119654315	Enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119597400-119613800	Weak transcription	Aorta	Aorta
2	chr12:119598400-119613800	Weak transcription	Right Atrium	heart
3	chr12:119604400-119613600	Enhancers	Placenta	Placenta
4	chr12:119609000-119616000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr12:119609200-119612600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr12:119609400-119613800	Weak transcription	Esophagus	oesophagus
7	chr12:119609400-119614000	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr12:119609800-119615800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr12:119610000-119613200	Weak transcription	Hela-S3	cervix
10	chr12:119610200-119613800	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr12:119610200-119614000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr12:119611200-119614000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr12:119611200-119614200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr12:119611400-119612600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr12:119611400-119616000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr12:119611600-119613800	Enhancers	Fetal Muscle Leg	muscle
17	chr12:119612200-119612600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr12:119612200-119612600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr12:119612200-119612800	Enhancers	Fetal Muscle Trunk	muscle
20	chr12:119612200-119613000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr12:119612200-119613200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr12:119612200-119613400	Enhancers	Stomach Smooth Muscle	stomach
23	chr12:119612200-119615200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr12:119612400-119614000	Weak transcription	HUES6 Cell Line	embryonic stem cell

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