Variant report

Variant	rs2191783
Chromosome Location	chr7:121525484-121525485
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:121516663..121519300-chr7:121525306..121527311,2	MCF-7	breast:

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs12667535	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12669706	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12672519	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1916885	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2024251	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3801373	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3801374	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3801377	0.88[CEU][hapmap];0.94[JPT][hapmap];0.96[LWK][hapmap];0.88[MKK][hapmap];0.90[TSI][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3801380	0.94[JPT][hapmap]
rs56265902	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6946211	0.89[CHB][hapmap];0.84[JPT][hapmap];0.80[MEX][hapmap]
rs6971645	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];0.94[MEX][hapmap];0.88[MKK][hapmap];0.90[TSI][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73229136	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs740965	0.94[JPT][hapmap]
rs9641678	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];0.94[MEX][hapmap];0.88[MKK][hapmap];0.90[TSI][hapmap];0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429808	chr7:121384049-121600049	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr7:121515600-121543600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:121521600-121529800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr7:121522000-121530400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr7:121522400-121527600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:121522400-121528400	Enhancers	Fetal Brain Male	brain
6	chr7:121522600-121526800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr7:121522600-121550000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:121523200-121539800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr7:121523200-121552600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr7:121523600-121529800	Weak transcription	NHEK	skin
11	chr7:121523800-121527200	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr7:121524400-121525600	Genic enhancers	HUES6 Cell Line	embryonic stem cell
13	chr7:121524400-121526000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr7:121524400-121526200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr7:121524600-121525600	Genic enhancers	Cortex derived primary cultured neurospheres	brain
16	chr7:121524600-121525600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr7:121524600-121526200	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr7:121525000-121525600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr7:121525000-121525800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr7:121525000-121525800	Weak transcription	Fetal Brain Female	brain
21	chr7:121525000-121527000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr7:121525200-121526000	Genic enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr7:121525400-121525800	Genic enhancers	HUES48 Cell Line	embryonic stem cell
24	chr7:121525400-121531600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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