Variant report

Variant	rs6680068
Chromosome Location	chr1:192900657-192900658
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	chr1:192895816..192898455-chr1:192898887..192900802,2	MCF-7	breast:
2	chr1:192895978..192897609-chr1:192900333..192902139,2	MCF-7	breast:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10754036	0.98[EUR][1000 genomes]
rs10801165	0.81[EUR][1000 genomes]
rs10921300	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12117621	0.89[EUR][1000 genomes]
rs12118267	0.95[EUR][1000 genomes]
rs12124274	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12125252	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12132131	0.98[EUR][1000 genomes]
rs12133193	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12133295	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12138298	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12143913	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1339591	0.98[EUR][1000 genomes]
rs1339593	0.81[EUR][1000 genomes]
rs17525308	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2066216	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2486496	0.98[EUR][1000 genomes]
rs28461227	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35686688	0.84[EUR][1000 genomes]
rs710140	0.81[EUR][1000 genomes]
rs710141	0.81[EUR][1000 genomes]
rs72738564	0.98[EUR][1000 genomes]
rs72738565	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72738572	0.89[EUR][1000 genomes]
rs72738574	0.89[EUR][1000 genomes]
rs7415619	0.81[CEU][hapmap];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs842792	0.81[EUR][1000 genomes]
rs842793	0.81[EUR][1000 genomes]
rs842794	0.81[EUR][1000 genomes]
rs842798	0.81[EUR][1000 genomes]
rs842802	0.81[EUR][1000 genomes]
rs842803	0.81[EUR][1000 genomes]
rs842805	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs842812	0.81[EUR][1000 genomes]
rs842815	0.98[EUR][1000 genomes]
rs844528	0.81[EUR][1000 genomes]
rs946557	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532618	chr1:192537006-193149179	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
2	nsv548660	chr1:192609268-192945348	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:192897600-192903800	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr1:192898400-192901000	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr1:192898600-192900800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr1:192898800-192901400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr1:192899000-192901000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr1:192899600-192902200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr1:192899800-192900800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr1:192900600-192918600	Weak transcription	Psoas Muscle	Psoas

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