Variant report

Variant	rs67900982
Chromosome Location	chr2:208974831-208974832
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	chr2:208969150..208970998-chr2:208972838..208975738,2	K562	blood:
2	chr2:208973001..208975909-chr2:208979754..208981880,3	MCF-7	breast:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10188278	0.80[EUR][1000 genomes]
rs10188286	0.80[EUR][1000 genomes]
rs1020581	0.84[ASN][1000 genomes]
rs10497893	0.88[ASN][1000 genomes]
rs11677829	0.81[ASN][1000 genomes]
rs11684908	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11690797	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13006347	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13034094	0.84[ASN][1000 genomes]
rs1806338	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2084872	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34274138	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34577840	0.84[ASN][1000 genomes]
rs34589201	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34765959	0.84[ASN][1000 genomes]
rs35960349	0.85[ASN][1000 genomes]
rs55770589	0.84[ASN][1000 genomes]
rs60163320	0.89[ASN][1000 genomes]
rs6435411	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6709879	0.84[ASN][1000 genomes]
rs6716279	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6745137	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6745370	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6747966	0.82[EUR][1000 genomes]
rs6751131	0.82[ASN][1000 genomes]
rs6758319	0.80[EUR][1000 genomes]
rs6759995	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6761316	0.82[EUR][1000 genomes]
rs732008	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs732009	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7349197	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7586866	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7586953	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7587397	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7590593	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7604207	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010531	chr2:208610639-209176782	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv536130	chr2:208610639-209176782	Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv534496	chr2:208814372-209302791	Strong transcription Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	nsv875744	chr2:208952810-208994045	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv875745	chr2:208969865-208994045	Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv875746	chr2:208971007-208989708	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:208965000-208976600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr2:208967400-208976800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:208969400-208976600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr2:208972600-208976200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr2:208972600-208976600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr2:208973000-208975600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr2:208973000-208976200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr2:208973200-208975600	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr2:208973200-208976600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr2:208973200-208976800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr2:208973200-208989000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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