Variant report

Variant	rs4527446
Chromosome Location	chr4:93420293-93420294
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	chr4:93384358..93386319-chr4:93419609..93421147,2	K562	blood:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10000919	0.93[EUR][1000 genomes]
rs11930169	0.91[EUR][1000 genomes]
rs11940024	0.82[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs11945497	0.94[EUR][1000 genomes]
rs12331640	0.83[ASN][1000 genomes]
rs12643954	0.94[EUR][1000 genomes]
rs28480343	0.80[ASN][1000 genomes]
rs2870626	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34183174	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35400056	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs57390091	0.94[EUR][1000 genomes]
rs62310672	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62312219	0.80[EUR][1000 genomes]
rs6532370	0.91[EUR][1000 genomes]
rs6835375	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7658053	0.93[EUR][1000 genomes]
rs7659159	0.92[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7676323	0.92[EUR][1000 genomes]
rs7677007	0.91[EUR][1000 genomes]
rs7678325	0.91[EUR][1000 genomes]
rs7681461	0.80[EUR][1000 genomes]
rs7683035	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948712	chr4:93007985-93740409	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1000700	chr4:93270083-93425831	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv537182	chr4:93270083-93425831	Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv997925	chr4:93270083-93464386	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv537183	chr4:93270083-93464386	Enhancers Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv1005500	chr4:93359923-93590452	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv537184	chr4:93359923-93590452	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv879605	chr4:93376231-93740409	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1006957	chr4:93389054-93511561	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv879606	chr4:93391251-93479275	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv1013199	chr4:93395509-93511052	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:93409800-93421600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:93410200-93421400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr4:93410200-93421600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr4:93414600-93421800	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr4:93414800-93434400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr4:93417600-93420800	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr4:93418400-93421600	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr4:93419000-93421000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr4:93419400-93421600	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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