Variant report

Variant	rs17167732
Chromosome Location	chr7:14035652-14035653
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	chr7:14034847..14037750-chr7:14053463..14055035,2	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10275495	0.81[ASN][1000 genomes]
rs10454309	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16878059	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17167695	1.00[EUR][1000 genomes]
rs17167746	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17167750	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17167772	1.00[AFR][1000 genomes]
rs17167778	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs17167783	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17167784	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17167806	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17167809	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17167812	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17167842	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17167848	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17167853	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2079353	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2190063	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35291842	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3919485	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4719388	0.97[AMR][1000 genomes]
rs58567888	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60718708	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs62452789	0.89[AMR][1000 genomes]
rs73057909	0.89[AMR][1000 genomes]
rs9639173	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9639174	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9639175	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9639176	1.00[AFR][1000 genomes];1.00[EUR][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	nsv1019873	chr7:13707148-14133367	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv887698	chr7:13841798-14056075	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv949467	chr7:13938464-14279074	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv887700	chr7:13948517-14042702	Flanking Active TSS Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv1030645	chr7:14015533-14078153	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv538739	chr7:14015533-14078153	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer 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:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14032200-14038400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:14032400-14037800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr7:14032400-14038400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:14032800-14038200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr7:14033000-14038200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:14033000-14038200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr7:14033000-14038400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr7:14033200-14038200	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr7:14033200-14038400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr7:14033200-14038400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr7:14033200-14038400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr7:14033200-14038400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr7:14033200-14041600	Weak transcription	K562	blood

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