Variant report

Variant	rs74017545
Chromosome Location	chr16:31935460-31935461
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:31930170..31932707-chr16:31934024..31936447,2	K562	blood:
2	chr16:31931465..31935999-chr16:31936605..31940603,7	K562	blood:
3	chr16:31932903..31935520-chr16:31946813..31948460,2	K562	blood:
4	chr16:31929972..31932646-chr16:31933691..31936236,4	MCF-7	breast:
5	chr16:31932491..31936311-chr16:31936605..31941493,6	K562	blood:
6	chr16:31929792..31932707-chr16:31934299..31936447,2	K562	blood:

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs28784931	1.00[EUR][1000 genomes]
rs28798712	1.00[EUR][1000 genomes]
rs28803931	1.00[EUR][1000 genomes]
rs28813790	1.00[EUR][1000 genomes]
rs28829329	1.00[EUR][1000 genomes]
rs28838657	1.00[EUR][1000 genomes]
rs28845565	1.00[EUR][1000 genomes]
rs28847351	1.00[EUR][1000 genomes]
rs28847575	1.00[EUR][1000 genomes]
rs28855454	1.00[EUR][1000 genomes]
rs28870502	1.00[EUR][1000 genomes]
rs28874939	1.00[EUR][1000 genomes]
rs28897501	1.00[EUR][1000 genomes]
rs3907736	1.00[EUR][1000 genomes]
rs3907737	1.00[EUR][1000 genomes]
rs4584827	1.00[EUR][1000 genomes]
rs56051141	1.00[EUR][1000 genomes]
rs57379260	1.00[EUR][1000 genomes]
rs58693542	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60327897	1.00[EUR][1000 genomes]
rs60788729	1.00[EUR][1000 genomes]
rs61321146	1.00[EUR][1000 genomes]
rs61444575	1.00[EUR][1000 genomes]
rs7205954	1.00[EUR][1000 genomes]
rs7339438	1.00[EUR][1000 genomes]
rs7339445	1.00[EUR][1000 genomes]
rs73526430	1.00[EUR][1000 genomes]
rs73526472	1.00[EUR][1000 genomes]
rs74017544	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74017550	1.00[EUR][1000 genomes]
rs74017570	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1067321	chr16:31652036-31959992	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
2	nsv1066522	chr16:31831196-31959992	ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv1057300	chr16:31862900-31959992	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	nsv833196	chr16:31897381-32068953	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	esv1850460	chr16:31905688-32097085	Strong transcription ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv974735	chr16:31933472-31947343	ZNF genes & repeats Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv1848653	chr16:31934245-32394874	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31931200-31936600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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