Variant report

Variant	rs4653831
Chromosome Location	chr1:227553319-227553320
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:227504024..227506366-chr1:227550798..227554388,3	MCF-7	breast:
2	chr1:227551558..227554150-chr1:227559420..227561744,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000143776	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10458380	0.80[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs10753434	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10799412	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10916123	0.85[ASN][1000 genomes]
rs10916124	0.85[ASN][1000 genomes]
rs10916127	0.87[ASN][1000 genomes]
rs10916128	0.88[ASN][1000 genomes]
rs10916129	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10916133	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12022275	0.85[ASN][1000 genomes]
rs12023427	0.94[ASN][1000 genomes]
rs12028523	0.92[ASN][1000 genomes]
rs12047964	0.90[ASN][1000 genomes]
rs12057466	0.93[ASN][1000 genomes]
rs12062358	0.93[ASN][1000 genomes]
rs12081061	0.86[ASN][1000 genomes]
rs16847682	0.92[ASN][1000 genomes]
rs16847690	0.92[ASN][1000 genomes]
rs28654860	0.82[ASN][1000 genomes]
rs4075196	0.92[ASN][1000 genomes]
rs4075861	0.92[ASN][1000 genomes]
rs4531260	0.93[ASN][1000 genomes]
rs4653497	0.92[ASN][1000 genomes]
rs4653498	0.92[ASN][1000 genomes]
rs4653828	0.85[ASN][1000 genomes]
rs59718661	0.86[ASN][1000 genomes]
rs61833060	0.92[ASN][1000 genomes]
rs6690898	0.92[ASN][1000 genomes]
rs67343057	0.86[ASN][1000 genomes]
rs7519870	0.90[ASN][1000 genomes]
rs7541775	0.85[ASN][1000 genomes]
rs7553358	0.90[ASN][1000 genomes]
rs7555764	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7556096	0.85[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	nsv1003656	chr1:227034700-227559665	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv535318	chr1:227034700-227559665	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv534002	chr1:227315186-228047108	Bivalent/Poised TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
4	nsv873242	chr1:227371906-227579344	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv549271	chr1:227411003-227581017	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv1001353	chr1:227474785-227660691	Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227545800-227571200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:227552400-227553800	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr1:227552600-227553800	Enhancers	Rectal Mucosa Donor 29	rectum
4	chr1:227552600-227556400	Weak transcription	K562	blood
5	chr1:227553200-227553800	Enhancers	Duodenum Mucosa	Duodenum

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