Variant report

Variant	rs1745420
Chromosome Location	chr1:228251732-228251733
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:228241595..228245026-chr1:228250966..228253620,3	MCF-7	breast:
2	chr1:228223566..228226544-chr1:228251359..228253705,2	MCF-7	breast:
3	chr1:228241062..228243243-chr1:228249965..228251823,3	K562	blood:
4	chr1:228251281..228254071-chr1:228258113..228259786,2	MCF-7	breast:
5	chr1:228230710..228233813-chr1:228249288..228252101,3	MCF-7	breast:
6	chr1:228249900..228252116-chr1:228255479..228257281,2	MCF-7	breast:
7	chr1:228249620..228252604-chr1:228254168..228256020,2	MCF-7	breast:
8	chr1:228248925..228252171-chr1:228258918..228261969,3	MCF-7	breast:

No data

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1034792	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1048503	0.86[JPT][hapmap]
rs10916261	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10916262	0.84[CEU][hapmap];0.92[EUR][1000 genomes]
rs1094602	0.82[ASN][1000 genomes]
rs11584499	0.84[CEU][hapmap];0.86[JPT][hapmap];0.90[EUR][1000 genomes]
rs11589513	0.92[CEU][hapmap];0.92[EUR][1000 genomes]
rs1188975	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1188977	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12033088	0.94[EUR][1000 genomes]
rs12048010	0.92[EUR][1000 genomes]
rs13374948	0.91[CEU][hapmap];0.84[CHB][hapmap];0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1620734	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1745422	0.94[EUR][1000 genomes]
rs2107905	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3738680	0.86[JPT][hapmap]
rs3738681	0.86[JPT][hapmap]
rs41270175	0.94[EUR][1000 genomes]
rs41270177	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4653533	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4653897	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4653906	0.93[CHB][hapmap]
rs57146523	0.92[EUR][1000 genomes]
rs57657087	0.92[EUR][1000 genomes]
rs61825125	0.84[AMR][1000 genomes]
rs61825130	0.92[EUR][1000 genomes]
rs61825131	0.94[EUR][1000 genomes]
rs61825133	0.88[EUR][1000 genomes]
rs6668719	0.85[CHB][hapmap]
rs708126	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72756204	0.92[EUR][1000 genomes]
rs72756209	0.88[EUR][1000 genomes]
rs7537552	0.92[CHB][hapmap]
rs7539664	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs822727	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs860301	0.97[ASN][1000 genomes]
rs882451	0.84[CEU][hapmap];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010605	chr1:227770415-228332690	Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	esv32853	chr1:227880116-228806209	Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	187 gene(s)	inside rSNPs	diseases
3	nsv427952	chr1:227881664-228308629	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
4	nsv826908	chr1:227895386-228691100	Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
5	nsv516409	chr1:228035131-228296745	Enhancers Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
6	nsv523935	chr1:228038124-228681749	Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	137 gene(s)	inside rSNPs	diseases
7	nsv832803	chr1:228155118-228313681	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
8	nsv873252	chr1:228174528-228371551	Strong transcription Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
9	esv1814215	chr1:228231601-228259932	Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
10	esv1844252	chr1:228231601-228259932	Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
11	nsv873253	chr1:228231601-228537942	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
12	nsv873254	chr1:228231601-228543800	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228248200-228269000	Weak transcription	Right Atrium	heart
2	chr1:228251200-228254200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:228251400-228253000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
4	chr1:228251600-228251800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
5	chr1:228251600-228251800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
6	chr1:228251600-228251800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
7	chr1:228251600-228251800	Bivalent Enhancer	Stomach Mucosa	stomach
8	chr1:228251600-228252200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell

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