Variant report

Variant	rs1901520
Chromosome Location	chr5:101754661-101754662
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	chr5:101754300..101756641-chr5:101769503..101772313,2	K562	blood:

Extended variants
information (count: 119 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:107)

rs_ID	r²[population]
rs10038809	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs10041507	0.92[CHB][hapmap];0.92[JPT][hapmap]
rs10041525	0.92[CHB][hapmap];0.92[JPT][hapmap]
rs10041806	0.91[CHB][hapmap];0.83[JPT][hapmap]
rs10053573	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10055023	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs10062613	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs10065821	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs10069193	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs10073052	0.85[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs10223273	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs10463981	0.89[YRI][hapmap]
rs10479216	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs10515326	1.00[YRI][hapmap]
rs1078338	0.82[ASN][1000 genomes]
rs1117130	0.86[ASN][1000 genomes]
rs1118008	0.91[CHB][hapmap];0.92[JPT][hapmap]
rs11242471	0.91[CHB][hapmap];0.92[JPT][hapmap]
rs11746217	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs12658397	1.00[YRI][hapmap]
rs13353915	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1376894	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs1376898	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs1376907	0.89[YRI][hapmap]
rs1376910	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs1376911	0.92[CHB][hapmap];0.91[JPT][hapmap]
rs1452057	0.92[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs1452060	0.82[ASN][1000 genomes]
rs1452065	0.86[ASN][1000 genomes]
rs1542296	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs1545487	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs1545488	0.86[CHB][hapmap];0.91[JPT][hapmap]
rs1562960	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs1562961	0.92[CHB][hapmap];0.91[JPT][hapmap]
rs1597771	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs17273466	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs1823694	0.82[ASN][1000 genomes]
rs1875634	0.91[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs1901512	0.92[CHB][hapmap];0.91[JPT][hapmap]
rs1901521	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs1901522	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs2010590	0.80[ASN][1000 genomes]
rs2060833	0.95[CHB][hapmap];0.85[JPT][hapmap]
rs2060836	0.86[ASN][1000 genomes]
rs2060837	0.86[ASN][1000 genomes]
rs2084826	0.92[CHB][hapmap];0.91[JPT][hapmap]
rs2123133	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs2123135	0.91[JPT][hapmap]
rs2167586	0.91[ASN][1000 genomes]
rs2400795	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs2400796	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap]
rs2400797	0.92[CHB][hapmap];0.91[JPT][hapmap]
rs2400798	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs2400801	0.91[CHB][hapmap];0.92[JPT][hapmap]
rs2600831	0.83[JPT][hapmap]
rs28532891	0.82[ASN][1000 genomes]
rs3114660	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs3114661	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs4085107	0.92[CHB][hapmap];0.91[JPT][hapmap]
rs4386713	1.00[YRI][hapmap]
rs4703226	0.92[CHB][hapmap];0.91[JPT][hapmap]
rs4703230	0.92[CHB][hapmap];0.92[JPT][hapmap]
rs4703232	0.92[CHB][hapmap];0.92[JPT][hapmap]
rs56358831	0.91[ASN][1000 genomes]
rs6596482	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs6596486	1.00[YRI][hapmap]
rs6596493	0.91[CHB][hapmap];0.87[JPT][hapmap]
rs6596495	0.86[CHB][hapmap];0.91[JPT][hapmap]
rs6860720	0.91[ASN][1000 genomes]
rs6866255	0.91[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs6871070	0.92[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs6871966	0.91[CHB][hapmap];0.92[JPT][hapmap]
rs6873305	0.91[CHB][hapmap];0.83[JPT][hapmap]
rs6873738	0.92[CHB][hapmap];0.91[JPT][hapmap]
rs6877722	0.92[CHB][hapmap];0.92[JPT][hapmap]
rs6878326	0.91[ASN][1000 genomes]
rs6881112	0.83[YRI][hapmap]
rs6884162	0.82[ASN][1000 genomes]
rs6885800	0.90[CHB][hapmap];0.90[JPT][hapmap]
rs6890130	0.92[CHB][hapmap];0.91[JPT][hapmap]
rs6893391	0.86[ASN][1000 genomes]
rs6893723	0.87[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs6895200	0.92[CHB][hapmap];0.92[JPT][hapmap]
rs709369	0.82[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs709372	0.92[CHB][hapmap];0.92[JPT][hapmap]
rs7356647	0.92[CHB][hapmap];0.91[JPT][hapmap]
rs7702418	0.82[ASN][1000 genomes]
rs7711687	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs7715217	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs7719316	0.91[CHB][hapmap];0.94[JPT][hapmap]
rs7721084	0.87[CHB][hapmap]
rs7721548	0.82[ASN][1000 genomes]
rs7722680	0.82[ASN][1000 genomes]
rs7731256	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs7731310	0.92[CHB][hapmap];0.91[JPT][hapmap]
rs7732942	0.92[CHB][hapmap];0.92[JPT][hapmap]
rs7733253	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs7736579	0.91[CHB][hapmap];0.92[JPT][hapmap]
rs7737204	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs841924	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs841928	0.85[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs841931	0.85[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs841933	0.83[JPT][hapmap]
rs896545	0.85[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs9285943	0.90[CHB][hapmap]
rs9327859	0.92[CHB][hapmap];0.92[JPT][hapmap]
rs9327860	0.91[CHB][hapmap];0.92[JPT][hapmap]

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	nsv817537	chr5:101489151-101992104	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1016176	chr5:101534391-102333606	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv537831	chr5:101534391-102333606	Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	nsv522882	chr5:101596633-101782930	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1029894	chr5:101620079-102516827	Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
6	nsv830427	chr5:101651510-101849723	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv882511	chr5:101669015-101819981	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv882514	chr5:101672238-101795490	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv882515	chr5:101672238-101816104	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv882516	chr5:101672238-101819981	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv519686	chr5:101701924-101795490	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv526352	chr5:101701924-101795490	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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