Variant report

Variant	rs4437922
Chromosome Location	chr1:92581818-92581819
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 149 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:116)

rs_ID	r²[population]
rs1014415	1.00[JPT][hapmap]
rs10159094	0.88[CEU][hapmap];1.00[JPT][hapmap]
rs1023041	1.00[JPT][hapmap]
rs10747503	0.90[ASN][1000 genomes]
rs10783109	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10783112	0.86[EUR][1000 genomes]
rs10875204	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];0.88[MKK][hapmap];0.95[TSI][hapmap];0.97[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10875209	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10875214	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10875237	0.90[ASN][1000 genomes]
rs10875319	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs10875349	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs11165984	1.00[JPT][hapmap]
rs11166042	1.00[JPT][hapmap]
rs11166141	0.83[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.84[MKK][hapmap];0.90[TSI][hapmap];0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11166144	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11166184	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11166218	0.88[EUR][1000 genomes]
rs1157469	0.96[CEU][hapmap];0.93[GIH][hapmap];0.80[TSI][hapmap];0.88[EUR][1000 genomes]
rs1157470	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11577572	1.00[JPT][hapmap]
rs11585255	1.00[JPT][hapmap]
rs11588153	1.00[JPT][hapmap]
rs12119246	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1226179	0.90[ASN][1000 genomes]
rs1226183	0.80[CEU][hapmap];1.00[JPT][hapmap]
rs1226187	0.87[CEU][hapmap];1.00[JPT][hapmap];0.93[TSI][hapmap];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12404806	1.00[JPT][hapmap]
rs12729867	1.00[JPT][hapmap]
rs1483022	0.92[CEU][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1487540	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs1542685	1.00[JPT][hapmap]
rs1601020	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1601021	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1601023	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1872007	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs1982720	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2046620	1.00[JPT][hapmap]
rs2087194	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs2093879	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.85[MKK][hapmap];0.93[TSI][hapmap];0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2128645	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2128646	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2181897	0.90[ASN][1000 genomes]
rs2209337	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2391114	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2391116	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2839877	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2893200	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.80[TSI][hapmap];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3103176	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs3103178	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs3103181	1.00[JPT][hapmap]
rs3118137	0.90[ASN][1000 genomes]
rs3131814	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs3131828	1.00[JPT][hapmap]
rs3851271	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.80[TSI][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3851272	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.80[TSI][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3851273	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4261159	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4623754	1.00[CHB][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4658127	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4658128	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.81[MKK][hapmap];0.95[TSI][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4658129	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4658289	1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4658290	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4658291	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4658294	1.00[JPT][hapmap]
rs4658298	1.00[JPT][hapmap]
rs4658299	1.00[JPT][hapmap]
rs488288	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs488849	0.88[CEU][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs490800	0.81[CEU][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs492164	0.88[CEU][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs493595	0.92[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs504606	1.00[JPT][hapmap]
rs506375	0.88[CEU][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs507452	0.81[CEU][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs511546	0.81[CEU][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs515280	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs519343	0.90[ASN][1000 genomes]
rs519623	0.90[ASN][1000 genomes]
rs519932	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs527412	0.92[CEU][hapmap];1.00[JPT][hapmap];0.93[TSI][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs529135	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs534547	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs547699	0.92[CEU][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs551909	0.92[CEU][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs553861	0.92[CEU][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs556980	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs560389	0.84[CEU][hapmap]
rs563113	0.88[CEU][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs563606	1.00[JPT][hapmap];0.90[TSI][hapmap];0.90[ASN][1000 genomes]
rs564971	0.90[ASN][1000 genomes]
rs569178	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs569593	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs570368	0.83[CEU][hapmap];1.00[JPT][hapmap]
rs573044	0.85[CEU][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs575805	0.88[CEU][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs6604080	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6604082	0.92[CEU][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6604090	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs6661384	0.85[CHD][hapmap]
rs6663278	1.00[JPT][hapmap]
rs6677184	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6684317	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6699855	0.87[CEU][hapmap];1.00[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.90[ASN][1000 genomes]
rs6702267	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs7529835	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7533077	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.80[TSI][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7541482	0.91[CEU][hapmap];0.80[YRI][hapmap];0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7542358	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.84[MKK][hapmap];0.93[TSI][hapmap];0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7542373	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7545076	0.88[CEU][hapmap];1.00[JPT][hapmap];0.80[TSI][hapmap];0.90[ASN][1000 genomes]
rs7549158	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7549516	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9661633	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs981583	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:33 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012864	chr1:92067100-92827761	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv535029	chr1:92067100-92827761	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv530438	chr1:92091957-92827760	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1010179	chr1:92140209-92655952	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv535030	chr1:92140209-92655952	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv949449	chr1:92211020-92585831	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv524845	chr1:92215725-92598705	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
8	nsv462517	chr1:92215725-92598705	Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv546810	chr1:92215725-92598705	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv1006318	chr1:92216408-92608324	Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	nsv432498	chr1:92218245-92618323	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
12	nsv1004570	chr1:92220544-92622129	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv1007661	chr1:92220544-92655952	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
14	nsv1014837	chr1:92233905-92618839	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
15	nsv535031	chr1:92233905-92618839	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
16	nsv1012134	chr1:92235485-92598800	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	nsv530046	chr1:92277460-92799794	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
18	nsv1007270	chr1:92289298-92598800	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
19	nsv871415	chr1:92340684-92641607	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
20	nsv871144	chr1:92380302-92641607	Enhancers Strong transcription Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
21	nsv871508	chr1:92478130-92781579	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
22	nsv1009079	chr1:92525630-92595669	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
23	nsv546821	chr1:92525678-92650349	ZNF genes & repeats Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
24	nsv870471	chr1:92568263-92604114	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
25	nsv871948	chr1:92574745-92607997	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
26	esv3452381	chr1:92579071-92585148	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
27	esv3452380	chr1:92579087-92585131	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
28	esv3452379	chr1:92579096-92585168	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
29	esv3452382	chr1:92579199-92585022	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
30	nsv441700	chr1:92579244-92584515	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	inside rSNPs	diseases
31	esv1850566	chr1:92579244-92584519	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
32	esv2762159	chr1:92579244-92586079	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	inside rSNPs	diseases
33	nsv946074	chr1:92580215-92588466	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92552200-92583800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr1:92552400-92586000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr1:92552400-92595200	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr1:92552600-92582400	Weak transcription	Duodenum Mucosa	Duodenum
5	chr1:92552600-92590000	Weak transcription	Brain Angular Gyrus	brain
6	chr1:92552600-92591600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr1:92552600-92613400	Weak transcription	Stomach Smooth Muscle	stomach
8	chr1:92552800-92613600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr1:92554400-92583200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr1:92555200-92620400	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr1:92556000-92613600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:92556600-92613400	Weak transcription	Fetal Brain Female	brain
13	chr1:92557400-92598000	Weak transcription	Spleen	Spleen
14	chr1:92558000-92583000	Weak transcription	Primary hematopoietic stem cells	blood
15	chr1:92558000-92604000	Weak transcription	Left Ventricle	heart
16	chr1:92560000-92613600	Weak transcription	Brain Anterior Caudate	brain
17	chr1:92560600-92590800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr1:92561200-92619600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr1:92561600-92590000	Weak transcription	Brain Substantia Nigra	brain
20	chr1:92562600-92582800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr1:92565600-92583000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:92567200-92624200	Weak transcription	Fetal Stomach	stomach
23	chr1:92567400-92618000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr1:92568000-92583200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr1:92568200-92616400	Weak transcription	Colon Smooth Muscle	Colon
26	chr1:92569400-92595600	Weak transcription	Brain Germinal Matrix	brain
27	chr1:92569600-92583000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr1:92569800-92613600	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr1:92570000-92619600	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr1:92570400-92589400	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr1:92570800-92594800	Weak transcription	Fetal Intestine Large	intestine
32	chr1:92571800-92601600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr1:92571800-92613400	Weak transcription	Dnd41	blood
34	chr1:92572000-92613400	Weak transcription	Brain Hippocampus Middle	brain
35	chr1:92574000-92613400	Weak transcription	Fetal Lung	lung
36	chr1:92576200-92583000	Weak transcription	Primary T cells from cord blood	blood
37	chr1:92576200-92595800	Weak transcription	Adipose Nuclei	Adipose
38	chr1:92580800-92590800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr1:92580800-92595200	Weak transcription	Ovary	ovary
40	chr1:92580800-92615200	Weak transcription	Lung	lung
41	chr1:92580800-92619000	Weak transcription	Pancreas	Pancrea
42	chr1:92581000-92590800	Weak transcription	Aorta	Aorta
43	chr1:92581400-92583000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:92581400-92597200	Weak transcription	Fetal Intestine Small	intestine
45	chr1:92581400-92613600	Weak transcription	Liver	Liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links