Variant report

Variant	rs1583188
Chromosome Location	chr4:151899626-151899627
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	chr4:151898127..151900327-chr4:151908207..151910681,2	K562	blood:
2	chr4:151899256..151901793-chr4:151906070..151908890,2	K562	blood:

Extended variants
information (count: 157 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:125)

rs_ID	r²[population]
rs10000557	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs10011421	1.00[JPT][hapmap]
rs10030785	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs10034173	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10222881	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1046168	1.00[JPT][hapmap]
rs10857250	0.82[EUR][1000 genomes]
rs10857254	1.00[JPT][hapmap]
rs10964	1.00[JPT][hapmap]
rs11099782	1.00[JPT][hapmap]
rs11099783	1.00[JPT][hapmap]
rs11099788	1.00[JPT][hapmap]
rs1148631	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1148633	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1148634	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1148636	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1148641	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1148644	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1148646	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1148650	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1148651	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1148655	0.88[EUR][1000 genomes]
rs11734095	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11734586	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs11737590	0.82[EUR][1000 genomes]
rs11938266	1.00[JPT][hapmap]
rs1201197	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1201199	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1201200	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1201208	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1201209	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1201210	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1201216	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1212119	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12501829	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12507657	1.00[JPT][hapmap]
rs1273329	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1273331	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1273332	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1298678	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13146584	1.00[JPT][hapmap]
rs1583189	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1615230	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17027155	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17027197	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17027226	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1782360	0.88[EUR][1000 genomes]
rs1782365	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs186080	0.87[EUR][1000 genomes]
rs1975112	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2154349	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2198191	0.82[EUR][1000 genomes]
rs2198192	0.82[EUR][1000 genomes]
rs2218899	0.82[EUR][1000 genomes]
rs2407440	1.00[JPT][hapmap]
rs2897660	1.00[JPT][hapmap]
rs2912477	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2915451	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs294530	0.87[EUR][1000 genomes]
rs294532	0.88[EUR][1000 genomes]
rs294533	0.88[EUR][1000 genomes]
rs294535	0.82[EUR][1000 genomes]
rs2952814	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2952817	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2952818	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2952819	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3990470	0.82[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4524364	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4696226	1.00[JPT][hapmap]
rs4696229	1.00[JPT][hapmap]
rs4696634	0.82[EUR][1000 genomes]
rs4696648	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57003564	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57029739	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57218449	0.87[AFR][1000 genomes]
rs57518605	0.90[AFR][1000 genomes]
rs59572961	0.94[AFR][1000 genomes]
rs60102523	0.86[AFR][1000 genomes]
rs62344571	0.86[AFR][1000 genomes]
rs62344572	0.85[AFR][1000 genomes]
rs62344578	0.89[AFR][1000 genomes]
rs62344579	0.89[AFR][1000 genomes]
rs62344598	0.92[AFR][1000 genomes]
rs62344602	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344619	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344622	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344623	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62344624	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6535750	0.82[EUR][1000 genomes]
rs6535756	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6535757	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6535760	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6535763	1.00[JPT][hapmap]
rs6535765	1.00[JPT][hapmap]
rs6535766	1.00[JPT][hapmap]
rs6812083	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6817726	0.82[EUR][1000 genomes]
rs6819599	1.00[JPT][hapmap]
rs6819868	0.94[AFR][1000 genomes]
rs6820819	0.82[EUR][1000 genomes]
rs6825613	1.00[JPT][hapmap]
rs6826863	1.00[JPT][hapmap]
rs6829963	1.00[JPT][hapmap]
rs6833956	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6837905	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs6838286	0.82[EUR][1000 genomes]
rs6839352	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6853215	1.00[JPT][hapmap]
rs6855472	0.83[EUR][1000 genomes]
rs73859291	0.81[AFR][1000 genomes]
rs73859295	0.94[AFR][1000 genomes]
rs7436602	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7656796	0.82[EUR][1000 genomes]
rs7657953	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7659146	1.00[JPT][hapmap]
rs7668154	1.00[JPT][hapmap]
rs7671635	0.82[EUR][1000 genomes]
rs7677374	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7678748	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7683092	1.00[JPT][hapmap]
rs7683377	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7684325	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7693282	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs891689	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9999064	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:32 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024820	chr4:151364078-151943561	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv1034948	chr4:151590115-152202687	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv537302	chr4:151590115-152202687	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	nsv530159	chr4:151624865-152203910	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	nsv1018404	chr4:151664438-152067409	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
6	nsv1017850	chr4:151664438-152071876	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
7	esv2763837	chr4:151664438-152071888	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
8	nsv870257	chr4:151665349-152072867	Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
9	nsv1015387	chr4:151673751-152071876	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
10	nsv526976	chr4:151675819-152055073	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
11	nsv1025077	chr4:151682266-152035733	Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
12	nsv537303	chr4:151682266-152035733	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
13	nsv949066	chr4:151693149-152069566	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
14	nsv949002	chr4:151693149-152095109	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
15	nsv948719	chr4:151693149-152161625	Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
16	nsv1031720	chr4:151708502-152071876	Strong transcription Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
17	nsv880262	chr4:151712054-152519899	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
18	nsv1031516	chr4:151718614-152065644	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
19	nsv537304	chr4:151718614-152065644	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
20	nsv1022884	chr4:151718814-152065505	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
21	nsv537305	chr4:151718814-152065505	Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
22	nsv880576	chr4:151751369-151936149	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
23	nsv595689	chr4:151788955-152015704	Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
24	nsv595690	chr4:151788955-152109552	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
25	nsv881254	chr4:151829824-151936149	Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
26	nsv880429	chr4:151844476-151936149	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
27	nsv1026416	chr4:151847403-152105879	Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
28	nsv461678	chr4:151865522-151980636	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
29	nsv595692	chr4:151865522-151980636	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
30	nsv4548	chr4:151867014-151908030	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
31	nsv595699	chr4:151880765-151968295	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
32	nsv869553	chr4:151892289-152003402	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:151876800-151902000	Weak transcription	Esophagus	oesophagus
2	chr4:151880400-151914400	Weak transcription	Primary B cells from cord blood	blood
3	chr4:151880400-151922000	Weak transcription	Thymus	Thymus
4	chr4:151883600-151925000	Weak transcription	NHEK	skin
5	chr4:151883800-151924000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr4:151888800-151933400	Weak transcription	Fetal Lung	lung
7	chr4:151891600-151922000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr4:151892400-151925000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:151893800-151903600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr4:151894000-151920400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr4:151894000-151933200	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr4:151894200-151922200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr4:151894600-151901600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr4:151895200-151903800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr4:151895600-151903800	Weak transcription	Fetal Kidney	kidney
16	chr4:151895600-151907600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr4:151896000-151924600	Weak transcription	Fetal Thymus	thymus
18	chr4:151896400-151912400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:151896400-151921800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr4:151896600-151901600	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr4:151896600-151901600	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr4:151896600-151903200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr4:151896600-151903400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr4:151896600-151903600	Weak transcription	Small Intestine	intestine
25	chr4:151896600-151903800	Weak transcription	Primary B cells from peripheral blood	blood
26	chr4:151896600-151903800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr4:151896600-151907600	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr4:151896600-151907600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr4:151898200-151899800	Strong transcription	Primary T cells from cord blood	blood
30	chr4:151898400-151904200	Weak transcription	Left Ventricle	heart
31	chr4:151898600-151903600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr4:151898600-151903600	Weak transcription	GM12878-XiMat	blood
33	chr4:151898600-151903800	Weak transcription	K562	blood
34	chr4:151898600-151908000	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr4:151898600-151908400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr4:151898600-151922200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr4:151898800-151905000	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr4:151899000-151900000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr4:151899000-151903600	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr4:151899000-151908600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr4:151899000-151921600	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr4:151899200-151900200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr4:151899200-151900200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr4:151899200-151909600	Weak transcription	Fetal Intestine Small	intestine
45	chr4:151899400-151901800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
46	chr4:151899600-151919400	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr4:151899600-151920000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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