Variant report

Variant	rs1805058
Chromosome Location	chr22:23438191-23438192
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr22:23433414..23435124-chr22:23436092..23438297,2	MCF-7	breast:
2	chr22:23435451..23438238-chr22:23506678..23508386,2	K562	blood:
3	chr22:23436752..23438822-chr22:23487240..23488966,2	K562	blood:
4	chr22:23426024..23426653-chr22:23437564..23438367,2	K562	blood:

Variant related genes	Relation type
ENSG00000100228	Chromatin interaction

Extended variants
information (count: 146 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs1051875	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs12167308	0.92[CEU][hapmap];0.89[JPT][hapmap]
rs13054985	0.81[CHB][hapmap];0.89[JPT][hapmap]
rs1858745	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1858746	0.96[CEU][hapmap];0.86[CHB][hapmap];0.85[JPT][hapmap];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1858747	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1989776	1.00[CHB][hapmap];0.95[JPT][hapmap];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1989777	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1989778	1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2071431	0.88[CEU][hapmap];0.84[JPT][hapmap]
rs2157710	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs2249692	0.90[JPT][hapmap]
rs2266995	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2266996	0.91[CHB][hapmap];0.85[JPT][hapmap];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2266997	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2266998	0.96[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2266999	1.00[CEU][hapmap];0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2267000	0.90[CHB][hapmap];0.85[JPT][hapmap]
rs2267001	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs2267003	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs2267004	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs2267005	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs2267006	0.90[JPT][hapmap]
rs2267007	0.89[JPT][hapmap]
rs2267009	0.87[CEU][hapmap];0.84[JPT][hapmap]
rs2283802	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2283803	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs2283804	0.90[JPT][hapmap]
rs2301554	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs2330336	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2330338	0.96[CEU][hapmap];0.86[CHB][hapmap];0.85[JPT][hapmap];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2330361	0.89[JPT][hapmap]
rs3761418	0.88[CEU][hapmap];0.84[JPT][hapmap]
rs3788342	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3788343	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3788345	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3788346	1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3788347	0.81[CHB][hapmap];0.90[JPT][hapmap]
rs3788348	0.90[JPT][hapmap]
rs3788350	0.81[CHB][hapmap];0.95[JPT][hapmap]
rs3810614	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3827315	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4820536	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4820537	0.90[JPT][hapmap]
rs4820538	0.84[AMR][1000 genomes]
rs4820539	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs4820541	0.92[CEU][hapmap];0.89[JPT][hapmap]
rs4820542	0.87[CEU][hapmap];0.84[JPT][hapmap]
rs4822354	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4822357	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs4822359	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs4822360	0.81[CHB][hapmap];0.90[JPT][hapmap]
rs4822361	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs4822362	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs4822369	0.88[CEU][hapmap];0.81[CHB][hapmap];0.89[JPT][hapmap]
rs5751576	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs5751578	0.96[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs5751579	0.96[CEU][hapmap];0.90[CHB][hapmap];0.90[JPT][hapmap];0.81[YRI][hapmap];0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs5751587	0.82[CHB][hapmap];0.88[JPT][hapmap]
rs5751589	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs5751593	0.89[JPT][hapmap]
rs5751596	0.89[JPT][hapmap]
rs5751603	0.88[CEU][hapmap];0.84[JPT][hapmap]
rs5751606	0.88[CEU][hapmap]
rs5759580	0.88[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5759581	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5759583	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs5759584	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5759585	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5759587	0.86[ASN][1000 genomes]
rs5759593	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs5759598	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs5759600	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs5759604	0.93[JPT][hapmap]
rs5759607	0.92[CEU][hapmap];0.89[JPT][hapmap]
rs5759608	0.89[JPT][hapmap]
rs5759611	0.92[CEU][hapmap];0.89[JPT][hapmap]
rs5759612	0.89[JPT][hapmap]
rs5759613	0.89[JPT][hapmap]
rs5759614	0.89[JPT][hapmap]
rs5759615	0.89[JPT][hapmap]
rs5759619	0.89[JPT][hapmap]
rs5759620	0.89[JPT][hapmap]
rs5759621	0.89[JPT][hapmap]
rs5759631	0.88[CEU][hapmap];0.84[JPT][hapmap]
rs5996467	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs5996483	0.88[CEU][hapmap]
rs6003499	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6003501	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6003502	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6003518	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs6519411	0.96[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs713617	0.88[CEU][hapmap]
rs713682	0.89[JPT][hapmap]
rs72617225	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs737818	0.88[JPT][hapmap]
rs737819	0.89[JPT][hapmap]
rs739362	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs756631	0.81[CHB][hapmap];0.85[JPT][hapmap]
rs756633	0.89[JPT][hapmap]
rs8139380	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8139779	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8142746	0.89[JPT][hapmap]
rs874138	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs885962	1.00[CHB][hapmap];0.95[JPT][hapmap];0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs885963	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs885964	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs885965	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs916583	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs916584	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs916585	0.85[CHB][hapmap];0.87[JPT][hapmap]
rs9612230	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9612234	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs9612237	0.85[CHB][hapmap];0.89[JPT][hapmap]
rs9612248	0.85[JPT][hapmap]
rs9612252	0.89[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1803110	chr22:22731758-23497674	Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
2	nsv915235	chr22:22971768-23650987	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	101 gene(s)	inside rSNPs	diseases
3	esv3388845	chr22:22973346-23652447	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats 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	100 gene(s)	inside rSNPs	diseases
4	nsv531799	chr22:22993679-23642142	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
5	nsv1061433	chr22:22997799-23649107	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
6	nsv521695	chr22:22998337-23648009	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
7	nsv915236	chr22:22998337-23650987	Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
8	nsv588512	chr22:22998337-23667731	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
9	nsv531800	chr22:23002708-23648163	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
10	nsv916593	chr22:23002709-23648790	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers 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	97 gene(s)	inside rSNPs	diseases
11	nsv993496	chr22:23002709-23654222	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
12	nsv1067002	chr22:23007167-23643363	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
13	nsv1067324	chr22:23007367-23654223	Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
14	nsv533839	chr22:23012013-23643223	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
15	nsv916933	chr22:23012069-23654237	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
16	nsv531801	chr22:23028586-23657804	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription 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	92 gene(s)	inside rSNPs	diseases
17	nsv531802	chr22:23046186-23627391	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	85 gene(s)	inside rSNPs	diseases
18	nsv1060509	chr22:23055148-23648719	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS 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	83 gene(s)	inside rSNPs	diseases
19	nsv1056324	chr22:23055148-23750989	Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS 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	88 gene(s)	inside rSNPs	diseases
20	nsv1062780	chr22:23060449-23648719	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
21	nsv948942	chr22:23063178-23645718	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
22	nsv1063200	chr22:23097177-23643224	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	80 gene(s)	inside rSNPs	diseases
23	nsv949250	chr22:23157485-23645718	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
24	esv34158	chr22:23216762-23499513	Weak transcription Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
25	nsv914575	chr22:23399743-23467804	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Bivalent/Poised TSS Flanking Active 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	15 gene(s)	inside rSNPs	diseases
26	nsv914576	chr22:23399743-23469918	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
27	esv1806531	chr22:23400739-23448258	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
28	nsv544609	chr22:23400739-23455790	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
29	nsv1057659	chr22:23400739-24138788	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
30	esv1825944	chr22:23414398-23473840	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1805058	BCR	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23413600-23440600	Strong transcription	Right Atrium	heart
2	chr22:23416000-23452800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr22:23427800-23447600	Weak transcription	Fetal Intestine Small	intestine
4	chr22:23430600-23448600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr22:23431000-23444400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr22:23431400-23444400	Weak transcription	Primary B cells from peripheral blood	blood
7	chr22:23431600-23439800	Weak transcription	Pancreas	Pancrea
8	chr22:23431600-23440200	Weak transcription	Esophagus	oesophagus
9	chr22:23431600-23442000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr22:23432800-23439800	Weak transcription	Adipose Nuclei	Adipose
11	chr22:23433600-23442200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr22:23433600-23454400	Weak transcription	Primary B cells from cord blood	blood
13	chr22:23433800-23439200	Weak transcription	Stomach Smooth Muscle	stomach
14	chr22:23434400-23438400	Weak transcription	HepG2	liver
15	chr22:23436400-23440600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr22:23436600-23440400	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr22:23437000-23438600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr22:23437000-23440400	Strong transcription	Fetal Stomach	stomach
19	chr22:23437200-23438400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr22:23437400-23441000	Weak transcription	Fetal Intestine Large	intestine
21	chr22:23437600-23438400	Strong transcription	Ovary	ovary
22	chr22:23437600-23439600	Strong transcription	Gastric	stomach
23	chr22:23437600-23439600	Weak transcription	Spleen	Spleen
24	chr22:23437600-23441200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr22:23437600-23458000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr22:23437800-23438200	Weak transcription	Brain Hippocampus Middle	brain
27	chr22:23437800-23438400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr22:23437800-23438400	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr22:23437800-23438400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr22:23437800-23438600	Weak transcription	Brain Angular Gyrus	brain
31	chr22:23437800-23438800	Strong transcription	Cortex derived primary cultured neurospheres	brain
32	chr22:23437800-23438800	Strong transcription	Brain Anterior Caudate	brain
33	chr22:23437800-23439000	Genic enhancers	Brain Cingulate Gyrus	brain
34	chr22:23437800-23439000	Strong transcription	Brain Germinal Matrix	brain
35	chr22:23437800-23439800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr22:23438000-23438600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr22:23438000-23438600	Weak transcription	Brain Substantia Nigra	brain
38	chr22:23438000-23438800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr22:23438000-23438800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr22:23438000-23439400	Strong transcription	Fetal Brain Female	brain
41	chr22:23438000-23439600	Weak transcription	Fetal Brain Male	brain
42	chr22:23438000-23440400	Weak transcription	Colon Smooth Muscle	Colon

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