Variant report

Variant	rs6601523
Chromosome Location	chr8:10635141-10635142
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:10628530..10631997-chr8:10633640..10636320,4	K562	blood:
2	chr8:10633410..10636281-chr8:10695946..10698229,2	K562	blood:
3	chr8:10634439..10636776-chr8:10637920..10639941,2	K562	blood:

Variant related genes	Relation type
ENSG00000253695	Chromatin interaction
ENSG00000254093	Chromatin interaction
ENSG00000258724	Chromatin interaction

Extended variants
information (count: 159 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:135)

rs_ID	r²[population]
rs10089615	0.95[CHB][hapmap];0.94[JPT][hapmap];0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10091836	0.85[ASN][1000 genomes]
rs10092781	0.90[CHB][hapmap];0.84[ASN][1000 genomes]
rs10093774	0.84[CEU][hapmap];0.81[GIH][hapmap];0.84[TSI][hapmap]
rs10094907	0.81[CHB][hapmap]
rs10095737	0.84[ASN][1000 genomes]
rs10097283	0.86[CHB][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10097531	0.80[CHB][hapmap]
rs10098699	0.92[CEU][hapmap]
rs10099021	0.81[CHB][hapmap]
rs10099907	0.82[ASN][1000 genomes]
rs10100209	0.88[CEU][hapmap]
rs10100265	0.88[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10105487	0.95[JPT][hapmap];0.80[ASN][1000 genomes]
rs10107180	0.86[CHB][hapmap];0.80[ASN][1000 genomes]
rs10107289	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10113332	0.81[CHB][hapmap]
rs10113343	0.91[CHB][hapmap];0.85[ASN][1000 genomes]
rs10481451	0.92[CEU][hapmap];0.91[GIH][hapmap];0.81[JPT][hapmap];0.96[MEX][hapmap];0.98[TSI][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1073913	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10903330	0.90[JPT][hapmap];0.91[MEX][hapmap];0.87[TSI][hapmap]
rs1115866	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1115867	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1124010	0.81[ASN][1000 genomes]
rs11250069	0.84[ASN][1000 genomes]
rs11250070	0.82[ASN][1000 genomes]
rs11250071	0.81[ASN][1000 genomes]
rs11250073	0.88[CEU][hapmap];0.87[CHB][hapmap];0.94[JPT][hapmap];0.92[YRI][hapmap]
rs11250074	0.87[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11250076	0.81[YRI][hapmap];0.85[EUR][1000 genomes]
rs11250077	0.92[CEU][hapmap];0.91[CHB][hapmap];0.91[GIH][hapmap];0.90[JPT][hapmap];0.96[MEX][hapmap];0.98[TSI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11250078	0.83[JPT][hapmap];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11250080	0.85[JPT][hapmap]
rs11993903	0.85[JPT][hapmap]
rs12542888	0.96[CEU][hapmap];0.87[CHB][hapmap];0.91[GIH][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12550169	0.81[CHB][hapmap]
rs12676417	0.92[CEU][hapmap];0.87[GIH][hapmap];0.90[JPT][hapmap];0.82[LWK][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13276026	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1430867	0.82[ASN][1000 genomes]
rs17152302	0.83[ASN][1000 genomes]
rs17152305	0.84[ASN][1000 genomes]
rs1821001	0.83[ASN][1000 genomes]
rs1821002	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1897207	0.92[ASN][1000 genomes]
rs1968400	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1968401	0.94[ASN][1000 genomes]
rs1991651	0.83[ASW][hapmap];0.84[CEU][hapmap];0.82[LWK][hapmap];0.84[TSI][hapmap]
rs2005309	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2005311	0.81[CHB][hapmap]
rs2033369	0.86[CHB][hapmap];0.84[ASN][1000 genomes]
rs2116092	0.82[ASN][1000 genomes]
rs2116093	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2116095	0.91[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2116096	0.84[ASN][1000 genomes]
rs2277130	0.92[CEU][hapmap]
rs2280047	0.84[ASN][1000 genomes]
rs2409658	0.80[ASN][1000 genomes]
rs2409663	0.95[CHB][hapmap];0.84[JPT][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2409669	0.91[ASW][hapmap];0.92[CEU][hapmap];0.95[CHB][hapmap];0.91[GIH][hapmap];0.90[JPT][hapmap];1.00[LWK][hapmap];0.82[MEX][hapmap];0.93[TSI][hapmap];0.86[YRI][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2409672	0.81[ASN][1000 genomes]
rs2409674	0.80[ASN][1000 genomes]
rs2409675	0.81[ASN][1000 genomes]
rs28570522	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2898248	0.85[CEU][hapmap];1.00[CHB][hapmap];0.85[GIH][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs2898251	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4240669	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4240670	0.88[JPT][hapmap];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4321967	0.84[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4504595	0.94[CEU][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4551304	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4593498	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4840512	0.81[ASN][1000 genomes]
rs4840513	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4840516	0.96[CEU][hapmap];0.91[GIH][hapmap];0.90[JPT][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4840517	0.90[JPT][hapmap];0.80[ASN][1000 genomes]
rs4841437	0.81[ASN][1000 genomes]
rs4841441	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4841452	0.95[CEU][hapmap];0.83[YRI][hapmap]
rs6601513	0.80[ASN][1000 genomes]
rs6601520	0.84[ASN][1000 genomes]
rs6601521	0.91[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs6601522	0.88[CEU][hapmap];0.91[CHB][hapmap];0.89[GIH][hapmap];0.95[JPT][hapmap];0.88[LWK][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap];0.81[YRI][hapmap];0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6601524	0.86[CHB][hapmap];0.84[ASN][1000 genomes]
rs6601525	0.91[CHB][hapmap];0.86[ASN][1000 genomes]
rs6601527	0.80[ASN][1000 genomes]
rs6601529	0.92[CEU][hapmap];0.83[GIH][hapmap];0.90[JPT][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.81[EUR][1000 genomes]
rs6601530	0.84[CEU][hapmap];0.90[JPT][hapmap]
rs6980805	0.92[CEU][hapmap]
rs6981530	0.83[ASN][1000 genomes]
rs6984744	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6985218	0.81[CHB][hapmap]
rs6989072	0.86[ASN][1000 genomes]
rs6989160	0.84[CEU][hapmap]
rs6989370	0.95[ASN][1000 genomes]
rs6993841	0.88[CEU][hapmap];0.86[CHB][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6994595	0.85[ASN][1000 genomes]
rs7002117	0.94[ASN][1000 genomes]
rs7002137	0.84[ASN][1000 genomes]
rs7002282	0.92[CEU][hapmap];0.91[GIH][hapmap];0.90[JPT][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7005905	0.84[CEU][hapmap];0.81[CHB][hapmap];0.85[JPT][hapmap]
rs7010926	0.84[ASN][1000 genomes]
rs7014168	0.84[ASN][1000 genomes]
rs7014285	0.84[ASN][1000 genomes]
rs7015129	0.84[ASN][1000 genomes]
rs7018334	0.83[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs718741	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs718742	0.93[ASN][1000 genomes]
rs733395	0.84[ASN][1000 genomes]
rs733396	0.84[ASN][1000 genomes]
rs73542560	0.83[ASN][1000 genomes]
rs73544343	0.86[ASN][1000 genomes]
rs736668	0.84[ASN][1000 genomes]
rs736669	0.84[ASN][1000 genomes]
rs752446	0.91[CHB][hapmap];0.85[JPT][hapmap];0.92[ASN][1000 genomes]
rs7813706	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7814142	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7814757	0.92[CEU][hapmap];0.89[JPT][hapmap]
rs7823088	0.84[ASN][1000 genomes]
rs7826180	0.86[CHB][hapmap];0.85[ASN][1000 genomes]
rs7826189	0.81[CHB][hapmap];0.84[ASN][1000 genomes]
rs7826218	0.85[ASN][1000 genomes]
rs7826392	0.84[ASN][1000 genomes]
rs7830431	0.84[CEU][hapmap]
rs7830528	0.84[ASN][1000 genomes]
rs7833945	0.84[CEU][hapmap]
rs7834466	0.83[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7836194	0.82[CHB][hapmap]
rs7836366	0.84[CEU][hapmap]
rs7836833	0.80[ASN][1000 genomes]
rs891554	0.81[CHB][hapmap]
rs891556	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs919555	0.84[ASN][1000 genomes]
rs9329231	0.95[ASN][1000 genomes]
rs9644730	0.81[CHB][hapmap]
rs9969626	0.92[CEU][hapmap];0.90[JPT][hapmap];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022994	chr8:10190618-10660122	Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv539466	chr8:10190618-10660122	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv917085	chr8:10237508-10828204	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv1022582	chr8:10571218-10636162	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv539468	chr8:10571218-10636162	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Genic enhancers Flanking Active TSS Active 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
6	nsv1026802	chr8:10576444-10754489	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
7	nsv539469	chr8:10576444-10754489	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
8	nsv1017836	chr8:10591801-10803617	Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
9	nsv1034988	chr8:10591801-10804243	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer 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	14 gene(s)	inside rSNPs	diseases
10	nsv519768	chr8:10600254-10691993	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
11	nsv1024806	chr8:10605438-10662555	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv831232	chr8:10606053-10774948	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
13	nsv1031709	chr8:10610545-10657726	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	esv2764105	chr8:10610557-10657726	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
15	nsv519376	chr8:10611708-10691993	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
16	nsv429860	chr8:10615990-10685890	Strong transcription Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
17	nsv1023085	chr8:10617908-10657584	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
18	nsv539470	chr8:10617908-10657584	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
19	nsv1019754	chr8:10617908-10700140	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
20	nsv539471	chr8:10617908-10700140	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
21	nsv1026230	chr8:10618928-10652924	Bivalent Enhancer Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
22	nsv539472	chr8:10618928-10652924	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
23	nsv1031726	chr8:10627742-10749369	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
24	nsv522226	chr8:10628947-10635317	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs6601523	CLDN23	cis	multi-tissue	Pritchard
rs6601523	C8orf13	cis	multi-tissue	Pritchard
rs6601523	SOX7	cis	multi-tissue	Pritchard

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10610800-10662000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr8:10618800-10636400	Weak transcription	Psoas Muscle	Psoas
3	chr8:10618800-10646200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr8:10618800-10665200	Weak transcription	Fetal Brain Female	brain
5	chr8:10619000-10636400	Weak transcription	HSMM	muscle
6	chr8:10619200-10635800	Weak transcription	Brain Angular Gyrus	brain
7	chr8:10619200-10644800	Weak transcription	Small Intestine	intestine
8	chr8:10619200-10656400	Weak transcription	Rectal Smooth Muscle	rectum
9	chr8:10619400-10661600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr8:10620000-10669800	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr8:10620200-10645000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr8:10621200-10662000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr8:10621400-10656000	Weak transcription	HepG2	liver
14	chr8:10622000-10639000	Weak transcription	HMEC	breast
15	chr8:10622800-10641000	Weak transcription	Hela-S3	cervix
16	chr8:10622800-10656000	Weak transcription	A549	lung
17	chr8:10623200-10650000	Weak transcription	Duodenum Mucosa	Duodenum
18	chr8:10623400-10646400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr8:10623400-10656800	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr8:10623400-10662600	Weak transcription	Fetal Thymus	thymus
21	chr8:10623400-10662800	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr8:10623400-10665000	Weak transcription	Fetal Intestine Large	intestine
23	chr8:10623600-10643800	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr8:10623600-10644200	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr8:10623600-10648800	Weak transcription	Fetal Intestine Small	intestine
26	chr8:10623600-10667000	Weak transcription	Thymus	Thymus
27	chr8:10623800-10639200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr8:10623800-10648800	Weak transcription	Primary B cells from peripheral blood	blood
29	chr8:10623800-10649600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr8:10623800-10656800	Weak transcription	Gastric	stomach
31	chr8:10624000-10639400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr8:10624000-10649600	Weak transcription	Pancreas	Pancrea
33	chr8:10624200-10644000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr8:10624800-10642400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr8:10624800-10646800	Weak transcription	Brain Germinal Matrix	brain
36	chr8:10625000-10639200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr8:10628800-10639200	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr8:10629200-10641000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr8:10629800-10637600	Weak transcription	Primary T cells from cord blood	blood
40	chr8:10629800-10639000	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr8:10629800-10639200	Weak transcription	Stomach Smooth Muscle	stomach
42	chr8:10629800-10639400	Weak transcription	Primary B cells from cord blood	blood
43	chr8:10630000-10639200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr8:10630000-10639200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr8:10630000-10639400	Weak transcription	Aorta	Aorta
46	chr8:10630400-10646200	Weak transcription	GM12878-XiMat	blood
47	chr8:10631000-10639000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr8:10631000-10639800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr8:10631400-10635200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr8:10631400-10637800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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