Variant report

Variant	rs6601633
Chromosome Location	chr8:11805173-11805174
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:11658805..11661004-chr8:11802756..11805427,2	K562	blood:
2	chr8:11798435..11800299-chr8:11803537..11805187,2	K562	blood:
3	chr8:11801089..11802817-chr8:11804319..11806900,3	K562	blood:

Variant related genes	Relation type
ENSG00000079459	Chromatin interaction
ENSG00000255046	Chromatin interaction

Extended variants
information (count: 137 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:105)

rs_ID	r²[population]
rs10087494	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10089712	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10092340	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10103485	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10112958	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10113042	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10113062	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10113145	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10216773	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10903345	0.83[AMR][1000 genomes]
rs11250175	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11250176	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11250177	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11250178	0.96[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11250179	0.96[CEU][hapmap];0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11250182	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11996277	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12681142	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12719914	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12719915	0.96[CEU][hapmap];0.83[CHD][hapmap];0.95[GIH][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13252853	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13252854	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13261205	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13264994	0.85[CEU][hapmap]
rs13265816	0.80[AMR][1000 genomes]
rs13268030	0.96[CEU][hapmap]
rs13269417	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13275143	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13276433	0.96[CEU][hapmap];0.83[CHD][hapmap];0.93[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs13279577	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13281077	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13281315	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs28510449	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs28838382	0.80[EUR][1000 genomes]
rs34012738	0.86[AMR][1000 genomes]
rs34117651	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34266352	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34419349	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34465618	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34535807	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34583868	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34657250	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35251245	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35391955	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35647515	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35657308	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35778860	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35905106	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35995176	0.80[EUR][1000 genomes]
rs36100659	0.82[AMR][1000 genomes]
rs4240678	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4367597	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4840597	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4840599	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.87[YRI][hapmap];0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4841639	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4841641	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4841642	0.80[AMR][1000 genomes]
rs4841644	0.80[AMR][1000 genomes]
rs4841645	0.84[CEU][hapmap];0.83[CHD][hapmap];0.91[GIH][hapmap];0.85[MEX][hapmap];0.80[AMR][1000 genomes]
rs4841646	0.80[AMR][1000 genomes]
rs56001613	0.80[EUR][1000 genomes]
rs56102998	0.83[EUR][1000 genomes]
rs57356272	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs57597334	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs58049869	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs58202536	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs58325983	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs58556886	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs58869268	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs59423463	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62493601	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62493617	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6601634	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6985792	0.81[EUR][1000 genomes]
rs6998690	0.80[AMR][1000 genomes]
rs6999030	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7006538	0.86[ASW][hapmap];1.00[CEU][hapmap];0.95[GIH][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7011924	0.84[CEU][hapmap]
rs7012446	0.84[CEU][hapmap]
rs7014580	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7459545	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7459983	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7461273	0.82[EUR][1000 genomes]
rs7812563	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7815179	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7815186	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7815572	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7815595	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7816182	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7820338	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7821336	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7824267	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7824564	0.84[CEU][hapmap]
rs7825529	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7830734	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7833079	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7833685	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7842810	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9329251	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9692662	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9692668	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9693925	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9694940	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9694967	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9886639	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[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	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv1018978	chr8:11438267-11858466	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv1027378	chr8:11541739-11858466	Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv1028229	chr8:11575762-11805961	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv539475	chr8:11575762-11805961	Flanking Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv1034014	chr8:11602337-11858466	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
7	nsv1034132	chr8:11657033-12198242	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers 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	52 gene(s)	inside rSNPs	diseases
8	nsv890366	chr8:11666451-11900847	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription 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	20 gene(s)	inside rSNPs	diseases
9	nsv1018042	chr8:11667496-11882385	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
10	nsv890369	chr8:11671041-11840011	Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
11	nsv1016952	chr8:11679271-11849955	Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
12	nsv1029093	chr8:11679271-11858466	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv539478	chr8:11679271-11858466	Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv1031972	chr8:11696393-11805961	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
15	nsv539481	chr8:11696393-11805961	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
16	nsv610293	chr8:11698747-11929734	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
17	nsv516685	chr8:11698747-12570199	Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	74 gene(s)	inside rSNPs	diseases
18	nsv1029694	chr8:11727357-11858466	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
19	esv2758148	chr8:11741558-12567301	ZNF genes & repeats Active TSS Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	70 gene(s)	inside rSNPs	diseases
20	nsv427815	chr8:11741558-12567301	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	70 gene(s)	inside rSNPs	diseases
21	nsv428195	chr8:11741558-12567301	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	70 gene(s)	inside rSNPs	diseases
22	esv2759593	chr8:11741558-12601971	Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer 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	73 gene(s)	inside rSNPs	diseases
23	nsv1029934	chr8:11747133-11858466	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
24	nsv1016332	chr8:11751798-11861797	Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
25	nsv1016544	chr8:11754663-11849955	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
26	nsv539482	chr8:11754663-11849955	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
27	nsv890370	chr8:11755513-11900847	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
28	nsv491752	chr8:11758865-12467543	Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
29	nsv890371	chr8:11771089-11896831	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
30	nsv1026344	chr8:11786255-11897177	Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
31	nsv1019536	chr8:11788237-11828263	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
32	nsv1019489	chr8:11802328-11858466	Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs6601633	NEIL2	cis	Nerve Tibial	GTEx
rs6601633	FLJ10661	cis	cerebellum	SCAN
rs6601633	TDH	cis	cerebellum	SCAN
rs6601633	CTSB	cis	cerebellum	SCAN
rs6601633	CLDN23	cis	multi-tissue	Pritchard
rs6601633	PRSS55	cis	cerebellum	SCAN
rs6601633	TDH	cis	parietal	SCAN
rs6601633	DEFB134	cis	cerebellum	SCAN
rs6601633	MFHAS1	cis	cerebellum	SCAN
rs6601633	FLJ10661	cis	parietal	SCAN

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11800800-11807200	Weak transcription	Right Atrium	heart
2	chr8:11801600-11806800	Weak transcription	Fetal Heart	heart
3	chr8:11804800-11805400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr8:11804800-11805800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin

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