Variant report

Variant	rs1037004
Chromosome Location	chr7:153084998-153084999
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:153077274..153079986-chr7:153084409..153086483,3	K562	blood:
2	chr7:153073552..153076060-chr7:153082257..153085199,2	K562	blood:
3	chr7:153080633..153085077-chr7:153085115..153088222,5	K562	blood:

Extended variants
information (count: 89 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10239341	0.92[CEU][hapmap];0.87[CHD][hapmap];0.83[GIH][hapmap];0.94[JPT][hapmap];0.95[TSI][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10246632	0.89[CEU][hapmap];0.89[TSI][hapmap];0.89[EUR][1000 genomes]
rs10278147	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11760609	0.92[CEU][hapmap];0.94[JPT][hapmap];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12154671	0.89[EUR][1000 genomes]
rs12703288	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12703290	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12703295	0.89[EUR][1000 genomes]
rs12703296	0.89[EUR][1000 genomes]
rs12703297	0.89[EUR][1000 genomes]
rs12703298	0.89[EUR][1000 genomes]
rs12703299	0.89[EUR][1000 genomes]
rs12703300	0.88[EUR][1000 genomes]
rs12703301	0.89[EUR][1000 genomes]
rs12703302	0.89[EUR][1000 genomes]
rs12703303	0.89[EUR][1000 genomes]
rs12703304	0.89[CEU][hapmap];0.80[MEX][hapmap];0.89[TSI][hapmap];0.89[EUR][1000 genomes]
rs12703305	0.89[CEU][hapmap];0.80[MEX][hapmap];0.89[TSI][hapmap];0.89[EUR][1000 genomes]
rs12703306	0.89[CEU][hapmap];0.80[MEX][hapmap];0.89[TSI][hapmap];0.89[EUR][1000 genomes]
rs1319653	0.89[EUR][1000 genomes]
rs13223314	0.92[CEU][hapmap];0.94[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13226467	0.82[CEU][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs13230671	0.88[CEU][hapmap];0.89[TSI][hapmap];0.89[EUR][1000 genomes]
rs13231619	0.89[EUR][1000 genomes]
rs13231707	0.89[EUR][1000 genomes]
rs13233777	0.89[CEU][hapmap];0.89[TSI][hapmap];0.89[EUR][1000 genomes]
rs13234416	0.89[EUR][1000 genomes]
rs13235094	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13238866	0.89[EUR][1000 genomes]
rs13242507	0.82[EUR][1000 genomes]
rs13245532	0.87[EUR][1000 genomes]
rs1444458	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1444462	0.88[EUR][1000 genomes]
rs1444463	0.89[CEU][hapmap];0.89[EUR][1000 genomes]
rs1992624	0.89[EUR][1000 genomes]
rs2312352	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28648695	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28671105	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28675346	0.83[EUR][1000 genomes]
rs2872011	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34123236	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34726402	0.86[EUR][1000 genomes]
rs35444218	0.89[EUR][1000 genomes]
rs4563798	0.82[EUR][1000 genomes]
rs55838859	0.89[EUR][1000 genomes]
rs6955304	0.89[EUR][1000 genomes]
rs6965505	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6966291	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6971281	0.89[CEU][hapmap];0.89[EUR][1000 genomes]
rs6971902	0.89[CEU][hapmap];0.89[EUR][1000 genomes]
rs6974731	0.89[CEU][hapmap];0.80[MEX][hapmap];0.89[TSI][hapmap];0.89[EUR][1000 genomes]
rs7779733	0.89[EUR][1000 genomes]
rs7780839	0.83[EUR][1000 genomes]
rs7784310	0.89[EUR][1000 genomes]
rs7785341	0.87[EUR][1000 genomes]
rs7785383	0.89[EUR][1000 genomes]
rs7785473	0.89[EUR][1000 genomes]
rs7787854	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7798819	0.89[EUR][1000 genomes]
rs7800637	0.89[CEU][hapmap];0.89[EUR][1000 genomes]
rs7800865	0.89[EUR][1000 genomes]
rs7803966	0.89[EUR][1000 genomes]
rs7804377	0.89[EUR][1000 genomes]
rs7805371	0.87[EUR][1000 genomes]
rs7805698	0.89[EUR][1000 genomes]
rs884852	0.88[EUR][1000 genomes]
rs884853	0.88[CEU][hapmap];0.89[EUR][1000 genomes]
rs987673	0.89[EUR][1000 genomes]
rs987674	0.89[EUR][1000 genomes]
rs987675	0.89[EUR][1000 genomes]
rs989754	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532222	chr7:152504090-153450290	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv1031602	chr7:152889661-153100643	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1034031	chr7:152894293-153099991	Strong transcription ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv539210	chr7:152894293-153099991	Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1027502	chr7:152895275-153100643	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv609071	chr7:152898417-153101151	Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1034277	chr7:152932263-153526276	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
8	nsv1023927	chr7:152938365-153526276	Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
9	nsv609072	chr7:152942680-153527304	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
10	nsv1028109	chr7:152945148-153526276	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
11	nsv1034036	chr7:152954795-153379878	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
12	nsv539211	chr7:152954795-153379878	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
13	nsv1032443	chr7:152988419-153450150	Enhancers ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
14	nsv539212	chr7:152988419-153450150	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
15	esv2758141	chr7:153001173-153298779	Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
16	esv2759576	chr7:153001173-153298779	Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
17	nsv889510	chr7:153050837-153413046	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
18	nsv889511	chr7:153076838-153201572	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs1037004	KRBA1	cis	parietal	SCAN
rs1037004	ATG9B	cis	parietal	SCAN
rs1037004	ZNF212	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:153082000-153086000	Weak transcription	Colon Smooth Muscle	Colon
2	chr7:153083200-153085800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr7:153084400-153089600	Strong transcription	K562	blood

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