Variant report

Variant	rs6584033
Chromosome Location	chr10:97578453-97578454
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr10:97577581-97578825	GM12892	blood:	n/a	n/a
2	POLR2A	chr10:97576705-97578856	GM18505	blood:	n/a	n/a
3	FOSL2	chr10:97578388-97578799	HepG2	liver:	n/a	chr10:97578702-97578711
4	POLR2A	chr10:97574937-97578880	GM12891	blood:	n/a	n/a
5	BATF	chr10:97578397-97578868	GM12878	blood:	n/a	chr10:97578700-97578710 chr10:97578704-97578714
6	ATF2	chr10:97578269-97578936	GM12878	blood:	n/a	n/a
7	MTA3	chr10:97578134-97578804	GM12878	blood:	n/a	n/a
8	POLR2A	chr10:97578408-97578624	GM12878	blood:	n/a	n/a
9	EP300	chr10:97578240-97579048	ECC-1	luminal epithelium:	n/a	chr10:97578703-97578712 chr10:97578595-97578605
10	FOXA1	chr10:97578396-97578772	T-47D	breast:	n/a	n/a
11	POLR2A	chr10:97577744-97578815	GM12878	blood:	n/a	n/a
12	FOXA2	chr10:97578445-97578686	A549	lung:	n/a	n/a
13	TEAD4	chr10:97578316-97578895	HepG2	liver:	n/a	n/a
14	FOXA2	chr10:97578447-97578699	A549	lung:	n/a	n/a
15	POLR2A	chr10:97577868-97580068	GM12878	blood:	n/a	n/a
16	PML	chr10:97577579-97579044	GM12878	blood:	n/a	n/a
17	POLR2A	chr10:97578211-97578921	HUVEC	blood vessel:	n/a	n/a
18	POLR2A	chr10:97574825-97578894	GM12891	blood:	n/a	n/a
19	RCOR1	chr10:97578069-97578901	IMR90	lung:	n/a	n/a
20	FOXA1	chr10:97578377-97578781	ECC-1	luminal epithelium:	n/a	n/a
21	NFATC1	chr10:97577508-97578895	GM12878	blood:	n/a	n/a
22	ELK1	chr10:97578447-97578635	GM12878	blood:	n/a	n/a
23	FOXA1	chr10:97578416-97578910	HepG2	liver:	n/a	n/a
24	TCF12	chr10:97578226-97578907	ECC-1	luminal epithelium:	n/a	chr10:97578632-97578641 chr10:97578596-97578605
25	FOXA1	chr10:97578443-97578777	HepG2	liver:	n/a	n/a
26	BCLAF1	chr10:97578374-97578884	GM12878	blood:	n/a	n/a
27	POLR2A	chr10:97578318-97578652	GM12878	blood:	n/a	n/a
28	NFIC	chr10:97578274-97578913	GM12878	blood:	n/a	n/a
29	POLR2A	chr10:97576591-97578817	GM12891	blood:	n/a	n/a
30	POLR2A	chr10:97578443-97578503	HUVEC	blood vessel:	n/a	n/a
31	FOXA1	chr10:97578422-97578822	T-47D	breast:	n/a	n/a
32	WRNIP1	chr10:97578168-97578654	GM12878	blood:	n/a	n/a
33	NFATC1	chr10:97575708-97578846	GM12878	blood:	n/a	n/a
34	POLR2A	chr10:97577731-97578518	GM12892	blood:	n/a	n/a
35	TEAD4	chr10:97578284-97578955	ECC-1	luminal epithelium:	n/a	n/a
36	POLR2A	chr10:97577815-97579311	GM12892	blood:	n/a	n/a
37	JUN	chr10:97578310-97578869	HUVEC	blood vessel:	n/a	chr10:97578702-97578711
38	FOXA1	chr10:97578343-97578754	ECC-1	luminal epithelium:	n/a	n/a
39	NFIC	chr10:97578342-97578942	ECC-1	luminal epithelium:	n/a	n/a
40	FOXA2	chr10:97578415-97578741	HepG2	liver:	n/a	n/a
41	POLR2A	chr10:97574871-97578865	GM12891	blood:	n/a	n/a
42	RUNX3	chr10:97578398-97578921	GM12878	blood:	n/a	n/a
43	FOXA1	chr10:97578419-97578803	HepG2	liver:	n/a	n/a
44	POLR2A	chr10:97577641-97578804	GM12891	blood:	n/a	n/a
45	GATA2	chr10:97578156-97578757	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr10:97578328-97578767	HUVEC	blood vessel:	n/a	n/a
47	NR3C1	chr10:97578450-97578725	ECC-1	luminal epithelium:	n/a	n/a
48	FOXA1	chr10:97578361-97578841	HepG2	liver:	n/a	n/a
49	POLR2A	chr10:97574823-97579264	GM12878	blood:	n/a	n/a
50	FOS	chr10:97578435-97578903	HUVEC	blood vessel:	n/a	chr10:97578702-97578711

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:97572611..97574483-chr10:97578100..97579949,2	K562	blood:

Variant related genes	Relation type
ENTPD1	TF binding region

Extended variants
information (count: 83 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10159941	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs10509687	0.92[CHB][hapmap];0.85[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];0.88[MEX][hapmap];0.88[MKK][hapmap];0.96[YRI][hapmap]
rs10748634	0.84[CHB][hapmap]
rs10748635	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap]
rs10748637	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs10748638	0.86[CHB][hapmap]
rs10748641	0.81[AFR][1000 genomes]
rs10786230	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs10786235	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10786238	0.87[ASN][1000 genomes]
rs10882646	0.83[CHB][hapmap]
rs10882653	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs10882664	0.92[CHB][hapmap]
rs10882665	0.92[CHB][hapmap]
rs10882670	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10882681	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10882682	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10882683	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1113881	0.81[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs11188459	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11188468	0.85[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs11188470	0.90[AFR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11188482	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11188485	1.00[CHB][hapmap];0.90[CHD][hapmap];0.93[JPT][hapmap];0.87[ASN][1000 genomes]
rs11188488	1.00[CHB][hapmap];0.92[JPT][hapmap];0.87[ASN][1000 genomes]
rs11498722	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11528098	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12240959	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12262943	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs1340837	0.86[JPT][hapmap]
rs1342791	0.92[CHB][hapmap]
rs1933166	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs1933169	0.92[CHB][hapmap]
rs1933171	0.81[AFR][1000 genomes]
rs1953710	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.81[ASN][1000 genomes]
rs2211002	0.84[CHB][hapmap]
rs2225893	1.00[ASW][hapmap];0.88[CEU][hapmap];0.92[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap]
rs2225894	0.81[AFR][1000 genomes]
rs2861149	0.86[CHB][hapmap]
rs2901873	0.92[CHB][hapmap]
rs2901874	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3176883	0.94[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3181123	0.92[CHB][hapmap]
rs3793748	0.88[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap]
rs3938778	0.87[AFR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3949478	0.92[CHB][hapmap]
rs4075311	0.82[CHD][hapmap];0.93[JPT][hapmap];0.98[LWK][hapmap];0.97[MKK][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs4290159	0.82[CHB][hapmap]
rs4409759	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4457685	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes]
rs4501930	0.94[ASW][hapmap];0.92[CHB][hapmap];0.82[CHD][hapmap];0.91[GIH][hapmap];0.86[JPT][hapmap]
rs4641390	0.80[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs4918950	0.84[CHB][hapmap]
rs4918964	0.86[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.80[AFR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs60227189	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6584014	0.81[AFR][1000 genomes]
rs6584015	0.81[AFR][1000 genomes]
rs6584026	0.94[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6584028	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6584031	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7069234	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7073723	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs7081414	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7090320	0.87[ASN][1000 genomes]
rs7098750	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7100137	0.89[ASN][1000 genomes]
rs7897988	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7901116	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7902190	1.00[CHB][hapmap]
rs7905653	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs7909569	0.83[CHB][hapmap]
rs7910565	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7911400	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7912508	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7915345	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs7919773	0.80[AFR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7920850	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap]
rs945958	0.84[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531923	chr10:97366055-97725757	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 miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv895905	chr10:97513362-97686064	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv895906	chr10:97513362-97703650	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic 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	10 gene(s)	inside rSNPs	diseases
4	nsv895907	chr10:97529318-97686064	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv895908	chr10:97544513-97724247	Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs6584033	TCTN3	cis	lymphoblastoid	seeQTL
rs6584033	ENTPD1	cis	lymphoblastoid	seeQTL

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97573200-97580000	Enhancers	HUVEC	blood vessel
2	chr10:97573800-97584400	Weak transcription	Brain Cingulate Gyrus	brain
3	chr10:97574200-97583000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr10:97574400-97580800	Weak transcription	Small Intestine	intestine
5	chr10:97574400-97581000	Weak transcription	Spleen	Spleen
6	chr10:97574400-97581400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr10:97574800-97590800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr10:97575000-97580400	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr10:97575400-97579400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr10:97575400-97579600	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr10:97575600-97596600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr10:97575800-97579600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr10:97575800-97579800	Weak transcription	Left Ventricle	heart
14	chr10:97575800-97592000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr10:97575800-97597000	Weak transcription	Brain Hippocampus Middle	brain
16	chr10:97576000-97579400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr10:97576800-97580000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr10:97577000-97578600	Genic enhancers	Monocytes-CD14+_RO01746	blood
19	chr10:97577000-97580000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr10:97577200-97578800	Genic enhancers	GM12878-XiMat	blood
21	chr10:97577200-97580000	Enhancers	NHDF-Ad	bronchial
22	chr10:97577200-97587200	Weak transcription	Lung	lung
23	chr10:97577200-97591400	Weak transcription	Stomach Smooth Muscle	stomach
24	chr10:97577600-97583000	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr10:97577800-97580000	Enhancers	HepG2	liver
26	chr10:97578000-97578600	Enhancers	Aorta	Aorta
27	chr10:97578000-97579200	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr10:97578000-97580600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr10:97578200-97578600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr10:97578200-97578600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr10:97578200-97579200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr10:97578200-97579200	Weak transcription	Primary B cells from cord blood	blood
33	chr10:97578200-97579600	Enhancers	NH-A	brain
34	chr10:97578200-97579800	Enhancers	Muscle Satellite Cultured Cells	--
35	chr10:97578200-97579800	Enhancers	HMEC	breast
36	chr10:97578200-97579800	Enhancers	NHLF	lung
37	chr10:97578200-97580000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr10:97578200-97583000	Enhancers	Primary B cells from peripheral blood	blood
39	chr10:97578400-97578600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr10:97578400-97578600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr10:97578400-97578600	Enhancers	Fetal Stomach	stomach
42	chr10:97578400-97579000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr10:97578400-97579200	Enhancers	Osteobl	bone
44	chr10:97578400-97579400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr10:97578400-97580400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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