Variant report

Variant	rs2974999
Chromosome Location	chr17:17997547-17997548
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:142)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:142 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr17:17997400-17997550	AG04449	skin:	n/a	n/a
2	POLR2A	chr17:17997099-17997584	K562	blood:	n/a	n/a
3	BHLHE40	chr17:17997396-17997698	HepG2	liver:	n/a	n/a
4	CTCF	chr17:17997420-17997570	NHDF-neo	bronchial:	n/a	n/a
5	CTCF	chr17:17997400-17997550	SAEC	small airway:	n/a	n/a
6	CTCF	chr17:17997222-17997753	MCF-7	breast:	n/a	n/a
7	CTCF	chr17:17997400-17997550	NHLF	lung:	n/a	n/a
8	POLR2A	chr17:17997438-17997740	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr17:17997340-17997584	A549	lung:	n/a	n/a
10	CTCF	chr17:17997440-17997590	GM12872	blood:	n/a	n/a
11	CTCF	chr17:17997355-17997602	Hela-S3	cervix:	n/a	n/a
12	MXI1	chr17:17997236-17997841	IMR90	lung:	n/a	n/a
13	CTCF	chr17:17997400-17997550	BE2_C	brain:	n/a	n/a
14	CTCF	chr17:17997366-17997574	MCF-7	breast:	n/a	n/a
15	FOS	chr17:17997420-17997586	MCF10A-Er-Src	breast:	n/a	n/a
16	YY1	chr17:17997291-17997622	A549	lung:	n/a	n/a
17	CTCF	chr17:17997354-17997565	ProgFib	skin:	n/a	n/a
18	CTCF	chr17:17997403-17997551	GM10266	blood:	n/a	n/a
19	CTCF	chr17:17997420-17997570	HA-sp	spinal cord:	n/a	n/a
20	MAZ	chr17:17997243-17997834	IMR90	lung:	n/a	n/a
21	CTCF	chr17:17997440-17997590	HCFaa	heart:	n/a	n/a
22	CTCF	chr17:17997336-17997613	NHEK	skin:	n/a	n/a
23	CTCF	chr17:17997400-17997550	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr17:17997400-17997550	HL-60	blood:	n/a	n/a
25	MYC	chr17:17997430-17997621	K562	blood:	n/a	n/a
26	CTCF	chr17:17997280-17997660	K562	blood:	n/a	n/a
27	CTCF	chr17:17997400-17997550	GM12865	blood:	n/a	n/a
28	CTCF	chr17:17997420-17997570	GM12873	blood:	n/a	n/a
29	CTCF	chr17:17997378-17997561	MCF-7	breast:	n/a	n/a
30	CTCF	chr17:17997420-17997570	AG09309	skin:	n/a	n/a
31	CTCF	chr17:17997460-17997610	WI-38	lung:	n/a	n/a
32	ZNF143	chr17:17997401-17997625	K562	blood:	n/a	n/a
33	CTCF	chr17:17997400-17997550	HMEC	breast:	n/a	n/a
34	CTCF	chr17:17997393-17997561	GM12892	blood:	n/a	n/a
35	FOS	chr17:17997439-17997647	MCF10A-Er-Src	breast:	n/a	n/a
36	CTCF	chr17:17997420-17997570	GM12875	blood:	n/a	n/a
37	MYC	chr17:17997417-17997647	MCF10A-Er-Src	breast:	n/a	n/a
38	CTCF	chr17:17997400-17997550	HMF	breast:	n/a	n/a
39	CTCF	chr17:17997400-17997550	HRE	kidney:	n/a	n/a
40	CTCF	chr17:17997431-17997547	GM10248	blood:	n/a	n/a
41	POLR2A	chr17:17996659-17997549	HepG2	liver:	n/a	n/a
42	CTCF	chr17:17997395-17997549	Medullo	brain:	n/a	n/a
43	CTCF	chr17:17997400-17997550	AG10803	skin:	n/a	n/a
44	CTCF	chr17:17997420-17997570	MCF-7	breast:	n/a	n/a
45	CTCF	chr17:17997292-17997674	HepG2	liver:	n/a	n/a
46	CTCF	chr17:17997400-17997550	GM12872	blood:	n/a	n/a
47	POLR2A	chr17:17997231-17997899	PFSK-1	brain:	n/a	n/a
48	CTCF	chr17:17997400-17997550	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr17:17997359-17997599	HepG2	liver:	n/a	n/a
50	RAD21	chr17:17997320-17997658	HepG2	liver:	n/a	n/a

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:17944377..17946429-chr17:17996253..17997823,2	K562	blood:
2	chr17:17991646..17993233-chr17:17995608..17997950,2	K562	blood:
3	chr17:17991305..17993918-chr17:17994644..17998089,4	K562	blood:
4	chr17:17996047..17999029-chr17:18001413..18005397,3	MCF-7	breast:
5	chr17:17989607..17991385-chr17:17997337..17999008,2	MCF-7	breast:
6	chr17:17942903..17946429-chr17:17996253..17997904,3	K562	blood:
7	chr17:17997353..17998976-chr17:18004637..18006664,2	K562	blood:
8	chr17:17995313..17997784-chr17:18005282..18007698,2	K562	blood:
9	chr17:17989895..17993133-chr17:17993965..17998692,5	MCF-7	breast:

No data

Variant related genes	Relation type
DRG2	TF binding region
ENSG00000108591	Chromatin interaction

Extended variants
information (count: 108 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs1008135	0.96[EUR][1000 genomes]
rs1101727	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11078408	0.85[CEU][hapmap]
rs11078410	0.92[EUR][1000 genomes]
rs11650021	0.83[EUR][1000 genomes]
rs11867241	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11870660	0.85[CEU][hapmap]
rs12939020	0.82[EUR][1000 genomes]
rs2056842	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2955350	0.81[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs2955353	0.82[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs2955354	0.95[CEU][hapmap];0.86[YRI][hapmap];0.82[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs2955355	0.95[CEU][hapmap];0.85[EUR][1000 genomes]
rs2955356	0.95[CEU][hapmap];0.85[EUR][1000 genomes]
rs2955357	0.95[CEU][hapmap];0.85[EUR][1000 genomes]
rs2955358	0.95[CEU][hapmap];0.85[EUR][1000 genomes]
rs2955359	0.95[CEU][hapmap];0.85[YRI][hapmap];0.81[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs2955365	0.85[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2955366	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2955367	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2955368	0.84[EUR][1000 genomes]
rs2955370	0.95[CEU][hapmap];0.86[YRI][hapmap];0.84[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs2955372	0.95[CEU][hapmap];0.86[EUR][1000 genomes]
rs2955377	0.90[CEU][hapmap];0.81[YRI][hapmap];0.81[EUR][1000 genomes]
rs2955378	0.95[CEU][hapmap];0.82[YRI][hapmap];0.81[EUR][1000 genomes]
rs2955380	0.95[CEU][hapmap];0.85[YRI][hapmap];0.82[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs2955381	0.94[CEU][hapmap];0.86[YRI][hapmap];0.84[EUR][1000 genomes]
rs2955383	0.95[CEU][hapmap];0.83[EUR][1000 genomes]
rs2955384	0.95[CEU][hapmap];0.82[YRI][hapmap];0.80[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs2955385	0.95[CEU][hapmap];0.82[YRI][hapmap];0.80[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs2974998	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2975003	0.82[ASN][1000 genomes]
rs2975004	0.82[ASN][1000 genomes]
rs2975005	0.82[ASN][1000 genomes]
rs4072738	0.90[CEU][hapmap]
rs4072739	0.89[CEU][hapmap]
rs4299203	0.85[CEU][hapmap]
rs4365346	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4368210	0.95[CEU][hapmap];0.82[YRI][hapmap]
rs4410135	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4426402	1.00[CEU][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4459604	0.95[CEU][hapmap]
rs4506967	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4506969	0.90[CEU][hapmap];0.83[YRI][hapmap]
rs4561528	0.93[EUR][1000 genomes]
rs4584886	0.95[CEU][hapmap];0.82[YRI][hapmap]
rs4643387	0.85[EUR][1000 genomes]
rs4924832	0.95[CEU][hapmap]
rs4925135	0.84[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs4925136	0.84[EUR][1000 genomes]
rs59518074	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62073573	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6502632	0.95[CEU][hapmap]
rs6502633	0.80[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs6502634	0.81[EUR][1000 genomes]
rs6502636	1.00[CEU][hapmap];0.90[CHB][hapmap];0.90[JPT][hapmap];0.90[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6502637	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6826	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs712267	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs712268	0.96[EUR][1000 genomes]
rs7207461	0.82[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs7207821	0.95[CEU][hapmap];0.83[YRI][hapmap]
rs7209003	0.95[CEU][hapmap]
rs7210400	0.85[EUR][1000 genomes]
rs7211714	1.00[CEU][hapmap];0.93[YRI][hapmap];0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7212167	0.95[CEU][hapmap]
rs7212447	1.00[CEU][hapmap];0.89[CHB][hapmap];0.86[JPT][hapmap];0.89[YRI][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7214002	0.80[YRI][hapmap]
rs7215524	0.81[EUR][1000 genomes]
rs721669	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7219324	0.89[CEU][hapmap]
rs7224047	0.82[EUR][1000 genomes]
rs7406744	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7406982	0.95[CEU][hapmap];0.85[YRI][hapmap];0.82[EUR][1000 genomes]
rs741782	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7503738	0.82[EUR][1000 genomes]
rs8066764	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8068175	0.85[CEU][hapmap]
rs8069811	0.80[EUR][1000 genomes]
rs8075189	0.95[CEU][hapmap]
rs8080602	0.95[CEU][hapmap];0.84[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs854763	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.93[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs854767	1.00[CEU][hapmap];0.85[CHB][hapmap];0.86[JPT][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs854768	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs854769	1.00[CEU][hapmap];0.85[CHB][hapmap];0.86[JPT][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs854770	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs854789	0.96[EUR][1000 genomes]
rs854790	1.00[CEU][hapmap];0.85[CHB][hapmap];0.86[JPT][hapmap];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs854791	1.00[CEU][hapmap];0.85[CHB][hapmap];0.86[JPT][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs854792	0.85[EUR][1000 genomes]
rs854808	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs854809	1.00[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs854814	1.00[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs854817	1.00[CEU][hapmap];0.85[CHB][hapmap];0.86[JPT][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs854818	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9303144	1.00[CEU][hapmap];0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9894138	0.85[EUR][1000 genomes]
rs9896837	0.95[CEU][hapmap];0.82[YRI][hapmap];0.81[EUR][1000 genomes]
rs9897761	0.95[CEU][hapmap]
rs9899355	0.89[CEU][hapmap]
rs9913277	0.95[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531183	chr17:17571035-18205309	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
2	nsv916653	chr17:17651916-18454952	Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
3	nsv533142	chr17:17691726-18236686	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
4	nsv960429	chr17:17951047-18027679	Strong transcription Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
5	nsv482491	chr17:17959577-18153920	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription 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	38 gene(s)	inside rSNPs	diseases
6	nsv1061162	chr17:17978838-18259234	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
7	nsv492305	chr17:17980441-18424702	Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2974999	SREBF1	cis	Whole Blood	GTEx

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17991800-18009800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr17:17992000-18000600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr17:17992200-18000800	Weak transcription	Psoas Muscle	Psoas
4	chr17:17992200-18002400	Weak transcription	Fetal Brain Male	brain
5	chr17:17992200-18014000	Weak transcription	Right Atrium	heart
6	chr17:17992400-17998400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr17:17992400-17998800	Weak transcription	HUVEC	blood vessel
8	chr17:17992400-17999000	Weak transcription	Primary hematopoietic stem cells	blood
9	chr17:17992400-17999800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr17:17992400-18001000	Weak transcription	Colon Smooth Muscle	Colon
11	chr17:17992400-18005600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr17:17993000-18004800	Weak transcription	Small Intestine	intestine
13	chr17:17993000-18012000	Strong transcription	Fetal Muscle Trunk	muscle
14	chr17:17993200-17997600	Weak transcription	Left Ventricle	heart
15	chr17:17993200-17999200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr17:17993200-18011200	Strong transcription	Fetal Stomach	stomach
17	chr17:17993400-17999200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr17:17993800-18005200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr17:17994000-18005400	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr17:17994000-18005600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr17:17994000-18006000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr17:17994000-18010800	Strong transcription	Dnd41	blood
23	chr17:17994200-18005400	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr17:17994200-18005600	Strong transcription	Primary T cells from cord blood	blood
25	chr17:17994200-18010800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr17:17994200-18010800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr17:17994200-18011000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr17:17994200-18011000	Strong transcription	Sigmoid Colon	Sigmoid Colon
29	chr17:17994200-18011600	Strong transcription	Fetal Muscle Leg	muscle
30	chr17:17994200-18011800	Strong transcription	Stomach Smooth Muscle	stomach
31	chr17:17994200-18012000	Strong transcription	Fetal Intestine Small	intestine
32	chr17:17994400-17998200	Strong transcription	Rectal Smooth Muscle	rectum
33	chr17:17994400-18005600	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr17:17994400-18005600	Strong transcription	Fetal Thymus	thymus
35	chr17:17994400-18011000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr17:17994400-18011400	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr17:17994600-18011200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr17:17994600-18012800	Strong transcription	Thymus	Thymus
39	chr17:17994800-18004600	Strong transcription	Liver	Liver
40	chr17:17994800-18005400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr17:17995000-18005600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr17:17995000-18010800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr17:17995000-18011200	Strong transcription	Placenta	Placenta
44	chr17:17995200-17998000	Strong transcription	HSMM	muscle
45	chr17:17995200-17998200	Strong transcription	Gastric	stomach
46	chr17:17995200-18005600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr17:17995200-18011000	Strong transcription	Ovary	ovary
48	chr17:17995200-18011000	Strong transcription	Rectal Mucosa Donor 29	rectum
49	chr17:17995200-18011000	Strong transcription	NHLF	lung
50	chr17:17995200-18011400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links