Variant report

Variant	rs4925084
Chromosome Location	chr17:19998958-19998959
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	RAD21	chr17:19998520-19999091	MCF-7	breast:	n/a	chr17:19998781-19998795 chr17:19998728-19998740
2	POLR2A	chr17:19998717-19999006	MCF-7	breast:	n/a	n/a
3	CTCF	chr17:19998920-19999070	Hela-S3	cervix:	n/a	n/a
4	FOXA1	chr17:19998612-19999313	A549	lung:	n/a	n/a
5	CTCF	chr17:19998820-19998970	NHLF	lung:	n/a	n/a
6	NR3C1	chr17:19998694-19999335	A549	lung:	n/a	chr17:19998918-19998931 chr17:19999074-19999083 chr17:19998982-19998995
7	RAD21	chr17:19998608-19998997	SK-N-SH_RA	brain:	n/a	chr17:19998781-19998795 chr17:19998728-19998740
8	MAX	chr17:19998482-19999121	A549	lung:	n/a	n/a
9	CREB1	chr17:19998684-19999285	A549	lung:	n/a	n/a
10	POLR2A	chr17:19998869-19999028	MCF-7	breast:	n/a	n/a
11	CTCF	chr17:19998516-19999051	MCF-7	breast:	n/a	n/a
12	CTCF	chr17:19998583-19998977	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr17:19998637-19998967	MCF-7	breast:	n/a	n/a
14	RAD21	chr17:19998627-19999036	H1-hESC	embryonic stem cell:	n/a	chr17:19998781-19998795 chr17:19998728-19998740
15	MAX	chr17:19998554-19999011	SK-N-SH	brain:	n/a	n/a
16	RAD21	chr17:19998514-19998975	HCT-116	colon:	n/a	chr17:19998781-19998795 chr17:19998728-19998740
17	CTCF	chr17:19998496-19999071	MCF-7	breast:	n/a	n/a
18	SMC3	chr17:19998607-19998962	Hela-S3	cervix:	n/a	chr17:19998781-19998788
19	NR3C1	chr17:19998636-19999403	A549	lung:	n/a	chr17:19998918-19998931 chr17:19999074-19999083 chr17:19998982-19998995
20	CTCF	chr17:19998679-19999007	Fibrobl	skin:	n/a	n/a
21	NR3C1	chr17:19998696-19999312	A549	lung:	n/a	chr17:19998918-19998931 chr17:19999074-19999083 chr17:19998982-19998995
22	SMC3	chr17:19998550-19999448	SK-N-SH	brain:	n/a	chr17:19998781-19998788
23	CTCF	chr17:19998549-19999001	HCT-116	colon:	n/a	n/a
24	POLR2A	chr17:19998675-19998996	A549	lung:	n/a	n/a
25	CTCF	chr17:19998644-19998966	MCF-7	breast:	n/a	n/a
26	RAD21	chr17:19998444-19999234	A549	lung:	n/a	chr17:19998781-19998795 chr17:19998728-19998740
27	CTCF	chr17:19998648-19998979	MCF-7	breast:	n/a	n/a
28	RAD21	chr17:19998577-19998987	HepG2	liver:	n/a	chr17:19998781-19998795 chr17:19998728-19998740
29	RAD21	chr17:19998159-19999582	SK-N-SH	brain:	n/a	chr17:19998781-19998795 chr17:19998728-19998740
30	CTCF	chr17:19998585-19998977	A549	lung:	n/a	n/a
31	KAP1	chr17:19998316-19999070	HEK293	kidney:	n/a	n/a
32	RAD21	chr17:19998483-19999032	A549	lung:	n/a	chr17:19998781-19998795 chr17:19998728-19998740
33	MYC	chr17:19998944-19998964	MCF-7	breast:	n/a	n/a
34	CTCF	chr17:19998423-19999522	SK-N-SH	brain:	n/a	n/a
35	NR3C1	chr17:19998645-19999332	A549	lung:	n/a	chr17:19998918-19998931 chr17:19999074-19999083 chr17:19998982-19998995
36	CTCF	chr17:19998620-19998999	K562	blood:	n/a	n/a
37	RAD21	chr17:19998486-19998986	MCF-7	breast:	n/a	chr17:19998781-19998795 chr17:19998728-19998740
38	CTCF	chr17:19998840-19998990	WI-38	lung:	n/a	n/a
39	KAP1	chr17:19998430-19999216	U2OS	brain:	n/a	n/a
40	MXI1	chr17:19998190-19999434	SK-N-SH	brain:	n/a	chr17:19998462-19998477
41	FOXA2	chr17:19998645-19999404	A549	lung:	n/a	n/a
42	CTCF	chr17:19998509-19999073	A549	lung:	n/a	n/a
43	CTCF	chr17:19998181-19999885	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:19998939-19998989	PrEC	prostate:	n/a
2	chr17:19998939-19998989	K562	blood:	n/a
3	chr17:19998939-19998989	HUVEC	blood vessel:	n/a
4	chr17:19998939-19998989	HNPCEpiC	eye:	n/a
5	chr17:19998939-19998989	ovcar-3	ovarian:	n/a
6	chr17:19998939-19998989	AG09319	gingival:	n/a
7	chr17:19998939-19998989	GM12892	blood:	n/a
8	chr17:19998939-19998989	HCF	heart:	n/a
9	chr17:19998939-19998989	AG04450	lung:	fetal
10	chr17:19998939-19998989	SK-N-MC	brain:	n/a
11	chr17:19998939-19998989	GM06990	blood:	n/a
12	chr17:19998939-19998989	HL-60	blood:	n/a
13	chr17:19998939-19998989	GM19239	blood:	n/a
14	chr17:19998939-19998989	Jurkat	blood:	n/a
15	chr17:19998939-19998989	CMK	blood:	n/a
16	chr17:19998939-19998989	MCF10A-Er-Src	breast:	n/a
17	chr17:19998939-19998989	BE2_C	brain:	n/a
18	chr17:19998939-19998989	NHDF-neo	bronchial:	n/a
19	chr17:19998939-19998989	MCF-7	breast:	n/a
20	chr17:19998939-19998989	ECC-1	luminal epithelium:	n/a
21	chr17:19998939-19998989	AG10803	skin:	n/a
22	chr17:19998939-19998989	HepG2	liver:	n/a
23	chr17:19998939-19998989	HPAEpiC	pulmonary alveolar:	n/a
24	chr17:19998939-19998989	SKMC	muscle:	n/a
25	chr17:19998939-19998989	U87	brain:	n/a
26	chr17:19998939-19998989	LNCaP	prostate:	n/a
27	chr17:19998939-19998989	NHBE	bronchial:	n/a
28	chr17:19998939-19998989	AG04449	skin:	fetal
29	chr17:19998939-19998989	NT2-D1	testis:	n/a
30	chr17:19998939-19998989	A549	lung:	n/a
31	chr17:19998939-19998989	PFSK-1	brain:	n/a
32	chr17:19998939-19998989	HAEpiC	amniotic membrane:	n/a
33	chr17:19998939-19998989	SK-N-SH	brain:	n/a
34	chr17:19998939-19998989	Caco-2	colon:	n/a
35	chr17:19998939-19998989	BJ	skin:	n/a
36	chr17:19998939-19998989	HRPEpiC	eye:	n/a
37	chr17:19998939-19998989	HMEC	breast:	n/a
38	chr17:19998939-19998989	AoSMC	blood vessel:	n/a
39	chr17:19998939-19998989	NH-A	brain:	n/a
40	chr17:19998939-19998989	SK-N-SH_RA	brain:	n/a
41	chr17:19998939-19998989	RPTEC	kidney:	n/a
42	chr17:19998939-19998989	IMR90	lung:	fetal
43	chr17:19998939-19998989	HCM	heart:	n/a
44	chr17:19998939-19998989	HEK293	kidney:	embryo
45	chr17:19998939-19998989	GM12891	blood:	n/a
46	chr17:19998939-19998989	HCPEpiC	choroid plexus:	n/a
47	chr17:19998939-19998989	Hela-S3	cervix:	n/a
48	chr17:19998939-19998989	Hepatocyte	liver:	n/a
49	chr17:19998939-19998989	HRCEpiC	kidney:	n/a
50	chr17:19998939-19998989	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:19912973..19913861-chr17:19998764..19999738,2	K562	blood:
2	chr17:19912162..19913083-chr17:19998469..19999472,3	MCF-7	breast:

Variant related genes	Relation type
SPECC1	TF binding region
SPECC1	CpG island
ENSG00000261033	Chromatin interaction
ENSG00000128487	Chromatin interaction

Extended variants
information (count: 120 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:111)

rs_ID	r²[population]
rs1009082	1.00[CHB][hapmap]
rs10438824	1.00[CHB][hapmap]
rs11204422	0.84[CEU][hapmap]
rs11869931	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12449914	0.95[AMR][1000 genomes]
rs12450857	1.00[CHB][hapmap]
rs12451841	0.84[CEU][hapmap]
rs12453332	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12453720	1.00[CHB][hapmap]
rs12937327	0.93[AMR][1000 genomes]
rs12943904	0.93[AMR][1000 genomes]
rs12947713	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12947950	1.00[CHB][hapmap]
rs12949485	1.00[CHB][hapmap]
rs12949710	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1468953	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1544421	1.00[CHB][hapmap]
rs1561974	1.00[CHB][hapmap]
rs1638527	1.00[CHB][hapmap]
rs17604987	1.00[CHB][hapmap]
rs17685923	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17686622	1.00[CHB][hapmap]
rs17686839	1.00[CHB][hapmap]
rs17759041	0.90[AMR][1000 genomes]
rs17759609	1.00[CHB][hapmap];0.94[AMR][1000 genomes]
rs1812934	1.00[CHB][hapmap]
rs2013576	1.00[CHB][hapmap]
rs203467	1.00[CHB][hapmap]
rs203475	1.00[CHB][hapmap]
rs203480	1.00[CHB][hapmap]
rs2107566	1.00[CHB][hapmap]
rs2108981	1.00[CHB][hapmap]
rs2158473	1.00[CHB][hapmap]
rs2189710	1.00[CHB][hapmap]
rs2263175	1.00[CHB][hapmap]
rs2386485	1.00[CHB][hapmap]
rs2526460	1.00[CHB][hapmap]
rs2526462	1.00[CHB][hapmap]
rs2526467	1.00[CHB][hapmap]
rs2526468	1.00[CHB][hapmap]
rs2526469	1.00[CHB][hapmap]
rs2526471	1.00[CHB][hapmap]
rs2526474	1.00[CHB][hapmap]
rs2526475	1.00[CHB][hapmap]
rs2526480	1.00[CHB][hapmap]
rs2526484	1.00[CHB][hapmap]
rs2526491	1.00[CHB][hapmap]
rs2703772	1.00[CHB][hapmap]
rs2703773	1.00[CHB][hapmap]
rs2703774	1.00[CHB][hapmap]
rs2703782	1.00[CHB][hapmap]
rs2703790	1.00[CHB][hapmap]
rs2703791	1.00[CHB][hapmap]
rs2703792	1.00[CHB][hapmap]
rs2703794	1.00[CHB][hapmap]
rs2703799	1.00[CHB][hapmap]
rs2703801	1.00[CHB][hapmap]
rs2703802	1.00[CHB][hapmap]
rs2703804	1.00[CHB][hapmap]
rs2703806	1.00[CHB][hapmap]
rs2703808	1.00[CHB][hapmap]
rs2703813	1.00[CHB][hapmap]
rs2703815	1.00[CHB][hapmap]
rs2703816	1.00[CHB][hapmap]
rs2703817	1.00[CHB][hapmap]
rs2703818	1.00[CHB][hapmap]
rs2703821	1.00[CHB][hapmap]
rs34089239	1.00[CHB][hapmap]
rs34756775	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35124809	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35156798	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35191778	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35244101	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35317166	0.93[AMR][1000 genomes]
rs35493088	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35770292	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35915823	0.93[AMR][1000 genomes]
rs3850783	1.00[CHB][hapmap]
rs3850784	1.00[CHB][hapmap]
rs3850785	1.00[CHB][hapmap]
rs3862151	1.00[CHB][hapmap];0.90[AMR][1000 genomes]
rs4341795	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4346259	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4350625	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4471741	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4588033	1.00[CHB][hapmap]
rs4924802	1.00[CHB][hapmap];0.93[AMR][1000 genomes]
rs4924809	1.00[CHB][hapmap]
rs4924810	1.00[CHB][hapmap]
rs4925054	1.00[CHB][hapmap]
rs4925071	0.90[AMR][1000 genomes]
rs4925074	0.90[AMR][1000 genomes]
rs4925075	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4925076	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4925078	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4925082	0.84[CEU][hapmap]
rs56371654	0.93[AMR][1000 genomes]
rs62067488	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7215803	0.84[CEU][hapmap]
rs7503407	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs8068484	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8075343	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8080827	1.00[CHB][hapmap]
rs8081817	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs888424	0.84[CEU][hapmap]
rs9325894	1.00[CHB][hapmap]
rs9896221	1.00[CHB][hapmap]
rs9896709	1.00[CHB][hapmap]
rs9897328	1.00[CHB][hapmap]
rs9904928	1.00[CHB][hapmap]
rs9905493	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062853	chr17:19547912-20206601	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
2	nsv907868	chr17:19768924-20217122	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv833394	chr17:19827714-19999577	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv1060337	chr17:19828636-20204872	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv543257	chr17:19828636-20204872	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv907870	chr17:19871922-20001612	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv907871	chr17:19927699-20088492	Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv482438	chr17:19934376-20089005	Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv833395	chr17:19969959-20124084	Genic enhancers Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4925084	SPECC1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:19978800-20000000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr17:19993400-20006400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr17:19993600-20000000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr17:19993600-20003600	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr17:19993800-20000600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr17:19993800-20001600	Weak transcription	Lung	lung
7	chr17:19993800-20006400	Weak transcription	Esophagus	oesophagus
8	chr17:19993800-20008800	Weak transcription	GM12878-XiMat	blood
9	chr17:19995000-20000000	Weak transcription	Right Ventricle	heart
10	chr17:19995000-20001200	Weak transcription	Primary hematopoietic stem cells	blood
11	chr17:19996600-20000800	Weak transcription	Aorta	Aorta
12	chr17:19996800-19999600	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr17:19997600-19999600	Enhancers	Fetal Muscle Leg	muscle
14	chr17:19997800-19999000	Enhancers	NHLF	lung
15	chr17:19997800-19999200	Enhancers	Brain Germinal Matrix	brain
16	chr17:19997800-19999200	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr17:19998200-19999000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr17:19998200-19999000	Enhancers	Duodenum Smooth Muscle	Duodenum
19	chr17:19998200-19999200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr17:19998200-19999200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr17:19998200-19999200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr17:19998200-20000000	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr17:19998200-20000000	Enhancers	Brain Substantia Nigra	brain
24	chr17:19998400-19999000	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr17:19998400-19999000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr17:19998400-19999000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr17:19998400-19999000	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr17:19998400-19999000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr17:19998400-19999000	Flanking Active TSS	Brain Angular Gyrus	brain
30	chr17:19998400-19999200	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr17:19998400-19999200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr17:19998400-19999200	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr17:19998400-19999200	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr17:19998400-19999200	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr17:19998400-19999200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
36	chr17:19998400-19999200	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr17:19998400-19999200	Flanking Active TSS	A549	lung
38	chr17:19998400-19999400	Flanking Active TSS	Brain Anterior Caudate	brain
39	chr17:19998600-19999000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr17:19998600-19999000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr17:19998600-19999000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr17:19998600-19999000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr17:19998600-19999000	Flanking Active TSS	Adipose Nuclei	Adipose
44	chr17:19998600-19999000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
45	chr17:19998600-19999000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
46	chr17:19998600-19999000	Enhancers	Hela-S3	cervix
47	chr17:19998600-19999000	Flanking Active TSS	NHDF-Ad	bronchial
48	chr17:19998600-19999200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr17:19998600-19999200	Enhancers	Fetal Brain Male	brain
50	chr17:19998600-19999400	Enhancers	HUES6 Cell Line	embryonic stem cell

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