Variant report

Variant	nsv981560
Chromosome Location	chr7:100929810-100935291
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:358)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr7:100933704-100933944	GM12878	blood:	n/a	n/a
2	BHLHE40	chr7:100933720-100933933	K562	blood:	n/a	n/a
3	BHLHE40	chr7:100933740-100933907	HepG2	liver:	n/a	n/a
4	CEBPB	chr7:100931396-100931555	IMR90	lung:	n/a	n/a
5	CEBPB	chr7:100930489-100930562	K562	blood:	n/a	n/a
6	CTCF	chr7:100933580-100933730	AG10803	skin:	n/a	n/a
7	CTCF	chr7:100934380-100934530	AoAF	blood vessel:	n/a	n/a
8	CTCF	chr7:100933560-100933710	HEK293	kidney:	n/a	n/a
9	CTCF	chr7:100933580-100933730	K562	blood:	n/a	n/a
10	CTCF	chr7:100933579-100933647	Medullo	brain:	n/a	n/a
11	CTCF	chr7:100933600-100933750	HRE	kidney:	n/a	n/a
12	CTCF	chr7:100933880-100934030	GM12874	blood:	n/a	n/a
13	CTCF	chr7:100934108-100934268	GM19238	blood:	n/a	n/a
14	CTCF	chr7:100933666-100934021	GM19240	blood:	n/a	n/a
15	CTCF	chr7:100933820-100933970	HVMF	connective:	n/a	n/a
16	CTCF	chr7:100933580-100933730	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr7:100933880-100934030	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr7:100933820-100933970	NHLF	lung:	n/a	n/a
19	CTCF	chr7:100933773-100933994	GM13976	blood:	n/a	n/a
20	CTCF	chr7:100933920-100934070	WI-38	lung:	n/a	n/a
21	CTCF	chr7:100933820-100933970	GM12870	blood:	n/a	n/a
22	CTCF	chr7:100933580-100933730	HCM	heart:	n/a	n/a
23	CTCF	chr7:100933580-100933730	AG09319	gingival:	n/a	n/a
24	CTCF	chr7:100934320-100934470	GM12866	blood:	n/a	n/a
25	CTCF	chr7:100933880-100934030	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr7:100933661-100934004	GM19239	blood:	n/a	n/a
27	CTCF	chr7:100933820-100933970	NB4	blood:	n/a	n/a
28	CTCF	chr7:100933707-100933999	MCF-7	breast:	n/a	n/a
29	CTCF	chr7:100934122-100934250	GM12891	blood:	n/a	n/a
30	CTCF	chr7:100933820-100933970	GM12866	blood:	n/a	n/a
31	CTCF	chr7:100933665-100934018	Gliobla	brain:	n/a	n/a
32	CTCF	chr7:100933610-100933621	GM19238	blood:	n/a	n/a
33	CTCF	chr7:100933549-100933669	Lung_OC	lung:	n/a	n/a
34	CTCF	chr7:100933580-100933730	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr7:100933512-100934199	K562	blood:	n/a	n/a
36	CTCF	chr7:100933880-100934030	HCFaa	heart:	n/a	n/a
37	CTCF	chr7:100933721-100934014	LNCaP	prostate:	n/a	n/a
38	CTCF	chr7:100933734-100934033	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr7:100930213-100930239	GM13977	blood:	n/a	n/a
40	CTCF	chr7:100933820-100933970	HMEC	breast:	n/a	n/a
41	CTCF	chr7:100933820-100933970	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr7:100933880-100934030	AG09309	skin:	n/a	n/a
43	CTCF	chr7:100933657-100934010	A549	lung:	n/a	n/a
44	CTCF	chr7:100933600-100933750	GM12871	blood:	n/a	n/a
45	CTCF	chr7:100933560-100933710	GM12875	blood:	n/a	n/a
46	CTCF	chr7:100933739-100934002	LNCaP	prostate:	n/a	n/a
47	CTCF	chr7:100933580-100933730	BJ	skin:	n/a	n/a
48	CTCF	chr7:100933580-100933730	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr7:100933600-100933750	NHEK	skin:	n/a	n/a
50	CTCF	chr7:100933692-100933995	Fibrobl	skin:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100782339..100784727-chr7:100935145..100937630,2	K562	blood:
2	chr7:100886578..100888503-chr7:100932125..100933912,2	MCF-7	breast:
3	chr7:100926499..100928031-chr7:100930619..100932209,2	K562	blood:
4	chr7:100933432..100934555-chr7:101150641..101151287,4	MCF-7	breast:
5	chr7:99577726..99579955-chr7:100932141..100934760,2	MCF-7	breast:
6	chr7:100886674..100889462-chr7:100928835..100931897,3	MCF-7	breast:
7	chr7:100933411..100934409-chr7:101150803..101151635,3	K562	blood:

No data

Variant related genes	Relation type
AZGP1P2	TF binding region
ENSG00000214313	chromatin interactions
ENSG00000214253	chromatin interactions

Extended variants
information (count: 262 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375980958	chr7:100929853-100929854	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs370200587	chr7:100929869-100929870	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs373193975	chr7:100929875-100929876	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs577371509	chr7:100929897-100929898	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs56125283	chr7:100929917-100929918	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs191759112	chr7:100929942-100929943	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs553548847	chr7:100929947-100929948	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs148005004	chr7:100929974-100929975	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs185217936	chr7:100929992-100929993	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs546537152	chr7:100929996-100929997	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs113226225	chr7:100930001-100930002	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs190063691	chr7:100930017-100930018	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs557596803	chr7:100930036-100930037	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs575871640	chr7:100930093-100930094	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs545738740	chr7:100930132-100930133	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs563750709	chr7:100930135-100930136	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs528118477	chr7:100930150-100930151	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs141687570	chr7:100930178-100930179	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs561475773	chr7:100930193-100930194	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs374677092	chr7:100930223-100930224	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs75129268	chr7:100930257-100930258	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs12536711	chr7:100930265-100930266	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs569085069	chr7:100930303-100930304	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs182215128	chr7:100930306-100930307	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs551694466	chr7:100930354-100930355	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs570855593	chr7:100930384-100930385	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs535042221	chr7:100930431-100930432	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs553485579	chr7:100930458-100930459	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs568582140	chr7:100930472-100930473	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs370975941	chr7:100930495-100930496	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs536017946	chr7:100930497-100930498	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs557278120	chr7:100930516-100930517	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs138536698	chr7:100930526-100930527	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs141812819	chr7:100930576-100930577	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs115455297	chr7:100930613-100930614	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs117178589	chr7:100930620-100930621	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs539878409	chr7:100930664-100930665	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs187247366	chr7:100930685-100930686	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs200073281	chr7:100930744-100930745	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs528981755	chr7:100930745-100930746	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs544352145	chr7:100930746-100930747	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs562534187	chr7:100930794-100930795	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs139436783	chr7:100930853-100930854	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551677030	chr7:100930884-100930885	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs189265985	chr7:100930900-100930901	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs528458751	chr7:100930914-100930915	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs547036576	chr7:100930931-100930932	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs568521827	chr7:100930934-100930935	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs180946911	chr7:100930935-100930936	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs185067243	chr7:100930952-100930953	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100917200-100932800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:100919600-100935200	Weak transcription	Right Atrium	heart
3	chr7:100926200-100932400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr7:100926400-100930000	Weak transcription	Fetal Thymus	thymus
5	chr7:100926400-100930400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr7:100926400-100931600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr7:100926400-100932200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:100926400-100932400	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr7:100926400-100932400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:100926400-100932800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr7:100928600-100931000	Strong transcription	H1 Cell Line	embryonic stem cell
12	chr7:100929400-100930000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr7:100929400-100930800	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr7:100929600-100930600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr7:100929600-100930600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:100929600-100930800	Enhancers	Dnd41	blood
17	chr7:100929800-100930000	Flanking Active TSS	Liver	Liver
18	chr7:100930000-100930400	Enhancers	Liver	Liver
19	chr7:100930000-100930800	Enhancers	Fetal Thymus	thymus
20	chr7:100930000-100932400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr7:100930200-100930600	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr7:100930200-100930600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr7:100930200-100931000	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr7:100930200-100932400	Weak transcription	HepG2	liver
25	chr7:100930400-100930800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr7:100930400-100932000	Flanking Active TSS	Liver	Liver
27	chr7:100930600-100931000	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr7:100930800-100932800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr7:100930800-100933600	Weak transcription	Dnd41	blood
30	chr7:100931000-100931600	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr7:100931600-100931800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
32	chr7:100931600-100933000	Active TSS	HUES64 Cell Line	embryonic stem cell
33	chr7:100931600-100933200	Active TSS	H1 Cell Line	embryonic stem cell
34	chr7:100931800-100932400	Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr7:100932000-100933200	Active TSS	Liver	Liver
36	chr7:100932200-100932400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:100932400-100932600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
38	chr7:100932400-100932600	Flanking Active TSS	HepG2	liver
39	chr7:100932400-100932800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
40	chr7:100932400-100933600	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr7:100932400-100933800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr7:100932400-100934200	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr7:100932400-100934200	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr7:100932400-100935600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr7:100932600-100932800	Enhancers	HepG2	liver
46	chr7:100932600-100933000	Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr7:100932800-100933600	Enhancers	GM12878-XiMat	blood
48	chr7:100932800-100933800	Flanking Active TSS	HepG2	liver
49	chr7:100932800-100934000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr7:100932800-100934200	Enhancers	H9 Cell Line	embryonic stem cell

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