Variant report

Variant	esv2757736
Chromosome Location	chr1:73613099-73775684
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:237)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:237 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr1:73649075-73649509	GM12878	blood:	n/a	chr1:73649321-73649332 chr1:73649293-73649304 chr1:73649265-73649276
2	CEBPB	chr1:73621875-73622188	K562	blood:	n/a	n/a
3	CEBPB	chr1:73618610-73618934	H1-hESC	embryonic stem cell:	n/a	chr1:73618778-73618789
4	CEBPB	chr1:73760044-73760362	HepG2	liver:	n/a	chr1:73760197-73760208
5	CEBPB	chr1:73621990-73622190	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr1:73672624-73672710	K562	blood:	n/a	n/a
7	CEBPB	chr1:73641068-73641268	HepG2	liver:	n/a	n/a
8	CEBPB	chr1:73643000-73643227	H1-hESC	embryonic stem cell:	n/a	chr1:73643106-73643117
9	CEBPB	chr1:73618648-73618936	A549	lung:	n/a	chr1:73618778-73618789
10	CEBPB	chr1:73618626-73618958	IMR90	lung:	n/a	chr1:73618778-73618789
11	CEBPB	chr1:73642956-73643192	HepG2	liver:	n/a	chr1:73643106-73643117
12	CEBPB	chr1:73686066-73686343	HepG2	liver:	n/a	chr1:73686199-73686212 chr1:73686201-73686210 chr1:73686200-73686211 chr1:73686199-73686210
13	CEBPB	chr1:73621888-73622181	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr1:73621882-73622201	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:73621845-73622196	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:73618647-73618856	HepG2	liver:	n/a	chr1:73618778-73618789
17	CEBPB	chr1:73647386-73647575	HepG2	liver:	n/a	n/a
18	CTCF	chr1:73671401-73671580	MCF-7	breast:	n/a	n/a
19	CTCF	chr1:73671580-73671730	RPTEC	kidney:	n/a	n/a
20	CTCF	chr1:73639740-73639890	HAc	cerebellar:	n/a	n/a
21	CTCF	chr1:73671360-73671510	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr1:73671380-73671530	GM12878	blood:	n/a	n/a
23	CTCF	chr1:73671460-73671610	GM12875	blood:	n/a	n/a
24	CTCF	chr1:73711680-73711830	GM12866	blood:	n/a	n/a
25	CTCF	chr1:73671440-73671590	HepG2	liver:	n/a	n/a
26	CTCF	chr1:73671420-73671570	GM12870	blood:	n/a	n/a
27	CTCF	chr1:73671423-73671536	LNCaP	prostate:	n/a	n/a
28	CTCF	chr1:73671428-73671503	MCF-7	breast:	n/a	n/a
29	CTCF	chr1:73670856-73670888	Fibrobl	skin:	n/a	n/a
30	CTCF	chr1:73671420-73671570	NHEK	skin:	n/a	n/a
31	CTCF	chr1:73671420-73671570	MCF-7	breast:	n/a	n/a
32	CTCF	chr1:73668921-73668931	ProgFib	skin:	n/a	n/a
33	CTCF	chr1:73671380-73671530	GM12866	blood:	n/a	n/a
34	CTCF	chr1:73687730-73687779	Lung_OC	lung:	n/a	n/a
35	CTCF	chr1:73671408-73671510	MCF-7	breast:	n/a	n/a
36	CTCF	chr1:73730377-73730445	GM13976	blood:	n/a	n/a
37	CTCF	chr1:73671420-73671570	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr1:73687129-73687179	GM10248	blood:	n/a	n/a
39	CTCF	chr1:73671400-73671550	GM12868	blood:	n/a	n/a
40	CTCF	chr1:73671309-73671671	GM12878	blood:	n/a	n/a
41	CTCF	chr1:73671440-73671590	HEK293	kidney:	n/a	n/a
42	CTCF	chr1:73671425-73671557	GM12878	blood:	n/a	n/a
43	CTCF	chr1:73671400-73671550	MCF-7	breast:	n/a	n/a
44	CTCF	chr1:73650000-73650150	HCM	heart:	n/a	n/a
45	CTCF	chr1:73671380-73671530	GM12865	blood:	n/a	n/a
46	CTCF	chr1:73671360-73671510	GM06990	blood:	n/a	n/a
47	CTCF	chr1:73671460-73671610	NB4	blood:	n/a	n/a
48	CTCF	chr1:73671401-73671584	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr1:73671420-73671570	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr1:73671400-73671550	GM12872	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr1:73623181..73625541-chr16:30564814..30567773,2	MCF-7	breast:
2	chr1:73719821..73721687-chr1:73728566..73730529,2	K562	blood:
3	chr1:73719821..73721687-chr1:73728566..73730529,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FPGT-3	chr1:73771821-73771980	XLOC_000256
2	lnc-FPGT-3	chr1:73772851-73773046	XLOC_000256
3	lnc-FPGT-3	chr1:73771922-73771957	XLOC_000256
4	lnc-FPGT-3	chr1:73771912-73771957	XLOC_000256
5	lnc-FPGT-3	chr1:73771821-73771980	XLOC_000256
6	lnc-FPGT-3	chr1:73771634-73771980	NONHSAT003934
7	lnc-FPGT-3	chr1:73771821-73771980	XLOC_000256
8	lnc-FPGT-3	chr1:73771917-73771957	XLOC_000256
9	lnc-FPGT-3	chr1:73771853-73771957	XLOC_000256
10	lnc-FPGT-3	chr1:73772850-73773255	NONHSAT003934
11	lnc-FPGT-3	chr1:73772899-73773046	XLOC_000256
12	lnc-FPGT-3	chr1:73772851-73773046	ENSG00000233973
13	lnc-FPGT-3	chr1:73771635-73771957	XLOC_000256
14	lnc-LRRIQ3-1	chr1:73657287-73657538	NONHSAT003933
15	lnc-FPGT-3	chr1:73771821-73771957	XLOC_000256
16	lnc-FPGT-3	chr1:73771853-73771957	ENSG00000233973
17	lnc-FPGT-3	chr1:73772851-73773255	XLOC_000256

No data

Variant related genes	Relation type
RN7SKP19	TF binding region
ENSG00000233973	TF binding region
CEP350	miRNA target sites

Extended variants
information (count: 1286 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1286 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35446706	chr1:73626418-73626419	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs35489458	chr1:73626421-73626422	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs183319829	chr1:73626423-73626424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs60439400	chr1:73626443-73626444	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs543343592	chr1:73626455-73626456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs71586995	chr1:73626498-73626499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs72175967	chr1:73626499-73626500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6672279	chr1:73626527-73626528	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs532156428	chr1:73626556-73626557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560209824	chr1:73626576-73626577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559040097	chr1:73626590-73626591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs532209279	chr1:73626621-73626622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs550532575	chr1:73626626-73626627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548212740	chr1:73626654-73626655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112404414	chr1:73626697-73626698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146633049	chr1:73626707-73626708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532401258	chr1:73626731-73626732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs6659790	chr1:73626753-73626754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs11210155	chr1:73626794-73626795	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs539250091	chr1:73626796-73626797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189224950	chr1:73626807-73626808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375371600	chr1:73626874-73626875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566183228	chr1:73626906-73626907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74091950	chr1:73626910-73626911	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs368940423	chr1:73626940-73626941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554989025	chr1:73626953-73626954	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372197212	chr1:73626976-73626977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11210156	chr1:73627002-73627003	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs11210157	chr1:73627058-73627059	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs552313419	chr1:73627081-73627082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545715252	chr1:73627110-73627111	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371409843	chr1:73627112-73627113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76336626	chr1:73627130-73627131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576693828	chr1:73627144-73627145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs72347272	chr1:73627164-73627165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545604854	chr1:73627165-73627166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375379968	chr1:73627167-73627168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35413294	chr1:73627224-73627225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11210159	chr1:73627225-73627226	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs373729121	chr1:73627338-73627339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537845451	chr1:73627363-73627364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541542334	chr1:73627376-73627377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561748912	chr1:73627437-73627438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs530444690	chr1:73627479-73627480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs371069832	chr1:73627555-73627556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550515540	chr1:73627583-73627584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563980340	chr1:73627587-73627588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556151614	chr1:73627636-73627637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532806740	chr1:73627646-73627647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192893710	chr1:73627744-73627745	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:73626400-73626600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr1:73626600-73627000	Enhancers	Ovary	ovary
3	chr1:73626600-73627800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:73626600-73628600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr1:73626800-73627400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr1:73627000-73627400	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr1:73627000-73627400	Weak transcription	Ovary	ovary
8	chr1:73627000-73627600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr1:73627400-73628400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr1:73627400-73628600	Enhancers	Ovary	ovary
11	chr1:73627600-73628600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr1:73628000-73629000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:73628400-73641800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr1:73635000-73635200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr1:73635200-73636600	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr1:73635400-73636000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr1:73636000-73636200	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr1:73636200-73642200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr1:73636600-73641600	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr1:73641600-73643000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr1:73641800-73642000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr1:73641800-73642800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr1:73642000-73642400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr1:73642200-73642400	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr1:73642200-73643000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr1:73642400-73642600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr1:73642400-73642800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
28	chr1:73642400-73642800	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr1:73642400-73643000	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr1:73642600-73651000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr1:73642800-73653600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr1:73651000-73651200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr1:73651200-73651400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr1:73651400-73652800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:73652800-73653400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr1:73653200-73653600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr1:73653200-73653600	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr1:73653200-73653800	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr1:73653400-73653800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr1:73653600-73653800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr1:73653800-73654000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr1:73664600-73665400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr1:73671000-73671200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr1:73693600-73694000	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr1:73693800-73694400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr1:73693800-73695200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr1:73745200-73745400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr1:73752800-73753000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr1:73766600-73766800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr1:73766800-73767000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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