Variant report

Variant	nsv523778
Chromosome Location	chr13:51755107-51768501
allele	n/a
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	ATF2	chr13:51753991-51755386	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr13:51755659-51756181	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr13:51752086-51755611	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr13:51754582-51755193	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr13:51755730-51756763	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr13:51751341-51755520	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr13:51757891-51758080	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr13:51759197-51759202	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr13:51762317-51762465	H1-hESC	embryonic stem cell:	n/a	n/a
10	E2F4	chr13:51760537-51760737	MCF10A-Er-Src	breast:	n/a	n/a
11	EP300	chr13:51765007-51765292	SK-N-SH_RA	brain:	n/a	n/a
12	EP300	chr13:51764953-51765300	SK-N-SH_RA	brain:	n/a	n/a
13	FOS	chr13:51766596-51766791	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr13:51766541-51766709	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr13:51766408-51766866	HUVEC	blood vessel:	n/a	n/a
16	FOS	chr13:51766594-51766740	MCF10A-Er-Src	breast:	n/a	n/a
17	GABPA	chr13:51765751-51766401	HL-60	blood:	n/a	n/a
18	GABPA	chr13:51765879-51766079	K562	blood:	n/a	n/a
19	GABPA	chr13:51765843-51766366	HL-60	blood:	n/a	n/a
20	GABPA	chr13:51765892-51766147	K562	blood:	n/a	n/a
21	GATA2	chr13:51766970-51767452	SH-SY5Y	brain:	n/a	n/a
22	GATA2	chr13:51764990-51765651	SH-SY5Y	brain:	n/a	chr13:51765222-51765232 chr13:51765221-51765233 chr13:51765559-51765569 chr13:51765221-51765234 chr13:51765223-51765230 chr13:51765223-51765232 chr13:51765445-51765455
23	GATA3	chr13:51767048-51767629	SH-SY5Y	brain:	n/a	chr13:51767559-51767566 chr13:51767559-51767566 chr13:51767505-51767512 chr13:51767559-51767569 chr13:51767557-51767566 chr13:51767559-51767566 chr13:51767552-51767573 chr13:51767499-51767511
24	GATA3	chr13:51764739-51765263	SH-SY5Y	brain:	n/a	chr13:51765222-51765232 chr13:51765221-51765233 chr13:51765221-51765234 chr13:51765223-51765230 chr13:51765223-51765232
25	GTF2F1	chr13:51765379-51765384	H1-hESC	embryonic stem cell:	n/a	n/a
26	GTF2F1	chr13:51765837-51765976	H1-hESC	embryonic stem cell:	n/a	n/a
27	GTF2F1	chr13:51763578-51763600	H1-hESC	embryonic stem cell:	n/a	n/a
28	GTF2F1	chr13:51754210-51755509	H1-hESC	embryonic stem cell:	n/a	n/a
29	GTF2F1	chr13:51755749-51756601	H1-hESC	embryonic stem cell:	n/a	n/a
30	JUN	chr13:51758052-51758077	H1-hESC	embryonic stem cell:	n/a	n/a
31	JUND	chr13:51754376-51755246	H1-hESC	embryonic stem cell:	n/a	chr13:51754478-51754488 chr13:51754479-51754486 chr13:51754478-51754488 chr13:51754477-51754489 chr13:51754479-51754487 chr13:51754479-51754487 chr13:51754478-51754488
32	JUND	chr13:51755108-51755355	H1-hESC	embryonic stem cell:	n/a	chr13:51755316-51755323
33	MAFF	chr13:51767584-51767886	HepG2	liver:	n/a	n/a
34	MAFF	chr13:51767581-51767795	K562	blood:	n/a	n/a
35	MAFK	chr13:51767575-51767873	IMR90	lung:	n/a	n/a
36	MAFK	chr13:51756828-51757060	H1-hESC	embryonic stem cell:	n/a	n/a
37	MAFK	chr13:51756711-51756821	HepG2	liver:	n/a	n/a
38	MAFK	chr13:51757943-51758004	H1-hESC	embryonic stem cell:	n/a	n/a
39	MAFK	chr13:51759380-51759580	H1-hESC	embryonic stem cell:	n/a	n/a
40	MAFK	chr13:51767543-51767886	HepG2	liver:	n/a	n/a
41	MAFK	chr13:51767568-51767871	HepG2	liver:	n/a	n/a
42	MAFK	chr13:51767550-51767735	K562	blood:	n/a	n/a
43	MAFK	chr13:51767575-51767879	H1-hESC	embryonic stem cell:	n/a	n/a
44	MYC	chr13:51760179-51760226	MCF10A-Er-Src	breast:	n/a	n/a
45	MYC	chr13:51754930-51755203	H1-hESC	embryonic stem cell:	n/a	n/a
46	NRF1	chr13:51755657-51755969	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr13:51755070-51755338	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr13:51762222-51762420	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr13:51755659-51756787	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr13:51762315-51762532	H1-hESC	embryonic stem cell:	n/a	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-INTS6-6	chr13:51762034-51762628	NONHSAT033889
2	lnc-INTS6-2	chr13:51764578-51765109	XLOC_010616
3	lnc-FAM124A-2	chr13:51754413-51755574	NONHSAT033887
4	lnc-FAM124A-2	chr13:51761389-51762080	NONHSAT033887
5	lnc-INTS6-6	chr13:51764015-51764080	NONHSAT033889
6	lnc-INTS6-2	chr13:51765817-51766020	XLOC_010616

Variant related genes	Relation type
SLMO2P2	TF binding region

Extended variants
information (count: 496 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17252034	chr13:51755107-51755108	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541497965	chr13:51755144-51755145	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs75476728	chr13:51755145-51755146	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs9535610	chr13:51755159-51755160	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs563922657	chr13:51755162-51755163	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs73488064	chr13:51755170-51755171	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs552837137	chr13:51755208-51755209	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs73488066	chr13:51755213-51755214	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs148160665	chr13:51755258-51755259	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs547083842	chr13:51755274-51755275	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs371188980	chr13:51755280-51755281	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs188958180	chr13:51755306-51755307	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs141986841	chr13:51755309-51755310	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs9535611	chr13:51755319-51755320	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs1361470	chr13:51755329-51755330	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs374085964	chr13:51755348-51755349	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs575940887	chr13:51755409-51755410	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs116127445	chr13:51755412-51755413	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs371155613	chr13:51755425-51755426	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs181957588	chr13:51755432-51755433	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs558824111	chr13:51755456-51755457	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs59816449	chr13:51755479-51755480	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs34864319	chr13:51755496-51755497	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs570558338	chr13:51755547-51755548	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs535066525	chr13:51755550-51755551	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs35517354	chr13:51755597-51755598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555079311	chr13:51755614-51755615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111476880	chr13:51755626-51755627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201729362	chr13:51755666-51755667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574951150	chr13:51755669-51755670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs150696754	chr13:51755692-51755693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183853301	chr13:51755694-51755695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531084465	chr13:51755720-51755721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs139834109	chr13:51755743-51755744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143261533	chr13:51755744-51755745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147164338	chr13:51755776-51755777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559665106	chr13:51755792-51755793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs57546351	chr13:51755848-51755849	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs116152509	chr13:51755864-51755865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs527832542	chr13:51755872-51755873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs112197393	chr13:51755914-51755915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs139604930	chr13:51755915-51755916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529729082	chr13:51755920-51755921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373484792	chr13:51755941-51755942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs549852870	chr13:51756019-51756020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569713284	chr13:51756072-51756073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538868653	chr13:51756106-51756107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570774659	chr13:51756114-51756115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7334124	chr13:51756153-51756154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552498301	chr13:51756158-51756159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21990379	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51750000-51755200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:51750000-51763000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr13:51750200-51755200	Strong transcription	HUES6 Cell Line	embryonic stem cell
4	chr13:51750200-51767000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr13:51752600-51755200	Genic enhancers	HUES48 Cell Line	embryonic stem cell
6	chr13:51753000-51757600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr13:51753200-51755200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr13:51753200-51757800	Weak transcription	Right Atrium	heart
9	chr13:51754000-51766000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr13:51754600-51770000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr13:51754800-51755200	Enhancers	Fetal Lung	lung
12	chr13:51754800-51756200	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr13:51755000-51757200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr13:51755000-51757400	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr13:51755000-51757400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr13:51755000-51765600	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr13:51755200-51755600	Weak transcription	Fetal Lung	lung
18	chr13:51755200-51756200	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr13:51755200-51757600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr13:51755200-51760400	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr13:51755600-51757000	Enhancers	Fetal Lung	lung
22	chr13:51755800-51756600	Enhancers	Fetal Brain Male	brain
23	chr13:51756200-51756400	Genic enhancers	H9 Cell Line	embryonic stem cell
24	chr13:51756200-51756600	Genic enhancers	HUES6 Cell Line	embryonic stem cell
25	chr13:51756200-51756600	Enhancers	Fetal Brain Female	brain
26	chr13:51756400-51756600	Strong transcription	H9 Cell Line	embryonic stem cell
27	chr13:51756600-51757200	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr13:51756600-51763800	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr13:51757200-51759800	Strong transcription	HUES6 Cell Line	embryonic stem cell
30	chr13:51757200-51760400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
31	chr13:51757400-51759000	Strong transcription	H1 Cell Line	embryonic stem cell
32	chr13:51757400-51759800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
33	chr13:51757600-51758600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr13:51758600-51761000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr13:51759000-51767800	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr13:51759800-51761400	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr13:51759800-51761400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr13:51760400-51761400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr13:51760400-51761800	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr13:51761000-51762400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr13:51761400-51761800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
42	chr13:51761400-51761800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
43	chr13:51761400-51762600	Strong transcription	HUES6 Cell Line	embryonic stem cell
44	chr13:51761800-51763600	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr13:51761800-51764600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr13:51761800-51766200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr13:51762400-51765000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr13:51762600-51765000	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr13:51766000-51766200	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr13:51766000-51767200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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