Variant report

Variant	nsv527876
Chromosome Location	chr8:118012265-118037316
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	ATF1	chr8:118022516-118022716	K562	blood:	n/a	n/a
2	ATF1	chr8:118020845-118021044	K562	blood:	n/a	n/a
3	CEBPB	chr8:118013646-118013892	IMR90	lung:	n/a	chr8:118013765-118013776
4	CEBPB	chr8:118013692-118013912	HepG2	liver:	n/a	chr8:118013765-118013776
5	CEBPB	chr8:118013598-118013930	Hela-S3	cervix:	n/a	chr8:118013765-118013776
6	CEBPB	chr8:118031492-118031968	MCF-7	breast:	n/a	chr8:118031801-118031812 chr8:118031678-118031689 chr8:118031676-118031689 chr8:118031678-118031689
7	CEBPB	chr8:118013672-118013901	A549	lung:	n/a	chr8:118013765-118013776
8	CEBPB	chr8:118031649-118032296	IMR90	lung:	n/a	chr8:118031801-118031812 chr8:118031678-118031689 chr8:118031676-118031689 chr8:118031678-118031689
9	CEBPB	chr8:118032015-118032280	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr8:118031703-118031883	HepG2	liver:	n/a	chr8:118031801-118031812
11	CEBPB	chr8:118031604-118031804	K562	blood:	n/a	chr8:118031678-118031689 chr8:118031676-118031689 chr8:118031678-118031689
12	CEBPB	chr8:118031502-118032316	Hela-S3	cervix:	n/a	chr8:118031801-118031812 chr8:118031678-118031689 chr8:118031676-118031689 chr8:118031678-118031689
13	CTCF	chr8:118031600-118031750	HEK293	kidney:	n/a	chr8:118031705-118031721
14	CTCF	chr8:118031620-118031770	AG09319	gingival:	n/a	chr8:118031705-118031721
15	CTCF	chr8:118031660-118031810	HRPEpiC	eye:	n/a	chr8:118031705-118031721
16	CTCF	chr8:118031640-118031790	HPAF	blood vessel:	n/a	chr8:118031705-118031721
17	CTCF	chr8:118031540-118031690	HCM	heart:	n/a	n/a
18	CTCF	chr8:118031640-118031790	Hela-S3	cervix:	n/a	chr8:118031705-118031721
19	CTCF	chr8:118031600-118031750	HCM	heart:	n/a	chr8:118031705-118031721
20	CTCF	chr8:118031660-118031810	RPTEC	kidney:	n/a	chr8:118031705-118031721
21	CTCF	chr8:118031620-118031770	Hela-S3	cervix:	n/a	chr8:118031705-118031721
22	CTCF	chr8:118031580-118031730	HMEC	breast:	n/a	chr8:118031705-118031721
23	CTCF	chr8:118031596-118031890	GM12878	blood:	n/a	chr8:118031705-118031721
24	CTCF	chr8:118031620-118031770	Caco-2	colon:	n/a	chr8:118031705-118031721
25	CTCF	chr8:118031580-118031730	GM12873	blood:	n/a	chr8:118031705-118031721
26	CTCF	chr8:118031664-118031766	MCF-7	breast:	n/a	chr8:118031705-118031721
27	CTCF	chr8:118031690-118031750	K562	blood:	n/a	chr8:118031705-118031721
28	CTCF	chr8:118031640-118031790	AG10803	skin:	n/a	chr8:118031705-118031721
29	CTCF	chr8:118031618-118031809	Hela-S3	cervix:	n/a	chr8:118031705-118031721
30	CTCF	chr8:118031494-118031968	MCF-7	breast:	n/a	chr8:118031705-118031721
31	CTCF	chr8:118031560-118031710	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:118031712-118031788	LNCaP	prostate:	n/a	n/a
33	CTCF	chr8:118031620-118031770	NB4	blood:	n/a	chr8:118031705-118031721
34	CTCF	chr8:118031540-118031830	HFF	foreskin:	n/a	chr8:118031705-118031721
35	CTCF	chr8:118031661-118031761	GM12878	blood:	n/a	chr8:118031705-118031721
36	CTCF	chr8:118031560-118031710	HVMF	connective:	n/a	n/a
37	CTCF	chr8:118031620-118031770	MCF-7	breast:	n/a	chr8:118031705-118031721
38	CTCF	chr8:118031660-118031810	HFF-Myc	foreskin:	n/a	chr8:118031705-118031721
39	CTCF	chr8:118031631-118031786	MCF-7	breast:	n/a	chr8:118031705-118031721
40	CTCF	chr8:118031692-118031811	K562	blood:	n/a	chr8:118031705-118031721
41	CTCF	chr8:118031640-118031790	HMF	breast:	n/a	chr8:118031705-118031721
42	CTCF	chr8:118031740-118031890	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr8:118031666-118031763	Medullo	brain:	n/a	chr8:118031705-118031721
44	CTCF	chr8:118031600-118031750	GM12864	blood:	n/a	chr8:118031705-118031721
45	CTCF	chr8:118031520-118031670	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr8:118031560-118031710	HCT-116	colon:	n/a	n/a
47	CTCF	chr8:118031620-118031770	HCFaa	heart:	n/a	chr8:118031705-118031721
48	CTCF	chr8:118031580-118031730	BJ	skin:	n/a	chr8:118031705-118031721
49	CTCF	chr8:118031678-118031737	HUVEC	blood vessel:	n/a	chr8:118031705-118031721
50	CTCF	chr8:118030746-118030822	Fibrobl	skin:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:118020240..118022931-chr8:118026040..118028339,2	K562	blood:
2	chr8:117753207..117755356-chr8:118019404..118021027,2	K562	blood:
3	chr8:118020240..118022931-chr8:118026040..118028339,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf85-3	chr8:118030185-118030485	NONHSAT128387
2	lnc-C8orf85-5	chr8:118019230-118019352	NONHSAT128385
3	lnc-RAD21-2	chr8:118017080-118019878	ncRnaDb_ncrna_FR361237_1

Variant related genes	Relation type
RN7SL228P	TF binding region

Extended variants
information (count: 950 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:950 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2938864	chr8:118012265-118012266	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147568094	chr8:118012277-118012278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562093115	chr8:118012290-118012291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188375555	chr8:118012325-118012326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569281052	chr8:118012332-118012333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141987725	chr8:118012368-118012369	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78759527	chr8:118012376-118012377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs75762565	chr8:118012391-118012392	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571103539	chr8:118012392-118012393	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535048516	chr8:118012406-118012407	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547131612	chr8:118012408-118012409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143019639	chr8:118012434-118012435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148230939	chr8:118012457-118012458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140194999	chr8:118012503-118012504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150351032	chr8:118012518-118012519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192696143	chr8:118012528-118012529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112526168	chr8:118012629-118012630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571184284	chr8:118012699-118012700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs117823183	chr8:118012718-118012719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75687197	chr8:118012724-118012725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs76761717	chr8:118012725-118012726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577055277	chr8:118012768-118012769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201445782	chr8:118012783-118012784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540974839	chr8:118012799-118012800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372904362	chr8:118012823-118012824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559072415	chr8:118012831-118012832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183009474	chr8:118012876-118012877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73312273	chr8:118012894-118012895	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs375805096	chr8:118012901-118012902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs187621841	chr8:118012938-118012939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs137982137	chr8:118012978-118012979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs78478105	chr8:118013020-118013021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191322908	chr8:118013036-118013037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs142681972	chr8:118013038-118013039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575446011	chr8:118013166-118013167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547339877	chr8:118013188-118013189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545134799	chr8:118013211-118013212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540807292	chr8:118013216-118013217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184978457	chr8:118013235-118013236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536043705	chr8:118013290-118013291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551226631	chr8:118013295-118013296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189408251	chr8:118013328-118013329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143123266	chr8:118013421-118013422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs377267900	chr8:118013443-118013444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35945960	chr8:118013444-118013445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs34639384	chr8:118013464-118013465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs397893098	chr8:118013465-118013466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146023317	chr8:118013533-118013534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554732505	chr8:118013572-118013573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs539586789	chr8:118013621-118013622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:137)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	20164920	CNVD
Breast cancer	20932292	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	17268525	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	19204574	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Colorectal cancer	21645411	CNVD
T-cell lymphomas	22341440	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:118010400-118014400	Weak transcription	Fetal Heart	heart
2	chr8:118011400-118012600	Enhancers	Stomach Smooth Muscle	stomach
3	chr8:118011600-118012600	Enhancers	Fetal Stomach	stomach
4	chr8:118011600-118012800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr8:118011600-118012800	Enhancers	Colon Smooth Muscle	Colon
6	chr8:118012200-118014600	Enhancers	Rectal Smooth Muscle	rectum
7	chr8:118012800-118016600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr8:118014400-118015200	Enhancers	Fetal Heart	heart
9	chr8:118015200-118016400	Weak transcription	Fetal Heart	heart
10	chr8:118016400-118016800	Enhancers	Fetal Heart	heart
11	chr8:118016600-118017600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr8:118017600-118019800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr8:118019600-118020000	Enhancers	Fetal Intestine Large	intestine
14	chr8:118019800-118021000	Enhancers	Fetal Intestine Small	intestine
15	chr8:118019800-118021600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr8:118021600-118022600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr8:118022400-118023000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr8:118022400-118023200	Enhancers	Lung	lung
19	chr8:118022600-118023600	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr8:118022800-118023000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr8:118022800-118023200	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr8:118023000-118023600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr8:118023400-118023600	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr8:118023600-118031600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr8:118028600-118028800	Enhancers	HSMMtube	muscle
26	chr8:118029200-118031400	Weak transcription	HSMMtube	muscle
27	chr8:118029600-118029800	Enhancers	Fetal Lung	lung
28	chr8:118031400-118031600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr8:118031400-118032200	Enhancers	Hela-S3	cervix
30	chr8:118031400-118032400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr8:118031400-118032400	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr8:118031400-118032400	Enhancers	HSMMtube	muscle
33	chr8:118031600-118031800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr8:118031600-118031800	Enhancers	Fetal Heart	heart
35	chr8:118031600-118032000	Enhancers	Colon Smooth Muscle	Colon
36	chr8:118031600-118032200	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr8:118031600-118032400	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr8:118031600-118032400	Enhancers	H9 Cell Line	embryonic stem cell
39	chr8:118031600-118032400	Enhancers	Duodenum Smooth Muscle	Duodenum
40	chr8:118031800-118032000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr8:118031800-118032200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr8:118031800-118032200	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr8:118031800-118032200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr8:118031800-118032200	Flanking Active TSS	Fetal Heart	heart
45	chr8:118031800-118032200	Bivalent Enhancer	Fetal Lung	lung
46	chr8:118031800-118032400	Enhancers	H1 Cell Line	embryonic stem cell
47	chr8:118031800-118032400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr8:118031800-118032400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr8:118031800-118032400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr8:118031800-118032400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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