Variant report

Variant	nsv876968
Chromosome Location	chr3:75361506-75437889
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:346)
CpG islands
(count:796)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:75390901-75391145	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr3:75411520-75411813	GM12878	blood:	n/a	n/a
3	BATF	chr3:75411604-75411874	GM12878	blood:	n/a	n/a
4	BATF	chr3:75386395-75386620	GM12878	blood:	n/a	n/a
5	BCL3	chr3:75417319-75417660	GM12878	blood:	n/a	n/a
6	BCL3	chr3:75429024-75429912	GM12878	blood:	n/a	n/a
7	BCL3	chr3:75407756-75407999	GM12878	blood:	n/a	n/a
8	BCL3	chr3:75395680-75395995	GM12878	blood:	n/a	n/a
9	BCL3	chr3:75417298-75417641	GM12878	blood:	n/a	n/a
10	BCL3	chr3:75416737-75417040	GM12878	blood:	n/a	n/a
11	BCL3	chr3:75428941-75429895	GM12878	blood:	n/a	n/a
12	BHLHE40	chr3:75429659-75429896	K562	blood:	n/a	n/a
13	CTCF	chr3:75390996-75391155	Fibrobl	skin:	n/a	n/a
14	CTCF	chr3:75411628-75411813	GM10248	blood:	n/a	n/a
15	CTCF	chr3:75391060-75391210	AG10803	skin:	n/a	n/a
16	CTCF	chr3:75411700-75411850	NHEK	skin:	n/a	n/a
17	CTCF	chr3:75390960-75391110	WERI-Rb-1	eye:	n/a	n/a
18	CTCF	chr3:75372463-75372558	Gliobla	brain:	n/a	n/a
19	CTCF	chr3:75390960-75391110	HEK293	kidney:	n/a	n/a
20	CTCF	chr3:75390970-75391178	MCF-7	breast:	n/a	n/a
21	CTCF	chr3:75411533-75411871	K562	blood:	n/a	n/a
22	CTCF	chr3:75367864-75367906	GM10248	blood:	n/a	n/a
23	CTCF	chr3:75408562-75408653	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr3:75430538-75430581	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr3:75411589-75411810	K562	blood:	n/a	n/a
26	CTCF	chr3:75411615-75411799	GM13977	blood:	n/a	n/a
27	CTCF	chr3:75411676-75411801	Spleen_OC	spleen:	n/a	n/a
28	CTCF	chr3:75391139-75391181	Lung_OC	lung:	n/a	n/a
29	CTCF	chr3:75411759-75411823	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chr3:75411597-75411820	GM19238	blood:	n/a	n/a
31	CTCF	chr3:75411580-75411790	GM12870	blood:	n/a	n/a
32	CTCF	chr3:75392448-75392477	GM13976	blood:	n/a	n/a
33	CTCF	chr3:75379784-75379903	HepG2	liver:	n/a	n/a
34	CTCF	chr3:75379719-75379937	Gliobla	brain:	n/a	n/a
35	CTCF	chr3:75411704-75411825	GM13976	blood:	n/a	n/a
36	CTCF	chr3:75411740-75411890	HFF	foreskin:	n/a	n/a
37	CTCF	chr3:75411640-75411790	GM12866	blood:	n/a	n/a
38	CTCF	chr3:75379735-75379916	GM12878	blood:	n/a	n/a
39	CTCF	chr3:75379710-75379923	A549	lung:	n/a	n/a
40	CTCF	chr3:75391033-75391109	NHEK	skin:	n/a	n/a
41	CTCF	chr3:75380108-75380114	GM12891	blood:	n/a	n/a
42	CTCF	chr3:75390946-75391197	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:75411620-75411770	GM12865	blood:	n/a	n/a
44	CTCF	chr3:75380073-75380152	GM12892	blood:	n/a	n/a
45	CTCF	chr3:75392436-75392447	GM13976	blood:	n/a	n/a
46	CTCF	chr3:75372419-75372592	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr3:75391060-75391210	Caco-2	colon:	n/a	n/a
48	CTCF	chr3:75379712-75379893	GM19239	blood:	n/a	n/a
49	CTCF	chr3:75379776-75379914	GM12892	blood:	n/a	n/a
50	CTCF	chr3:75390980-75391130	AG09309	skin:	n/a	n/a

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75412866-75412916	A549	lung:	n/a
2	chr3:75412866-75412916	HRCEpiC	kidney:	n/a
3	chr3:75415591-75415641	NB4	blood:	n/a
4	chr3:75412866-75412916	A549	lung:	n/a
5	chr3:75412866-75412916	HRCEpiC	kidney:	n/a
6	chr3:75415591-75415641	NB4	blood:	n/a
7	chr3:75415561-75415611	HCPEpiC	choroid plexus:	n/a
8	chr3:75414486-75414536	T-47D	breast:	n/a
9	chr3:75415561-75415611	GM19239	blood:	n/a
10	chr3:75413083-75413133	T-47D	breast:	n/a
11	chr3:75410747-75410797	MCF-7	breast:	n/a
12	chr3:75416171-75416221	GM12891	blood:	n/a
13	chr3:75415591-75415641	HCPEpiC	choroid plexus:	n/a
14	chr3:75411217-75411267	AG09309	skin:	n/a
15	chr3:75410747-75410797	PrEC	prostate:	n/a
16	chr3:75416171-75416221	AG09319	gingival:	n/a
17	chr3:75413083-75413133	HCPEpiC	choroid plexus:	n/a
18	chr3:75411217-75411267	GM12878	blood:	n/a
19	chr3:75414693-75414743	HRPEpiC	eye:	n/a
20	chr3:75412866-75412916	Caco-2	colon:	n/a
21	chr3:75414693-75414743	HCF	heart:	n/a
22	chr3:75415561-75415611	PFSK-1	brain:	n/a
23	chr3:75414486-75414536	ovcar-3	ovarian:	n/a
24	chr3:75414693-75414743	H1-hESC	embryonic stem cell:	embryo
25	chr3:75413083-75413133	AoSMC	blood vessel:	n/a
26	chr3:75412866-75412916	HCPEpiC	choroid plexus:	n/a
27	chr3:75411217-75411267	H1-hESC	embryonic stem cell:	embryo
28	chr3:75411217-75411267	HRE	kidney:	n/a
29	chr3:75410747-75410797	HIPEpiC	eye:	n/a
30	chr3:75414693-75414743	NHBE	bronchial:	n/a
31	chr3:75414693-75414743	Hepatocyte	liver:	n/a
32	chr3:75414486-75414536	SKMC	muscle:	n/a
33	chr3:75416171-75416221	Hela-S3	cervix:	n/a
34	chr3:75414693-75414743	PrEC	prostate:	n/a
35	chr3:75415561-75415611	AoSMC	blood vessel:	n/a
36	chr3:75414486-75414536	Hepatocyte	liver:	n/a
37	chr3:75411217-75411267	AoSMC	blood vessel:	n/a
38	chr3:75416171-75416221	AG09309	skin:	n/a
39	chr3:75414693-75414743	AG09309	skin:	n/a
40	chr3:75410747-75410797	AG10803	skin:	n/a
41	chr3:75411421-75411471	U87	brain:	n/a
42	chr3:75411421-75411471	BJ	skin:	n/a
43	chr3:75411421-75411471	GM12892	blood:	n/a
44	chr3:75415526-75415576	SK-N-MC	brain:	n/a
45	chr3:75415591-75415641	HRE	kidney:	n/a
46	chr3:75414486-75414536	NHBE	bronchial:	n/a
47	chr3:75410789-75410839	NHBE	bronchial:	n/a
48	chr3:75411038-75411088	AoSMC	blood vessel:	n/a
49	chr3:75410747-75410797	AG04450	lung:	fetal
50	chr3:75410747-75410797	HPAEpiC	pulmonary alveolar:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:75390707..75391392-chr3:75471007..75471537,3	MCF-7	breast:
2	chr3:75343455..75344253-chr3:75389889..75390567,2	MCF-7	breast:

No data

Variant related genes	Relation type
OR7E66P	TF binding region
MYLKP1	TF binding region
ENSG00000266685	TF binding region
OR7E55P	TF binding region
OR7E22P	TF binding region
ENSG00000263782	TF binding region
OR7E66P	CpG island
MYLKP1	CpG island
ENSG00000266685	CpG island
OR7E55P	CpG island
OR7E22P	CpG island
ENSG00000263782	CpG island

Extended variants
information (count: 2941 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2941 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2007444	chr3:75361506-75361507	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371286908	chr3:75361541-75361542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs575685337	chr3:75361542-75361543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543060745	chr3:75361552-75361553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558121742	chr3:75361615-75361616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375040723	chr3:75361622-75361623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541298141	chr3:75361641-75361642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559360390	chr3:75361643-75361644	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529918058	chr3:75361673-75361674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542007511	chr3:75361675-75361676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561374689	chr3:75361701-75361702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148209211	chr3:75361724-75361725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550230565	chr3:75361757-75361758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190843191	chr3:75361776-75361777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532372738	chr3:75361796-75361797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568449125	chr3:75361804-75361805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182368957	chr3:75361811-75361812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112599551	chr3:75361837-75361838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566200732	chr3:75361921-75361922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536450301	chr3:75361925-75361926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs367867301	chr3:75361926-75361927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs57324358	chr3:75361934-75361935	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs569452771	chr3:75361945-75361946	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536733849	chr3:75361968-75361969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186658312	chr3:75361972-75361973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372377165	chr3:75361978-75361979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576795446	chr3:75361989-75361990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534290640	chr3:75361998-75361999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192666369	chr3:75362017-75362018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536840217	chr3:75362030-75362031	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574600630	chr3:75362038-75362039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183119577	chr3:75362042-75362043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76230673	chr3:75362053-75362054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576635860	chr3:75362057-75362058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543953000	chr3:75362058-75362059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188254128	chr3:75362078-75362079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150718421	chr3:75362100-75362101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547427507	chr3:75362129-75362130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192985921	chr3:75362144-75362145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530319849	chr3:75362160-75362161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547835906	chr3:75362212-75362213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570814561	chr3:75362214-75362215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548409207	chr3:75362216-75362217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184205234	chr3:75362325-75362326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537221099	chr3:75362341-75362342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139061286	chr3:75362367-75362368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570413134	chr3:75362390-75362391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534616538	chr3:75362445-75362446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs11926609	chr3:75362456-75362457	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs535722990	chr3:75362496-75362497	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75359000-75374600	Weak transcription	Pancreas	Pancrea
2	chr3:75361600-75362200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr3:75361600-75362800	Enhancers	Primary hematopoietic stem cells	blood
4	chr3:75362800-75369800	Weak transcription	Primary hematopoietic stem cells	blood
5	chr3:75366000-75369800	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr3:75368800-75370200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr3:75369000-75370400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr3:75369200-75370000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr3:75369800-75370000	Enhancers	Primary hematopoietic stem cells	blood
10	chr3:75369800-75370600	Enhancers	H1 Cell Line	embryonic stem cell
11	chr3:75369800-75370600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr3:75369800-75373400	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr3:75370000-75370400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr3:75370000-75370600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr3:75370200-75370600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr3:75370200-75370800	Enhancers	H9 Cell Line	embryonic stem cell
17	chr3:75370200-75371400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr3:75370400-75372000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr3:75370600-75377200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr3:75370800-75373200	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr3:75371400-75371600	Enhancers	Right Atrium	heart
22	chr3:75371400-75372200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr3:75371400-75372200	Enhancers	Fetal Muscle Leg	muscle
24	chr3:75371600-75374600	Weak transcription	Right Atrium	heart
25	chr3:75372000-75372200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr3:75372200-75373600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr3:75373200-75373400	Enhancers	H9 Cell Line	embryonic stem cell
28	chr3:75373400-75374400	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr3:75373600-75373800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr3:75374600-75375000	Enhancers	Pancreas	Pancrea
31	chr3:75374600-75375000	Enhancers	Right Atrium	heart
32	chr3:75374600-75377600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:75374800-75375000	Enhancers	Gastric	stomach
34	chr3:75375000-75376000	Weak transcription	Pancreas	Pancrea
35	chr3:75375000-75382400	Weak transcription	Gastric	stomach
36	chr3:75375800-75376400	Enhancers	Fetal Stomach	stomach
37	chr3:75376000-75376200	Enhancers	Pancreas	Pancrea
38	chr3:75376000-75382800	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr3:75376200-75378200	Active TSS	Pancreas	Pancrea
40	chr3:75376400-75376800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr3:75376600-75376800	Enhancers	Right Atrium	heart
42	chr3:75376600-75377600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr3:75376600-75379400	Enhancers	Fetal Lung	lung
44	chr3:75376800-75377200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr3:75376800-75381600	Weak transcription	Right Atrium	heart
46	chr3:75377000-75377400	Enhancers	H1 Cell Line	embryonic stem cell
47	chr3:75377200-75377400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr3:75377200-75377600	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr3:75377200-75377800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr3:75377400-75377600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland

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