Variant report

Variant	nsv874340
Chromosome Location	chr2:77730014-77786509
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	BACH1	chr2:77750117-77750320	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr2:77740493-77740504	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr2:77735678-77735954	K562	blood:	n/a	chr2:77735834-77735845 chr2:77735832-77735849
4	CEBPB	chr2:77777482-77777812	HepG2	liver:	n/a	chr2:77777649-77777660
5	CEBPB	chr2:77733675-77734144	HepG2	liver:	n/a	chr2:77734044-77734055 chr2:77734043-77734054 chr2:77734043-77734056
6	CEBPB	chr2:77747356-77747682	IMR90	lung:	n/a	chr2:77747442-77747453 chr2:77747510-77747523 chr2:77747573-77747581 chr2:77747510-77747523
7	CEBPB	chr2:77749105-77749135	HepG2	liver:	n/a	chr2:77749110-77749119
8	CEBPB	chr2:77777488-77777779	A549	lung:	n/a	chr2:77777649-77777660
9	CEBPB	chr2:77740319-77740722	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr2:77735678-77735907	A549	lung:	n/a	chr2:77735834-77735845 chr2:77735832-77735849
11	CEBPB	chr2:77735714-77735914	H1-hESC	embryonic stem cell:	n/a	chr2:77735834-77735845 chr2:77735832-77735849
12	CEBPB	chr2:77750079-77750314	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr2:77748991-77749319	H1-hESC	embryonic stem cell:	n/a	chr2:77749110-77749119
14	CEBPB	chr2:77735694-77735970	HepG2	liver:	n/a	chr2:77735834-77735845 chr2:77735832-77735849
15	CHD1	chr2:77749631-77750561	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr2:77762060-77762210	HRE	kidney:	n/a	chr2:77762078-77762087
17	CTCF	chr2:77749420-77749570	SK-N-SH_RA	brain:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
18	CTCF	chr2:77749500-77749650	RPTEC	kidney:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
19	CTCF	chr2:77749433-77749604	MCF-7	breast:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
20	CTCF	chr2:77762000-77762150	RPTEC	kidney:	n/a	chr2:77762078-77762087
21	CTCF	chr2:77762020-77762170	HBMEC	blood vessel:	n/a	chr2:77762078-77762087
22	CTCF	chr2:77749420-77749570	WERI-Rb-1	eye:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
23	CTCF	chr2:77749324-77749650	MCF-7	breast:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
24	CTCF	chr2:77749422-77749583	Gliobla	brain:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
25	CTCF	chr2:77761940-77762090	Caco-2	colon:	n/a	chr2:77762078-77762087
26	CTCF	chr2:77777739-77777771	GM10266	blood:	n/a	n/a
27	CTCF	chr2:77749460-77749610	HRPEpiC	eye:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
28	CTCF	chr2:77742885-77742896	LNCaP	prostate:	n/a	n/a
29	CTCF	chr2:77749495-77749530	GM13977	blood:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
30	CTCF	chr2:77762061-77762113	HepG2	liver:	n/a	chr2:77762078-77762087
31	CTCF	chr2:77749472-77749582	MCF-7	breast:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
32	CTCF	chr2:77749360-77749510	HAc	cerebellar:	n/a	n/a
33	CTCF	chr2:77786130-77786161	GM10248	blood:	n/a	n/a
34	CTCF	chr2:77762041-77762099	H1-hESC	embryonic stem cell:	n/a	chr2:77762078-77762087
35	CTCF	chr2:77749415-77749559	SK-N-SH_RA	brain:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
36	CTCF	chr2:77749420-77749570	HBMEC	blood vessel:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
37	CTCF	chr2:77749400-77749550	Hela-S3	cervix:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
38	CTCF	chr2:77749340-77749490	BE2_C	brain:	n/a	n/a
39	CTCF	chr2:77749420-77749570	BE2_C	brain:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
40	CTCF	chr2:77749420-77749570	HepG2	liver:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
41	CTCF	chr2:77749580-77749730	HAc	cerebellar:	n/a	n/a
42	CTCF	chr2:77749368-77749683	GM12878	blood:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
43	CTCF	chr2:77762000-77762150	HRE	kidney:	n/a	chr2:77762078-77762087
44	CTCF	chr2:77749435-77749590	HepG2	liver:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
45	CTCF	chr2:77749388-77749636	LNCaP	prostate:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
46	CTCF	chr2:77749460-77749610	HAc	cerebellar:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
47	CTCF	chr2:77749440-77749590	RPTEC	kidney:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
48	CTCF	chr2:77749415-77749605	MCF-7	breast:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
49	CTCF	chr2:77749134-77749822	SK-N-SH	brain:	n/a	chr2:77749505-77749518 chr2:77749503-77749521
50	CTCF	chr2:77749387-77749630	Medullo	brain:	n/a	chr2:77749505-77749518 chr2:77749503-77749521

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:77748917-77748967	K562	blood:	n/a
2	chr2:77748917-77748967	K562	blood:	n/a
3	chr2:77750866-77750916	AG09319	gingival:	n/a
4	chr2:77750866-77750916	Hepatocyte	liver:	n/a
5	chr2:77747049-77747099	HRCEpiC	kidney:	n/a
6	chr2:77748917-77748967	H1-hESC	embryonic stem cell:	embryo
7	chr2:77750866-77750916	NHDF-neo	bronchial:	n/a
8	chr2:77748917-77748967	PANC-1	pancreas:	n/a
9	chr2:77748917-77748967	NH-A	brain:	n/a
10	chr2:77748917-77748967	AG09309	skin:	n/a
11	chr2:77750866-77750916	HRE	kidney:	n/a
12	chr2:77747049-77747099	GM12892	blood:	n/a
13	chr2:77747049-77747099	GM19239	blood:	n/a
14	chr2:77750866-77750916	NH-A	brain:	n/a
15	chr2:77750866-77750916	CMK	blood:	n/a
16	chr2:77750866-77750916	HNPCEpiC	eye:	n/a
17	chr2:77747049-77747099	IMR90	lung:	fetal
18	chr2:77747049-77747099	ProgFib	skin:	n/a
19	chr2:77750866-77750916	GM12892	blood:	n/a
20	chr2:77748917-77748967	NB4	blood:	n/a
21	chr2:77748917-77748967	HepG2	liver:	n/a
22	chr2:77747049-77747099	CMK	blood:	n/a
23	chr2:77750866-77750916	HEEpiC	esophagus:	n/a
24	chr2:77747049-77747099	AG04450	lung:	fetal
25	chr2:77747049-77747099	GM12878	blood:	n/a
26	chr2:77750866-77750916	HMEC	breast:	n/a
27	chr2:77748917-77748967	HCM	heart:	n/a
28	chr2:77750866-77750916	SKMC	muscle:	n/a
29	chr2:77747049-77747099	HUVEC	blood vessel:	n/a
30	chr2:77748917-77748967	IMR90	lung:	fetal
31	chr2:77750866-77750916	HCPEpiC	choroid plexus:	n/a
32	chr2:77747049-77747099	LNCaP	prostate:	n/a
33	chr2:77748917-77748967	SK-N-SH	brain:	n/a
34	chr2:77747049-77747099	ECC-1	luminal epithelium:	n/a
35	chr2:77748917-77748967	GM19239	blood:	n/a
36	chr2:77750866-77750916	H1-hESC	embryonic stem cell:	embryo
37	chr2:77748917-77748967	U87	brain:	n/a
38	chr2:77747049-77747099	AoSMC	blood vessel:	n/a
39	chr2:77747049-77747099	HCPEpiC	choroid plexus:	n/a
40	chr2:77747049-77747099	BE2_C	brain:	n/a
41	chr2:77748917-77748967	HCT-116	colon:	n/a
42	chr2:77750866-77750916	AG09309	skin:	n/a
43	chr2:77748917-77748967	Jurkat	blood:	n/a
44	chr2:77750866-77750916	MCF10A-Er-Src	breast:	n/a
45	chr2:77750866-77750916	RPTEC	kidney:	n/a
46	chr2:77748917-77748967	MCF10A-Er-Src	breast:	n/a
47	chr2:77748917-77748967	PFSK-1	brain:	n/a
48	chr2:77750866-77750916	AG10803	skin:	n/a
49	chr2:77747049-77747099	NHDF-neo	bronchial:	n/a
50	chr2:77750866-77750916	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:77747263..77749621-chr20:52208634..52211022,2	MCF-7	breast:
2	chr2:77726699..77728852-chr2:77733118..77735865,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REG3G-11	chr2:77752849-77752903	NONHSAT071828
2	lnc-REG1B-8	chr2:77733047-77733243	NONHSAT071827
3	lnc-REG3G-11	chr2:77753685-77754426	NONHSAT071828
4	lnc-REG1B-8	chr2:77735216-77735302	NONHSAT071827

Variant related genes	Relation type
LRRTM4	TF binding region
LRRTM4	CpG island
ENSG00000171940	chromatin interactions

Extended variants
information (count: 1726 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1726 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2204916	chr2:77730014-77730015	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs542824803	chr2:77730051-77730052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs367757763	chr2:77730054-77730055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs201267293	chr2:77730079-77730080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs140168011	chr2:77730080-77730081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562642658	chr2:77730107-77730108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143605410	chr2:77730111-77730112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs112405824	chr2:77730128-77730129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs186490482	chr2:77730189-77730190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1344257	chr2:77730225-77730226	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs62159463	chr2:77730243-77730244	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs55847661	chr2:77730247-77730248	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs536374990	chr2:77730278-77730279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368979145	chr2:77730288-77730289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs1344256	chr2:77730308-77730309	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs569875495	chr2:77730336-77730337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541124751	chr2:77730337-77730338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs570671322	chr2:77730360-77730361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368180534	chr2:77730361-77730362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539226874	chr2:77730421-77730422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148059623	chr2:77730441-77730442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs572741670	chr2:77730508-77730509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530907811	chr2:77730534-77730535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533541703	chr2:77730539-77730540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs1344255	chr2:77730541-77730542	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs370551881	chr2:77730547-77730548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573703331	chr2:77730548-77730549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189737051	chr2:77730569-77730570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs376606203	chr2:77730574-77730575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182683643	chr2:77730684-77730685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35286009	chr2:77730722-77730723	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs188198446	chr2:77730725-77730726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192785027	chr2:77730728-77730729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs13418152	chr2:77730773-77730774	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs141755848	chr2:77730778-77730779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs560912984	chr2:77730790-77730791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34827946	chr2:77730823-77730824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147189317	chr2:77730824-77730825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569862889	chr2:77730825-77730826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538850917	chr2:77730865-77730866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10198058	chr2:77730954-77730955	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs74338442	chr2:77730988-77730989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535299769	chr2:77730994-77730995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6761838	chr2:77730997-77730998	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs573637726	chr2:77731032-77731033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373587170	chr2:77731057-77731058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556287912	chr2:77731123-77731124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368386961	chr2:77731128-77731129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567118234	chr2:77731136-77731137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544859559	chr2:77731154-77731155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:77729800-77730200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:77729800-77730400	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr2:77729800-77730400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr2:77729800-77730400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr2:77729800-77730400	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr2:77729800-77730600	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr2:77729800-77730800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr2:77730000-77730400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:77730400-77739200	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr2:77730400-77739400	Weak transcription	Fetal Brain Male	brain
11	chr2:77730400-77740200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr2:77730800-77737000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr2:77734800-77735000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr2:77734800-77735200	Enhancers	H1 Cell Line	embryonic stem cell
15	chr2:77735000-77739000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr2:77735200-77740200	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr2:77737000-77737600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr2:77737600-77739000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr2:77738200-77738400	Enhancers	Fetal Brain Female	brain
20	chr2:77738400-77739200	Weak transcription	Fetal Brain Female	brain
21	chr2:77739000-77740600	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr2:77739000-77740600	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr2:77739200-77739800	Enhancers	Fetal Brain Female	brain
24	chr2:77739200-77740200	Enhancers	Brain Hippocampus Middle	brain
25	chr2:77739200-77740400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr2:77739200-77740400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr2:77739200-77740600	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr2:77739400-77740600	Enhancers	Fetal Brain Male	brain
29	chr2:77739400-77741000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr2:77739600-77739800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr2:77739600-77740200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr2:77739800-77740000	Flanking Active TSS	Fetal Brain Female	brain
33	chr2:77739800-77740200	Active TSS	Brain Anterior Caudate	brain
34	chr2:77739800-77740600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr2:77739800-77741000	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr2:77740000-77740600	Active TSS	Fetal Brain Female	brain
37	chr2:77740200-77740400	Flanking Active TSS	Brain Anterior Caudate	brain
38	chr2:77740200-77740600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr2:77740200-77740600	Active TSS	Brain Inferior Temporal Lobe	brain
40	chr2:77740200-77741000	Enhancers	H1 Cell Line	embryonic stem cell
41	chr2:77740200-77741000	Enhancers	H9 Cell Line	embryonic stem cell
42	chr2:77740200-77741000	Enhancers	NH-A	brain
43	chr2:77740200-77745400	Weak transcription	Brain Hippocampus Middle	brain
44	chr2:77740200-77746000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr2:77740400-77740600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:77740400-77740600	Active TSS	Brain Anterior Caudate	brain
47	chr2:77740400-77744800	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr2:77740400-77746200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr2:77740600-77741000	Enhancers	Brain Anterior Caudate	brain
50	chr2:77740600-77741000	Enhancers	Brain Inferior Temporal Lobe	brain

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