Variant report

Variant	nsv431013
Chromosome Location	chr2:50861049-50914485
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:199)
CpG islands
(count:244)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:199 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr2:50890728-50891191	HepG2	liver:	n/a	chr2:50890749-50890760 chr2:50891044-50891055
2	CTCF	chr2:50902120-50902270	GM12874	blood:	n/a	n/a
3	CTCF	chr2:50901960-50902110	RPTEC	kidney:	n/a	n/a
4	CTCF	chr2:50902200-50902350	HRPEpiC	eye:	n/a	n/a
5	CTCF	chr2:50889583-50889671	GM19238	blood:	n/a	n/a
6	CTCF	chr2:50902200-50902350	HCFaa	heart:	n/a	n/a
7	CTCF	chr2:50902200-50902350	HRE	kidney:	n/a	n/a
8	CTCF	chr2:50902128-50902354	IMR90	lung:	n/a	n/a
9	CTCF	chr2:50906100-50906250	GM12864	blood:	n/a	n/a
10	CTCF	chr2:50889589-50889673	MCF-7	breast:	n/a	n/a
11	CTCF	chr2:50902140-50902290	GM12871	blood:	n/a	n/a
12	CTCF	chr2:50902100-50902250	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr2:50902171-50902279	K562	blood:	n/a	n/a
14	CTCF	chr2:50902100-50902250	HMF	breast:	n/a	n/a
15	CTCF	chr2:50902140-50902290	HEK293	kidney:	n/a	n/a
16	CTCF	chr2:50889585-50889672	MCF-7	breast:	n/a	n/a
17	CTCF	chr2:50902001-50902362	HepG2	liver:	n/a	n/a
18	CTCF	chr2:50902106-50902258	A549	lung:	n/a	n/a
19	CTCF	chr2:50902140-50902290	NB4	blood:	n/a	n/a
20	CTCF	chr2:50902100-50902250	GM12874	blood:	n/a	n/a
21	CTCF	chr2:50902200-50902350	GM12869	blood:	n/a	n/a
22	CTCF	chr2:50902100-50902250	GM12864	blood:	n/a	n/a
23	CTCF	chr2:50902100-50902250	HFF-Myc	foreskin:	n/a	n/a
24	CTCF	chr2:50902120-50902270	K562	blood:	n/a	n/a
25	CTCF	chr2:50902180-50902330	HA-sp	spinal cord:	n/a	n/a
26	CTCF	chr2:50889625-50889634	Gliobla	brain:	n/a	n/a
27	CTCF	chr2:50902163-50902293	Gliobla	brain:	n/a	n/a
28	CTCF	chr2:50902320-50902470	A549	lung:	n/a	n/a
29	CTCF	chr2:50902076-50902365	GM12878	blood:	n/a	n/a
30	CTCF	chr2:50902119-50902292	GM19240	blood:	n/a	n/a
31	CTCF	chr2:50902120-50902270	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr2:50889610-50889663	GM12891	blood:	n/a	n/a
33	CTCF	chr2:50902220-50902370	A549	lung:	n/a	n/a
34	CTCF	chr2:50902140-50902290	GM06990	blood:	n/a	n/a
35	CTCF	chr2:50902100-50902250	SAEC	small airway:	n/a	n/a
36	CTCF	chr2:50902170-50902253	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:50902080-50902230	GM12875	blood:	n/a	n/a
38	CTCF	chr2:50902060-50902290	GM12864	blood:	n/a	n/a
39	CTCF	chr2:50902116-50902324	GM12892	blood:	n/a	n/a
40	CTCF	chr2:50902100-50902250	GM12870	blood:	n/a	n/a
41	CTCF	chr2:50902046-50902364	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr2:50902100-50902250	GM12873	blood:	n/a	n/a
43	CTCF	chr2:50902035-50902240	K562	blood:	n/a	n/a
44	CTCF	chr2:50902182-50902235	LNCaP	prostate:	n/a	n/a
45	CTCF	chr2:50889588-50889678	GM19239	blood:	n/a	n/a
46	CTCF	chr2:50902080-50902230	NHEK	skin:	n/a	n/a
47	CTCF	chr2:50902140-50902290	HMEC	breast:	n/a	n/a
48	CTCF	chr2:50902120-50902270	GM12866	blood:	n/a	n/a
49	CTCF	chr2:50889598-50889668	NHEK	skin:	n/a	n/a
50	CTCF	chr2:50902100-50902250	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50884693-50884743	HAEpiC	amniotic membrane:	n/a
2	chr2:50863603-50863653	GM19239	blood:	n/a
3	chr2:50876837-50876887	AG04450	lung:	fetal
4	chr2:50884693-50884743	RPTEC	kidney:	n/a
5	chr2:50884693-50884743	BJ	skin:	n/a
6	chr2:50876837-50876887	SAEC	small airway:	n/a
7	chr2:50863603-50863653	Caco-2	colon:	n/a
8	chr2:50884252-50884302	RPTEC	kidney:	n/a
9	chr2:50863603-50863653	ECC-1	luminal epithelium:	n/a
10	chr2:50884252-50884302	HUVEC	blood vessel:	n/a
11	chr2:50876837-50876887	LNCaP	prostate:	n/a
12	chr2:50863603-50863653	HEEpiC	esophagus:	n/a
13	chr2:50863603-50863653	NHDF-neo	bronchial:	n/a
14	chr2:50884693-50884743	AoSMC	blood vessel:	n/a
15	chr2:50884693-50884743	SK-N-SH	brain:	n/a
16	chr2:50876837-50876887	HPAEpiC	pulmonary alveolar:	n/a
17	chr2:50884693-50884743	Caco-2	colon:	n/a
18	chr2:50876837-50876887	MCF10A-Er-Src	breast:	n/a
19	chr2:50884693-50884743	NHBE	bronchial:	n/a
20	chr2:50863603-50863653	HCT-116	colon:	n/a
21	chr2:50863603-50863653	BJ	skin:	n/a
22	chr2:50884252-50884302	SK-N-MC	brain:	n/a
23	chr2:50884693-50884743	GM12892	blood:	n/a
24	chr2:50863603-50863653	AG10803	skin:	n/a
25	chr2:50884252-50884302	HNPCEpiC	eye:	n/a
26	chr2:50884252-50884302	NHDF-neo	bronchial:	n/a
27	chr2:50884693-50884743	LNCaP	prostate:	n/a
28	chr2:50876837-50876887	AG04449	skin:	fetal
29	chr2:50876837-50876887	HIPEpiC	eye:	n/a
30	chr2:50884693-50884743	Jurkat	blood:	n/a
31	chr2:50884252-50884302	ovcar-3	ovarian:	n/a
32	chr2:50863603-50863653	HNPCEpiC	eye:	n/a
33	chr2:50884252-50884302	GM12892	blood:	n/a
34	chr2:50884693-50884743	AG04449	skin:	fetal
35	chr2:50876837-50876887	A549	lung:	n/a
36	chr2:50884252-50884302	HAEpiC	amniotic membrane:	n/a
37	chr2:50876837-50876887	BJ	skin:	n/a
38	chr2:50884252-50884302	HCPEpiC	choroid plexus:	n/a
39	chr2:50876837-50876887	HUVEC	blood vessel:	n/a
40	chr2:50863603-50863653	AG04449	skin:	fetal
41	chr2:50876837-50876887	HRPEpiC	eye:	n/a
42	chr2:50876837-50876887	H1-hESC	embryonic stem cell:	embryo
43	chr2:50884252-50884302	NHBE	bronchial:	n/a
44	chr2:50884693-50884743	IMR90	lung:	fetal
45	chr2:50884693-50884743	AG09319	gingival:	n/a
46	chr2:50863603-50863653	SK-N-MC	brain:	n/a
47	chr2:50884693-50884743	AG09309	skin:	n/a
48	chr2:50884693-50884743	GM06990	blood:	n/a
49	chr2:50884252-50884302	HCM	heart:	n/a
50	chr2:50876837-50876887	HepG2	liver:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:
2	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:
3	chr2:50884111..50885778-chr2:50886770..50888521,2	MCF-7	breast:
4	chr2:50909775..50912434-chr2:50920496..50923402,2	MCF-7	breast:
5	chr2:50884111..50885778-chr2:50886770..50888521,2	MCF-7	breast:
6	chr2:50883231..50884999-chr2:50887642..50889397,2	MCF-7	breast:

No data

Variant related genes	Relation type
NRXN1	TF binding region
NRXN1	CpG island
ENSG00000216191	chromatin interactions
ENSG00000179915	chromatin interactions

Extended variants
information (count: 1791 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1791 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10176888	chr2:50861049-50861050	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115203072	chr2:50861081-50861082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111414673	chr2:50861132-50861133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148328906	chr2:50861140-50861141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141453576	chr2:50861148-50861149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577514440	chr2:50861172-50861173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534863311	chr2:50861182-50861183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150880532	chr2:50861187-50861188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368038408	chr2:50861206-50861207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574443131	chr2:50861226-50861227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140126793	chr2:50861259-50861260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562931561	chr2:50861274-50861275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs80097175	chr2:50861323-50861324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs143990171	chr2:50861327-50861328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562683656	chr2:50861348-50861349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531579110	chr2:50861359-50861360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563994101	chr2:50861369-50861370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528300259	chr2:50861375-50861376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548504196	chr2:50861376-50861377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78835232	chr2:50861390-50861391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs55956343	chr2:50861393-50861394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559845128	chr2:50861397-50861398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530121513	chr2:50861422-50861423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs17040907	chr2:50861450-50861451	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs79661127	chr2:50861464-50861465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537395624	chr2:50861469-50861470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552911646	chr2:50861488-50861489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375909526	chr2:50861500-50861501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527568024	chr2:50861501-50861502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189172320	chr2:50861549-50861550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535265328	chr2:50861615-50861616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553266808	chr2:50861638-50861639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574512167	chr2:50861639-50861640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147333797	chr2:50861642-50861643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556612485	chr2:50861679-50861680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574898916	chr2:50861701-50861702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545353609	chr2:50861715-50861716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564081998	chr2:50861768-50861769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141008922	chr2:50861769-50861770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149883068	chr2:50861782-50861783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561748431	chr2:50861832-50861833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529057435	chr2:50861859-50861860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74649397	chr2:50861864-50861865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs17480206	chr2:50861879-50861880	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs143858866	chr2:50861880-50861881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552599735	chr2:50861898-50861899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571149206	chr2:50861929-50861930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567624454	chr2:50861976-50861977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547241418	chr2:50861983-50861984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568584917	chr2:50862076-50862077	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	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
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Basal cell lymphoma	21115979	CNVD
Cognitive impairment	21505072	CNVD
Psychiatric disorder	19734545	CNVD
Autism	20844286	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Autism	19218893	CNVD
Autism	22209245	CNVD
Neuropsychiatric disorder	21827697	CNVD
Schizophrenia	22118685	CNVD
Autism	20663923	CNVD
Schizophrenia	21285140	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21990379	CNVD
Schizophrenia	22885689	CNVD
Autism	20964600	CNVD
Schizophrenia	19521646	CNVD
Attention deficit hyperactivity disorder	22214315	CNVD
Chronic motor tic disorder	22214315	CNVD
Schizophrenia	22214315	CNVD
Mental retardation	19896112	CNVD
Acute myeloid leukemia	20729466	CNVD
Bipolar disorder	19114987	CNVD
Autism	20841430	CNVD

Chromatin state (count:172 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50855200-50862600	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr2:50862000-50863600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:50862000-50863800	Enhancers	H1 Cell Line	embryonic stem cell
4	chr2:50862000-50864600	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr2:50862600-50863600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr2:50862600-50864000	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr2:50862600-50865800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr2:50862800-50863800	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr2:50862800-50865800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr2:50863000-50864200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr2:50863000-50864800	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr2:50863400-50863800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr2:50863400-50864000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:50863400-50864000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr2:50863600-50864000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr2:50863800-50865400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr2:50864000-50864600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr2:50864000-50865600	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr2:50864600-50864800	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr2:50864600-50866200	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr2:50865600-50865800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr2:50866200-50866400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr2:50868400-50868600	Enhancers	Fetal Brain Male	brain
24	chr2:50868600-50869000	Enhancers	Fetal Muscle Leg	muscle
25	chr2:50868600-50872200	Weak transcription	Fetal Brain Male	brain
26	chr2:50869000-50875600	Weak transcription	Fetal Muscle Leg	muscle
27	chr2:50872200-50877800	Enhancers	Fetal Brain Male	brain
28	chr2:50872600-50873200	Enhancers	Fetal Brain Female	brain
29	chr2:50872800-50873400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr2:50873000-50873200	Enhancers	Brain Cingulate Gyrus	brain
31	chr2:50873000-50873400	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr2:50873000-50873400	Enhancers	Brain Substantia Nigra	brain
33	chr2:50873200-50874000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr2:50873200-50875600	Weak transcription	Fetal Brain Female	brain
35	chr2:50873200-50875800	Weak transcription	Fetal Kidney	kidney
36	chr2:50873400-50874800	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr2:50873400-50875400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr2:50873400-50875400	Weak transcription	Brain Substantia Nigra	brain
39	chr2:50873600-50873800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr2:50873800-50876800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr2:50874000-50875600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr2:50874800-50878000	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr2:50875200-50876000	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr2:50875400-50876000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr2:50875400-50876000	Enhancers	Brain Substantia Nigra	brain
46	chr2:50875400-50877800	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr2:50875600-50876000	Enhancers	H1 Cell Line	embryonic stem cell
48	chr2:50875600-50876000	Enhancers	Brain Hippocampus Middle	brain
49	chr2:50875600-50876000	Enhancers	Fetal Brain Female	brain
50	chr2:50875600-50876000	Enhancers	Fetal Muscle Leg	muscle

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