Variant report

Variant	nsv994946
Chromosome Location	chr2:50881995-50947729
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:199)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
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	chr2:50919241-50919557	IMR90	lung:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
2	CEBPB	chr2:50890728-50891191	HepG2	liver:	n/a	chr2:50890749-50890760 chr2:50891044-50891055
3	CEBPB	chr2:50919242-50919552	HepG2	liver:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
4	CEBPB	chr2:50919262-50919518	K562	blood:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
5	CTCF	chr2:50902161-50902296	GM10266	blood:	n/a	n/a
6	CTCF	chr2:50902156-50902295	GM19239	blood:	n/a	n/a
7	CTCF	chr2:50902138-50902315	NHEK	skin:	n/a	n/a
8	CTCF	chr2:50902106-50902258	A549	lung:	n/a	n/a
9	CTCF	chr2:50902140-50902290	GM12872	blood:	n/a	n/a
10	CTCF	chr2:50902081-50902284	HepG2	liver:	n/a	n/a
11	CTCF	chr2:50902200-50902350	HRPEpiC	eye:	n/a	n/a
12	CTCF	chr2:50889603-50889665	GM19240	blood:	n/a	n/a
13	CTCF	chr2:50902139-50902314	GM12891	blood:	n/a	n/a
14	CTCF	chr2:50902120-50902270	HMEC	breast:	n/a	n/a
15	CTCF	chr2:50902080-50902230	NHEK	skin:	n/a	n/a
16	CTCF	chr2:50902100-50902250	NHEK	skin:	n/a	n/a
17	CTCF	chr2:50902001-50902362	HepG2	liver:	n/a	n/a
18	CTCF	chr2:50902100-50902250	HFF-Myc	foreskin:	n/a	n/a
19	CTCF	chr2:50902100-50902250	K562	blood:	n/a	n/a
20	CTCF	chr2:50902080-50902230	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr2:50902035-50902240	K562	blood:	n/a	n/a
22	CTCF	chr2:50902120-50902270	A549	lung:	n/a	n/a
23	CTCF	chr2:50886104-50886220	NHEK	skin:	n/a	n/a
24	CTCF	chr2:50902100-50902250	HCT-116	colon:	n/a	n/a
25	CTCF	chr2:50902140-50902290	NB4	blood:	n/a	n/a
26	CTCF	chr2:50902140-50902290	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr2:50902128-50902354	IMR90	lung:	n/a	n/a
28	CTCF	chr2:50902100-50902250	HepG2	liver:	n/a	n/a
29	CTCF	chr2:50902146-50902299	GM19238	blood:	n/a	n/a
30	CTCF	chr2:50902080-50902230	GM06990	blood:	n/a	n/a
31	CTCF	chr2:50902182-50902235	LNCaP	prostate:	n/a	n/a
32	CTCF	chr2:50902100-50902250	GM12873	blood:	n/a	n/a
33	CTCF	chr2:50902170-50902253	MCF-7	breast:	n/a	n/a
34	CTCF	chr2:50926700-50926850	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr2:50902155-50902284	GM13977	blood:	n/a	n/a
36	CTCF	chr2:50902080-50902230	GM12864	blood:	n/a	n/a
37	CTCF	chr2:50902220-50902370	A549	lung:	n/a	n/a
38	CTCF	chr2:50902100-50902250	GM12872	blood:	n/a	n/a
39	CTCF	chr2:50902120-50902270	K562	blood:	n/a	n/a
40	CTCF	chr2:50902320-50902470	A549	lung:	n/a	n/a
41	CTCF	chr2:50902100-50902250	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr2:50902120-50902270	GM12878	blood:	n/a	n/a
43	CTCF	chr2:50902180-50902330	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr2:50902100-50902250	HMF	breast:	n/a	n/a
45	CTCF	chr2:50902100-50902250	GM12865	blood:	n/a	n/a
46	CTCF	chr2:50902140-50902290	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr2:50902080-50902230	HL-60	blood:	n/a	n/a
48	CTCF	chr2:50889610-50889663	GM12891	blood:	n/a	n/a
49	CTCF	chr2:50902171-50902279	K562	blood:	n/a	n/a
50	CTCF	chr2:50902080-50902230	GM12869	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50884252-50884302	SK-N-MC	brain:	n/a
2	chr2:50884252-50884302	HEEpiC	esophagus:	n/a
3	chr2:50884252-50884302	SAEC	small airway:	n/a
4	chr2:50884252-50884302	PFSK-1	brain:	n/a
5	chr2:50884693-50884743	SKMC	muscle:	n/a
6	chr2:50884252-50884302	SKMC	muscle:	n/a
7	chr2:50884693-50884743	HEK293	kidney:	embryo
8	chr2:50884252-50884302	NT2-D1	testis:	n/a
9	chr2:50884252-50884302	NHBE	bronchial:	n/a
10	chr2:50884252-50884302	NB4	blood:	n/a
11	chr2:50884693-50884743	PrEC	prostate:	n/a
12	chr2:50884693-50884743	ovcar-3	ovarian:	n/a
13	chr2:50884693-50884743	MCF10A-Er-Src	breast:	n/a
14	chr2:50884252-50884302	Hela-S3	cervix:	n/a
15	chr2:50884693-50884743	SAEC	small airway:	n/a
16	chr2:50884252-50884302	GM19239	blood:	n/a
17	chr2:50884252-50884302	AG04449	skin:	fetal
18	chr2:50884252-50884302	HCF	heart:	n/a
19	chr2:50884693-50884743	NHBE	bronchial:	n/a
20	chr2:50884693-50884743	SK-N-MC	brain:	n/a
21	chr2:50884693-50884743	BJ	skin:	n/a
22	chr2:50884252-50884302	GM12878	blood:	n/a
23	chr2:50884252-50884302	AG10803	skin:	n/a
24	chr2:50884693-50884743	T-47D	breast:	n/a
25	chr2:50884252-50884302	Hepatocyte	liver:	n/a
26	chr2:50884252-50884302	BE2_C	brain:	n/a
27	chr2:50884693-50884743	CMK	blood:	n/a
28	chr2:50884252-50884302	RPTEC	kidney:	n/a
29	chr2:50884252-50884302	ovcar-3	ovarian:	n/a
30	chr2:50884693-50884743	HRE	kidney:	n/a
31	chr2:50884693-50884743	GM06990	blood:	n/a
32	chr2:50884693-50884743	H1-hESC	embryonic stem cell:	embryo
33	chr2:50884693-50884743	AG04449	skin:	fetal
34	chr2:50884693-50884743	A549	lung:	n/a
35	chr2:50884252-50884302	HCT-116	colon:	n/a
36	chr2:50884693-50884743	HCT-116	colon:	n/a
37	chr2:50884693-50884743	HRCEpiC	kidney:	n/a
38	chr2:50884693-50884743	GM12891	blood:	n/a
39	chr2:50884693-50884743	K562	blood:	n/a
40	chr2:50884693-50884743	HUVEC	blood vessel:	n/a
41	chr2:50884693-50884743	HCM	heart:	n/a
42	chr2:50884252-50884302	PrEC	prostate:	n/a
43	chr2:50884252-50884302	MCF10A-Er-Src	breast:	n/a
44	chr2:50884693-50884743	SK-N-SH_RA	brain:	n/a
45	chr2:50884252-50884302	HCM	heart:	n/a
46	chr2:50884252-50884302	HEK293	kidney:	embryo
47	chr2:50884252-50884302	MCF-7	breast:	n/a
48	chr2:50884252-50884302	H1-hESC	embryonic stem cell:	embryo
49	chr2:50884693-50884743	NHDF-neo	bronchial:	n/a
50	chr2:50884252-50884302	SK-N-SH	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:50883231..50884999-chr2:50887642..50889397,2	MCF-7	breast:
2	chr2:50946676..50947176-chr20:60981159..60981778,2	MCF-7	breast:
3	chr2:50884111..50885778-chr2:50886770..50888521,2	MCF-7	breast:
4	chr2:50909775..50912434-chr2:50920496..50923402,2	MCF-7	breast:
5	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:
6	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:
7	chr2:50884111..50885778-chr2:50886770..50888521,2	MCF-7	breast:

No data

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

Extended variants
information (count: 2284 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2284 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191325227	chr2:50882009-50882010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542728451	chr2:50882015-50882016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183706178	chr2:50882017-50882018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370823697	chr2:50882021-50882022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs34249591	chr2:50882056-50882057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371178087	chr2:50882094-50882095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374340679	chr2:50882106-50882107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1518550	chr2:50882140-50882141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144787642	chr2:50882147-50882148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75571104	chr2:50882151-50882152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1518551	chr2:50882153-50882154	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs528681315	chr2:50882204-50882205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532635428	chr2:50882236-50882237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113507486	chr2:50882250-50882251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566093717	chr2:50882310-50882311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536366205	chr2:50882317-50882318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570502365	chr2:50882328-50882329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547941976	chr2:50882329-50882330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs74715503	chr2:50882337-50882338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372338994	chr2:50882349-50882350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536625878	chr2:50882373-50882374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144895340	chr2:50882394-50882395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75184388	chr2:50882401-50882402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192897126	chr2:50882451-50882452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs1518552	chr2:50882468-50882469	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs185361204	chr2:50882469-50882470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111507176	chr2:50882482-50882483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553155657	chr2:50882535-50882536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190051589	chr2:50882540-50882541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371751836	chr2:50882552-50882553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555079217	chr2:50882638-50882639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182158889	chr2:50882652-50882653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs9752732	chr2:50882657-50882658	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs565238207	chr2:50882667-50882668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532843117	chr2:50882676-50882677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111673511	chr2:50882693-50882694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559910503	chr2:50882718-50882719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530214099	chr2:50882721-50882722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79765924	chr2:50882726-50882727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148182313	chr2:50882746-50882747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140081860	chr2:50882747-50882748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544916482	chr2:50882800-50882801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537440201	chr2:50882806-50882807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551760090	chr2:50882807-50882808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188240643	chr2:50882808-50882809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564904820	chr2:50882813-50882814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs151021418	chr2:50882814-50882815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527679150	chr2:50882884-50882885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547568559	chr2:50882885-50882886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552978482	chr2:50882944-50882945	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:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50879400-50885000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr2:50879800-50884400	Weak transcription	NHEK	skin
3	chr2:50879800-50888600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr2:50880000-50884600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr2:50884400-50886800	Enhancers	NHEK	skin
6	chr2:50884600-50885000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:50884600-50886400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr2:50884800-50885200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:50885000-50886400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr2:50885000-50888600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:50885200-50888400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:50885400-50886400	Enhancers	HMEC	breast
13	chr2:50885600-50886400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:50885800-50886400	Enhancers	H9 Cell Line	embryonic stem cell
15	chr2:50885800-50886400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr2:50886000-50886200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr2:50886000-50886400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr2:50886200-50888600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr2:50886400-50890400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr2:50886800-50890600	Weak transcription	NHEK	skin
21	chr2:50888400-50890800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr2:50888600-50889200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr2:50888600-50889400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr2:50888600-50889600	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr2:50888600-50890400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:50889000-50889200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr2:50889000-50889400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr2:50889400-50890800	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr2:50890400-50890800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr2:50890400-50899200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr2:50890600-50891400	Enhancers	NHEK	skin
32	chr2:50890800-50891000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr2:50890800-50895000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:50894800-50895800	Enhancers	Brain Angular Gyrus	brain
35	chr2:50895000-50895200	Enhancers	Brain Germinal Matrix	brain
36	chr2:50895000-50895600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:50895000-50895800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr2:50895200-50896200	Enhancers	Brain Substantia Nigra	brain
39	chr2:50895600-50896000	Enhancers	Brain Cingulate Gyrus	brain
40	chr2:50895800-50896000	Enhancers	Brain Germinal Matrix	brain
41	chr2:50896000-50896400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:50899200-50899600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:50899200-50899800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr2:50899600-50899800	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr2:50904200-50904600	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr2:50905400-50905800	Enhancers	Brain Hippocampus Middle	brain
47	chr2:50905600-50906200	Enhancers	Brain Anterior Caudate	brain
48	chr2:50905800-50906200	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr2:50913400-50914000	Enhancers	Brain Angular Gyrus	brain
50	chr2:50913400-50914600	Enhancers	iPS-20b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links