Variant report

Variant	nsv997865
Chromosome Location	chr2:50872939-50948407
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:235)
CpG islands
(count:184)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:235 , 50 per page) page: 1 2 3 4 5

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	chr2:50919242-50919552	HepG2	liver:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
3	CEBPB	chr2:50919262-50919518	K562	blood:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
4	CEBPB	chr2:50890728-50891191	HepG2	liver:	n/a	chr2:50890749-50890760 chr2:50891044-50891055
5	CHD2	chr2:50947884-50948198	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr2:50902180-50902330	HA-sp	spinal cord:	n/a	n/a
7	CTCF	chr2:50902001-50902362	HepG2	liver:	n/a	n/a
8	CTCF	chr2:50902140-50902290	GM12865	blood:	n/a	n/a
9	CTCF	chr2:50902100-50902250	BE2_C	brain:	n/a	n/a
10	CTCF	chr2:50902100-50902250	NHEK	skin:	n/a	n/a
11	CTCF	chr2:50902120-50902270	HBMEC	blood vessel:	n/a	n/a
12	CTCF	chr2:50902080-50902230	GM12875	blood:	n/a	n/a
13	CTCF	chr2:50902154-50902311	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr2:50902120-50902270	GM12867	blood:	n/a	n/a
15	CTCF	chr2:50902100-50902250	HCPEpiC	choroid plexus:	n/a	n/a
16	CTCF	chr2:50902100-50902250	HepG2	liver:	n/a	n/a
17	CTCF	chr2:50902128-50902354	IMR90	lung:	n/a	n/a
18	CTCF	chr2:50902180-50902330	GM12871	blood:	n/a	n/a
19	CTCF	chr2:50889579-50889662	MCF-7	breast:	n/a	n/a
20	CTCF	chr2:50902140-50902290	HRPEpiC	eye:	n/a	n/a
21	CTCF	chr2:50902140-50902290	NB4	blood:	n/a	n/a
22	CTCF	chr2:50902080-50902230	GM12873	blood:	n/a	n/a
23	CTCF	chr2:50902106-50902258	A549	lung:	n/a	n/a
24	CTCF	chr2:50902080-50902230	HL-60	blood:	n/a	n/a
25	CTCF	chr2:50902180-50902330	GM12878	blood:	n/a	n/a
26	CTCF	chr2:50906100-50906250	GM12864	blood:	n/a	n/a
27	CTCF	chr2:50889588-50889678	GM19239	blood:	n/a	n/a
28	CTCF	chr2:50902120-50902270	HMEC	breast:	n/a	n/a
29	CTCF	chr2:50902138-50902315	NHEK	skin:	n/a	n/a
30	CTCF	chr2:50901960-50902110	RPTEC	kidney:	n/a	n/a
31	CTCF	chr2:50902120-50902270	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr2:50902140-50902290	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr2:50902060-50902290	GM12864	blood:	n/a	n/a
34	CTCF	chr2:50902140-50902290	HEK293	kidney:	n/a	n/a
35	CTCF	chr2:50902120-50902270	HepG2	liver:	n/a	n/a
36	CTCF	chr2:50902100-50902250	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr2:50902171-50902279	K562	blood:	n/a	n/a
38	CTCF	chr2:50889603-50889665	GM19240	blood:	n/a	n/a
39	CTCF	chr2:50902080-50902230	GM12864	blood:	n/a	n/a
40	CTCF	chr2:50889625-50889634	Gliobla	brain:	n/a	n/a
41	CTCF	chr2:50902100-50902250	HMF	breast:	n/a	n/a
42	CTCF	chr2:50902140-50902290	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr2:50902173-50902283	HepG2	liver:	n/a	n/a
44	CTCF	chr2:50902100-50902250	K562	blood:	n/a	n/a
45	CTCF	chr2:50902120-50902270	K562	blood:	n/a	n/a
46	CTCF	chr2:50902080-50902230	GM12869	blood:	n/a	n/a
47	CTCF	chr2:50902145-50902298	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:50902156-50902295	GM19239	blood:	n/a	n/a
49	CTCF	chr2:50902170-50902253	MCF-7	breast:	n/a	n/a
50	CTCF	chr2:50902013-50902311	H1-hESC	embryonic stem cell:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50876837-50876887	H1-hESC	embryonic stem cell:	embryo
2	chr2:50876837-50876887	H1-hESC	embryonic stem cell:	embryo
3	chr2:50884252-50884302	MCF10A-Er-Src	breast:	n/a
4	chr2:50876837-50876887	PrEC	prostate:	n/a
5	chr2:50876837-50876887	AG04449	skin:	fetal
6	chr2:50876837-50876887	Caco-2	colon:	n/a
7	chr2:50884252-50884302	IMR90	lung:	fetal
8	chr2:50884252-50884302	HIPEpiC	eye:	n/a
9	chr2:50884252-50884302	HPAEpiC	pulmonary alveolar:	n/a
10	chr2:50876837-50876887	LNCaP	prostate:	n/a
11	chr2:50884693-50884743	RPTEC	kidney:	n/a
12	chr2:50884252-50884302	GM19239	blood:	n/a
13	chr2:50884252-50884302	U87	brain:	n/a
14	chr2:50884693-50884743	LNCaP	prostate:	n/a
15	chr2:50884252-50884302	SAEC	small airway:	n/a
16	chr2:50884693-50884743	AG09309	skin:	n/a
17	chr2:50884693-50884743	AG04449	skin:	fetal
18	chr2:50884693-50884743	SKMC	muscle:	n/a
19	chr2:50884252-50884302	ovcar-3	ovarian:	n/a
20	chr2:50884693-50884743	MCF-7	breast:	n/a
21	chr2:50884693-50884743	SK-N-SH	brain:	n/a
22	chr2:50884252-50884302	NHDF-neo	bronchial:	n/a
23	chr2:50884252-50884302	HL-60	blood:	n/a
24	chr2:50884252-50884302	AoSMC	blood vessel:	n/a
25	chr2:50884252-50884302	PrEC	prostate:	n/a
26	chr2:50876837-50876887	MCF10A-Er-Src	breast:	n/a
27	chr2:50884252-50884302	BJ	skin:	n/a
28	chr2:50884693-50884743	HEEpiC	esophagus:	n/a
29	chr2:50876837-50876887	Hepatocyte	liver:	n/a
30	chr2:50876837-50876887	HCPEpiC	choroid plexus:	n/a
31	chr2:50884252-50884302	HRPEpiC	eye:	n/a
32	chr2:50876837-50876887	HPAEpiC	pulmonary alveolar:	n/a
33	chr2:50876837-50876887	Hela-S3	cervix:	n/a
34	chr2:50884252-50884302	Jurkat	blood:	n/a
35	chr2:50884693-50884743	ProgFib	skin:	n/a
36	chr2:50884252-50884302	GM12891	blood:	n/a
37	chr2:50884693-50884743	HNPCEpiC	eye:	n/a
38	chr2:50884693-50884743	GM12891	blood:	n/a
39	chr2:50884693-50884743	HCT-116	colon:	n/a
40	chr2:50876837-50876887	A549	lung:	n/a
41	chr2:50884693-50884743	SAEC	small airway:	n/a
42	chr2:50884693-50884743	PrEC	prostate:	n/a
43	chr2:50876837-50876887	ProgFib	skin:	n/a
44	chr2:50884252-50884302	AG10803	skin:	n/a
45	chr2:50884693-50884743	PANC-1	pancreas:	n/a
46	chr2:50884252-50884302	NH-A	brain:	n/a
47	chr2:50876837-50876887	HRPEpiC	eye:	n/a
48	chr2:50884693-50884743	HRCEpiC	kidney:	n/a
49	chr2:50876837-50876887	HUVEC	blood vessel:	n/a
50	chr2:50876837-50876887	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr2:50884111..50885778-chr2:50886770..50888521,2	MCF-7	breast:
2	chr2:50883231..50884999-chr2:50887642..50889397,2	MCF-7	breast:
3	chr2:50946676..50947176-chr20:60981159..60981778,2	MCF-7	breast:
4	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:
5	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:
6	chr2:50909775..50912434-chr2:50920496..50923402,2	MCF-7	breast:
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: 2732 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2732 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17040914	chr2:50872939-50872940	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556723067	chr2:50872963-50872964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531250521	chr2:50873028-50873029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74466633	chr2:50873056-50873057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373156472	chr2:50873058-50873059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77421195	chr2:50873064-50873065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs17040916	chr2:50873107-50873108	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs184481136	chr2:50873115-50873116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145370415	chr2:50873219-50873220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147655979	chr2:50873230-50873231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550535941	chr2:50873235-50873236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539328401	chr2:50873262-50873263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568727712	chr2:50873295-50873296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539745341	chr2:50873301-50873302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12988828	chr2:50873312-50873313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12988848	chr2:50873353-50873354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12989376	chr2:50873361-50873362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs13015779	chr2:50873368-50873369	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12989016	chr2:50873369-50873370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1989595	chr2:50873413-50873414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558039473	chr2:50873429-50873430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1989594	chr2:50873436-50873437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs566684600	chr2:50873449-50873450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142446198	chr2:50873505-50873506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs75178938	chr2:50873511-50873512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs574968758	chr2:50873514-50873515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541924053	chr2:50873531-50873532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557347407	chr2:50873608-50873609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375933370	chr2:50873635-50873636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116038267	chr2:50873636-50873637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564431650	chr2:50873665-50873666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2018909	chr2:50873666-50873667	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs550707430	chr2:50873716-50873717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564229423	chr2:50873745-50873746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76162951	chr2:50873751-50873752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573116621	chr2:50873766-50873767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146631704	chr2:50873779-50873780	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188922296	chr2:50873818-50873819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs72885655	chr2:50873838-50873839	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs552231598	chr2:50873846-50873847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs377118131	chr2:50873847-50873848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540834627	chr2:50873868-50873869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532753735	chr2:50873916-50873917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551744929	chr2:50873998-50873999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs566750338	chr2:50874006-50874007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs534009270	chr2:50874054-50874055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs17480512	chr2:50874084-50874085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567319530	chr2:50874119-50874120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs535948319	chr2:50874134-50874135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs557133219	chr2:50874141-50874142	Weak transcription Enhancers	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:295 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50869000-50875600	Weak transcription	Fetal Muscle Leg	muscle
2	chr2:50872200-50877800	Enhancers	Fetal Brain Male	brain
3	chr2:50872600-50873200	Enhancers	Fetal Brain Female	brain
4	chr2:50872800-50873400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr2:50873000-50873200	Enhancers	Brain Cingulate Gyrus	brain
6	chr2:50873000-50873400	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr2:50873000-50873400	Enhancers	Brain Substantia Nigra	brain
8	chr2:50873200-50874000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr2:50873200-50875600	Weak transcription	Fetal Brain Female	brain
10	chr2:50873200-50875800	Weak transcription	Fetal Kidney	kidney
11	chr2:50873400-50874800	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr2:50873400-50875400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr2:50873400-50875400	Weak transcription	Brain Substantia Nigra	brain
14	chr2:50873600-50873800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr2:50873800-50876800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr2:50874000-50875600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr2:50874800-50878000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr2:50875200-50876000	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr2:50875400-50876000	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr2:50875400-50876000	Enhancers	Brain Substantia Nigra	brain
21	chr2:50875400-50877800	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr2:50875600-50876000	Enhancers	H1 Cell Line	embryonic stem cell
23	chr2:50875600-50876000	Enhancers	Brain Hippocampus Middle	brain
24	chr2:50875600-50876000	Enhancers	Fetal Brain Female	brain
25	chr2:50875600-50876000	Enhancers	Fetal Muscle Leg	muscle
26	chr2:50875600-50876200	Enhancers	Brain Cingulate Gyrus	brain
27	chr2:50875600-50878000	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr2:50875800-50877000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr2:50875800-50877600	Enhancers	HSMMtube	muscle
30	chr2:50875800-50878000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr2:50876000-50876400	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr2:50876000-50877000	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr2:50876000-50877000	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr2:50876000-50877000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr2:50876000-50877000	Enhancers	NHEK	skin
36	chr2:50876000-50878800	Weak transcription	Brain Hippocampus Middle	brain
37	chr2:50876000-50878800	Weak transcription	Brain Substantia Nigra	brain
38	chr2:50876000-50878800	Weak transcription	Fetal Brain Female	brain
39	chr2:50876200-50879200	Weak transcription	Brain Cingulate Gyrus	brain
40	chr2:50876400-50878200	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr2:50876400-50879800	Enhancers	HMEC	breast
42	chr2:50876600-50877200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr2:50876600-50877600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr2:50876600-50877800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr2:50876600-50877800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:50876800-50877400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr2:50876800-50877400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr2:50876800-50878000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:50876800-50878000	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr2:50877000-50877400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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