Variant report

Variant	nsv933499
Chromosome Location	chr2:50878329-50938310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:191)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:191 , 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	CEBPB	chr2:50919241-50919557	IMR90	lung:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
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	chr2:50902106-50902258	A549	lung:	n/a	n/a
6	CTCF	chr2:50902081-50902284	HepG2	liver:	n/a	n/a
7	CTCF	chr2:50902197-50902266	Medullo	brain:	n/a	n/a
8	CTCF	chr2:50889625-50889634	Gliobla	brain:	n/a	n/a
9	CTCF	chr2:50902140-50902290	NB4	blood:	n/a	n/a
10	CTCF	chr2:50902200-50902350	HCFaa	heart:	n/a	n/a
11	CTCF	chr2:50902173-50902283	HepG2	liver:	n/a	n/a
12	CTCF	chr2:50902100-50902250	AG04449	skin:	n/a	n/a
13	CTCF	chr2:50902080-50902230	HL-60	blood:	n/a	n/a
14	CTCF	chr2:50902100-50902250	GM12870	blood:	n/a	n/a
15	CTCF	chr2:50902140-50902290	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr2:50902180-50902330	GM12878	blood:	n/a	n/a
17	CTCF	chr2:50902320-50902470	A549	lung:	n/a	n/a
18	CTCF	chr2:50902100-50902250	HepG2	liver:	n/a	n/a
19	CTCF	chr2:50902100-50902250	K562	blood:	n/a	n/a
20	CTCF	chr2:50902171-50902279	K562	blood:	n/a	n/a
21	CTCF	chr2:50902013-50902311	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr2:50902154-50902311	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr2:50902100-50902250	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr2:50902146-50902299	GM19238	blood:	n/a	n/a
25	CTCF	chr2:50902100-50902250	HMF	breast:	n/a	n/a
26	CTCF	chr2:50902120-50902270	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr2:50886104-50886220	NHEK	skin:	n/a	n/a
28	CTCF	chr2:50902100-50902250	GM12865	blood:	n/a	n/a
29	CTCF	chr2:50902182-50902235	LNCaP	prostate:	n/a	n/a
30	CTCF	chr2:50902140-50902290	GM12871	blood:	n/a	n/a
31	CTCF	chr2:50902120-50902270	GM12874	blood:	n/a	n/a
32	CTCF	chr2:50902138-50902315	NHEK	skin:	n/a	n/a
33	CTCF	chr2:50902100-50902250	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr2:50902100-50902250	GM12874	blood:	n/a	n/a
35	CTCF	chr2:50907104-50907160	GM20000	blood:	n/a	n/a
36	CTCF	chr2:50902176-50902276	GM10248	blood:	n/a	n/a
37	CTCF	chr2:50902080-50902230	GM12864	blood:	n/a	n/a
38	CTCF	chr2:50902100-50902250	NHEK	skin:	n/a	n/a
39	CTCF	chr2:50902080-50902230	GM12875	blood:	n/a	n/a
40	CTCF	chr2:50902140-50902290	GM12865	blood:	n/a	n/a
41	CTCF	chr2:50902120-50902270	K562	blood:	n/a	n/a
42	CTCF	chr2:50902220-50902370	A549	lung:	n/a	n/a
43	CTCF	chr2:50902080-50902230	GM06990	blood:	n/a	n/a
44	CTCF	chr2:50902140-50902290	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr2:50889583-50889671	GM19238	blood:	n/a	n/a
46	CTCF	chr2:50902120-50902270	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr2:50902100-50902250	SAEC	small airway:	n/a	n/a
48	CTCF	chr2:50902120-50902270	HepG2	liver:	n/a	n/a
49	CTCF	chr2:50902161-50902296	GM10266	blood:	n/a	n/a
50	CTCF	chr2:50902080-50902230	NHEK	skin:	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	PrEC	prostate:	n/a
2	chr2:50884693-50884743	H1-hESC	embryonic stem cell:	embryo
3	chr2:50884693-50884743	AG04450	lung:	fetal
4	chr2:50884252-50884302	PFSK-1	brain:	n/a
5	chr2:50884693-50884743	GM12878	blood:	n/a
6	chr2:50884252-50884302	Hepatocyte	liver:	n/a
7	chr2:50884693-50884743	AG09309	skin:	n/a
8	chr2:50884252-50884302	ECC-1	luminal epithelium:	n/a
9	chr2:50884693-50884743	SAEC	small airway:	n/a
10	chr2:50884252-50884302	GM12891	blood:	n/a
11	chr2:50884252-50884302	SKMC	muscle:	n/a
12	chr2:50884693-50884743	BE2_C	brain:	n/a
13	chr2:50884693-50884743	GM06990	blood:	n/a
14	chr2:50884693-50884743	ovcar-3	ovarian:	n/a
15	chr2:50884252-50884302	AG04449	skin:	fetal
16	chr2:50884252-50884302	HEK293	kidney:	embryo
17	chr2:50884693-50884743	RPTEC	kidney:	n/a
18	chr2:50884693-50884743	HAEpiC	amniotic membrane:	n/a
19	chr2:50884693-50884743	Hela-S3	cervix:	n/a
20	chr2:50884693-50884743	NHDF-neo	bronchial:	n/a
21	chr2:50884693-50884743	Hepatocyte	liver:	n/a
22	chr2:50884252-50884302	SK-N-SH	brain:	n/a
23	chr2:50884252-50884302	T-47D	breast:	n/a
24	chr2:50884252-50884302	BE2_C	brain:	n/a
25	chr2:50884693-50884743	ECC-1	luminal epithelium:	n/a
26	chr2:50884693-50884743	NB4	blood:	n/a
27	chr2:50884252-50884302	AG09309	skin:	n/a
28	chr2:50884252-50884302	ovcar-3	ovarian:	n/a
29	chr2:50884693-50884743	HUVEC	blood vessel:	n/a
30	chr2:50884693-50884743	AG09319	gingival:	n/a
31	chr2:50884693-50884743	Caco-2	colon:	n/a
32	chr2:50884252-50884302	GM12878	blood:	n/a
33	chr2:50884693-50884743	MCF10A-Er-Src	breast:	n/a
34	chr2:50884693-50884743	LNCaP	prostate:	n/a
35	chr2:50884693-50884743	HEK293	kidney:	embryo
36	chr2:50884693-50884743	AG10803	skin:	n/a
37	chr2:50884252-50884302	K562	blood:	n/a
38	chr2:50884693-50884743	SK-N-MC	brain:	n/a
39	chr2:50884693-50884743	HMEC	breast:	n/a
40	chr2:50884252-50884302	HAEpiC	amniotic membrane:	n/a
41	chr2:50884693-50884743	SKMC	muscle:	n/a
42	chr2:50884252-50884302	NHBE	bronchial:	n/a
43	chr2:50884252-50884302	HCF	heart:	n/a
44	chr2:50884693-50884743	NH-A	brain:	n/a
45	chr2:50884252-50884302	MCF-7	breast:	n/a
46	chr2:50884693-50884743	CMK	blood:	n/a
47	chr2:50884252-50884302	NHDF-neo	bronchial:	n/a
48	chr2:50884693-50884743	GM12891	blood:	n/a
49	chr2:50884693-50884743	AoSMC	blood vessel:	n/a
50	chr2:50884252-50884302	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:50884111..50885778-chr2:50886770..50888521,2	MCF-7	breast:
2	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:
3	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:
4	chr2:50884111..50885778-chr2:50886770..50888521,2	MCF-7	breast:
5	chr2:50909775..50912434-chr2:50920496..50923402,2	MCF-7	breast:
6	chr2:50883231..50884999-chr2:50887642..50889397,2	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: 2085 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2085 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569114985	chr2:50878334-50878335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs539643428	chr2:50878407-50878408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559124408	chr2:50878429-50878430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577403483	chr2:50878437-50878438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs193236299	chr2:50878480-50878481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs554309360	chr2:50878500-50878501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557867186	chr2:50878513-50878514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184503000	chr2:50878516-50878517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371763620	chr2:50878554-50878555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs117360738	chr2:50878560-50878561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542547805	chr2:50878577-50878578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542866571	chr2:50878603-50878604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs72224726	chr2:50878611-50878612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200996594	chr2:50878615-50878616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563822249	chr2:50878625-50878626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79714080	chr2:50878630-50878631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs545971680	chr2:50878635-50878636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564305348	chr2:50878640-50878641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201818448	chr2:50878645-50878646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552235633	chr2:50878646-50878647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs528195376	chr2:50878648-50878649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs386645993	chr2:50878650-50878651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs62142333	chr2:50878655-50878656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs62142334	chr2:50878660-50878661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528873447	chr2:50878665-50878666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550901208	chr2:50878677-50878678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569153661	chr2:50878715-50878716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188111413	chr2:50878740-50878741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558002183	chr2:50878754-50878755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs566646799	chr2:50878761-50878762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75544411	chr2:50878771-50878772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553180735	chr2:50878791-50878792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574821587	chr2:50878805-50878806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140836029	chr2:50878837-50878838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs72837003	chr2:50878844-50878845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557668552	chr2:50878872-50878873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575547795	chr2:50878895-50878896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150079078	chr2:50878948-50878949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114007911	chr2:50878950-50878951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573060594	chr2:50878964-50878965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138489983	chr2:50878968-50878969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561626820	chr2:50879009-50879010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs858956	chr2:50879012-50879013	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs149259490	chr2:50879017-50879018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184041710	chr2:50879019-50879020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533289513	chr2:50879029-50879030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564461560	chr2:50879052-50879053	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566711547	chr2:50879081-50879082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189167274	chr2:50879083-50879084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547097171	chr2:50879105-50879106	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:169 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50876000-50878800	Weak transcription	Brain Hippocampus Middle	brain
2	chr2:50876000-50878800	Weak transcription	Brain Substantia Nigra	brain
3	chr2:50876000-50878800	Weak transcription	Fetal Brain Female	brain
4	chr2:50876200-50879200	Weak transcription	Brain Cingulate Gyrus	brain
5	chr2:50876400-50879800	Enhancers	HMEC	breast
6	chr2:50877000-50879200	Enhancers	Brain Germinal Matrix	brain
7	chr2:50877400-50879000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:50877600-50879000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr2:50877800-50878800	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr2:50878000-50879000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr2:50878000-50879400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr2:50878000-50879800	Enhancers	NHEK	skin
13	chr2:50878200-50878800	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr2:50878200-50880000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr2:50878600-50879200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
16	chr2:50878800-50879000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr2:50878800-50879000	Enhancers	Brain Substantia Nigra	brain
18	chr2:50878800-50879400	Enhancers	Brain Hippocampus Middle	brain
19	chr2:50878800-50879400	Enhancers	Fetal Brain Female	brain
20	chr2:50878800-50879800	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr2:50879000-50879200	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr2:50879000-50879400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr2:50879000-50879400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr2:50879000-50879400	Weak transcription	Brain Substantia Nigra	brain
25	chr2:50879000-50879800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr2:50879200-50879400	Enhancers	HSMMtube	muscle
27	chr2:50879400-50879600	Enhancers	Brain Cingulate Gyrus	brain
28	chr2:50879400-50879800	Enhancers	Brain Substantia Nigra	brain
29	chr2:50879400-50885000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr2:50879800-50884400	Weak transcription	NHEK	skin
31	chr2:50879800-50888600	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr2:50880000-50884600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr2:50884400-50886800	Enhancers	NHEK	skin
34	chr2:50884600-50885000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr2:50884600-50886400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr2:50884800-50885200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:50885000-50886400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr2:50885000-50888600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr2:50885200-50888400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr2:50885400-50886400	Enhancers	HMEC	breast
41	chr2:50885600-50886400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr2:50885800-50886400	Enhancers	H9 Cell Line	embryonic stem cell
43	chr2:50885800-50886400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr2:50886000-50886200	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr2:50886000-50886400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr2:50886200-50888600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr2:50886400-50890400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr2:50886800-50890600	Weak transcription	NHEK	skin
49	chr2:50888400-50890800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr2:50888600-50889200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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