Variant report

Variant	nsv1014726
Chromosome Location	chr2:187036909-187213113
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:731)
CpG islands
(count:122)
Chromatin interactive
region (count:20)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:731 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:187206787-187207142	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:187046339-187046834	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:187168763-187169293	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:187173020-187173545	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:187164433-187164716	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:187121356-187121642	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:187062701-187063034	HepG2	liver:	n/a	n/a
8	BATF	chr2:187212171-187212425	GM12878	blood:	n/a	chr2:187212330-187212340 chr2:187212329-187212340
9	BHLHE40	chr2:187172649-187173008	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:187168871-187169071	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:187198053-187198290	A549	lung:	n/a	chr2:187198180-187198191
12	CEBPB	chr2:187049017-187049033	A549	lung:	n/a	n/a
13	CEBPB	chr2:187101886-187102131	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:187173024-187173481	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:187205988-187206512	HepG2	liver:	n/a	chr2:187206388-187206399
16	CEBPB	chr2:187060629-187060771	H1-hESC	embryonic stem cell:	n/a	chr2:187060674-187060685 chr2:187060674-187060687
17	CEBPB	chr2:187173060-187173458	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:187101217-187101408	A549	lung:	n/a	n/a
19	CEBPB	chr2:187076965-187077188	HepG2	liver:	n/a	chr2:187077137-187077148 chr2:187077058-187077069
20	CEBPB	chr2:187197140-187197143	A549	lung:	n/a	n/a
21	CEBPB	chr2:187119718-187119844	HepG2	liver:	n/a	chr2:187119776-187119787
22	CEBPB	chr2:187160429-187160719	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:187139715-187140087	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:187173092-187173343	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:187198051-187198316	HepG2	liver:	n/a	chr2:187198180-187198191
26	CEBPB	chr2:187047299-187047519	HepG2	liver:	n/a	chr2:187047425-187047436
27	CEBPB	chr2:187211925-187212181	IMR90	lung:	n/a	n/a
28	CEBPB	chr2:187194952-187195104	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr2:187046357-187046763	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:187160425-187160666	A549	lung:	n/a	n/a
31	CEBPB	chr2:187173089-187173381	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr2:187046418-187046647	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:187173048-187173341	MCF-7	breast:	n/a	n/a
34	CEBPB	chr2:187163228-187163470	HepG2	liver:	n/a	chr2:187163337-187163348
35	CEBPB	chr2:187211903-187212201	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:187046375-187046652	HepG2	liver:	n/a	n/a
37	CEBPB	chr2:187101181-187102157	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:187060567-187060855	HepG2	liver:	n/a	chr2:187060674-187060685 chr2:187060674-187060687
39	CEBPB	chr2:187212025-187212177	A549	lung:	n/a	n/a
40	CEBPB	chr2:187046402-187046754	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:187173018-187173453	HCT-116	colon:	n/a	n/a
42	CEBPB	chr2:187173103-187173303	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr2:187101857-187102129	A549	lung:	n/a	n/a
44	CEBPB	chr2:187197705-187198263	IMR90	lung:	n/a	chr2:187198180-187198191
45	CEBPD	chr2:187173048-187173375	HepG2	liver:	n/a	n/a
46	CHD2	chr2:187121341-187121365	GM12878	blood:	n/a	n/a
47	CTCF	chr2:187121207-187121618	HepG2	liver:	n/a	chr2:187121466-187121484 chr2:187121467-187121483 chr2:187121461-187121482
48	CTCF	chr2:187081150-187081226	MCF-7	breast:	n/a	n/a
49	CTCF	chr2:187106700-187106850	Caco-2	colon:	n/a	n/a
50	CTCF	chr2:187121440-187121590	MCF-7	breast:	n/a	chr2:187121466-187121484 chr2:187121467-187121483 chr2:187121461-187121482

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:187120710-187120760	HEK293	kidney:	embryo
2	chr2:187081534-187081584	PrEC	prostate:	n/a
3	chr2:187081534-187081584	AG04450	lung:	fetal
4	chr2:187081534-187081584	A549	lung:	n/a
5	chr2:187120710-187120760	SK-N-SH	brain:	n/a
6	chr2:187081534-187081584	IMR90	lung:	fetal
7	chr2:187081534-187081584	HCPEpiC	choroid plexus:	n/a
8	chr2:187081534-187081584	HRPEpiC	eye:	n/a
9	chr2:187081534-187081584	MCF-7	breast:	n/a
10	chr2:187120710-187120760	HRE	kidney:	n/a
11	chr2:187081534-187081584	Hepatocyte	liver:	n/a
12	chr2:187120710-187120760	HCM	heart:	n/a
13	chr2:187120710-187120760	Hepatocyte	liver:	n/a
14	chr2:187120710-187120760	PrEC	prostate:	n/a
15	chr2:187120710-187120760	AG09319	gingival:	n/a
16	chr2:187081534-187081584	HPAEpiC	pulmonary alveolar:	n/a
17	chr2:187081534-187081584	NHBE	bronchial:	n/a
18	chr2:187081534-187081584	GM19239	blood:	n/a
19	chr2:187081534-187081584	NB4	blood:	n/a
20	chr2:187120710-187120760	PANC-1	pancreas:	n/a
21	chr2:187120710-187120760	HNPCEpiC	eye:	n/a
22	chr2:187120710-187120760	ProgFib	skin:	n/a
23	chr2:187120710-187120760	SK-N-SH_RA	brain:	n/a
24	chr2:187120710-187120760	Caco-2	colon:	n/a
25	chr2:187081534-187081584	SK-N-SH_RA	brain:	n/a
26	chr2:187120710-187120760	SAEC	small airway:	n/a
27	chr2:187081534-187081584	GM06990	blood:	n/a
28	chr2:187120710-187120760	LNCaP	prostate:	n/a
29	chr2:187081534-187081584	NHDF-neo	bronchial:	n/a
30	chr2:187120710-187120760	NHBE	bronchial:	n/a
31	chr2:187081534-187081584	AG04449	skin:	fetal
32	chr2:187120710-187120760	HRCEpiC	kidney:	n/a
33	chr2:187081534-187081584	HEEpiC	esophagus:	n/a
34	chr2:187120710-187120760	HCF	heart:	n/a
35	chr2:187120710-187120760	HCT-116	colon:	n/a
36	chr2:187081534-187081584	ECC-1	luminal epithelium:	n/a
37	chr2:187120710-187120760	NHDF-neo	bronchial:	n/a
38	chr2:187081534-187081584	NT2-D1	testis:	n/a
39	chr2:187081534-187081584	H1-hESC	embryonic stem cell:	embryo
40	chr2:187081534-187081584	T-47D	breast:	n/a
41	chr2:187081534-187081584	HEK293	kidney:	embryo
42	chr2:187081534-187081584	HNPCEpiC	eye:	n/a
43	chr2:187081534-187081584	ProgFib	skin:	n/a
44	chr2:187120710-187120760	A549	lung:	n/a
45	chr2:187081534-187081584	GM12892	blood:	n/a
46	chr2:187120710-187120760	H1-hESC	embryonic stem cell:	embryo
47	chr2:187081534-187081584	GM12891	blood:	n/a
48	chr2:187081534-187081584	CMK	blood:	n/a
49	chr2:187081534-187081584	AG10803	skin:	n/a
50	chr2:187081534-187081584	SAEC	small airway:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:186819232..186820505-chr2:187121247..187122132,3	MCF-7	breast:
2	chr2:187144221..187146013-chr2:187148146..187151029,2	K562	blood:
3	chr2:187111432..187114258-chr2:187118686..187120723,2	MCF-7	breast:
4	chr2:186493563..186494107-chr2:187121512..187122407,2	MCF-7	breast:
5	chr2:187121005..187121910-chr2:187323354..187324097,2	MCF-7	breast:
6	chr2:187111432..187114258-chr2:187118686..187120723,2	MCF-7	breast:
7	chr2:187080091..187081693-chr2:187086828..187089165,2	K562	blood:
8	chr2:186844422..186846233-chr2:187042627..187045441,2	K562	blood:
9	chr2:186603700..186604546-chr2:187121410..187122246,2	MCF-7	breast:
10	chr2:187144221..187146013-chr2:187148146..187151029,2	K562	blood:
11	chr2:187205041..187207847-chr2:187331696..187333365,2	K562	blood:
12	chr2:187046232..187048383-chr2:187048758..187051703,2	MCF-7	breast:
13	chr2:187077199..187079062-chr2:187349198..187350991,2	K562	blood:
14	chr14:59949728..59952600-chr2:187172098..187173850,2	MCF-7	breast:
15	chr2:187168079..187170910-chr2:187226806..187228664,2	K562	blood:
16	chr10:23092682..23094839-chr2:187127661..187130019,2	MCF-7	breast:
17	chr2:186948418..186950441-chr2:187047439..187049579,2	K562	blood:
18	chr2:186603423..186604198-chr2:187120988..187121931,3	MCF-7	breast:
19	chr2:187046232..187048383-chr2:187048758..187051703,2	MCF-7	breast:
20	chr2:187080091..187081693-chr2:187086828..187089165,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM2-3	chr2:187126284-187126336	NONHSAT075981
2	lnc-ZSWIM2-3	chr2:187079525-187079817	NONHSAT075981
3	lnc-ZSWIM2-3	chr2:187166504-187166849	NONHSAT075981
4	lnc-ZSWIM2-3	chr2:187205652-187206185	NONHSAT075981

No data

Variant related genes	Relation type
RPL23AP35	TF binding region
RPL23AP35	CpG island
ENSG00000126790	chromatin interactions
ENSG00000226747	chromatin interactions
ENSG00000188738	chromatin interactions
ENSG00000065548	chromatin interactions
ENSG00000050130	chromatin interactions

Extended variants
information (count: 6160 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:6160 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577098997	chr2:187036918-187036919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs535019841	chr2:187036949-187036950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553082977	chr2:187036959-187036960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574823848	chr2:187036987-187036988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567066373	chr2:187037094-187037095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568816652	chr2:187037181-187037182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571410197	chr2:187037186-187037187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs77974267	chr2:187037194-187037195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539197551	chr2:187037213-187037214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369224542	chr2:187037236-187037237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182675136	chr2:187037246-187037247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533751060	chr2:187037282-187037283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs35122314	chr2:187037296-187037297	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs368708785	chr2:187037297-187037298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565107611	chr2:187037310-187037311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35209494	chr2:187037324-187037325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532436190	chr2:187037331-187037332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541381407	chr2:187037345-187037346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192210620	chr2:187037365-187037366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185162094	chr2:187037378-187037379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547942085	chr2:187037436-187037437	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs567449989	chr2:187037444-187037445	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs569753264	chr2:187037471-187037472	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs369000911	chr2:187037474-187037475	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs530548096	chr2:187037480-187037481	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs552337204	chr2:187037491-187037492	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs59528603	chr2:187037523-187037524	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs188875003	chr2:187037524-187037525	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs576340461	chr2:187037525-187037526	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs534070835	chr2:187037643-187037644	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs553633181	chr2:187037689-187037690	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs4331467	chr2:187037698-187037699	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs2887815	chr2:187037747-187037748	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs535858819	chr2:187037749-187037750	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs557149395	chr2:187037755-187037756	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs12327903	chr2:187037784-187037785	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs374371770	chr2:187037824-187037825	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs139613974	chr2:187037846-187037847	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs573936588	chr2:187037849-187037850	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs12327910	chr2:187037976-187037977	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs111967974	chr2:187037985-187037986	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs559611627	chr2:187038004-187038005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529628096	chr2:187038069-187038070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541786290	chr2:187038075-187038076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374533973	chr2:187038109-187038110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs193235451	chr2:187038118-187038119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184509124	chr2:187038150-187038151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551900402	chr2:187038166-187038167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559531655	chr2:187038211-187038212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139755216	chr2:187038228-187038229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:385 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:187025000-187049800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr2:187029400-187044400	Weak transcription	Aorta	Aorta
3	chr2:187029600-187037400	Weak transcription	Fetal Intestine Small	intestine
4	chr2:187037400-187038000	ZNF genes & repeats	Fetal Intestine Small	intestine
5	chr2:187044000-187045400	Enhancers	Rectal Smooth Muscle	rectum
6	chr2:187044400-187044600	Enhancers	Aorta	Aorta
7	chr2:187044400-187044600	Enhancers	Pancreas	Pancrea
8	chr2:187044400-187045400	Enhancers	Colon Smooth Muscle	Colon
9	chr2:187044600-187053600	Weak transcription	Pancreas	Pancrea
10	chr2:187046200-187047600	Enhancers	HepG2	liver
11	chr2:187046600-187047000	Enhancers	Liver	Liver
12	chr2:187052600-187054800	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr2:187052800-187054000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:187053000-187053800	Enhancers	Aorta	Aorta
15	chr2:187053400-187053800	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr2:187053600-187053800	Enhancers	Pancreas	Pancrea
17	chr2:187053800-187087600	Weak transcription	Aorta	Aorta
18	chr2:187054800-187055000	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
19	chr2:187056200-187057200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr2:187059000-187059400	Enhancers	Placenta Amnion	Placenta Amnion
21	chr2:187059200-187060800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr2:187060800-187061000	Enhancers	HepG2	liver
23	chr2:187061200-187062600	Weak transcription	HepG2	liver
24	chr2:187062600-187063000	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr2:187062600-187063000	Enhancers	HepG2	liver
26	chr2:187063200-187064000	Enhancers	Fetal Intestine Large	intestine
27	chr2:187066000-187066600	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr2:187066200-187066800	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr2:187066600-187070200	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr2:187066800-187070400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr2:187066800-187070400	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr2:187070000-187070400	Enhancers	Brain Substantia Nigra	brain
33	chr2:187070000-187070400	Enhancers	Fetal Brain Female	brain
34	chr2:187070200-187070600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr2:187070200-187070600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr2:187070200-187070600	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr2:187070200-187070600	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr2:187070200-187070800	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr2:187070400-187070600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr2:187070400-187070800	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr2:187070600-187075200	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr2:187074200-187074400	Enhancers	Liver	Liver
43	chr2:187074400-187074800	Flanking Active TSS	Liver	Liver
44	chr2:187074800-187075000	Enhancers	Liver	Liver
45	chr2:187075200-187075600	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr2:187076800-187077600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr2:187077200-187078000	Enhancers	Placenta Amnion	Placenta Amnion
48	chr2:187079800-187080000	Enhancers	Esophagus	oesophagus
49	chr2:187081000-187091400	Weak transcription	Primary hematopoietic stem cells	blood
50	chr2:187081400-187081800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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