Variant report

Variant	esv2757886
Chromosome Location	chr3:116142130-116307542
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:116142157-116142669	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr3:116163624-116163632	GM12878	blood:	n/a	n/a
3	BHLHE40	chr3:116284778-116284791	GM12878	blood:	n/a	n/a
4	CEBPB	chr3:116248962-116249228	A549	lung:	n/a	chr3:116249121-116249132 chr3:116249042-116249053 chr3:116249119-116249132 chr3:116249121-116249130
5	CEBPB	chr3:116161595-116161795	H1-hESC	embryonic stem cell:	n/a	chr3:116161693-116161704
6	CEBPB	chr3:116168826-116169096	HepG2	liver:	n/a	chr3:116168957-116168970 chr3:116168946-116168957 chr3:116168957-116168970 chr3:116168958-116168969
7	CEBPB	chr3:116180965-116181264	A549	lung:	n/a	n/a
8	CEBPB	chr3:116243582-116243871	HepG2	liver:	n/a	chr3:116243710-116243723 chr3:116243710-116243723 chr3:116243712-116243723 chr3:116243710-116243721 chr3:116243710-116243723
9	CEBPB	chr3:116168817-116169054	A549	lung:	n/a	chr3:116168957-116168970 chr3:116168946-116168957 chr3:116168957-116168970 chr3:116168958-116168969
10	CEBPB	chr3:116168782-116169095	IMR90	lung:	n/a	chr3:116168957-116168970 chr3:116168946-116168957 chr3:116168957-116168970 chr3:116168958-116168969
11	CEBPB	chr3:116169510-116169797	HepG2	liver:	n/a	chr3:116169612-116169623 chr3:116169612-116169625
12	CEBPB	chr3:116243294-116243886	IMR90	lung:	n/a	chr3:116243710-116243723 chr3:116243710-116243723 chr3:116243712-116243723 chr3:116243710-116243721 chr3:116243710-116243723
13	CEBPB	chr3:116243704-116243708	A549	lung:	n/a	n/a
14	CEBPB	chr3:116161516-116161847	HepG2	liver:	n/a	chr3:116161693-116161704
15	CEBPB	chr3:116252009-116252060	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr3:116161665-116161827	K562	blood:	n/a	chr3:116161693-116161704
17	CEBPB	chr3:116260129-116260421	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr3:116260161-116260361	HepG2	liver:	n/a	n/a
19	CEBPB	chr3:116161505-116161893	IMR90	lung:	n/a	chr3:116161693-116161704
20	CHD1	chr3:116161465-116161544	GM12878	blood:	n/a	n/a
21	CHD2	chr3:116148024-116148036	GM12878	blood:	n/a	n/a
22	CHD2	chr3:116142636-116142670	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr3:116298696-116299024	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr3:116298753-116299076	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTBP2	chr3:116163661-116164948	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr3:116236260-116236410	GM12871	blood:	n/a	chr3:116236334-116236355 chr3:116236339-116236357
27	CTCF	chr3:116236200-116236350	NHDF-neo	bronchial:	n/a	n/a
28	CTCF	chr3:116152440-116152769	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr3:116236320-116236470	HFF-Myc	foreskin:	n/a	chr3:116236334-116236355 chr3:116236339-116236357
30	CTCF	chr3:116236280-116236430	HPAF	blood vessel:	n/a	chr3:116236334-116236355 chr3:116236339-116236357
31	CTCF	chr3:116236500-116236650	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr3:116236140-116236290	GM12872	blood:	n/a	n/a
33	CTCF	chr3:116236240-116236390	GM12865	blood:	n/a	chr3:116236334-116236355 chr3:116236339-116236357
34	CTCF	chr3:116172912-116173056	LNCaP	prostate:	n/a	chr3:116172987-116173005
35	CTCF	chr3:116236400-116236550	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr3:116236240-116236390	HCT-116	colon:	n/a	chr3:116236334-116236355 chr3:116236339-116236357
37	CTCF	chr3:116236180-116236330	GM12868	blood:	n/a	n/a
38	CTCF	chr3:116189252-116189303	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr3:116236232-116236407	HepG2	liver:	n/a	chr3:116236334-116236355 chr3:116236339-116236357
40	CTCF	chr3:116172920-116173070	HCFaa	heart:	n/a	chr3:116172987-116173005
41	CTCF	chr3:116172860-116173010	AoAF	blood vessel:	n/a	chr3:116172987-116173005
42	CTCF	chr3:116236280-116236430	GM12878	blood:	n/a	chr3:116236334-116236355 chr3:116236339-116236357
43	CTCF	chr3:116173020-116173170	HCM	heart:	n/a	n/a
44	CTCF	chr3:116172940-116173090	NHDF-neo	bronchial:	n/a	chr3:116172987-116173005
45	CTCF	chr3:116172940-116173090	SK-N-SH_RA	brain:	n/a	chr3:116172987-116173005
46	CTCF	chr3:116236300-116236450	HMEC	breast:	n/a	chr3:116236334-116236355 chr3:116236339-116236357
47	CTCF	chr3:116236220-116236370	GM12866	blood:	n/a	chr3:116236334-116236355 chr3:116236339-116236357
48	CTCF	chr3:116236240-116236390	Caco-2	colon:	n/a	chr3:116236334-116236355 chr3:116236339-116236357
49	CTCF	chr3:116236136-116236557	GM12878	blood:	n/a	chr3:116236334-116236355 chr3:116236339-116236357
50	CTCF	chr3:116172920-116173070	BJ	skin:	n/a	chr3:116172987-116173005

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:116158857-116158907	HRE	kidney:	n/a
2	chr3:116158857-116158907	GM06990	blood:	n/a
3	chr3:116158857-116158907	HRE	kidney:	n/a
4	chr3:116158857-116158907	GM06990	blood:	n/a
5	chr3:116164576-116164626	GM12891	blood:	n/a
6	chr3:116163858-116163908	Jurkat	blood:	n/a
7	chr3:116163765-116163815	HEK293	kidney:	embryo
8	chr3:116164035-116164085	Hela-S3	cervix:	n/a
9	chr3:116164512-116164562	NH-A	brain:	n/a
10	chr3:116164512-116164562	HPAEpiC	pulmonary alveolar:	n/a
11	chr3:116164242-116164292	HPAEpiC	pulmonary alveolar:	n/a
12	chr3:116164943-116164993	HRPEpiC	eye:	n/a
13	chr3:116164035-116164085	K562	blood:	n/a
14	chr3:116164035-116164085	HEEpiC	esophagus:	n/a
15	chr3:116163694-116163744	HRPEpiC	eye:	n/a
16	chr3:116163925-116163975	SKMC	muscle:	n/a
17	chr3:116164943-116164993	Hepatocyte	liver:	n/a
18	chr3:116163765-116163815	AG04450	lung:	fetal
19	chr3:116163858-116163908	BE2_C	brain:	n/a
20	chr3:116163694-116163744	HCF	heart:	n/a
21	chr3:116142557-116142607	HRPEpiC	eye:	n/a
22	chr3:116163694-116163744	MCF-7	breast:	n/a
23	chr3:116158857-116158907	GM12892	blood:	n/a
24	chr3:116164035-116164085	HCF	heart:	n/a
25	chr3:116164242-116164292	HMEC	breast:	n/a
26	chr3:116164242-116164292	U87	brain:	n/a
27	chr3:116164512-116164562	HNPCEpiC	eye:	n/a
28	chr3:116163765-116163815	PrEC	prostate:	n/a
29	chr3:116164943-116164993	SK-N-SH_RA	brain:	n/a
30	chr3:116163694-116163744	AG09319	gingival:	n/a
31	chr3:116164512-116164562	HCPEpiC	choroid plexus:	n/a
32	chr3:116163925-116163975	HEK293	kidney:	embryo
33	chr3:116163858-116163908	AG10803	skin:	n/a
34	chr3:116158857-116158907	HAEpiC	amniotic membrane:	n/a
35	chr3:116163858-116163908	A549	lung:	n/a
36	chr3:116163765-116163815	MCF-7	breast:	n/a
37	chr3:116164512-116164562	AG09309	skin:	n/a
38	chr3:116164512-116164562	AoSMC	blood vessel:	n/a
39	chr3:116164035-116164085	NB4	blood:	n/a
40	chr3:116163858-116163908	AG04450	lung:	fetal
41	chr3:116163925-116163975	Jurkat	blood:	n/a
42	chr3:116163858-116163908	HAEpiC	amniotic membrane:	n/a
43	chr3:116164576-116164626	SKMC	muscle:	n/a
44	chr3:116164576-116164626	PrEC	prostate:	n/a
45	chr3:116142557-116142607	PANC-1	pancreas:	n/a
46	chr3:116164035-116164085	Caco-2	colon:	n/a
47	chr3:116163925-116163975	GM12892	blood:	n/a
48	chr3:116164576-116164626	SK-N-MC	brain:	n/a
49	chr3:116163925-116163975	HCF	heart:	n/a
50	chr3:116164576-116164626	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:64779766..64782316-chr3:116274576..116276076,2	MCF-7	breast:
2	chr3:116240379..116243344-chr3:116243558..116245234,2	MCF-7	breast:
3	chr3:116183757..116185826-chr3:116200230..116203090,2	K562	blood:
4	chr3:116240379..116243344-chr3:116243558..116245234,2	MCF-7	breast:
5	chr3:116191901..116194742-chr3:116200549..116202358,2	K562	blood:
6	chr3:116191901..116194742-chr3:116200549..116202358,2	K562	blood:
7	chr3:116183757..116185826-chr3:116200230..116203090,2	K562	blood:
8	chr3:115858909..115859556-chr3:116235958..116236759,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GAP43-5	chr3:116271320-116271367	XLOC_002767
2	lnc-ZBTB20-7	chr3:116301401-116301677	NONHSAT091312
3	lnc-GAP43-5	chr3:116286937-116287111	XLOC_002767

Variant related genes	Relation type
LINC00903	TF binding region
RN7SL582P	TF binding region
LSAMP	TF binding region
LINC00903	CpG island
RN7SL582P	CpG island
LSAMP	CpG island
RB1	miRNA target sites

Extended variants
information (count: 3260 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3260 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570193852	chr3:116142153-116142154	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs114719082	chr3:116142210-116142211	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs552794046	chr3:116142258-116142259	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs564538369	chr3:116142283-116142284	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs16824895	chr3:116142313-116142314	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs550085215	chr3:116142322-116142323	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs568249681	chr3:116142351-116142352	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs576199372	chr3:116142371-116142372	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs535544580	chr3:116142398-116142399	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs190543655	chr3:116142492-116142493	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs565692578	chr3:116142533-116142534	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs143536809	chr3:116142561-116142562	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs558782239	chr3:116142571-116142572	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs181682977	chr3:116142633-116142634	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs559672368	chr3:116142634-116142635	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs1920175	chr3:116142646-116142647	Flanking Active TSS Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs186247079	chr3:116142673-116142674	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs559417544	chr3:116142735-116142736	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs375166376	chr3:116142742-116142743	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs144285700	chr3:116142781-116142782	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs34636793	chr3:116142896-116142897	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs192056089	chr3:116142936-116142937	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs371086767	chr3:116142965-116142966	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs61000976	chr3:116142976-116142977	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs114358817	chr3:116142993-116142994	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs116140388	chr3:116142996-116142997	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs146819367	chr3:116143009-116143010	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs564828816	chr3:116143018-116143019	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs531895409	chr3:116143038-116143039	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs77375418	chr3:116143040-116143041	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs561941465	chr3:116143137-116143138	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs182770481	chr3:116143171-116143172	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs187650772	chr3:116143271-116143272	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs547446225	chr3:116143277-116143278	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs565751684	chr3:116143287-116143288	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs533331667	chr3:116143333-116143334	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs551466349	chr3:116143379-116143380	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs148525087	chr3:116143387-116143388	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs537742505	chr3:116143393-116143394	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs541073211	chr3:116143433-116143434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556372228	chr3:116143465-116143466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568218614	chr3:116143514-116143515	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535558132	chr3:116143518-116143519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553871067	chr3:116143717-116143718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368887960	chr3:116143728-116143729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572147159	chr3:116143762-116143763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573678372	chr3:116143792-116143793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545818227	chr3:116143799-116143800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6767942	chr3:116143809-116143810	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs76821358	chr3:116143861-116143862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Ovarian cancer	22174824	CNVD
Myelofibrosis	22110671	CNVD
Characteristic facial feature	22180640	CNVD
hypoplastic male genitals	22180640	CNVD
postnatal overgrowth	22180640	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:657 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:116140800-116142200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr3:116141600-116142200	Enhancers	Colon Smooth Muscle	Colon
3	chr3:116141800-116142200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr3:116141800-116142200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr3:116141800-116142200	Enhancers	Brain Anterior Caudate	brain
6	chr3:116141800-116142200	Enhancers	Brain Hippocampus Middle	brain
7	chr3:116141800-116142200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
8	chr3:116141800-116142400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr3:116141800-116142400	Flanking Active TSS	Brain Cingulate Gyrus	brain
10	chr3:116141800-116142600	Enhancers	Duodenum Smooth Muscle	Duodenum
11	chr3:116141800-116142800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr3:116141800-116143200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr3:116141800-116143400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:116141800-116143400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr3:116141800-116143600	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr3:116141800-116143600	Enhancers	Brain Germinal Matrix	brain
17	chr3:116141800-116143800	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr3:116142000-116142200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr3:116142000-116142200	Enhancers	Brain Angular Gyrus	brain
20	chr3:116142000-116142200	Flanking Active TSS	Brain Substantia Nigra	brain
21	chr3:116142000-116142400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr3:116142000-116142400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
23	chr3:116142000-116142600	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr3:116142000-116142800	Active TSS	Stomach Smooth Muscle	stomach
25	chr3:116142000-116143000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr3:116142000-116143000	Active TSS	Brain Inferior Temporal Lobe	brain
27	chr3:116142000-116143200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr3:116142000-116143600	Enhancers	Rectal Smooth Muscle	rectum
29	chr3:116142000-116143800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr3:116142000-116143800	Enhancers	Fetal Lung	lung
31	chr3:116142200-116142400	Flanking Active TSS	Colon Smooth Muscle	Colon
32	chr3:116142200-116142600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr3:116142200-116142600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr3:116142200-116142600	Active TSS	Brain Angular Gyrus	brain
35	chr3:116142200-116142600	Enhancers	Fetal Brain Male	brain
36	chr3:116142200-116142800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr3:116142200-116142800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr3:116142200-116142800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr3:116142200-116142800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr3:116142200-116143000	Active TSS	Brain Anterior Caudate	brain
41	chr3:116142200-116143000	Active TSS	Brain Substantia Nigra	brain
42	chr3:116142200-116143200	Flanking Active TSS	Brain Hippocampus Middle	brain
43	chr3:116142200-116143800	Enhancers	Fetal Stomach	stomach
44	chr3:116142200-116144200	Enhancers	Stomach Mucosa	stomach
45	chr3:116142400-116142800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr3:116142400-116142800	Active TSS	Brain Cingulate Gyrus	brain
47	chr3:116142400-116142800	Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr3:116142400-116143000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr3:116142400-116143000	Active TSS	Colon Smooth Muscle	Colon
50	chr3:116142400-116143200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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