Variant report

Variant	nsv1010032
Chromosome Location	chr3:23408985-23469063
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:272)
CpG islands
(count:123)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:272 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr3:23436607-23436931	GM12878	blood:	n/a	chr3:23436755-23436764
2	BATF	chr3:23463964-23464237	GM12878	blood:	n/a	n/a
3	BCLAF1	chr3:23463910-23464435	GM12878	blood:	n/a	n/a
4	BHLHE40	chr3:23429181-23429214	GM12878	blood:	n/a	n/a
5	BHLHE40	chr3:23446575-23446933	GM12878	blood:	n/a	n/a
6	BRCA1	chr3:23445745-23446118	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr3:23466068-23466225	A549	lung:	n/a	n/a
8	CEBPB	chr3:23438341-23438541	HepG2	liver:	n/a	chr3:23438451-23438464 chr3:23438451-23438464 chr3:23438451-23438462
9	CEBPB	chr3:23438328-23438606	Hela-S3	cervix:	n/a	chr3:23438451-23438464 chr3:23438451-23438464 chr3:23438451-23438462
10	CEBPB	chr3:23445735-23446103	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr3:23425510-23425634	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr3:23454462-23454480	HepG2	liver:	n/a	n/a
13	CEBPB	chr3:23466027-23466260	HepG2	liver:	n/a	n/a
14	CEBPB	chr3:23438342-23438564	A549	lung:	n/a	chr3:23438451-23438464 chr3:23438451-23438464 chr3:23438451-23438462
15	CEBPB	chr3:23466021-23466291	IMR90	lung:	n/a	n/a
16	CHD1	chr3:23446784-23446957	GM12878	blood:	n/a	n/a
17	CHD2	chr3:23429199-23429204	GM12878	blood:	n/a	n/a
18	CTCF	chr3:23412040-23412190	MCF-7	breast:	n/a	n/a
19	CTCF	chr3:23412100-23412250	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr3:23413880-23414030	HAc	cerebellar:	n/a	n/a
21	CTCF	chr3:23413980-23414130	HCM	heart:	n/a	n/a
22	CTCF	chr3:23412180-23412330	AG09309	skin:	n/a	n/a
23	CTCF	chr3:23413880-23414030	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr3:23412200-23412350	RPTEC	kidney:	n/a	n/a
25	CTCF	chr3:23413880-23414030	BJ	skin:	n/a	n/a
26	CTCF	chr3:23412120-23412270	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr3:23412216-23412270	HUVEC	blood vessel:	n/a	n/a
28	CTCF	chr3:23412100-23412250	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr3:23413840-23413990	AG10803	skin:	n/a	n/a
30	CTCF	chr3:23413880-23414030	HCM	heart:	n/a	n/a
31	CTCF	chr3:23412140-23412290	A549	lung:	n/a	n/a
32	CTCF	chr3:23412080-23412230	HFF	foreskin:	n/a	n/a
33	CTCF	chr3:23413860-23414010	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr3:23412060-23412210	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr3:23412160-23412310	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr3:23411980-23412130	A549	lung:	n/a	n/a
37	CTCF	chr3:23431100-23431250	GM12872	blood:	n/a	n/a
38	CTCF	chr3:23413840-23413990	AG04449	skin:	n/a	n/a
39	CTCF	chr3:23412180-23412330	GM12872	blood:	n/a	n/a
40	CTCF	chr3:23410380-23410530	HPF	lung:	n/a	n/a
41	CTCF	chr3:23451260-23451410	MCF-7	breast:	n/a	n/a
42	CTCF	chr3:23412111-23412325	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:23412116-23412302	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr3:23432114-23432127	ProgFib	skin:	n/a	n/a
45	CTCF	chr3:23413880-23414030	NHLF	lung:	n/a	n/a
46	CTCF	chr3:23412140-23412290	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr3:23432120-23432270	GM12871	blood:	n/a	n/a
48	CTCF	chr3:23412200-23412350	MCF-7	breast:	n/a	n/a
49	CTCF	chr3:23413880-23414030	HMF	breast:	n/a	n/a
50	CTCF	chr3:23412080-23412230	HBMEC	blood vessel:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:23415040-23415090	RPTEC	kidney:	n/a
2	chr3:23415040-23415090	RPTEC	kidney:	n/a
3	chr3:23448023-23448073	BE2_C	brain:	n/a
4	chr3:23415040-23415090	HCT-116	colon:	n/a
5	chr3:23448023-23448073	ProgFib	skin:	n/a
6	chr3:23415040-23415090	SK-N-MC	brain:	n/a
7	chr3:23415040-23415090	PANC-1	pancreas:	n/a
8	chr3:23415040-23415090	SAEC	small airway:	n/a
9	chr3:23448023-23448073	HUVEC	blood vessel:	n/a
10	chr3:23415040-23415090	CMK	blood:	n/a
11	chr3:23448023-23448073	HMEC	breast:	n/a
12	chr3:23448023-23448073	MCF10A-Er-Src	breast:	n/a
13	chr3:23415040-23415090	SK-N-SH	brain:	n/a
14	chr3:23448023-23448073	Caco-2	colon:	n/a
15	chr3:23415040-23415090	AG04450	lung:	fetal
16	chr3:23415040-23415090	HRE	kidney:	n/a
17	chr3:23415040-23415090	ProgFib	skin:	n/a
18	chr3:23415040-23415090	HUVEC	blood vessel:	n/a
19	chr3:23415040-23415090	BE2_C	brain:	n/a
20	chr3:23415040-23415090	HL-60	blood:	n/a
21	chr3:23448023-23448073	A549	lung:	n/a
22	chr3:23448023-23448073	GM12891	blood:	n/a
23	chr3:23448023-23448073	NHBE	bronchial:	n/a
24	chr3:23448023-23448073	Jurkat	blood:	n/a
25	chr3:23415040-23415090	AG09319	gingival:	n/a
26	chr3:23448023-23448073	HepG2	liver:	n/a
27	chr3:23415040-23415090	MCF-7	breast:	n/a
28	chr3:23415040-23415090	T-47D	breast:	n/a
29	chr3:23415040-23415090	GM12878	blood:	n/a
30	chr3:23415040-23415090	PrEC	prostate:	n/a
31	chr3:23448023-23448073	HAEpiC	amniotic membrane:	n/a
32	chr3:23448023-23448073	GM19239	blood:	n/a
33	chr3:23448023-23448073	SK-N-SH	brain:	n/a
34	chr3:23415040-23415090	Hepatocyte	liver:	n/a
35	chr3:23448023-23448073	NH-A	brain:	n/a
36	chr3:23448023-23448073	SAEC	small airway:	n/a
37	chr3:23415040-23415090	NT2-D1	testis:	n/a
38	chr3:23448023-23448073	PANC-1	pancreas:	n/a
39	chr3:23415040-23415090	GM12892	blood:	n/a
40	chr3:23415040-23415090	AoSMC	blood vessel:	n/a
41	chr3:23448023-23448073	LNCaP	prostate:	n/a
42	chr3:23448023-23448073	HRCEpiC	kidney:	n/a
43	chr3:23448023-23448073	NT2-D1	testis:	n/a
44	chr3:23415040-23415090	ovcar-3	ovarian:	n/a
45	chr3:23448023-23448073	H1-hESC	embryonic stem cell:	embryo
46	chr3:23448023-23448073	NHDF-neo	bronchial:	n/a
47	chr3:23448023-23448073	HRPEpiC	eye:	n/a
48	chr3:23415040-23415090	PFSK-1	brain:	n/a
49	chr3:23448023-23448073	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:23448023-23448073	T-47D	breast:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:23429124..23431176-chr3:23435283..23438143,3	MCF-7	breast:
2	chr3:23447289..23448831-chr3:23450533..23452284,2	K562	blood:
3	chr3:23442881..23445228-chr3:23445484..23447259,2	K562	blood:
4	chr3:23442881..23445378-chr3:23445759..23448586,2	K562	blood:
5	chr3:23413992..23416641-chr3:23420982..23423774,2	MCF-7	breast:
6	chr3:23447289..23448831-chr3:23450533..23452284,2	K562	blood:
7	chr3:23443862..23447627-chr3:23449749..23452969,4	MCF-7	breast:
8	chr3:23413992..23416641-chr3:23420982..23423774,2	MCF-7	breast:
9	chr3:23436371..23438292-chr3:23438375..23440407,2	MCF-7	breast:
10	chr3:23429124..23431176-chr3:23435283..23438143,3	MCF-7	breast:
11	chr3:23442881..23445378-chr3:23445759..23448586,2	K562	blood:
12	chr3:23436579..23438931-chr3:23441202..23443899,2	K562	blood:
13	chr3:23442881..23445228-chr3:23445484..23447259,2	K562	blood:
14	chr3:23436579..23438931-chr3:23441202..23443899,2	K562	blood:
15	chr3:23443862..23447627-chr3:23449749..23452969,4	MCF-7	breast:
16	chr3:23436371..23438292-chr3:23438375..23440407,2	MCF-7	breast:
17	chr3:23466052..23468838-chr3:23474911..23476655,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NKIRAS1-5	chr3:23431152-23431400	NONHSAT088668

No data

Variant related genes	Relation type
ENSG00000221506	TF binding region
ENSG00000228171	TF binding region
ENSG00000221506	CpG island
ENSG00000228171	CpG island

Extended variants
information (count: 2277 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2277 , 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	rs549563604	chr3:23408996-23408997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs139020074	chr3:23409021-23409022	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs117059303	chr3:23409041-23409042	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149911880	chr3:23409054-23409055	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558259957	chr3:23409055-23409056	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs554720132	chr3:23409058-23409059	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs534463811	chr3:23409093-23409094	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs185504903	chr3:23409142-23409143	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189634594	chr3:23409153-23409154	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538237645	chr3:23409158-23409159	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs75162636	chr3:23409209-23409210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs578038217	chr3:23409214-23409215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545200586	chr3:23409222-23409223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553904438	chr3:23409247-23409248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571925019	chr3:23409282-23409283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192326617	chr3:23409315-23409316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183480391	chr3:23409324-23409325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575975671	chr3:23409379-23409380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs144945405	chr3:23409420-23409421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139940189	chr3:23409439-23409440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs386659348	chr3:23409505-23409506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113237927	chr3:23409506-23409507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs2359760	chr3:23409507-23409508	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs188603487	chr3:23409516-23409517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79875326	chr3:23409542-23409543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181090607	chr3:23409573-23409574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185975425	chr3:23409576-23409577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567952854	chr3:23409580-23409581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538192625	chr3:23409582-23409583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189923549	chr3:23409589-23409590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571573605	chr3:23409614-23409615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200210230	chr3:23409626-23409627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539089455	chr3:23409637-23409638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573177325	chr3:23409645-23409646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553857700	chr3:23409678-23409679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182566411	chr3:23409685-23409686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187173178	chr3:23409722-23409723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539164671	chr3:23409750-23409751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554382436	chr3:23409759-23409760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192104984	chr3:23409900-23409901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs71322174	chr3:23409907-23409908	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs561853146	chr3:23409923-23409924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530765003	chr3:23409956-23409957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74709254	chr3:23409976-23409977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564866744	chr3:23410008-23410009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs202105403	chr3:23410026-23410027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs75872459	chr3:23410119-23410120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541076504	chr3:23410126-23410127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559489314	chr3:23410135-23410136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529857567	chr3:23410145-23410146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23398400-23413000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr3:23398600-23414600	Weak transcription	Psoas Muscle	Psoas
3	chr3:23404200-23418000	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr3:23404400-23418000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr3:23407000-23411000	Weak transcription	Primary B cells from peripheral blood	blood
6	chr3:23408800-23409600	Enhancers	GM12878-XiMat	blood
7	chr3:23409000-23409200	ZNF genes & repeats	Aorta	Aorta
8	chr3:23409000-23409400	Enhancers	Spleen	Spleen
9	chr3:23409200-23431800	Weak transcription	Aorta	Aorta
10	chr3:23409600-23411400	Weak transcription	GM12878-XiMat	blood
11	chr3:23410600-23410800	Enhancers	Brain Cingulate Gyrus	brain
12	chr3:23410800-23426800	Weak transcription	Brain Cingulate Gyrus	brain
13	chr3:23411000-23411200	Enhancers	Primary B cells from peripheral blood	blood
14	chr3:23411200-23413400	Weak transcription	Primary B cells from peripheral blood	blood
15	chr3:23411400-23411600	Enhancers	GM12878-XiMat	blood
16	chr3:23411600-23411800	Weak transcription	GM12878-XiMat	blood
17	chr3:23412200-23412400	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr3:23412600-23413800	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr3:23413000-23415200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr3:23413800-23415000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr3:23413800-23415000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr3:23413800-23415000	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr3:23413800-23415000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr3:23413800-23415200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr3:23414000-23414200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr3:23414000-23414600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr3:23414000-23415000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr3:23414000-23415000	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr3:23414000-23415000	Enhancers	Adipose Nuclei	Adipose
30	chr3:23414000-23415000	Enhancers	Brain Hippocampus Middle	brain
31	chr3:23414000-23415400	Enhancers	Fetal Lung	lung
32	chr3:23414400-23415000	Enhancers	H1 Cell Line	embryonic stem cell
33	chr3:23414400-23415000	Enhancers	H9 Cell Line	embryonic stem cell
34	chr3:23414400-23415200	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr3:23414600-23415000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr3:23414600-23415000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr3:23414600-23415000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr3:23414600-23415000	Genic enhancers	Psoas Muscle	Psoas
39	chr3:23414800-23415000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr3:23414800-23415000	Enhancers	Brain Substantia Nigra	brain
41	chr3:23414800-23415200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr3:23415000-23416000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr3:23415000-23418000	Weak transcription	Left Ventricle	heart
44	chr3:23415000-23418000	Weak transcription	Psoas Muscle	Psoas
45	chr3:23415000-23418400	Weak transcription	Brain Substantia Nigra	brain
46	chr3:23415000-23422000	Weak transcription	Brain Hippocampus Middle	brain
47	chr3:23415400-23418400	Weak transcription	Fetal Lung	lung
48	chr3:23416000-23416200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr3:23416000-23417000	Enhancers	Liver	Liver
50	chr3:23417000-23418000	Weak transcription	Primary B cells from peripheral blood	blood

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