Variant report

Variant	nsv508213
Chromosome Location	chr3:25206150-25326196
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:195)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:195 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:25271771-25271866	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr3:25288457-25288786	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr3:25276044-25276091	A549	lung:	n/a	n/a
4	CEBPB	chr3:25212341-25212643	H1-hESC	embryonic stem cell:	n/a	chr3:25212458-25212469
5	CEBPB	chr3:25212335-25212578	A549	lung:	n/a	chr3:25212458-25212469
6	CEBPB	chr3:25274155-25274231	K562	blood:	n/a	chr3:25274184-25274195
7	CEBPB	chr3:25274108-25274276	HepG2	liver:	n/a	chr3:25274184-25274195
8	CEBPB	chr3:25212333-25212577	HepG2	liver:	n/a	chr3:25212458-25212469
9	CTCF	chr3:25285013-25285072	GM13977	blood:	n/a	n/a
10	CTCF	chr3:25315424-25315458	GM12891	blood:	n/a	n/a
11	CTCF	chr3:25283030-25283078	GM20000	blood:	n/a	n/a
12	CTCF	chr3:25244324-25244357	GM13976	blood:	n/a	n/a
13	CTCF	chr3:25215896-25215964	MCF-7	breast:	n/a	n/a
14	CTCF	chr3:25223904-25223960	GM13976	blood:	n/a	chr3:25223940-25223948
15	CTCF	chr3:25219060-25219210	GM12878	blood:	n/a	n/a
16	CTCF	chr3:25223896-25223899	GM13976	blood:	n/a	n/a
17	CTCF	chr3:25215965-25215967	MCF-7	breast:	n/a	n/a
18	CTCF	chr3:25284775-25284834	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr3:25308996-25309084	GM13976	blood:	n/a	n/a
20	CTCF	chr3:25289074-25289136	A549	lung:	n/a	n/a
21	E2F4	chr3:25236725-25236749	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr3:25296342-25296479	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr3:25248809-25248947	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr3:25222675-25222850	MCF10A-Er-Src	breast:	n/a	n/a
25	EP300	chr3:25213501-25213811	SK-N-SH_RA	brain:	n/a	n/a
26	EP300	chr3:25277149-25277262	GM12878	blood:	n/a	n/a
27	EP300	chr3:25213543-25213823	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr3:25322722-25323065	SK-N-SH_RA	brain:	n/a	n/a
29	EP300	chr3:25212226-25214085	SK-N-SH	brain:	n/a	chr3:25213135-25213149 chr3:25213137-25213151 chr3:25213138-25213152 chr3:25213452-25213462 chr3:25213136-25213150 chr3:25212704-25212714
30	EP300	chr3:25212538-25213287	SK-N-SH_RA	brain:	n/a	chr3:25213135-25213149 chr3:25213137-25213151 chr3:25213138-25213152 chr3:25213136-25213150 chr3:25212704-25212714
31	EP300	chr3:25322750-25323109	SK-N-SH_RA	brain:	n/a	n/a
32	EP300	chr3:25212547-25213299	SK-N-SH_RA	brain:	n/a	chr3:25213135-25213149 chr3:25213137-25213151 chr3:25213138-25213152 chr3:25213136-25213150 chr3:25212704-25212714
33	ESR1	chr3:25302139-25302403	T-47D	breast:	n/a	n/a
34	ESR1	chr3:25266761-25267041	T-47D	breast:	n/a	chr3:25266947-25266964 chr3:25266946-25266963
35	ESR1	chr3:25302125-25302423	T-47D	breast:	n/a	n/a
36	ESR1	chr3:25302151-25302464	T-47D	breast:	n/a	n/a
37	ESR1	chr3:25266821-25267039	T-47D	breast:	n/a	chr3:25266947-25266964 chr3:25266946-25266963
38	FAM48A	chr3:25308734-25308829	GM12878	blood:	n/a	n/a
39	FOS	chr3:25325852-25326052	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr3:25317531-25317702	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr3:25325853-25326160	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr3:25298531-25298802	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr3:25325807-25326061	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr3:25298593-25298748	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr3:25294264-25294484	MCF10A-Er-Src	breast:	n/a	chr3:25294336-25294345 chr3:25294333-25294344 chr3:25294335-25294346 chr3:25294338-25294345
46	FOS	chr3:25298562-25298762	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr3:25315110-25315181	MCF10A-Er-Src	breast:	n/a	n/a
48	FOSL2	chr3:25325707-25326218	A549	lung:	n/a	n/a
49	FOXA1	chr3:25276530-25276784	T-47D	breast:	n/a	chr3:25276683-25276698
50	FOXA1	chr3:25301425-25301693	T-47D	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:25215914-25215964	AG04450	lung:	fetal
2	chr3:25215914-25215964	CMK	blood:	n/a
3	chr3:25215914-25215964	ProgFib	skin:	n/a
4	chr3:25215914-25215964	BJ	skin:	n/a
5	chr3:25215914-25215964	AoSMC	blood vessel:	n/a
6	chr3:25215914-25215964	HPAEpiC	pulmonary alveolar:	n/a
7	chr3:25215914-25215964	Jurkat	blood:	n/a
8	chr3:25215914-25215964	SKMC	muscle:	n/a
9	chr3:25215914-25215964	HepG2	liver:	n/a
10	chr3:25215914-25215964	AG09319	gingival:	n/a
11	chr3:25215914-25215964	AG10803	skin:	n/a
12	chr3:25215914-25215964	HNPCEpiC	eye:	n/a
13	chr3:25215914-25215964	GM06990	blood:	n/a
14	chr3:25215914-25215964	PrEC	prostate:	n/a
15	chr3:25215914-25215964	HRPEpiC	eye:	n/a
16	chr3:25215914-25215964	H1-hESC	embryonic stem cell:	embryo
17	chr3:25215914-25215964	AG04449	skin:	fetal
18	chr3:25215914-25215964	ECC-1	luminal epithelium:	n/a
19	chr3:25215914-25215964	HCT-116	colon:	n/a
20	chr3:25215914-25215964	ovcar-3	ovarian:	n/a
21	chr3:25215914-25215964	HMEC	breast:	n/a
22	chr3:25215914-25215964	Hepatocyte	liver:	n/a
23	chr3:25215914-25215964	RPTEC	kidney:	n/a
24	chr3:25215914-25215964	NT2-D1	testis:	n/a
25	chr3:25215914-25215964	MCF10A-Er-Src	breast:	n/a
26	chr3:25215914-25215964	HRCEpiC	kidney:	n/a
27	chr3:25215914-25215964	SK-N-SH	brain:	n/a
28	chr3:25215914-25215964	IMR90	lung:	fetal
29	chr3:25215914-25215964	GM12892	blood:	n/a
30	chr3:25215914-25215964	HRE	kidney:	n/a
31	chr3:25215914-25215964	NHBE	bronchial:	n/a
32	chr3:25215914-25215964	HEK293	kidney:	embryo
33	chr3:25215914-25215964	HUVEC	blood vessel:	n/a
34	chr3:25215914-25215964	HEEpiC	esophagus:	n/a
35	chr3:25215914-25215964	AG09309	skin:	n/a
36	chr3:25215914-25215964	LNCaP	prostate:	n/a
37	chr3:25215914-25215964	HAEpiC	amniotic membrane:	n/a
38	chr3:25215914-25215964	HCPEpiC	choroid plexus:	n/a
39	chr3:25215914-25215964	Caco-2	colon:	n/a
40	chr3:25215914-25215964	PANC-1	pancreas:	n/a
41	chr3:25215914-25215964	K562	blood:	n/a
42	chr3:25215914-25215964	GM12878	blood:	n/a
43	chr3:25215914-25215964	A549	lung:	n/a
44	chr3:25215914-25215964	SAEC	small airway:	n/a
45	chr3:25215914-25215964	GM19239	blood:	n/a
46	chr3:25215914-25215964	SK-N-SH_RA	brain:	n/a
47	chr3:25215914-25215964	NHDF-neo	bronchial:	n/a
48	chr3:25215914-25215964	Hela-S3	cervix:	n/a
49	chr3:25215914-25215964	HCM	heart:	n/a
50	chr3:25215914-25215964	NB4	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:25268545..25270522-chr3:25294614..25297344,2	K562	blood:
2	chr3:25309716..25310544-chr7:113865351..113866074,2	MCF-7	breast:
3	chr3:25304103..25305628-chr3:25307690..25309808,2	K562	blood:
4	chr3:25273667..25275678-chr3:25276657..25278966,2	K562	blood:
5	chr3:25201532..25204868-chr3:25206067..25208834,3	K562	blood:
6	chr3:25200008..25202995-chr3:25206457..25208830,2	MCF-7	breast:
7	chr3:25268545..25270522-chr3:25294614..25297344,2	K562	blood:
8	chr3:25273667..25275678-chr3:25276657..25278966,2	K562	blood:
9	chr3:25304103..25305628-chr3:25307690..25309808,2	K562	blood:
10	chr3:25295460..25296960-chr8:144924480..144925983,2	K562	blood:
11	chr3:25262575..25264631-chr3:25265325..25268274,2	K562	blood:
12	chr3:25262575..25264631-chr3:25265325..25268274,2	K562	blood:
13	chr3:25224245..25226447-chr3:25227786..25229605,2	K562	blood:
14	chr3:25224245..25226447-chr3:25227786..25229605,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RARB-1	chr3:25215610-25215796	ENSG00000237838

No data

Variant related genes	Relation type
RARB	TF binding region
RARB	CpG island

Extended variants
information (count: 3961 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3961 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138057010	chr3:25206166-25206167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs78433279	chr3:25206174-25206175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534660979	chr3:25206195-25206196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372610316	chr3:25206207-25206208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554549708	chr3:25206250-25206251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141628827	chr3:25206255-25206256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187993875	chr3:25206256-25206257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs79481947	chr3:25206277-25206278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577408615	chr3:25206282-25206283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs80223246	chr3:25206289-25206290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553350424	chr3:25206316-25206317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150517626	chr3:25206344-25206345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs367579537	chr3:25206362-25206363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs79938267	chr3:25206382-25206383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560881401	chr3:25206414-25206415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138634967	chr3:25206421-25206422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112430878	chr3:25206468-25206469	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369233953	chr3:25206472-25206473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540042863	chr3:25206506-25206507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532248640	chr3:25206514-25206515	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs74467766	chr3:25206522-25206523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548006125	chr3:25206578-25206579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573327653	chr3:25206579-25206580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs78550012	chr3:25206582-25206583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528393952	chr3:25206583-25206584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74566656	chr3:25206588-25206589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548160451	chr3:25206590-25206591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553492739	chr3:25206637-25206638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537547325	chr3:25206661-25206662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191128478	chr3:25206664-25206665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs59296535	chr3:25206678-25206679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539599525	chr3:25206690-25206691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375095650	chr3:25206712-25206713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553624672	chr3:25206733-25206734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573542326	chr3:25206761-25206762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542574800	chr3:25206770-25206771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149327577	chr3:25206777-25206778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76990455	chr3:25206837-25206838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183765918	chr3:25206845-25206846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs115879447	chr3:25206851-25206852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189319594	chr3:25206852-25206853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs321517	chr3:25206864-25206865	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs73145379	chr3:25206886-25206887	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs146234328	chr3:25206888-25206889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548123972	chr3:25206912-25206913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549704353	chr3:25206945-25206946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139305238	chr3:25206971-25206972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs321518	chr3:25206975-25206976	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs116762997	chr3:25206996-25206997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs181977344	chr3:25207050-25207051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Squamous cell cancer	20885788	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:25194000-25211800	Weak transcription	Aorta	Aorta
2	chr3:25198600-25211200	Weak transcription	Fetal Stomach	stomach
3	chr3:25198800-25207000	Weak transcription	Fetal Lung	lung
4	chr3:25200600-25214600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr3:25205200-25206600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr3:25206600-25211800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr3:25207000-25208000	Enhancers	Fetal Lung	lung
8	chr3:25208000-25215200	Weak transcription	Fetal Lung	lung
9	chr3:25210400-25211200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:25210600-25211000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
11	chr3:25211000-25211600	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr3:25211200-25212000	Enhancers	Fetal Stomach	stomach
13	chr3:25211200-25212600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:25211600-25211800	Enhancers	H1 Cell Line	embryonic stem cell
15	chr3:25211600-25211800	Enhancers	H9 Cell Line	embryonic stem cell
16	chr3:25211600-25213800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr3:25211600-25213800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr3:25211600-25214000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr3:25211800-25212000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr3:25211800-25212000	Enhancers	Aorta	Aorta
21	chr3:25211800-25212200	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr3:25211800-25212600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr3:25211800-25212800	Enhancers	Fetal Muscle Leg	muscle
24	chr3:25211800-25216800	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr3:25212000-25215800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr3:25212200-25212400	Enhancers	H1 Cell Line	embryonic stem cell
27	chr3:25212400-25213000	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr3:25212400-25215800	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr3:25212600-25212800	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr3:25212600-25213000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr3:25212600-25213400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr3:25212600-25213600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr3:25212600-25215600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr3:25212800-25216400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr3:25213000-25213400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr3:25213000-25215600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:25213400-25213600	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr3:25213400-25213800	Enhancers	Brain Anterior Caudate	brain
39	chr3:25213600-25215000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr3:25213600-25218800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr3:25213800-25214800	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr3:25213800-25215200	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr3:25214000-25218000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr3:25214600-25216000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr3:25214800-25215400	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr3:25215000-25217400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr3:25215200-25215400	Enhancers	Fetal Lung	lung
48	chr3:25215200-25215600	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr3:25215600-25215800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr3:25215600-25216800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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