Variant report

Variant	nsv876930
Chromosome Location	chr3:68844213-68961010
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	ARID3A	chr3:68925289-68925627	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:68942935-68943109	K562	blood:	n/a	chr3:68943078-68943094
3	BACH1	chr3:68910069-68910337	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr3:68932592-68932613	GM12878	blood:	n/a	n/a
5	BRCA1	chr3:68915390-68915620	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr3:68940433-68940716	H1-hESC	embryonic stem cell:	n/a	chr3:68940436-68940447 chr3:68940552-68940563 chr3:68940552-68940565
7	CEBPB	chr3:68851229-68851424	HepG2	liver:	n/a	chr3:68851285-68851298 chr3:68851286-68851297
8	CEBPB	chr3:68900744-68900944	HepG2	liver:	n/a	chr3:68900823-68900836 chr3:68900823-68900836 chr3:68900825-68900834 chr3:68900823-68900834 chr3:68900825-68900836
9	CEBPB	chr3:68940514-68940708	HepG2	liver:	n/a	chr3:68940552-68940563 chr3:68940552-68940565
10	CEBPB	chr3:68952840-68953265	HepG2	liver:	n/a	chr3:68953134-68953147 chr3:68953135-68953146
11	CEBPB	chr3:68939993-68940250	HepG2	liver:	n/a	chr3:68940076-68940089 chr3:68940076-68940087
12	CEBPB	chr3:68952844-68953221	A549	lung:	n/a	chr3:68953134-68953147 chr3:68953135-68953146
13	CEBPB	chr3:68952832-68953256	IMR90	lung:	n/a	chr3:68953134-68953147 chr3:68953135-68953146
14	CEBPB	chr3:68921692-68922073	HepG2	liver:	n/a	n/a
15	CTCF	chr3:68927620-68927770	HFF-Myc	foreskin:	n/a	chr3:68927663-68927681 chr3:68927658-68927679
16	CTCF	chr3:68942860-68943010	SAEC	small airway:	n/a	chr3:68942972-68942993 chr3:68942977-68942995
17	CTCF	chr3:68915464-68915571	NHEK	skin:	n/a	n/a
18	CTCF	chr3:68925380-68925530	HFF-Myc	foreskin:	n/a	chr3:68925447-68925468
19	CTCF	chr3:68925380-68925530	SAEC	small airway:	n/a	chr3:68925447-68925468
20	CTCF	chr3:68925360-68925510	NHLF	lung:	n/a	chr3:68925447-68925468
21	CTCF	chr3:68927395-68927894	HCT-116	colon:	n/a	chr3:68927663-68927681 chr3:68927658-68927679
22	CTCF	chr3:68942780-68942930	RPTEC	kidney:	n/a	n/a
23	CTCF	chr3:68925320-68925470	WI-38	lung:	n/a	chr3:68925447-68925468
24	CTCF	chr3:68927580-68927730	RPTEC	kidney:	n/a	chr3:68927663-68927681 chr3:68927658-68927679
25	CTCF	chr3:68927568-68927804	MCF-7	breast:	n/a	chr3:68927663-68927681 chr3:68927658-68927679
26	CTCF	chr3:68942940-68943090	AG10803	skin:	n/a	chr3:68942972-68942993 chr3:68942977-68942995
27	CTCF	chr3:68942778-68943068	HepG2	liver:	n/a	chr3:68942972-68942993 chr3:68942977-68942995
28	CTCF	chr3:68943040-68943190	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr3:68925225-68925641	HepG2	liver:	n/a	chr3:68925447-68925468
30	CTCF	chr3:68927620-68927770	WI-38	lung:	n/a	chr3:68927663-68927681 chr3:68927658-68927679
31	CTCF	chr3:68942820-68942970	RPTEC	kidney:	n/a	n/a
32	CTCF	chr3:68927600-68927750	HVMF	connective:	n/a	chr3:68927663-68927681 chr3:68927658-68927679
33	CTCF	chr3:68927580-68927730	WERI-Rb-1	eye:	n/a	chr3:68927663-68927681 chr3:68927658-68927679
34	CTCF	chr3:68927620-68927770	NHEK	skin:	n/a	chr3:68927663-68927681 chr3:68927658-68927679
35	CTCF	chr3:68925360-68925510	HMF	breast:	n/a	chr3:68925447-68925468
36	CTCF	chr3:68942900-68943050	HA-sp	spinal cord:	n/a	chr3:68942972-68942993 chr3:68942977-68942995
37	CTCF	chr3:68925400-68925550	AG04449	skin:	n/a	chr3:68925447-68925468
38	CTCF	chr3:68942847-68943102	HUVEC	blood vessel:	n/a	chr3:68942972-68942993 chr3:68942977-68942995
39	CTCF	chr3:68942880-68943030	HEEpiC	esophagus:	n/a	chr3:68942972-68942993 chr3:68942977-68942995
40	CTCF	chr3:68925380-68925530	HRE	kidney:	n/a	chr3:68925447-68925468
41	CTCF	chr3:68927601-68927768	A549	lung:	n/a	chr3:68927663-68927681 chr3:68927658-68927679
42	CTCF	chr3:68942840-68942990	GM12865	blood:	n/a	n/a
43	CTCF	chr3:68927620-68927770	SK-N-SH_RA	brain:	n/a	chr3:68927663-68927681 chr3:68927658-68927679
44	CTCF	chr3:68925310-68925531	ECC-1	luminal epithelium:	n/a	chr3:68925447-68925468
45	CTCF	chr3:68927600-68927750	HMF	breast:	n/a	chr3:68927663-68927681 chr3:68927658-68927679
46	CTCF	chr3:68927587-68927785	K562	blood:	n/a	chr3:68927663-68927681 chr3:68927658-68927679
47	CTCF	chr3:68925380-68925530	HPAF	blood vessel:	n/a	chr3:68925447-68925468
48	CTCF	chr3:68927560-68927710	NHLF	lung:	n/a	chr3:68927663-68927681 chr3:68927658-68927679
49	CTCF	chr3:68942860-68943010	GM12872	blood:	n/a	chr3:68942972-68942993 chr3:68942977-68942995
50	CTCF	chr3:68925340-68925490	HMEC	breast:	n/a	chr3:68925447-68925468

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:68925535-68925585	Hepatocyte	liver:	n/a
2	chr3:68938451-68938501	MCF10A-Er-Src	breast:	n/a
3	chr3:68925535-68925585	HEK293	kidney:	embryo
4	chr3:68925535-68925585	HepG2	liver:	n/a
5	chr3:68938451-68938501	HUVEC	blood vessel:	n/a
6	chr3:68925535-68925585	HNPCEpiC	eye:	n/a
7	chr3:68925535-68925585	HCPEpiC	choroid plexus:	n/a
8	chr3:68925535-68925585	RPTEC	kidney:	n/a
9	chr3:68925535-68925585	AoSMC	blood vessel:	n/a
10	chr3:68938451-68938501	SKMC	muscle:	n/a
11	chr3:68925535-68925585	HIPEpiC	eye:	n/a
12	chr3:68938451-68938501	AG10803	skin:	n/a
13	chr3:68938451-68938501	HepG2	liver:	n/a
14	chr3:68938451-68938501	HRCEpiC	kidney:	n/a
15	chr3:68938451-68938501	GM12878	blood:	n/a
16	chr3:68938451-68938501	GM12892	blood:	n/a
17	chr3:68925535-68925585	NHBE	bronchial:	n/a
18	chr3:68938451-68938501	AG04450	lung:	fetal
19	chr3:68925535-68925585	Caco-2	colon:	n/a
20	chr3:68938451-68938501	HRPEpiC	eye:	n/a
21	chr3:68938451-68938501	T-47D	breast:	n/a
22	chr3:68938451-68938501	HPAEpiC	pulmonary alveolar:	n/a
23	chr3:68925535-68925585	SK-N-SH_RA	brain:	n/a
24	chr3:68938451-68938501	GM12891	blood:	n/a
25	chr3:68925535-68925585	HL-60	blood:	n/a
26	chr3:68925535-68925585	HAEpiC	amniotic membrane:	n/a
27	chr3:68938451-68938501	NHDF-neo	bronchial:	n/a
28	chr3:68938451-68938501	HNPCEpiC	eye:	n/a
29	chr3:68938451-68938501	GM19239	blood:	n/a
30	chr3:68925535-68925585	AG04450	lung:	fetal
31	chr3:68925535-68925585	AG04449	skin:	fetal
32	chr3:68938451-68938501	Hela-S3	cervix:	n/a
33	chr3:68925535-68925585	MCF10A-Er-Src	breast:	n/a
34	chr3:68938451-68938501	HAEpiC	amniotic membrane:	n/a
35	chr3:68938451-68938501	Caco-2	colon:	n/a
36	chr3:68938451-68938501	HCF	heart:	n/a
37	chr3:68938451-68938501	NT2-D1	testis:	n/a
38	chr3:68925535-68925585	PrEC	prostate:	n/a
39	chr3:68925535-68925585	U87	brain:	n/a
40	chr3:68925535-68925585	SK-N-MC	brain:	n/a
41	chr3:68938451-68938501	SK-N-SH_RA	brain:	n/a
42	chr3:68925535-68925585	LNCaP	prostate:	n/a
43	chr3:68925535-68925585	AG09309	skin:	n/a
44	chr3:68925535-68925585	HPAEpiC	pulmonary alveolar:	n/a
45	chr3:68925535-68925585	AG10803	skin:	n/a
46	chr3:68938451-68938501	BE2_C	brain:	n/a
47	chr3:68938451-68938501	Hepatocyte	liver:	n/a
48	chr3:68938451-68938501	ProgFib	skin:	n/a
49	chr3:68925535-68925585	GM19239	blood:	n/a
50	chr3:68938451-68938501	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:66988494..66989399-chr3:68925421..68925952,2	K562	blood:
2	chr3:68940824..68942525-chr3:69056629..69058801,2	K562	blood:
3	chr3:68927239..68928502-chr3:69021583..69022148,4	MCF-7	breast:
4	chr3:67022337..67023183-chr3:68925421..68925921,2	K562	blood:
5	chr3:68942591..68943252-chr3:69021152..69021724,2	K562	blood:
6	chr3:67159823..67160870-chr3:68924556..68925868,3	MCF-7	breast:
7	chr3:68954906..68957314-chr3:68959873..68962850,2	K562	blood:
8	chr3:67159850..67160749-chr3:68927123..68927995,3	MCF-7	breast:
9	chr3:67869561..67870138-chr3:68927224..68928400,3	MCF-7	breast:
10	chr3:68927346..68928063-chr4:97807302..97808145,2	MCF-7	breast:
11	chr3:66988749..66989610-chr3:68927193..68927742,2	K562	blood:
12	chr3:67952201..67952773-chr3:68925063..68925992,2	MCF-7	breast:
13	chr3:68954906..68957314-chr3:68959873..68962850,2	K562	blood:

Variant related genes	Relation type
RNA5SP135	TF binding region
RNA5SP135	CpG island
ENSG00000163378	chromatin interactions

Extended variants
information (count: 1773 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1773 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1873264	chr3:68844213-68844214	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565326862	chr3:68844239-68844240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530657466	chr3:68844278-68844279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544302672	chr3:68844334-68844335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541747663	chr3:68844351-68844352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112099642	chr3:68844355-68844356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529680443	chr3:68844372-68844373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141592598	chr3:68844382-68844383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566713319	chr3:68844394-68844395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186825899	chr3:68844395-68844396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147033747	chr3:68844400-68844401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568698598	chr3:68844428-68844429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368116381	chr3:68844468-68844469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537179882	chr3:68844472-68844473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556999084	chr3:68844491-68844492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567329061	chr3:68844522-68844523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79102323	chr3:68844569-68844570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553087054	chr3:68844571-68844572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377473991	chr3:68844630-68844631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113934811	chr3:68844645-68844646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575181648	chr3:68844719-68844720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545739019	chr3:68844741-68844742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1489998	chr3:68844752-68844753	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs544341435	chr3:68844789-68844790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373510935	chr3:68844794-68844795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74823032	chr3:68844796-68844797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540271235	chr3:68844811-68844812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547877521	chr3:68844812-68844813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559886644	chr3:68844841-68844842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs13321204	chr3:68844861-68844862	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs13320444	chr3:68844865-68844866	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs138253674	chr3:68844898-68844899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531360393	chr3:68844918-68844919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550661430	chr3:68844926-68844927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183150765	chr3:68844947-68844948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75273213	chr3:68844999-68845000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539331723	chr3:68845011-68845012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549981657	chr3:68845029-68845030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553365867	chr3:68845032-68845033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142638749	chr3:68845045-68845046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs386662042	chr3:68845047-68845048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113489998	chr3:68845048-68845049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200876552	chr3:68845054-68845055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs150263290	chr3:68845083-68845084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs544770513	chr3:68845089-68845090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6804313	chr3:68845091-68845092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs1387730	chr3:68845092-68845093	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs138899673	chr3:68845097-68845098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560124499	chr3:68845105-68845106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs72925150	chr3:68845120-68845121	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	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
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	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
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	21509527	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Prostate cancer	17217626	CNVD
Urothelial cell carcinoma	18451213	CNVD
Alzheimer''s disease	22166940	CNVD
Mental retardation	20848658	CNVD
Breast cancer	17142309	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:68843800-68845000	Weak transcription	Fetal Brain Male	brain
2	chr3:68844200-68846600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr3:68845000-68845400	Enhancers	Fetal Brain Male	brain
4	chr3:68850600-68852800	Enhancers	Fetal Brain Male	brain
5	chr3:68850800-68851000	Enhancers	Fetal Brain Female	brain
6	chr3:68851000-68851800	Weak transcription	Fetal Brain Female	brain
7	chr3:68851800-68852600	Enhancers	Stomach Smooth Muscle	stomach
8	chr3:68851800-68852800	Enhancers	Fetal Brain Female	brain
9	chr3:68852000-68852800	Enhancers	Brain Angular Gyrus	brain
10	chr3:68856000-68856400	Enhancers	Brain Substantia Nigra	brain
11	chr3:68859000-68859800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr3:68859400-68859600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr3:68859400-68860000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
14	chr3:68866000-68866400	Enhancers	HUVEC	blood vessel
15	chr3:68866400-68868200	Weak transcription	HUVEC	blood vessel
16	chr3:68867200-68872800	Weak transcription	Aorta	Aorta
17	chr3:68868200-68868400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr3:68868200-68868400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr3:68868200-68868600	Enhancers	H9 Cell Line	embryonic stem cell
20	chr3:68868200-68869000	Enhancers	HUVEC	blood vessel
21	chr3:68868400-68869400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr3:68868600-68869000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:68868600-68869200	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr3:68868600-68869400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr3:68869000-68869200	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr3:68869000-68869800	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr3:68869400-68869800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr3:68871600-68871800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr3:68875000-68875200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr3:68875400-68882000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr3:68881600-68882200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr3:68882000-68882200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr3:68882000-68882200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr3:68882000-68882200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr3:68882000-68882200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr3:68882000-68882200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr3:68882000-68882400	Enhancers	Gastric	stomach
38	chr3:68887800-68888000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr3:68889000-68889400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr3:68904600-68905400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr3:68904600-68905400	Enhancers	HMEC	breast
42	chr3:68904800-68905200	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr3:68910200-68912000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr3:68910800-68911200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr3:68924000-68924200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
46	chr3:68925200-68925400	Enhancers	Colon Smooth Muscle	Colon
47	chr3:68925200-68925400	Enhancers	Fetal Kidney	kidney
48	chr3:68925400-68933600	Weak transcription	Colon Smooth Muscle	Colon
49	chr3:68926800-68930200	Active TSS	Stomach Smooth Muscle	stomach
50	chr3:68927600-68928200	Enhancers	HUES48 Cell Line	embryonic stem cell

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