Variant report

Variant	nsv455679
Chromosome Location	chr12:85908396-86024749
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	chr12:85943398-85943797	HepG2	liver:	n/a	n/a
2	ATF2	chr12:85920866-85921402	GM12878	blood:	n/a	n/a
3	BATF	chr12:85929686-85929979	GM12878	blood:	n/a	n/a
4	BHLHE40	chr12:85925172-85925543	GM12878	blood:	n/a	n/a
5	BRCA1	chr12:86019903-86020631	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr12:86020121-86020665	HCT-116	colon:	n/a	n/a
7	CEBPB	chr12:86020007-86020716	HCT-116	colon:	n/a	chr12:86020651-86020662
8	CEBPB	chr12:86019722-86020633	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:85957585-85957738	Hela-S3	cervix:	n/a	chr12:85957676-85957689 chr12:85957676-85957689 chr12:85957676-85957687 chr12:85957676-85957689 chr12:85957676-85957687
10	CEBPB	chr12:86002098-86002319	A549	lung:	n/a	n/a
11	CEBPB	chr12:85981876-85982197	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr12:86021300-86021775	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:85948898-85949146	HepG2	liver:	n/a	chr12:85949046-85949057 chr12:85949018-85949029
14	CEBPB	chr12:85943405-85943769	HepG2	liver:	n/a	n/a
15	CEBPB	chr12:86020158-86020619	A549	lung:	n/a	n/a
16	CEBPB	chr12:85943425-85943748	A549	lung:	n/a	n/a
17	CEBPB	chr12:86002046-86002376	HepG2	liver:	n/a	n/a
18	CEBPB	chr12:86020186-86020596	A549	lung:	n/a	n/a
19	CEBPB	chr12:85916987-85917438	Hela-S3	cervix:	n/a	chr12:85917175-85917188
20	CEBPB	chr12:85966835-85967062	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr12:85942491-85942784	A549	lung:	n/a	n/a
22	CEBPB	chr12:85948894-85949140	A549	lung:	n/a	chr12:85949046-85949057 chr12:85949018-85949029
23	CEBPB	chr12:86019830-86021039	IMR90	lung:	n/a	chr12:86020651-86020662
24	CEBPB	chr12:85981944-85982144	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr12:85978878-85979088	A549	lung:	n/a	chr12:85978973-85978986 chr12:85978973-85978984 chr12:85978975-85978984 chr12:85978974-85978985 chr12:85978973-85978986 chr12:85978975-85978984 chr12:85978975-85978984 chr12:85978973-85978986 chr12:85978975-85978984
26	CEBPB	chr12:85978809-85979116	HepG2	liver:	n/a	chr12:85978973-85978986 chr12:85978973-85978984 chr12:85978975-85978984 chr12:85978974-85978985 chr12:85978973-85978986 chr12:85978975-85978984 chr12:85978975-85978984 chr12:85978973-85978986 chr12:85978975-85978984
27	CEBPB	chr12:86020105-86020665	HCT-116	colon:	n/a	chr12:86020651-86020662
28	CEBPB	chr12:85942503-85942765	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr12:85942408-85942794	A549	lung:	n/a	chr12:85942416-85942428
30	CEBPB	chr12:86021336-86021743	IMR90	lung:	n/a	n/a
31	CEBPB	chr12:85942473-85942800	HepG2	liver:	n/a	n/a
32	CEBPB	chr12:86020204-86020533	A549	lung:	n/a	n/a
33	CHD2	chr12:85925018-85925442	GM12878	blood:	n/a	n/a
34	CHD2	chr12:86020187-86020626	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr12:85926171-85926219	GM12878	blood:	n/a	n/a
36	CREB1	chr12:85929762-85930042	GM12878	blood:	n/a	n/a
37	CTCF	chr12:85969580-85969730	GM12864	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
38	CTCF	chr12:85969516-85969836	K562	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
39	CTCF	chr12:85969100-85969250	GM06990	blood:	n/a	n/a
40	CTCF	chr12:85969520-85969793	ECC-1	luminal epithelium:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
41	CTCF	chr12:85969180-85969330	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr12:85969519-85969813	HepG2	liver:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
43	CTCF	chr12:85969560-85969710	GM12865	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
44	CTCF	chr12:85969516-85969794	MCF-7	breast:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
45	CTCF	chr12:85969600-85969750	GM12867	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
46	CTCF	chr12:85969560-85969710	AG09319	gingival:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
47	CTCF	chr12:85969548-85969782	Pancreas_OC	pancreas:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
48	CTCF	chr12:85969528-85969783	ProgFib	skin:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
49	CTCF	chr12:85969580-85969730	K562	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
50	CTCF	chr12:85969560-85969710	HepG2	liver:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:85945089-85945139	H1-hESC	embryonic stem cell:	embryo
2	chr12:85945089-85945139	SKMC	muscle:	n/a
3	chr12:85945089-85945139	AG04449	skin:	fetal
4	chr12:85945089-85945139	RPTEC	kidney:	n/a
5	chr12:85945089-85945139	HRCEpiC	kidney:	n/a
6	chr12:85945089-85945139	NH-A	brain:	n/a
7	chr12:85945089-85945139	PANC-1	pancreas:	n/a
8	chr12:85945089-85945139	CMK	blood:	n/a
9	chr12:85945089-85945139	GM19239	blood:	n/a
10	chr12:85945089-85945139	MCF10A-Er-Src	breast:	n/a
11	chr12:85945089-85945139	HCPEpiC	choroid plexus:	n/a
12	chr12:85945089-85945139	NHDF-neo	bronchial:	n/a
13	chr12:85945089-85945139	Jurkat	blood:	n/a
14	chr12:85945089-85945139	A549	lung:	n/a
15	chr12:85945089-85945139	K562	blood:	n/a
16	chr12:85945089-85945139	NT2-D1	testis:	n/a
17	chr12:85945089-85945139	AoSMC	blood vessel:	n/a
18	chr12:85945089-85945139	BJ	skin:	n/a
19	chr12:85945089-85945139	HIPEpiC	eye:	n/a
20	chr12:85945089-85945139	HEK293	kidney:	embryo
21	chr12:85945089-85945139	HPAEpiC	pulmonary alveolar:	n/a
22	chr12:85945089-85945139	PFSK-1	brain:	n/a
23	chr12:85945089-85945139	ECC-1	luminal epithelium:	n/a
24	chr12:85945089-85945139	GM12891	blood:	n/a
25	chr12:85945089-85945139	LNCaP	prostate:	n/a
26	chr12:85945089-85945139	GM12878	blood:	n/a
27	chr12:85945089-85945139	AG04450	lung:	fetal
28	chr12:85945089-85945139	MCF-7	breast:	n/a
29	chr12:85945089-85945139	HUVEC	blood vessel:	n/a
30	chr12:85945089-85945139	AG10803	skin:	n/a
31	chr12:85945089-85945139	SAEC	small airway:	n/a
32	chr12:85945089-85945139	HL-60	blood:	n/a
33	chr12:85945089-85945139	Hela-S3	cervix:	n/a
34	chr12:85945089-85945139	HCM	heart:	n/a
35	chr12:85945089-85945139	HNPCEpiC	eye:	n/a
36	chr12:85945089-85945139	Caco-2	colon:	n/a
37	chr12:85945089-85945139	HCF	heart:	n/a
38	chr12:85945089-85945139	HRPEpiC	eye:	n/a
39	chr12:85945089-85945139	IMR90	lung:	fetal
40	chr12:85945089-85945139	T-47D	breast:	n/a
41	chr12:85945089-85945139	ProgFib	skin:	n/a
42	chr12:85945089-85945139	HepG2	liver:	n/a
43	chr12:85945089-85945139	Hepatocyte	liver:	n/a
44	chr12:85945089-85945139	SK-N-SH_RA	brain:	n/a
45	chr12:85945089-85945139	NB4	blood:	n/a
46	chr12:85945089-85945139	ovcar-3	ovarian:	n/a
47	chr12:85945089-85945139	HMEC	breast:	n/a
48	chr12:85945089-85945139	SK-N-MC	brain:	n/a
49	chr12:85945089-85945139	GM12892	blood:	n/a
50	chr12:85945089-85945139	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:85908005..85909863-chr12:85911172..85913825,2	MCF-7	breast:
2	chr12:85940120..85942691-chr12:85944053..85946791,2	MCF-7	breast:
3	chr12:85969213..85970141-chr12:86036344..86037184,4	MCF-7	breast:
4	chr12:86014804..86017595-chr12:86018520..86021053,2	MCF-7	breast:
5	chr12:86002253..86004144-chr12:86006143..86008700,2	MCF-7	breast:
6	chr12:85930199..85932678-chr12:85934950..85937006,2	K562	blood:
7	chr12:85940120..85942691-chr12:85944053..85946791,2	MCF-7	breast:
8	chr12:85908005..85909863-chr12:85911172..85913825,2	MCF-7	breast:
9	chr12:85972333..85972969-chr12:86260657..86261419,2	MCF-7	breast:
10	chr12:86008021..86010789-chr12:86012957..86015625,2	MCF-7	breast:
11	chr12:85972231..85974209-chr12:85975781..85977996,2	MCF-7	breast:
12	chr12:85930199..85932678-chr12:85934950..85937006,2	K562	blood:
13	chr12:85916869..85918658-chr12:85921402..85924342,2	K562	blood:
14	chr12:85905968..85908916-chr17:58676509..58679332,2	MCF-7	breast:
15	chr12:85916869..85918658-chr12:85921402..85924342,2	K562	blood:
16	chr12:85956037..85957820-chr12:85959579..85961160,2	K562	blood:
17	chr12:85972231..85974209-chr12:85975781..85977996,2	MCF-7	breast:
18	chr12:86002253..86004144-chr12:86006143..86008700,2	MCF-7	breast:
19	chr12:85969245..85970171-chr12:86260729..86261622,3	MCF-7	breast:
20	chr12:86008021..86010789-chr12:86012957..86015625,2	MCF-7	breast:
21	chr12:85949711..85951775-chr12:85954587..85956542,2	K562	blood:
22	chr12:85956037..85957820-chr12:85959579..85961160,2	K562	blood:
23	chr12:85949711..85951775-chr12:85954587..85956542,2	K562	blood:
24	chr12:86014804..86017595-chr12:86018520..86021053,2	MCF-7	breast:
25	chr12:85968890..85970646-chr12:86260113..86261752,8	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALX1-2	chr12:85988245-85988373	NONHSAT029750

Variant related genes	Relation type
ENSG00000257855	TF binding region
ENSG00000257855	CpG island
ENSG00000170836	chromatin interactions

Extended variants
information (count: 2813 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2813 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10862989	chr12:85908396-85908397	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551717121	chr12:85908421-85908422	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs114345528	chr12:85908450-85908451	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs80073056	chr12:85908457-85908458	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs146124155	chr12:85908474-85908475	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs376952036	chr12:85908483-85908484	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs140108748	chr12:85908503-85908504	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs142480443	chr12:85908524-85908525	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs11116853	chr12:85908657-85908658	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs570315033	chr12:85908714-85908715	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs190972527	chr12:85908715-85908716	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs558884112	chr12:85908722-85908723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs577198372	chr12:85908727-85908728	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs535104110	chr12:85908739-85908740	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs182405990	chr12:85908764-85908765	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs553234136	chr12:85908766-85908767	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574291348	chr12:85908831-85908832	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs151326037	chr12:85908841-85908842	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs12307956	chr12:85908885-85908886	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs534191444	chr12:85908936-85908937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113989614	chr12:85908967-85908968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76555873	chr12:85908981-85908982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575159471	chr12:85908992-85908993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187852460	chr12:85909024-85909025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368485410	chr12:85909049-85909050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564085766	chr12:85909066-85909067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533546393	chr12:85909149-85909150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528106608	chr12:85909161-85909162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs116655101	chr12:85909175-85909176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561678251	chr12:85909178-85909179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529001813	chr12:85909261-85909262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374315600	chr12:85909275-85909276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs149662998	chr12:85909290-85909291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs78898085	chr12:85909296-85909297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139145799	chr12:85909343-85909344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs552630986	chr12:85909392-85909393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570816245	chr12:85909423-85909424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115970708	chr12:85909425-85909426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530092636	chr12:85909439-85909440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553337275	chr12:85909461-85909462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568178673	chr12:85909617-85909618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376117234	chr12:85909637-85909638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535571558	chr12:85909694-85909695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141248776	chr12:85909798-85909799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539488371	chr12:85909829-85909830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575120954	chr12:85909908-85909909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs78794234	chr12:85909944-85909945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs74112086	chr12:85909987-85909988	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs192380804	chr12:85910023-85910024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539798164	chr12:85910060-85910061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:85903600-85911400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:85908200-85908600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr12:85908600-85908800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr12:85908600-85912400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr12:85909200-85909400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr12:85909400-85912200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr12:85910000-85913000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr12:85910600-85911000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr12:85910600-85911000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr12:85910600-85911000	Enhancers	NHEK	skin
11	chr12:85910600-85911200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
12	chr12:85910800-85911000	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr12:85910800-85911000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr12:85910800-85911200	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr12:85911000-85912200	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr12:85911000-85912400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr12:85911000-85912600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr12:85911200-85912200	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr12:85911200-85912200	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr12:85911200-85912400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr12:85911400-85912800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr12:85912200-85912800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr12:85912200-85913800	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr12:85912200-85913800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr12:85912200-85913800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr12:85912400-85912600	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr12:85912400-85912800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr12:85912400-85913200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr12:85912400-85913200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr12:85912400-85914000	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr12:85912600-85913000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr12:85912600-85913800	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr12:85912800-85913000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr12:85912800-85913200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr12:85913000-85913200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr12:85913000-85913400	Enhancers	H1 Cell Line	embryonic stem cell
37	chr12:85913000-85913400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr12:85913000-85913800	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr12:85913200-85913400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
40	chr12:85913200-85913600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr12:85913400-85913800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr12:85916200-85916800	Enhancers	GM12878-XiMat	blood
43	chr12:85916800-85920200	Weak transcription	GM12878-XiMat	blood
44	chr12:85920200-85920600	Enhancers	GM12878-XiMat	blood
45	chr12:85920400-85921800	Enhancers	Primary B cells from peripheral blood	blood
46	chr12:85920600-85921800	Flanking Active TSS	GM12878-XiMat	blood
47	chr12:85920800-85921600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr12:85920800-85921600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr12:85920800-85922400	Enhancers	Primary hematopoietic stem cells	blood
50	chr12:85921000-85921600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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