Variant report

Variant	nsv1050959
Chromosome Location	chr12:85941487-85999874
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	CEBPB	chr12:85957585-85957738	Hela-S3	cervix:	n/a	chr12:85957676-85957689 chr12:85957676-85957689 chr12:85957676-85957687 chr12:85957676-85957689 chr12:85957676-85957687
3	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
4	CEBPB	chr12:85948894-85949140	A549	lung:	n/a	chr12:85949046-85949057 chr12:85949018-85949029
5	CEBPB	chr12:85981876-85982197	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr12:85942473-85942800	HepG2	liver:	n/a	n/a
7	CEBPB	chr12:85943405-85943769	HepG2	liver:	n/a	n/a
8	CEBPB	chr12:85966835-85967062	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:85948898-85949146	HepG2	liver:	n/a	chr12:85949046-85949057 chr12:85949018-85949029
10	CEBPB	chr12:85942491-85942784	A549	lung:	n/a	n/a
11	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
12	CEBPB	chr12:85981944-85982144	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr12:85943425-85943748	A549	lung:	n/a	n/a
14	CEBPB	chr12:85942503-85942765	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr12:85942408-85942794	A549	lung:	n/a	chr12:85942416-85942428
16	CTCF	chr12:85969180-85969330	HPAF	blood vessel:	n/a	n/a
17	CTCF	chr12:85969580-85969730	HBMEC	blood vessel:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
18	CTCF	chr12:85969541-85969759	GM10266	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
19	CTCF	chr12:85969600-85969750	GM12869	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
20	CTCF	chr12:85969600-85969750	GM12874	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
21	CTCF	chr12:85969560-85969710	HEK293	kidney:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
22	CTCF	chr12:85969600-85969750	AG04449	skin:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
23	CTCF	chr12:85969520-85969670	K562	blood:	n/a	n/a
24	CTCF	chr12:85969560-85969710	NHEK	skin:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
25	CTCF	chr12:85969560-85969710	HL-60	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
26	CTCF	chr12:85969620-85969770	HRPEpiC	eye:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
27	CTCF	chr12:85969640-85969790	HAc	cerebellar:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
28	CTCF	chr12:85969601-85969742	MCF-7	breast:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
29	CTCF	chr12:85969020-85969170	HVMF	connective:	n/a	n/a
30	CTCF	chr12:85969530-85969788	A549	lung:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
31	CTCF	chr12:85969560-85969823	A549	lung:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
32	CTCF	chr12:85969580-85969730	HAc	cerebellar:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
33	CTCF	chr12:85969200-85969350	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr12:85969540-85969690	HVMF	connective:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
35	CTCF	chr12:85969351-85969893	GM12878	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
36	CTCF	chr12:85969560-85969710	HA-sp	spinal cord:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
37	CTCF	chr12:85969580-85969730	RPTEC	kidney:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
38	CTCF	chr12:85969532-85969780	Fibrobl	skin:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
39	CTCF	chr12:85969543-85969785	Spleen_OC	spleen:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
40	CTCF	chr12:85969620-85969770	AG09319	gingival:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
41	CTCF	chr12:85960200-85960350	HFF	foreskin:	n/a	n/a
42	CTCF	chr12:85969496-85969835	T-47D	breast:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
43	CTCF	chr12:85969560-85969710	HRPEpiC	eye:	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	chr12:85980356-85980428	GM13977	blood:	n/a	n/a
46	CTCF	chr12:85969445-85970048	HCT-116	colon:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
47	CTCF	chr12:85969560-85969710	GM12801	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
48	CTCF	chr12:85969620-85969770	GM12870	blood:	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	AG09319	gingival:	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	ovcar-3	ovarian:	n/a
2	chr12:85945089-85945139	HCF	heart:	n/a
3	chr12:85945089-85945139	Hela-S3	cervix:	n/a
4	chr12:85945089-85945139	ECC-1	luminal epithelium:	n/a
5	chr12:85945089-85945139	SK-N-SH_RA	brain:	n/a
6	chr12:85945089-85945139	PrEC	prostate:	n/a
7	chr12:85945089-85945139	ProgFib	skin:	n/a
8	chr12:85945089-85945139	AoSMC	blood vessel:	n/a
9	chr12:85945089-85945139	HRE	kidney:	n/a
10	chr12:85945089-85945139	BE2_C	brain:	n/a
11	chr12:85945089-85945139	A549	lung:	n/a
12	chr12:85945089-85945139	Caco-2	colon:	n/a
13	chr12:85945089-85945139	NT2-D1	testis:	n/a
14	chr12:85945089-85945139	HEEpiC	esophagus:	n/a
15	chr12:85945089-85945139	HIPEpiC	eye:	n/a
16	chr12:85945089-85945139	HL-60	blood:	n/a
17	chr12:85945089-85945139	T-47D	breast:	n/a
18	chr12:85945089-85945139	AG09309	skin:	n/a
19	chr12:85945089-85945139	SAEC	small airway:	n/a
20	chr12:85945089-85945139	RPTEC	kidney:	n/a
21	chr12:85945089-85945139	GM12892	blood:	n/a
22	chr12:85945089-85945139	AG04449	skin:	fetal
23	chr12:85945089-85945139	HepG2	liver:	n/a
24	chr12:85945089-85945139	GM12891	blood:	n/a
25	chr12:85945089-85945139	GM12878	blood:	n/a
26	chr12:85945089-85945139	CMK	blood:	n/a
27	chr12:85945089-85945139	AG10803	skin:	n/a
28	chr12:85945089-85945139	HCT-116	colon:	n/a
29	chr12:85945089-85945139	BJ	skin:	n/a
30	chr12:85945089-85945139	HRCEpiC	kidney:	n/a
31	chr12:85945089-85945139	HRPEpiC	eye:	n/a
32	chr12:85945089-85945139	U87	brain:	n/a
33	chr12:85945089-85945139	HCM	heart:	n/a
34	chr12:85945089-85945139	IMR90	lung:	fetal
35	chr12:85945089-85945139	GM06990	blood:	n/a
36	chr12:85945089-85945139	SK-N-SH	brain:	n/a
37	chr12:85945089-85945139	Hepatocyte	liver:	n/a
38	chr12:85945089-85945139	NHDF-neo	bronchial:	n/a
39	chr12:85945089-85945139	HMEC	breast:	n/a
40	chr12:85945089-85945139	K562	blood:	n/a
41	chr12:85945089-85945139	MCF-7	breast:	n/a
42	chr12:85945089-85945139	SK-N-MC	brain:	n/a
43	chr12:85945089-85945139	LNCaP	prostate:	n/a
44	chr12:85945089-85945139	PANC-1	pancreas:	n/a
45	chr12:85945089-85945139	HPAEpiC	pulmonary alveolar:	n/a
46	chr12:85945089-85945139	Jurkat	blood:	n/a
47	chr12:85945089-85945139	NB4	blood:	n/a
48	chr12:85945089-85945139	NHBE	bronchial:	n/a
49	chr12:85945089-85945139	H1-hESC	embryonic stem cell:	embryo
50	chr12:85945089-85945139	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:85968890..85970646-chr12:86260113..86261752,8	MCF-7	breast:
2	chr12:85940120..85942691-chr12:85944053..85946791,2	MCF-7	breast:
3	chr12:85949711..85951775-chr12:85954587..85956542,2	K562	blood:
4	chr12:85972231..85974209-chr12:85975781..85977996,2	MCF-7	breast:
5	chr12:85956037..85957820-chr12:85959579..85961160,2	K562	blood:
6	chr12:85972231..85974209-chr12:85975781..85977996,2	MCF-7	breast:
7	chr12:85956037..85957820-chr12:85959579..85961160,2	K562	blood:
8	chr12:85969213..85970141-chr12:86036344..86037184,4	MCF-7	breast:
9	chr12:85940120..85942691-chr12:85944053..85946791,2	MCF-7	breast:
10	chr12:85949711..85951775-chr12:85954587..85956542,2	K562	blood:
11	chr12:85972333..85972969-chr12:86260657..86261419,2	MCF-7	breast:
12	chr12:85969245..85970171-chr12:86260729..86261622,3	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

Extended variants
information (count: 1479 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1479 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11116873	chr12:85941487-85941488	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535783115	chr12:85941495-85941496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556931558	chr12:85941567-85941568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563755649	chr12:85941580-85941581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs75135948	chr12:85941581-85941582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530157173	chr12:85941621-85941622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546186127	chr12:85941630-85941631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557937141	chr12:85941644-85941645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573309572	chr12:85941659-85941660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs540407804	chr12:85941680-85941681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568847770	chr12:85941703-85941704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529194572	chr12:85941739-85941740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182467176	chr12:85941780-85941781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562805872	chr12:85941816-85941817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs34575353	chr12:85941991-85941992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187103060	chr12:85942015-85942016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191257526	chr12:85942016-85942017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs73367251	chr12:85942047-85942048	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs115329897	chr12:85942057-85942058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546778261	chr12:85942076-85942077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561111454	chr12:85942085-85942086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568360487	chr12:85942156-85942157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs10779167	chr12:85942177-85942178	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs557191087	chr12:85942203-85942204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs7485590	chr12:85942225-85942226	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs115754020	chr12:85942231-85942232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558159818	chr12:85942237-85942238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs534097700	chr12:85942315-85942316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558426625	chr12:85942330-85942331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs183762657	chr12:85942349-85942350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs77243753	chr12:85942397-85942398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs144342550	chr12:85942424-85942425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577010270	chr12:85942428-85942429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544378022	chr12:85942464-85942465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556269075	chr12:85942478-85942479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78308203	chr12:85942498-85942499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574478496	chr12:85942532-85942533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541789791	chr12:85942588-85942589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs151123144	chr12:85942594-85942595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189205296	chr12:85942616-85942617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs566677360	chr12:85942626-85942627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs142865377	chr12:85942630-85942631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560137917	chr12:85942647-85942648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs111625845	chr12:85942701-85942702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs12814689	chr12:85942705-85942706	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs560132361	chr12:85942737-85942738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143296600	chr12:85942743-85942744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs527379577	chr12:85942749-85942750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74112227	chr12:85942753-85942754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548618487	chr12:85942860-85942861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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	21293372	CNVD

Chromatin state (count:149 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:85938800-85943800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr12:85939000-85944000	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr12:85939000-85944200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr12:85939000-85944200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:85939200-85943600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr12:85939200-85944800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr12:85939400-85943800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr12:85939600-85942400	Weak transcription	Fetal Intestine Small	intestine
9	chr12:85940400-85942000	Weak transcription	Fetal Intestine Large	intestine
10	chr12:85942000-85945600	Enhancers	Fetal Intestine Large	intestine
11	chr12:85942400-85942600	Enhancers	Duodenum Mucosa	Duodenum
12	chr12:85942400-85945600	Enhancers	Fetal Intestine Small	intestine
13	chr12:85942600-85943600	Weak transcription	Duodenum Mucosa	Duodenum
14	chr12:85943600-85943800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr12:85943600-85944800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr12:85943600-85945400	Enhancers	Duodenum Mucosa	Duodenum
17	chr12:85943600-85947000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr12:85943800-85944600	Enhancers	H9 Cell Line	embryonic stem cell
19	chr12:85943800-85944600	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr12:85943800-85944800	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr12:85943800-85945200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr12:85943800-85946800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr12:85943800-85947000	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr12:85944000-85947000	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr12:85944200-85947000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr12:85944200-85947000	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr12:85944200-85947000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:85944400-85945200	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr12:85944600-85945000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr12:85944600-85945200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr12:85944800-85945400	Enhancers	H1 Cell Line	embryonic stem cell
32	chr12:85944800-85946400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr12:85945200-85946200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr12:85945200-85947000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr12:85945400-85946800	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr12:85945400-85952200	Weak transcription	Duodenum Mucosa	Duodenum
37	chr12:85946200-85946400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr12:85946400-85946600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr12:85946400-85946800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr12:85946800-85947000	Enhancers	H1 Cell Line	embryonic stem cell
41	chr12:85952200-85952600	Enhancers	Duodenum Mucosa	Duodenum
42	chr12:85952200-85952800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr12:85952400-85952800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr12:85952400-85952800	Enhancers	Fetal Intestine Small	intestine
45	chr12:85952600-85953000	Enhancers	Osteobl	bone
46	chr12:85952800-85953000	Weak transcription	Fetal Intestine Small	intestine
47	chr12:85952800-85953400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr12:85953000-85953400	Enhancers	Fetal Intestine Small	intestine
49	chr12:85953400-85954000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr12:85954000-85955400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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