Variant report

Variant	nsv1043663
Chromosome Location	chr12:85934317-85999874
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	chr12:85978809-85979116	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
3	CEBPB	chr12:85957585-85957738	Hela-S3	cervix:	n/a	chr12:85957676-85957689 chr12:85957676-85957689 chr12:85957676-85957687 chr12:85957676-85957689 chr12:85957676-85957687
4	CEBPB	chr12:85942503-85942765	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr12:85942473-85942800	HepG2	liver:	n/a	n/a
6	CEBPB	chr12:85942408-85942794	A549	lung:	n/a	chr12:85942416-85942428
7	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
8	CEBPB	chr12:85943405-85943769	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:85948898-85949146	HepG2	liver:	n/a	chr12:85949046-85949057 chr12:85949018-85949029
10	CEBPB	chr12:85943425-85943748	A549	lung:	n/a	n/a
11	CEBPB	chr12:85981876-85982197	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr12:85942491-85942784	A549	lung:	n/a	n/a
13	CEBPB	chr12:85966835-85967062	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr12:85948894-85949140	A549	lung:	n/a	chr12:85949046-85949057 chr12:85949018-85949029
15	CEBPB	chr12:85981944-85982144	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr12:85969580-85969730	Hela-S3	cervix:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
17	CTCF	chr12:85969580-85969730	HPF	lung:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
18	CTCF	chr12:85969516-85969836	K562	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
19	CTCF	chr12:85969220-85969370	HEK293	kidney:	n/a	n/a
20	CTCF	chr12:85969520-85969793	ECC-1	luminal epithelium:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
21	CTCF	chr12:85969560-85969710	GM12872	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
22	CTCF	chr12:85969497-85969847	ECC-1	luminal epithelium:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
23	CTCF	chr12:85969600-85969750	HMEC	breast:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
24	CTCF	chr12:85969302-85969343	GM12892	blood:	n/a	n/a
25	CTCF	chr12:85969600-85969750	HPF	lung:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
26	CTCF	chr12:85980356-85980428	GM13977	blood:	n/a	n/a
27	CTCF	chr12:85969532-85969780	Fibrobl	skin:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
28	CTCF	chr12:85969543-85969780	LNCaP	prostate:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
29	CTCF	chr12:85969560-85969710	HEK293	kidney:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
30	CTCF	chr12:85960200-85960350	HFF	foreskin:	n/a	n/a
31	CTCF	chr12:85969580-85969730	HPAF	blood vessel:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
32	CTCF	chr12:85969508-85969804	Gliobla	brain:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
33	CTCF	chr12:85969580-85969730	HVMF	connective:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
34	CTCF	chr12:85969517-85969816	Medullo	brain:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
35	CTCF	chr12:85969600-85969750	Caco-2	colon:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
36	CTCF	chr12:85969519-85969813	HepG2	liver:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
37	CTCF	chr12:85969312-85969401	ProgFib	skin:	n/a	n/a
38	CTCF	chr12:85969620-85969770	AG09319	gingival:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
39	CTCF	chr12:85969520-85969670	GM12878	blood:	n/a	n/a
40	CTCF	chr12:85969560-85969710	HA-sp	spinal cord:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
41	CTCF	chr12:85969560-85969710	HRPEpiC	eye:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
42	CTCF	chr12:85969200-85969350	NB4	blood:	n/a	n/a
43	CTCF	chr12:85969540-85969690	HRE	kidney:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
44	CTCF	chr12:85969600-85969750	HEEpiC	esophagus:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
45	CTCF	chr12:85969600-85969750	HBMEC	blood vessel:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
46	CTCF	chr12:85969541-85969728	A549	lung:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
47	CTCF	chr12:85969620-85969770	GM12869	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
48	CTCF	chr12:85969560-85969710	SK-N-SH_RA	brain:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
49	CTCF	chr12:85969580-85969730	GM12864	blood:	n/a	chr12:85969661-85969677 chr12:85969663-85969676 chr12:85969660-85969678 chr12:85969662-85969683
50	CTCF	chr12:85969602-85969743	MCF-7	breast:	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	HepG2	liver:	n/a
2	chr12:85945089-85945139	Hepatocyte	liver:	n/a
3	chr12:85945089-85945139	PFSK-1	brain:	n/a
4	chr12:85945089-85945139	HCT-116	colon:	n/a
5	chr12:85945089-85945139	GM12892	blood:	n/a
6	chr12:85945089-85945139	MCF10A-Er-Src	breast:	n/a
7	chr12:85945089-85945139	HEK293	kidney:	embryo
8	chr12:85945089-85945139	Jurkat	blood:	n/a
9	chr12:85945089-85945139	Caco-2	colon:	n/a
10	chr12:85945089-85945139	BE2_C	brain:	n/a
11	chr12:85945089-85945139	SK-N-SH	brain:	n/a
12	chr12:85945089-85945139	HIPEpiC	eye:	n/a
13	chr12:85945089-85945139	Hela-S3	cervix:	n/a
14	chr12:85945089-85945139	HL-60	blood:	n/a
15	chr12:85945089-85945139	MCF-7	breast:	n/a
16	chr12:85945089-85945139	LNCaP	prostate:	n/a
17	chr12:85945089-85945139	NB4	blood:	n/a
18	chr12:85945089-85945139	U87	brain:	n/a
19	chr12:85945089-85945139	HMEC	breast:	n/a
20	chr12:85945089-85945139	SK-N-SH_RA	brain:	n/a
21	chr12:85945089-85945139	GM06990	blood:	n/a
22	chr12:85945089-85945139	GM12891	blood:	n/a
23	chr12:85945089-85945139	IMR90	lung:	fetal
24	chr12:85945089-85945139	AG04449	skin:	fetal
25	chr12:85945089-85945139	ProgFib	skin:	n/a
26	chr12:85945089-85945139	HRE	kidney:	n/a
27	chr12:85945089-85945139	RPTEC	kidney:	n/a
28	chr12:85945089-85945139	AG10803	skin:	n/a
29	chr12:85945089-85945139	HUVEC	blood vessel:	n/a
30	chr12:85945089-85945139	HPAEpiC	pulmonary alveolar:	n/a
31	chr12:85945089-85945139	CMK	blood:	n/a
32	chr12:85945089-85945139	T-47D	breast:	n/a
33	chr12:85945089-85945139	NH-A	brain:	n/a
34	chr12:85945089-85945139	HAEpiC	amniotic membrane:	n/a
35	chr12:85945089-85945139	AG04450	lung:	fetal
36	chr12:85945089-85945139	HNPCEpiC	eye:	n/a
37	chr12:85945089-85945139	GM19239	blood:	n/a
38	chr12:85945089-85945139	HCM	heart:	n/a
39	chr12:85945089-85945139	ovcar-3	ovarian:	n/a
40	chr12:85945089-85945139	GM12878	blood:	n/a
41	chr12:85945089-85945139	SK-N-MC	brain:	n/a
42	chr12:85945089-85945139	NHBE	bronchial:	n/a
43	chr12:85945089-85945139	AG09319	gingival:	n/a
44	chr12:85945089-85945139	ECC-1	luminal epithelium:	n/a
45	chr12:85945089-85945139	NHDF-neo	bronchial:	n/a
46	chr12:85945089-85945139	HRPEpiC	eye:	n/a
47	chr12:85945089-85945139	PANC-1	pancreas:	n/a
48	chr12:85945089-85945139	HCPEpiC	choroid plexus:	n/a
49	chr12:85945089-85945139	A549	lung:	n/a
50	chr12:85945089-85945139	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:85956037..85957820-chr12:85959579..85961160,2	K562	blood:
2	chr12:85972231..85974209-chr12:85975781..85977996,2	MCF-7	breast:
3	chr12:85940120..85942691-chr12:85944053..85946791,2	MCF-7	breast:
4	chr12:85972231..85974209-chr12:85975781..85977996,2	MCF-7	breast:
5	chr12:85968890..85970646-chr12:86260113..86261752,8	MCF-7	breast:
6	chr12:85956037..85957820-chr12:85959579..85961160,2	K562	blood:
7	chr12:85949711..85951775-chr12:85954587..85956542,2	K562	blood:
8	chr12:85972333..85972969-chr12:86260657..86261419,2	MCF-7	breast:
9	chr12:85949711..85951775-chr12:85954587..85956542,2	K562	blood:
10	chr12:85969245..85970171-chr12:86260729..86261622,3	MCF-7	breast:
11	chr12:85940120..85942691-chr12:85944053..85946791,2	MCF-7	breast:
12	chr12:85969213..85970141-chr12:86036344..86037184,4	MCF-7	breast:
13	chr12:85930199..85932678-chr12:85934950..85937006,2	K562	blood:

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: 1693 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1693 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573204850	chr12:85934372-85934373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs138576453	chr12:85934398-85934399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551239539	chr12:85934517-85934518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562000010	chr12:85934571-85934572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs563521981	chr12:85934621-85934622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200312721	chr12:85934630-85934631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544394397	chr12:85934694-85934695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569415212	chr12:85934700-85934701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533251252	chr12:85934754-85934755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551429259	chr12:85934834-85934835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369102565	chr12:85934859-85934860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs10779166	chr12:85934870-85934871	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs149261885	chr12:85934875-85934876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370769051	chr12:85934889-85934890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548975664	chr12:85934939-85934940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs566994284	chr12:85934981-85934982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs186316413	chr12:85934982-85934983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs191507961	chr12:85934992-85934993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs182076825	chr12:85935061-85935062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566733154	chr12:85935080-85935081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534405110	chr12:85935126-85935127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558122429	chr12:85935179-85935180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs375585334	chr12:85935216-85935217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144559789	chr12:85935217-85935218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73367235	chr12:85935223-85935224	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs555757250	chr12:85935225-85935226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12367484	chr12:85935263-85935264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76373921	chr12:85935285-85935286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs544753195	chr12:85935286-85935287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs80071690	chr12:85935314-85935315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148442998	chr12:85935363-85935364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186337104	chr12:85935368-85935369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191581865	chr12:85935389-85935390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141809382	chr12:85935435-85935436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542237148	chr12:85935497-85935498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182707632	chr12:85935539-85935540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150588228	chr12:85935544-85935545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549511843	chr12:85935580-85935581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571014656	chr12:85935581-85935582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533324761	chr12:85935586-85935587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140743478	chr12:85935651-85935652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567026775	chr12:85935678-85935679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534540478	chr12:85935703-85935704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544831469	chr12:85935723-85935724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567706073	chr12:85935837-85935838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538342336	chr12:85935876-85935877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556652565	chr12:85935924-85935925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73367237	chr12:85935952-85935953	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs575561226	chr12:85936026-85936027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs74112222	chr12:85936035-85936036	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:165 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:85934200-85934400	Enhancers	Fetal Intestine Large	intestine
2	chr12:85934200-85935400	Enhancers	Fetal Intestine Small	intestine
3	chr12:85934400-85938600	Weak transcription	Fetal Intestine Large	intestine
4	chr12:85935400-85938200	Weak transcription	Fetal Intestine Small	intestine
5	chr12:85938200-85939600	Enhancers	Fetal Intestine Small	intestine
6	chr12:85938400-85938800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr12:85938400-85938800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr12:85938400-85939000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr12:85938400-85939400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr12:85938600-85939000	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr12:85938600-85939000	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr12:85938600-85939200	Enhancers	H1 Cell Line	embryonic stem cell
13	chr12:85938600-85939200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr12:85938600-85939800	Enhancers	Fetal Intestine Large	intestine
15	chr12:85938800-85943800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr12:85939000-85944000	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr12:85939000-85944200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr12:85939000-85944200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:85939200-85943600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr12:85939200-85944800	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr12:85939400-85943800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr12:85939600-85942400	Weak transcription	Fetal Intestine Small	intestine
23	chr12:85939800-85940200	Weak transcription	Fetal Intestine Large	intestine
24	chr12:85940200-85940400	Enhancers	Fetal Intestine Large	intestine
25	chr12:85940400-85942000	Weak transcription	Fetal Intestine Large	intestine
26	chr12:85942000-85945600	Enhancers	Fetal Intestine Large	intestine
27	chr12:85942400-85942600	Enhancers	Duodenum Mucosa	Duodenum
28	chr12:85942400-85945600	Enhancers	Fetal Intestine Small	intestine
29	chr12:85942600-85943600	Weak transcription	Duodenum Mucosa	Duodenum
30	chr12:85943600-85943800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr12:85943600-85944800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr12:85943600-85945400	Enhancers	Duodenum Mucosa	Duodenum
33	chr12:85943600-85947000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr12:85943800-85944600	Enhancers	H9 Cell Line	embryonic stem cell
35	chr12:85943800-85944600	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr12:85943800-85944800	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr12:85943800-85945200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr12:85943800-85946800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr12:85943800-85947000	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr12:85944000-85947000	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr12:85944200-85947000	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr12:85944200-85947000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr12:85944200-85947000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr12:85944400-85945200	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr12:85944600-85945000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr12:85944600-85945200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr12:85944800-85945400	Enhancers	H1 Cell Line	embryonic stem cell
48	chr12:85944800-85946400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr12:85945200-85946200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr12:85945200-85947000	Enhancers	iPS-20b Cell Line	embryonic stem cell

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