Variant report

Variant	esv2761758
Chromosome Location	chr12:85906092-86045137
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	chr12:86036581-86037005	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:85943398-85943797	HepG2	liver:	n/a	n/a
3	ATF2	chr12:85920866-85921402	GM12878	blood:	n/a	n/a
4	BATF	chr12:85929686-85929979	GM12878	blood:	n/a	n/a
5	BHLHE40	chr12:85925172-85925543	GM12878	blood:	n/a	n/a
6	BRCA1	chr12:86019903-86020631	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr12:86020121-86020665	HCT-116	colon:	n/a	n/a
8	CEBPB	chr12:85942503-85942765	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr12:86036533-86037022	MCF-7	breast:	n/a	chr12:86036746-86036757
10	CEBPB	chr12:85966835-85967062	Hela-S3	cervix:	n/a	n/a
11	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
12	CEBPB	chr12:86021300-86021775	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:86036462-86037083	HCT-116	colon:	n/a	chr12:86036746-86036757
14	CEBPB	chr12:85943425-85943748	A549	lung:	n/a	n/a
15	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
16	CEBPB	chr12:86036559-86036960	HepG2	liver:	n/a	chr12:86036746-86036757
17	CEBPB	chr12:85948898-85949146	HepG2	liver:	n/a	chr12:85949046-85949057 chr12:85949018-85949029
18	CEBPB	chr12:86020158-86020619	A549	lung:	n/a	n/a
19	CEBPB	chr12:86032813-86033108	HepG2	liver:	n/a	chr12:86033071-86033083
20	CEBPB	chr12:86036545-86036953	IMR90	lung:	n/a	chr12:86036746-86036757
21	CEBPB	chr12:86036609-86036880	HepG2	liver:	n/a	chr12:86036746-86036757
22	CEBPB	chr12:86002098-86002319	A549	lung:	n/a	n/a
23	CEBPB	chr12:86036618-86036904	HepG2	liver:	n/a	chr12:86036746-86036757
24	CEBPB	chr12:85942408-85942794	A549	lung:	n/a	chr12:85942416-85942428
25	CEBPB	chr12:85981876-85982197	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr12:86036576-86036938	A549	lung:	n/a	chr12:86036746-86036757
27	CEBPB	chr12:86036612-86036933	H1-hESC	embryonic stem cell:	n/a	chr12:86036746-86036757
28	CEBPB	chr12:86002046-86002376	HepG2	liver:	n/a	n/a
29	CEBPB	chr12:86020007-86020716	HCT-116	colon:	n/a	chr12:86020651-86020662
30	CEBPB	chr12:86019830-86021039	IMR90	lung:	n/a	chr12:86020651-86020662
31	CEBPB	chr12:86020186-86020596	A549	lung:	n/a	n/a
32	CEBPB	chr12:86027250-86027714	HCT-116	colon:	n/a	n/a
33	CEBPB	chr12:86020204-86020533	A549	lung:	n/a	n/a
34	CEBPB	chr12:85942473-85942800	HepG2	liver:	n/a	n/a
35	CEBPB	chr12:85916987-85917438	Hela-S3	cervix:	n/a	chr12:85917175-85917188
36	CEBPB	chr12:85948894-85949140	A549	lung:	n/a	chr12:85949046-85949057 chr12:85949018-85949029
37	CEBPB	chr12:86020105-86020665	HCT-116	colon:	n/a	chr12:86020651-86020662
38	CEBPB	chr12:85942491-85942784	A549	lung:	n/a	n/a
39	CEBPB	chr12:86028843-86029069	HepG2	liver:	n/a	n/a
40	CEBPB	chr12:86036542-86036989	Hela-S3	cervix:	n/a	chr12:86036746-86036757
41	CEBPB	chr12:86036562-86036986	A549	lung:	n/a	chr12:86036746-86036757
42	CEBPB	chr12:85943405-85943769	HepG2	liver:	n/a	n/a
43	CEBPB	chr12:86036563-86036936	MCF-7	breast:	n/a	chr12:86036746-86036757
44	CEBPB	chr12:86036541-86036964	HepG2	liver:	n/a	chr12:86036746-86036757
45	CEBPB	chr12:86021336-86021743	IMR90	lung:	n/a	n/a
46	CEBPB	chr12:86019722-86020633	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr12:85981944-85982144	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr12:85957585-85957738	Hela-S3	cervix:	n/a	chr12:85957676-85957689 chr12:85957676-85957689 chr12:85957676-85957687 chr12:85957676-85957689 chr12:85957676-85957687
49	CEBPD	chr12:86036657-86036867	HepG2	liver:	n/a	chr12:86036747-86036758
50	CEBPD	chr12:86036667-86036892	HepG2	liver:	n/a	chr12:86036747-86036758

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:85945089-85945139	PrEC	prostate:	n/a
2	chr12:85945089-85945139	SKMC	muscle:	n/a
3	chr12:86040467-86040517	HAEpiC	amniotic membrane:	n/a
4	chr12:86040467-86040517	AoSMC	blood vessel:	n/a
5	chr12:85945089-85945139	GM12892	blood:	n/a
6	chr12:85945089-85945139	HMEC	breast:	n/a
7	chr12:85945089-85945139	AG09309	skin:	n/a
8	chr12:86040467-86040517	Caco-2	colon:	n/a
9	chr12:85945089-85945139	RPTEC	kidney:	n/a
10	chr12:85945089-85945139	HCT-116	colon:	n/a
11	chr12:85945089-85945139	SK-N-SH	brain:	n/a
12	chr12:86040467-86040517	GM12892	blood:	n/a
13	chr12:86040467-86040517	HEK293	kidney:	embryo
14	chr12:85945089-85945139	PANC-1	pancreas:	n/a
15	chr12:85945089-85945139	NB4	blood:	n/a
16	chr12:85945089-85945139	HNPCEpiC	eye:	n/a
17	chr12:85945089-85945139	A549	lung:	n/a
18	chr12:86040467-86040517	HRPEpiC	eye:	n/a
19	chr12:86040467-86040517	H1-hESC	embryonic stem cell:	embryo
20	chr12:85945089-85945139	GM19239	blood:	n/a
21	chr12:85945089-85945139	H1-hESC	embryonic stem cell:	embryo
22	chr12:86040467-86040517	GM12891	blood:	n/a
23	chr12:86040467-86040517	RPTEC	kidney:	n/a
24	chr12:86040467-86040517	LNCaP	prostate:	n/a
25	chr12:86040467-86040517	HNPCEpiC	eye:	n/a
26	chr12:85945089-85945139	AG04450	lung:	fetal
27	chr12:85945089-85945139	SK-N-SH_RA	brain:	n/a
28	chr12:86040467-86040517	HCPEpiC	choroid plexus:	n/a
29	chr12:86040467-86040517	T-47D	breast:	n/a
30	chr12:85945089-85945139	NHBE	bronchial:	n/a
31	chr12:86040467-86040517	GM19239	blood:	n/a
32	chr12:85945089-85945139	HL-60	blood:	n/a
33	chr12:85945089-85945139	ovcar-3	ovarian:	n/a
34	chr12:85945089-85945139	GM06990	blood:	n/a
35	chr12:85945089-85945139	AG09319	gingival:	n/a
36	chr12:86040467-86040517	GM12878	blood:	n/a
37	chr12:85945089-85945139	HRCEpiC	kidney:	n/a
38	chr12:85945089-85945139	Jurkat	blood:	n/a
39	chr12:86040467-86040517	CMK	blood:	n/a
40	chr12:85945089-85945139	BE2_C	brain:	n/a
41	chr12:86040467-86040517	AG09309	skin:	n/a
42	chr12:85945089-85945139	MCF-7	breast:	n/a
43	chr12:86040467-86040517	Jurkat	blood:	n/a
44	chr12:85945089-85945139	IMR90	lung:	fetal
45	chr12:86040467-86040517	HRE	kidney:	n/a
46	chr12:86040467-86040517	PFSK-1	brain:	n/a
47	chr12:86040467-86040517	SAEC	small airway:	n/a
48	chr12:85945089-85945139	HUVEC	blood vessel:	n/a
49	chr12:85945089-85945139	NHDF-neo	bronchial:	n/a
50	chr12:85945089-85945139	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:85969213..85970141-chr12:86036344..86037184,4	MCF-7	breast:
2	chr12:85972231..85974209-chr12:85975781..85977996,2	MCF-7	breast:
3	chr12:85930199..85932678-chr12:85934950..85937006,2	K562	blood:
4	chr12:85905968..85908916-chr17:58676509..58679332,2	MCF-7	breast:
5	chr12:86036224..86038282-chr12:86040678..86042966,2	MCF-7	breast:
6	chr12:85956037..85957820-chr12:85959579..85961160,2	K562	blood:
7	chr12:85916869..85918658-chr12:85921402..85924342,2	K562	blood:
8	chr12:85969213..85970141-chr12:86036344..86037184,4	MCF-7	breast:
9	chr12:86014804..86017595-chr12:86018520..86021053,2	MCF-7	breast:
10	chr12:85972231..85974209-chr12:85975781..85977996,2	MCF-7	breast:
11	chr12:85956037..85957820-chr12:85959579..85961160,2	K562	blood:
12	chr12:85972333..85972969-chr12:86260657..86261419,2	MCF-7	breast:
13	chr12:86008021..86010789-chr12:86012957..86015625,2	MCF-7	breast:
14	chr12:85949711..85951775-chr12:85954587..85956542,2	K562	blood:
15	chr12:85969245..85970171-chr12:86260729..86261622,3	MCF-7	breast:
16	chr12:86002253..86004144-chr12:86006143..86008700,2	MCF-7	breast:
17	chr12:85949711..85951775-chr12:85954587..85956542,2	K562	blood:
18	chr12:85916869..85918658-chr12:85921402..85924342,2	K562	blood:
19	chr12:85940120..85942691-chr12:85944053..85946791,2	MCF-7	breast:
20	chr12:86002253..86004144-chr12:86006143..86008700,2	MCF-7	breast:
21	chr12:85908005..85909863-chr12:85911172..85913825,2	MCF-7	breast:
22	chr12:85930199..85932678-chr12:85934950..85937006,2	K562	blood:
23	chr12:85940120..85942691-chr12:85944053..85946791,2	MCF-7	breast:
24	chr12:85968890..85970646-chr12:86260113..86261752,8	MCF-7	breast:
25	chr12:85908005..85909863-chr12:85911172..85913825,2	MCF-7	breast:
26	chr12:86014804..86017595-chr12:86018520..86021053,2	MCF-7	breast:
27	chr12:86008021..86010789-chr12:86012957..86015625,2	MCF-7	breast:
28	chr12:86031568..86033990-chr12:86035290..86037133,2	K562	blood:
29	chr12:86031568..86033990-chr12:86035290..86037133,2	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
ENSG00000263449	TF binding region
ENSG00000257855	CpG island
ENSG00000263449	CpG island
ENSG00000170836	chromatin interactions
ENSG00000263449	chromatin interactions

Extended variants
information (count: 3416 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:3416 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540392237	chr12:85906096-85906097	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs565095573	chr12:85906103-85906104	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs569073264	chr12:85906104-85906105	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs144747399	chr12:85906135-85906136	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs547906243	chr12:85906148-85906149	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs140527253	chr12:85906171-85906172	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs538528095	chr12:85906177-85906178	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs55936484	chr12:85906180-85906181	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs139633912	chr12:85906191-85906192	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs536283900	chr12:85906197-85906198	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs58340016	chr12:85906219-85906220	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs575693395	chr12:85906234-85906235	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs536765538	chr12:85906254-85906255	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs556311775	chr12:85906260-85906261	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs181005937	chr12:85906323-85906324	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs545364660	chr12:85906427-85906428	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs560883648	chr12:85906433-85906434	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs532590147	chr12:85906449-85906450	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs572348150	chr12:85906451-85906452	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs550807752	chr12:85906496-85906497	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs561275058	chr12:85906514-85906515	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs531802396	chr12:85906610-85906611	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs57190868	chr12:85906668-85906669	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs565051785	chr12:85906677-85906678	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs79858393	chr12:85906686-85906687	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs79662918	chr12:85906700-85906701	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs547363937	chr12:85906756-85906757	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs73167835	chr12:85906766-85906767	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs529955631	chr12:85906769-85906770	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs547750595	chr12:85906775-85906776	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs186164878	chr12:85906804-85906805	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs536727791	chr12:85906839-85906840	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs558267197	chr12:85906862-85906863	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs80253016	chr12:85906922-85906923	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs57967740	chr12:85906960-85906961	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs139107274	chr12:85906964-85906965	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs34641784	chr12:85906965-85906966	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs71076126	chr12:85906966-85906967	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs191082242	chr12:85907010-85907011	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs572656379	chr12:85907025-85907026	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs181538506	chr12:85907075-85907076	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs144264225	chr12:85907172-85907173	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs566858455	chr12:85907184-85907185	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs572225930	chr12:85907213-85907214	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs576533684	chr12:85907256-85907257	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs559071806	chr12:85907269-85907270	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs141999945	chr12:85907337-85907338	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs76974243	chr12:85907383-85907384	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs558699408	chr12:85907397-85907398	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs185716487	chr12:85907415-85907416	Weak transcription	Chromatin interactive region	1 gene(s)	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:382 , 50 per page) page: 1 2 3 4 5 6 7 8

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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