Variant report

Variant	nsv559667
Chromosome Location	chr12:86318004-86416212
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	CEBPB	chr12:86373817-86374059	A549	lung:	n/a	n/a
2	CEBPB	chr12:86401103-86401271	HepG2	liver:	n/a	chr12:86401153-86401164
3	CEBPB	chr12:86339876-86340044	HepG2	liver:	n/a	n/a
4	CEBPB	chr12:86373808-86374132	HepG2	liver:	n/a	n/a
5	CEBPB	chr12:86397242-86397397	HepG2	liver:	n/a	n/a
6	CHD2	chr12:86398858-86398899	HepG2	liver:	n/a	n/a
7	CTCF	chr12:86345780-86345930	HEEpiC	esophagus:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
8	CTCF	chr12:86349020-86349170	AG10803	skin:	n/a	chr12:86349074-86349092 chr12:86349075-86349091 chr12:86349076-86349097 chr12:86349079-86349087 chr12:86349077-86349090
9	CTCF	chr12:86348940-86349090	BJ	skin:	n/a	chr12:86349079-86349087 chr12:86349077-86349090
10	CTCF	chr12:86348980-86349130	NHDF-neo	bronchial:	n/a	chr12:86349074-86349092 chr12:86349075-86349091 chr12:86349076-86349097 chr12:86349079-86349087 chr12:86349077-86349090
11	CTCF	chr12:86348980-86349230	HVMF	connective:	n/a	chr12:86349074-86349092 chr12:86349075-86349091 chr12:86349076-86349097 chr12:86349079-86349087 chr12:86349077-86349090
12	CTCF	chr12:86345740-86345890	HMEC	breast:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
13	CTCF	chr12:86345820-86345970	GM12874	blood:	n/a	n/a
14	CTCF	chr12:86348900-86349050	HMEC	breast:	n/a	n/a
15	CTCF	chr12:86365760-86365910	HCM	heart:	n/a	n/a
16	CTCF	chr12:86345960-86346110	HepG2	liver:	n/a	n/a
17	CTCF	chr12:86365600-86365750	HMEC	breast:	n/a	n/a
18	CTCF	chr12:86345780-86345930	NHDF-neo	bronchial:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
19	CTCF	chr12:86348985-86349160	Hela-S3	cervix:	n/a	chr12:86349074-86349092 chr12:86349075-86349091 chr12:86349076-86349097 chr12:86349079-86349087 chr12:86349077-86349090
20	CTCF	chr12:86345727-86345909	LNCaP	prostate:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
21	CTCF	chr12:86345780-86345930	HCT-116	colon:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
22	CTCF	chr12:86345680-86345830	NB4	blood:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
23	CTCF	chr12:86349020-86349170	HUVEC	blood vessel:	n/a	chr12:86349074-86349092 chr12:86349075-86349091 chr12:86349076-86349097 chr12:86349079-86349087 chr12:86349077-86349090
24	CTCF	chr12:86345780-86345930	GM12871	blood:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
25	CTCF	chr12:86345720-86345870	HCFaa	heart:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
26	CTCF	chr12:86346060-86346210	AG04450	lung:	n/a	n/a
27	CTCF	chr12:86349000-86349150	HPF	lung:	n/a	chr12:86349074-86349092 chr12:86349075-86349091 chr12:86349076-86349097 chr12:86349079-86349087 chr12:86349077-86349090
28	CTCF	chr12:86345720-86345870	Caco-2	colon:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
29	CTCF	chr12:86398480-86398710	K562	blood:	n/a	n/a
30	CTCF	chr12:86345760-86345910	GM12865	blood:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
31	CTCF	chr12:86345720-86345870	HVMF	connective:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
32	CTCF	chr12:86345760-86345910	HCT-116	colon:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
33	CTCF	chr12:86349000-86349133	LNCaP	prostate:	n/a	chr12:86349074-86349092 chr12:86349075-86349091 chr12:86349076-86349097 chr12:86349079-86349087 chr12:86349077-86349090
34	CTCF	chr12:86345720-86345870	Hela-S3	cervix:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
35	CTCF	chr12:86345700-86345850	HRPEpiC	eye:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
36	CTCF	chr12:86348940-86349090	HPF	lung:	n/a	chr12:86349079-86349087 chr12:86349077-86349090
37	CTCF	chr12:86345740-86345890	GM12873	blood:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
38	CTCF	chr12:86348978-86349134	A549	lung:	n/a	chr12:86349074-86349092 chr12:86349075-86349091 chr12:86349076-86349097 chr12:86349079-86349087 chr12:86349077-86349090
39	CTCF	chr12:86345740-86345890	HEK293	kidney:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
40	CTCF	chr12:86345780-86345930	BE2_C	brain:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
41	CTCF	chr12:86345740-86345890	AoAF	blood vessel:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
42	CTCF	chr12:86345760-86345910	HA-sp	spinal cord:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
43	CTCF	chr12:86345660-86345810	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr12:86345700-86345850	HCM	heart:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
45	CTCF	chr12:86345468-86346295	SK-N-SH	brain:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
46	CTCF	chr12:86345700-86345850	HUVEC	blood vessel:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
47	CTCF	chr12:86348980-86349130	RPTEC	kidney:	n/a	chr12:86349074-86349092 chr12:86349075-86349091 chr12:86349076-86349097 chr12:86349079-86349087 chr12:86349077-86349090
48	CTCF	chr12:86317463-86318082	SK-N-SH	brain:	n/a	chr12:86317699-86317717 chr12:86317700-86317716 chr12:86317703-86317710 chr12:86317701-86317722
49	CTCF	chr12:86345747-86345867	HepG2	liver:	n/a	chr12:86345797-86345818 chr12:86345802-86345820
50	CTCF	chr12:86349000-86349150	HPAF	blood vessel:	n/a	chr12:86349074-86349092 chr12:86349075-86349091 chr12:86349076-86349097 chr12:86349079-86349087 chr12:86349077-86349090

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:86342281-86342331	HRPEpiC	eye:	n/a
2	chr12:86342281-86342331	HCM	heart:	n/a
3	chr12:86342281-86342331	HEEpiC	esophagus:	n/a
4	chr12:86342281-86342331	AG09309	skin:	n/a
5	chr12:86342281-86342331	SK-N-MC	brain:	n/a
6	chr12:86342281-86342331	SKMC	muscle:	n/a
7	chr12:86342281-86342331	NB4	blood:	n/a
8	chr12:86342281-86342331	AG10803	skin:	n/a
9	chr12:86342281-86342331	BJ	skin:	n/a
10	chr12:86342281-86342331	HMEC	breast:	n/a
11	chr12:86342281-86342331	HPAEpiC	pulmonary alveolar:	n/a
12	chr12:86342281-86342331	GM06990	blood:	n/a
13	chr12:86342281-86342331	HL-60	blood:	n/a
14	chr12:86342281-86342331	IMR90	lung:	fetal
15	chr12:86342281-86342331	ECC-1	luminal epithelium:	n/a
16	chr12:86342281-86342331	NHBE	bronchial:	n/a
17	chr12:86342281-86342331	ovcar-3	ovarian:	n/a
18	chr12:86342281-86342331	PrEC	prostate:	n/a
19	chr12:86342281-86342331	GM19239	blood:	n/a
20	chr12:86342281-86342331	NT2-D1	testis:	n/a
21	chr12:86342281-86342331	PANC-1	pancreas:	n/a
22	chr12:86342281-86342331	HNPCEpiC	eye:	n/a
23	chr12:86342281-86342331	NH-A	brain:	n/a
24	chr12:86342281-86342331	SK-N-SH	brain:	n/a
25	chr12:86342281-86342331	HCPEpiC	choroid plexus:	n/a
26	chr12:86342281-86342331	MCF10A-Er-Src	breast:	n/a
27	chr12:86342281-86342331	CMK	blood:	n/a
28	chr12:86342281-86342331	HepG2	liver:	n/a
29	chr12:86342281-86342331	Hepatocyte	liver:	n/a
30	chr12:86342281-86342331	LNCaP	prostate:	n/a
31	chr12:86342281-86342331	GM12891	blood:	n/a
32	chr12:86342281-86342331	NHDF-neo	bronchial:	n/a
33	chr12:86342281-86342331	HRCEpiC	kidney:	n/a
34	chr12:86342281-86342331	SAEC	small airway:	n/a
35	chr12:86342281-86342331	PFSK-1	brain:	n/a
36	chr12:86342281-86342331	AG04450	lung:	fetal
37	chr12:86342281-86342331	AG09319	gingival:	n/a
38	chr12:86342281-86342331	SK-N-SH_RA	brain:	n/a
39	chr12:86342281-86342331	RPTEC	kidney:	n/a
40	chr12:86342281-86342331	ProgFib	skin:	n/a
41	chr12:86342281-86342331	Jurkat	blood:	n/a
42	chr12:86342281-86342331	HCT-116	colon:	n/a
43	chr12:86342281-86342331	K562	blood:	n/a
44	chr12:86342281-86342331	T-47D	breast:	n/a
45	chr12:86342281-86342331	MCF-7	breast:	n/a
46	chr12:86342281-86342331	U87	brain:	n/a
47	chr12:86342281-86342331	HRE	kidney:	n/a
48	chr12:86342281-86342331	GM12878	blood:	n/a
49	chr12:86342281-86342331	HAEpiC	amniotic membrane:	n/a
50	chr12:86342281-86342331	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr12:86365669..86366250-chr12:86579981..86580554,2	MCF-7	breast:
2	chr12:86317858..86318633-chr12:86345266..86346124,2	MCF-7	breast:
3	chr12:86348557..86349487-chr12:88241812..88242801,2	MCF-7	breast:
4	chr12:86398397..86398897-chr12:93280846..93281597,2	K562	blood:
5	chr12:86317272..86318172-chr12:86345555..86346156,3	MCF-7	breast:
6	chr12:86317272..86318172-chr12:86345555..86346156,3	MCF-7	breast:
7	chr12:86317858..86318633-chr12:86345266..86346124,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NTS-1	chr12:86352465-86353340	ENSG00000258178
2	lnc-MGAT4C-1	chr12:86396130-86396256	NONHSAT029759
3	lnc-NTS-1	chr12:86354344-86354725	ENSG00000258178
4	lnc-MGAT4C-1	chr12:86405578-86405680	NONHSAT029760
5	lnc-NTS-2	chr12:86409475-86410219	NONHSAT029761
6	lnc-MGAT4C-1	chr12:86407459-86407536	NONHSAT029760
7	lnc-MGAT4C-1	chr12:86407459-86407536	NONHSAT029759

Variant related genes	Relation type
ENSG00000258178	TF binding region
ENSG00000257897	TF binding region
ENSG00000258178	CpG island
ENSG00000257897	CpG island

Extended variants
information (count: 1708 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1708 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17348032	chr12:86318004-86318005	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563185994	chr12:86318016-86318017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533217112	chr12:86318031-86318032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535605386	chr12:86318034-86318035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543849606	chr12:86318094-86318095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139127425	chr12:86318102-86318103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527793412	chr12:86318162-86318163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549034403	chr12:86318179-86318180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs144693573	chr12:86318205-86318206	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs186974989	chr12:86318218-86318219	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs537643866	chr12:86318233-86318234	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs143245096	chr12:86318236-86318237	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs571523323	chr12:86318244-86318245	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs538517898	chr12:86318245-86318246	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs566715912	chr12:86318369-86318370	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs571919656	chr12:86318387-86318388	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs728753	chr12:86318405-86318406	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs572849842	chr12:86318431-86318432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73177167	chr12:86318460-86318461	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs574323801	chr12:86318468-86318469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200534416	chr12:86318470-86318471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544815774	chr12:86318486-86318487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562892811	chr12:86318500-86318501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191445535	chr12:86318537-86318538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147510300	chr12:86318548-86318549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73177169	chr12:86318554-86318555	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs527654481	chr12:86318593-86318594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376694232	chr12:86318604-86318605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184762013	chr12:86318630-86318631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs716882	chr12:86318683-86318684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549109802	chr12:86318689-86318690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369985594	chr12:86318701-86318702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561046358	chr12:86318802-86318803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140231919	chr12:86318833-86318834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549959167	chr12:86318835-86318836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75175855	chr12:86318843-86318844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12099914	chr12:86318857-86318858	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs532460245	chr12:86318872-86318873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547353628	chr12:86318880-86318881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565714174	chr12:86318881-86318882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149642235	chr12:86318917-86318918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575274427	chr12:86318931-86318932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554751690	chr12:86318951-86318952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189127959	chr12:86318996-86318997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537100010	chr12:86319002-86319003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552298518	chr12:86319096-86319097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556729985	chr12:86319119-86319120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144364414	chr12:86319129-86319130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs11117105	chr12:86319157-86319158	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs554163143	chr12:86319166-86319167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:161 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86317800-86318400	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr12:86317800-86318400	Enhancers	Muscle Satellite Cultured Cells	--
3	chr12:86317800-86318600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr12:86317800-86318800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr12:86317800-86318800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr12:86318000-86318400	Enhancers	Osteobl	bone
7	chr12:86318000-86319000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr12:86318200-86318400	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr12:86318200-86318800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr12:86318600-86324600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr12:86318800-86319400	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr12:86319600-86319800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
13	chr12:86321400-86321800	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr12:86330200-86332000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr12:86330400-86331000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
16	chr12:86332000-86338200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr12:86337400-86338400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr12:86337400-86339200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr12:86338000-86338200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr12:86338000-86338400	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr12:86338200-86338400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
22	chr12:86338200-86338800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:86338400-86339400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr12:86338400-86339400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr12:86338400-86339600	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr12:86338400-86339600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr12:86338800-86339200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:86339200-86339600	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr12:86339200-86340000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr12:86339400-86339600	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr12:86339400-86340800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
32	chr12:86339600-86339800	Enhancers	H1 Cell Line	embryonic stem cell
33	chr12:86339600-86340000	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr12:86339600-86340200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr12:86339600-86340600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
36	chr12:86339600-86341200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
37	chr12:86339800-86340400	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr12:86339800-86342800	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr12:86340000-86341400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
40	chr12:86340200-86340800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
41	chr12:86340400-86340600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
42	chr12:86340600-86341000	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr12:86340600-86341200	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr12:86340600-86341200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr12:86340800-86341000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr12:86340800-86342200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr12:86341000-86342000	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr12:86341000-86342800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr12:86341200-86341400	Enhancers	H1 Cell Line	embryonic stem cell
50	chr12:86341200-86341400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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