Variant report

Variant	nsv898578
Chromosome Location	chr12:876288-909731
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	chr12:904508-904691	K562	blood:	n/a	n/a
2	ARID3A	chr12:899446-899520	K562	blood:	n/a	n/a
3	ARID3A	chr12:888927-889307	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:899820-900011	K562	blood:	n/a	n/a
5	ARID3A	chr12:886012-886221	HepG2	liver:	n/a	n/a
6	BATF	chr12:888854-889213	GM12878	blood:	n/a	chr12:889023-889034
7	BATF	chr12:888884-889145	GM12878	blood:	n/a	chr12:889023-889034
8	BATF	chr12:898909-899396	GM12878	blood:	n/a	chr12:899377-899386
9	BATF	chr12:901667-901904	GM12878	blood:	n/a	chr12:901756-901767
10	BCLAF1	chr12:886788-887257	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:899138-899144	GM12878	blood:	n/a	n/a
12	BRCA1	chr12:889560-889696	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:888782-889449	A549	lung:	n/a	chr12:889117-889128 chr12:889116-889129
14	CEBPB	chr12:905298-905813	MCF-7	breast:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
15	CEBPB	chr12:905392-905755	HepG2	liver:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
16	CEBPB	chr12:897304-897610	IMR90	lung:	n/a	chr12:897445-897456
17	CEBPB	chr12:897329-897508	K562	blood:	n/a	chr12:897445-897456
18	CEBPB	chr12:902966-903085	A549	lung:	n/a	n/a
19	CEBPB	chr12:905390-905757	H1-hESC	embryonic stem cell:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
20	CEBPB	chr12:905354-905723	K562	blood:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
21	CEBPB	chr12:877930-877946	Hela-S3	cervix:	n/a	chr12:877931-877942 chr12:877933-877944 chr12:877933-877942 chr12:877931-877944
22	CEBPB	chr12:905367-905856	ECC-1	luminal epithelium:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
23	CEBPB	chr12:883175-883531	Hela-S3	cervix:	n/a	chr12:883369-883380 chr12:883369-883380
24	CEBPB	chr12:877842-878030	A549	lung:	n/a	chr12:877931-877942 chr12:877933-877944 chr12:877933-877942 chr12:877931-877944
25	CEBPB	chr12:905401-905800	MCF-7	breast:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
26	CEBPB	chr12:905298-905804	ECC-1	luminal epithelium:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
27	CEBPB	chr12:877787-878039	HepG2	liver:	n/a	chr12:877931-877942 chr12:877933-877944 chr12:877933-877942 chr12:877931-877944
28	CEBPB	chr12:905454-905615	K562	blood:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
29	CEBPB	chr12:905381-905772	K562	blood:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
30	CEBPB	chr12:905381-905768	IMR90	lung:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
31	CEBPB	chr12:888925-889760	IMR90	lung:	n/a	chr12:889117-889128 chr12:889116-889129
32	CEBPB	chr12:905382-905775	Hela-S3	cervix:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
33	CEBPB	chr12:882285-882467	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr12:897314-897616	HepG2	liver:	n/a	chr12:897445-897456
35	CEBPB	chr12:888929-889313	A549	lung:	n/a	chr12:889117-889128 chr12:889116-889129
36	CEBPB	chr12:888908-889383	A549	lung:	n/a	chr12:889117-889128 chr12:889116-889129
37	CEBPB	chr12:902952-903073	K562	blood:	n/a	n/a
38	CEBPB	chr12:905352-905829	HCT-116	colon:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
39	CEBPB	chr12:905352-905808	A549	lung:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
40	CEBPB	chr12:897316-897544	A549	lung:	n/a	chr12:897445-897456
41	CEBPB	chr12:905259-905893	A549	lung:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
42	CEBPB	chr12:888917-889759	Hela-S3	cervix:	n/a	chr12:889117-889128 chr12:889116-889129
43	CEBPB	chr12:888933-889293	HepG2	liver:	n/a	chr12:889117-889128 chr12:889116-889129
44	CEBPB	chr12:905390-905769	A549	lung:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
45	CHD1	chr12:890234-890263	GM12878	blood:	n/a	n/a
46	CHD2	chr12:877061-877162	GM12878	blood:	n/a	n/a
47	CTCF	chr12:879780-879930	HL-60	blood:	n/a	chr12:879818-879839 chr12:879823-879841
48	CTCF	chr12:879760-879910	AG04449	skin:	n/a	chr12:879818-879839 chr12:879823-879841
49	CTCF	chr12:879780-879930	BJ	skin:	n/a	chr12:879818-879839 chr12:879823-879841
50	CTCF	chr12:887507-887582	GM20000	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:886615-886665	Jurkat	blood:	n/a
2	chr12:886615-886665	NB4	blood:	n/a
3	chr12:886615-886665	GM19239	blood:	n/a
4	chr12:886615-886665	HCPEpiC	choroid plexus:	n/a
5	chr12:886615-886665	MCF10A-Er-Src	breast:	n/a
6	chr12:886615-886665	AG09319	gingival:	n/a
7	chr12:886615-886665	BE2_C	brain:	n/a
8	chr12:886615-886665	HRE	kidney:	n/a
9	chr12:886615-886665	ProgFib	skin:	n/a
10	chr12:886615-886665	SKMC	muscle:	n/a
11	chr12:886615-886665	LNCaP	prostate:	n/a
12	chr12:886615-886665	NT2-D1	testis:	n/a
13	chr12:886615-886665	Hepatocyte	liver:	n/a
14	chr12:886615-886665	T-47D	breast:	n/a
15	chr12:886615-886665	NHDF-neo	bronchial:	n/a
16	chr12:886615-886665	MCF-7	breast:	n/a
17	chr12:886615-886665	AG04450	lung:	fetal
18	chr12:886615-886665	HMEC	breast:	n/a
19	chr12:886615-886665	HepG2	liver:	n/a
20	chr12:886615-886665	RPTEC	kidney:	n/a
21	chr12:886615-886665	BJ	skin:	n/a
22	chr12:886615-886665	GM12878	blood:	n/a
23	chr12:886615-886665	HRPEpiC	eye:	n/a
24	chr12:886615-886665	HRCEpiC	kidney:	n/a
25	chr12:886615-886665	H1-hESC	embryonic stem cell:	embryo
26	chr12:886615-886665	SK-N-MC	brain:	n/a
27	chr12:886615-886665	AoSMC	blood vessel:	n/a
28	chr12:886615-886665	HCM	heart:	n/a
29	chr12:886615-886665	AG04449	skin:	fetal
30	chr12:886615-886665	Hela-S3	cervix:	n/a
31	chr12:886615-886665	IMR90	lung:	fetal
32	chr12:886615-886665	HIPEpiC	eye:	n/a
33	chr12:886615-886665	HEK293	kidney:	embryo
34	chr12:886615-886665	HUVEC	blood vessel:	n/a
35	chr12:886615-886665	ECC-1	luminal epithelium:	n/a
36	chr12:886615-886665	HCF	heart:	n/a
37	chr12:886615-886665	Caco-2	colon:	n/a
38	chr12:886615-886665	AG09309	skin:	n/a
39	chr12:886615-886665	HNPCEpiC	eye:	n/a
40	chr12:886615-886665	CMK	blood:	n/a
41	chr12:886615-886665	U87	brain:	n/a
42	chr12:886615-886665	A549	lung:	n/a
43	chr12:886615-886665	ovcar-3	ovarian:	n/a
44	chr12:886615-886665	HL-60	blood:	n/a
45	chr12:886615-886665	HEEpiC	esophagus:	n/a
46	chr12:886615-886665	SK-N-SH_RA	brain:	n/a
47	chr12:886615-886665	HCT-116	colon:	n/a
48	chr12:886615-886665	NH-A	brain:	n/a
49	chr12:886615-886665	K562	blood:	n/a
50	chr12:886615-886665	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:876367..879119-chr12:880594..883556,3	K562	blood:
2	chr12:678017..679838-chr12:873854..876600,2	K562	blood:
3	chr12:906517..908148-chr12:911108..913048,2	K562	blood:
4	chr12:862374..864096-chr12:909523..912296,2	MCF-7	breast:
5	chr12:860489..863381-chr12:877011..880566,3	MCF-7	breast:
6	chr12:902748..905210-chr12:909004..911043,2	K562	blood:
7	chr12:881327..883755-chr12:895131..898641,3	K562	blood:
8	chr12:876367..879119-chr12:880594..883556,3	K562	blood:
9	chr12:902748..905210-chr12:909004..911043,2	K562	blood:
10	chr12:876294..878971-chr12:885168..888118,2	K562	blood:
11	chr12:899602..901917-chr13:59262650..59264676,2	MCF-7	breast:
12	chr12:864103..866169-chr12:883528..885181,2	K562	blood:
13	chr12:881327..883755-chr12:895131..898641,3	K562	blood:
14	chr12:689801..692487-chr12:897629..900163,2	K562	blood:
15	chr12:881327..884915-chr12:893641..898608,4	K562	blood:
16	chr12:881327..884915-chr12:893641..898608,4	K562	blood:
17	chr12:876294..878971-chr12:885168..888118,2	K562	blood:
18	chr12:860587..863557-chr12:905754..908662,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NINJ2-3	chr12:890139-890879	predAs_chen_BU787457_1

Variant related genes	Relation type
RNU4ATAC16P	TF binding region
RNU4ATAC16P	CpG island
ENSG00000060237	chromatin interactions

Extended variants
information (count: 1249 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1249 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12310089	chr12:876288-876289	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565440233	chr12:876290-876291	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551597091	chr12:876334-876335	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534086735	chr12:876354-876355	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs71051382	chr12:876426-876427	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555580125	chr12:876478-876479	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs12424624	chr12:876493-876494	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150198524	chr12:876511-876512	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544924392	chr12:876540-876541	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs56299520	chr12:876546-876547	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs556596357	chr12:876552-876553	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs145691232	chr12:876563-876564	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545078978	chr12:876564-876565	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs560532889	chr12:876565-876566	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs527829612	chr12:876567-876568	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542843240	chr12:876586-876587	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs71449108	chr12:876603-876604	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181737108	chr12:876605-876606	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570162848	chr12:876606-876607	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531618992	chr12:876608-876609	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537602135	chr12:876627-876628	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113397742	chr12:876660-876661	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184203576	chr12:876663-876664	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547086384	chr12:876678-876679	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567916409	chr12:876708-876709	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535055864	chr12:876741-876742	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553383250	chr12:876743-876744	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565426185	chr12:876825-876826	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535987533	chr12:876838-876839	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549150849	chr12:876951-876952	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567487343	chr12:876961-876962	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537831974	chr12:876968-876969	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35839781	chr12:876986-876987	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556770625	chr12:876990-876991	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs578195873	chr12:877011-877012	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs145507062	chr12:877022-877023	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs554256689	chr12:877078-877079	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs188707461	chr12:877087-877088	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs12310187	chr12:877088-877089	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs556145190	chr12:877090-877091	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs561381194	chr12:877095-877096	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs549657037	chr12:877154-877155	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs576155517	chr12:877164-877165	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs181192394	chr12:877190-877191	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs565145917	chr12:877245-877246	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs532342976	chr12:877250-877251	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs546986443	chr12:877265-877266	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs553388826	chr12:877293-877294	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs558950782	chr12:877295-877296	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs529657084	chr12:877302-877303	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22844521	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1413 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:863800-876600	Weak transcription	Spleen	Spleen
2	chr12:864400-883200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:864600-884600	Weak transcription	Aorta	Aorta
4	chr12:865200-883200	Weak transcription	Placenta	Placenta
5	chr12:865200-884600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr12:865200-884600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr12:865200-884600	Weak transcription	Lung	lung
8	chr12:865200-895600	Weak transcription	Pancreas	Pancrea
9	chr12:866000-883400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr12:866000-889200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr12:866200-877000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr12:866200-883200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr12:866200-885000	Weak transcription	Stomach Smooth Muscle	stomach
14	chr12:866400-877000	Weak transcription	Fetal Muscle Leg	muscle
15	chr12:866400-878800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr12:866400-880000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr12:866400-881400	Weak transcription	Duodenum Mucosa	Duodenum
18	chr12:866400-881600	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr12:866400-883000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr12:866400-883000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr12:866400-883000	Weak transcription	Fetal Lung	lung
22	chr12:866400-883200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr12:866400-888800	Weak transcription	HMEC	breast
24	chr12:866600-882800	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr12:866800-876800	Weak transcription	Brain Cingulate Gyrus	brain
26	chr12:866800-877000	Weak transcription	Brain Anterior Caudate	brain
27	chr12:866800-883000	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr12:866800-888800	Weak transcription	Fetal Intestine Large	intestine
29	chr12:867000-881400	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr12:867600-887200	Weak transcription	Fetal Brain Female	brain
31	chr12:868000-883200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr12:869000-881600	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr12:869200-883200	Weak transcription	HepG2	liver
34	chr12:869400-883000	Weak transcription	Hela-S3	cervix
35	chr12:870800-879000	Weak transcription	Brain Hippocampus Middle	brain
36	chr12:870800-883200	Weak transcription	Rectal Smooth Muscle	rectum
37	chr12:870800-886600	Weak transcription	NHLF	lung
38	chr12:871000-881400	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr12:871000-883000	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr12:871000-883000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr12:871000-883000	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr12:871000-888800	Weak transcription	NH-A	brain
43	chr12:871200-876800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr12:871200-879400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr12:871200-882800	Weak transcription	Osteobl	bone
46	chr12:872400-876400	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr12:872400-876600	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr12:872400-876800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr12:872400-877000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr12:872400-888000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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