Variant report

Variant	nsv916611
Chromosome Location	chr12:33822204-34079869
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:522)
CpG islands
(count:122)
Chromatin interactive
region (count:39)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:522 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:33905885-33906235	K562	blood:	n/a	n/a
2	ARID3A	chr12:33831095-33831857	K562	blood:	n/a	n/a
3	ATF1	chr12:33905799-33906217	K562	blood:	n/a	n/a
4	ATF1	chr12:33918231-33918238	K562	blood:	n/a	n/a
5	ATF1	chr12:33837952-33838076	K562	blood:	n/a	n/a
6	BACH1	chr12:33854735-33854758	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr12:33905912-33906117	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr12:33847319-33847363	K562	blood:	n/a	n/a
9	BHLHE40	chr12:33867451-33867477	K562	blood:	n/a	n/a
10	BHLHE40	chr12:33905773-33906139	K562	blood:	n/a	n/a
11	BRCA1	chr12:34046005-34046050	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr12:33905727-33906205	K562	blood:	n/a	n/a
13	CEBPB	chr12:33985871-33986186	A549	lung:	n/a	chr12:33986016-33986029 chr12:33986016-33986027 chr12:33986018-33986029
14	CEBPB	chr12:33985877-33986165	H1-hESC	embryonic stem cell:	n/a	chr12:33986016-33986029 chr12:33986016-33986027 chr12:33986018-33986029
15	CEBPB	chr12:34017618-34017682	HepG2	liver:	n/a	chr12:34017650-34017661
16	CEBPB	chr12:33884520-33884677	K562	blood:	n/a	chr12:33884579-33884590
17	CEBPB	chr12:33830997-33831470	K562	blood:	n/a	n/a
18	CEBPB	chr12:33901844-33902079	IMR90	lung:	n/a	n/a
19	CEBPB	chr12:33839411-33839655	K562	blood:	n/a	n/a
20	CEBPB	chr12:34017562-34017665	A549	lung:	n/a	chr12:34017650-34017661
21	CEBPB	chr12:34063911-34064203	HepG2	liver:	n/a	chr12:34064049-34064060
22	CEBPB	chr12:34035643-34035942	A549	lung:	n/a	n/a
23	CEBPB	chr12:33864469-33864773	HepG2	liver:	n/a	chr12:33864636-33864653 chr12:33864641-33864652 chr12:33864639-33864650 chr12:33864639-33864652 chr12:33864641-33864652 chr12:33864639-33864652
24	CEBPB	chr12:33843303-33843542	HepG2	liver:	n/a	chr12:33843373-33843384
25	CEBPB	chr12:33859879-33860243	K562	blood:	n/a	n/a
26	CEBPB	chr12:33884502-33884721	HepG2	liver:	n/a	chr12:33884579-33884590
27	CEBPB	chr12:33981274-33981584	K562	blood:	n/a	n/a
28	CEBPB	chr12:34045385-34045711	HepG2	liver:	n/a	chr12:34045544-34045555
29	CEBPB	chr12:33864515-33864805	K562	blood:	n/a	chr12:33864636-33864653 chr12:33864641-33864652 chr12:33864639-33864650 chr12:33864639-33864652 chr12:33864641-33864652 chr12:33864639-33864652
30	CEBPB	chr12:34035721-34035955	MCF-7	breast:	n/a	n/a
31	CEBPB	chr12:33985843-33986208	HepG2	liver:	n/a	chr12:33986016-33986029 chr12:33986016-33986027 chr12:33986018-33986029
32	CEBPB	chr12:33911428-33911698	K562	blood:	n/a	chr12:33911549-33911560 chr12:33911547-33911560 chr12:33911547-33911558 chr12:33911547-33911560
33	CEBPB	chr12:33859919-33860228	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr12:33869924-33870124	HepG2	liver:	n/a	chr12:33869980-33869991
35	CEBPB	chr12:33939585-33939878	K562	blood:	n/a	chr12:33939709-33939720
36	CEBPB	chr12:33874543-33874787	Hela-S3	cervix:	n/a	chr12:33874667-33874676
37	CEBPB	chr12:33884519-33884734	IMR90	lung:	n/a	chr12:33884579-33884590
38	CEBPB	chr12:34044510-34044724	HepG2	liver:	n/a	chr12:34044643-34044654 chr12:34044640-34044657
39	CEBPB	chr12:33859895-33860215	IMR90	lung:	n/a	n/a
40	CEBPB	chr12:34045370-34045733	IMR90	lung:	n/a	chr12:34045544-34045555
41	CEBPB	chr12:33843240-33843532	A549	lung:	n/a	chr12:33843373-33843384
42	CEBPB	chr12:33956359-33956503	HepG2	liver:	n/a	chr12:33956423-33956434
43	CEBPB	chr12:34045415-34045710	K562	blood:	n/a	chr12:34045544-34045555
44	CEBPB	chr12:34045411-34045695	A549	lung:	n/a	chr12:34045544-34045555
45	CEBPB	chr12:34075757-34076029	HepG2	liver:	n/a	chr12:34075905-34075916
46	CEBPB	chr12:33911471-33911677	HepG2	liver:	n/a	chr12:33911549-33911560 chr12:33911547-33911560 chr12:33911547-33911558 chr12:33911547-33911560
47	CEBPB	chr12:33985801-33986171	IMR90	lung:	n/a	chr12:33986016-33986029 chr12:33986016-33986027 chr12:33986018-33986029
48	CEBPB	chr12:34075788-34076026	A549	lung:	n/a	chr12:34075905-34075916
49	CEBPB	chr12:33859890-33860233	HepG2	liver:	n/a	n/a
50	CEBPB	chr12:34035659-34035858	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:34001319-34001369	SK-N-SH_RA	brain:	n/a
2	chr12:34061681-34061731	U87	brain:	n/a
3	chr12:34001319-34001369	A549	lung:	n/a
4	chr12:34001319-34001369	HRE	kidney:	n/a
5	chr12:34001319-34001369	NH-A	brain:	n/a
6	chr12:34061681-34061731	NHDF-neo	bronchial:	n/a
7	chr12:34001319-34001369	HMEC	breast:	n/a
8	chr12:34001319-34001369	Caco-2	colon:	n/a
9	chr12:34061681-34061731	NH-A	brain:	n/a
10	chr12:34001319-34001369	HEK293	kidney:	embryo
11	chr12:34061681-34061731	HNPCEpiC	eye:	n/a
12	chr12:34001319-34001369	HL-60	blood:	n/a
13	chr12:34061681-34061731	HCF	heart:	n/a
14	chr12:34001319-34001369	RPTEC	kidney:	n/a
15	chr12:34061681-34061731	Caco-2	colon:	n/a
16	chr12:34001319-34001369	HCF	heart:	n/a
17	chr12:34001319-34001369	BJ	skin:	n/a
18	chr12:34061681-34061731	AoSMC	blood vessel:	n/a
19	chr12:34001319-34001369	SAEC	small airway:	n/a
20	chr12:34061681-34061731	Hepatocyte	liver:	n/a
21	chr12:34001319-34001369	HNPCEpiC	eye:	n/a
22	chr12:34061681-34061731	GM12891	blood:	n/a
23	chr12:34001319-34001369	H1-hESC	embryonic stem cell:	embryo
24	chr12:34061681-34061731	SAEC	small airway:	n/a
25	chr12:34001319-34001369	BE2_C	brain:	n/a
26	chr12:34001319-34001369	U87	brain:	n/a
27	chr12:34001319-34001369	AG04449	skin:	fetal
28	chr12:34001319-34001369	HepG2	liver:	n/a
29	chr12:34001319-34001369	HAEpiC	amniotic membrane:	n/a
30	chr12:34061681-34061731	Jurkat	blood:	n/a
31	chr12:34061681-34061731	HRPEpiC	eye:	n/a
32	chr12:34001319-34001369	MCF10A-Er-Src	breast:	n/a
33	chr12:34001319-34001369	K562	blood:	n/a
34	chr12:34061681-34061731	HCM	heart:	n/a
35	chr12:34061681-34061731	HL-60	blood:	n/a
36	chr12:34061681-34061731	GM19239	blood:	n/a
37	chr12:34061681-34061731	GM12892	blood:	n/a
38	chr12:34001319-34001369	AG09309	skin:	n/a
39	chr12:34001319-34001369	SK-N-MC	brain:	n/a
40	chr12:34061681-34061731	ProgFib	skin:	n/a
41	chr12:34061681-34061731	AG09309	skin:	n/a
42	chr12:34061681-34061731	HMEC	breast:	n/a
43	chr12:34061681-34061731	AG09319	gingival:	n/a
44	chr12:34061681-34061731	HUVEC	blood vessel:	n/a
45	chr12:34061681-34061731	NT2-D1	testis:	n/a
46	chr12:34061681-34061731	HEEpiC	esophagus:	n/a
47	chr12:34001319-34001369	GM06990	blood:	n/a
48	chr12:34061681-34061731	AG04449	skin:	fetal
49	chr12:34001319-34001369	ProgFib	skin:	n/a
50	chr12:34001319-34001369	SK-N-SH	brain:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:33983313..33984854-chr12:33986265..33988102,2	MCF-7	breast:
2	chr12:33828843..33831342-chr12:33831748..33833892,2	MCF-7	breast:
3	chr12:33975803..33979098-chr12:33979674..33983619,4	MCF-7	breast:
4	chr12:33830515..33832081-chr12:33832328..33834300,2	K562	blood:
5	chr12:33901002..33902516-chr12:33905016..33907291,2	MCF-7	breast:
6	chr12:33828756..33830899-chr12:33837528..33839909,2	MCF-7	breast:
7	chr12:33934409..33936900-chr12:33939410..33941605,3	K562	blood:
8	chr12:33990071..33993034-chr8:42750325..42752539,2	MCF-7	breast:
9	chr12:34053367..34054987-chr12:34055066..34057564,2	MCF-7	breast:
10	chr12:33825675..33828123-chr8:42750828..42752625,2	MCF-7	breast:
11	chr12:33977547..33980480-chr12:33992605..33994282,2	K562	blood:
12	chr12:33975803..33979098-chr12:33979674..33983619,4	MCF-7	breast:
13	chr12:34009182..34012663-chr12:34013902..34015537,3	MCF-7	breast:
14	chr12:33983313..33984854-chr12:33986265..33988102,2	MCF-7	breast:
15	chr12:34017264..34017766-chr13:48856661..48857204,2	MCF-7	breast:
16	chr12:33587036..33589098-chr12:33993044..33994546,2	MCF-7	breast:
17	chr12:33809313..33810966-chr12:33832220..33835115,2	K562	blood:
18	chr12:33829191..33832015-chr12:33832800..33835417,2	K562	blood:
19	chr12:33916761..33918446-chr16:3069457..3072448,2	MCF-7	breast:
20	chr12:33817225..33819690-chr12:33823230..33824769,2	MCF-7	breast:
21	chr12:33977547..33980480-chr12:33992605..33994282,2	K562	blood:
22	chr12:33828843..33831342-chr12:33831748..33833892,2	MCF-7	breast:
23	chr12:33829191..33832015-chr12:33832800..33835417,2	K562	blood:
24	chr12:34008981..34009786-chr2:33211553..33212456,2	MCF-7	breast:
25	chr12:33828756..33830899-chr12:33837528..33839909,2	MCF-7	breast:
26	chr12:33903835..33905859-chr12:33907919..33910698,2	MCF-7	breast:
27	chr12:33984638..33987420-chr12:33995374..33998517,3	MCF-7	breast:
28	chr12:34053367..34054987-chr12:34055066..34057564,2	MCF-7	breast:
29	chr12:33851368..33853439-chr12:33854297..33856163,2	K562	blood:
30	chr12:33851368..33853439-chr12:33854297..33856163,2	K562	blood:
31	chr12:33815236..33817568-chr12:33820316..33823181,2	K562	blood:
32	chr12:33984638..33987420-chr12:33995374..33998517,3	MCF-7	breast:
33	chr12:33901002..33902516-chr12:33905016..33907291,2	MCF-7	breast:
34	chr12:33903835..33905859-chr12:33907919..33910698,2	MCF-7	breast:
35	chr12:33831200..33833987-chr12:33837460..33839264,2	K562	blood:
36	chr12:33831200..33833987-chr12:33837460..33839264,2	K562	blood:
37	chr12:33830515..33832081-chr12:33832328..33834300,2	K562	blood:
38	chr12:33934409..33936900-chr12:33939410..33941605,3	K562	blood:
39	chr12:34009182..34012663-chr12:34013902..34015537,3	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG10-6	chr12:33870788-33871152	NONHSAT027645

No data

Variant related genes	Relation type
ENSG00000270807	TF binding region
RNU6-472P	TF binding region
ENSG00000270807	CpG island
RNU6-472P	CpG island
ENSG00000120925	chromatin interactions
ENSG00000184697	chromatin interactions
ENSG00000168172	chromatin interactions
ENSG00000006327	chromatin interactions
ENSG00000266044	chromatin interactions

Extended variants
information (count: 2290 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2290 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372930378	chr12:33822228-33822229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs571723151	chr12:33822244-33822245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145794518	chr12:33822248-33822249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs376687670	chr12:33822273-33822274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140728467	chr12:33822288-33822289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550066982	chr12:33822290-33822291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563910619	chr12:33822293-33822294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532624687	chr12:33822314-33822315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552721696	chr12:33822325-33822326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566214173	chr12:33822341-33822342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115601957	chr12:33822351-33822352	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548613301	chr12:33822456-33822457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs567435999	chr12:33822457-33822458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555880378	chr12:33822477-33822478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs145910409	chr12:33822504-33822505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544827672	chr12:33822521-33822522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185275522	chr12:33822539-33822540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs372280583	chr12:33822541-33822542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs11052830	chr12:33822562-33822563	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs534077841	chr12:33822580-33822581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533467845	chr12:33822677-33822678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571835639	chr12:33822739-33822740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs199944464	chr12:33822769-33822770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115598146	chr12:33822809-33822810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554558626	chr12:33822837-33822838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369044259	chr12:33822853-33822854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574986183	chr12:33822927-33822928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544116236	chr12:33822963-33822964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563836718	chr12:33822970-33822971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557734761	chr12:33823038-33823039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532735305	chr12:33823051-33823052	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34964520	chr12:33823096-33823097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs397776575	chr12:33823103-33823104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs397849994	chr12:33823104-33823105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201573921	chr12:33823108-33823109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78776911	chr12:33823129-33823130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141258040	chr12:33823151-33823152	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376884102	chr12:33823202-33823203	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs529363759	chr12:33823226-33823227	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs541138417	chr12:33823266-33823267	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs527739623	chr12:33823271-33823272	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs143236310	chr12:33823291-33823292	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs567787559	chr12:33823408-33823409	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs559721332	chr12:33823463-33823464	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs111782579	chr12:33823467-33823468	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs148325870	chr12:33823475-33823476	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs568447497	chr12:33823490-33823491	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs190152478	chr12:33823507-33823508	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs550066388	chr12:33823514-33823515	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs569650472	chr12:33823554-33823555	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Chronic lymphocytic leukemia	21546498	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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chordoma	18071362	CNVD
Lung cancer	18438408	CNVD
Cancer	21272361	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Tetralogy of Fallot	22912587	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:33820800-33823400	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr12:33821000-33824200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr12:33821600-33822400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr12:33821600-33822400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr12:33821600-33823800	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr12:33821800-33822800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:33822200-33822400	Enhancers	H9 Cell Line	embryonic stem cell
8	chr12:33822400-33823200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr12:33822400-33823600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr12:33822400-33825000	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr12:33822400-33825800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr12:33822600-33825800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr12:33822800-33823000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr12:33823000-33823400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr12:33823200-33823800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr12:33823400-33823600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr12:33823400-33823800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
18	chr12:33823600-33825400	Enhancers	H9 Cell Line	embryonic stem cell
19	chr12:33823600-33825800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:33823800-33824000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr12:33823800-33824200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr12:33823800-33826600	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr12:33824000-33824400	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr12:33824200-33824600	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr12:33824200-33825800	Enhancers	H1 Cell Line	embryonic stem cell
26	chr12:33824200-33826200	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr12:33824400-33825400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr12:33824400-33826400	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr12:33824600-33827000	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr12:33825600-33826200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr12:33825800-33826200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr12:33826200-33831400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr12:33830000-33831600	Enhancers	HSMMtube	muscle
34	chr12:33830800-33831000	Enhancers	K562	blood
35	chr12:33831000-33831800	Flanking Active TSS	K562	blood
36	chr12:33831400-33832000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr12:33831800-33832000	Enhancers	K562	blood
38	chr12:33836800-33837400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr12:33850000-33850400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr12:33850000-33851000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr12:33850400-33850800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chr12:33850600-33850800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr12:33850800-33852400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr12:33851000-33852600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:33852200-33852800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr12:33852200-33853000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr12:33852400-33852600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr12:33857800-33858200	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr12:33872600-33873000	Active TSS	Spleen	Spleen
50	chr12:33905400-33906600	Enhancers	K562	blood

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