Variant report

Variant	nsv558188
Chromosome Location	chr12:32531220-32587465
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:750)
CpG islands
(count:793)
Chromatin interactive
region (count:31)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:750 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:32575802-32575932	K562	blood:	n/a	n/a
2	ARID3A	chr12:32552458-32552646	K562	blood:	n/a	n/a
3	ATF1	chr12:32558644-32558694	K562	blood:	n/a	n/a
4	ATF1	chr12:32576643-32576728	K562	blood:	n/a	n/a
5	ATF1	chr12:32575757-32575985	K562	blood:	n/a	n/a
6	ATF2	chr12:32552787-32553894	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr12:32552294-32553761	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr12:32575689-32575885	K562	blood:	n/a	n/a
9	BACH1	chr12:32553857-32553865	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr12:32532678-32532869	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr12:32552426-32553010	K562	blood:	n/a	chr12:32552448-32552464
12	BHLHE40	chr12:32552607-32552709	GM12878	blood:	n/a	n/a
13	BHLHE40	chr12:32575853-32575968	K562	blood:	n/a	n/a
14	BHLHE40	chr12:32572669-32573020	K562	blood:	n/a	n/a
15	BRCA1	chr12:32552404-32552930	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr12:32552322-32552751	K562	blood:	n/a	n/a
17	CCNT2	chr12:32552175-32552976	K562	blood:	n/a	n/a
18	CEBPB	chr12:32587090-32587153	H1-hESC	embryonic stem cell:	n/a	chr12:32587109-32587118 chr12:32587109-32587120
19	CEBPB	chr12:32563476-32563682	HepG2	liver:	n/a	chr12:32563553-32563564
20	CEBPB	chr12:32532224-32532493	K562	blood:	n/a	chr12:32532327-32532338 chr12:32532326-32532339
21	CEBPB	chr12:32532134-32532505	K562	blood:	n/a	chr12:32532327-32532338 chr12:32532326-32532339
22	CEBPB	chr12:32550543-32550989	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr12:32553319-32553779	H1-hESC	embryonic stem cell:	n/a	chr12:32553629-32553640
24	CEBPB	chr12:32538469-32538621	A549	lung:	n/a	n/a
25	CEBPB	chr12:32544773-32544800	A549	lung:	n/a	chr12:32544785-32544796 chr12:32544787-32544796
26	CEBPB	chr12:32551931-32553167	ECC-1	luminal epithelium:	n/a	chr12:32552412-32552420
27	CEBPB	chr12:32552136-32552847	Hela-S3	cervix:	n/a	chr12:32552412-32552420
28	CEBPB	chr12:32587058-32587194	A549	lung:	n/a	chr12:32587109-32587118 chr12:32587109-32587120
29	CEBPB	chr12:32532173-32532459	HepG2	liver:	n/a	chr12:32532327-32532338 chr12:32532326-32532339
30	CEBPB	chr12:32554622-32554995	K562	blood:	n/a	n/a
31	CEBPB	chr12:32554611-32554951	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPZ	chr12:32548074-32548130	HepG2	liver:	n/a	n/a
33	CHD1	chr12:32555412-32555523	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr12:32552453-32554107	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr12:32543855-32544140	HepG2	liver:	n/a	n/a
36	CHD2	chr12:32552448-32553561	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr12:32543808-32543841	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr12:32552779-32552962	HepG2	liver:	n/a	n/a
39	CHD2	chr12:32552571-32552749	GM12878	blood:	n/a	n/a
40	CHD2	chr12:32551982-32553310	Hela-S3	cervix:	n/a	chr12:32552385-32552395
41	CREB1	chr12:32551959-32552863	A549	lung:	n/a	n/a
42	CREB1	chr12:32552177-32552959	K562	blood:	n/a	n/a
43	CREB1	chr12:32552258-32553434	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTBP2	chr12:32551946-32553418	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr12:32555120-32555270	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr12:32552560-32552710	GM12871	blood:	n/a	chr12:32552660-32552673 chr12:32552660-32552669
47	CTCF	chr12:32552440-32552590	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr12:32552600-32552750	GM12878	blood:	n/a	chr12:32552660-32552673 chr12:32552660-32552669
49	CTCF	chr12:32552560-32552710	HMEC	breast:	n/a	chr12:32552660-32552673 chr12:32552660-32552669
50	CTCF	chr12:32552493-32552743	ProgFib	skin:	n/a	chr12:32552660-32552673 chr12:32552660-32552669

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:32553273-32553323	AG04449	skin:	fetal
2	chr12:32552526-32552576	HUVEC	blood vessel:	n/a
3	chr12:32552279-32552329	AG09309	skin:	n/a
4	chr12:32553273-32553323	AG04450	lung:	fetal
5	chr12:32548874-32548924	AoSMC	blood vessel:	n/a
6	chr12:32555628-32555678	SK-N-MC	brain:	n/a
7	chr12:32552899-32552949	H1-hESC	embryonic stem cell:	embryo
8	chr12:32552526-32552576	GM19239	blood:	n/a
9	chr12:32548874-32548924	HAEpiC	amniotic membrane:	n/a
10	chr12:32571851-32571901	CMK	blood:	n/a
11	chr12:32552765-32552815	RPTEC	kidney:	n/a
12	chr12:32552765-32552815	SK-N-SH_RA	brain:	n/a
13	chr12:32552279-32552329	GM12891	blood:	n/a
14	chr12:32553295-32553345	RPTEC	kidney:	n/a
15	chr12:32571851-32571901	RPTEC	kidney:	n/a
16	chr12:32543849-32543899	GM06990	blood:	n/a
17	chr12:32551988-32552038	HCF	heart:	n/a
18	chr12:32553295-32553345	HL-60	blood:	n/a
19	chr12:32553273-32553323	ovcar-3	ovarian:	n/a
20	chr12:32552066-32552116	LNCaP	prostate:	n/a
21	chr12:32548874-32548924	HIPEpiC	eye:	n/a
22	chr12:32552526-32552576	NT2-D1	testis:	n/a
23	chr12:32555628-32555678	HEEpiC	esophagus:	n/a
24	chr12:32553295-32553345	BE2_C	brain:	n/a
25	chr12:32552279-32552329	AG09319	gingival:	n/a
26	chr12:32552279-32552329	BE2_C	brain:	n/a
27	chr12:32552765-32552815	SKMC	muscle:	n/a
28	chr12:32553033-32553083	HL-60	blood:	n/a
29	chr12:32552765-32552815	HRPEpiC	eye:	n/a
30	chr12:32552279-32552329	MCF10A-Er-Src	breast:	n/a
31	chr12:32552066-32552116	Hepatocyte	liver:	n/a
32	chr12:32543849-32543899	SK-N-SH_RA	brain:	n/a
33	chr12:32553295-32553345	ProgFib	skin:	n/a
34	chr12:32543849-32543899	Caco-2	colon:	n/a
35	chr12:32552899-32552949	GM12892	blood:	n/a
36	chr12:32553033-32553083	U87	brain:	n/a
37	chr12:32543849-32543899	HIPEpiC	eye:	n/a
38	chr12:32552279-32552329	Caco-2	colon:	n/a
39	chr12:32553273-32553323	Caco-2	colon:	n/a
40	chr12:32552066-32552116	GM19239	blood:	n/a
41	chr12:32571851-32571901	HUVEC	blood vessel:	n/a
42	chr12:32555628-32555678	H1-hESC	embryonic stem cell:	embryo
43	chr12:32552899-32552949	HEK293	kidney:	embryo
44	chr12:32552526-32552576	RPTEC	kidney:	n/a
45	chr12:32552526-32552576	GM12892	blood:	n/a
46	chr12:32543849-32543899	AG04450	lung:	fetal
47	chr12:32552899-32552949	HEEpiC	esophagus:	n/a
48	chr12:32543849-32543899	RPTEC	kidney:	n/a
49	chr12:32553033-32553083	K562	blood:	n/a
50	chr12:32552765-32552815	HCF	heart:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:32533618..32535853-chr12:32541374..32543080,2	MCF-7	breast:
2	chr12:32580165..32582932-chr12:32583223..32584880,2	K562	blood:
3	chr12:32534948..32536924-chr12:32539453..32542087,2	K562	blood:
4	chr12:32550852..32553049-chr12:32831118..32832629,2	MCF-7	breast:
5	chr12:32552822..32553411-chr3:169306373..169306873,2	HCT-116	colon:
6	chr12:32552199..32553014-chr7:48018664..48019299,2	HCT-116	colon:
7	chr12:32521160..32523381-chr12:32570318..32572312,2	MCF-7	breast:
8	chr12:32539085..32541375-chr12:32544139..32545933,2	K562	blood:
9	chr12:32552467..32553163-chr2:113403051..113404044,2	Hela-S3	cervix:
10	chr12:32552355..32553211-chrX:77359577..77360122,2	Hela-S3	cervix:
11	chr12:32534188..32536796-chr12:32561079..32564068,2	MCF-7	breast:
12	chr12:32534459..32536924-chr12:32539453..32542230,3	K562	blood:
13	chr12:32552095..32552992-chr19:18391097..18392504,4	Hela-S3	cervix:
14	chr12:32522485..32524048-chr12:32531384..32533676,2	K562	blood:
15	chr12:32551367..32553605-chr12:32570827..32573292,2	MCF-7	breast:
16	chr12:32539085..32541375-chr12:32544139..32545933,2	K562	blood:
17	chr12:32533618..32535853-chr12:32541374..32543080,2	MCF-7	breast:
18	chr12:32547740..32549812-chr12:32551795..32554175,2	MCF-7	breast:
19	chr12:32552514..32555337-chr12:32557035..32560074,3	MCF-7	breast:
20	chr12:32580165..32582932-chr12:32583223..32584880,2	K562	blood:
21	chr12:32534948..32536924-chr12:32539453..32542087,2	K562	blood:
22	chr12:32551819..32553534-chr12:32555515..32557617,2	MCF-7	breast:
23	chr12:32534188..32536796-chr12:32561079..32564068,2	MCF-7	breast:
24	chr12:32550694..32554059-chr12:32587426..32590293,5	MCF-7	breast:
25	chr12:32585117..32587361-chr12:32596940..32599478,2	MCF-7	breast:
26	chr12:32534459..32536924-chr12:32539453..32542230,3	K562	blood:
27	chr12:32551025..32552744-chr12:32831132..32833604,2	K562	blood:
28	chr12:32547740..32549812-chr12:32551795..32554175,2	MCF-7	breast:
29	chr12:32519761..32521890-chr12:32532145..32533928,2	K562	blood:
30	chr12:32530472..32534353-chr12:32830607..32833580,3	K562	blood:
31	chr12:32535707..32537411-chr12:32551451..32553487,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BICD1-3	chr12:32558027-32558182	NONHSAT027612
2	lnc-BICD1-3	chr12:32583267-32583630	NONHSAT027612
3	lnc-BICD1-3	chr12:32557462-32557481	NONHSAT027612
4	lnc-BICD1-3	chr12:32573758-32574475	NONHSAT027612
5	lnc-BICD1-3	chr12:32557113-32557450	NONHSAT027612
6	lnc-BICD1-3	chr12:32560576-32560852	NONHSAT027612
7	lnc-BICD1-1	chr12:32534220-32536567	NONHSAT027609
8	lnc-BICD1-3	chr12:32572878-32573361	NONHSAT027612
9	lnc-BICD1-3	chr12:32564376-32564483	NONHSAT027612
10	lnc-BICD1-3	chr12:32586545-32587362	NONHSAT027612

No data

Variant related genes	Relation type
FGD4	TF binding region
ENSG00000207176	TF binding region
FGD4	CpG island
ENSG00000207176	CpG island
ENSG00000130522	chromatin interactions
ENSG00000102144	chromatin interactions
ENSG00000136273	chromatin interactions
ENSG00000237753	chromatin interactions
ENSG00000207176	chromatin interactions
ENSG00000087470	chromatin interactions
ENSG00000144136	chromatin interactions
ENSG00000139132	chromatin interactions

Extended variants
information (count: 2228 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2228 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12229856	chr12:32531220-32531221	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190030615	chr12:32531227-32531228	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs571333165	chr12:32531234-32531235	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs533903765	chr12:32531310-32531311	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs554057497	chr12:32531324-32531325	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs567822394	chr12:32531429-32531430	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs536855649	chr12:32531445-32531446	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs11051967	chr12:32531450-32531451	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs370972458	chr12:32531480-32531481	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs34913988	chr12:32531511-32531512	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs141142286	chr12:32531512-32531513	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs537974193	chr12:32531533-32531534	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs16919819	chr12:32531539-32531540	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs577737438	chr12:32531548-32531549	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs540202550	chr12:32531558-32531559	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs368272310	chr12:32531562-32531563	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs145699993	chr12:32531653-32531654	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs560408045	chr12:32531661-32531662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs146194809	chr12:32531678-32531679	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs542907767	chr12:32531679-32531680	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs568560150	chr12:32531686-32531687	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs182258902	chr12:32531714-32531715	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs115196471	chr12:32531725-32531726	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs185152158	chr12:32531799-32531800	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs191047037	chr12:32531802-32531803	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs140806853	chr12:32531881-32531882	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs144016348	chr12:32531956-32531957	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs368741622	chr12:32532037-32532038	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547427446	chr12:32532045-32532046	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs535916170	chr12:32532063-32532064	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs183932618	chr12:32532077-32532078	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs17600381	chr12:32532105-32532106	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs570291633	chr12:32532143-32532144	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs145971740	chr12:32532256-32532257	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs139659006	chr12:32532284-32532285	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs76879297	chr12:32532348-32532349	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs533776114	chr12:32532360-32532361	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553537101	chr12:32532406-32532407	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs573564008	chr12:32532415-32532416	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs16919821	chr12:32532431-32532432	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs150040798	chr12:32532439-32532440	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs550532482	chr12:32532448-32532449	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs145397413	chr12:32532450-32532451	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs80108042	chr12:32532451-32532452	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs563397667	chr12:32532468-32532469	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs188425884	chr12:32532488-32532489	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs6488050	chr12:32532499-32532500	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs149228293	chr12:32532505-32532506	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs78927598	chr12:32532559-32532560	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs191768775	chr12:32532582-32532583	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
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
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	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	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1205 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32475600-32532400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:32492400-32532000	Weak transcription	Brain Angular Gyrus	brain
3	chr12:32494200-32533800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr12:32518800-32531800	Weak transcription	Stomach Smooth Muscle	stomach
5	chr12:32519200-32532000	Weak transcription	NHDF-Ad	bronchial
6	chr12:32520800-32532400	Weak transcription	Fetal Intestine Small	intestine
7	chr12:32522400-32532200	Weak transcription	Osteobl	bone
8	chr12:32522600-32535800	Weak transcription	Fetal Brain Female	brain
9	chr12:32522800-32532400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr12:32529800-32532000	Weak transcription	Ovary	ovary
11	chr12:32530600-32532000	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr12:32530600-32532400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr12:32530600-32534000	Weak transcription	HSMM	muscle
14	chr12:32530800-32531600	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr12:32530800-32531800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr12:32530800-32531800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr12:32530800-32532000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr12:32530800-32532000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr12:32530800-32532000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr12:32530800-32532000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr12:32530800-32532200	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr12:32530800-32532200	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr12:32531000-32532000	Weak transcription	K562	blood
24	chr12:32531000-32533400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr12:32531600-32532800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr12:32531800-32532800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr12:32532000-32532200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr12:32532000-32532200	Enhancers	K562	blood
29	chr12:32532000-32532400	Enhancers	Ovary	ovary
30	chr12:32532000-32532600	Enhancers	H1 Cell Line	embryonic stem cell
31	chr12:32532000-32532600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr12:32532000-32532800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr12:32532000-32533000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr12:32532200-32532400	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr12:32532200-32532400	Flanking Active TSS	HepG2	liver
36	chr12:32532200-32532600	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr12:32532200-32532800	Enhancers	H9 Cell Line	embryonic stem cell
38	chr12:32532200-32532800	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr12:32532200-32532800	Flanking Active TSS	K562	blood
40	chr12:32532400-32532600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr12:32532400-32532600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr12:32532400-32532600	Active TSS	HepG2	liver
43	chr12:32532600-32532800	Flanking Active TSS	HepG2	liver
44	chr12:32532600-32543400	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr12:32532800-32533200	Active TSS	K562	blood
46	chr12:32532800-32533400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr12:32532800-32533400	Enhancers	HepG2	liver
48	chr12:32536400-32536600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr12:32536600-32537600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr12:32536600-32538200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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