Variant report

Variant	esv3430375
Chromosome Location	chr12:8693691-8718887
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	BACH1	chr12:8707101-8707369	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr12:8696791-8696806	K562	blood:	n/a	n/a
3	BATF	chr12:8709541-8709799	GM12878	blood:	n/a	n/a
4	BCLAF1	chr12:8696744-8697287	GM12878	blood:	n/a	chr12:8697034-8697047
5	BRCA1	chr12:8696893-8697200	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr12:8696742-8697029	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr12:8696866-8697144	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr12:8696610-8696750	GM12892	blood:	n/a	n/a
9	CTCF	chr12:8696920-8697070	NHDF-neo	bronchial:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
10	CTCF	chr12:8696940-8697090	GM12872	blood:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
11	CTCF	chr12:8696920-8697070	HRPEpiC	eye:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
12	CTCF	chr12:8715037-8715168	A549	lung:	n/a	n/a
13	CTCF	chr12:8715040-8715190	GM12871	blood:	n/a	n/a
14	CTCF	chr12:8705980-8706130	GM12867	blood:	n/a	chr12:8706013-8706022
15	CTCF	chr12:8696900-8697050	AG04450	lung:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
16	CTCF	chr12:8714960-8715110	GM12870	blood:	n/a	n/a
17	CTCF	chr12:8697020-8697170	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr12:8696865-8697169	A549	lung:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
19	CTCF	chr12:8696940-8697090	NB4	blood:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
20	CTCF	chr12:8715041-8715176	GM12891	blood:	n/a	n/a
21	CTCF	chr12:8696823-8697171	Medullo	brain:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
22	CTCF	chr12:8714980-8715130	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr12:8696520-8696670	WI-38	lung:	n/a	n/a
24	CTCF	chr12:8696920-8697070	GM12870	blood:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
25	CTCF	chr12:8696904-8697158	GM19238	blood:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
26	CTCF	chr12:8696900-8697132	HepG2	liver:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
27	CTCF	chr12:8696895-8697164	A549	lung:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
28	CTCF	chr12:8715060-8715210	GM12878	blood:	n/a	n/a
29	CTCF	chr12:8705990-8706002	MCF-7	breast:	n/a	n/a
30	CTCF	chr12:8696900-8697155	GM19240	blood:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
31	CTCF	chr12:8696940-8697090	HA-sp	spinal cord:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
32	CTCF	chr12:8696960-8697110	GM12864	blood:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
33	CTCF	chr12:8715120-8715144	LNCaP	prostate:	n/a	n/a
34	CTCF	chr12:8705920-8706070	WERI-Rb-1	eye:	n/a	chr12:8706013-8706022
35	CTCF	chr12:8715060-8715210	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr12:8696890-8697146	K562	blood:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
37	CTCF	chr12:8696820-8696970	HAc	cerebellar:	n/a	n/a
38	CTCF	chr12:8715000-8715150	GM12864	blood:	n/a	n/a
39	CTCF	chr12:8715052-8715166	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr12:8715020-8715170	BE2_C	brain:	n/a	n/a
41	CTCF	chr12:8696960-8697110	HUVEC	blood vessel:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
42	CTCF	chr12:8715020-8715170	HMF	breast:	n/a	n/a
43	CTCF	chr12:8696940-8697090	HepG2	liver:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
44	CTCF	chr12:8705960-8706110	GM12864	blood:	n/a	chr12:8706013-8706022
45	CTCF	chr12:8696626-8696776	ProgFib	skin:	n/a	n/a
46	CTCF	chr12:8715031-8715157	MCF-7	breast:	n/a	n/a
47	CTCF	chr12:8696896-8697112	GM13976	blood:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
48	CTCF	chr12:8696667-8696779	GM19239	blood:	n/a	n/a
49	CTCF	chr12:8696896-8697141	LNCaP	prostate:	n/a	chr12:8697007-8697028 chr12:8697005-8697023 chr12:8697008-8697021 chr12:8697009-8697016 chr12:8697006-8697022
50	CTCF	chr12:8715045-8715139	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8717467-8717517	MCF10A-Er-Src	breast:	n/a
2	chr12:8694468-8694518	MCF10A-Er-Src	breast:	n/a
3	chr12:8717467-8717517	CMK	blood:	n/a
4	chr12:8717487-8717537	HCT-116	colon:	n/a
5	chr12:8716899-8716949	SK-N-MC	brain:	n/a
6	chr12:8717487-8717537	GM12891	blood:	n/a
7	chr12:8717467-8717517	BJ	skin:	n/a
8	chr12:8717487-8717537	HMEC	breast:	n/a
9	chr12:8716899-8716949	LNCaP	prostate:	n/a
10	chr12:8694468-8694518	HRPEpiC	eye:	n/a
11	chr12:8717467-8717517	Hela-S3	cervix:	n/a
12	chr12:8717467-8717517	GM06990	blood:	n/a
13	chr12:8717467-8717517	AG10803	skin:	n/a
14	chr12:8717487-8717537	ECC-1	luminal epithelium:	n/a
15	chr12:8694216-8694266	HNPCEpiC	eye:	n/a
16	chr12:8717487-8717537	BE2_C	brain:	n/a
17	chr12:8717467-8717517	HCPEpiC	choroid plexus:	n/a
18	chr12:8717391-8717441	HCF	heart:	n/a
19	chr12:8694468-8694518	Hela-S3	cervix:	n/a
20	chr12:8716899-8716949	AG09319	gingival:	n/a
21	chr12:8717391-8717441	HPAEpiC	pulmonary alveolar:	n/a
22	chr12:8716899-8716949	SKMC	muscle:	n/a
23	chr12:8717391-8717441	HL-60	blood:	n/a
24	chr12:8694216-8694266	Hela-S3	cervix:	n/a
25	chr12:8716899-8716949	NHBE	bronchial:	n/a
26	chr12:8716899-8716949	HPAEpiC	pulmonary alveolar:	n/a
27	chr12:8694468-8694518	GM12891	blood:	n/a
28	chr12:8717487-8717537	GM12878	blood:	n/a
29	chr12:8717487-8717537	AG04449	skin:	fetal
30	chr12:8694468-8694518	PFSK-1	brain:	n/a
31	chr12:8717391-8717441	HRE	kidney:	n/a
32	chr12:8717487-8717537	GM19239	blood:	n/a
33	chr12:8694216-8694266	HEK293	kidney:	embryo
34	chr12:8694216-8694266	GM12878	blood:	n/a
35	chr12:8694468-8694518	HL-60	blood:	n/a
36	chr12:8694468-8694518	Jurkat	blood:	n/a
37	chr12:8716899-8716949	HEK293	kidney:	embryo
38	chr12:8694468-8694518	IMR90	lung:	fetal
39	chr12:8694468-8694518	NHDF-neo	bronchial:	n/a
40	chr12:8694216-8694266	MCF-7	breast:	n/a
41	chr12:8717487-8717537	Jurkat	blood:	n/a
42	chr12:8717487-8717537	RPTEC	kidney:	n/a
43	chr12:8717487-8717537	HepG2	liver:	n/a
44	chr12:8717391-8717441	HEEpiC	esophagus:	n/a
45	chr12:8694468-8694518	HEK293	kidney:	embryo
46	chr12:8717487-8717537	HUVEC	blood vessel:	n/a
47	chr12:8717467-8717517	GM19239	blood:	n/a
48	chr12:8694468-8694518	SKMC	muscle:	n/a
49	chr12:8716899-8716949	RPTEC	kidney:	n/a
50	chr12:8694216-8694266	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:8696425..8698519-chr12:8700227..8702565,2	MCF-7	breast:
2	chr12:8696556..8697442-chr12:9201824..9202588,3	K562	blood:
3	chr12:8696425..8698519-chr12:8700227..8702565,2	MCF-7	breast:
4	chr12:8699767..8702661-chr12:8703535..8705829,2	MCF-7	breast:
5	chr12:8703161..8706323-chr12:8710096..8711893,3	K562	blood:
6	chr12:8696893..8697412-chr12:8756185..8756692,2	MCF-7	breast:
7	chr12:8703161..8706323-chr12:8710096..8711893,3	K562	blood:
8	chr12:8699767..8702661-chr12:8703535..8705829,2	MCF-7	breast:
9	chr12:8696479..8697067-chr12:8761332..8762088,2	K562	blood:
10	chr12:8696589..8697753-chr12:8761269..8762276,7	MCF-7	breast:
11	chr12:8697584..8700120-chr12:8760238..8761960,2	MCF-7	breast:
12	chr12:8696628..8697485-chr12:8760059..8760765,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC4D-1	chr12:8717334-8717612	XLOC_009643
2	lnc-CLEC4D-1	chr12:8718119-8718789	XLOC_009643
3	lnc-CLEC4D-1	chr12:8718119-8718668	NONHSAT026348
4	lnc-CLEC4D-1	chr12:8717266-8717612	NONHSAT026348
5	lnc-CLEC4D-1	chr12:8718512-8718789	XLOC_009643
6	lnc-CLEC4D-1	chr12:8717523-8717612	XLOC_009643
7	lnc-CLEC4E-1	chr12:8704596-8704736	ENSG00000255801
8	lnc-CLEC4D-1	chr12:8718119-8718282	XLOC_009643
9	lnc-CLEC4D-1	chr12:8716835-8717177	NONHSAT026348
10	lnc-CLEC4E-1	chr12:8700957-8701257	ENSG00000255801
11	lnc-CLEC4D-1	chr12:8717333-8717612	NONHSAT026349
12	lnc-CLEC4D-1	chr12:8718118-8718789	NONHSAT026349

Variant related genes	Relation type
CLEC4E	TF binding region
CLEC4E	CpG island

Extended variants
information (count: 684 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:684 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144884702	chr12:8693709-8693710	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs148698222	chr12:8693711-8693712	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs10605488	chr12:8693732-8693733	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs398097977	chr12:8693741-8693742	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7132177	chr12:8693789-8693790	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs7306903	chr12:8693807-8693808	Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs373544240	chr12:8693839-8693840	Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs12312546	chr12:8693843-8693844	Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs60863721	chr12:8693967-8693968	Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377328164	chr12:8693968-8693969	Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372843480	chr12:8694018-8694019	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs192895401	chr12:8694041-8694042	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs531329080	chr12:8694105-8694106	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs543628174	chr12:8694118-8694119	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs549929164	chr12:8694160-8694161	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs182980111	chr12:8694171-8694172	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs4883166	chr12:8694195-8694196	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs372960484	chr12:8694219-8694220	Enhancers Flanking Active TSS Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs4883167	chr12:8694267-8694268	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs186938640	chr12:8694284-8694285	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs191530445	chr12:8694287-8694288	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs369876662	chr12:8694413-8694414	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140320681	chr12:8694422-8694423	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184061928	chr12:8694652-8694653	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs61405779	chr12:8694743-8694744	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371397808	chr12:8694909-8694910	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs71042393	chr12:8694910-8694911	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs370721602	chr12:8694928-8694929	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs4883168	chr12:8694984-8694985	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs188979161	chr12:8695007-8695008	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs11046143	chr12:8695017-8695018	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs140980682	chr12:8695041-8695042	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs150199738	chr12:8695042-8695043	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs544992424	chr12:8695047-8695048	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs73049982	chr12:8695307-8695308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs10770845	chr12:8695310-8695311	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs551179781	chr12:8695405-8695406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs76204349	chr12:8695481-8695482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574285090	chr12:8695502-8695503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185552191	chr12:8695516-8695517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375727601	chr12:8695560-8695561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs116494403	chr12:8695616-8695617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200125776	chr12:8695621-8695622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs79637610	chr12:8695622-8695623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35678901	chr12:8695627-8695628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs201533036	chr12:8695628-8695629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs138691667	chr12:8695698-8695699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149434997	chr12:8695700-8695701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs4315136	chr12:8695808-8695809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7485954	chr12:8695818-8695819	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:76)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	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
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8691800-8693800	Active TSS	Primary hematopoietic stem cells	blood
2	chr12:8691800-8694000	Active TSS	Primary B cells from cord blood	blood
3	chr12:8692400-8694800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
4	chr12:8693000-8693800	Enhancers	Adipose Nuclei	Adipose
5	chr12:8693200-8693800	Active TSS	Primary monocytes fromperipheralblood	blood
6	chr12:8693200-8693800	Active TSS	Monocytes-CD14+_RO01746	blood
7	chr12:8693400-8694000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
8	chr12:8693400-8694000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr12:8693600-8694000	Active TSS	Primary hematopoietic stem cells short term culture	blood
10	chr12:8693600-8694000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr12:8693800-8694000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
12	chr12:8693800-8694200	Flanking Active TSS	Primary hematopoietic stem cells	blood
13	chr12:8693800-8694600	Enhancers	GM12878-XiMat	blood
14	chr12:8693800-8694600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
15	chr12:8694000-8694200	Flanking Active TSS	Primary B cells from cord blood	blood
16	chr12:8694000-8694400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr12:8694000-8694600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr12:8694000-8695200	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr12:8694200-8694400	Active TSS	Primary B cells from cord blood	blood
20	chr12:8694200-8694400	Active TSS	Primary hematopoietic stem cells	blood
21	chr12:8694400-8694600	Enhancers	Primary B cells from cord blood	blood
22	chr12:8694400-8697000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:8694600-8695200	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr12:8694600-8697200	Weak transcription	GM12878-XiMat	blood
25	chr12:8694800-8697600	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr12:8695000-8695200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr12:8695200-8696600	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr12:8695200-8696600	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr12:8696600-8697400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr12:8696600-8697400	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr12:8696600-8697400	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr12:8696600-8697400	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr12:8696600-8697800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr12:8696800-8697000	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
35	chr12:8696800-8697000	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr12:8696800-8697600	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr12:8697000-8697200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr12:8697000-8697200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr12:8697000-8697200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr12:8697000-8697200	Active TSS	Hela-S3	cervix
41	chr12:8697000-8697400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr12:8697000-8697400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr12:8697000-8697400	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr12:8697000-8697400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr12:8697000-8697400	Enhancers	Fetal Thymus	thymus
46	chr12:8697000-8697400	Active TSS	Ovary	ovary
47	chr12:8697000-8697600	Enhancers	Primary T cells from cord blood	blood
48	chr12:8697000-8697600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr12:8697200-8697400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr12:8697200-8697400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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