Variant report

Variant	nsv558589
Chromosome Location	chr12:39667861-39768356
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:630)
CpG islands
(count:306)
Chromatin interactive
region (count:74)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:630 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:39713017-39713303	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:39734843-39735216	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:39708632-39708643	K562	blood:	n/a	n/a
4	ARID3A	chr12:39726981-39727045	K562	blood:	n/a	n/a
5	ATF1	chr12:39681654-39681982	K562	blood:	n/a	n/a
6	ATF2	chr12:39734914-39735478	GM12878	blood:	n/a	n/a
7	ATF3	chr12:39748780-39749070	K562	blood:	n/a	n/a
8	BACH1	chr12:39713137-39713293	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr12:39671281-39671667	GM12878	blood:	n/a	n/a
10	BATF	chr12:39734939-39735488	GM12878	blood:	n/a	n/a
11	BATF	chr12:39766731-39767112	GM12878	blood:	n/a	chr12:39766904-39766915
12	BATF	chr12:39734956-39735511	GM12878	blood:	n/a	n/a
13	BATF	chr12:39671306-39671625	GM12878	blood:	n/a	n/a
14	BATF	chr12:39693284-39693435	GM12878	blood:	n/a	n/a
15	BATF	chr12:39693282-39693429	GM12878	blood:	n/a	n/a
16	BCL11A	chr12:39734955-39735370	GM12878	blood:	n/a	n/a
17	BCLAF1	chr12:39766698-39767293	GM12878	blood:	n/a	n/a
18	BHLHE40	chr12:39671371-39671521	GM12878	blood:	n/a	n/a
19	BRCA1	chr12:39694055-39694061	GM12878	blood:	n/a	n/a
20	CEBPB	chr12:39681643-39682028	HepG2	liver:	n/a	chr12:39681826-39681837
21	CEBPB	chr12:39681563-39682066	ECC-1	luminal epithelium:	n/a	chr12:39681826-39681837
22	CEBPB	chr12:39681629-39681971	K562	blood:	n/a	chr12:39681826-39681837
23	CEBPB	chr12:39712964-39713245	MCF-7	breast:	n/a	chr12:39713116-39713127
24	CEBPB	chr12:39671094-39671647	Hela-S3	cervix:	n/a	chr12:39671434-39671447 chr12:39671239-39671252 chr12:39671434-39671447 chr12:39671434-39671445 chr12:39671436-39671447
25	CEBPB	chr12:39709737-39709804	A549	lung:	n/a	n/a
26	CEBPB	chr12:39724202-39724401	HepG2	liver:	n/a	chr12:39724314-39724325 chr12:39724316-39724327
27	CEBPB	chr12:39671259-39671594	MCF-7	breast:	n/a	chr12:39671434-39671447 chr12:39671434-39671447 chr12:39671434-39671445 chr12:39671436-39671447
28	CEBPB	chr12:39681542-39682062	K562	blood:	n/a	chr12:39681826-39681837
29	CEBPB	chr12:39707718-39707730	K562	blood:	n/a	n/a
30	CEBPB	chr12:39681640-39682014	H1-hESC	embryonic stem cell:	n/a	chr12:39681826-39681837
31	CEBPB	chr12:39681689-39681935	HepG2	liver:	n/a	chr12:39681826-39681837
32	CEBPB	chr12:39681660-39682018	K562	blood:	n/a	chr12:39681826-39681837
33	CEBPB	chr12:39681517-39682075	A549	lung:	n/a	chr12:39681826-39681837
34	CEBPB	chr12:39713048-39713212	HepG2	liver:	n/a	chr12:39713116-39713127
35	CEBPB	chr12:39735556-39735740	HepG2	liver:	n/a	chr12:39735638-39735649
36	CEBPB	chr12:39681650-39682021	IMR90	lung:	n/a	chr12:39681826-39681837
37	CEBPB	chr12:39708398-39708605	HepG2	liver:	n/a	chr12:39708518-39708529
38	CEBPB	chr12:39681644-39682034	A549	lung:	n/a	chr12:39681826-39681837
39	CEBPB	chr12:39671277-39671610	HepG2	liver:	n/a	chr12:39671434-39671447 chr12:39671434-39671447 chr12:39671434-39671445 chr12:39671436-39671447
40	CEBPB	chr12:39671272-39671617	A549	lung:	n/a	chr12:39671434-39671447 chr12:39671434-39671447 chr12:39671434-39671445 chr12:39671436-39671447
41	CEBPB	chr12:39708432-39708620	A549	lung:	n/a	chr12:39708518-39708529
42	CEBPB	chr12:39681203-39682057	Hela-S3	cervix:	n/a	chr12:39681826-39681837
43	CEBPB	chr12:39724245-39724382	A549	lung:	n/a	chr12:39724314-39724325 chr12:39724316-39724327
44	CEBPB	chr12:39681567-39682036	ECC-1	luminal epithelium:	n/a	chr12:39681826-39681837
45	CEBPB	chr12:39712949-39713260	HepG2	liver:	n/a	chr12:39713116-39713127
46	CEBPB	chr12:39681618-39681998	MCF-7	breast:	n/a	chr12:39681826-39681837
47	CEBPB	chr12:39681603-39682092	MCF-7	breast:	n/a	chr12:39681826-39681837
48	CEBPB	chr12:39681750-39681908	HepG2	liver:	n/a	chr12:39681826-39681837
49	CEBPB	chr12:39681602-39681955	A549	lung:	n/a	chr12:39681826-39681837
50	CEBPB	chr12:39671251-39671626	K562	blood:	n/a	chr12:39671434-39671447 chr12:39671434-39671447 chr12:39671434-39671445 chr12:39671436-39671447

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:39687917-39687967	PFSK-1	brain:	n/a
2	chr12:39687917-39687967	PFSK-1	brain:	n/a
3	chr12:39727030-39727080	SK-N-SH_RA	brain:	n/a
4	chr12:39687917-39687967	HMEC	breast:	n/a
5	chr12:39726715-39726765	IMR90	lung:	fetal
6	chr12:39726715-39726765	BE2_C	brain:	n/a
7	chr12:39727030-39727080	HRCEpiC	kidney:	n/a
8	chr12:39706834-39706884	HEEpiC	esophagus:	n/a
9	chr12:39687917-39687967	H1-hESC	embryonic stem cell:	embryo
10	chr12:39763210-39763260	A549	lung:	n/a
11	chr12:39706834-39706884	NHDF-neo	bronchial:	n/a
12	chr12:39687917-39687967	AG09309	skin:	n/a
13	chr12:39726715-39726765	GM19239	blood:	n/a
14	chr12:39727030-39727080	NHBE	bronchial:	n/a
15	chr12:39726715-39726765	Hela-S3	cervix:	n/a
16	chr12:39726715-39726765	U87	brain:	n/a
17	chr12:39727030-39727080	AG04449	skin:	fetal
18	chr12:39727030-39727080	HCPEpiC	choroid plexus:	n/a
19	chr12:39687917-39687967	HRE	kidney:	n/a
20	chr12:39706834-39706884	Hepatocyte	liver:	n/a
21	chr12:39687917-39687967	Jurkat	blood:	n/a
22	chr12:39687917-39687967	ECC-1	luminal epithelium:	n/a
23	chr12:39763210-39763260	HCF	heart:	n/a
24	chr12:39687917-39687967	BJ	skin:	n/a
25	chr12:39687917-39687967	NHDF-neo	bronchial:	n/a
26	chr12:39687917-39687967	HNPCEpiC	eye:	n/a
27	chr12:39706834-39706884	HL-60	blood:	n/a
28	chr12:39687917-39687967	HCM	heart:	n/a
29	chr12:39727030-39727080	GM06990	blood:	n/a
30	chr12:39727030-39727080	CMK	blood:	n/a
31	chr12:39726715-39726765	ProgFib	skin:	n/a
32	chr12:39706834-39706884	MCF10A-Er-Src	breast:	n/a
33	chr12:39706834-39706884	NHBE	bronchial:	n/a
34	chr12:39706834-39706884	HRCEpiC	kidney:	n/a
35	chr12:39687917-39687967	ProgFib	skin:	n/a
36	chr12:39727030-39727080	RPTEC	kidney:	n/a
37	chr12:39726715-39726765	MCF10A-Er-Src	breast:	n/a
38	chr12:39687917-39687967	MCF-7	breast:	n/a
39	chr12:39726715-39726765	H1-hESC	embryonic stem cell:	embryo
40	chr12:39706834-39706884	HNPCEpiC	eye:	n/a
41	chr12:39687917-39687967	HPAEpiC	pulmonary alveolar:	n/a
42	chr12:39687917-39687967	SK-N-MC	brain:	n/a
43	chr12:39727030-39727080	PANC-1	pancreas:	n/a
44	chr12:39687917-39687967	HEEpiC	esophagus:	n/a
45	chr12:39706834-39706884	NH-A	brain:	n/a
46	chr12:39763210-39763260	HCM	heart:	n/a
47	chr12:39727030-39727080	Hela-S3	cervix:	n/a
48	chr12:39763210-39763260	T-47D	breast:	n/a
49	chr12:39726715-39726765	AG10803	skin:	n/a
50	chr12:39687917-39687967	SKMC	muscle:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:39708222..39708926-chr12:39836719..39837524,2	MCF-7	breast:
2	chr12:39766807..39768997-chr12:39769052..39771333,2	MCF-7	breast:
3	chr12:39721304..39723929-chr12:39731222..39733567,2	K562	blood:
4	chr12:39716315..39719529-chr12:39835472..39838157,3	K562	blood:
5	chr12:39741674..39745219-chr12:39746773..39748556,3	K562	blood:
6	chr12:39690972..39693239-chr12:39694761..39697625,2	MCF-7	breast:
7	chr12:39736502..39739070-chr12:39744339..39745945,2	K562	blood:
8	chr12:39757176..39762110-chr12:39835391..39838507,4	MCF-7	breast:
9	chr12:39701709..39705031-chr12:39707216..39710861,3	K562	blood:
10	chr12:39685600..39687183-chr12:39700503..39702703,2	K562	blood:
11	chr12:39752339..39754010-chr12:39754627..39757326,2	K562	blood:
12	chr12:39756404..39758819-chr12:39835044..39837136,2	MCF-7	breast:
13	chr12:39707343..39709850-chr12:39833796..39835957,2	K562	blood:
14	chr12:39701621..39703209-chr12:39709361..39712125,2	K562	blood:
15	chr12:39709526..39712296-chr12:39716470..39718844,2	MCF-7	breast:
16	chr12:39738067..39741527-chr12:39743955..39747329,3	MCF-7	breast:
17	chr12:39762097..39763744-chr12:39766808..39769516,2	MCF-7	breast:
18	chr12:39751967..39753839-chr12:39754682..39757326,2	K562	blood:
19	chr12:39747712..39750921-chr12:39754829..39757616,3	K562	blood:
20	chr12:39746719..39749261-chr12:39836622..39838192,2	MCF-7	breast:
21	chr12:39719395..39721529-chr12:39835962..39838768,2	MCF-7	breast:
22	chr12:39694207..39696152-chr12:39837237..39840087,2	K562	blood:
23	chr12:39747731..39750258-chr12:39836308..39838380,2	K562	blood:
24	chr12:39708198..39710149-chr12:39835781..39837977,2	MCF-7	breast:
25	chr12:39725322..39729241-chr12:39730380..39734731,5	K562	blood:
26	chr12:39685600..39687183-chr12:39700503..39702703,2	K562	blood:
27	chr12:39742374..39745219-chr12:39747056..39748871,3	K562	blood:
28	chr12:39743968..39746775-chr12:39830107..39832162,2	K562	blood:
29	chr12:39708405..39711742-chr12:39713944..39715751,3	K562	blood:
30	chr12:39706735..39709135-chr12:39713252..39715316,2	K562	blood:
31	chr12:39701435..39705436-chr12:39706649..39711644,6	MCF-7	breast:
32	chr12:39705679..39708570-chr12:39709976..39712207,2	MCF-7	breast:
33	chr12:39725322..39729241-chr12:39730380..39734731,5	K562	blood:
34	chr12:39709526..39712296-chr12:39716470..39718844,2	MCF-7	breast:
35	chr12:39708256..39710912-chr12:39833762..39835679,2	MCF-7	breast:
36	chr12:39707021..39709923-chr12:39830984..39833005,2	K562	blood:
37	chr12:39743944..39745971-chr12:39833401..39836053,2	K562	blood:
38	chr12:39711735..39712649-chr12:40077357..40078312,2	K562	blood:
39	chr12:39736502..39739070-chr12:39744339..39745945,2	K562	blood:
40	chr12:39741674..39745219-chr12:39746773..39748556,3	K562	blood:
41	chr12:39701435..39705436-chr12:39706649..39711644,6	MCF-7	breast:
42	chr12:39762097..39763744-chr12:39766808..39769516,2	MCF-7	breast:
43	chr12:39738067..39741527-chr12:39743955..39747329,3	MCF-7	breast:
44	chr12:38722084..38722866-chr12:39667246..39667987,2	MCF-7	breast:
45	chr12:39679471..39682455-chr12:39683067..39685661,2	MCF-7	breast:
46	chr12:39759346..39760264-chr12:39836545..39837409,2	MCF-7	breast:
47	chr12:39708828..39711217-chr12:39835849..39838225,2	K562	blood:
48	chr12:39748533..39750921-chr12:39755964..39757616,2	K562	blood:
49	chr12:39751967..39753839-chr12:39754682..39757326,2	K562	blood:
50	chr12:39698698..39701515-chr12:39705485..39708006,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCD2-5	chr12:39751050-39751089	NONHSAT027704
2	lnc-C12orf40-3	chr12:39721472-39721634	NONHSAT027701
3	lnc-ABCD2-5	chr12:39750402-39750697	NONHSAT027704
4	lnc-C12orf40-3	chr12:39721472-39721634	NONHSAT027700
5	lnc-C12orf40-3	chr12:39720075-39720147	NONHSAT027700
6	lnc-C12orf40-3	chr12:39720338-39720424	NONHSAT027701
7	lnc-C12orf40-3	chr12:39721864-39722713	NONHSAT027701
8	lnc-C12orf40-3	chr12:39721864-39722713	NONHSAT027700
9	lnc-C12orf40-3	chr12:39721864-39722713	NONHSAT027702
10	lnc-C12orf40-3	chr12:39721452-39721634	NONHSAT027702

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KIF21A	hsa-miR-186-5p	chr12:39688170-39688191
2	KIF21A	hsa-miR-186-5p	chr12:39687380-39687401

Variant related genes	Relation type
KIF21A	TF binding region
KIF21A	CpG island
ENSG00000252974	chromatin interactions
ENSG00000139116	chromatin interactions

Extended variants
information (count: 3326 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:3326 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537539371	chr12:39669442-39669443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs17120051	chr12:39669497-39669498	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs574254512	chr12:39669546-39669547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541644773	chr12:39669561-39669562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs145621288	chr12:39669575-39669576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553660447	chr12:39669646-39669647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs578247425	chr12:39669647-39669648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs545424343	chr12:39669662-39669663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545227330	chr12:39669687-39669688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1512942	chr12:39669705-39669706	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs191026582	chr12:39669723-39669724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs111851514	chr12:39669742-39669743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs561450687	chr12:39669756-39669757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs111308644	chr12:39669781-39669782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545198504	chr12:39669783-39669784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559171010	chr12:39669785-39669786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533235725	chr12:39669806-39669807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs202011205	chr12:39669839-39669840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs117370925	chr12:39669846-39669847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574681214	chr12:39669851-39669852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182408543	chr12:39669872-39669873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549449682	chr12:39669902-39669903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567767577	chr12:39669907-39669908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs74498365	chr12:39669942-39669943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541948147	chr12:39669972-39669973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547364736	chr12:39674847-39674848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565974635	chr12:39674880-39674881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs74892512	chr12:39674940-39674941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557990565	chr12:39674945-39674946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576532050	chr12:39675045-39675046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs74805853	chr12:39675049-39675050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556034734	chr12:39675068-39675069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572588036	chr12:39675098-39675099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146233976	chr12:39675120-39675121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34990089	chr12:39675123-39675124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560081930	chr12:39675213-39675214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571963020	chr12:39675256-39675257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545857384	chr12:39675270-39675271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372244586	chr12:39675272-39675273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543014953	chr12:39675362-39675363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138631379	chr12:39675435-39675436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79172616	chr12:39675444-39675445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12321574	chr12:39675488-39675489	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs547390799	chr12:39675589-39675590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1955314	chr12:39675600-39675601	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs149309729	chr12:39675607-39675608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182789333	chr12:39675619-39675620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186519769	chr12:39675678-39675679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537586661	chr12:39675697-39675698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555971768	chr12:39675703-39675704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
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
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
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	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
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:983 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:39669400-39670000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr12:39674800-39690200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr12:39681200-39682000	Enhancers	Hela-S3	cervix
4	chr12:39681400-39681600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:39681400-39682200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr12:39681600-39687600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:39682000-39699200	Weak transcription	Hela-S3	cervix
8	chr12:39682400-39688800	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr12:39683200-39696000	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr12:39683400-39685600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr12:39683400-39686000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr12:39684400-39695400	Weak transcription	A549	lung
13	chr12:39684600-39688000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr12:39684600-39688200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr12:39685200-39697400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr12:39685200-39714400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr12:39685600-39688800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:39686000-39688200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr12:39686200-39686600	Enhancers	Brain Germinal Matrix	brain
20	chr12:39686400-39686600	Enhancers	Fetal Brain Male	brain
21	chr12:39686400-39699600	Weak transcription	HMEC	breast
22	chr12:39686600-39686800	Enhancers	Pancreas	Pancrea
23	chr12:39686600-39688000	Weak transcription	Brain Germinal Matrix	brain
24	chr12:39686600-39688400	Weak transcription	Fetal Brain Male	brain
25	chr12:39686600-39722400	Weak transcription	GM12878-XiMat	blood
26	chr12:39686600-39725400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr12:39686800-39729800	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr12:39686800-39738800	Weak transcription	Pancreas	Pancrea
29	chr12:39687200-39696800	Weak transcription	Stomach Smooth Muscle	stomach
30	chr12:39687200-39726400	Weak transcription	Fetal Intestine Small	intestine
31	chr12:39687600-39688800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr12:39687600-39723800	Weak transcription	Duodenum Mucosa	Duodenum
33	chr12:39687800-39688200	Enhancers	Brain Anterior Caudate	brain
34	chr12:39688000-39688400	Enhancers	Brain Germinal Matrix	brain
35	chr12:39688000-39688800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr12:39688000-39689600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr12:39688000-39690400	Weak transcription	Liver	Liver
38	chr12:39688200-39688600	Weak transcription	Brain Anterior Caudate	brain
39	chr12:39688200-39689000	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr12:39688200-39689200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr12:39688400-39688600	Enhancers	Fetal Brain Male	brain
42	chr12:39688400-39688800	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr12:39688400-39688800	Enhancers	Brain Substantia Nigra	brain
44	chr12:39688400-39689000	Enhancers	Brain Angular Gyrus	brain
45	chr12:39688400-39689400	Enhancers	Brain Cingulate Gyrus	brain
46	chr12:39688400-39689400	Enhancers	Brain Hippocampus Middle	brain
47	chr12:39688400-39689400	Enhancers	Fetal Brain Female	brain
48	chr12:39688400-39694000	Weak transcription	Brain Germinal Matrix	brain
49	chr12:39688400-39709800	Weak transcription	Ovary	ovary
50	chr12:39688400-39724600	Weak transcription	Esophagus	oesophagus

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