Variant report

Variant	esv1810729
Chromosome Location	chr12:64234926-64268005
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1162)
CpG islands
(count:915)
Chromatin interactive
region (count:48)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:64237560-64237994	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:64256027-64256474	HepG2	liver:	n/a	n/a
3	ATF3	chr12:64237371-64238069	A549	lung:	n/a	n/a
4	ATF3	chr12:64237449-64238018	A549	lung:	n/a	n/a
5	ATF3	chr12:64255861-64256565	A549	lung:	n/a	n/a
6	BACH1	chr12:64237368-64237963	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr12:64238672-64238907	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr12:64237690-64237925	GM12878	blood:	n/a	n/a
9	BATF	chr12:64247807-64248068	GM12878	blood:	n/a	n/a
10	BCL3	chr12:64238356-64239146	A549	lung:	n/a	n/a
11	BCL3	chr12:64255893-64256921	A549	lung:	n/a	chr12:64256368-64256377 chr12:64256297-64256305
12	BCL3	chr12:64251477-64252236	A549	lung:	n/a	n/a
13	BCL3	chr12:64255849-64256807	A549	lung:	n/a	chr12:64256368-64256377 chr12:64256297-64256305
14	BCL3	chr12:64237582-64237909	GM12878	blood:	n/a	chr12:64237583-64237596
15	BCLAF1	chr12:64237422-64238113	GM12878	blood:	n/a	chr12:64238031-64238044 chr12:64237583-64237596
16	BCLAF1	chr12:64237576-64238031	GM12878	blood:	n/a	chr12:64237583-64237596
17	BHLHE40	chr12:64237495-64238031	GM12878	blood:	n/a	chr12:64237962-64237978 chr12:64237615-64237631 chr12:64237744-64237760
18	BHLHE40	chr12:64237536-64237987	K562	blood:	n/a	chr12:64237962-64237978 chr12:64237615-64237631 chr12:64237744-64237760
19	BHLHE40	chr12:64237474-64238007	HepG2	liver:	n/a	chr12:64237962-64237978 chr12:64237615-64237631 chr12:64237744-64237760
20	BHLHE40	chr12:64256012-64256392	A549	lung:	n/a	n/a
21	BHLHE40	chr12:64237602-64237918	A549	lung:	n/a	chr12:64237615-64237631 chr12:64237744-64237760
22	BRCA1	chr12:64239678-64239728	GM12878	blood:	n/a	n/a
23	BRCA1	chr12:64256000-64256388	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr12:64237390-64237914	HepG2	liver:	n/a	n/a
25	BRCA1	chr12:64237631-64237909	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr12:64237499-64237992	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr12:64237584-64237913	K562	blood:	n/a	n/a
28	CCNT2	chr12:64237380-64238051	K562	blood:	n/a	n/a
29	CEBPB	chr12:64251514-64252190	A549	lung:	n/a	n/a
30	CEBPB	chr12:64237457-64237971	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr12:64256017-64256507	A549	lung:	n/a	n/a
32	CEBPB	chr12:64238686-64238825	HepG2	liver:	n/a	n/a
33	CEBPB	chr12:64251737-64252152	A549	lung:	n/a	n/a
34	CEBPB	chr12:64240159-64240495	A549	lung:	n/a	chr12:64240324-64240337
35	CEBPB	chr12:64243578-64243697	K562	blood:	n/a	n/a
36	CEBPB	chr12:64237678-64237919	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr12:64240177-64240470	IMR90	lung:	n/a	chr12:64240324-64240337
38	CEBPB	chr12:64257878-64258197	IMR90	lung:	n/a	chr12:64258023-64258034
39	CEBPB	chr12:64252487-64252618	IMR90	lung:	n/a	n/a
40	CEBPB	chr12:64255986-64256930	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr12:64255500-64255629	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr12:64243469-64243658	IMR90	lung:	n/a	n/a
43	CEBPB	chr12:64252223-64252644	A549	lung:	n/a	n/a
44	CEBPB	chr12:64239534-64239862	HepG2	liver:	n/a	chr12:64239667-64239684
45	CEBPB	chr12:64252427-64252637	A549	lung:	n/a	n/a
46	CEBPB	chr12:64255357-64255680	IMR90	lung:	n/a	n/a
47	CEBPB	chr12:64257966-64258066	HepG2	liver:	n/a	chr12:64258023-64258034
48	CEBPB	chr12:64255830-64256935	A549	lung:	n/a	n/a
49	CEBPB	chr12:64256047-64256479	A549	lung:	n/a	n/a
50	CEBPB	chr12:64257868-64258148	A549	lung:	n/a	chr12:64258023-64258034

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:64237202-64237252	GM12891	blood:	n/a
2	chr12:64238503-64238553	HPAEpiC	pulmonary alveolar:	n/a
3	chr12:64238424-64238474	K562	blood:	n/a
4	chr12:64240787-64240837	AG09319	gingival:	n/a
5	chr12:64238503-64238553	IMR90	lung:	fetal
6	chr12:64238503-64238553	Jurkat	blood:	n/a
7	chr12:64263169-64263219	GM12878	blood:	n/a
8	chr12:64238538-64238588	GM06990	blood:	n/a
9	chr12:64238043-64238093	GM12892	blood:	n/a
10	chr12:64238607-64238657	HAEpiC	amniotic membrane:	n/a
11	chr12:64238366-64238416	SK-N-MC	brain:	n/a
12	chr12:64238424-64238474	RPTEC	kidney:	n/a
13	chr12:64238503-64238553	CMK	blood:	n/a
14	chr12:64238325-64238375	Hela-S3	cervix:	n/a
15	chr12:64238538-64238588	SK-N-MC	brain:	n/a
16	chr12:64238424-64238474	NT2-D1	testis:	n/a
17	chr12:64238424-64238474	HPAEpiC	pulmonary alveolar:	n/a
18	chr12:64240787-64240837	HIPEpiC	eye:	n/a
19	chr12:64264894-64264944	NB4	blood:	n/a
20	chr12:64238396-64238446	HRPEpiC	eye:	n/a
21	chr12:64263169-64263219	HNPCEpiC	eye:	n/a
22	chr12:64238379-64238429	NHBE	bronchial:	n/a
23	chr12:64264894-64264944	U87	brain:	n/a
24	chr12:64238396-64238446	Hepatocyte	liver:	n/a
25	chr12:64238379-64238429	SK-N-SH	brain:	n/a
26	chr12:64238366-64238416	Jurkat	blood:	n/a
27	chr12:64238424-64238474	HL-60	blood:	n/a
28	chr12:64238325-64238375	HIPEpiC	eye:	n/a
29	chr12:64240787-64240837	HUVEC	blood vessel:	n/a
30	chr12:64240787-64240837	Jurkat	blood:	n/a
31	chr12:64238503-64238553	HUVEC	blood vessel:	n/a
32	chr12:64237202-64237252	HUVEC	blood vessel:	n/a
33	chr12:64264894-64264944	ovcar-3	ovarian:	n/a
34	chr12:64237202-64237252	IMR90	lung:	fetal
35	chr12:64237202-64237252	HNPCEpiC	eye:	n/a
36	chr12:64264894-64264944	PANC-1	pancreas:	n/a
37	chr12:64238396-64238446	H1-hESC	embryonic stem cell:	embryo
38	chr12:64264894-64264944	BJ	skin:	n/a
39	chr12:64238043-64238093	Hepatocyte	liver:	n/a
40	chr12:64238424-64238474	PrEC	prostate:	n/a
41	chr12:64238396-64238446	HCM	heart:	n/a
42	chr12:64238043-64238093	IMR90	lung:	fetal
43	chr12:64238607-64238657	GM12892	blood:	n/a
44	chr12:64263169-64263219	NT2-D1	testis:	n/a
45	chr12:64238424-64238474	A549	lung:	n/a
46	chr12:64263169-64263219	MCF10A-Er-Src	breast:	n/a
47	chr12:64237202-64237252	SK-N-SH	brain:	n/a
48	chr12:64238538-64238588	SKMC	muscle:	n/a
49	chr12:64238607-64238657	HCT-116	colon:	n/a
50	chr12:64237202-64237252	BE2_C	brain:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:64248653..64250464-chr12:64256025..64258029,2	MCF-7	breast:
2	chr12:64243123..64244682-chr12:64261360..64263267,2	MCF-7	breast:
3	chr12:64238646..64240219-chr12:64329765..64332123,2	MCF-7	breast:
4	chr12:64246806..64249435-chr12:64262805..64265409,2	K562	blood:
5	chr12:50505708..50506336-chr12:64237320..64237922,2	Hela-S3	cervix:
6	chr12:64257915..64259746-chr12:64264033..64266487,2	K562	blood:
7	chr12:64234725..64235387-chr12:64629309..64629959,2	MCF-7	breast:
8	chr12:64241662..64243647-chr12:64288984..64291005,2	MCF-7	breast:
9	chr12:64240320..64243216-chr12:64291651..64293921,2	MCF-7	breast:
10	chr12:64260075..64262066-chr12:64596655..64599026,2	MCF-7	breast:
11	chr12:64235952..64238772-chr12:64614485..64617363,3	K562	blood:
12	chr12:64254678..64258025-chr12:64259314..64262432,3	MCF-7	breast:
13	chr12:64257945..64259859-chr12:64259892..64262492,3	MCF-7	breast:
14	chr12:64236758..64238491-chr12:64513269..64515825,2	MCF-7	breast:
15	chr12:64254678..64258025-chr12:64259314..64262432,3	MCF-7	breast:
16	chr12:64259856..64261721-chr12:64265461..64267447,2	MCF-7	breast:
17	chr12:64246806..64249435-chr12:64262805..64265409,2	K562	blood:
18	chr12:64254946..64256892-chr12:64282588..64284962,2	MCF-7	breast:
19	chr12:64257643..64259888-chr12:64403526..64405520,2	MCF-7	breast:
20	chr12:64238158..64239661-chr12:64250605..64253293,2	MCF-7	breast:
21	chr12:64237577..64240346-chr12:64245227..64250030,4	MCF-7	breast:
22	chr12:64237925..64239667-chr12:64240036..64242683,2	K562	blood:
23	chr12:64263588..64265669-chr12:64273685..64275675,2	MCF-7	breast:
24	chr12:64240146..64242509-chr12:64254956..64256783,2	MCF-7	breast:
25	chr12:64243148..64249002-chr12:64249405..64253780,7	MCF-7	breast:
26	chr12:64265884..64268355-chr12:64269681..64272144,3	MCF-7	breast:
27	chr12:64243148..64249002-chr12:64249405..64253780,7	MCF-7	breast:
28	chr12:64262850..64264983-chr12:64404690..64407382,2	MCF-7	breast:
29	chr12:64263544..64264431-chr12:64474734..64475281,2	MCF-7	breast:
30	chr12:64240146..64242509-chr12:64254956..64256783,2	MCF-7	breast:
31	chr12:64240035..64242114-chr12:64615625..64617239,2	MCF-7	breast:
32	chr12:64248021..64249552-chr12:64270096..64271954,2	MCF-7	breast:
33	chr12:64243123..64244682-chr12:64261360..64263267,2	MCF-7	breast:
34	chr12:64237199..64239425-chr12:64240324..64242683,2	K562	blood:
35	chr12:64233673..64240233-chr12:64613167..64618011,13	MCF-7	breast:
36	chr12:64234247..64239748-chr12:64612699..64616990,14	MCF-7	breast:
37	chr12:64235522..64237444-chr12:64652638..64654533,2	K562	blood:
38	chr12:64234749..64237107-chr12:64586923..64589437,2	MCF-7	breast:
39	chr12:64235116..64240404-chr12:64242494..64248805,7	MCF-7	breast:
40	chr12:64231966..64234951-chr12:64236615..64238882,2	MCF-7	breast:
41	chr12:64238988..64240941-chr12:64313933..64315670,2	MCF-7	breast:
42	chr12:64240054..64242405-chr12:64482423..64484975,2	MCF-7	breast:
43	chr12:64237304..64239476-chr12:64424891..64426645,2	MCF-7	breast:
44	chr12:64257945..64259859-chr12:64259892..64262492,3	MCF-7	breast:
45	chr12:64239389..64242178-chr12:64352043..64353568,2	MCF-7	breast:
46	chr12:64240094..64242329-chr12:64649536..64651426,2	MCF-7	breast:
47	chr12:64172802..64174995-chr12:64236940..64239856,2	MCF-7	breast:
48	chr12:64248653..64250464-chr12:64256025..64258029,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DPY19L2-6	chr12:64265519-64265824	NONHSAT029123

No data

Variant related genes	Relation type
RPL36AP41	TF binding region
SRGAP1	TF binding region
ENSG00000256571	TF binding region
RPL36AP41	CpG island
SRGAP1	CpG island
ENSG00000256571	CpG island
ENSG00000272368	chromatin interactions
ENSG00000242087	chromatin interactions
ENSG00000212298	chromatin interactions
ENSG00000255817	chromatin interactions
ENSG00000243024	chromatin interactions
ENSG00000178449	chromatin interactions
ENSG00000174206	chromatin interactions
ENSG00000118600	chromatin interactions
ENSG00000255780	chromatin interactions
ENSG00000196935	chromatin interactions

Extended variants
information (count: 1126 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1126 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17099872	chr12:64234926-64234927	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545109337	chr12:64235003-64235004	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs144406847	chr12:64235010-64235011	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs527261627	chr12:64235076-64235077	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs547017037	chr12:64235096-64235097	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs560841225	chr12:64235102-64235103	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs79155309	chr12:64235116-64235117	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs76703851	chr12:64235117-64235118	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs57618488	chr12:64235183-64235184	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs397951033	chr12:64235192-64235193	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs557813471	chr12:64235227-64235228	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs549518216	chr12:64235240-64235241	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs60069860	chr12:64235244-64235245	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs187721310	chr12:64235319-64235320	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs537920709	chr12:64235338-64235339	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs551839867	chr12:64235372-64235373	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs571680590	chr12:64235375-64235376	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs556722323	chr12:64235436-64235437	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs549146509	chr12:64235481-64235482	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs534192414	chr12:64235534-64235535	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs148793512	chr12:64235535-64235536	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs574340146	chr12:64235595-64235596	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs536946479	chr12:64235677-64235678	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs577963332	chr12:64235678-64235679	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs192753025	chr12:64235712-64235713	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs545305160	chr12:64235736-64235737	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs564971102	chr12:64235747-64235748	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs558640124	chr12:64235749-64235750	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs73313475	chr12:64235765-64235766	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs185433749	chr12:64235785-64235786	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs529911423	chr12:64235821-64235822	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs539820087	chr12:64235823-64235824	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs187898379	chr12:64235847-64235848	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs200432214	chr12:64236001-64236002	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs12819035	chr12:64236002-64236003	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs78788297	chr12:64236004-64236005	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs56321914	chr12:64236024-64236025	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs532314325	chr12:64236111-64236112	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs552136435	chr12:64236120-64236121	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs191985809	chr12:64236168-64236169	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs12298689	chr12:64236192-64236193	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs534295796	chr12:64236299-64236300	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs547764283	chr12:64236309-64236310	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs7958627	chr12:64236349-64236350	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs184686162	chr12:64236474-64236475	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs544872030	chr12:64236492-64236493	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs7958845	chr12:64236511-64236512	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs142083744	chr12:64236514-64236515	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs12298928	chr12:64236529-64236530	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs556879695	chr12:64236551-64236552	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD

Chromatin state (count:1189 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:64216200-64237000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr12:64228200-64235800	Enhancers	Fetal Brain Male	brain
3	chr12:64230600-64237000	Weak transcription	Right Atrium	heart
4	chr12:64230800-64237000	Weak transcription	Brain Germinal Matrix	brain
5	chr12:64231000-64237000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:64232200-64236800	Weak transcription	Fetal Brain Female	brain
7	chr12:64234600-64236200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr12:64234800-64236000	Enhancers	NHLF	lung
9	chr12:64234800-64236800	Weak transcription	A549	lung
10	chr12:64235000-64235600	Enhancers	NHDF-Ad	bronchial
11	chr12:64235200-64235400	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr12:64235400-64235600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr12:64235400-64237000	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr12:64235600-64235800	Enhancers	Brain Hippocampus Middle	brain
15	chr12:64235600-64235800	Enhancers	HepG2	liver
16	chr12:64235600-64237000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr12:64235600-64237000	Weak transcription	NHDF-Ad	bronchial
18	chr12:64235800-64236600	Weak transcription	Fetal Brain Male	brain
19	chr12:64235800-64236800	Weak transcription	HepG2	liver
20	chr12:64235800-64237000	Weak transcription	Brain Hippocampus Middle	brain
21	chr12:64236000-64237000	Weak transcription	NHLF	lung
22	chr12:64236200-64236600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr12:64236600-64236800	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr12:64236600-64237000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr12:64236600-64237000	Enhancers	Fetal Brain Male	brain
26	chr12:64236800-64237000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr12:64236800-64237000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
28	chr12:64236800-64237000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr12:64236800-64237000	Enhancers	Muscle Satellite Cultured Cells	--
30	chr12:64236800-64237000	Active TSS	Adipose Nuclei	Adipose
31	chr12:64236800-64237000	Enhancers	Liver	Liver
32	chr12:64236800-64237000	Enhancers	Brain Angular Gyrus	brain
33	chr12:64236800-64237000	Enhancers	Fetal Heart	heart
34	chr12:64236800-64237000	Enhancers	Fetal Intestine Large	intestine
35	chr12:64236800-64237000	Enhancers	Fetal Muscle Trunk	muscle
36	chr12:64236800-64237000	Flanking Active TSS	A549	lung
37	chr12:64236800-64237000	Active TSS	Hela-S3	cervix
38	chr12:64236800-64237000	Enhancers	HepG2	liver
39	chr12:64236800-64237000	Active TSS	HUVEC	blood vessel
40	chr12:64236800-64237200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr12:64236800-64238400	Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr12:64236800-64238400	Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr12:64236800-64238400	Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr12:64236800-64238600	Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr12:64236800-64238800	Active TSS	Fetal Brain Female	brain
46	chr12:64236800-64239600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr12:64236800-64239600	Active TSS	Brain Substantia Nigra	brain
48	chr12:64236800-64239600	Active TSS	Pancreatic Islets	Pancreatic Islet
49	chr12:64236800-64240200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr12:64236800-64240800	Active TSS	ES-I3 Cell Line	embryonic stem cell

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