Variant report

Variant	esv1811918
Chromosome Location	chr12:46965257-47033254
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:336)
CpG islands
(count:62)
Chromatin interactive
region (count:31)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:46973105-46973651	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:46970849-46971198	HepG2	liver:	n/a	n/a
3	ATF1	chr12:47002940-47003079	K562	blood:	n/a	n/a
4	ATF1	chr12:46979675-46979881	K562	blood:	n/a	n/a
5	BCL3	chr12:47023574-47023851	GM12878	blood:	n/a	n/a
6	BHLHE40	chr12:47004620-47004796	GM12878	blood:	n/a	n/a
7	CBX3	chr12:46979624-46980018	K562	blood:	n/a	n/a
8	CEBPB	chr12:46974260-46974597	A549	lung:	n/a	chr12:46974404-46974415
9	CEBPB	chr12:46974247-46974582	IMR90	lung:	n/a	chr12:46974404-46974415
10	CEBPB	chr12:47017356-47017408	HepG2	liver:	n/a	chr12:47017382-47017393
11	CEBPB	chr12:46997588-46997829	HepG2	liver:	n/a	chr12:46997711-46997722
12	CEBPB	chr12:46965497-46965774	A549	lung:	n/a	chr12:46965614-46965625 chr12:46965616-46965627 chr12:46965614-46965627 chr12:46965614-46965627
13	CEBPB	chr12:47010915-47011283	IMR90	lung:	n/a	chr12:47011097-47011108 chr12:47011095-47011108 chr12:47011095-47011106 chr12:47011095-47011108
14	CEBPB	chr12:46974306-46974570	H1-hESC	embryonic stem cell:	n/a	chr12:46974404-46974415
15	CEBPB	chr12:46974243-46974591	Hela-S3	cervix:	n/a	chr12:46974404-46974415
16	CEBPB	chr12:46974260-46974615	MCF-7	breast:	n/a	chr12:46974404-46974415
17	CEBPB	chr12:46973446-46973680	MCF-7	breast:	n/a	n/a
18	CEBPB	chr12:47010986-47011221	HepG2	liver:	n/a	chr12:47011097-47011108 chr12:47011095-47011108 chr12:47011095-47011106 chr12:47011095-47011108
19	CEBPB	chr12:47010942-47011127	A549	lung:	n/a	chr12:47011097-47011108 chr12:47011095-47011108 chr12:47011095-47011106 chr12:47011095-47011108
20	CEBPB	chr12:47017288-47017415	IMR90	lung:	n/a	chr12:47017382-47017393
21	CEBPB	chr12:47017356-47017523	K562	blood:	n/a	chr12:47017382-47017393
22	CEBPB	chr12:47026097-47026116	HepG2	liver:	n/a	n/a
23	CEBPB	chr12:46973214-46973596	HepG2	liver:	n/a	n/a
24	CEBPB	chr12:46965507-46965773	IMR90	lung:	n/a	chr12:46965614-46965625 chr12:46965616-46965627 chr12:46965614-46965627 chr12:46965614-46965627
25	CEBPB	chr12:46974260-46974533	K562	blood:	n/a	chr12:46974404-46974415
26	CEBPB	chr12:47005123-47005296	K562	blood:	n/a	n/a
27	CEBPB	chr12:46970787-46971390	HepG2	liver:	n/a	chr12:46971231-46971242
28	CEBPB	chr12:46966912-46967141	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr12:46974227-46974574	K562	blood:	n/a	chr12:46974404-46974415
30	CEBPB	chr12:46965485-46965685	K562	blood:	n/a	chr12:46965614-46965625 chr12:46965616-46965627 chr12:46965614-46965627 chr12:46965614-46965627
31	CEBPB	chr12:46965487-46965708	HepG2	liver:	n/a	chr12:46965614-46965625 chr12:46965616-46965627 chr12:46965614-46965627 chr12:46965614-46965627
32	CEBPB	chr12:46974302-46974450	HepG2	liver:	n/a	chr12:46974404-46974415
33	CEBPB	chr12:46974231-46974602	HepG2	liver:	n/a	chr12:46974404-46974415
34	CEBPB	chr12:47010968-47011269	Hela-S3	cervix:	n/a	chr12:47011097-47011108 chr12:47011095-47011108 chr12:47011095-47011106 chr12:47011095-47011108
35	CHD2	chr12:46979775-46979865	K562	blood:	n/a	n/a
36	CTCF	chr12:46998200-46998350	GM12873	blood:	n/a	n/a
37	CTCF	chr12:46985580-46985730	GM12868	blood:	n/a	n/a
38	CTCF	chr12:47002220-47002370	AG04449	skin:	n/a	n/a
39	CTCF	chr12:46998140-46998290	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:47009099-47009176	GM20000	blood:	n/a	n/a
41	CTCF	chr12:46998180-46998330	GM12871	blood:	n/a	n/a
42	CTCF	chr12:46998005-46998040	GM13976	blood:	n/a	n/a
43	CTCF	chr12:46998020-46998170	GM12869	blood:	n/a	n/a
44	CTCF	chr12:47024640-47024790	GM12875	blood:	n/a	chr12:47024775-47024784
45	CTCF	chr12:47024620-47024770	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr12:46998080-46998230	GM12872	blood:	n/a	n/a
47	CTCF	chr12:47024640-47024790	GM12873	blood:	n/a	chr12:47024775-47024784
48	CTCF	chr12:47018580-47018730	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr12:47024660-47024810	MCF-7	breast:	n/a	chr12:47024775-47024784
50	CTCF	chr12:46998211-46998293	H1-hESC	embryonic stem cell:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:47022795-47022845	HRE	kidney:	n/a
2	chr12:47022795-47022845	HRE	kidney:	n/a
3	chr12:47022795-47022845	ECC-1	luminal epithelium:	n/a
4	chr12:47022795-47022845	HEEpiC	esophagus:	n/a
5	chr12:47022795-47022845	RPTEC	kidney:	n/a
6	chr12:47022795-47022845	GM06990	blood:	n/a
7	chr12:47022795-47022845	SK-N-SH	brain:	n/a
8	chr12:47022795-47022845	PrEC	prostate:	n/a
9	chr12:47022795-47022845	HIPEpiC	eye:	n/a
10	chr12:47022795-47022845	AG09319	gingival:	n/a
11	chr12:47022795-47022845	PANC-1	pancreas:	n/a
12	chr12:47022795-47022845	IMR90	lung:	fetal
13	chr12:47022795-47022845	NT2-D1	testis:	n/a
14	chr12:47022795-47022845	HEK293	kidney:	embryo
15	chr12:47022795-47022845	NHBE	bronchial:	n/a
16	chr12:47022795-47022845	HRCEpiC	kidney:	n/a
17	chr12:47022795-47022845	PFSK-1	brain:	n/a
18	chr12:47022795-47022845	ovcar-3	ovarian:	n/a
19	chr12:47022795-47022845	HAEpiC	amniotic membrane:	n/a
20	chr12:47022795-47022845	NH-A	brain:	n/a
21	chr12:47022795-47022845	SAEC	small airway:	n/a
22	chr12:47022795-47022845	AG04449	skin:	fetal
23	chr12:47022795-47022845	HL-60	blood:	n/a
24	chr12:47022795-47022845	CMK	blood:	n/a
25	chr12:47022795-47022845	Hepatocyte	liver:	n/a
26	chr12:47022795-47022845	LNCaP	prostate:	n/a
27	chr12:47022795-47022845	BE2_C	brain:	n/a
28	chr12:47022795-47022845	BJ	skin:	n/a
29	chr12:47022795-47022845	K562	blood:	n/a
30	chr12:47022795-47022845	HPAEpiC	pulmonary alveolar:	n/a
31	chr12:47022795-47022845	NB4	blood:	n/a
32	chr12:47022795-47022845	ProgFib	skin:	n/a
33	chr12:47022795-47022845	GM12878	blood:	n/a
34	chr12:47022795-47022845	GM12892	blood:	n/a
35	chr12:47022795-47022845	HCF	heart:	n/a
36	chr12:47022795-47022845	HCM	heart:	n/a
37	chr12:47022795-47022845	HUVEC	blood vessel:	n/a
38	chr12:47022795-47022845	AG09309	skin:	n/a
39	chr12:47022795-47022845	HCPEpiC	choroid plexus:	n/a
40	chr12:47022795-47022845	HRPEpiC	eye:	n/a
41	chr12:47022795-47022845	HCT-116	colon:	n/a
42	chr12:47022795-47022845	HNPCEpiC	eye:	n/a
43	chr12:47022795-47022845	SK-N-SH_RA	brain:	n/a
44	chr12:47022795-47022845	SK-N-MC	brain:	n/a
45	chr12:47022795-47022845	AG04450	lung:	fetal
46	chr12:47022795-47022845	H1-hESC	embryonic stem cell:	embryo
47	chr12:47022795-47022845	T-47D	breast:	n/a
48	chr12:47022795-47022845	AG10803	skin:	n/a
49	chr12:47022795-47022845	AoSMC	blood vessel:	n/a
50	chr12:47022795-47022845	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:46760405..46763047-chr12:46997167..46998956,2	K562	blood:
2	chr12:46760939..46762662-chr12:46964793..46967282,2	K562	blood:
3	chr12:46965755..46967970-chr12:46969956..46972326,2	MCF-7	breast:
4	chr12:47018512..47021454-chr12:47022647..47024563,2	K562	blood:
5	chr12:46997151..46999304-chr12:47001117..47002975,2	K562	blood:
6	chr12:47004476..47006389-chr12:47019123..47021406,2	K562	blood:
7	chr12:47004476..47006389-chr12:47019123..47021406,2	K562	blood:
8	chr12:46972689..46974788-chr12:47053934..47056734,2	MCF-7	breast:
9	chr12:46996986..46999798-chr12:47001476..47004365,3	MCF-7	breast:
10	chr12:46963166..46965349-chr12:46968243..46970653,2	K562	blood:
11	chr12:46996953..46999304-chr12:47001117..47002975,3	K562	blood:
12	chr12:46765212..46766815-chr12:46968840..46971660,2	MCF-7	breast:
13	chr12:46963166..46965705-chr12:46969153..46971844,2	K562	blood:
14	chr12:47018512..47021454-chr12:47022647..47024563,3	K562	blood:
15	chr12:47018512..47021454-chr12:47022647..47024563,2	K562	blood:
16	chr12:46997151..46999304-chr12:47001117..47002975,2	K562	blood:
17	chr12:46761162..46768544-chr12:46964631..46969835,8	K562	blood:
18	chr12:46965755..46967970-chr12:46969956..46972326,2	MCF-7	breast:
19	chr12:46996953..46999304-chr12:47001117..47002975,3	K562	blood:
20	chr12:47025079..47028602-chr12:47029579..47033419,4	MCF-7	breast:
21	chr12:46923109..46925590-chr12:46988951..46990498,2	MCF-7	breast:
22	chr12:47018512..47021454-chr12:47022647..47024563,3	K562	blood:
23	chr12:46657106..46659743-chr12:47006995..47009851,2	MCF-7	breast:
24	chr12:46764440..46766646-chr12:46971360..46973081,2	MCF-7	breast:
25	chr12:46963166..46965349-chr12:46968243..46970653,2	K562	blood:
26	chr12:46764555..46766598-chr12:47004748..47006262,2	MCF-7	breast:
27	chr12:46996986..46999798-chr12:47001476..47004365,3	MCF-7	breast:
28	chr12:46777368..46779670-chr12:46992247..46995085,2	MCF-7	breast:
29	chr12:46963166..46965705-chr12:46969153..46971844,2	K562	blood:
30	chr12:47025079..47028602-chr12:47029579..47033419,4	MCF-7	breast:
31	chr12:46887354..46888000-chr12:46973431..46973941,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC38A2-3	chr12:46968827-46968899	NONHSAT027883

No data

Variant related genes	Relation type
OR7A19P	TF binding region
OR7A19P	CpG island
ENSG00000257261	chromatin interactions
ENSG00000258096	chromatin interactions
ENSG00000134294	chromatin interactions

Extended variants
information (count: 2413 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2413 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11831929	chr12:46965257-46965258	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs139272299	chr12:46965318-46965319	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs367616447	chr12:46965341-46965342	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs541764668	chr12:46965417-46965418	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs562015625	chr12:46965446-46965447	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs12318411	chr12:46965470-46965471	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs547372999	chr12:46965478-46965479	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs185488115	chr12:46965586-46965587	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs533270394	chr12:46965631-46965632	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs550211614	chr12:46965655-46965656	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs539900099	chr12:46965667-46965668	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs147157141	chr12:46965674-46965675	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs190348015	chr12:46965717-46965718	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs549457531	chr12:46965752-46965753	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs566492068	chr12:46965824-46965825	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs182946529	chr12:46965825-46965826	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs553825957	chr12:46965830-46965831	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs534152076	chr12:46965882-46965883	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs555592213	chr12:46965883-46965884	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs368523152	chr12:46965892-46965893	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs576874875	chr12:46965894-46965895	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs140412310	chr12:46965935-46965936	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs538092591	chr12:46965939-46965940	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs187647216	chr12:46966129-46966130	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs576207935	chr12:46966155-46966156	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs542000795	chr12:46966213-46966214	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs149233021	chr12:46966226-46966227	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs372421721	chr12:46966241-46966242	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs35542017	chr12:46966329-46966330	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs571988500	chr12:46966354-46966355	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs2408578	chr12:46966366-46966367	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs564153545	chr12:46966384-46966385	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs533113513	chr12:46966411-46966412	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs144467359	chr12:46966463-46966464	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs193058761	chr12:46966705-46966706	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs529502866	chr12:46966707-46966708	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs184187804	chr12:46966730-46966731	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs73291969	chr12:46966773-46966774	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs187569318	chr12:46966803-46966804	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs528812169	chr12:46966807-46966808	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs577689555	chr12:46966813-46966814	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs112484127	chr12:46966841-46966842	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs150048839	chr12:46966846-46966847	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs560201342	chr12:46966861-46966862	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs539418318	chr12:46966876-46966877	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs556029046	chr12:46966930-46966931	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs376738620	chr12:46966974-46966975	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs192811218	chr12:46967036-46967037	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs11836940	chr12:46967064-46967065	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs561207956	chr12:46967110-46967111	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Neurodevelopmental disorder	22521361	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21542898	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:605 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:46961600-46970800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:46963000-46971200	Weak transcription	Primary B cells from cord blood	blood
3	chr12:46963200-46966400	Weak transcription	Hela-S3	cervix
4	chr12:46963400-46965600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr12:46963800-46970800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr12:46963800-46971000	Weak transcription	Aorta	Aorta
7	chr12:46964000-46979400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr12:46964800-46965800	Enhancers	NHDF-Ad	bronchial
9	chr12:46964800-46969400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr12:46965000-46967800	Enhancers	HSMMtube	muscle
11	chr12:46965200-46975200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr12:46965200-46977600	Weak transcription	Primary hematopoietic stem cells	blood
13	chr12:46965600-46965800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr12:46965800-46966800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr12:46965800-46972200	Weak transcription	NHDF-Ad	bronchial
16	chr12:46966600-46967000	Enhancers	HepG2	liver
17	chr12:46966600-46967200	Enhancers	HSMM	muscle
18	chr12:46966600-46967600	Enhancers	Osteobl	bone
19	chr12:46966600-46967800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr12:46966600-46967800	Enhancers	Psoas Muscle	Psoas
21	chr12:46966600-46968000	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr12:46966800-46967000	Enhancers	Hela-S3	cervix
23	chr12:46966800-46967200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr12:46966800-46967600	Enhancers	Adipose Nuclei	Adipose
25	chr12:46966800-46967800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr12:46966800-46967800	Enhancers	Liver	Liver
27	chr12:46966800-46967800	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr12:46966800-46968600	Enhancers	Fetal Lung	lung
29	chr12:46967000-46968600	Weak transcription	HepG2	liver
30	chr12:46967200-46967600	Enhancers	Fetal Muscle Leg	muscle
31	chr12:46967600-46967800	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr12:46967600-46968600	Weak transcription	Adipose Nuclei	Adipose
33	chr12:46967600-46972600	Weak transcription	Primary B cells from peripheral blood	blood
34	chr12:46967800-46968200	Weak transcription	Liver	Liver
35	chr12:46967800-46968800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr12:46967800-46968800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr12:46967800-46972000	Weak transcription	HSMMtube	muscle
38	chr12:46967800-46972400	Weak transcription	Psoas Muscle	Psoas
39	chr12:46967800-46972400	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr12:46968000-46969000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr12:46968000-46972400	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr12:46968200-46969400	Enhancers	Liver	Liver
43	chr12:46968600-46969400	Enhancers	Adipose Nuclei	Adipose
44	chr12:46968600-46969600	Enhancers	HepG2	liver
45	chr12:46968800-46969400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr12:46968800-46969400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr12:46968800-46969400	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr12:46968800-46969600	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr12:46969000-46969400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr12:46969000-46969400	Enhancers	HUES48 Cell Line	embryonic stem cell

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