Variant report

Variant	nsv5513
Chromosome Location	chr6:144068006-144102028
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	ATF1	chr6:144068421-144069008	K562	blood:	n/a	n/a
2	ATF1	chr6:144099907-144100043	K562	blood:	n/a	n/a
3	ATF1	chr6:144078467-144078874	K562	blood:	n/a	n/a
4	ATF2	chr6:144067075-144068247	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr6:144067217-144068081	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:144067444-144068191	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:144072409-144072444	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr6:144078994-144079337	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:144068428-144069066	K562	blood:	n/a	n/a
10	BRCA1	chr6:144068926-144068968	H1-hESC	embryonic stem cell:	n/a	n/a
11	CCNT2	chr6:144100153-144100166	K562	blood:	n/a	n/a
12	CCNT2	chr6:144068444-144068865	K562	blood:	n/a	n/a
13	CCNT2	chr6:144079096-144079286	K562	blood:	n/a	n/a
14	CEBPB	chr6:144094728-144095051	A549	lung:	n/a	chr6:144094867-144094880 chr6:144094867-144094878 chr6:144094869-144094878 chr6:144094867-144094878 chr6:144094868-144094879 chr6:144094869-144094878 chr6:144094867-144094880 chr6:144094867-144094880 chr6:144094869-144094878 chr6:144094869-144094878
15	CEBPB	chr6:144094785-144094901	H1-hESC	embryonic stem cell:	n/a	chr6:144094867-144094880 chr6:144094867-144094878 chr6:144094869-144094878 chr6:144094867-144094878 chr6:144094868-144094879 chr6:144094869-144094878 chr6:144094867-144094880 chr6:144094867-144094880 chr6:144094869-144094878 chr6:144094869-144094878
16	CEBPB	chr6:144094699-144095054	K562	blood:	n/a	chr6:144094867-144094880 chr6:144094867-144094878 chr6:144094869-144094878 chr6:144094867-144094878 chr6:144094868-144094879 chr6:144094869-144094878 chr6:144094867-144094880 chr6:144094867-144094880 chr6:144094869-144094878 chr6:144094869-144094878
17	CEBPB	chr6:144076338-144076685	IMR90	lung:	n/a	n/a
18	CEBPB	chr6:144094699-144095061	IMR90	lung:	n/a	chr6:144094867-144094880 chr6:144094867-144094878 chr6:144094869-144094878 chr6:144094867-144094878 chr6:144094868-144094879 chr6:144094869-144094878 chr6:144094867-144094880 chr6:144094867-144094880 chr6:144094869-144094878 chr6:144094869-144094878
19	CEBPB	chr6:144094708-144095041	HepG2	liver:	n/a	chr6:144094867-144094880 chr6:144094867-144094878 chr6:144094869-144094878 chr6:144094867-144094878 chr6:144094868-144094879 chr6:144094869-144094878 chr6:144094867-144094880 chr6:144094867-144094880 chr6:144094869-144094878 chr6:144094869-144094878
20	CEBPB	chr6:144094761-144095037	Hela-S3	cervix:	n/a	chr6:144094867-144094880 chr6:144094867-144094878 chr6:144094869-144094878 chr6:144094867-144094878 chr6:144094868-144094879 chr6:144094869-144094878 chr6:144094867-144094880 chr6:144094867-144094880 chr6:144094869-144094878 chr6:144094869-144094878
21	CEBPB	chr6:144076349-144076711	A549	lung:	n/a	n/a
22	CEBPB	chr6:144076365-144076724	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr6:144076303-144076809	A549	lung:	n/a	n/a
24	CEBPB	chr6:144078457-144078860	K562	blood:	n/a	chr6:144078776-144078789
25	CEBPB	chr6:144076343-144076682	HepG2	liver:	n/a	n/a
26	CHD2	chr6:144067598-144068133	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr6:144068710-144068771	HepG2	liver:	n/a	n/a
28	CREB1	chr6:144076435-144076680	A549	lung:	n/a	n/a
29	CTBP2	chr6:144067459-144068072	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr6:144094828-144094852	Lung_OC	lung:	n/a	n/a
31	CTCF	chr6:144082339-144082377	Lung_OC	lung:	n/a	n/a
32	CTCF	chr6:144076495-144076544	Gliobla	brain:	n/a	n/a
33	CTCF	chr6:144093220-144093370	BJ	skin:	n/a	n/a
34	CTCF	chr6:144086768-144086799	ProgFib	skin:	n/a	n/a
35	CTCF	chr6:144076486-144076569	MCF-7	breast:	n/a	n/a
36	CTCF	chr6:144093280-144093430	BJ	skin:	n/a	n/a
37	CTCF	chr6:144096400-144096550	GM12866	blood:	n/a	n/a
38	CUX1	chr6:144079860-144079986	K562	blood:	n/a	chr6:144079938-144079947
39	EP300	chr6:144076331-144076625	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr6:144067510-144068119	H1-hESC	embryonic stem cell:	n/a	n/a
41	EP300	chr6:144068465-144068781	K562	blood:	n/a	chr6:144068589-144068599
42	EP300	chr6:144076252-144076895	A549	lung:	n/a	n/a
43	EP300	chr6:144076308-144076684	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr6:144079643-144080001	HepG2	liver:	n/a	n/a
45	EP300	chr6:144068546-144069044	HepG2	liver:	n/a	chr6:144068589-144068599
46	EP300	chr6:144065464-144068008	HepG2	liver:	n/a	chr6:144066048-144066062 chr6:144066134-144066143 chr6:144066133-144066142
47	EP300	chr6:144073565-144073982	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr6:144079777-144079922	HepG2	liver:	n/a	n/a
49	EP300	chr6:144068249-144069125	HepG2	liver:	n/a	chr6:144068589-144068599
50	EP300	chr6:144068350-144068850	HepG2	liver:	n/a	chr6:144068589-144068599

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:144074925-144074975	HUVEC	blood vessel:	n/a
2	chr6:144074925-144074975	HepG2	liver:	n/a
3	chr6:144074925-144074975	CMK	blood:	n/a
4	chr6:144074617-144074667	U87	brain:	n/a
5	chr6:144074925-144074975	SKMC	muscle:	n/a
6	chr6:144074925-144074975	HPAEpiC	pulmonary alveolar:	n/a
7	chr6:144074925-144074975	AG09309	skin:	n/a
8	chr6:144074617-144074667	PrEC	prostate:	n/a
9	chr6:144074925-144074975	HL-60	blood:	n/a
10	chr6:144074925-144074975	Hepatocyte	liver:	n/a
11	chr6:144074925-144074975	PrEC	prostate:	n/a
12	chr6:144074617-144074667	NH-A	brain:	n/a
13	chr6:144074617-144074667	RPTEC	kidney:	n/a
14	chr6:144074617-144074667	HRE	kidney:	n/a
15	chr6:144074925-144074975	Jurkat	blood:	n/a
16	chr6:144074617-144074667	Caco-2	colon:	n/a
17	chr6:144074925-144074975	IMR90	lung:	fetal
18	chr6:144074617-144074667	AG04449	skin:	fetal
19	chr6:144074925-144074975	HRPEpiC	eye:	n/a
20	chr6:144074617-144074667	MCF-7	breast:	n/a
21	chr6:144074617-144074667	HL-60	blood:	n/a
22	chr6:144074617-144074667	HAEpiC	amniotic membrane:	n/a
23	chr6:144074617-144074667	GM12878	blood:	n/a
24	chr6:144074617-144074667	ProgFib	skin:	n/a
25	chr6:144074925-144074975	HEK293	kidney:	embryo
26	chr6:144074925-144074975	AoSMC	blood vessel:	n/a
27	chr6:144074617-144074667	NT2-D1	testis:	n/a
28	chr6:144074617-144074667	HUVEC	blood vessel:	n/a
29	chr6:144074617-144074667	HepG2	liver:	n/a
30	chr6:144074925-144074975	BE2_C	brain:	n/a
31	chr6:144074925-144074975	RPTEC	kidney:	n/a
32	chr6:144074617-144074667	K562	blood:	n/a
33	chr6:144074925-144074975	MCF10A-Er-Src	breast:	n/a
34	chr6:144074617-144074667	CMK	blood:	n/a
35	chr6:144074925-144074975	HRE	kidney:	n/a
36	chr6:144074617-144074667	NHDF-neo	bronchial:	n/a
37	chr6:144074925-144074975	Caco-2	colon:	n/a
38	chr6:144074617-144074667	HPAEpiC	pulmonary alveolar:	n/a
39	chr6:144074617-144074667	SKMC	muscle:	n/a
40	chr6:144074617-144074667	AG09309	skin:	n/a
41	chr6:144074617-144074667	AG09319	gingival:	n/a
42	chr6:144074617-144074667	HMEC	breast:	n/a
43	chr6:144074617-144074667	HNPCEpiC	eye:	n/a
44	chr6:144074925-144074975	K562	blood:	n/a
45	chr6:144074925-144074975	U87	brain:	n/a
46	chr6:144074617-144074667	BE2_C	brain:	n/a
47	chr6:144074925-144074975	HCF	heart:	n/a
48	chr6:144074925-144074975	NH-A	brain:	n/a
49	chr6:144074617-144074667	GM12891	blood:	n/a
50	chr6:144074617-144074667	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:144085424..144087844-chr6:144169297..144171955,2	K562	blood:
2	chr6:144083699..144085965-chr6:144088536..144091208,2	K562	blood:
3	chr6:144075659..144077408-chr6:144078604..144081076,2	K562	blood:
4	chr6:144076102..144076905-chr8:128588687..128589603,2	MCF-7	breast:
5	chr6:144076953..144079572-chr6:144081415..144086815,4	K562	blood:
6	chr6:143831076..143832888-chr6:144092613..144094642,2	MCF-7	breast:
7	chr6:144071724..144073521-chr6:144074905..144077250,2	MCF-7	breast:
8	chr6:144074038..144075721-chr6:144077621..144079711,2	K562	blood:
9	chr6:144037482..144039752-chr6:144079011..144080855,2	K562	blood:
10	chr6:144078322..144080514-chr6:144163039..144165218,2	K562	blood:
11	chr6:144091837..144094429-chr6:144095791..144097571,2	K562	blood:
12	chr6:144083699..144085965-chr6:144088536..144091208,2	K562	blood:
13	chr6:144076953..144079572-chr6:144081415..144086815,4	K562	blood:
14	chr6:144080993..144084686-chr6:144086462..144088347,3	K562	blood:
15	chr6:144094412..144096220-chr6:144126094..144128720,2	K562	blood:
16	chr6:144071798..144073720-chr6:144082492..144084536,2	MCF-7	breast:
17	chr6:144071732..144074823-chr6:144075904..144078859,3	MCF-7	breast:
18	chr6:144071724..144073521-chr6:144074905..144077250,2	MCF-7	breast:
19	chr6:144059361..144061589-chr6:144086524..144088312,2	K562	blood:
20	chr6:144063490..144065500-chr6:144068197..144069773,2	K562	blood:
21	chr6:144074038..144075721-chr6:144077621..144079711,2	K562	blood:
22	chr6:143831191..143834659-chr6:144066379..144069896,4	MCF-7	breast:
23	chr6:144071732..144074823-chr6:144075904..144078859,3	MCF-7	breast:
24	chr6:144069372..144071037-chr6:144077042..144078678,2	MCF-7	breast:
25	chr6:144080993..144084686-chr6:144086462..144088347,3	K562	blood:
26	chr6:143998734..144000526-chr6:144065898..144068139,2	MCF-7	breast:
27	chr6:144075659..144077408-chr6:144078604..144081076,2	K562	blood:
28	chr6:144091837..144094429-chr6:144095791..144097571,2	K562	blood:
29	chr6:143993282..143995063-chr6:144073784..144075986,2	MCF-7	breast:
30	chr6:144071798..144073720-chr6:144082492..144084536,2	MCF-7	breast:

Variant related genes	Relation type
PHACTR2	TF binding region
PHACTR2	CpG island
ENSG00000001036	chromatin interactions
ENSG00000112419	chromatin interactions
ENSG00000257065	chromatin interactions
ENSG00000135521	chromatin interactions

Extended variants
information (count: 1224 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1224 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535232828	chr6:144068048-144068049	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs1935496	chr6:144068066-144068067	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs370340689	chr6:144068141-144068142	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs575199513	chr6:144068148-144068149	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs575198073	chr6:144068210-144068211	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs2235996	chr6:144068259-144068260	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs557640932	chr6:144068285-144068286	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs186906744	chr6:144068327-144068328	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs537921502	chr6:144068400-144068401	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs1935497	chr6:144068453-144068454	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs577778709	chr6:144068468-144068469	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs370686247	chr6:144068477-144068478	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs561768596	chr6:144068504-144068505	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs142889010	chr6:144068505-144068506	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs11962678	chr6:144068641-144068642	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs542001989	chr6:144068647-144068648	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs144280895	chr6:144068676-144068677	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs549987243	chr6:144068692-144068693	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs148676428	chr6:144068715-144068716	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs527245613	chr6:144068733-144068734	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs191931917	chr6:144068735-144068736	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs560365870	chr6:144068741-144068742	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs564793609	chr6:144068763-144068764	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs528824599	chr6:144068776-144068777	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs142145237	chr6:144068910-144068911	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs568603619	chr6:144068940-144068941	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs529487351	chr6:144068965-144068966	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs76157782	chr6:144068975-144068976	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs111741045	chr6:144068989-144068990	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs570712127	chr6:144069028-144069029	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs568573644	chr6:144069057-144069058	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs539062668	chr6:144069067-144069068	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs574003560	chr6:144069082-144069083	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs557358803	chr6:144069088-144069089	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs142599644	chr6:144069203-144069204	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs558150591	chr6:144069206-144069207	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs533874359	chr6:144069209-144069210	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs150802540	chr6:144069266-144069267	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs539651681	chr6:144069305-144069306	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs573754925	chr6:144069318-144069319	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs187053394	chr6:144069368-144069369	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs139736409	chr6:144069383-144069384	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs575782968	chr6:144069419-144069420	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs546298961	chr6:144069450-144069451	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs556074073	chr6:144069452-144069453	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs528487485	chr6:144069466-144069467	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs540618331	chr6:144069485-144069486	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs147572112	chr6:144069492-144069493	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs529474817	chr6:144069575-144069576	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs189689853	chr6:144069729-144069730	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1193 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:144038600-144075400	Weak transcription	NHEK	skin
2	chr6:144046200-144074600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr6:144053400-144076600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr6:144053600-144073600	Weak transcription	Osteobl	bone
5	chr6:144053600-144075400	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr6:144053600-144075600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr6:144053800-144079800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr6:144056200-144080200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr6:144059800-144077000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr6:144060200-144078400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr6:144060600-144074600	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr6:144060800-144074400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr6:144061000-144079800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr6:144061000-144086600	Weak transcription	Primary T cells from cord blood	blood
15	chr6:144063000-144075400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:144063400-144069000	Enhancers	Left Ventricle	heart
17	chr6:144063400-144069200	Enhancers	Fetal Heart	heart
18	chr6:144063400-144070600	Enhancers	H9 Cell Line	embryonic stem cell
19	chr6:144063400-144071400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:144063600-144068800	Enhancers	Right Ventricle	heart
21	chr6:144063600-144069000	Enhancers	Placenta Amnion	Placenta Amnion
22	chr6:144063600-144076600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr6:144063800-144075000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr6:144063800-144086400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr6:144064400-144071400	Enhancers	H1 Cell Line	embryonic stem cell
26	chr6:144064400-144074400	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr6:144064600-144069000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr6:144064600-144076800	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr6:144064800-144071000	Enhancers	Fetal Intestine Large	intestine
30	chr6:144064800-144075400	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr6:144064800-144086600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr6:144065600-144069800	Enhancers	Placenta	Placenta
33	chr6:144066400-144068400	Weak transcription	Small Intestine	intestine
34	chr6:144066400-144076400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr6:144066600-144075400	Weak transcription	Liver	Liver
36	chr6:144066600-144081000	Weak transcription	Esophagus	oesophagus
37	chr6:144066800-144068600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr6:144066800-144080600	Weak transcription	Spleen	Spleen
39	chr6:144067000-144068600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr6:144067000-144069000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr6:144067000-144069000	Enhancers	Fetal Stomach	stomach
42	chr6:144067000-144069000	Enhancers	Stomach Mucosa	stomach
43	chr6:144067000-144075800	Weak transcription	HUVEC	blood vessel
44	chr6:144067000-144076400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr6:144067000-144077200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr6:144067000-144081000	Weak transcription	Brain Angular Gyrus	brain
47	chr6:144067000-144083000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr6:144067200-144069200	Enhancers	Fetal Muscle Leg	muscle
49	chr6:144067200-144070000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr6:144067200-144070000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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