Variant report

Variant	nsv602958
Chromosome Location	chr6:38362024-38446634
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	ARID3A	chr6:38372214-38373086	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:38418438-38418909	HepG2	liver:	n/a	n/a
3	ATF1	chr6:38411596-38411926	K562	blood:	n/a	n/a
4	ATF2	chr6:38445534-38446002	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr6:38395485-38396059	GM12878	blood:	n/a	n/a
6	ATF2	chr6:38445535-38446087	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr6:38385354-38385551	HepG2	liver:	n/a	n/a
8	BHLHE40	chr6:38372154-38372381	GM12878	blood:	n/a	n/a
9	BRCA1	chr6:38411408-38411424	GM12878	blood:	n/a	n/a
10	BRCA1	chr6:38372302-38372439	GM12878	blood:	n/a	n/a
11	CEBPB	chr6:38402959-38403241	HepG2	liver:	n/a	chr6:38403067-38403078
12	CEBPB	chr6:38372576-38373089	A549	lung:	n/a	chr6:38372895-38372908 chr6:38372896-38372907 chr6:38372895-38372906 chr6:38372897-38372906
13	CEBPB	chr6:38372620-38373229	Hela-S3	cervix:	n/a	chr6:38372895-38372908 chr6:38372896-38372907 chr6:38372895-38372906 chr6:38372897-38372906
14	CEBPB	chr6:38404623-38404982	HepG2	liver:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
15	CEBPB	chr6:38372716-38373072	A549	lung:	n/a	chr6:38372895-38372908 chr6:38372896-38372907 chr6:38372895-38372906 chr6:38372897-38372906
16	CEBPB	chr6:38404599-38405042	MCF-7	breast:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
17	CEBPB	chr6:38404452-38405116	HCT-116	colon:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
18	CEBPB	chr6:38372676-38373136	ECC-1	luminal epithelium:	n/a	chr6:38372895-38372908 chr6:38372896-38372907 chr6:38372895-38372906 chr6:38372897-38372906
19	CEBPB	chr6:38372694-38373102	HepG2	liver:	n/a	chr6:38372895-38372908 chr6:38372896-38372907 chr6:38372895-38372906 chr6:38372897-38372906
20	CEBPB	chr6:38404559-38405061	A549	lung:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
21	CEBPB	chr6:38404748-38404953	H1-hESC	embryonic stem cell:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
22	CEBPB	chr6:38385365-38385623	H1-hESC	embryonic stem cell:	n/a	chr6:38385499-38385510
23	CEBPB	chr6:38372784-38373110	HepG2	liver:	n/a	chr6:38372895-38372908 chr6:38372896-38372907 chr6:38372895-38372906 chr6:38372897-38372906
24	CEBPB	chr6:38372687-38373133	A549	lung:	n/a	chr6:38372895-38372908 chr6:38372896-38372907 chr6:38372895-38372906 chr6:38372897-38372906
25	CEBPB	chr6:38385415-38385606	HepG2	liver:	n/a	chr6:38385499-38385510
26	CEBPB	chr6:38372632-38373185	MCF-7	breast:	n/a	chr6:38372895-38372908 chr6:38372896-38372907 chr6:38372895-38372906 chr6:38372897-38372906
27	CEBPB	chr6:38372464-38373277	MCF-7	breast:	n/a	chr6:38372895-38372908 chr6:38372896-38372907 chr6:38372895-38372906 chr6:38372897-38372906
28	CEBPB	chr6:38372766-38372960	HepG2	liver:	n/a	chr6:38372895-38372908 chr6:38372896-38372907 chr6:38372895-38372906 chr6:38372897-38372906
29	CEBPB	chr6:38385427-38385694	ECC-1	luminal epithelium:	n/a	chr6:38385499-38385510 chr6:38385686-38385694
30	CEBPB	chr6:38385339-38385668	MCF-7	breast:	n/a	chr6:38385499-38385510
31	CEBPB	chr6:38385354-38385599	HepG2	liver:	n/a	chr6:38385499-38385510
32	CEBPB	chr6:38385374-38385622	IMR90	lung:	n/a	chr6:38385499-38385510
33	CEBPB	chr6:38385924-38386459	HepG2	liver:	n/a	chr6:38386031-38386040 chr6:38386031-38386042 chr6:38386029-38386040 chr6:38386029-38386042
34	CEBPB	chr6:38404618-38404982	A549	lung:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
35	CEBPB	chr6:38368580-38368891	MCF-7	breast:	n/a	n/a
36	CEBPB	chr6:38372732-38373090	HepG2	liver:	n/a	chr6:38372895-38372908 chr6:38372896-38372907 chr6:38372895-38372906 chr6:38372897-38372906
37	CEBPB	chr6:38368411-38368892	MCF-7	breast:	n/a	n/a
38	CEBPB	chr6:38372652-38373172	ECC-1	luminal epithelium:	n/a	chr6:38372895-38372908 chr6:38372896-38372907 chr6:38372895-38372906 chr6:38372897-38372906
39	CEBPB	chr6:38385282-38385651	HCT-116	colon:	n/a	chr6:38385499-38385510
40	CEBPB	chr6:38445586-38445959	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr6:38385296-38385779	MCF-7	breast:	n/a	chr6:38385499-38385510 chr6:38385686-38385694
42	CEBPB	chr6:38372716-38373082	IMR90	lung:	n/a	chr6:38372895-38372908 chr6:38372896-38372907 chr6:38372895-38372906 chr6:38372897-38372906
43	CEBPB	chr6:38385352-38385628	Hela-S3	cervix:	n/a	chr6:38385499-38385510
44	CEBPB	chr6:38385284-38385708	HCT-116	colon:	n/a	chr6:38385499-38385510 chr6:38385686-38385694
45	CEBPB	chr6:38385886-38386476	IMR90	lung:	n/a	chr6:38386031-38386040 chr6:38386031-38386042 chr6:38386029-38386040 chr6:38386029-38386042
46	CEBPB	chr6:38385945-38386423	K562	blood:	n/a	chr6:38386031-38386040 chr6:38386031-38386042 chr6:38386029-38386040 chr6:38386029-38386042
47	CEBPB	chr6:38404552-38404999	IMR90	lung:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
48	CEBPB	chr6:38404527-38405019	MCF-7	breast:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
49	CEBPB	chr6:38404606-38404974	Hela-S3	cervix:	n/a	chr6:38404798-38404811 chr6:38404800-38404809 chr6:38404800-38404811 chr6:38404798-38404809
50	CEBPD	chr6:38372741-38373054	HepG2	liver:	n/a	chr6:38372896-38372907 chr6:38372895-38372906

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:38394278-38394328	ECC-1	luminal epithelium:	n/a
2	chr6:38394278-38394328	MCF10A-Er-Src	breast:	n/a
3	chr6:38394278-38394328	HUVEC	blood vessel:	n/a
4	chr6:38373578-38373628	HRCEpiC	kidney:	n/a
5	chr6:38394278-38394328	NB4	blood:	n/a
6	chr6:38373578-38373628	SK-N-SH_RA	brain:	n/a
7	chr6:38394278-38394328	Jurkat	blood:	n/a
8	chr6:38373578-38373628	GM12891	blood:	n/a
9	chr6:38445981-38446031	MCF10A-Er-Src	breast:	n/a
10	chr6:38394278-38394328	GM19239	blood:	n/a
11	chr6:38394278-38394328	IMR90	lung:	fetal
12	chr6:38373578-38373628	HIPEpiC	eye:	n/a
13	chr6:38373578-38373628	HCM	heart:	n/a
14	chr6:38394278-38394328	AG04450	lung:	fetal
15	chr6:38445981-38446031	H1-hESC	embryonic stem cell:	embryo
16	chr6:38373578-38373628	AoSMC	blood vessel:	n/a
17	chr6:38394278-38394328	Hepatocyte	liver:	n/a
18	chr6:38445981-38446031	AG09319	gingival:	n/a
19	chr6:38373578-38373628	ovcar-3	ovarian:	n/a
20	chr6:38394278-38394328	AoSMC	blood vessel:	n/a
21	chr6:38373578-38373628	MCF-7	breast:	n/a
22	chr6:38373578-38373628	Hela-S3	cervix:	n/a
23	chr6:38445981-38446031	AG04450	lung:	fetal
24	chr6:38445981-38446031	Caco-2	colon:	n/a
25	chr6:38394278-38394328	HCF	heart:	n/a
26	chr6:38373578-38373628	NHBE	bronchial:	n/a
27	chr6:38373578-38373628	GM06990	blood:	n/a
28	chr6:38394278-38394328	HRE	kidney:	n/a
29	chr6:38445981-38446031	Hela-S3	cervix:	n/a
30	chr6:38394278-38394328	SK-N-SH_RA	brain:	n/a
31	chr6:38394278-38394328	BJ	skin:	n/a
32	chr6:38394278-38394328	SKMC	muscle:	n/a
33	chr6:38394278-38394328	Caco-2	colon:	n/a
34	chr6:38445981-38446031	NT2-D1	testis:	n/a
35	chr6:38394278-38394328	HIPEpiC	eye:	n/a
36	chr6:38373578-38373628	Hepatocyte	liver:	n/a
37	chr6:38373578-38373628	GM12878	blood:	n/a
38	chr6:38445981-38446031	HCF	heart:	n/a
39	chr6:38445981-38446031	HRPEpiC	eye:	n/a
40	chr6:38373578-38373628	HUVEC	blood vessel:	n/a
41	chr6:38394278-38394328	GM12892	blood:	n/a
42	chr6:38394278-38394328	HEK293	kidney:	embryo
43	chr6:38445981-38446031	BE2_C	brain:	n/a
44	chr6:38445981-38446031	IMR90	lung:	fetal
45	chr6:38394278-38394328	HNPCEpiC	eye:	n/a
46	chr6:38373578-38373628	HEEpiC	esophagus:	n/a
47	chr6:38445981-38446031	SK-N-MC	brain:	n/a
48	chr6:38445981-38446031	GM06990	blood:	n/a
49	chr6:38445981-38446031	HRCEpiC	kidney:	n/a
50	chr6:38445981-38446031	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:38357729..38359260-chr6:38373840..38376265,2	MCF-7	breast:
2	chr6:38423292..38425801-chr6:38436010..38438215,2	K562	blood:
3	chr6:38411269..38413093-chr6:38413488..38416191,2	K562	blood:
4	chr6:38421940..38424040-chr6:38426250..38428177,2	K562	blood:
5	chr6:38229115..38229659-chr6:38404798..38405463,2	MCF-7	breast:
6	chr6:38382277..38384906-chr6:38386748..38389388,2	MCF-7	breast:
7	chr6:38435448..38438389-chr6:38439030..38441795,2	MCF-7	breast:
8	chr6:38368148..38369962-chr6:38370893..38373695,3	K562	blood:
9	chr6:38409873..38411784-chr6:38412186..38413893,2	MCF-7	breast:
10	chr6:38382277..38384906-chr6:38386748..38389388,2	MCF-7	breast:
11	chr6:38411269..38413093-chr6:38413488..38416191,2	K562	blood:
12	chr6:38421940..38424040-chr6:38426250..38428177,2	K562	blood:
13	chr6:38375672..38377894-chr6:38379334..38382033,2	MCF-7	breast:
14	chr6:38375672..38377894-chr6:38379334..38382033,2	MCF-7	breast:
15	chr6:38441969..38444159-chr6:38445659..38447643,2	K562	blood:
16	chr6:38441969..38444159-chr6:38445659..38447643,2	K562	blood:
17	chr6:38350378..38352979-chr6:38364532..38367157,2	K562	blood:
18	chr6:38406164..38407857-chr6:38442817..38445173,2	K562	blood:
19	chr6:38415370..38417878-chr6:38418782..38420645,2	MCF-7	breast:
20	chr6:38435448..38438389-chr6:38439030..38441795,2	MCF-7	breast:
21	chr6:38443341..38445345-chr6:38445490..38448475,2	MCF-7	breast:
22	chr6:38415370..38417878-chr6:38418782..38420645,2	MCF-7	breast:
23	chr6:38406164..38407857-chr6:38442817..38445173,2	K562	blood:
24	chr6:38409873..38411784-chr6:38412186..38413893,2	MCF-7	breast:
25	chr6:38423292..38425801-chr6:38436010..38438215,2	K562	blood:
26	chr6:38371909..38373449-chr6:38395704..38397463,2	K562	blood:
27	chr6:38443341..38445345-chr6:38445490..38448475,2	MCF-7	breast:
28	chr6:38371909..38373449-chr6:38395704..38397463,2	K562	blood:
29	chr6:38410346..38413041-chr6:38421338..38423278,2	MCF-7	breast:
30	chr6:38410346..38413041-chr6:38421338..38423278,2	MCF-7	breast:
31	chr6:38368148..38369962-chr6:38370893..38373695,3	K562	blood:

Variant related genes	Relation type
BTBD9-AS1	TF binding region
BTBD9-AS1	CpG island

Extended variants
information (count: 3168 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3168 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11962576	chr6:38362024-38362025	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs561548415	chr6:38362099-38362100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575087361	chr6:38362102-38362103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191222334	chr6:38362125-38362126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564584745	chr6:38362150-38362151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374721464	chr6:38362161-38362162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533242030	chr6:38362193-38362194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs546989860	chr6:38362194-38362195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560480762	chr6:38362202-38362203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79356356	chr6:38362242-38362243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182672615	chr6:38362250-38362251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147469985	chr6:38362277-38362278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186052060	chr6:38362282-38362283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550430531	chr6:38362304-38362305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs74890993	chr6:38362313-38362314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539126743	chr6:38362344-38362345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs371831215	chr6:38362346-38362347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35095110	chr6:38362437-38362438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372757091	chr6:38362442-38362443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572458599	chr6:38362443-38362444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535405517	chr6:38362444-38362445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79239481	chr6:38362453-38362454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554339638	chr6:38362503-38362504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145472662	chr6:38362509-38362510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575124795	chr6:38362531-38362532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs375783934	chr6:38362570-38362571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115678618	chr6:38362584-38362585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369038033	chr6:38362603-38362604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs78794428	chr6:38362643-38362644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs529292473	chr6:38362658-38362659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543375214	chr6:38362722-38362723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs568940282	chr6:38362736-38362737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs62397040	chr6:38362739-38362740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs202194147	chr6:38362742-38362743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs397734305	chr6:38362752-38362753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs79182655	chr6:38362753-38362754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs531881086	chr6:38362771-38362772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs139970624	chr6:38362826-38362827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571708600	chr6:38362842-38362843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35374525	chr6:38362853-38362854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11967720	chr6:38362855-38362856	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs145475391	chr6:38362870-38362871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs58303939	chr6:38362905-38362906	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs373318104	chr6:38362946-38362947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116742329	chr6:38363016-38363017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554915844	chr6:38363041-38363042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569150216	chr6:38363048-38363049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11969412	chr6:38363053-38363054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557938168	chr6:38363054-38363055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577762366	chr6:38363083-38363084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	21693616	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Breast cancer	16397240	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38343000-38367800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:38350200-38366200	Weak transcription	Lung	lung
3	chr6:38354000-38376000	Weak transcription	Primary T cells from cord blood	blood
4	chr6:38354800-38370800	Weak transcription	Primary B cells from cord blood	blood
5	chr6:38358800-38362200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr6:38358800-38362800	Enhancers	HUVEC	blood vessel
7	chr6:38359600-38367200	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr6:38359800-38363800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr6:38359800-38365200	Weak transcription	Fetal Heart	heart
10	chr6:38360000-38372200	Weak transcription	Psoas Muscle	Psoas
11	chr6:38360400-38365200	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr6:38360400-38372800	Weak transcription	Left Ventricle	heart
13	chr6:38361400-38372400	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr6:38361800-38362200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr6:38361800-38362400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:38361800-38362400	Enhancers	HMEC	breast
17	chr6:38361800-38362600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:38361800-38362600	Enhancers	NHEK	skin
19	chr6:38362000-38362400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr6:38362200-38371800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr6:38362400-38363800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr6:38362400-38363800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:38362400-38364200	Weak transcription	HMEC	breast
24	chr6:38362600-38364000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr6:38362600-38364000	Weak transcription	NHEK	skin
26	chr6:38363000-38372000	Weak transcription	Brain Substantia Nigra	brain
27	chr6:38363800-38364400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr6:38363800-38364600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr6:38364000-38364400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr6:38364000-38364600	Enhancers	NHEK	skin
31	chr6:38364000-38365400	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr6:38364200-38364400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr6:38364200-38364400	Enhancers	HMEC	breast
34	chr6:38364200-38366600	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr6:38365200-38365800	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr6:38365200-38366400	Enhancers	Fetal Heart	heart
37	chr6:38365400-38365800	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr6:38365600-38365800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:38365800-38368200	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr6:38365800-38372600	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr6:38366200-38366400	Enhancers	Lung	lung
42	chr6:38367200-38367400	Enhancers	Primary T helper cells PMA-I stimulated	--
43	chr6:38367200-38372000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr6:38367800-38368200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr6:38367800-38368200	Enhancers	Stomach Mucosa	stomach
46	chr6:38367800-38368400	Enhancers	Fetal Thymus	thymus
47	chr6:38367800-38368400	Enhancers	Gastric	stomach
48	chr6:38367800-38368600	Enhancers	Fetal Intestine Large	intestine
49	chr6:38368000-38368400	Enhancers	Thymus	Thymus
50	chr6:38368000-38369200	Enhancers	Adipose Nuclei	Adipose

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