Variant report

Variant	nsv886736
Chromosome Location	chr6:142365171-142523865
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2035)
CpG islands
(count:1835)
Chromatin interactive
region (count:126)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2035 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:142509681-142509718	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:142467784-142468437	K562	blood:	n/a	n/a
3	ARID3A	chr6:142467802-142468560	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:142433634-142433971	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:142492534-142492795	HepG2	liver:	n/a	n/a
6	ATF1	chr6:142468043-142468605	K562	blood:	n/a	n/a
7	ATF2	chr6:142468046-142468707	GM12878	blood:	n/a	n/a
8	ATF2	chr6:142409951-142410378	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr6:142468022-142468453	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr6:142467959-142468503	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr6:142467908-142468724	GM12878	blood:	n/a	n/a
12	ATF3	chr6:142468001-142468494	K562	blood:	n/a	n/a
13	ATF3	chr6:142467971-142468588	A549	lung:	n/a	chr6:142468553-142468562
14	ATF3	chr6:142468119-142468361	K562	blood:	n/a	n/a
15	ATF3	chr6:142467960-142468496	A549	lung:	n/a	n/a
16	BACH1	chr6:142409948-142410277	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:142468027-142468472	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:142409357-142409582	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr6:142376411-142376651	GM12878	blood:	n/a	n/a
20	BATF	chr6:142413775-142414012	GM12878	blood:	n/a	chr6:142413927-142413938
21	BATF	chr6:142413816-142414046	GM12878	blood:	n/a	chr6:142413927-142413938
22	BATF	chr6:142468038-142468452	GM12878	blood:	n/a	n/a
23	BCLAF1	chr6:142467983-142468766	K562	blood:	n/a	chr6:142468374-142468383
24	BCLAF1	chr6:142467910-142468518	K562	blood:	n/a	chr6:142468374-142468383
25	BCLAF1	chr6:142467982-142468621	GM12878	blood:	n/a	chr6:142468374-142468383
26	BCLAF1	chr6:142467900-142468691	GM12878	blood:	n/a	chr6:142468374-142468383
27	BHLHE40	chr6:142467972-142468783	K562	blood:	n/a	n/a
28	BHLHE40	chr6:142366123-142366493	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:142468016-142468729	HepG2	liver:	n/a	n/a
30	BHLHE40	chr6:142366125-142366500	HepG2	liver:	n/a	n/a
31	BHLHE40	chr6:142468001-142468591	GM12878	blood:	n/a	n/a
32	BRCA1	chr6:142366297-142366496	GM12878	blood:	n/a	n/a
33	BRCA1	chr6:142468138-142468553	HepG2	liver:	n/a	n/a
34	BRCA1	chr6:142477078-142477284	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr6:142467983-142468692	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr6:142467973-142468795	HCT-116	colon:	n/a	n/a
37	CBX3	chr6:142467860-142468694	HCT-116	colon:	n/a	n/a
38	CBX3	chr6:142467960-142468578	K562	blood:	n/a	n/a
39	CBX3	chr6:142467944-142468815	K562	blood:	n/a	n/a
40	CCNT2	chr6:142504511-142504674	K562	blood:	n/a	n/a
41	CCNT2	chr6:142468141-142468647	K562	blood:	n/a	chr6:142468620-142468629
42	CEBPB	chr6:142460224-142460502	K562	blood:	n/a	chr6:142460384-142460395 chr6:142460382-142460393
43	CEBPB	chr6:142468065-142468498	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr6:142366530-142366841	A549	lung:	n/a	chr6:142366690-142366701 chr6:142366685-142366702 chr6:142366688-142366701 chr6:142366688-142366699 chr6:142366690-142366701
45	CEBPB	chr6:142460241-142460536	HepG2	liver:	n/a	chr6:142460384-142460395 chr6:142460382-142460393
46	CEBPB	chr6:142366475-142366821	MCF-7	breast:	n/a	chr6:142366690-142366701 chr6:142366685-142366702 chr6:142366688-142366701 chr6:142366688-142366699 chr6:142366690-142366701
47	CEBPB	chr6:142433588-142433936	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr6:142423620-142423897	HepG2	liver:	n/a	chr6:142423731-142423742
49	CEBPB	chr6:142433602-142433922	A549	lung:	n/a	n/a
50	CEBPB	chr6:142433576-142433959	MCF-7	breast:	n/a	n/a

(count:1835 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:142410098-142410148	LNCaP	prostate:	n/a
2	chr6:142465233-142465283	HepG2	liver:	n/a
3	chr6:142409630-142409680	HepG2	liver:	n/a
4	chr6:142468432-142468482	PANC-1	pancreas:	n/a
5	chr6:142409417-142409467	PrEC	prostate:	n/a
6	chr6:142410098-142410148	LNCaP	prostate:	n/a
7	chr6:142465233-142465283	HepG2	liver:	n/a
8	chr6:142409630-142409680	HepG2	liver:	n/a
9	chr6:142468432-142468482	PANC-1	pancreas:	n/a
10	chr6:142409417-142409467	PrEC	prostate:	n/a
11	chr6:142410216-142410266	HIPEpiC	eye:	n/a
12	chr6:142468362-142468412	IMR90	lung:	fetal
13	chr6:142468512-142468562	AoSMC	blood vessel:	n/a
14	chr6:142467043-142467093	Hepatocyte	liver:	n/a
15	chr6:142468191-142468241	GM19239	blood:	n/a
16	chr6:142468350-142468400	HCF	heart:	n/a
17	chr6:142409202-142409252	AG09319	gingival:	n/a
18	chr6:142468354-142468404	Caco-2	colon:	n/a
19	chr6:142409993-142410043	HIPEpiC	eye:	n/a
20	chr6:142468354-142468404	IMR90	lung:	fetal
21	chr6:142476640-142476690	HPAEpiC	pulmonary alveolar:	n/a
22	chr6:142468318-142468368	HRE	kidney:	n/a
23	chr6:142409630-142409680	HCT-116	colon:	n/a
24	chr6:142468318-142468368	AG10803	skin:	n/a
25	chr6:142468197-142468247	PANC-1	pancreas:	n/a
26	chr6:142468191-142468241	NHDF-neo	bronchial:	n/a
27	chr6:142468197-142468247	AoSMC	blood vessel:	n/a
28	chr6:142410216-142410266	GM12878	blood:	n/a
29	chr6:142410098-142410148	HNPCEpiC	eye:	n/a
30	chr6:142409202-142409252	HNPCEpiC	eye:	n/a
31	chr6:142409202-142409252	Hela-S3	cervix:	n/a
32	chr6:142465233-142465283	AG09319	gingival:	n/a
33	chr6:142409993-142410043	Jurkat	blood:	n/a
34	chr6:142409630-142409680	Hela-S3	cervix:	n/a
35	chr6:142468432-142468482	AG09309	skin:	n/a
36	chr6:142409993-142410043	GM19239	blood:	n/a
37	chr6:142476640-142476690	HRPEpiC	eye:	n/a
38	chr6:142410216-142410266	U87	brain:	n/a
39	chr6:142468362-142468412	AG09319	gingival:	n/a
40	chr6:142409507-142409557	HNPCEpiC	eye:	n/a
41	chr6:142409756-142409806	AG04450	lung:	fetal
42	chr6:142410216-142410266	SK-N-SH_RA	brain:	n/a
43	chr6:142468350-142468400	HCM	heart:	n/a
44	chr6:142468656-142468706	RPTEC	kidney:	n/a
45	chr6:142409202-142409252	HCT-116	colon:	n/a
46	chr6:142409630-142409680	HNPCEpiC	eye:	n/a
47	chr6:142409993-142410043	LNCaP	prostate:	n/a
48	chr6:142468318-142468368	T-47D	breast:	n/a
49	chr6:142409993-142410043	U87	brain:	n/a
50	chr6:142468656-142468706	PFSK-1	brain:	n/a

(count:126 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr21:43172983..43173483-chr6:142366294..142366805,2	Hela-S3	cervix:
2	chr6:142470468..142472219-chr6:144162798..144164527,2	K562	blood:
3	chr6:142470533..142472236-chr6:142476885..142478577,2	K562	blood:
4	chr5:137649363..137650864-chr6:142364815..142366317,2	K562	blood:
5	chr4:153845959..153847477-chr6:142366299..142367825,2	K562	blood:
6	chr2:20500446..20501966-chr6:142366297..142367819,2	MCF-7	breast:
7	chr17:41399314..41402537-chr6:142366296..142367823,5	MCF-7	breast:
8	chr6:142310160..142310940-chr6:142392407..142393314,2	MCF-7	breast:
9	chr6:142476386..142478985-chr6:142483280..142485789,2	MCF-7	breast:
10	chr17:41462135..41468687-chr6:142364795..142367816,19	K562	blood:
11	chr6:142475480..142477535-chr6:142483300..142485466,2	K562	blood:
12	chr6:142365543..142367464-chr6:142370102..142372383,2	K562	blood:
13	chr6:141996747..141997654-chr6:142433323..142434142,3	MCF-7	breast:
14	chr20:18807037..18808557-chr6:142364804..142366320,2	MCF-7	breast:
15	chr20:51476079..51477599-chr6:142364799..142367796,2	MCF-7	breast:
16	chr6:141998840..141999399-chr6:142365802..142366506,2	MCF-7	breast:
17	chr17:41463781..41464354-chr6:142366301..142366821,2	MCF-7	breast:
18	chr6:142474084..142476668-chr6:142479494..142481093,2	K562	blood:
19	chr6:142379089..142381222-chr6:142382597..142385230,2	K562	blood:
20	chr6:142470687..142472679-chr6:142481549..142483699,2	K562	blood:
21	chr3:73158440..73161632-chr6:142364819..142367821,7	K562	blood:
22	chr17:41445015..41446827-chr6:142364795..142366297,2	K562	blood:
23	chr6:142480480..142482070-chr6:142484857..142487134,2	MCF-7	breast:
24	chr13:58066693..58068213-chr6:142366296..142367819,2	K562	blood:
25	chr6:142509860..142511893-chr6:142513753..142515292,2	K562	blood:
26	chr6:142476386..142478985-chr6:142483280..142485789,2	MCF-7	breast:
27	chr4:103260693..103262213-chr6:142364799..142366317,2	K562	blood:
28	chr19:49942464..49945484-chr6:142364799..142367795,4	K562	blood:
29	chr6:142468629..142470840-chr6:142474904..142476440,2	K562	blood:
30	chr6:141998099..141999007-chr6:142433461..142433965,2	MCF-7	breast:
31	chr6:142366297..142366801-chrX:77931321..77931822,2	MCF-7	breast:
32	chr3:73158440..73162071-chr6:142364794..142367821,11	K562	blood:
33	chr11:62607631..62609197-chr6:142364799..142366321,4	MCF-7	breast:
34	chr6:141962578..141963250-chr6:142366256..142367149,2	MCF-7	breast:
35	chr2:137557381..137558381-chr6:142365795..142366315,2	Hela-S3	cervix:
36	chr11:62608630..62609650-chr6:142365799..142366321,3	HCT-116	colon:
37	chr10:111980949..111982469-chr6:142364799..142366321,4	K562	blood:
38	chr3:115770645..115772165-chr6:142364804..142366315,2	MCF-7	breast:
39	chr6:142492670..142496237-chr6:142496854..142499913,3	K562	blood:
40	chr6:142482644..142484421-chr6:142484812..142486415,2	MCF-7	breast:
41	chr6:142364797..142367795-chrX:77930320..77931841,2	K562	blood:
42	chr11:62607617..62610628-chr6:142364795..142367820,5	K562	blood:
43	chr17:41398699..41402637-chr6:142364804..142367821,8	MCF-7	breast:
44	chr11:62607617..62609155-chr6:142364815..142367815,4	K562	blood:
45	chr17:41380090..41383896-chr6:142364797..142367825,21	K562	blood:
46	chr17:41391026..41393127-chr6:142366322..142367825,2	K562	blood:
47	chr6:142489018..142492180-chr6:142492773..142495963,3	K562	blood:
48	chr2:169365139..169366658-chr6:142364815..142367814,2	K562	blood:
49	chr10:103124607..103126128-chr6:142364797..142367796,2	K562	blood:
50	chr16:9513156..9513676-chr6:142365801..142366324,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GJE1-6	chr6:142383854-142384190	NONHSAT115302
2	lnc-GJE1-4	chr6:142495920-142496027	NONHSAT115305
3	lnc-GJE1-4	chr6:142496680-142496862	NONHSAT115305
4	lnc-GJE1-4	chr6:142497360-142497981	NONHSAT115305

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	VTA1	hsa-miR-455-5p	chr6:142510580-142510603

Variant related genes	Relation type
ENSG00000270983	TF binding region
GJE1	TF binding region
VTA1	TF binding region
ENSG00000236822	TF binding region
NMBR	TF binding region
ENSG00000270983	CpG island
GJE1	CpG island
VTA1	CpG island
ENSG00000236822	CpG island
NMBR	CpG island
ENSG00000134294	chromatin interactions
ENSG00000104907	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000009844	chromatin interactions
ENSG00000158815	chromatin interactions
ENSG00000257199	chromatin interactions
ENSG00000222414	chromatin interactions
ENSG00000104888	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000270983	chromatin interactions
ENSG00000147454	chromatin interactions
ENSG00000136932	chromatin interactions
ENSG00000135521	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000112414	chromatin interactions
ENSG00000236383	chromatin interactions

Extended variants
information (count: 3254 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:3254 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7776318	chr6:142365171-142365172	Weak transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550384360	chr6:142365175-142365176	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs573044149	chr6:142365188-142365189	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs73573663	chr6:142365309-142365310	Weak transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs538976622	chr6:142365332-142365333	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs73573665	chr6:142365357-142365358	Weak transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs570116842	chr6:142365420-142365421	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs529294657	chr6:142365509-142365510	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs549048656	chr6:142365592-142365593	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs188972157	chr6:142365618-142365619	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs17071411	chr6:142365619-142365620	Weak transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs557521620	chr6:142365680-142365681	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs9496236	chr6:142365776-142365777	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs530779597	chr6:142365837-142365838	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs565776485	chr6:142365932-142365933	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs577229774	chr6:142365933-142365934	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs377448770	chr6:142365940-142365941	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs192464518	chr6:142365956-142365957	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs34391792	chr6:142365968-142365969	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs546354706	chr6:142366039-142366040	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs372174944	chr6:142366062-142366063	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs535117850	chr6:142366097-142366098	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs556872892	chr6:142366125-142366126	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs561301341	chr6:142366139-142366140	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs569209395	chr6:142366169-142366170	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs371754458	chr6:142366177-142366178	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs535011999	chr6:142366220-142366221	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs573081038	chr6:142366263-142366264	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs540794425	chr6:142366266-142366267	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs78304200	chr6:142366295-142366296	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs555597001	chr6:142366297-142366298	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs149662113	chr6:142366299-142366300	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
33	rs544283588	chr6:142366306-142366307	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs201835203	chr6:142366327-142366328	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs368164597	chr6:142366331-142366332	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs562867900	chr6:142366351-142366352	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs75390039	chr6:142366401-142366402	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs546103215	chr6:142366413-142366414	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs374831796	chr6:142366416-142366417	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs553352050	chr6:142366429-142366430	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs528295273	chr6:142366468-142366469	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs573628266	chr6:142366511-142366512	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs184443186	chr6:142366512-142366513	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs13215043	chr6:142366529-142366530	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
45	rs9496237	chr6:142366538-142366539	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs13215046	chr6:142366539-142366540	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs561635122	chr6:142366541-142366542	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs528932615	chr6:142366595-142366596	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs373299473	chr6:142366605-142366606	Enhancers Weak transcription Active TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs550204858	chr6:142366617-142366618	Enhancers Weak transcription Active TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Gastric cancer	17908304	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
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
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Burkitt''s lymphoma	19759907	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2020 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142360600-142366200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr6:142360600-142366200	Weak transcription	Osteobl	bone
3	chr6:142360800-142366200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:142360800-142366200	Weak transcription	NHLF	lung
5	chr6:142361000-142366200	Weak transcription	NHDF-Ad	bronchial
6	chr6:142362200-142376600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:142366200-142366400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr6:142366200-142366400	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr6:142366200-142366400	Flanking Active TSS	Osteobl	bone
10	chr6:142366200-142366600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr6:142366200-142366600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr6:142366200-142366600	Enhancers	Adipose Nuclei	Adipose
13	chr6:142366200-142366600	Enhancers	Liver	Liver
14	chr6:142366200-142366800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr6:142366200-142367000	Enhancers	NHDF-Ad	bronchial
16	chr6:142366200-142367200	Enhancers	NHLF	lung
17	chr6:142366400-142366600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr6:142366400-142366800	Active TSS	Osteobl	bone
19	chr6:142366600-142367400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr6:142366800-142369000	Weak transcription	Osteobl	bone
21	chr6:142367000-142367200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr6:142367200-142370600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr6:142369000-142369600	Active TSS	Osteobl	bone
24	chr6:142369400-142369600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr6:142369400-142369800	Active TSS	Brain Inferior Temporal Lobe	brain
26	chr6:142369600-142370000	Active TSS	Brain Angular Gyrus	brain
27	chr6:142376600-142377400	Enhancers	Fetal Stomach	stomach
28	chr6:142376600-142377400	Enhancers	HMEC	breast
29	chr6:142376600-142377600	Enhancers	Stomach Smooth Muscle	stomach
30	chr6:142376600-142377600	Enhancers	NHEK	skin
31	chr6:142376600-142377800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr6:142377600-142378000	Weak transcription	Stomach Smooth Muscle	stomach
33	chr6:142377800-142382000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr6:142378000-142378200	Enhancers	Stomach Smooth Muscle	stomach
35	chr6:142378200-142379600	Weak transcription	Stomach Smooth Muscle	stomach
36	chr6:142379000-142379200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr6:142379200-142379400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr6:142379200-142379600	Active TSS	NHDF-Ad	bronchial
39	chr6:142379400-142381000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr6:142379600-142379800	Enhancers	Stomach Smooth Muscle	stomach
41	chr6:142379600-142379800	Flanking Active TSS	NHDF-Ad	bronchial
42	chr6:142379800-142380400	Enhancers	NHDF-Ad	bronchial
43	chr6:142380400-142381600	Weak transcription	NHDF-Ad	bronchial
44	chr6:142381000-142382000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr6:142381800-142382000	Enhancers	NHDF-Ad	bronchial
46	chr6:142393400-142393600	Enhancers	HepG2	liver
47	chr6:142396400-142397400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr6:142396600-142397000	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
49	chr6:142396600-142397400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr6:142396800-142397000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood

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