Variant report

Variant	nsv885821
Chromosome Location	chr6:38843970-39039503
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1679)
CpG islands
(count:1343)
Chromatin interactive
region (count:122)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1679 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:38901263-38901545	K562	blood:	n/a	n/a
2	ARID3A	chr6:38901288-38901576	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:38941052-38941287	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:38975330-38975634	K562	blood:	n/a	n/a
5	ARID3A	chr6:38877137-38877544	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:38936310-38936447	K562	blood:	n/a	n/a
7	ARID3A	chr6:38940983-38941393	K562	blood:	n/a	chr6:38941372-38941388 chr6:38941371-38941387
8	ATF1	chr6:38936497-38936730	K562	blood:	n/a	n/a
9	ATF1	chr6:38907941-38908103	K562	blood:	n/a	n/a
10	ATF1	chr6:38919623-38919663	K562	blood:	n/a	n/a
11	ATF1	chr6:38975339-38975740	K562	blood:	n/a	n/a
12	ATF1	chr6:39004705-39005449	K562	blood:	n/a	n/a
13	BACH1	chr6:38997248-38997532	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr6:38936526-38936631	H1-hESC	embryonic stem cell:	n/a	n/a
15	BHLHE40	chr6:38877338-38877466	HepG2	liver:	n/a	n/a
16	BHLHE40	chr6:38975311-38975785	K562	blood:	n/a	n/a
17	BHLHE40	chr6:39004752-39005119	K562	blood:	n/a	n/a
18	BHLHE40	chr6:39008820-39009201	GM12878	blood:	n/a	n/a
19	BRCA1	chr6:38997350-38997514	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr6:38965049-38965205	H1-hESC	embryonic stem cell:	n/a	n/a
21	CBX3	chr6:38975301-38975702	K562	blood:	n/a	n/a
22	CBX3	chr6:38940911-38941419	HCT-116	colon:	n/a	n/a
23	CCNT2	chr6:39016546-39016774	K562	blood:	n/a	n/a
24	CCNT2	chr6:39004558-39005133	K562	blood:	n/a	chr6:39004951-39004971
25	CCNT2	chr6:38975289-38975683	K562	blood:	n/a	n/a
26	CEBPB	chr6:38873049-38873362	K562	blood:	n/a	chr6:38873206-38873215 chr6:38873204-38873217 chr6:38873204-38873217 chr6:38873206-38873215 chr6:38873206-38873215 chr6:38873204-38873215 chr6:38873206-38873217 chr6:38873206-38873215
27	CEBPB	chr6:38988768-38988964	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr6:38873099-38873318	A549	lung:	n/a	chr6:38873206-38873215 chr6:38873204-38873217 chr6:38873204-38873217 chr6:38873206-38873215 chr6:38873206-38873215 chr6:38873204-38873215 chr6:38873206-38873217 chr6:38873206-38873215
29	CEBPB	chr6:38936660-38936909	K562	blood:	n/a	chr6:38936813-38936824
30	CEBPB	chr6:38877059-38877302	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:38877082-38877357	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr6:38877070-38877471	HepG2	liver:	n/a	n/a
33	CEBPB	chr6:38876989-38877363	HepG2	liver:	n/a	n/a
34	CEBPB	chr6:38989658-38989814	K562	blood:	n/a	chr6:38989736-38989747 chr6:38989738-38989749 chr6:38989736-38989749
35	CEBPB	chr6:38995915-38996015	K562	blood:	n/a	chr6:38995941-38995952
36	CEBPB	chr6:39004818-39005206	K562	blood:	n/a	chr6:39005009-39005020
37	CEBPB	chr6:38936699-38936899	A549	lung:	n/a	chr6:38936813-38936824
38	CEBPB	chr6:38878012-38878350	K562	blood:	n/a	n/a
39	CEBPB	chr6:38878047-38878243	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:38873228-38873259	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr6:38886888-38887081	K562	blood:	n/a	chr6:38886956-38886969
42	CEBPB	chr6:38878073-38878262	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr6:38936672-38936956	HepG2	liver:	n/a	chr6:38936813-38936824
44	CEBPB	chr6:39038220-39038357	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr6:38995870-38995998	HepG2	liver:	n/a	chr6:38995941-38995952
46	CEBPB	chr6:38915477-38915639	K562	blood:	n/a	chr6:38915498-38915509
47	CEBPB	chr6:38873071-38873395	HepG2	liver:	n/a	chr6:38873206-38873215 chr6:38873204-38873217 chr6:38873204-38873217 chr6:38873206-38873215 chr6:38873206-38873215 chr6:38873204-38873215 chr6:38873206-38873217 chr6:38873206-38873215
48	CEBPB	chr6:38950341-38950628	MCF-7	breast:	n/a	chr6:38950442-38950459 chr6:38950445-38950456
49	CEBPB	chr6:38989536-38989904	HepG2	liver:	n/a	chr6:38989540-38989553 chr6:38989736-38989747 chr6:38989738-38989749 chr6:38989736-38989749
50	CEBPB	chr6:38915428-38915641	HepG2	liver:	n/a	chr6:38915498-38915509

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:39017116-39017166	BJ	skin:	n/a
2	chr6:39017116-39017166	BJ	skin:	n/a
3	chr6:39016479-39016529	GM12892	blood:	n/a
4	chr6:39016262-39016312	NHBE	bronchial:	n/a
5	chr6:38976072-38976122	NH-A	brain:	n/a
6	chr6:38945383-38945433	NB4	blood:	n/a
7	chr6:39004623-39004673	HEK293	kidney:	embryo
8	chr6:39017116-39017166	ProgFib	skin:	n/a
9	chr6:38976072-38976122	H1-hESC	embryonic stem cell:	embryo
10	chr6:39011018-39011068	NHDF-neo	bronchial:	n/a
11	chr6:39016470-39016520	AG09319	gingival:	n/a
12	chr6:39016776-39016826	HPAEpiC	pulmonary alveolar:	n/a
13	chr6:38998315-38998365	NHDF-neo	bronchial:	n/a
14	chr6:38945383-38945433	PrEC	prostate:	n/a
15	chr6:38998315-38998365	HPAEpiC	pulmonary alveolar:	n/a
16	chr6:39004623-39004673	AG10803	skin:	n/a
17	chr6:38945383-38945433	K562	blood:	n/a
18	chr6:39016326-39016376	AG04450	lung:	fetal
19	chr6:39016590-39016640	HRE	kidney:	n/a
20	chr6:39016363-39016413	SKMC	muscle:	n/a
21	chr6:38896772-38896822	T-47D	breast:	n/a
22	chr6:38997395-38997445	Hepatocyte	liver:	n/a
23	chr6:39013152-39013202	GM12891	blood:	n/a
24	chr6:39011018-39011068	GM12891	blood:	n/a
25	chr6:39016326-39016376	HPAEpiC	pulmonary alveolar:	n/a
26	chr6:39015339-39015389	HRCEpiC	kidney:	n/a
27	chr6:39022380-39022430	HAEpiC	amniotic membrane:	n/a
28	chr6:39016262-39016312	ECC-1	luminal epithelium:	n/a
29	chr6:38896772-38896822	AG04450	lung:	fetal
30	chr6:39016479-39016529	NH-A	brain:	n/a
31	chr6:39011018-39011068	HCT-116	colon:	n/a
32	chr6:39011018-39011068	CMK	blood:	n/a
33	chr6:39022380-39022430	AG04449	skin:	fetal
34	chr6:39020986-39021036	AG04450	lung:	fetal
35	chr6:38945383-38945433	RPTEC	kidney:	n/a
36	chr6:38976072-38976122	MCF10A-Er-Src	breast:	n/a
37	chr6:38998315-38998365	AG04450	lung:	fetal
38	chr6:39011018-39011068	RPTEC	kidney:	n/a
39	chr6:39015339-39015389	Hepatocyte	liver:	n/a
40	chr6:39022380-39022430	LNCaP	prostate:	n/a
41	chr6:39016326-39016376	U87	brain:	n/a
42	chr6:39020986-39021036	Hela-S3	cervix:	n/a
43	chr6:38998315-38998365	Caco-2	colon:	n/a
44	chr6:38921683-38921733	HRE	kidney:	n/a
45	chr6:39016470-39016520	HRCEpiC	kidney:	n/a
46	chr6:38998315-38998365	AG09309	skin:	n/a
47	chr6:38976072-38976122	Caco-2	colon:	n/a
48	chr6:38945383-38945433	IMR90	lung:	fetal
49	chr6:38896772-38896822	HRPEpiC	eye:	n/a
50	chr6:39016363-39016413	HRCEpiC	kidney:	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:38998521..39000063-chr6:39004182..39006109,2	MCF-7	breast:
2	chr6:38896535..38899367-chr6:38900906..38902876,2	MCF-7	breast:
3	chr6:39008195..39010703-chr6:39012915..39015347,2	K562	blood:
4	chr6:38973623..38975732-chr6:38976644..38979495,2	K562	blood:
5	chr6:38998521..39000063-chr6:39004182..39006109,2	MCF-7	breast:
6	chr6:38949259..38950815-chr6:38952793..38955307,2	MCF-7	breast:
7	chr6:38939906..38942695-chr6:38942827..38945177,2	K562	blood:
8	chr6:38877103..38879677-chr6:38880412..38883023,2	K562	blood:
9	chr6:39014216..39015762-chr6:39017423..39020213,2	K562	blood:
10	chr6:38970568..38971494-chr6:39127178..39128129,2	K562	blood:
11	chr6:38940723..38941491-chr6:39055376..39056317,2	MCF-7	breast:
12	chr6:38964813..38965597-chr6:39269534..39270104,3	K562	blood:
13	chr6:39025094..39027190-chr6:39031133..39033531,2	K562	blood:
14	chr6:38976194..38979423-chr6:38983493..38987225,3	K562	blood:
15	chr6:38970965..38971472-chr6:39270578..39271231,2	K562	blood:
16	chr6:38861067..38863812-chr6:38904075..38906920,2	MCF-7	breast:
17	chr6:38851556..38854549-chr6:38855510..38859290,4	K562	blood:
18	chr6:38983654..38986496-chr6:38995790..38997665,2	K562	blood:
19	chr6:38839518..38840375-chr6:38900813..38901849,3	MCF-7	breast:
20	chr6:38839463..38840459-chr6:38901033..38901837,4	MCF-7	breast:
21	chr6:38861067..38863812-chr6:38904075..38906920,2	MCF-7	breast:
22	chr6:38960673..38962363-chr6:38963725..38966028,2	MCF-7	breast:
23	chr6:38901364..38904102-chr6:38904353..38906720,2	K562	blood:
24	chr6:38868758..38870496-chr6:38873013..38875836,2	K562	blood:
25	chr6:39032106..39033612-chr6:39039523..39041550,2	K562	blood:
26	chr6:38902804..38905532-chr6:38908040..38910496,2	K562	blood:
27	chr6:38973623..38975925-chr6:38976644..38978356,2	K562	blood:
28	chr6:38964768..38966045-chr6:39059915..39060630,3	MCF-7	breast:
29	chr6:38940690..38941643-chr6:39133929..39134512,2	MCF-7	breast:
30	chr6:38949259..38950815-chr6:38952793..38955307,2	MCF-7	breast:
31	chr6:38984460..38985977-chr6:38987498..38989238,2	K562	blood:
32	chr6:38975629..38979423-chr6:38983493..38987291,5	K562	blood:
33	chr6:39009574..39011759-chr6:39155267..39157602,2	K562	blood:
34	chr6:38877864..38879774-chr6:38880204..38883069,2	K562	blood:
35	chr6:38970479..38971603-chr6:39058514..39059664,3	K562	blood:
36	chr6:39008195..39010703-chr6:39012915..39015347,2	K562	blood:
37	chr6:38901364..38904102-chr6:38904353..38906720,2	K562	blood:
38	chr6:38858466..38860453-chr6:38860487..38863310,2	K562	blood:
39	chr6:38839504..38840084-chr6:38897171..38897919,2	MCF-7	breast:
40	chr6:38838915..38841250-chr6:38844804..38847506,2	MCF-7	breast:
41	chr6:38901008..38902530-chr6:38905671..38907488,2	K562	blood:
42	chr6:38885137..38887248-chr6:38897981..38900186,2	K562	blood:
43	chr4:134215031..134215860-chr6:38986253..38986839,2	K562	blood:
44	chr6:38882569..38884990-chr6:38896928..38898795,2	K562	blood:
45	chr6:38914946..38917394-chr6:38943758..38945918,2	MCF-7	breast:
46	chr6:38877864..38879774-chr6:38880204..38883069,2	K562	blood:
47	chr6:38914946..38917394-chr6:38943758..38945918,2	MCF-7	breast:
48	chr6:38990306..38992412-chr6:38998180..39000571,2	K562	blood:
49	chr6:38934741..38936465-chr6:38939691..38941854,2	K562	blood:
50	chr6:39016643..39019473-chr6:39022041..39023583,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SAYSD1-1	chr6:38904069-38904168	NONHSAT112341
2	lnc-SAYSD1-1	chr6:38899109-38899149	NONHSAT112341
3	lnc-SAYSD1-1	chr6:38914899-38915050	NONHSAT112341
4	lnc-SAYSD1-1	chr6:38900773-38900879	NONHSAT112341
5	lnc-SAYSD1-2	chr6:39007379-39007761	NONHSAT112342

No data

Variant related genes	Relation type
ENSG00000220556	TF binding region
ENSG00000220076	TF binding region
ENSG00000231150	TF binding region
GLP1R	TF binding region
ENSG00000220556	CpG island
ENSG00000220076	CpG island
ENSG00000231150	CpG island
GLP1R	CpG island
ENSG00000112164	chromatin interactions
ENSG00000217165	chromatin interactions
ENSG00000220556	chromatin interactions
ENSG00000231150	chromatin interactions
ENSG00000112167	chromatin interactions

Extended variants
information (count: 4949 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:4949 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs862427	chr6:38843970-38843971	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs138296070	chr6:38843982-38843983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149194613	chr6:38844055-38844056	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs546284269	chr6:38844069-38844070	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs373543599	chr6:38844070-38844071	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs190041241	chr6:38844073-38844074	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs182412757	chr6:38844115-38844116	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs567442004	chr6:38844116-38844117	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs201036079	chr6:38844136-38844137	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs201161782	chr6:38844139-38844140	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs530053104	chr6:38844152-38844153	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs36123074	chr6:38844330-38844331	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs111639657	chr6:38844331-38844332	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs542469930	chr6:38844385-38844386	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs370829028	chr6:38844386-38844387	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs9366982	chr6:38844390-38844391	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs538263314	chr6:38844408-38844409	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs558203427	chr6:38844442-38844443	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs565446869	chr6:38844494-38844495	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs534879766	chr6:38844495-38844496	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs555189399	chr6:38844519-38844520	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs575010136	chr6:38844637-38844638	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs537615788	chr6:38844672-38844673	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs11752596	chr6:38844709-38844710	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs4711558	chr6:38844716-38844717	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs187091345	chr6:38844756-38844757	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs538191854	chr6:38844835-38844836	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs4711559	chr6:38844867-38844868	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs192136253	chr6:38844880-38844881	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs559847783	chr6:38844887-38844888	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs34774645	chr6:38844894-38844895	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs142960937	chr6:38844946-38844947	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs540866520	chr6:38845036-38845037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs561166587	chr6:38845069-38845070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs529931610	chr6:38845098-38845099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs6942142	chr6:38845116-38845117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs201995443	chr6:38845177-38845178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs199676669	chr6:38845178-38845179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564195272	chr6:38845233-38845234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs4380739	chr6:38845314-38845315	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs79039423	chr6:38845328-38845329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs531934827	chr6:38845333-38845334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs4302660	chr6:38845359-38845360	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs531951753	chr6:38845382-38845383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138371550	chr6:38845433-38845434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs534743399	chr6:38845489-38845490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143937932	chr6:38845492-38845493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568603110	chr6:38845531-38845532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537267797	chr6:38845532-38845533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs34625234	chr6:38845549-38845550	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:98)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Glioblastoma multiforme	21510904	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:819 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38840200-38845400	Enhancers	Fetal Thymus	thymus
2	chr6:38841000-38844000	Weak transcription	Primary T cells from cord blood	blood
3	chr6:38842200-38844000	Enhancers	Thymus	Thymus
4	chr6:38842200-38845400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr6:38842200-38845800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr6:38842800-38844000	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr6:38842800-38845400	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr6:38843400-38845400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr6:38843400-38845600	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr6:38843600-38845000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr6:38843600-38845400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
12	chr6:38843600-38845400	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr6:38843600-38845400	Enhancers	Dnd41	blood
14	chr6:38843800-38844000	Enhancers	Brain Anterior Caudate	brain
15	chr6:38843800-38844200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr6:38843800-38844400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr6:38843800-38844600	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr6:38843800-38844800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
19	chr6:38843800-38845000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr6:38843800-38845200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr6:38843800-38845200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr6:38843800-38845200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr6:38843800-38845200	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr6:38843800-38845200	Enhancers	Adipose Nuclei	Adipose
25	chr6:38843800-38845400	Enhancers	Primary T cells fromperipheralblood	blood
26	chr6:38843800-38845400	Enhancers	Primary hematopoietic stem cells	blood
27	chr6:38843800-38845800	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr6:38844000-38844400	Enhancers	GM12878-XiMat	blood
29	chr6:38844000-38844600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
30	chr6:38844000-38844600	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr6:38844000-38844800	Enhancers	Primary T cells from cord blood	blood
32	chr6:38844000-38845000	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr6:38844000-38845000	Flanking Active TSS	Thymus	Thymus
34	chr6:38844000-38845200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr6:38844200-38844600	Enhancers	Primary B cells from peripheral blood	blood
36	chr6:38844200-38844800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr6:38844200-38844800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr6:38844200-38845200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr6:38844400-38844800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr6:38844600-38845400	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr6:38844800-38845400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr6:38845000-38845800	Enhancers	Thymus	Thymus
43	chr6:38863600-38864200	Enhancers	Fetal Intestine Small	intestine
44	chr6:38869600-38869800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr6:38869600-38869800	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr6:38869600-38870400	Enhancers	H1 Cell Line	embryonic stem cell
47	chr6:38869600-38870400	Enhancers	H9 Cell Line	embryonic stem cell
48	chr6:38869600-38870400	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr6:38869600-38870400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr6:38869600-38870600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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