Variant report

Variant	nsv432984
Chromosome Location	chr6:167018915-167181613
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1825)
CpG islands
(count:5074)
Chromatin interactive
region (count:81)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1825 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167089914-167090051	K562	blood:	n/a	n/a
2	ATF1	chr6:167106355-167106363	K562	blood:	n/a	n/a
3	ATF1	chr6:167047252-167047515	K562	blood:	n/a	n/a
4	ATF1	chr6:167043173-167043565	K562	blood:	n/a	n/a
5	ATF1	chr6:167091973-167092242	K562	blood:	n/a	n/a
6	ATF2	chr6:167041056-167041381	GM12878	blood:	n/a	n/a
7	ATF2	chr6:167041025-167041424	GM12878	blood:	n/a	n/a
8	ATF3	chr6:167047221-167047476	K562	blood:	n/a	n/a
9	BACH1	chr6:167174931-167175059	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr6:167039835-167042182	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr6:167080570-167080599	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr6:167085611-167085744	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr6:167108688-167108908	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr6:167164829-167164988	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr6:167051743-167051753	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr6:167101913-167101935	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:167180403-167180549	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:167063736-167063868	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr6:167069823-167070312	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL11A	chr6:167070244-167070488	GM12878	blood:	n/a	n/a
21	BCL3	chr6:167136250-167136646	GM12878	blood:	n/a	chr6:167136381-167136389
22	BCL3	chr6:167073673-167073994	GM12878	blood:	n/a	n/a
23	BCL3	chr6:167056191-167056497	GM12878	blood:	n/a	n/a
24	BCL3	chr6:167061042-167061975	GM12878	blood:	n/a	n/a
25	BCL3	chr6:167073691-167073910	GM12878	blood:	n/a	n/a
26	BCL3	chr6:167061092-167062010	GM12878	blood:	n/a	n/a
27	BCLAF1	chr6:167041029-167041717	GM12878	blood:	n/a	chr6:167041543-167041556 chr6:167041144-167041152 chr6:167041389-167041402 chr6:167041101-167041114 chr6:167041582-167041589 chr6:167041047-167041060
28	BHLHE40	chr6:167161600-167161832	HepG2	liver:	n/a	chr6:167161698-167161707 chr6:167161698-167161707
29	BHLHE40	chr6:167094952-167094986	K562	blood:	n/a	n/a
30	BHLHE40	chr6:167161530-167161893	K562	blood:	n/a	chr6:167161698-167161707 chr6:167161698-167161707
31	BHLHE40	chr6:167040617-167041306	GM12878	blood:	n/a	chr6:167040795-167040811 chr6:167041145-167041161
32	BHLHE40	chr6:167047156-167047572	K562	blood:	n/a	n/a
33	BHLHE40	chr6:167040650-167041533	K562	blood:	n/a	chr6:167040795-167040811 chr6:167041145-167041161 chr6:167041505-167041521
34	BHLHE40	chr6:167047279-167047479	GM12878	blood:	n/a	n/a
35	BHLHE40	chr6:167171667-167171890	K562	blood:	n/a	chr6:167171784-167171793
36	BHLHE40	chr6:167047239-167047538	HepG2	liver:	n/a	n/a
37	BHLHE40	chr6:167164681-167164961	GM12878	blood:	n/a	chr6:167164821-167164837
38	BRCA1	chr6:167041101-167041127	HepG2	liver:	n/a	n/a
39	BRCA1	chr6:167041185-167042165	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr6:167040157-167040300	H1-hESC	embryonic stem cell:	n/a	n/a
41	CBX3	chr6:167104382-167105236	HCT-116	colon:	n/a	chr6:167104487-167104498
42	CBX3	chr6:167040659-167041117	K562	blood:	n/a	n/a
43	CBX3	chr6:167149947-167151156	HCT-116	colon:	n/a	n/a
44	CBX3	chr6:167104434-167105358	HCT-116	colon:	n/a	chr6:167104487-167104498
45	CCNT2	chr6:167040540-167041740	K562	blood:	n/a	chr6:167041047-167041056
46	CEBPB	chr6:167094606-167094920	A549	lung:	n/a	chr6:167094766-167094775 chr6:167094764-167094775
47	CEBPB	chr6:167089197-167089344	HepG2	liver:	n/a	n/a
48	CEBPB	chr6:167043274-167043509	K562	blood:	n/a	n/a
49	CEBPB	chr6:167095515-167095744	IMR90	lung:	n/a	n/a
50	CEBPB	chr6:167039650-167039996	H1-hESC	embryonic stem cell:	n/a	chr6:167039824-167039835

(count:5074 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167104601-167104651	HRPEpiC	eye:	n/a
2	chr6:167040675-167040725	U87	brain:	n/a
3	chr6:167136367-167136417	HEEpiC	esophagus:	n/a
4	chr6:167104761-167104811	SK-N-SH	brain:	n/a
5	chr6:167173257-167173307	CMK	blood:	n/a
6	chr6:167031411-167031461	SK-N-SH	brain:	n/a
7	chr6:167040440-167040490	PrEC	prostate:	n/a
8	chr6:167032502-167032552	HPAEpiC	pulmonary alveolar:	n/a
9	chr6:167041940-167041990	K562	blood:	n/a
10	chr6:167070053-167070103	NT2-D1	testis:	n/a
11	chr6:167117898-167117948	HAEpiC	amniotic membrane:	n/a
12	chr6:167104601-167104651	HRPEpiC	eye:	n/a
13	chr6:167040675-167040725	U87	brain:	n/a
14	chr6:167136367-167136417	HEEpiC	esophagus:	n/a
15	chr6:167104761-167104811	SK-N-SH	brain:	n/a
16	chr6:167173257-167173307	CMK	blood:	n/a
17	chr6:167031411-167031461	SK-N-SH	brain:	n/a
18	chr6:167040440-167040490	PrEC	prostate:	n/a
19	chr6:167032502-167032552	HPAEpiC	pulmonary alveolar:	n/a
20	chr6:167041940-167041990	K562	blood:	n/a
21	chr6:167070053-167070103	NT2-D1	testis:	n/a
22	chr6:167117898-167117948	HAEpiC	amniotic membrane:	n/a
23	chr6:167117898-167117948	AG09309	skin:	n/a
24	chr6:167152254-167152304	PANC-1	pancreas:	n/a
25	chr6:167041940-167041990	HUVEC	blood vessel:	n/a
26	chr6:167032331-167032381	T-47D	breast:	n/a
27	chr6:167051781-167051831	PANC-1	pancreas:	n/a
28	chr6:167032331-167032381	HCF	heart:	n/a
29	chr6:167104903-167104953	HRE	kidney:	n/a
30	chr6:167032403-167032453	HL-60	blood:	n/a
31	chr6:167136367-167136417	CMK	blood:	n/a
32	chr6:167065429-167065479	HRE	kidney:	n/a
33	chr6:167093129-167093179	HNPCEpiC	eye:	n/a
34	chr6:167051518-167051568	T-47D	breast:	n/a
35	chr6:167033966-167034016	AG09319	gingival:	n/a
36	chr6:167032443-167032493	HNPCEpiC	eye:	n/a
37	chr6:167173343-167173393	ovcar-3	ovarian:	n/a
38	chr6:167065376-167065426	NH-A	brain:	n/a
39	chr6:167051744-167051794	GM06990	blood:	n/a
40	chr6:167063318-167063368	HCF	heart:	n/a
41	chr6:167070616-167070666	A549	lung:	n/a
42	chr6:167062226-167062276	HPAEpiC	pulmonary alveolar:	n/a
43	chr6:167178830-167178880	GM12891	blood:	n/a
44	chr6:167136367-167136417	SKMC	muscle:	n/a
45	chr6:167104601-167104651	NT2-D1	testis:	n/a
46	chr6:167062226-167062276	ovcar-3	ovarian:	n/a
47	chr6:167041530-167041580	U87	brain:	n/a
48	chr6:167040735-167040785	BJ	skin:	n/a
49	chr6:167040440-167040490	HRE	kidney:	n/a
50	chr6:167026505-167026555	HUVEC	blood vessel:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:167042473..167044859-chr6:167051026..167053525,2	MCF-7	breast:
2	chr6:167118192..167119844-chr6:167123770..167126237,2	MCF-7	breast:
3	chr6:167062835..167064756-chr6:167066345..167069061,2	K562	blood:
4	chr6:167146144..167148491-chr6:167149549..167152414,3	K562	blood:
5	chr6:167105343..167108325-chr6:167108497..167110048,2	MCF-7	breast:
6	chr6:167095053..167097754-chr6:167110301..167112969,2	K562	blood:
7	chr6:167045626..167049988-chr6:167051387..167056754,6	K562	blood:
8	chr6:167099352..167102037-chr6:167146508..167149347,2	MCF-7	breast:
9	chr6:167040717..167042560-chr6:167055383..167058084,2	MCF-7	breast:
10	chr6:167094171..167096219-chr6:167102346..167104221,2	K562	blood:
11	chr6:167050618..167053160-chr6:167077513..167080245,2	K562	blood:
12	chr6:167082807..167084979-chr6:167087135..167090920,3	K562	blood:
13	chr6:167035604..167038235-chr6:167040017..167042758,3	K562	blood:
14	chr6:167173252..167177821-chr6:167180840..167184779,4	K562	blood:
15	chr6:167137568..167139295-chr6:167143450..167146444,2	K562	blood:
16	chr6:167146144..167148491-chr6:167149549..167153230,4	K562	blood:
17	chr6:167027136..167029744-chr6:167037956..167040696,2	K562	blood:
18	chr6:167074591..167076523-chr6:167109521..167111565,2	K562	blood:
19	chr6:167027450..167030161-chr6:167032275..167034525,2	MCF-7	breast:
20	chr6:167172216..167176506-chr6:167180840..167185522,4	K562	blood:
21	chr6:167120732..167121236-chr6:167185691..167186290,2	MCF-7	breast:
22	chr6:167059027..167061692-chr6:167062613..167064872,3	K562	blood:
23	chr6:167021736..167024085-chr6:167052097..167054804,2	K562	blood:
24	chr6:167044666..167049346-chr6:167050228..167055763,8	K562	blood:
25	chr6:167019640..167022664-chr6:167027634..167030471,3	K562	blood:
26	chr6:167042473..167044859-chr6:167051026..167053525,2	MCF-7	breast:
27	chr6:167045626..167049988-chr6:167051387..167056754,6	K562	blood:
28	chr6:167097647..167099488-chr6:167100247..167103727,3	K562	blood:
29	chr6:167059027..167061692-chr6:167062613..167064872,3	K562	blood:
30	chr6:167040743..167042771-chr6:167090423..167092035,2	MCF-7	breast:
31	chr6:167042665..167045576-chr6:167045886..167047673,3	K562	blood:
32	chr6:167177178..167179780-chr6:167180212..167183134,2	MCF-7	breast:
33	chr6:167075814..167078811-chr6:167080757..167083595,2	MCF-7	breast:
34	chr6:167173252..167177821-chr6:167180840..167184779,4	K562	blood:
35	chr6:167097647..167100107-chr6:167101291..167103727,2	K562	blood:
36	chr6:167044666..167049346-chr6:167050228..167055763,8	K562	blood:
37	chr6:167105343..167108325-chr6:167108497..167110048,2	MCF-7	breast:
38	chr6:167062835..167064756-chr6:167066345..167069061,2	K562	blood:
39	chr6:167173631..167176313-chr6:167188907..167191189,2	K562	blood:
40	chr6:167021736..167024085-chr6:167052097..167054804,2	K562	blood:
41	chr6:167094171..167096219-chr6:167102346..167104221,2	K562	blood:
42	chr6:167042665..167045576-chr6:167045886..167047673,3	K562	blood:
43	chr6:167027450..167030161-chr6:167032275..167034525,2	MCF-7	breast:
44	chr6:167160489..167162374-chr6:167163032..167165986,2	K562	blood:
45	chr6:167059230..167061692-chr6:167062688..167064872,2	K562	blood:
46	chr6:167050618..167053160-chr6:167077513..167080245,2	K562	blood:
47	chr6:167041071..167042766-chr6:167149110..167150856,2	MCF-7	breast:
48	chr6:167179347..167182239-chr6:167183994..167186208,2	K562	blood:
49	chr6:167083479..167085354-chr6:167089213..167090920,2	K562	blood:
50	chr6:167097647..167100107-chr6:167101291..167103727,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGFR1OP-12	chr6:167064994-167067133	NONHSAT116054

No data

Variant related genes	Relation type
ENSG00000235008	TF binding region
RPS6KA2	TF binding region
ENSG00000235008	CpG island
RPS6KA2	CpG island
ENSG00000071242	chromatin interactions
ENSG00000235272	chromatin interactions

Extended variants
information (count: 7171 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:7171 , 50 per page) page: 1 2 3 4 5 6 7 ... 144

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4710074	chr6:167018915-167018916	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185681430	chr6:167018956-167018957	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs545520227	chr6:167019052-167019053	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560584519	chr6:167019096-167019097	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs3799584	chr6:167019126-167019127	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs540430703	chr6:167019140-167019141	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561924554	chr6:167019147-167019148	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576130921	chr6:167019148-167019149	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534158994	chr6:167019168-167019169	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529226500	chr6:167019181-167019182	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs116673693	chr6:167019206-167019207	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs115324334	chr6:167019212-167019213	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189998663	chr6:167019219-167019220	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140580179	chr6:167019237-167019238	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs180692762	chr6:167019244-167019245	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs3799583	chr6:167019290-167019291	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs144410408	chr6:167019295-167019296	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186448080	chr6:167019355-167019356	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147835331	chr6:167019363-167019364	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548095880	chr6:167019367-167019368	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191867537	chr6:167019371-167019372	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79217618	chr6:167019374-167019375	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs3799582	chr6:167019378-167019379	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs578048255	chr6:167019388-167019389	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545096199	chr6:167019403-167019404	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12203879	chr6:167019491-167019492	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs3799581	chr6:167019533-167019534	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs371976001	chr6:167019557-167019558	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572582123	chr6:167019584-167019585	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540420678	chr6:167019614-167019615	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141332148	chr6:167019621-167019622	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs142580223	chr6:167019647-167019648	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs3799580	chr6:167019648-167019649	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs16899233	chr6:167019675-167019676	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs183731849	chr6:167019738-167019739	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs188508080	chr6:167019767-167019768	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562654622	chr6:167019843-167019844	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532911632	chr6:167019891-167019892	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573151036	chr6:167019911-167019912	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531481660	chr6:167019922-167019923	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540467219	chr6:167019934-167019935	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559772528	chr6:167019968-167019969	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530108583	chr6:167019970-167019971	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs28391640	chr6:167019999-167020000	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs527433709	chr6:167020088-167020089	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375362749	chr6:167020140-167020141	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs35646789	chr6:167020156-167020157	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs191755340	chr6:167020225-167020226	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs567885357	chr6:167020280-167020281	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs150954141	chr6:167020285-167020286	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
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
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	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
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	22549408	CNVD

Chromatin state (count:3582 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167011000-167021000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:167012000-167023600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:167012200-167023400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr6:167012400-167025000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:167012400-167034400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr6:167012600-167025000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr6:167012600-167027600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr6:167012800-167027800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr6:167013200-167031000	Weak transcription	Fetal Intestine Small	intestine
10	chr6:167013400-167028800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:167013600-167027800	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr6:167013600-167028200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr6:167013800-167022400	Weak transcription	Brain Cingulate Gyrus	brain
14	chr6:167013800-167027000	Weak transcription	Esophagus	oesophagus
15	chr6:167013800-167027400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr6:167014000-167022200	Weak transcription	Brain Hippocampus Middle	brain
17	chr6:167014000-167025200	Weak transcription	Right Atrium	heart
18	chr6:167014000-167028000	Weak transcription	Brain Anterior Caudate	brain
19	chr6:167014200-167023400	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr6:167014200-167028400	Weak transcription	Stomach Mucosa	stomach
21	chr6:167014400-167027600	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr6:167015000-167021000	Weak transcription	NHDF-Ad	bronchial
23	chr6:167015000-167028400	Weak transcription	Osteobl	bone
24	chr6:167015200-167021600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr6:167016000-167019400	Weak transcription	Pancreas	Pancrea
26	chr6:167016000-167021200	Weak transcription	Left Ventricle	heart
27	chr6:167016000-167022400	Weak transcription	Ovary	ovary
28	chr6:167016000-167027400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr6:167016000-167027800	Weak transcription	Brain Angular Gyrus	brain
30	chr6:167016000-167028200	Weak transcription	Gastric	stomach
31	chr6:167016000-167034400	Weak transcription	Aorta	Aorta
32	chr6:167016200-167019600	Weak transcription	NHLF	lung
33	chr6:167016200-167025800	Weak transcription	Spleen	Spleen
34	chr6:167016200-167028400	Weak transcription	NH-A	brain
35	chr6:167016600-167032800	Weak transcription	Colon Smooth Muscle	Colon
36	chr6:167016800-167030200	Weak transcription	Brain Germinal Matrix	brain
37	chr6:167017200-167019400	Weak transcription	Psoas Muscle	Psoas
38	chr6:167017200-167023600	Weak transcription	Fetal Muscle Leg	muscle
39	chr6:167017200-167023600	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr6:167017200-167028600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:167017200-167032200	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr6:167017400-167019200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr6:167017400-167019400	Weak transcription	Right Ventricle	heart
44	chr6:167017400-167021200	Weak transcription	Fetal Muscle Trunk	muscle
45	chr6:167017400-167022400	Weak transcription	Stomach Smooth Muscle	stomach
46	chr6:167017400-167025000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr6:167017400-167030400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:167017600-167021200	Weak transcription	Fetal Stomach	stomach
49	chr6:167017600-167028400	Weak transcription	HSMM	muscle
50	chr6:167018200-167020400	Enhancers	Lung	lung

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