Variant report

Variant	nsv538403
Chromosome Location	chr6:106667748-106802072
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	chr6:106748826-106749149	K562	blood:	n/a	n/a
2	ARID3A	chr6:106709625-106709909	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:106735188-106735492	K562	blood:	n/a	n/a
4	ARID3A	chr6:106763794-106764192	K562	blood:	n/a	n/a
5	ARID3A	chr6:106758767-106758886	K562	blood:	n/a	n/a
6	ARID3A	chr6:106760548-106761365	K562	blood:	n/a	n/a
7	ARID3A	chr6:106705069-106705352	K562	blood:	n/a	n/a
8	ARID3A	chr6:106787182-106787615	K562	blood:	n/a	n/a
9	ARID3A	chr6:106773456-106774033	K562	blood:	n/a	n/a
10	ARID3A	chr6:106673530-106673875	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:106773317-106773989	HepG2	liver:	n/a	n/a
12	ATF1	chr6:106763820-106764204	K562	blood:	n/a	n/a
13	ATF1	chr6:106760631-106761360	K562	blood:	n/a	n/a
14	ATF1	chr6:106773303-106773985	K562	blood:	n/a	n/a
15	ATF2	chr6:106668286-106668769	GM12878	blood:	n/a	n/a
16	ATF2	chr6:106773128-106774123	GM12878	blood:	n/a	n/a
17	ATF2	chr6:106720930-106721470	GM12878	blood:	n/a	n/a
18	ATF2	chr6:106773241-106773877	GM12878	blood:	n/a	n/a
19	ATF2	chr6:106760955-106761360	GM12878	blood:	n/a	n/a
20	ATF2	chr6:106787194-106787679	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr6:106760955-106761437	GM12878	blood:	n/a	n/a
22	ATF2	chr6:106773236-106773875	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr6:106668333-106668763	GM12878	blood:	n/a	n/a
24	ATF2	chr6:106773242-106773922	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr6:106773453-106773878	K562	blood:	n/a	chr6:106773675-106773695 chr6:106773685-106773696 chr6:106773684-106773694 chr6:106773687-106773694 chr6:106773685-106773696 chr6:106773686-106773694 chr6:106773683-106773696 chr6:106773685-106773698 chr6:106773683-106773698 chr6:106773687-106773695
26	ATF3	chr6:106773440-106773885	K562	blood:	n/a	chr6:106773675-106773695 chr6:106773685-106773696 chr6:106773684-106773694 chr6:106773687-106773694 chr6:106773685-106773696 chr6:106773686-106773694 chr6:106773683-106773696 chr6:106773685-106773698 chr6:106773683-106773698 chr6:106773687-106773695
27	ATF3	chr6:106773502-106773828	GM12878	blood:	n/a	chr6:106773675-106773695 chr6:106773685-106773696 chr6:106773684-106773694 chr6:106773687-106773694 chr6:106773685-106773696 chr6:106773686-106773694 chr6:106773683-106773696 chr6:106773685-106773698 chr6:106773683-106773698 chr6:106773687-106773695
28	ATF3	chr6:106773438-106773872	HepG2	liver:	n/a	chr6:106773675-106773695 chr6:106773685-106773696 chr6:106773684-106773694 chr6:106773687-106773694 chr6:106773685-106773696 chr6:106773686-106773694 chr6:106773683-106773696 chr6:106773685-106773698 chr6:106773683-106773698 chr6:106773687-106773695
29	ATF3	chr6:106773451-106773868	H1-hESC	embryonic stem cell:	n/a	chr6:106773675-106773695 chr6:106773685-106773696 chr6:106773684-106773694 chr6:106773687-106773694 chr6:106773685-106773696 chr6:106773686-106773694 chr6:106773683-106773696 chr6:106773685-106773698 chr6:106773683-106773698 chr6:106773687-106773695
30	ATF3	chr6:106773391-106773906	K562	blood:	n/a	chr6:106773675-106773695 chr6:106773685-106773696 chr6:106773684-106773694 chr6:106773687-106773694 chr6:106773685-106773696 chr6:106773686-106773694 chr6:106773683-106773696 chr6:106773685-106773698 chr6:106773683-106773698 chr6:106773687-106773695
31	ATF3	chr6:106760800-106761326	K562	blood:	n/a	n/a
32	ATF3	chr6:106773377-106773968	GM12878	blood:	n/a	chr6:106773675-106773695 chr6:106773685-106773696 chr6:106773684-106773694 chr6:106773687-106773694 chr6:106773685-106773696 chr6:106773686-106773694 chr6:106773683-106773696 chr6:106773685-106773698 chr6:106773683-106773698 chr6:106773687-106773695
33	ATF3	chr6:106773423-106773971	A549	lung:	n/a	chr6:106773675-106773695 chr6:106773685-106773696 chr6:106773684-106773694 chr6:106773687-106773694 chr6:106773685-106773696 chr6:106773686-106773694 chr6:106773683-106773696 chr6:106773685-106773698 chr6:106773683-106773698 chr6:106773687-106773695
34	ATF3	chr6:106773430-106773936	H1-hESC	embryonic stem cell:	n/a	chr6:106773675-106773695 chr6:106773685-106773696 chr6:106773684-106773694 chr6:106773687-106773694 chr6:106773685-106773696 chr6:106773686-106773694 chr6:106773683-106773696 chr6:106773685-106773698 chr6:106773683-106773698 chr6:106773687-106773695
35	ATF3	chr6:106773377-106774002	HepG2	liver:	n/a	chr6:106773675-106773695 chr6:106773685-106773696 chr6:106773684-106773694 chr6:106773687-106773694 chr6:106773685-106773696 chr6:106773686-106773694 chr6:106773683-106773696 chr6:106773685-106773698 chr6:106773683-106773698 chr6:106773687-106773695
36	BACH1	chr6:106772962-106773991	K562	blood:	n/a	n/a
37	BACH1	chr6:106739765-106739776	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr6:106773015-106774021	H1-hESC	embryonic stem cell:	n/a	n/a
39	BATF	chr6:106773358-106773882	GM12878	blood:	n/a	chr6:106773684-106773697
40	BATF	chr6:106761101-106761350	GM12878	blood:	n/a	n/a
41	BATF	chr6:106695714-106696014	GM12878	blood:	n/a	chr6:106695843-106695854
42	BATF	chr6:106764315-106764568	GM12878	blood:	n/a	n/a
43	BATF	chr6:106764297-106764512	GM12878	blood:	n/a	n/a
44	BATF	chr6:106761071-106761369	GM12878	blood:	n/a	n/a
45	BATF	chr6:106692790-106693105	GM12878	blood:	n/a	chr6:106692813-106692822
46	BATF	chr6:106692789-106693117	GM12878	blood:	n/a	chr6:106692813-106692822 chr6:106693099-106693108
47	BCL11A	chr6:106695732-106696000	GM12878	blood:	n/a	n/a
48	BCL3	chr6:106773405-106773889	A549	lung:	n/a	chr6:106773564-106773573 chr6:106773593-106773602 chr6:106773472-106773481
49	BCL3	chr6:106773261-106773712	A549	lung:	n/a	chr6:106773564-106773573 chr6:106773593-106773602 chr6:106773472-106773481
50	BCLAF1	chr6:106773081-106773827	GM12878	blood:	n/a	chr6:106773564-106773573 chr6:106773593-106773602 chr6:106773472-106773481

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:106720478-106720528	HUVEC	blood vessel:	n/a
2	chr6:106676237-106676287	ProgFib	skin:	n/a
3	chr6:106720478-106720528	HUVEC	blood vessel:	n/a
4	chr6:106676237-106676287	ProgFib	skin:	n/a
5	chr6:106773719-106773769	IMR90	lung:	fetal
6	chr6:106773726-106773776	HEEpiC	esophagus:	n/a
7	chr6:106773695-106773745	ECC-1	luminal epithelium:	n/a
8	chr6:106773140-106773190	SKMC	muscle:	n/a
9	chr6:106709978-106710028	ECC-1	luminal epithelium:	n/a
10	chr6:106773780-106773830	AG04450	lung:	fetal
11	chr6:106702170-106702220	ovcar-3	ovarian:	n/a
12	chr6:106773726-106773776	SKMC	muscle:	n/a
13	chr6:106773140-106773190	AG09319	gingival:	n/a
14	chr6:106773188-106773238	NH-A	brain:	n/a
15	chr6:106676568-106676618	NHDF-neo	bronchial:	n/a
16	chr6:106720478-106720528	Hepatocyte	liver:	n/a
17	chr6:106773188-106773238	HEK293	kidney:	embryo
18	chr6:106720478-106720528	CMK	blood:	n/a
19	chr6:106773227-106773277	ECC-1	luminal epithelium:	n/a
20	chr6:106773726-106773776	BJ	skin:	n/a
21	chr6:106773719-106773769	PFSK-1	brain:	n/a
22	chr6:106774172-106774222	Caco-2	colon:	n/a
23	chr6:106773188-106773238	SKMC	muscle:	n/a
24	chr6:106774064-106774114	IMR90	lung:	fetal
25	chr6:106773695-106773745	SK-N-SH	brain:	n/a
26	chr6:106773705-106773755	AG10803	skin:	n/a
27	chr6:106709978-106710028	Hepatocyte	liver:	n/a
28	chr6:106676381-106676431	HepG2	liver:	n/a
29	chr6:106773705-106773755	GM12892	blood:	n/a
30	chr6:106676237-106676287	MCF-7	breast:	n/a
31	chr6:106773726-106773776	HRCEpiC	kidney:	n/a
32	chr6:106676237-106676287	AG09319	gingival:	n/a
33	chr6:106774064-106774114	ovcar-3	ovarian:	n/a
34	chr6:106773518-106773568	H1-hESC	embryonic stem cell:	embryo
35	chr6:106676237-106676287	GM12892	blood:	n/a
36	chr6:106676381-106676431	Jurkat	blood:	n/a
37	chr6:106774064-106774114	SK-N-MC	brain:	n/a
38	chr6:106773949-106773999	HNPCEpiC	eye:	n/a
39	chr6:106720478-106720528	HAEpiC	amniotic membrane:	n/a
40	chr6:106676381-106676431	ECC-1	luminal epithelium:	n/a
41	chr6:106676237-106676287	AoSMC	blood vessel:	n/a
42	chr6:106676568-106676618	HCPEpiC	choroid plexus:	n/a
43	chr6:106773705-106773755	Caco-2	colon:	n/a
44	chr6:106773695-106773745	HL-60	blood:	n/a
45	chr6:106770753-106770803	HRPEpiC	eye:	n/a
46	chr6:106676568-106676618	GM12878	blood:	n/a
47	chr6:106676568-106676618	Caco-2	colon:	n/a
48	chr6:106773140-106773190	BE2_C	brain:	n/a
49	chr6:106773949-106773999	SK-N-SH	brain:	n/a
50	chr6:106773518-106773568	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:106757150..106763241-chr6:106770428..106774915,9	MCF-7	breast:
2	chr17:41380326..41382145-chr6:106715204..106716723,3	K562	blood:
3	chr6:106583091..106583601-chr6:106673236..106673766,2	MCF-7	breast:
4	chr15:85523523..85524519-chr6:106773164..106773768,2	Hela-S3	cervix:
5	chr6:106750271..106753940-chr6:106760573..106763415,3	K562	blood:
6	chr6:106763853..106765922-chr6:106766260..106768887,2	MCF-7	breast:
7	chr6:106759060..106762188-chr6:106770312..106774543,4	MCF-7	breast:
8	chr6:106702821..106705726-chr6:106719179..106721244,2	K562	blood:
9	chr6:106782985..106783505-chr6:106892625..106893417,2	K562	blood:
10	chr6:106181287..106182030-chr6:106671102..106671759,4	MCF-7	breast:
11	chr10:12110899..12111464-chr6:106773211..106773850,2	Hela-S3	cervix:
12	chr17:41398972..41400831-chr6:106715223..106716723,3	K562	blood:
13	chr6:106768044..106771696-chr6:106771990..106774923,9	K562	blood:
14	chr6:106702743..106704638-chr6:106718970..106721930,2	MCF-7	breast:
15	chr6:31782559..31783446-chr6:106772863..106773513,2	Hela-S3	cervix:
16	chr6:106790394..106792499-chr6:106794390..106797153,2	K562	blood:
17	chr6:106726791..106729704-chr6:106731608..106734552,2	K562	blood:
18	chr6:106783081..106786779-chr6:106807913..106810095,3	MCF-7	breast:
19	chr6:106702583..106704653-chr6:106707003..106708997,2	K562	blood:
20	chr5:90678707..90679279-chr6:106773660..106774372,2	Hela-S3	cervix:
21	chr6:106797423..106799839-chr6:106808275..106811190,3	MCF-7	breast:
22	chr6:106788817..106792867-chr6:106807861..106810730,3	MCF-7	breast:
23	chr6:106792903..106794497-chr6:106796166..106798717,2	K562	blood:
24	chr6:106702743..106704638-chr6:106718970..106721930,2	MCF-7	breast:
25	chr6:106756472..106759441-chr6:106761621..106763989,2	K562	blood:
26	chr6:106537660..106538682-chr6:106670948..106671779,3	MCF-7	breast:
27	chr6:106761297..106762894-chr6:106764655..106766235,2	K562	blood:
28	chr6:106751067..106754037-chr6:106772364..106773866,2	MCF-7	breast:
29	chr6:106758694..106760423-chr6:106769043..106771248,2	K562	blood:
30	chr1:17231229..17231894-chr6:106773149..106773914,2	Hela-S3	cervix:
31	chr6:106665518..106668104-chr6:106669011..106671673,2	K562	blood:
32	chr6:106738772..106740659-chr6:106743750..106745285,2	K562	blood:
33	chr6:106687715..106690914-chr6:106691161..106694111,3	K562	blood:
34	chr17:41464871..41467659-chr6:106716704..106718204,2	MCF-7	breast:
35	chr6:106720896..106722569-chr6:106772183..106774793,2	MCF-7	breast:
36	chr17:41390684..41392218-chr6:106715223..106718203,2	K562	blood:
37	chr11:9482492..9483098-chr6:106773115..106773897,2	Hela-S3	cervix:
38	chr6:106751067..106754037-chr6:106772364..106773866,2	MCF-7	breast:
39	chr6:105851042..105852609-chr6:106764911..106766996,2	K562	blood:
40	chr6:106783098..106785023-chr6:106786459..106788185,2	K562	blood:
41	chr6:106786932..106787612-chr6:106892577..106893519,3	MCF-7	breast:
42	chr6:106722037..106723570-chr6:106735430..106737690,2	MCF-7	breast:
43	chr6:106757707..106762317-chr6:106772062..106775183,5	K562	blood:
44	chr6:106702821..106705726-chr6:106719179..106721244,2	K562	blood:
45	chr6:106798884..106801370-chr6:106805167..106807841,2	K562	blood:
46	chr6:106752268..106754671-chr6:106754790..106756847,2	MCF-7	breast:
47	chr13:111365187..111365888-chr6:106773147..106773877,2	Hela-S3	cervix:
48	chr6:106758694..106760423-chr6:106769043..106771248,2	K562	blood:
49	chr6:106772845..106775200-chr6:106775290..106778006,2	K562	blood:
50	chr6:106728937..106730967-chr6:106732037..106733829,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RTN4IP1-4	chr6:106731290-106731586	NONHSAT114231

Variant related genes	Relation type
RNU6-344P	TF binding region
ATG5	TF binding region
RN7SL47P	TF binding region
RNU6-344P	CpG island
ATG5	CpG island
RN7SL47P	CpG island
ENSG00000236383	chromatin interactions
ENSG00000106100	chromatin interactions
ENSG00000175727	chromatin interactions
ENSG00000233016	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000166478	chromatin interactions
ENSG00000204390	chromatin interactions
ENSG00000181192	chromatin interactions
ENSG00000073417	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000057663	chromatin interactions
ENSG00000113369	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000272426	chromatin interactions
ENSG00000197956	chromatin interactions
ENSG00000233941	chromatin interactions
ENSG00000204389	chromatin interactions
ENSG00000252444	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000030066	chromatin interactions

Extended variants
information (count: 4913 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:4913 , 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	rs558971792	chr6:106667748-106667749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs568968623	chr6:106667770-106667771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2299863	chr6:106667806-106667807	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs538232275	chr6:106667845-106667846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368290118	chr6:106667855-106667856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs112279096	chr6:106667877-106667878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376835180	chr6:106667890-106667891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529915154	chr6:106667898-106667899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554961138	chr6:106667905-106667906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs56244906	chr6:106667934-106667935	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs1769963	chr6:106667991-106667992	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs2299864	chr6:106667994-106667995	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs150480917	chr6:106668059-106668060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545213691	chr6:106668110-106668111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565029323	chr6:106668139-106668140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs144842037	chr6:106668151-106668152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs57178542	chr6:106668180-106668181	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs139046333	chr6:106668202-106668203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544111320	chr6:106668227-106668228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560503284	chr6:106668230-106668231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138292952	chr6:106668242-106668243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546344309	chr6:106668245-106668246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142936634	chr6:106668282-106668283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139676068	chr6:106668306-106668307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532576869	chr6:106668309-106668310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552785725	chr6:106668343-106668344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs138848450	chr6:106668354-106668355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192441054	chr6:106668393-106668394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs555322731	chr6:106668456-106668457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568429766	chr6:106668491-106668492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534229963	chr6:106668492-106668493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs562555626	chr6:106668641-106668642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184809705	chr6:106668670-106668671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs73775392	chr6:106668707-106668708	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs544865298	chr6:106668777-106668778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs113206177	chr6:106668834-106668835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1626224	chr6:106668839-106668840	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs189421832	chr6:106668935-106668936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs192192917	chr6:106668945-106668946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs141966896	chr6:106669105-106669106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs184516435	chr6:106669120-106669121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540252018	chr6:106669134-106669135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs17587319	chr6:106669139-106669140	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs73775393	chr6:106669197-106669198	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs551989101	chr6:106669217-106669218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569445553	chr6:106669260-106669261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549410184	chr6:106669271-106669272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs75364358	chr6:106669289-106669290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs189388204	chr6:106669319-106669320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs568795296	chr6:106669325-106669326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	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
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
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Developmental delay	21147756	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Autism	17483303	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
abnormal development	18461090	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2813 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:106626800-106674800	Weak transcription	K562	blood
2	chr6:106628400-106675200	Weak transcription	Stomach Mucosa	stomach
3	chr6:106628800-106671200	Weak transcription	Fetal Intestine Small	intestine
4	chr6:106645800-106695400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr6:106647400-106695200	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr6:106649200-106695200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:106649200-106695400	Weak transcription	HMEC	breast
8	chr6:106649400-106682400	Weak transcription	Primary T cells from cord blood	blood
9	chr6:106649600-106683000	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr6:106650000-106674200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr6:106650000-106674600	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr6:106650000-106695200	Weak transcription	NHEK	skin
13	chr6:106650400-106674800	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr6:106650400-106682600	Weak transcription	Dnd41	blood
15	chr6:106650600-106671600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr6:106657400-106673600	Weak transcription	HSMM	muscle
17	chr6:106657400-106674200	Weak transcription	Primary hematopoietic stem cells	blood
18	chr6:106657400-106675000	Weak transcription	Primary B cells from cord blood	blood
19	chr6:106657800-106683200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr6:106658200-106667800	Weak transcription	GM12878-XiMat	blood
21	chr6:106658200-106689000	Weak transcription	Primary B cells from peripheral blood	blood
22	chr6:106662400-106683000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr6:106662800-106671000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr6:106663400-106683800	Weak transcription	NHDF-Ad	bronchial
25	chr6:106664800-106683000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr6:106664800-106693800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr6:106665400-106689600	Weak transcription	Aorta	Aorta
28	chr6:106665400-106695200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr6:106666800-106671200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr6:106667200-106668000	Enhancers	Fetal Heart	heart
31	chr6:106667600-106673400	Weak transcription	HepG2	liver
32	chr6:106667800-106671200	Enhancers	GM12878-XiMat	blood
33	chr6:106668000-106671400	Weak transcription	Fetal Heart	heart
34	chr6:106668200-106683200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr6:106670400-106671600	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr6:106670600-106671600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr6:106671000-106671600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr6:106671000-106671600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr6:106671000-106671600	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr6:106671200-106671600	Enhancers	Fetal Intestine Small	intestine
41	chr6:106671200-106671800	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr6:106671200-106673600	Enhancers	A549	lung
43	chr6:106671200-106690000	Weak transcription	GM12878-XiMat	blood
44	chr6:106671400-106671800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr6:106671400-106672000	Enhancers	Fetal Heart	heart
46	chr6:106671600-106671800	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr6:106671600-106672400	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr6:106671600-106672600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr6:106671600-106675600	Weak transcription	Fetal Intestine Small	intestine
50	chr6:106671600-106677200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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