Variant report

Variant	nsv538401
Chromosome Location	chr6:106570926-106802072
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4051)
CpG islands
(count:2201)
Chromatin interactive
region (count:202)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4051 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:106673530-106673875	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:106758767-106758886	K562	blood:	n/a	n/a
3	ARID3A	chr6:106705069-106705352	K562	blood:	n/a	n/a
4	ARID3A	chr6:106773456-106774033	K562	blood:	n/a	n/a
5	ARID3A	chr6:106748826-106749149	K562	blood:	n/a	n/a
6	ARID3A	chr6:106636324-106636583	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:106787182-106787615	K562	blood:	n/a	n/a
8	ARID3A	chr6:106574041-106574231	K562	blood:	n/a	n/a
9	ARID3A	chr6:106735188-106735492	K562	blood:	n/a	n/a
10	ARID3A	chr6:106773317-106773989	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:106760548-106761365	K562	blood:	n/a	n/a
12	ARID3A	chr6:106763794-106764192	K562	blood:	n/a	n/a
13	ARID3A	chr6:106588539-106588816	K562	blood:	n/a	n/a
14	ARID3A	chr6:106583219-106583320	HepG2	liver:	n/a	n/a
15	ARID3A	chr6:106709625-106709909	HepG2	liver:	n/a	n/a
16	ARID3A	chr6:106583035-106583528	K562	blood:	n/a	n/a
17	ATF1	chr6:106573975-106574311	K562	blood:	n/a	n/a
18	ATF1	chr6:106773303-106773985	K562	blood:	n/a	n/a
19	ATF1	chr6:106603056-106603580	K562	blood:	n/a	n/a
20	ATF1	chr6:106597339-106597634	K562	blood:	n/a	n/a
21	ATF1	chr6:106763820-106764204	K562	blood:	n/a	n/a
22	ATF1	chr6:106760631-106761360	K562	blood:	n/a	n/a
23	ATF2	chr6:106773241-106773877	GM12878	blood:	n/a	n/a
24	ATF2	chr6:106760955-106761437	GM12878	blood:	n/a	n/a
25	ATF2	chr6:106593407-106593978	GM12878	blood:	n/a	n/a
26	ATF2	chr6:106573797-106574450	GM12878	blood:	n/a	n/a
27	ATF2	chr6:106760955-106761360	GM12878	blood:	n/a	n/a
28	ATF2	chr6:106611107-106612808	GM12878	blood:	n/a	n/a
29	ATF2	chr6:106629860-106630899	GM12878	blood:	n/a	n/a
30	ATF2	chr6:106594501-106595049	GM12878	blood:	n/a	n/a
31	ATF2	chr6:106615135-106615849	GM12878	blood:	n/a	n/a
32	ATF2	chr6:106773236-106773875	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF2	chr6:106589540-106590135	GM12878	blood:	n/a	n/a
34	ATF2	chr6:106615027-106615847	GM12878	blood:	n/a	n/a
35	ATF2	chr6:106773242-106773922	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF2	chr6:106654727-106655254	GM12878	blood:	n/a	n/a
37	ATF2	chr6:106611454-106613014	GM12878	blood:	n/a	n/a
38	ATF2	chr6:106787194-106787679	H1-hESC	embryonic stem cell:	n/a	n/a
39	ATF2	chr6:106629867-106630945	GM12878	blood:	n/a	n/a
40	ATF2	chr6:106589082-106590326	GM12878	blood:	n/a	n/a
41	ATF2	chr6:106573741-106574547	GM12878	blood:	n/a	n/a
42	ATF2	chr6:106668286-106668769	GM12878	blood:	n/a	n/a
43	ATF2	chr6:106634504-106634960	GM12878	blood:	n/a	n/a
44	ATF2	chr6:106720930-106721470	GM12878	blood:	n/a	n/a
45	ATF2	chr6:106773128-106774123	GM12878	blood:	n/a	n/a
46	ATF2	chr6:106572246-106572749	GM12878	blood:	n/a	n/a
47	ATF2	chr6:106668333-106668763	GM12878	blood:	n/a	n/a
48	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
49	ATF3	chr6:106583063-106583283	K562	blood:	n/a	n/a
50	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

(count:2201 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:106702170-106702220	Caco-2	colon:	n/a
2	chr6:106592760-106592810	ECC-1	luminal epithelium:	n/a
3	chr6:106583161-106583211	PANC-1	pancreas:	n/a
4	chr6:106774064-106774114	AG10803	skin:	n/a
5	chr6:106582669-106582719	LNCaP	prostate:	n/a
6	chr6:106702170-106702220	Caco-2	colon:	n/a
7	chr6:106592760-106592810	ECC-1	luminal epithelium:	n/a
8	chr6:106583161-106583211	PANC-1	pancreas:	n/a
9	chr6:106774064-106774114	AG10803	skin:	n/a
10	chr6:106582669-106582719	LNCaP	prostate:	n/a
11	chr6:106612002-106612052	SKMC	muscle:	n/a
12	chr6:106773705-106773755	AoSMC	blood vessel:	n/a
13	chr6:106770753-106770803	MCF-7	breast:	n/a
14	chr6:106773949-106773999	H1-hESC	embryonic stem cell:	embryo
15	chr6:106603209-106603259	PANC-1	pancreas:	n/a
16	chr6:106614417-106614467	Caco-2	colon:	n/a
17	chr6:106592760-106592810	HEK293	kidney:	embryo
18	chr6:106596012-106596062	SK-N-SH	brain:	n/a
19	chr6:106774064-106774114	NT2-D1	testis:	n/a
20	chr6:106583218-106583268	GM12878	blood:	n/a
21	chr6:106720478-106720528	RPTEC	kidney:	n/a
22	chr6:106614417-106614467	HEEpiC	esophagus:	n/a
23	chr6:106720478-106720528	HEEpiC	esophagus:	n/a
24	chr6:106770753-106770803	AoSMC	blood vessel:	n/a
25	chr6:106612002-106612052	NHDF-neo	bronchial:	n/a
26	chr6:106596012-106596062	LNCaP	prostate:	n/a
27	chr6:106583218-106583268	AG10803	skin:	n/a
28	chr6:106594431-106594481	HRE	kidney:	n/a
29	chr6:106709978-106710028	SKMC	muscle:	n/a
30	chr6:106773518-106773568	BJ	skin:	n/a
31	chr6:106770753-106770803	NHBE	bronchial:	n/a
32	chr6:106630507-106630557	ECC-1	luminal epithelium:	n/a
33	chr6:106773227-106773277	SK-N-MC	brain:	n/a
34	chr6:106676381-106676431	K562	blood:	n/a
35	chr6:106773518-106773568	HCF	heart:	n/a
36	chr6:106634304-106634354	HL-60	blood:	n/a
37	chr6:106773719-106773769	AG09309	skin:	n/a
38	chr6:106773712-106773762	K562	blood:	n/a
39	chr6:106592760-106592810	SKMC	muscle:	n/a
40	chr6:106596012-106596062	ProgFib	skin:	n/a
41	chr6:106702170-106702220	T-47D	breast:	n/a
42	chr6:106720478-106720528	PANC-1	pancreas:	n/a
43	chr6:106614417-106614467	SK-N-SH_RA	brain:	n/a
44	chr6:106773726-106773776	AoSMC	blood vessel:	n/a
45	chr6:106773140-106773190	AG09309	skin:	n/a
46	chr6:106614417-106614467	HL-60	blood:	n/a
47	chr6:106773140-106773190	NT2-D1	testis:	n/a
48	chr6:106594431-106594481	NHBE	bronchial:	n/a
49	chr6:106676237-106676287	T-47D	breast:	n/a
50	chr6:106773712-106773762	NHDF-neo	bronchial:	n/a

(count:202 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr6:106582685..106586548-chr6:106586639..106589895,5	K562	blood:
2	chr6:106583091..106583601-chr6:106673236..106673766,2	MCF-7	breast:
3	chr6:106571937..106574658-chr6:106760869..106763793,2	MCF-7	breast:
4	chr6:106758772..106760743-chr6:106761718..106763978,2	MCF-7	breast:
5	chr6:106761253..106763189-chr6:106763924..106766498,3	MCF-7	breast:
6	chr6:106587956..106591795-chr6:106592518..106598079,7	K562	blood:
7	chr6:106759165..106761053-chr6:106765599..106767778,3	MCF-7	breast:
8	chr6:106543067..106545717-chr6:106603091..106604835,2	K562	blood:
9	chr6:106571937..106574658-chr6:106760869..106763793,2	MCF-7	breast:
10	chr6:106607762..106610551-chr6:106612440..106614274,2	MCF-7	breast:
11	chr6:106626394..106628287-chr6:106631327..106633229,2	MCF-7	breast:
12	chr6:106782985..106783505-chr6:106892625..106893417,2	K562	blood:
13	chr6:106609627..106612260-chr6:106633159..106635604,2	MCF-7	breast:
14	chr11:73660702..73662934-chr6:106607356..106609610,2	MCF-7	breast:
15	chr6:106576961..106578620-chr6:106582173..106584108,2	MCF-7	breast:
16	chr6:106650293..106651927-chr6:106653289..106654803,2	K562	blood:
17	chr6:106668437..106670221-chr6:106672893..106674435,2	K562	blood:
18	chr6:106738772..106740659-chr6:106743750..106745285,2	K562	blood:
19	chr6:106786963..106787925-chr6:107318573..107319426,3	K562	blood:
20	chr1:153508168..153508824-chr6:106773337..106774109,2	Hela-S3	cervix:
21	chr6:106583091..106583601-chr6:106673236..106673766,2	MCF-7	breast:
22	chr6:106582718..106583982-chr6:106633824..106634839,9	MCF-7	breast:
23	chr6:106565935..106568775-chr6:106582626..106585270,2	MCF-7	breast:
24	chr6:106606541..106608998-chr6:106613812..106616904,3	MCF-7	breast:
25	chr6:106554917..106557278-chr6:106588143..106590911,3	K562	blood:
26	chr6:106702743..106704638-chr6:106718970..106721930,2	MCF-7	breast:
27	chr6:106597065..106599830-chr6:106759450..106761439,2	MCF-7	breast:
28	chr13:111365187..111365888-chr6:106773147..106773877,2	Hela-S3	cervix:
29	chr6:106752268..106754671-chr6:106754790..106756847,2	MCF-7	breast:
30	chr6:106616343..106618346-chr6:106620512..106623483,2	K562	blood:
31	chr6:105967746..105968312-chr6:106582748..106583466,3	MCF-7	breast:
32	chr10:12110899..12111464-chr6:106773211..106773850,2	Hela-S3	cervix:
33	chr17:60964482..60966018-chr6:106662776..106664412,2	MCF-7	breast:
34	chr6:106583053..106583633-chr6:106633874..106634792,3	MCF-7	breast:
35	chr6:106754483..106756426-chr6:106762936..106765537,2	K562	blood:
36	chr6:106722037..106723570-chr6:106735430..106737690,2	MCF-7	breast:
37	chr1:17231229..17231894-chr6:106773149..106773914,2	Hela-S3	cervix:
38	chr6:106538022..106538531-chr6:106748723..106749447,2	MCF-7	breast:
39	chr6:106783098..106785023-chr6:106786459..106788185,2	K562	blood:
40	chr6:106582685..106586548-chr6:106586639..106589895,5	K562	blood:
41	chr6:106738772..106740659-chr6:106743750..106745285,2	K562	blood:
42	chr6:106702583..106704653-chr6:106707003..106708997,2	K562	blood:
43	chr6:106560644..106566595-chr6:106567704..106572815,8	K562	blood:
44	chr6:106582718..106583982-chr6:106633824..106634839,9	MCF-7	breast:
45	chr6:106596720..106599715-chr6:106600989..106603238,3	K562	blood:
46	chr15:85523523..85524519-chr6:106773164..106773768,2	Hela-S3	cervix:
47	chr6:106761297..106762894-chr6:106764655..106766235,2	K562	blood:
48	chr6:106562594..106564776-chr6:106574919..106578759,3	K562	blood:
49	chr6:106797423..106799839-chr6:106808275..106811190,3	MCF-7	breast:
50	chr6:106687715..106690914-chr6:106691161..106694111,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRDM1-2	chr6:106629113-106629165	XLOC_005411
2	lnc-PRDM1-3	chr6:106580260-106580525	NONHSAT114228
3	lnc-PRDM1-2	chr6:106616369-106616946	XLOC_005411
4	lnc-PRDM1-3	chr6:106581991-106582034	NONHSAT114228
5	lnc-RTN4IP1-4	chr6:106731290-106731586	NONHSAT114231

No data

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
ENSG00000030066	chromatin interactions
ENSG00000272426	chromatin interactions
ENSG00000233016	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000073417	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000233941	chromatin interactions
ENSG00000175727	chromatin interactions
ENSG00000057657	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000166478	chromatin interactions
ENSG00000269919	chromatin interactions
ENSG00000113369	chromatin interactions
ENSG00000106100	chromatin interactions
ENSG00000187726	chromatin interactions
ENSG00000197956	chromatin interactions
ENSG00000204390	chromatin interactions
ENSG00000252444	chromatin interactions
ENSG00000204389	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000057663	chromatin interactions
ENSG00000181192	chromatin interactions
ENSG00000188825	chromatin interactions
PCDHA3	miRNA target sites

Extended variants
information (count: 8375 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:8375 , 50 per page) page: 1 2 3 4 5 6 7 ... 168

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140448265	chr6:106570935-106570936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs145449159	chr6:106570984-106570985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555596087	chr6:106570996-106570997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568975300	chr6:106571003-106571004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531936209	chr6:106571007-106571008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182047737	chr6:106571021-106571022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572407013	chr6:106571025-106571026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116568304	chr6:106571032-106571033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534252188	chr6:106571132-106571133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187596373	chr6:106571199-106571200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200175180	chr6:106571246-106571247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570478475	chr6:106571247-106571248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541300268	chr6:106571250-106571251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs137973546	chr6:106571338-106571339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs79647944	chr6:106571352-106571353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576176678	chr6:106571367-106571368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532961699	chr6:106571437-106571438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78702734	chr6:106571438-106571439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563964787	chr6:106571453-106571454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6910707	chr6:106571460-106571461	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs574657682	chr6:106571474-106571475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144692513	chr6:106571520-106571521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12205855	chr6:106571533-106571534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11152965	chr6:106571543-106571544	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs532936294	chr6:106571566-106571567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545860273	chr6:106571607-106571608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548415600	chr6:106571683-106571684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs9486283	chr6:106571699-106571700	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs192026527	chr6:106571708-106571709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549637137	chr6:106571721-106571722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs143929454	chr6:106571746-106571747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148226434	chr6:106571749-106571750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138717668	chr6:106571769-106571770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547733427	chr6:106571788-106571789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570813509	chr6:106571792-106571793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539446317	chr6:106571808-106571809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549806605	chr6:106571829-106571830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs569801577	chr6:106571860-106571861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs11969705	chr6:106571906-106571907	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs555854117	chr6:106571985-106571986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574504446	chr6:106571998-106571999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533992379	chr6:106572008-106572009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs553777278	chr6:106572053-106572054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577249062	chr6:106572187-106572188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545799378	chr6:106572191-106572192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs141139260	chr6:106572238-106572239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576128018	chr6:106572282-106572283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs548091767	chr6:106572358-106572359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561830772	chr6:106572403-106572404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs527835068	chr6:106572518-106572519	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:4597 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:106553600-106584000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:106559200-106574200	Weak transcription	Small Intestine	intestine
3	chr6:106565800-106572600	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr6:106567200-106573800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr6:106567400-106572800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr6:106567400-106573400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr6:106567800-106571000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:106568000-106576800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr6:106568200-106573000	Weak transcription	Fetal Intestine Large	intestine
10	chr6:106568400-106573400	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr6:106568600-106573000	Weak transcription	Fetal Intestine Small	intestine
12	chr6:106568600-106576800	Weak transcription	NHDF-Ad	bronchial
13	chr6:106568600-106577000	Weak transcription	HSMMtube	muscle
14	chr6:106568800-106571000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr6:106568800-106578000	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr6:106570200-106571400	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr6:106570400-106574800	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr6:106570600-106571400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:106570600-106571800	Weak transcription	GM12878-XiMat	blood
20	chr6:106570600-106573000	Weak transcription	Lung	lung
21	chr6:106570800-106572000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr6:106571000-106571200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr6:106571000-106571600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr6:106571200-106571400	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr6:106571400-106572400	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr6:106571400-106572800	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr6:106571800-106573800	Enhancers	GM12878-XiMat	blood
28	chr6:106572000-106572200	Enhancers	Primary B cells from cord blood	blood
29	chr6:106572000-106574600	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr6:106572200-106573200	Weak transcription	Primary B cells from cord blood	blood
31	chr6:106572200-106574600	Enhancers	Primary B cells from peripheral blood	blood
32	chr6:106572400-106573000	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr6:106572400-106574000	Enhancers	K562	blood
34	chr6:106572600-106573800	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr6:106572800-106573000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr6:106572800-106573800	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr6:106573000-106573200	Enhancers	Lung	lung
38	chr6:106573000-106573200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr6:106573000-106573800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr6:106573000-106573800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr6:106573000-106574000	Enhancers	Fetal Intestine Large	intestine
42	chr6:106573000-106574400	Enhancers	Fetal Intestine Small	intestine
43	chr6:106573200-106573600	Enhancers	Rectal Mucosa Donor 29	rectum
44	chr6:106573200-106573600	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr6:106573200-106573800	Enhancers	Primary B cells from cord blood	blood
46	chr6:106573200-106573800	Weak transcription	Lung	lung
47	chr6:106573400-106573600	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr6:106573400-106574000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr6:106573600-106573800	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr6:106573600-106573800	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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