Variant report

Variant	esv3428128
Chromosome Location	chr6:35150524-35225843
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1242)
CpG islands
(count:1406)
Chromatin interactive
region (count:151)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1242 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:35215709-35215952	K562	blood:	n/a	n/a
2	ARID3A	chr6:35153047-35153074	K562	blood:	n/a	n/a
3	ARID3A	chr6:35208936-35209172	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:35172889-35173142	K562	blood:	n/a	n/a
5	ARID3A	chr6:35151660-35152219	K562	blood:	n/a	n/a
6	ATF1	chr6:35151871-35151999	K562	blood:	n/a	n/a
7	ATF1	chr6:35161082-35161231	K562	blood:	n/a	n/a
8	ATF2	chr6:35206485-35206933	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr6:35216131-35216460	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr6:35181762-35182008	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr6:35216115-35216416	K562	blood:	n/a	n/a
12	BACH1	chr6:35181238-35181438	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr6:35183349-35183361	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL3	chr6:35196237-35196582	GM12878	blood:	n/a	n/a
15	BCL3	chr6:35196263-35196552	GM12878	blood:	n/a	n/a
16	BCLAF1	chr6:35215580-35215932	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:35179062-35179141	K562	blood:	n/a	chr6:35179110-35179119 chr6:35179110-35179119
18	BHLHE40	chr6:35179047-35179214	HepG2	liver:	n/a	chr6:35179110-35179119 chr6:35179110-35179119
19	BHLHE40	chr6:35172961-35173119	K562	blood:	n/a	n/a
20	BRCA1	chr6:35208914-35209098	HepG2	liver:	n/a	n/a
21	BRCA1	chr6:35170042-35170063	GM12878	blood:	n/a	n/a
22	BRCA1	chr6:35181736-35181822	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr6:35208911-35209234	H1-hESC	embryonic stem cell:	n/a	n/a
24	CBX3	chr6:35202712-35203014	K562	blood:	n/a	n/a
25	CBX3	chr6:35202658-35203116	K562	blood:	n/a	n/a
26	CCNT2	chr6:35151650-35152051	K562	blood:	n/a	n/a
27	CCNT2	chr6:35161113-35161260	K562	blood:	n/a	n/a
28	CEBPB	chr6:35169415-35169522	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr6:35208624-35209196	K562	blood:	n/a	chr6:35208801-35208812
30	CEBPB	chr6:35184154-35184386	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr6:35172893-35173233	HepG2	liver:	n/a	n/a
32	CEBPB	chr6:35152861-35153402	MCF-7	breast:	n/a	chr6:35153142-35153153
33	CEBPB	chr6:35151701-35152118	MCF-7	breast:	n/a	chr6:35151876-35151887
34	CEBPB	chr6:35153020-35153243	HepG2	liver:	n/a	chr6:35153142-35153153
35	CEBPB	chr6:35152926-35153314	HepG2	liver:	n/a	chr6:35153142-35153153
36	CEBPB	chr6:35152951-35153325	HepG2	liver:	n/a	chr6:35153142-35153153
37	CEBPB	chr6:35152902-35153348	Hela-S3	cervix:	n/a	chr6:35153142-35153153
38	CEBPB	chr6:35221054-35221417	HepG2	liver:	n/a	chr6:35221233-35221244 chr6:35221232-35221245
39	CEBPB	chr6:35172891-35173235	K562	blood:	n/a	n/a
40	CEBPB	chr6:35151711-35152056	Hela-S3	cervix:	n/a	chr6:35151876-35151887
41	CEBPB	chr6:35208630-35209293	IMR90	lung:	n/a	chr6:35208801-35208812
42	CEBPB	chr6:35155586-35155695	K562	blood:	n/a	n/a
43	CEBPB	chr6:35208578-35209457	MCF-7	breast:	n/a	chr6:35208801-35208812
44	CEBPB	chr6:35172803-35173198	A549	lung:	n/a	n/a
45	CEBPB	chr6:35221059-35221407	IMR90	lung:	n/a	chr6:35221233-35221244 chr6:35221232-35221245
46	CEBPB	chr6:35151652-35152108	K562	blood:	n/a	chr6:35151876-35151887
47	CEBPB	chr6:35152956-35153305	A549	lung:	n/a	chr6:35153142-35153153
48	CEBPB	chr6:35151742-35152050	A549	lung:	n/a	chr6:35151876-35151887
49	CEBPB	chr6:35208663-35209346	Hela-S3	cervix:	n/a	chr6:35208801-35208812
50	CEBPB	chr6:35152881-35153342	A549	lung:	n/a	chr6:35153142-35153153

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:35181924-35181974	GM12892	blood:	n/a
2	chr6:35153213-35153263	Jurkat	blood:	n/a
3	chr6:35181113-35181163	SKMC	muscle:	n/a
4	chr6:35181924-35181974	GM12892	blood:	n/a
5	chr6:35153213-35153263	Jurkat	blood:	n/a
6	chr6:35181113-35181163	SKMC	muscle:	n/a
7	chr6:35182910-35182960	GM12892	blood:	n/a
8	chr6:35185397-35185447	MCF10A-Er-Src	breast:	n/a
9	chr6:35208807-35208857	NHBE	bronchial:	n/a
10	chr6:35181888-35181938	HRCEpiC	kidney:	n/a
11	chr6:35183390-35183440	BJ	skin:	n/a
12	chr6:35153213-35153263	HEEpiC	esophagus:	n/a
13	chr6:35160575-35160625	Jurkat	blood:	n/a
14	chr6:35181924-35181974	AG09319	gingival:	n/a
15	chr6:35198848-35198898	SK-N-MC	brain:	n/a
16	chr6:35177616-35177666	PrEC	prostate:	n/a
17	chr6:35181113-35181163	U87	brain:	n/a
18	chr6:35173534-35173584	HUVEC	blood vessel:	n/a
19	chr6:35216799-35216849	SK-N-SH	brain:	n/a
20	chr6:35173534-35173584	SK-N-SH	brain:	n/a
21	chr6:35153213-35153263	A549	lung:	n/a
22	chr6:35170850-35170900	NHBE	bronchial:	n/a
23	chr6:35170850-35170900	GM12892	blood:	n/a
24	chr6:35153213-35153263	SK-N-SH_RA	brain:	n/a
25	chr6:35180909-35180959	HEK293	kidney:	embryo
26	chr6:35181924-35181974	U87	brain:	n/a
27	chr6:35182508-35182558	HCM	heart:	n/a
28	chr6:35206618-35206668	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:35173534-35173584	GM12878	blood:	n/a
30	chr6:35181113-35181163	AG04450	lung:	fetal
31	chr6:35181113-35181163	HIPEpiC	eye:	n/a
32	chr6:35181924-35181974	PrEC	prostate:	n/a
33	chr6:35177616-35177666	HUVEC	blood vessel:	n/a
34	chr6:35173534-35173584	BE2_C	brain:	n/a
35	chr6:35153213-35153263	AG09309	skin:	n/a
36	chr6:35160575-35160625	HRE	kidney:	n/a
37	chr6:35206618-35206668	NT2-D1	testis:	n/a
38	chr6:35181113-35181163	ovcar-3	ovarian:	n/a
39	chr6:35170850-35170900	HCM	heart:	n/a
40	chr6:35182910-35182960	PFSK-1	brain:	n/a
41	chr6:35182508-35182558	ovcar-3	ovarian:	n/a
42	chr6:35173534-35173584	Jurkat	blood:	n/a
43	chr6:35170850-35170900	ProgFib	skin:	n/a
44	chr6:35181113-35181163	HepG2	liver:	n/a
45	chr6:35182910-35182960	HIPEpiC	eye:	n/a
46	chr6:35198848-35198898	HepG2	liver:	n/a
47	chr6:35153213-35153263	HL-60	blood:	n/a
48	chr6:35160575-35160625	HRCEpiC	kidney:	n/a
49	chr6:35198848-35198898	AG04449	skin:	fetal
50	chr6:35185397-35185447	NHBE	bronchial:	n/a

(count:151 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:35118710..35120443-chr6:35162484..35164592,2	MCF-7	breast:
2	chr6:35178562..35181407-chr6:35198838..35201388,2	MCF-7	breast:
3	chr6:35086962..35089707-chr6:35186817..35189390,2	K562	blood:
4	chr6:35172567..35174119-chr6:35186872..35189196,2	MCF-7	breast:
5	chr6:35113907..35114851-chr6:35172520..35173065,3	K562	blood:
6	chr6:35203262..35205063-chr6:35205452..35207429,2	K562	blood:
7	chr6:35152047..35154652-chr6:35168732..35171108,2	MCF-7	breast:
8	chr6:35148681..35155694-chr6:35156262..35164857,12	MCF-7	breast:
9	chr6:35192773..35195560-chr6:35195988..35198811,2	MCF-7	breast:
10	chr6:35167248..35168898-chr6:35172556..35174347,2	MCF-7	breast:
11	chr6:35160680..35162385-chr6:35165533..35168085,2	MCF-7	breast:
12	chr6:35182167..35187066-chr6:35187567..35191599,8	K562	blood:
13	chr6:35209581..35211812-chr6:35214275..35216515,3	K562	blood:
14	chr6:35168653..35170985-chr6:35173621..35175811,2	MCF-7	breast:
15	chr6:35213830..35215728-chr6:35248385..35249951,2	K562	blood:
16	chr6:35186126..35189088-chr6:35223923..35225540,2	K562	blood:
17	chr6:35147410..35151273-chr6:35169982..35172318,3	MCF-7	breast:
18	chr6:35205769..35207687-chr6:35225072..35226945,2	K562	blood:
19	chr6:35127079..35138793-chr6:35145525..35157743,32	MCF-7	breast:
20	chr6:35211520..35214360-chr6:35225180..35229197,4	K562	blood:
21	chr6:35202209..35206634-chr6:35208195..35211678,7	K562	blood:
22	chr6:35178562..35181407-chr6:35198838..35201388,2	MCF-7	breast:
23	chr6:35188260..35190147-chr6:35205667..35207207,2	K562	blood:
24	chr6:35159595..35161669-chr6:35171600..35173649,2	K562	blood:
25	chr6:35177824..35181731-chr6:35185438..35190079,5	K562	blood:
26	chr6:35196327..35198090-chr6:35203601..35206096,2	MCF-7	breast:
27	chr6:35196232..35199243-chr6:35200230..35204307,5	K562	blood:
28	chr6:35167248..35168898-chr6:35172556..35174347,2	MCF-7	breast:
29	chr6:35195991..35200691-chr6:35207151..35212650,5	K562	blood:
30	chr6:35222206..35224519-chr6:35228928..35230958,2	K562	blood:
31	chr6:35153852..35155613-chr6:35168335..35170361,2	MCF-7	breast:
32	chr6:35129806..35132792-chr6:35197170..35199424,2	MCF-7	breast:
33	chr6:35141167..35143005-chr6:35157807..35160174,2	MCF-7	breast:
34	chr6:35150577..35155004-chr6:35155292..35158233,5	MCF-7	breast:
35	chr6:35173439..35175719-chr6:35204862..35206490,2	K562	blood:
36	chr6:35146928..35151829-chr6:35162484..35168348,5	K562	blood:
37	chr6:35107772..35108596-chr6:35208578..35209321,2	MCF-7	breast:
38	chr6:35203567..35205850-chr6:35210606..35213440,2	MCF-7	breast:
39	chr6:35210963..35213081-chr6:35462686..35465229,2	K562	blood:
40	chr6:35147410..35151273-chr6:35169982..35172318,3	MCF-7	breast:
41	chr6:34938891..34940598-chr6:35202108..35204116,2	K562	blood:
42	chr6:35131417..35136766-chr6:35169545..35174762,6	MCF-7	breast:
43	chr6:35195991..35200691-chr6:35207151..35212650,5	K562	blood:
44	chr6:35190929..35192629-chr6:35194228..35196176,2	K562	blood:
45	chr6:35192627..35195181-chr6:35418062..35420714,2	K562	blood:
46	chr6:35178452..35180834-chr6:35183642..35187997,3	MCF-7	breast:
47	chr6:35147825..35149730-chr6:35166517..35168770,2	MCF-7	breast:
48	chr6:35196232..35199243-chr6:35200230..35204307,5	K562	blood:
49	chr6:35016477..35017231-chr6:35208580..35209106,2	MCF-7	breast:
50	chr6:35203262..35205063-chr6:35205452..35207429,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCP11-2	chr6:35188147-35189134	NONHSAT112168
2	lnc-TCP11-2	chr6:35188147-35192407	ENSG00000272374.1
3	lnc-SCUBE3-2	chr6:35167125-35167995	NONHSAT112164
4	lnc-SCUBE3-1	chr6:35170798-35171095	NONHSAT112165
5	lnc-TCP11-1	chr6:35178593-35178950	NONHSAT112166
6	lnc-TCP11-1	chr6:35172923-35173184	NONHSAT112166
7	lnc-SCUBE3-3	chr6:35166103-35166815	NONHSAT112163

No data

Variant related genes	Relation type
SCUBE3	TF binding region
ENSG00000272374	TF binding region
ZNF76	TF binding region
SCUBE3	CpG island
ENSG00000272374	CpG island
ZNF76	CpG island
ENSG00000112033	chromatin interactions
ENSG00000065029	chromatin interactions
ENSG00000064999	chromatin interactions
ENSG00000272374	chromatin interactions
ENSG00000064995	chromatin interactions
ENSG00000112039	chromatin interactions
ENSG00000146197	chromatin interactions
ENSG00000124678	chromatin interactions
ENSG00000007866	chromatin interactions

Extended variants
information (count: 2616 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:2616 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs398048438	chr6:35150524-35150525	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs369290336	chr6:35150618-35150619	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs547728490	chr6:35150635-35150636	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs186001523	chr6:35150638-35150639	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs576206072	chr6:35150655-35150656	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs557212746	chr6:35150661-35150662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs567594032	chr6:35150743-35150744	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs12189669	chr6:35150800-35150801	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs556409546	chr6:35150808-35150809	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs190294126	chr6:35150812-35150813	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs573242839	chr6:35150828-35150829	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs555424637	chr6:35150843-35150844	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs556075774	chr6:35150865-35150866	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs182502598	chr6:35150897-35150898	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544783708	chr6:35150903-35150904	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs144408764	chr6:35150932-35150933	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs148791088	chr6:35151020-35151021	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs544743833	chr6:35151087-35151088	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs560128403	chr6:35151091-35151092	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs6904339	chr6:35151106-35151107	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs548911607	chr6:35151130-35151131	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs142428189	chr6:35151144-35151145	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs531458920	chr6:35151147-35151148	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs56809926	chr6:35151205-35151206	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs571328292	chr6:35151253-35151254	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs191902751	chr6:35151342-35151343	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs551571149	chr6:35151352-35151353	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs566901981	chr6:35151402-35151403	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs534182499	chr6:35151476-35151477	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs556137286	chr6:35151500-35151501	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs574396147	chr6:35151511-35151512	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs555244426	chr6:35151634-35151635	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs371273808	chr6:35151692-35151693	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559198610	chr6:35151768-35151769	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184151828	chr6:35151794-35151795	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs572738292	chr6:35151836-35151837	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs146360863	chr6:35151882-35151883	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs556276134	chr6:35152002-35152003	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs188628709	chr6:35152053-35152054	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs377126855	chr6:35152080-35152081	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs571747449	chr6:35152106-35152107	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs542223880	chr6:35152215-35152216	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs529138509	chr6:35152226-35152227	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs34058747	chr6:35152252-35152253	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs3220904	chr6:35152257-35152258	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs35624395	chr6:35152271-35152272	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs537043962	chr6:35152272-35152273	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs34365688	chr6:35152273-35152274	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs13198649	chr6:35152275-35152276	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs201794381	chr6:35152277-35152278	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Esophageal adenocarcinoma	18820669	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
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	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
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21510904	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
small cell lung cancer	17426248	CNVD
Oligozoospermia	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD

Chromatin state (count:1952 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35146800-35154400	Enhancers	Fetal Heart	heart
2	chr6:35147600-35152400	Weak transcription	Lung	lung
3	chr6:35148000-35151200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:35148200-35151000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:35148200-35151000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr6:35149800-35151000	Weak transcription	Osteobl	bone
7	chr6:35149800-35154200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr6:35149800-35154400	Enhancers	Muscle Satellite Cultured Cells	--
9	chr6:35149800-35158000	Weak transcription	Aorta	Aorta
10	chr6:35150000-35150800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr6:35150000-35151000	Weak transcription	Fetal Lung	lung
12	chr6:35150000-35151000	Weak transcription	HSMMtube	muscle
13	chr6:35150000-35151000	Weak transcription	K562	blood
14	chr6:35150000-35151200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:35150000-35151800	Weak transcription	HepG2	liver
16	chr6:35150000-35152600	Weak transcription	NHLF	lung
17	chr6:35150000-35153000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr6:35150000-35153000	Weak transcription	HSMM	muscle
19	chr6:35150000-35153400	Weak transcription	Spleen	Spleen
20	chr6:35150200-35150600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr6:35150200-35151000	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr6:35150200-35151400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr6:35150200-35152000	Weak transcription	NHEK	skin
24	chr6:35150200-35152400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr6:35150200-35152400	Weak transcription	Fetal Intestine Large	intestine
26	chr6:35150200-35152400	Enhancers	A549	lung
27	chr6:35150200-35152400	Weak transcription	NH-A	brain
28	chr6:35150200-35152400	Weak transcription	NHDF-Ad	bronchial
29	chr6:35150200-35152600	Weak transcription	Fetal Intestine Small	intestine
30	chr6:35150200-35152600	Weak transcription	Stomach Mucosa	stomach
31	chr6:35150200-35153000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr6:35150200-35153400	Weak transcription	Right Atrium	heart
33	chr6:35150200-35154000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr6:35150200-35154200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr6:35150200-35156600	Weak transcription	Esophagus	oesophagus
36	chr6:35150400-35150600	Weak transcription	Hela-S3	cervix
37	chr6:35150400-35152000	Weak transcription	Placenta	Placenta
38	chr6:35150400-35152000	Weak transcription	Left Ventricle	heart
39	chr6:35150400-35152200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr6:35150400-35152200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr6:35150400-35152400	Weak transcription	HMEC	breast
42	chr6:35150400-35153200	Weak transcription	Right Ventricle	heart
43	chr6:35150600-35151400	Enhancers	Hela-S3	cervix
44	chr6:35150600-35154200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr6:35150800-35154000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr6:35151000-35151200	Enhancers	Fetal Lung	lung
47	chr6:35151000-35151200	Enhancers	HSMMtube	muscle
48	chr6:35151000-35151600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr6:35151000-35151600	Enhancers	Placenta Amnion	Placenta Amnion
50	chr6:35151000-35151800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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