Variant report

Variant	nsv1016703
Chromosome Location	chr6:34784801-34827693
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:357)
CpG islands
(count:61)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34807829-34807953	K562	blood:	n/a	n/a
2	ARID3A	chr6:34802936-34803203	K562	blood:	n/a	n/a
3	ATF1	chr6:34827687-34828162	K562	blood:	n/a	n/a
4	ATF1	chr6:34803008-34803279	K562	blood:	n/a	n/a
5	BACH1	chr6:34807689-34808041	K562	blood:	n/a	n/a
6	BACH1	chr6:34787485-34787796	K562	blood:	n/a	n/a
7	BACH1	chr6:34807714-34807998	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr6:34803129-34803186	K562	blood:	n/a	n/a
9	BRCA1	chr6:34787549-34787562	GM12878	blood:	n/a	n/a
10	CCNT2	chr6:34803911-34804270	K562	blood:	n/a	n/a
11	CCNT2	chr6:34802973-34803202	K562	blood:	n/a	n/a
12	CEBPB	chr6:34800246-34800346	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr6:34802629-34803187	K562	blood:	n/a	chr6:34802997-34803008 chr6:34802715-34802727
14	CEBPB	chr6:34802890-34803079	K562	blood:	n/a	chr6:34802997-34803008
15	CEBPB	chr6:34802639-34803162	HepG2	liver:	n/a	chr6:34802997-34803008 chr6:34802715-34802727
16	CEBPB	chr6:34802689-34802861	K562	blood:	n/a	chr6:34802715-34802727
17	CEBPB	chr6:34802598-34803234	IMR90	lung:	n/a	chr6:34802997-34803008 chr6:34802715-34802727
18	CEBPB	chr6:34820249-34820448	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr6:34802648-34803041	Hela-S3	cervix:	n/a	chr6:34802997-34803008 chr6:34802715-34802727
20	CEBPB	chr6:34804376-34804565	K562	blood:	n/a	n/a
21	CEBPB	chr6:34789037-34789212	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:34813922-34814087	K562	blood:	n/a	chr6:34813977-34813988
23	CEBPB	chr6:34802587-34803257	K562	blood:	n/a	chr6:34802997-34803008 chr6:34802715-34802727
24	CEBPB	chr6:34813914-34814088	IMR90	lung:	n/a	chr6:34813977-34813988
25	CEBPB	chr6:34820393-34820475	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr6:34802575-34803279	MCF-7	breast:	n/a	chr6:34802997-34803008 chr6:34802715-34802727
27	CEBPB	chr6:34813927-34814067	HepG2	liver:	n/a	chr6:34813977-34813988
28	CEBPD	chr6:34784310-34784939	K562	blood:	n/a	n/a
29	CEBPD	chr6:34802808-34803358	K562	blood:	n/a	n/a
30	CEBPD	chr6:34784301-34784928	K562	blood:	n/a	n/a
31	CHD2	chr6:34820417-34820458	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr6:34826520-34826670	RPTEC	kidney:	n/a	n/a
33	CTCF	chr6:34826540-34826690	MCF-7	breast:	n/a	n/a
34	CTCF	chr6:34826556-34826727	MCF-7	breast:	n/a	n/a
35	CTCF	chr6:34823340-34823490	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr6:34826549-34826752	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr6:34826560-34826710	HMF	breast:	n/a	n/a
38	CTCF	chr6:34826500-34826650	GM12864	blood:	n/a	n/a
39	CTCF	chr6:34823340-34823490	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr6:34826580-34826730	HCFaa	heart:	n/a	n/a
41	CTCF	chr6:34826560-34826710	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr6:34823320-34823470	SAEC	small airway:	n/a	n/a
43	CTCF	chr6:34826562-34826740	HepG2	liver:	n/a	n/a
44	CTCF	chr6:34826627-34826719	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr6:34826600-34826750	K562	blood:	n/a	n/a
46	CTCF	chr6:34826540-34826690	GM12878	blood:	n/a	n/a
47	CTCF	chr6:34826567-34826722	Gliobla	brain:	n/a	n/a
48	CTCF	chr6:34823380-34823507	NHEK	skin:	n/a	n/a
49	CTCF	chr6:34823260-34823410	BE2_C	brain:	n/a	n/a
50	CTCF	chr6:34826620-34826770	GM12874	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34802849-34802899	AG04450	lung:	fetal
2	chr6:34802849-34802899	NB4	blood:	n/a
3	chr6:34802849-34802899	HL-60	blood:	n/a
4	chr6:34802849-34802899	GM06990	blood:	n/a
5	chr6:34802849-34802899	K562	blood:	n/a
6	chr6:34802849-34802899	PFSK-1	brain:	n/a
7	chr6:34802849-34802899	HRCEpiC	kidney:	n/a
8	chr6:34802849-34802899	U87	brain:	n/a
9	chr6:34802849-34802899	T-47D	breast:	n/a
10	chr6:34802849-34802899	LNCaP	prostate:	n/a
11	chr6:34802849-34802899	CMK	blood:	n/a
12	chr6:34802849-34802899	HUVEC	blood vessel:	n/a
13	chr6:34802849-34802899	GM12892	blood:	n/a
14	chr6:34802849-34802899	NHBE	bronchial:	n/a
15	chr6:34802849-34802899	GM19239	blood:	n/a
16	chr6:34802849-34802899	MCF-7	breast:	n/a
17	chr6:34802849-34802899	HNPCEpiC	eye:	n/a
18	chr6:34802849-34802899	HCM	heart:	n/a
19	chr6:34802849-34802899	Hepatocyte	liver:	n/a
20	chr6:34802849-34802899	AG09319	gingival:	n/a
21	chr6:34802849-34802899	BE2_C	brain:	n/a
22	chr6:34802849-34802899	PANC-1	pancreas:	n/a
23	chr6:34802849-34802899	NHDF-neo	bronchial:	n/a
24	chr6:34802849-34802899	HRPEpiC	eye:	n/a
25	chr6:34802849-34802899	HEEpiC	esophagus:	n/a
26	chr6:34802849-34802899	AG09309	skin:	n/a
27	chr6:34802849-34802899	HepG2	liver:	n/a
28	chr6:34802849-34802899	HCT-116	colon:	n/a
29	chr6:34802849-34802899	GM12891	blood:	n/a
30	chr6:34802849-34802899	NT2-D1	testis:	n/a
31	chr6:34802849-34802899	GM12878	blood:	n/a
32	chr6:34802849-34802899	SK-N-SH_RA	brain:	n/a
33	chr6:34802849-34802899	AG10803	skin:	n/a
34	chr6:34802849-34802899	Hela-S3	cervix:	n/a
35	chr6:34802849-34802899	SK-N-SH	brain:	n/a
36	chr6:34802849-34802899	AoSMC	blood vessel:	n/a
37	chr6:34802849-34802899	HIPEpiC	eye:	n/a
38	chr6:34802849-34802899	PrEC	prostate:	n/a
39	chr6:34802849-34802899	SK-N-MC	brain:	n/a
40	chr6:34802849-34802899	HRE	kidney:	n/a
41	chr6:34802849-34802899	H1-hESC	embryonic stem cell:	embryo
42	chr6:34802849-34802899	HCPEpiC	choroid plexus:	n/a
43	chr6:34802849-34802899	ovcar-3	ovarian:	n/a
44	chr6:34802849-34802899	HEK293	kidney:	embryo
45	chr6:34802849-34802899	SKMC	muscle:	n/a
46	chr6:34802849-34802899	HCF	heart:	n/a
47	chr6:34802849-34802899	IMR90	lung:	fetal
48	chr6:34802849-34802899	Jurkat	blood:	n/a
49	chr6:34802849-34802899	HMEC	breast:	n/a
50	chr6:34802849-34802899	MCF10A-Er-Src	breast:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:34759201..34762395-chr6:34788232..34791970,5	MCF-7	breast:
2	chr6:34803354..34806111-chr6:34854404..34857374,3	K562	blood:
3	chr6:34765154..34767029-chr6:34793754..34796653,2	K562	blood:
4	chr6:34763985..34766654-chr6:34795153..34797244,4	K562	blood:
5	chr6:34822875..34823681-chr6:34855389..34856282,2	MCF-7	breast:
6	chr6:34776624..34779636-chr6:34782424..34785536,4	K562	blood:
7	chr6:34758599..34760857-chr6:34787566..34790962,3	K562	blood:
8	chr6:34759673..34761787-chr6:34787706..34790146,2	MCF-7	breast:
9	chr6:34776609..34778206-chr6:34824620..34826578,2	K562	blood:
10	chr6:34803335..34805787-chr6:34806399..34809385,2	K562	blood:
11	chr6:34803335..34805787-chr6:34806399..34809385,2	K562	blood:
12	chr6:34782930..34784591-chr6:34786044..34787965,3	K562	blood:
13	chr6:34825507..34827584-chr6:34840818..34842443,2	MCF-7	breast:
14	chr6:34779065..34780836-chr6:34797089..34799244,2	K562	blood:
15	chr6:34767361..34769871-chr6:34784104..34787037,2	K562	blood:
16	chr6:34822969..34823913-chr6:35208985..35209580,2	MCF-7	breast:
17	chr6:34779962..34782219-chr6:34783114..34784979,2	K562	blood:
18	chr6:34824500..34828463-chr6:34854420..34857556,3	MCF-7	breast:
19	chr6:34758169..34761129-chr6:34802765..34804303,2	K562	blood:
20	chr6:34786614..34789043-chr6:34809197..34812183,2	K562	blood:
21	chr6:34780723..34782615-chr6:34786684..34789139,2	K562	blood:
22	chr6:34759204..34760846-chr6:34788555..34790886,2	K562	blood:
23	chr6:34795232..34797224-chr6:34825817..34828260,2	K562	blood:
24	chr6:34786614..34789043-chr6:34809197..34812183,2	K562	blood:
25	chr6:34795232..34797224-chr6:34825817..34828260,2	K562	blood:
26	chr6:34757536..34760018-chr6:34783052..34787037,5	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	UHRF1BP1	hsa-let-7e-5p	chr6:34825126-34825148

Variant related genes	Relation type
ENSG00000206717	TF binding region
ENSG00000206717	CpG island
ENSG00000064999	chromatin interactions
ENSG00000064995	chromatin interactions
ENSG00000065060	chromatin interactions

Extended variants
information (count: 1662 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1662 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138071868	chr6:34784805-34784806	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs111647353	chr6:34784806-34784807	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs558834414	chr6:34784826-34784827	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs368591241	chr6:34784850-34784851	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs141006157	chr6:34784866-34784867	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs577969246	chr6:34784882-34784883	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs541322960	chr6:34784897-34784898	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs559561717	chr6:34784904-34784905	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs530298301	chr6:34784916-34784917	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs374628322	chr6:34784935-34784936	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs189565486	chr6:34785045-34785046	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs73419621	chr6:34785079-34785080	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs182099570	chr6:34785114-34785115	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs374737036	chr6:34785141-34785142	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs10552272	chr6:34785270-34785271	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs72301239	chr6:34785275-34785276	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs537181454	chr6:34785293-34785294	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs552158648	chr6:34785305-34785306	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs78910466	chr6:34785421-34785422	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs186679322	chr6:34785437-34785438	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs370711967	chr6:34785446-34785447	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs189520274	chr6:34785452-34785453	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs568193417	chr6:34785493-34785494	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs554251848	chr6:34785509-34785510	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs181827127	chr6:34785540-34785541	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs570091707	chr6:34785581-34785582	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs546040519	chr6:34785593-34785594	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs537050864	chr6:34785620-34785621	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs552109265	chr6:34785629-34785630	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs374679191	chr6:34785645-34785646	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs60772060	chr6:34785646-34785647	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs573164479	chr6:34785661-34785662	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs558574413	chr6:34785664-34785665	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs576816930	chr6:34785687-34785688	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs535017957	chr6:34785738-34785739	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs148321098	chr6:34785755-34785756	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs574953633	chr6:34785756-34785757	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs185315104	chr6:34785820-34785821	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs368996075	chr6:34785836-34785837	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs374412104	chr6:34785857-34785858	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs575251420	chr6:34785878-34785879	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs545907500	chr6:34785941-34785942	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs564107314	chr6:34785950-34785951	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs528072546	chr6:34785960-34785961	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs189685682	chr6:34785968-34785969	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs368562891	chr6:34785995-34785996	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs561781868	chr6:34786067-34786068	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182536036	chr6:34786164-34786165	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs529088078	chr6:34786176-34786177	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs550704619	chr6:34786186-34786187	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1279 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34761400-34787200	Weak transcription	Fetal Muscle Leg	muscle
2	chr6:34761400-34789400	Weak transcription	Fetal Stomach	stomach
3	chr6:34761400-34789400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr6:34761400-34790800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr6:34762000-34788400	Weak transcription	Fetal Muscle Trunk	muscle
6	chr6:34764000-34803800	Weak transcription	HSMM	muscle
7	chr6:34764200-34785000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:34764600-34787400	Weak transcription	Liver	Liver
9	chr6:34772600-34789400	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr6:34773200-34791400	Weak transcription	Gastric	stomach
11	chr6:34775400-34787200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr6:34775400-34787200	Weak transcription	Right Ventricle	heart
13	chr6:34775400-34802400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr6:34776600-34789600	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr6:34777800-34789000	Weak transcription	Primary T cells from cord blood	blood
16	chr6:34778600-34787200	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr6:34779200-34797000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr6:34779200-34807400	Weak transcription	A549	lung
19	chr6:34779400-34787400	Weak transcription	HUVEC	blood vessel
20	chr6:34779400-34789400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr6:34779400-34789400	Weak transcription	Hela-S3	cervix
22	chr6:34779400-34796400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr6:34779400-34841000	Weak transcription	NH-A	brain
24	chr6:34779600-34791000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr6:34779600-34791400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr6:34779600-34796200	Weak transcription	NHEK	skin
27	chr6:34779800-34787400	Weak transcription	Left Ventricle	heart
28	chr6:34779800-34789400	Weak transcription	Fetal Intestine Small	intestine
29	chr6:34780400-34787200	Weak transcription	Right Atrium	heart
30	chr6:34780800-34794000	Weak transcription	Aorta	Aorta
31	chr6:34781000-34787200	Weak transcription	Brain Cingulate Gyrus	brain
32	chr6:34781000-34790800	Weak transcription	Brain Angular Gyrus	brain
33	chr6:34781000-34797000	Weak transcription	Colon Smooth Muscle	Colon
34	chr6:34781200-34789400	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr6:34781400-34790800	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr6:34781600-34785200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr6:34781600-34785200	Weak transcription	Fetal Brain Female	brain
38	chr6:34781600-34786400	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr6:34781600-34787400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr6:34781600-34787400	Weak transcription	Brain Hippocampus Middle	brain
41	chr6:34781600-34787400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr6:34781600-34787600	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr6:34781600-34788000	Weak transcription	HSMMtube	muscle
44	chr6:34781600-34791000	Weak transcription	Brain Anterior Caudate	brain
45	chr6:34781600-34791400	Weak transcription	Brain Substantia Nigra	brain
46	chr6:34781600-34824000	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr6:34781800-34790600	Weak transcription	Brain Germinal Matrix	brain
48	chr6:34782600-34789400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr6:34782800-34790800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr6:34783200-34807400	Weak transcription	Psoas Muscle	Psoas

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