Variant report

Variant	nsv885858
Chromosome Location	chr6:44385441-44421240
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:484)
CpG islands
(count:183)
Chromatin interactive
region (count:45)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:1)

(count:484 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:44398919-44399179	K562	blood:	n/a	n/a
2	ATF3	chr6:44416907-44417223	K562	blood:	n/a	n/a
3	BCL11A	chr6:44396560-44396746	GM12878	blood:	n/a	n/a
4	CEBPB	chr6:44414680-44415070	IMR90	lung:	n/a	n/a
5	CEBPB	chr6:44414619-44415124	A549	lung:	n/a	n/a
6	CEBPB	chr6:44420331-44420840	Hela-S3	cervix:	n/a	chr6:44420588-44420599
7	CEBPB	chr6:44420458-44420757	HepG2	liver:	n/a	chr6:44420588-44420599
8	CEBPB	chr6:44420394-44421207	IMR90	lung:	n/a	chr6:44420588-44420599
9	CEBPB	chr6:44420397-44420863	MCF-7	breast:	n/a	chr6:44420588-44420599
10	CEBPB	chr6:44407455-44407789	IMR90	lung:	n/a	n/a
11	CEBPB	chr6:44406548-44406821	IMR90	lung:	n/a	chr6:44406678-44406689
12	CEBPB	chr6:44414736-44415000	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:44414882-44414919	K562	blood:	n/a	n/a
14	CEBPB	chr6:44420475-44420743	A549	lung:	n/a	chr6:44420588-44420599
15	CEBPB	chr6:44406587-44406859	HepG2	liver:	n/a	chr6:44406678-44406689
16	CEBPB	chr6:44398209-44398460	IMR90	lung:	n/a	n/a
17	CEBPB	chr6:44414414-44415004	MCF-7	breast:	n/a	n/a
18	CEBPB	chr6:44414500-44415076	MCF-7	breast:	n/a	n/a
19	CEBPB	chr6:44414359-44415072	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr6:44404150-44404374	HepG2	liver:	n/a	n/a
21	CHD1	chr6:44398728-44399236	IMR90	lung:	n/a	n/a
22	CTCF	chr6:44398960-44399110	BE2_C	brain:	n/a	n/a
23	CTCF	chr6:44398912-44399207	Medullo	brain:	n/a	n/a
24	CTCF	chr6:44398600-44398750	GM12872	blood:	n/a	n/a
25	CTCF	chr6:44398980-44399130	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr6:44399000-44399150	GM12869	blood:	n/a	n/a
27	CTCF	chr6:44398980-44399130	RPTEC	kidney:	n/a	n/a
28	CTCF	chr6:44398580-44398730	HMF	breast:	n/a	n/a
29	CTCF	chr6:44398935-44399129	T-47D	breast:	n/a	n/a
30	CTCF	chr6:44412700-44412850	HRE	kidney:	n/a	n/a
31	CTCF	chr6:44398840-44399170	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr6:44399000-44399150	BE2_C	brain:	n/a	n/a
33	CTCF	chr6:44398960-44399110	GM12865	blood:	n/a	n/a
34	CTCF	chr6:44398620-44398770	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr6:44403347-44403448	Gliobla	brain:	n/a	chr6:44403397-44403406 chr6:44403394-44403404 chr6:44403391-44403409 chr6:44403386-44403407
36	CTCF	chr6:44399012-44399108	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:44398957-44399138	ProgFib	skin:	n/a	n/a
38	CTCF	chr6:44403240-44403390	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr6:44398880-44399030	HCT-116	colon:	n/a	n/a
40	CTCF	chr6:44398980-44399130	HMF	breast:	n/a	n/a
41	CTCF	chr6:44398908-44399185	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr6:44398838-44399248	GM12878	blood:	n/a	n/a
43	CTCF	chr6:44398960-44399110	HL-60	blood:	n/a	n/a
44	CTCF	chr6:44398980-44399130	AG10803	skin:	n/a	n/a
45	CTCF	chr6:44398960-44399110	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr6:44403347-44403493	Hela-S3	cervix:	n/a	chr6:44403397-44403406 chr6:44403394-44403404 chr6:44403391-44403409 chr6:44403386-44403407
47	CTCF	chr6:44398933-44399183	A549	lung:	n/a	n/a
48	CTCF	chr6:44398980-44399130	GM12868	blood:	n/a	n/a
49	CTCF	chr6:44398934-44399165	Lung_OC	lung:	n/a	n/a
50	CTCF	chr6:44398940-44399090	HA-sp	spinal cord:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:44420555-44420605	AG04449	skin:	fetal
2	chr6:44396701-44396751	SAEC	small airway:	n/a
3	chr6:44420555-44420605	NH-A	brain:	n/a
4	chr6:44413609-44413659	HIPEpiC	eye:	n/a
5	chr6:44396701-44396751	T-47D	breast:	n/a
6	chr6:44420555-44420605	CMK	blood:	n/a
7	chr6:44413609-44413659	PFSK-1	brain:	n/a
8	chr6:44413609-44413659	T-47D	breast:	n/a
9	chr6:44413609-44413659	MCF-7	breast:	n/a
10	chr6:44396701-44396751	LNCaP	prostate:	n/a
11	chr6:44420555-44420605	GM12878	blood:	n/a
12	chr6:44396701-44396751	AoSMC	blood vessel:	n/a
13	chr6:44413609-44413659	HRPEpiC	eye:	n/a
14	chr6:44413609-44413659	A549	lung:	n/a
15	chr6:44413609-44413659	GM06990	blood:	n/a
16	chr6:44420555-44420605	NHDF-neo	bronchial:	n/a
17	chr6:44413609-44413659	HCT-116	colon:	n/a
18	chr6:44413609-44413659	K562	blood:	n/a
19	chr6:44413609-44413659	IMR90	lung:	fetal
20	chr6:44420555-44420605	PrEC	prostate:	n/a
21	chr6:44413609-44413659	BJ	skin:	n/a
22	chr6:44396701-44396751	PANC-1	pancreas:	n/a
23	chr6:44396701-44396751	NHDF-neo	bronchial:	n/a
24	chr6:44413609-44413659	HL-60	blood:	n/a
25	chr6:44420555-44420605	ProgFib	skin:	n/a
26	chr6:44413609-44413659	HCM	heart:	n/a
27	chr6:44396701-44396751	HRPEpiC	eye:	n/a
28	chr6:44420555-44420605	NT2-D1	testis:	n/a
29	chr6:44413609-44413659	ProgFib	skin:	n/a
30	chr6:44396701-44396751	ovcar-3	ovarian:	n/a
31	chr6:44413609-44413659	SKMC	muscle:	n/a
32	chr6:44413609-44413659	NB4	blood:	n/a
33	chr6:44413609-44413659	HAEpiC	amniotic membrane:	n/a
34	chr6:44420555-44420605	HAEpiC	amniotic membrane:	n/a
35	chr6:44420555-44420605	HRE	kidney:	n/a
36	chr6:44420555-44420605	SK-N-MC	brain:	n/a
37	chr6:44396701-44396751	MCF-7	breast:	n/a
38	chr6:44420555-44420605	BE2_C	brain:	n/a
39	chr6:44420555-44420605	SAEC	small airway:	n/a
40	chr6:44413609-44413659	HPAEpiC	pulmonary alveolar:	n/a
41	chr6:44420555-44420605	HCPEpiC	choroid plexus:	n/a
42	chr6:44413609-44413659	Hela-S3	cervix:	n/a
43	chr6:44396701-44396751	AG04450	lung:	fetal
44	chr6:44396701-44396751	GM12891	blood:	n/a
45	chr6:44396701-44396751	K562	blood:	n/a
46	chr6:44396701-44396751	HCPEpiC	choroid plexus:	n/a
47	chr6:44420555-44420605	HCT-116	colon:	n/a
48	chr6:44413609-44413659	PANC-1	pancreas:	n/a
49	chr6:44396701-44396751	H1-hESC	embryonic stem cell:	embryo
50	chr6:44413609-44413659	CMK	blood:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:44398616..44399525-chr6:44612781..44613634,2	MCF-7	breast:
2	chr6:44390673..44392350-chr6:44396444..44398249,2	K562	blood:
3	chr6:44387232..44389973-chr6:44398026..44400145,2	K562	blood:
4	chr6:44403977..44405888-chr6:44416360..44418391,2	K562	blood:
5	chr6:44389167..44391810-chr6:44391881..44393956,2	K562	blood:
6	chr6:44410364..44415906-chr6:44416897..44422592,7	K562	blood:
7	chr6:44390273..44393124-chr6:44394241..44396226,2	K562	blood:
8	chr4:56311038..56311651-chr6:44419905..44420425,3	MCF-7	breast:
9	chr6:44408746..44410322-chr6:44420941..44423520,2	MCF-7	breast:
10	chr6:44365878..44368641-chr6:44383402..44385534,2	K562	blood:
11	chr6:44397467..44399070-chr6:44423188..44424780,2	K562	blood:
12	chr6:44420357..44422515-chr6:44433684..44436230,2	K562	blood:
13	chr6:44403977..44405888-chr6:44416360..44418391,2	K562	blood:
14	chr6:44406091..44407637-chr6:44410068..44412209,2	K562	blood:
15	chr6:44389136..44391989-chr6:44402458..44405433,2	MCF-7	breast:
16	chr6:44391027..44393883-chr6:44436519..44438149,2	K562	blood:
17	chr6:44398593..44399479-chr6:44423901..44425088,5	MCF-7	breast:
18	chr6:44279048..44280754-chr6:44413022..44414721,2	MCF-7	breast:
19	chr6:44390273..44393124-chr6:44394241..44396226,2	K562	blood:
20	chr6:44398583..44399484-chr6:44437679..44438221,2	K562	blood:
21	chr6:44391748..44393635-chr6:44395811..44398462,2	MCF-7	breast:
22	chr6:44214200..44215858-chr6:44420760..44422389,2	K562	blood:
23	chr6:44398980..44399515-chr6:44437258..44438078,2	MCF-7	breast:
24	chr6:44412103..44413730-chr6:44418202..44421080,2	MCF-7	breast:
25	chr6:44408746..44410322-chr6:44420941..44423520,2	MCF-7	breast:
26	chr6:44392433..44394528-chr6:44420421..44422468,2	K562	blood:
27	chr6:44410364..44415906-chr6:44416897..44422592,7	K562	blood:
28	chr6:44390673..44392350-chr6:44396444..44398249,2	K562	blood:
29	chr6:44389167..44391810-chr6:44391881..44393956,2	K562	blood:
30	chr6:44405048..44409188-chr6:44409781..44413783,5	K562	blood:
31	chr6:44417252..44422229-chr6:44425424..44429511,4	K562	blood:
32	chr6:44396473..44398052-chr6:44398079..44400521,2	K562	blood:
33	chr6:44387232..44389973-chr6:44398026..44400145,2	K562	blood:
34	chr6:44405048..44409188-chr6:44409781..44413783,5	K562	blood:
35	chr6:44406091..44407637-chr6:44410068..44412209,2	K562	blood:
36	chr6:44397217..44399070-chr6:44421997..44424688,3	K562	blood:
37	chr6:44391748..44393635-chr6:44395811..44398462,2	MCF-7	breast:
38	chr6:44398603..44399105-chr6:44423995..44424580,2	MCF-7	breast:
39	chr6:44382268..44386801-chr6:44387364..44390498,4	MCF-7	breast:
40	chr6:44396473..44398052-chr6:44398079..44400521,2	K562	blood:
41	chr6:44398528..44400400-chr6:44423668..44424679,12	K562	blood:
42	chr6:44402998..44404546-chr6:44407688..44409189,2	K562	blood:
43	chr6:44392433..44394528-chr6:44420421..44422468,2	K562	blood:
44	chr6:44382268..44386801-chr6:44387364..44390498,4	MCF-7	breast:
45	chr6:44412103..44413730-chr6:44418202..44421080,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDC5L-3	chr6:44418311-44418898	NONHSAT112963

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4642	chr6:44403387-44403408	MIMAT0019702

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CDC5L	hsa-miR-16-5p	chr6:44414719-44414740

Variant related genes	Relation type
MIR4642	TF binding region
ENSG00000267849	TF binding region
MIR4642	CpG island
ENSG00000267849	CpG island
ENSG00000266619	chromatin interactions
ENSG00000096384	chromatin interactions

Extended variants
information (count: 1320 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1320 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13198841	chr6:44385441-44385442	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs527637044	chr6:44385446-44385447	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554099905	chr6:44385448-44385449	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549088366	chr6:44385473-44385474	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552153513	chr6:44385478-44385479	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570780588	chr6:44385485-44385486	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538162279	chr6:44385487-44385488	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs538217347	chr6:44385493-44385494	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553356170	chr6:44385498-44385499	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145344543	chr6:44385528-44385529	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535724269	chr6:44385607-44385608	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554642574	chr6:44385616-44385617	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs180682246	chr6:44385620-44385621	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372912962	chr6:44385650-44385651	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540188960	chr6:44385652-44385653	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574064717	chr6:44385654-44385655	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558609638	chr6:44385670-44385671	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577177051	chr6:44385737-44385738	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544472401	chr6:44385776-44385777	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs373682771	chr6:44385782-44385783	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562685278	chr6:44385838-44385839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574565288	chr6:44385839-44385840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541668917	chr6:44385889-44385890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560164186	chr6:44385946-44385947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7753693	chr6:44385953-44385954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552116524	chr6:44385978-44385979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs11571970	chr6:44385980-44385981	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11571971	chr6:44386093-44386094	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs11571972	chr6:44386108-44386109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568703039	chr6:44386175-44386176	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536010405	chr6:44386178-44386179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548014121	chr6:44386196-44386197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200667031	chr6:44386230-44386231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11571973	chr6:44386241-44386242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372008445	chr6:44386246-44386247	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558722059	chr6:44386247-44386248	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376758164	chr6:44386294-44386295	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369278779	chr6:44386304-44386305	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372241709	chr6:44386338-44386339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576903658	chr6:44386347-44386348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376521562	chr6:44386350-44386351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548229155	chr6:44386393-44386394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373072080	chr6:44386394-44386395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369881569	chr6:44386447-44386448	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373996631	chr6:44386514-44386515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537483596	chr6:44386535-44386536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200163586	chr6:44386573-44386574	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs556382460	chr6:44386577-44386578	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201844205	chr6:44386582-44386583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568223190	chr6:44386586-44386587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
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
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
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	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
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Ovarian cancer	20844748	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1523 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44356400-44393800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:44357600-44388200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:44358000-44385600	Strong transcription	HUES6 Cell Line	embryonic stem cell
4	chr6:44358000-44385600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
5	chr6:44358000-44385800	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr6:44358000-44386000	Strong transcription	HUES64 Cell Line	embryonic stem cell
7	chr6:44358200-44385600	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr6:44358400-44386000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr6:44358400-44403800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr6:44358800-44385600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr6:44359400-44386000	Strong transcription	Rectal Mucosa Donor 29	rectum
12	chr6:44368400-44386000	Strong transcription	Cortex derived primary cultured neurospheres	brain
13	chr6:44369400-44385600	Strong transcription	Liver	Liver
14	chr6:44371400-44385600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr6:44371400-44385600	Strong transcription	Fetal Muscle Trunk	muscle
16	chr6:44371400-44385600	Strong transcription	Fetal Muscle Leg	muscle
17	chr6:44371600-44385600	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr6:44371600-44385600	Strong transcription	Fetal Lung	lung
19	chr6:44371600-44385800	Strong transcription	Fetal Intestine Large	intestine
20	chr6:44371600-44386000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr6:44371800-44385600	Strong transcription	Fetal Brain Female	brain
22	chr6:44373200-44385600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr6:44374600-44388400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr6:44376800-44398200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr6:44376800-44424400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr6:44378200-44385600	Strong transcription	Brain Germinal Matrix	brain
27	chr6:44378200-44387800	Weak transcription	Fetal Heart	heart
28	chr6:44378400-44387200	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr6:44379000-44386000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr6:44379400-44385600	Strong transcription	Placenta	Placenta
31	chr6:44379600-44385600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr6:44379600-44385600	Strong transcription	Adipose Nuclei	Adipose
33	chr6:44379800-44385600	Strong transcription	Fetal Stomach	stomach
34	chr6:44380600-44385600	Strong transcription	HUES48 Cell Line	embryonic stem cell
35	chr6:44381000-44385600	Strong transcription	Stomach Smooth Muscle	stomach
36	chr6:44381000-44385600	Strong transcription	HSMM	muscle
37	chr6:44382000-44387200	Weak transcription	Esophagus	oesophagus
38	chr6:44382800-44385600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
39	chr6:44382800-44385600	Strong transcription	Primary B cells from cord blood	blood
40	chr6:44382800-44385600	Strong transcription	K562	blood
41	chr6:44383000-44385600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr6:44383000-44386000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr6:44383200-44385600	Strong transcription	Primary T cells from cord blood	blood
44	chr6:44383200-44385600	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr6:44383200-44385600	Strong transcription	Aorta	Aorta
46	chr6:44383200-44385600	Strong transcription	NHEK	skin
47	chr6:44383400-44385600	Strong transcription	H1 Cell Line	embryonic stem cell
48	chr6:44383400-44385600	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
49	chr6:44383400-44385600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr6:44383600-44385600	Strong transcription	Primary T cells fromperipheralblood	blood

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