Variant report

Variant	esv3400653
Chromosome Location	chr6:37787424-37788572
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:37785796-37787564	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:37785949-37787564	K562	blood:	n/a	n/a
3	ATF1	chr6:37788108-37788474	K562	blood:	n/a	n/a
4	ATF3	chr6:37788082-37788372	HepG2	liver:	n/a	n/a
5	ATF3	chr6:37788104-37788363	K562	blood:	n/a	n/a
6	ATF3	chr6:37788065-37788392	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr6:37788129-37788438	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr6:37787999-37788521	K562	blood:	n/a	n/a
9	ATF3	chr6:37787964-37788556	HCT-116	colon:	n/a	n/a
10	BATF	chr6:37788178-37788389	GM12878	blood:	n/a	n/a
11	BATF	chr6:37788053-37788351	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:37786297-37787703	K562	blood:	n/a	chr6:37787322-37787338 chr6:37787530-37787546
13	BHLHE40	chr6:37786652-37787792	HepG2	liver:	n/a	chr6:37787322-37787338 chr6:37787530-37787546
14	BHLHE40	chr6:37786223-37787696	GM12878	blood:	n/a	chr6:37787322-37787338 chr6:37787530-37787546
15	BHLHE40	chr6:37786847-37787610	A549	lung:	n/a	chr6:37787322-37787338 chr6:37787530-37787546
16	BHLHE40	chr6:37788044-37788696	GM12878	blood:	n/a	n/a
17	BRCA1	chr6:37786368-37787573	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr6:37786832-37787608	HepG2	liver:	n/a	n/a
19	BRCA1	chr6:37786708-37787619	GM12878	blood:	n/a	n/a
20	BRCA1	chr6:37786797-37787485	H1-hESC	embryonic stem cell:	n/a	n/a
21	CBX3	chr6:37786222-37787590	K562	blood:	n/a	n/a
22	CCNT2	chr6:37786457-37787667	K562	blood:	n/a	chr6:37787260-37787269
23	CCNT2	chr6:37788062-37788399	K562	blood:	n/a	n/a
24	CEBPB	chr6:37788066-37788449	H1-hESC	embryonic stem cell:	n/a	chr6:37788250-37788261
25	CEBPB	chr6:37787954-37788563	HCT-116	colon:	n/a	chr6:37788250-37788261
26	CEBPB	chr6:37788010-37788503	ECC-1	luminal epithelium:	n/a	chr6:37788250-37788261
27	CEBPB	chr6:37788080-37788452	A549	lung:	n/a	chr6:37788250-37788261
28	CEBPB	chr6:37786215-37787603	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr6:37788104-37788450	A549	lung:	n/a	chr6:37788250-37788261
30	CEBPB	chr6:37788022-37788520	MCF-7	breast:	n/a	chr6:37788250-37788261
31	CEBPB	chr6:37787977-37788544	ECC-1	luminal epithelium:	n/a	chr6:37788250-37788261
32	CEBPB	chr6:37788050-37788459	HepG2	liver:	n/a	chr6:37788250-37788261
33	CEBPB	chr6:37788137-37788304	HepG2	liver:	n/a	chr6:37788250-37788261
34	CEBPB	chr6:37788074-37788363	K562	blood:	n/a	chr6:37788250-37788261
35	CEBPB	chr6:37787956-37788622	HCT-116	colon:	n/a	chr6:37788250-37788261
36	CEBPB	chr6:37788066-37788460	K562	blood:	n/a	chr6:37788250-37788261
37	CEBPB	chr6:37788014-37788749	Hela-S3	cervix:	n/a	chr6:37788250-37788261
38	CEBPB	chr6:37788047-37788543	A549	lung:	n/a	chr6:37788250-37788261
39	CEBPB	chr6:37788066-37788466	IMR90	lung:	n/a	chr6:37788250-37788261
40	CEBPB	chr6:37788079-37788427	HepG2	liver:	n/a	chr6:37788250-37788261
41	CEBPB	chr6:37788081-37788435	HepG2	liver:	n/a	chr6:37788250-37788261
42	CEBPB	chr6:37787994-37788528	K562	blood:	n/a	chr6:37788250-37788261
43	CEBPB	chr6:37787962-37788533	MCF-7	breast:	n/a	chr6:37788250-37788261
44	CEBPD	chr6:37786460-37787712	HepG2	liver:	n/a	n/a
45	CHD1	chr6:37788436-37788441	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr6:37786580-37787651	H1-hESC	embryonic stem cell:	n/a	chr6:37787422-37787432
47	CHD1	chr6:37785753-37787786	IMR90	lung:	n/a	chr6:37787422-37787432
48	CHD1	chr6:37788124-37788891	GM12878	blood:	n/a	n/a
49	CHD1	chr6:37786330-37787691	GM12878	blood:	n/a	chr6:37787422-37787432
50	CHD2	chr6:37786401-37787554	H1-hESC	embryonic stem cell:	n/a	chr6:37787422-37787432

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:37788171-37788221	HNPCEpiC	eye:	n/a
2	chr6:37788018-37788068	GM06990	blood:	n/a
3	chr6:37788171-37788221	SK-N-SH_RA	brain:	n/a
4	chr6:37787739-37787789	HCT-116	colon:	n/a
5	chr6:37788171-37788221	PANC-1	pancreas:	n/a
6	chr6:37788018-37788068	HMEC	breast:	n/a
7	chr6:37787739-37787789	GM12891	blood:	n/a
8	chr6:37787739-37787789	PFSK-1	brain:	n/a
9	chr6:37788018-37788068	HAEpiC	amniotic membrane:	n/a
10	chr6:37788171-37788221	MCF-7	breast:	n/a
11	chr6:37787739-37787789	AoSMC	blood vessel:	n/a
12	chr6:37787739-37787789	Caco-2	colon:	n/a
13	chr6:37787739-37787789	ovcar-3	ovarian:	n/a
14	chr6:37788018-37788068	LNCaP	prostate:	n/a
15	chr6:37788171-37788221	U87	brain:	n/a
16	chr6:37788018-37788068	K562	blood:	n/a
17	chr6:37787739-37787789	SKMC	muscle:	n/a
18	chr6:37787739-37787789	HMEC	breast:	n/a
19	chr6:37788018-37788068	BJ	skin:	n/a
20	chr6:37788171-37788221	PrEC	prostate:	n/a
21	chr6:37787739-37787789	AG09319	gingival:	n/a
22	chr6:37788018-37788068	NB4	blood:	n/a
23	chr6:37787739-37787789	AG04450	lung:	fetal
24	chr6:37787739-37787789	PrEC	prostate:	n/a
25	chr6:37788018-37788068	PANC-1	pancreas:	n/a
26	chr6:37788018-37788068	IMR90	lung:	fetal
27	chr6:37787739-37787789	MCF10A-Er-Src	breast:	n/a
28	chr6:37788171-37788221	Caco-2	colon:	n/a
29	chr6:37787739-37787789	HNPCEpiC	eye:	n/a
30	chr6:37787739-37787789	ProgFib	skin:	n/a
31	chr6:37788171-37788221	HCM	heart:	n/a
32	chr6:37787739-37787789	HL-60	blood:	n/a
33	chr6:37788171-37788221	NH-A	brain:	n/a
34	chr6:37788018-37788068	RPTEC	kidney:	n/a
35	chr6:37787739-37787789	PANC-1	pancreas:	n/a
36	chr6:37788171-37788221	ovcar-3	ovarian:	n/a
37	chr6:37788171-37788221	Hela-S3	cervix:	n/a
38	chr6:37788018-37788068	A549	lung:	n/a
39	chr6:37788018-37788068	HIPEpiC	eye:	n/a
40	chr6:37787739-37787789	GM06990	blood:	n/a
41	chr6:37787739-37787789	HRE	kidney:	n/a
42	chr6:37788018-37788068	HRCEpiC	kidney:	n/a
43	chr6:37788171-37788221	HCF	heart:	n/a
44	chr6:37787739-37787789	Hela-S3	cervix:	n/a
45	chr6:37788171-37788221	GM19239	blood:	n/a
46	chr6:37788018-37788068	GM12891	blood:	n/a
47	chr6:37788171-37788221	HPAEpiC	pulmonary alveolar:	n/a
48	chr6:37787739-37787789	HEEpiC	esophagus:	n/a
49	chr6:37787739-37787789	H1-hESC	embryonic stem cell:	embryo
50	chr6:37788018-37788068	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:37787460..37788198-chr7:2559148..2559754,2	HCT-116	colon:
2	chr6:37786462..37787543-chr7:25164251..25165338,4	Hela-S3	cervix:
3	chr6:37787991..37789516-chr6:37789518..37791025,2	MCF-7	breast:
4	chr3:64084830..64086992-chr6:37787357..37789363,2	MCF-7	breast:

Variant related genes	Relation type
ZFAND3	TF binding region
ENSG00000225945	TF binding region
ZFAND3	CpG island
ENSG00000225945	CpG island
ENSG00000172115	chromatin interactions
ENSG00000106003	chromatin interactions
ENSG00000241572	chromatin interactions

Extended variants
information (count: 49 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:49 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151198619	chr6:37787433-37787434	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs140377502	chr6:37787450-37787451	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs542378164	chr6:37787457-37787458	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs556899782	chr6:37787463-37787464	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs573668592	chr6:37787476-37787477	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs576538329	chr6:37787479-37787480	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs371172618	chr6:37787530-37787531	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs11544071	chr6:37787585-37787586	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs191064172	chr6:37787602-37787603	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs182727321	chr6:37787623-37787624	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs532864475	chr6:37787628-37787629	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs539970158	chr6:37787640-37787641	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs535914302	chr6:37787811-37787812	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs111579710	chr6:37787821-37787822	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs185826547	chr6:37787822-37787823	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs556928213	chr6:37787906-37787907	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs548821142	chr6:37787978-37787979	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs77714510	chr6:37788004-37788005	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs115773136	chr6:37788048-37788049	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs551284222	chr6:37788057-37788058	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs571449537	chr6:37788066-37788067	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs369480982	chr6:37788069-37788070	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs554324023	chr6:37788088-37788089	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs374723353	chr6:37788093-37788094	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs555710969	chr6:37788158-37788159	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs536654912	chr6:37788197-37788198	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs556634259	chr6:37788210-37788211	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs259723	chr6:37788220-37788221	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs189753819	chr6:37788229-37788230	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs182467866	chr6:37788247-37788248	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs558866934	chr6:37788260-37788261	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs572612992	chr6:37788272-37788273	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs79156839	chr6:37788302-37788303	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs75553944	chr6:37788316-37788317	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs188728247	chr6:37788322-37788323	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs561833841	chr6:37788327-37788328	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs137997118	chr6:37788341-37788342	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs542208405	chr6:37788367-37788368	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs562551667	chr6:37788370-37788371	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs531041731	chr6:37788384-37788385	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs140784315	chr6:37788412-37788413	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs150098837	chr6:37788413-37788414	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs377485190	chr6:37788447-37788448	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs544232017	chr6:37788451-37788452	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs192317412	chr6:37788457-37788458	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs527485296	chr6:37788474-37788475	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs547870653	chr6:37788512-37788513	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs567752402	chr6:37788519-37788520	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs536789052	chr6:37788542-37788543	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
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
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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	21693616	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Breast cancer	16397240	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:37784800-37789000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:37785400-37789200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr6:37785800-37788400	Active TSS	HUES64 Cell Line	embryonic stem cell
4	chr6:37785800-37788400	Active TSS	Rectal Mucosa Donor 29	rectum
5	chr6:37785800-37788600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
6	chr6:37785800-37788600	Active TSS	iPS-15b Cell Line	embryonic stem cell
7	chr6:37785800-37788600	Active TSS	iPS-20b Cell Line	embryonic stem cell
8	chr6:37785800-37788600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:37785800-37788600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr6:37785800-37788800	Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr6:37785800-37788800	Active TSS	H1 Cell Line	embryonic stem cell
12	chr6:37785800-37788800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr6:37785800-37788800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr6:37785800-37788800	Active TSS	A549	lung
15	chr6:37785800-37789000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr6:37785800-37789200	Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr6:37786000-37788200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:37786000-37788400	Bivalent/Poised TSS	HepG2	liver
19	chr6:37786000-37788600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr6:37786000-37788600	Active TSS	NHDF-Ad	bronchial
21	chr6:37786000-37788800	Active TSS	H9 Cell Line	embryonic stem cell
22	chr6:37786000-37788800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr6:37786000-37788800	Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr6:37786000-37788800	Active TSS	Fetal Muscle Trunk	muscle
25	chr6:37786000-37789000	Active TSS	Stomach Smooth Muscle	stomach
26	chr6:37786000-37789200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr6:37786000-37789200	Active TSS	Fetal Intestine Large	intestine
28	chr6:37786000-37789200	Active TSS	Right Ventricle	heart
29	chr6:37786000-37789200	Active TSS	GM12878-XiMat	blood
30	chr6:37786000-37789800	Active TSS	Psoas Muscle	Psoas
31	chr6:37786000-37790000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr6:37786200-37788400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr6:37786200-37788400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr6:37786200-37788400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr6:37786200-37788400	Active TSS	Small Intestine	intestine
36	chr6:37786200-37788600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:37786200-37788600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr6:37786200-37788600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr6:37786200-37788600	Active TSS	Duodenum Smooth Muscle	Duodenum
40	chr6:37786200-37788800	Active TSS	Colonic Mucosa	Colon
41	chr6:37786200-37788800	Active TSS	Esophagus	oesophagus
42	chr6:37786200-37788800	Active TSS	Left Ventricle	heart
43	chr6:37786200-37788800	Active TSS	Ovary	ovary
44	chr6:37786200-37788800	Active TSS	Sigmoid Colon	Sigmoid Colon
45	chr6:37786200-37789000	Active TSS	Aorta	Aorta
46	chr6:37786200-37789200	Active TSS	Pancreas	Pancrea
47	chr6:37786400-37788200	Active TSS	Primary monocytes fromperipheralblood	blood
48	chr6:37786400-37788200	Active TSS	Primary T cells from cord blood	blood
49	chr6:37786400-37788200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
50	chr6:37786400-37788200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood

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