Variant report

Variant	esv3438069
Chromosome Location	chr6:4775703-4778001
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:613)
CpG islands
(count:366)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:4776552-4776682	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:4777479-4777700	K562	blood:	n/a	n/a
3	ARID3A	chr6:4776144-4776305	HepG2	liver:	n/a	n/a
4	ATF1	chr6:4777467-4777779	K562	blood:	n/a	n/a
5	ATF2	chr6:4777275-4777795	GM12878	blood:	n/a	n/a
6	BCL11A	chr6:4777411-4777750	GM12878	blood:	n/a	n/a
7	BCLAF1	chr6:4777389-4778122	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:4775622-4776738	GM12878	blood:	n/a	chr6:4776143-4776159 chr6:4776135-4776151 chr6:4775989-4776005 chr6:4775829-4775845
9	BHLHE40	chr6:4777336-4778808	GM12878	blood:	n/a	n/a
10	CBX3	chr6:4777367-4777799	K562	blood:	n/a	n/a
11	CCNT2	chr6:4775501-4775730	K562	blood:	n/a	n/a
12	CCNT2	chr6:4776162-4777050	K562	blood:	n/a	n/a
13	CEBPB	chr6:4776473-4776624	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:4776619-4776792	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr6:4776749-4776903	HepG2	liver:	n/a	n/a
16	CEBPB	chr6:4777403-4778870	GM12878	blood:	n/a	chr6:4778531-4778542 chr6:4778533-4778544
17	CEBPD	chr6:4776372-4776784	HepG2	liver:	n/a	n/a
18	CEBPD	chr6:4775751-4776115	HepG2	liver:	n/a	n/a
19	CHD1	chr6:4776772-4776949	GM12878	blood:	n/a	n/a
20	CHD1	chr6:4776143-4776309	GM12878	blood:	n/a	n/a
21	CHD2	chr6:4775581-4776727	GM12878	blood:	n/a	chr6:4775824-4775834
22	CHD2	chr6:4777138-4777677	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr6:4776502-4776688	K562	blood:	n/a	n/a
24	CHD2	chr6:4776892-4777056	K562	blood:	n/a	n/a
25	CHD2	chr6:4776552-4776633	HepG2	liver:	n/a	n/a
26	CHD2	chr6:4777462-4778287	GM12878	blood:	n/a	n/a
27	CHD2	chr6:4776399-4776923	Hela-S3	cervix:	n/a	n/a
28	CREB1	chr6:4775637-4776833	A549	lung:	n/a	n/a
29	CREB1	chr6:4777392-4777853	K562	blood:	n/a	n/a
30	CREB1	chr6:4777368-4777965	K562	blood:	n/a	n/a
31	CREB1	chr6:4775487-4777065	HepG2	liver:	n/a	n/a
32	CREB1	chr6:4777058-4778152	GM12878	blood:	n/a	n/a
33	CREB1	chr6:4777444-4777888	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr6:4777096-4777966	GM12878	blood:	n/a	n/a
35	CREB1	chr6:4777473-4777836	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr6:4776080-4776230	HEK293	kidney:	n/a	n/a
37	CTCF	chr6:4776045-4776252	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr6:4775994-4776214	HepG2	liver:	n/a	n/a
39	CTCF	chr6:4776041-4776236	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr6:4776102-4776108	GM13976	blood:	n/a	n/a
41	CTCF	chr6:4776120-4776270	AG04450	lung:	n/a	n/a
42	CTCF	chr6:4776020-4776170	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr6:4776060-4776210	HMEC	breast:	n/a	n/a
44	CTCF	chr6:4776120-4776270	GM12874	blood:	n/a	n/a
45	CTCF	chr6:4776040-4776190	A549	lung:	n/a	n/a
46	CTCF	chr6:4776040-4776190	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr6:4776060-4776210	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr6:4776020-4776170	AG04449	skin:	n/a	n/a
49	CTCF	chr6:4776060-4776210	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr6:4776080-4776230	GM12865	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:4776641-4776691	RPTEC	kidney:	n/a
2	chr6:4776995-4777045	LNCaP	prostate:	n/a
3	chr6:4776490-4776540	NB4	blood:	n/a
4	chr6:4776623-4776673	NT2-D1	testis:	n/a
5	chr6:4776490-4776540	HRCEpiC	kidney:	n/a
6	chr6:4776623-4776673	AG04449	skin:	fetal
7	chr6:4776490-4776540	HIPEpiC	eye:	n/a
8	chr6:4776669-4776719	SK-N-SH_RA	brain:	n/a
9	chr6:4777549-4777599	HMEC	breast:	n/a
10	chr6:4776490-4776540	IMR90	lung:	fetal
11	chr6:4776669-4776719	SKMC	muscle:	n/a
12	chr6:4776623-4776673	HRE	kidney:	n/a
13	chr6:4776623-4776673	HEEpiC	esophagus:	n/a
14	chr6:4776490-4776540	HEK293	kidney:	embryo
15	chr6:4776490-4776540	HPAEpiC	pulmonary alveolar:	n/a
16	chr6:4776995-4777045	SK-N-MC	brain:	n/a
17	chr6:4776995-4777045	ovcar-3	ovarian:	n/a
18	chr6:4776641-4776691	H1-hESC	embryonic stem cell:	embryo
19	chr6:4776641-4776691	PANC-1	pancreas:	n/a
20	chr6:4776669-4776719	MCF-7	breast:	n/a
21	chr6:4776641-4776691	GM19239	blood:	n/a
22	chr6:4777549-4777599	HAEpiC	amniotic membrane:	n/a
23	chr6:4776995-4777045	HepG2	liver:	n/a
24	chr6:4776641-4776691	AG09309	skin:	n/a
25	chr6:4776669-4776719	GM06990	blood:	n/a
26	chr6:4776995-4777045	AG04449	skin:	fetal
27	chr6:4776669-4776719	PrEC	prostate:	n/a
28	chr6:4777549-4777599	HNPCEpiC	eye:	n/a
29	chr6:4776995-4777045	Caco-2	colon:	n/a
30	chr6:4776669-4776719	HEEpiC	esophagus:	n/a
31	chr6:4776641-4776691	Hela-S3	cervix:	n/a
32	chr6:4776995-4777045	NHBE	bronchial:	n/a
33	chr6:4776641-4776691	AG10803	skin:	n/a
34	chr6:4776995-4777045	HEK293	kidney:	embryo
35	chr6:4776669-4776719	BE2_C	brain:	n/a
36	chr6:4777549-4777599	GM12891	blood:	n/a
37	chr6:4776995-4777045	BE2_C	brain:	n/a
38	chr6:4776641-4776691	GM12891	blood:	n/a
39	chr6:4776490-4776540	MCF-7	breast:	n/a
40	chr6:4777549-4777599	HIPEpiC	eye:	n/a
41	chr6:4776995-4777045	NHDF-neo	bronchial:	n/a
42	chr6:4776623-4776673	ECC-1	luminal epithelium:	n/a
43	chr6:4776623-4776673	HCM	heart:	n/a
44	chr6:4776623-4776673	NHBE	bronchial:	n/a
45	chr6:4776995-4777045	HNPCEpiC	eye:	n/a
46	chr6:4776641-4776691	NT2-D1	testis:	n/a
47	chr6:4776669-4776719	GM19239	blood:	n/a
48	chr6:4777549-4777599	ProgFib	skin:	n/a
49	chr6:4776641-4776691	GM12892	blood:	n/a
50	chr6:4776641-4776691	ovcar-3	ovarian:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:4488845..4492110-chr6:4777740..4781440,3	MCF-7	breast:
2	chr6:4775660..4776622-chr6:5030960..5031503,2	MCF-7	breast:
3	chr6:4775959..4776581-chr6:4790810..4791474,2	K562	blood:
4	chr6:4777710..4780092-chr6:4801744..4804702,2	K562	blood:
5	chr6:4773447..4776687-chr6:4777915..4782551,4	MCF-7	breast:
6	chr1:155196815..155197641-chr6:4776806..4777313,2	Hela-S3	cervix:
7	chr6:4776139..4778956-chr6:5002447..5004557,2	K562	blood:
8	chr6:4776830..4778493-chr6:4928400..4930186,2	MCF-7	breast:
9	chr6:4775727..4780301-chr6:4925378..4930668,5	K562	blood:
10	chr6:4775417..4779410-chr6:4834974..4837006,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000236336	TF binding region
CDYL	TF binding region
ENSG00000236336	CpG island
CDYL	CpG island
ENSG00000160766	chromatin interactions
ENSG00000236336	chromatin interactions
ENSG00000260239	chromatin interactions
ENSG00000153046	chromatin interactions
ENSG00000124787	chromatin interactions

Extended variants
information (count: 44 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:44 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372920121	chr6:4775747-4775748	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs179822	chr6:4775766-4775767	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs533321841	chr6:4775786-4775787	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs369071954	chr6:4775797-4775798	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs569819395	chr6:4775829-4775830	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs11963533	chr6:4775838-4775839	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs555318851	chr6:4775867-4775868	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs565855931	chr6:4776124-4776125	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs570558271	chr6:4776132-4776133	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs141547718	chr6:4776173-4776174	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs557383578	chr6:4776211-4776212	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs577239885	chr6:4776233-4776234	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs373302690	chr6:4776369-4776370	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs113444172	chr6:4776403-4776404	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs186106039	chr6:4776418-4776419	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs202138645	chr6:4776422-4776423	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs377185331	chr6:4776455-4776456	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs112262470	chr6:4776516-4776517	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs189012947	chr6:4777010-4777011	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs534300464	chr6:4777074-4777075	Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs181570806	chr6:4777254-4777255	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs200325395	chr6:4777264-4777265	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs542978796	chr6:4777291-4777292	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs556899520	chr6:4777326-4777327	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs62384849	chr6:4777343-4777344	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs62384850	chr6:4777353-4777354	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs562185757	chr6:4777404-4777405	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs527846750	chr6:4777406-4777407	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs114380137	chr6:4777415-4777416	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs13214607	chr6:4777442-4777443	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs143538444	chr6:4777460-4777461	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs61531947	chr6:4777462-4777463	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs549944175	chr6:4777498-4777499	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs76149946	chr6:4777550-4777551	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs114484994	chr6:4777652-4777653	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs58544878	chr6:4777680-4777681	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs565736887	chr6:4777686-4777687	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs562705055	chr6:4777756-4777757	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs115994571	chr6:4777788-4777789	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs116308244	chr6:4777938-4777939	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs531819448	chr6:4777943-4777944	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs186340260	chr6:4777953-4777954	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs556729005	chr6:4777969-4777970	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs548451452	chr6:4777993-4777994	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD
Ovarian cancer	19193619	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:320 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4772600-4776200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
2	chr6:4772800-4777200	Active TSS	H1 Cell Line	embryonic stem cell
3	chr6:4772800-4777800	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr6:4773000-4777400	Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr6:4773000-4777600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:4773200-4777400	Active TSS	H9 Cell Line	embryonic stem cell
7	chr6:4773200-4777400	Active TSS	iPS-18 Cell Line	embryonic stem cell
8	chr6:4773200-4777400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr6:4773200-4777600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr6:4773200-4778200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr6:4774200-4778000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr6:4774600-4775800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
13	chr6:4774600-4777400	Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr6:4774800-4775800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr6:4774800-4775800	Flanking Active TSS	Primary B cells from cord blood	blood
16	chr6:4774800-4775800	Flanking Active TSS	Primary hematopoietic stem cells	blood
17	chr6:4774800-4775800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
18	chr6:4774800-4775800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr6:4774800-4777800	Active TSS	Brain Inferior Temporal Lobe	brain
20	chr6:4774800-4778000	Active TSS	Stomach Smooth Muscle	stomach
21	chr6:4775000-4775800	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
22	chr6:4775000-4775800	Flanking Active TSS	Primary B cells from peripheral blood	blood
23	chr6:4775000-4775800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
24	chr6:4775000-4775800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
25	chr6:4775000-4775800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
26	chr6:4775000-4775800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
27	chr6:4775000-4775800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
28	chr6:4775000-4775800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr6:4775000-4775800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr6:4775000-4775800	Flanking Active TSS	Adipose Nuclei	Adipose
31	chr6:4775000-4775800	Flanking Active TSS	Liver	Liver
32	chr6:4775000-4775800	Flanking Active TSS	Duodenum Mucosa	Duodenum
33	chr6:4775000-4775800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
34	chr6:4775000-4775800	Flanking Active TSS	Pancreas	Pancrea
35	chr6:4775000-4775800	Flanking Bivalent TSS/Enh	HepG2	liver
36	chr6:4775000-4777000	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:4775000-4777000	Active TSS	Placenta Amnion	Placenta Amnion
38	chr6:4775000-4777600	Active TSS	Brain Substantia Nigra	brain
39	chr6:4775000-4777800	Active TSS	Brain Angular Gyrus	brain
40	chr6:4775000-4777800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr6:4775000-4777800	Active TSS	Colon Smooth Muscle	Colon
42	chr6:4775000-4777800	Active TSS	Esophagus	oesophagus
43	chr6:4775000-4777800	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr6:4775000-4777800	Active TSS	Gastric	stomach
45	chr6:4775000-4777800	Active TSS	Rectal Mucosa Donor 31	rectum
46	chr6:4775000-4777800	Active TSS	Rectal Smooth Muscle	rectum
47	chr6:4775000-4778000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:4775000-4778000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:4775000-4778000	Active TSS	Ovary	ovary
50	chr6:4775000-4778400	Active TSS	Brain Cingulate Gyrus	brain

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