Variant report

Variant	nsv820187
Chromosome Location	chr1:77331722-77334433
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:260)
CpG islands
(count:977)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:260 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:77333208-77333337	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr1:77333624-77334049	H1-hESC	embryonic stem cell:	n/a	n/a
3	CHD1	chr1:77333558-77334048	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD2	chr1:77332918-77333425	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr1:77333683-77334121	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTBP2	chr1:77332973-77335016	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr1:77333920-77334070	WERI-Rb-1	eye:	n/a	n/a
8	CTCF	chr1:77333874-77334311	ProgFib	skin:	n/a	n/a
9	CTCF	chr1:77333880-77334030	GM12874	blood:	n/a	n/a
10	CTCF	chr1:77333020-77333170	HEK293	kidney:	n/a	chr1:77333114-77333127 chr1:77333104-77333117
11	CTCF	chr1:77332980-77333130	HPF	lung:	n/a	chr1:77333114-77333127 chr1:77333104-77333117
12	CTCF	chr1:77333860-77334106	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr1:77333960-77334110	GM12866	blood:	n/a	n/a
14	CTCF	chr1:77333017-77333147	SK-N-SH_RA	brain:	n/a	chr1:77333114-77333127 chr1:77333104-77333117
15	CTCF	chr1:77333920-77334070	AG04450	lung:	n/a	n/a
16	CTCF	chr1:77333900-77334050	AG09319	gingival:	n/a	n/a
17	CTCF	chr1:77333480-77333630	HFF	foreskin:	n/a	n/a
18	CTCF	chr1:77333773-77334120	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr1:77333860-77334010	HFF	foreskin:	n/a	n/a
20	CTCF	chr1:77333060-77333210	HFF	foreskin:	n/a	chr1:77333114-77333127 chr1:77333104-77333117
21	CTCF	chr1:77332960-77333110	AG04450	lung:	n/a	n/a
22	CTCF	chr1:77333640-77333790	GM12872	blood:	n/a	n/a
23	CTCF	chr1:77333936-77334011	GM12892	blood:	n/a	n/a
24	CTCF	chr1:77333740-77333890	HMEC	breast:	n/a	n/a
25	CTCF	chr1:77333836-77334105	GM19238	blood:	n/a	n/a
26	CTCF	chr1:77333079-77333161	ProgFib	skin:	n/a	chr1:77333114-77333127 chr1:77333104-77333117
27	CTCF	chr1:77334214-77334223	Medullo	brain:	n/a	n/a
28	CTCF	chr1:77332900-77333190	HCM	heart:	n/a	chr1:77333114-77333127 chr1:77333104-77333117
29	CTCF	chr1:77334140-77334290	GM12869	blood:	n/a	n/a
30	CTCF	chr1:77333940-77334090	GM12865	blood:	n/a	n/a
31	CTCF	chr1:77333060-77333210	AG04450	lung:	n/a	chr1:77333114-77333127 chr1:77333104-77333117
32	CTCF	chr1:77333960-77334110	HMEC	breast:	n/a	n/a
33	CTCF	chr1:77333960-77334110	GM12878	blood:	n/a	n/a
34	CTCF	chr1:77333940-77334090	GM12873	blood:	n/a	n/a
35	CTCF	chr1:77333900-77334050	HMEC	breast:	n/a	n/a
36	CTCF	chr1:77333880-77334030	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr1:77333900-77334050	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr1:77333040-77333190	HRPEpiC	eye:	n/a	chr1:77333114-77333127 chr1:77333104-77333117
39	CTCF	chr1:77333900-77334050	HEK293	kidney:	n/a	n/a
40	CTCF	chr1:77333040-77333190	AG04449	skin:	n/a	chr1:77333114-77333127 chr1:77333104-77333117
41	CTCF	chr1:77333860-77334010	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:77333080-77333230	BJ	skin:	n/a	chr1:77333114-77333127 chr1:77333104-77333117
43	CTCF	chr1:77333940-77334090	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr1:77333060-77333210	AG09309	skin:	n/a	chr1:77333114-77333127 chr1:77333104-77333117
45	CTCF	chr1:77333120-77333270	HAc	cerebellar:	n/a	n/a
46	CTCF	chr1:77333872-77334076	GM20000	blood:	n/a	n/a
47	CTCF	chr1:77332980-77333130	AG04449	skin:	n/a	chr1:77333114-77333127 chr1:77333104-77333117
48	CTCF	chr1:77333900-77334050	HRE	kidney:	n/a	n/a
49	CTCF	chr1:77333777-77334230	MCF-7	breast:	n/a	n/a
50	CTCF	chr1:77333440-77333590	SK-N-SH_RA	brain:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:77333074-77333124	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:77333074-77333124	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:77334070-77334120	LNCaP	prostate:	n/a
4	chr1:77334177-77334227	GM12878	blood:	n/a
5	chr1:77331940-77331990	GM12892	blood:	n/a
6	chr1:77331940-77331990	AG04449	skin:	fetal
7	chr1:77333198-77333248	IMR90	lung:	fetal
8	chr1:77333074-77333124	PrEC	prostate:	n/a
9	chr1:77334207-77334257	GM12892	blood:	n/a
10	chr1:77333749-77333799	AoSMC	blood vessel:	n/a
11	chr1:77334207-77334257	H1-hESC	embryonic stem cell:	embryo
12	chr1:77333138-77333188	NH-A	brain:	n/a
13	chr1:77334070-77334120	HEK293	kidney:	embryo
14	chr1:77334045-77334095	NHBE	bronchial:	n/a
15	chr1:77334070-77334120	RPTEC	kidney:	n/a
16	chr1:77333074-77333124	SAEC	small airway:	n/a
17	chr1:77333749-77333799	HMEC	breast:	n/a
18	chr1:77333122-77333172	Jurkat	blood:	n/a
19	chr1:77333159-77333209	Hela-S3	cervix:	n/a
20	chr1:77332993-77333043	PANC-1	pancreas:	n/a
21	chr1:77333122-77333172	HNPCEpiC	eye:	n/a
22	chr1:77334177-77334227	ECC-1	luminal epithelium:	n/a
23	chr1:77333860-77333910	HRE	kidney:	n/a
24	chr1:77333860-77333910	AG10803	skin:	n/a
25	chr1:77332991-77333041	RPTEC	kidney:	n/a
26	chr1:77333074-77333124	K562	blood:	n/a
27	chr1:77332993-77333043	HEEpiC	esophagus:	n/a
28	chr1:77333159-77333209	HCT-116	colon:	n/a
29	chr1:77334070-77334120	A549	lung:	n/a
30	chr1:77333229-77333279	NHDF-neo	bronchial:	n/a
31	chr1:77333229-77333279	MCF10A-Er-Src	breast:	n/a
32	chr1:77333860-77333910	Hela-S3	cervix:	n/a
33	chr1:77334045-77334095	AG04450	lung:	fetal
34	chr1:77334070-77334120	GM12891	blood:	n/a
35	chr1:77333198-77333248	SK-N-MC	brain:	n/a
36	chr1:77333138-77333188	AG04449	skin:	fetal
37	chr1:77332993-77333043	T-47D	breast:	n/a
38	chr1:77333198-77333248	GM19239	blood:	n/a
39	chr1:77333229-77333279	H1-hESC	embryonic stem cell:	embryo
40	chr1:77334177-77334227	AoSMC	blood vessel:	n/a
41	chr1:77331940-77331990	NHBE	bronchial:	n/a
42	chr1:77333074-77333124	HMEC	breast:	n/a
43	chr1:77334177-77334227	NHDF-neo	bronchial:	n/a
44	chr1:77333860-77333910	GM19239	blood:	n/a
45	chr1:77333749-77333799	Hepatocyte	liver:	n/a
46	chr1:77334070-77334120	SKMC	muscle:	n/a
47	chr1:77333074-77333124	HEEpiC	esophagus:	n/a
48	chr1:77334045-77334095	NHDF-neo	bronchial:	n/a
49	chr1:77334070-77334120	NH-A	brain:	n/a
50	chr1:77334256-77334306	BE2_C	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:77326930..77328743-chr1:77330284..77333050,4	K562	blood:
2	chr1:77325804..77328743-chr1:77329882..77332282,4	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ST6GALNAC5	hsa-miR-148b-3p	chr1:77334423-77334427

Variant related genes	Relation type
ST6GALNAC5	TF binding region
ST6GALNAC5	CpG island

Extended variants
information (count: 101 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:101 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183921887	chr1:77331726-77331727	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs147713829	chr1:77331750-77331751	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs531907937	chr1:77331767-77331768	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs377760989	chr1:77331793-77331794	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs116705027	chr1:77331851-77331852	Weak transcription Bivalent Enhancer Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs540371313	chr1:77331874-77331875	Weak transcription Bivalent Enhancer Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs141277084	chr1:77331912-77331913	Weak transcription Bivalent Enhancer Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs532185078	chr1:77332001-77332002	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs200266779	chr1:77332011-77332012	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs186753935	chr1:77332039-77332040	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs568827117	chr1:77332056-77332057	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs529970012	chr1:77332091-77332092	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs377629252	chr1:77332105-77332106	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs567696602	chr1:77332131-77332132	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs534797502	chr1:77332275-77332276	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs142387456	chr1:77332357-77332358	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs553439436	chr1:77332383-77332384	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs112592844	chr1:77332394-77332395	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs191279456	chr1:77332395-77332396	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs9726090	chr1:77332398-77332399	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs557654983	chr1:77332419-77332420	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs575995471	chr1:77332427-77332428	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs562525821	chr1:77332438-77332439	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs543334691	chr1:77332499-77332500	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs367725903	chr1:77332595-77332596	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs1522618	chr1:77332627-77332628	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs572837149	chr1:77332630-77332631	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs539909630	chr1:77332678-77332679	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs114455411	chr1:77332763-77332764	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs532140241	chr1:77332792-77332793	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs199624931	chr1:77332876-77332877	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs562369776	chr1:77332905-77332906	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs184854076	chr1:77332972-77332973	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs548503210	chr1:77332992-77332993	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs567506017	chr1:77333081-77333082	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs528486905	chr1:77333108-77333109	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs547085131	chr1:77333133-77333134	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs565864042	chr1:77333175-77333176	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190680760	chr1:77333189-77333190	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539172474	chr1:77333230-77333231	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557569110	chr1:77333239-77333240	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569520345	chr1:77333284-77333285	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs377131012	chr1:77333300-77333301	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs113659117	chr1:77333301-77333302	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113208751	chr1:77333325-77333326	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs76305167	chr1:77333355-77333356	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572703660	chr1:77333367-77333368	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369888538	chr1:77333395-77333396	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs115959772	chr1:77333401-77333402	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558164719	chr1:77333431-77333432	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:304 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77319800-77333200	Weak transcription	Gastric	stomach
2	chr1:77320400-77333000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:77329600-77332800	Enhancers	HSMMtube	muscle
4	chr1:77330200-77332800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:77330600-77332800	Weak transcription	NH-A	brain
6	chr1:77330800-77332200	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr1:77330800-77332200	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr1:77330800-77332800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr1:77331000-77332800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr1:77331400-77332000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr1:77331400-77332400	Bivalent Enhancer	Brain Cingulate Gyrus	brain
12	chr1:77331400-77332800	Enhancers	Fetal Brain Female	brain
13	chr1:77331600-77331800	Enhancers	Duodenum Smooth Muscle	Duodenum
14	chr1:77331600-77332000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
15	chr1:77331600-77332000	Enhancers	Aorta	Aorta
16	chr1:77331600-77332000	Enhancers	Ovary	ovary
17	chr1:77331600-77332000	Enhancers	HSMM	muscle
18	chr1:77331600-77332200	Enhancers	Rectal Smooth Muscle	rectum
19	chr1:77331800-77332000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr1:77331800-77332000	Bivalent Enhancer	Colon Smooth Muscle	Colon
21	chr1:77331800-77332200	Enhancers	Fetal Brain Male	brain
22	chr1:77331800-77333200	Active TSS	Stomach Smooth Muscle	stomach
23	chr1:77332000-77332600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr1:77332000-77332600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
25	chr1:77332000-77332800	Weak transcription	Aorta	Aorta
26	chr1:77332000-77332800	Weak transcription	Ovary	ovary
27	chr1:77332000-77332800	Weak transcription	HSMM	muscle
28	chr1:77332200-77332600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
29	chr1:77332200-77332600	Weak transcription	Fetal Brain Male	brain
30	chr1:77332200-77332800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr1:77332200-77333000	Weak transcription	Rectal Smooth Muscle	rectum
32	chr1:77332200-77335800	Active TSS	Brain Anterior Caudate	brain
33	chr1:77332400-77332600	Enhancers	Brain Cingulate Gyrus	brain
34	chr1:77332400-77332600	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
35	chr1:77332400-77332600	Bivalent Enhancer	NHDF-Ad	bronchial
36	chr1:77332400-77332800	Enhancers	Brain Germinal Matrix	brain
37	chr1:77332600-77332800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
38	chr1:77332600-77332800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr1:77332600-77332800	Enhancers	Fetal Brain Male	brain
40	chr1:77332600-77334400	Active TSS	Cortex derived primary cultured neurospheres	brain
41	chr1:77332800-77333000	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr1:77332800-77333000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
43	chr1:77332800-77333000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
44	chr1:77332800-77333000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
45	chr1:77332800-77333000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr1:77332800-77333000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:77332800-77333000	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:77332800-77333000	Flanking Bivalent TSS/Enh	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr1:77332800-77333000	Bivalent/Poised TSS	Primary B cells from cord blood	blood
50	chr1:77332800-77333000	Bivalent Enhancer	Primary T cells from cord blood	blood

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