Variant report

Variant	nsv546661
Chromosome Location	chr1:80656114-81156849
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1659)
CpG islands
(count:367)
Chromatin interactive
region (count:26)
LncRNA
region (count:46)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1659 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:81121838-81122229	HepG2	liver:	n/a	n/a
2	ATF1	chr1:81022589-81022754	K562	blood:	n/a	n/a
3	ATF2	chr1:81105405-81105867	GM12878	blood:	n/a	n/a
4	ATF2	chr1:81105420-81105817	GM12878	blood:	n/a	n/a
5	BACH1	chr1:81107002-81107005	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:80883213-80883325	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:80998868-80999129	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr1:81122395-81122574	GM12878	blood:	n/a	chr1:81122490-81122501
9	BCL11A	chr1:80975728-80975960	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr1:81105502-81105716	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:81105434-81105812	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:80723225-80723289	K562	blood:	n/a	n/a
13	BHLHE40	chr1:81098882-81098995	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:81105461-81106142	GM12878	blood:	n/a	n/a
15	BRCA1	chr1:80910757-80911113	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr1:80996803-80997369	HCT-116	colon:	n/a	n/a
17	CBX3	chr1:81000531-81001133	HCT-116	colon:	n/a	n/a
18	CCNT2	chr1:80678816-80679016	K562	blood:	n/a	n/a
19	CEBPB	chr1:80858254-80858574	A549	lung:	n/a	n/a
20	CEBPB	chr1:81006283-81006695	Hela-S3	cervix:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
21	CEBPB	chr1:80936700-80937019	HepG2	liver:	n/a	chr1:80936873-80936882 chr1:80936873-80936884 chr1:80936871-80936884 chr1:80936871-80936882 chr1:80936871-80936884 chr1:80936871-80936884
22	CEBPB	chr1:81059645-81060123	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr1:80784586-80784803	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:81000600-81001165	HCT-116	colon:	n/a	n/a
25	CEBPB	chr1:80910689-80911261	HCT-116	colon:	n/a	n/a
26	CEBPB	chr1:81126319-81126668	HepG2	liver:	n/a	chr1:81126471-81126482
27	CEBPB	chr1:80716920-80717073	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:81004063-81004214	A549	lung:	n/a	chr1:81004073-81004086 chr1:81004075-81004086 chr1:81004073-81004086 chr1:81004073-81004086
29	CEBPB	chr1:81122766-81123072	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:81126320-81126664	IMR90	lung:	n/a	chr1:81126471-81126482
31	CEBPB	chr1:81141228-81141567	A549	lung:	n/a	n/a
32	CEBPB	chr1:80858020-80858759	MCF-7	breast:	n/a	n/a
33	CEBPB	chr1:80989649-80990016	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr1:81121533-81121868	HepG2	liver:	n/a	n/a
35	CEBPB	chr1:80846876-80847176	IMR90	lung:	n/a	chr1:80847004-80847015
36	CEBPB	chr1:80913237-80913619	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr1:81099887-81100415	MCF-7	breast:	n/a	chr1:81100133-81100144
38	CEBPB	chr1:80818747-80819048	HepG2	liver:	n/a	chr1:80818857-80818868
39	CEBPB	chr1:80991202-80991443	HepG2	liver:	n/a	chr1:80991301-80991314 chr1:80991302-80991313
40	CEBPB	chr1:81000182-81001093	HCT-116	colon:	n/a	n/a
41	CEBPB	chr1:80912499-80912558	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr1:80745251-80745589	HepG2	liver:	n/a	n/a
43	CEBPB	chr1:81006302-81006643	HepG2	liver:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
44	CEBPB	chr1:81141200-81141555	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr1:80784526-80784853	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr1:80923262-80923547	Hela-S3	cervix:	n/a	chr1:80923417-80923428 chr1:80923417-80923430
47	CEBPB	chr1:80846825-80847141	Hela-S3	cervix:	n/a	chr1:80847004-80847015
48	CEBPB	chr1:81141098-81141568	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr1:81141244-81141532	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr1:81090428-81090679	Hela-S3	cervix:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:81001617-81001667	CMK	blood:	n/a
2	chr1:81001617-81001667	CMK	blood:	n/a
3	chr1:80961776-80961826	HUVEC	blood vessel:	n/a
4	chr1:81124441-81124491	PrEC	prostate:	n/a
5	chr1:81124441-81124491	A549	lung:	n/a
6	chr1:80961906-80961956	HCF	heart:	n/a
7	chr1:81001617-81001667	LNCaP	prostate:	n/a
8	chr1:81001617-81001667	GM19239	blood:	n/a
9	chr1:80961769-80961819	HIPEpiC	eye:	n/a
10	chr1:80961776-80961826	AG09319	gingival:	n/a
11	chr1:80961776-80961826	HEEpiC	esophagus:	n/a
12	chr1:80961906-80961956	PFSK-1	brain:	n/a
13	chr1:81124441-81124491	HRE	kidney:	n/a
14	chr1:81124441-81124491	HEK293	kidney:	embryo
15	chr1:80961776-80961826	SK-N-MC	brain:	n/a
16	chr1:80961769-80961819	HAEpiC	amniotic membrane:	n/a
17	chr1:80923103-80923153	LNCaP	prostate:	n/a
18	chr1:81001617-81001667	NHDF-neo	bronchial:	n/a
19	chr1:80961906-80961956	ECC-1	luminal epithelium:	n/a
20	chr1:80961769-80961819	Caco-2	colon:	n/a
21	chr1:81124441-81124491	IMR90	lung:	fetal
22	chr1:80923103-80923153	H1-hESC	embryonic stem cell:	embryo
23	chr1:81001617-81001667	HEK293	kidney:	embryo
24	chr1:81001617-81001667	HRPEpiC	eye:	n/a
25	chr1:80961776-80961826	HCT-116	colon:	n/a
26	chr1:81124441-81124491	BE2_C	brain:	n/a
27	chr1:81124441-81124491	HRCEpiC	kidney:	n/a
28	chr1:80961769-80961819	Hepatocyte	liver:	n/a
29	chr1:81124441-81124491	GM19239	blood:	n/a
30	chr1:81001617-81001667	K562	blood:	n/a
31	chr1:80961906-80961956	HPAEpiC	pulmonary alveolar:	n/a
32	chr1:80923103-80923153	U87	brain:	n/a
33	chr1:81124441-81124491	RPTEC	kidney:	n/a
34	chr1:80961769-80961819	HCF	heart:	n/a
35	chr1:80961906-80961956	AG04450	lung:	fetal
36	chr1:80961906-80961956	Hepatocyte	liver:	n/a
37	chr1:80961906-80961956	HCM	heart:	n/a
38	chr1:81124441-81124491	PANC-1	pancreas:	n/a
39	chr1:80961769-80961819	NHDF-neo	bronchial:	n/a
40	chr1:81124441-81124491	SK-N-SH	brain:	n/a
41	chr1:81001617-81001667	HCM	heart:	n/a
42	chr1:80961769-80961819	ProgFib	skin:	n/a
43	chr1:80961776-80961826	HCPEpiC	choroid plexus:	n/a
44	chr1:80923103-80923153	HRE	kidney:	n/a
45	chr1:81001617-81001667	ECC-1	luminal epithelium:	n/a
46	chr1:81001617-81001667	GM12892	blood:	n/a
47	chr1:81001617-81001667	HRE	kidney:	n/a
48	chr1:80961776-80961826	RPTEC	kidney:	n/a
49	chr1:80961769-80961819	HMEC	breast:	n/a
50	chr1:80923103-80923153	CMK	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:80656975..80659221-chr1:80663008..80665270,2	K562	blood:
2	chr1:80717061..80719964-chr1:80721747..80724139,2	K562	blood:
3	chr1:80784427..80786663-chr1:80792675..80794437,2	K562	blood:
4	chr1:80908006..80910063-chr1:80913147..80915791,2	K562	blood:
5	chr1:80911280..80913153-chr1:81098711..81100773,2	MCF-7	breast:
6	chr1:80678626..80682159-chr1:80682380..80685207,3	K562	blood:
7	chr1:80928602..80929152-chr11:66112041..66112777,2	HCT-116	colon:
8	chr1:79962962..79963539-chr1:80683583..80684326,2	MCF-7	breast:
9	chr1:81001450..81003092-chr6:32940222..32942950,2	MCF-7	breast:
10	chr1:80968594..80969285-chr1:159113721..159114329,2	MCF-7	breast:
11	chr1:80678626..80682159-chr1:80682380..80685207,3	K562	blood:
12	chr1:80908006..80910063-chr1:80913147..80915791,2	K562	blood:
13	chr1:81105655..81106213-chr1:81121889..81122888,2	MCF-7	breast:
14	chr1:81070565..81072592-chr1:81090453..81092983,2	MCF-7	breast:
15	chr1:80754826..80757744-chr1:80760526..80762840,2	K562	blood:
16	chr1:80754826..80757744-chr1:80760526..80762840,2	K562	blood:
17	chr1:81105655..81106213-chr1:81121889..81122888,2	MCF-7	breast:
18	chr1:81070565..81072592-chr1:81090453..81092983,2	MCF-7	breast:
19	chr1:80380861..80381772-chr1:80785065..80785571,2	K562	blood:
20	chr1:80683192..80684047-chr1:82226087..82226734,2	MCF-7	breast:
21	chr1:80784427..80786663-chr1:80792675..80794437,2	K562	blood:
22	chr1:80656975..80659221-chr1:80663008..80665270,2	K562	blood:
23	chr1:80717061..80719964-chr1:80721747..80724139,2	K562	blood:
24	chr1:80911280..80913153-chr1:81098711..81100773,2	MCF-7	breast:
25	chr1:80879820..80881703-chr1:80888899..80891310,2	MCF-7	breast:
26	chr1:80879820..80881703-chr1:80888899..80891310,2	MCF-7	breast:

(count:46 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELTD1-8	chr1:81000663-81000937	XLOC_000883
2	lnc-LPHN2-1	chr1:81109910-81109980	XLOC_000268
3	lnc-LPHN2-1	chr1:81112248-81112471	NONHSAT004117
4	lnc-LPHN2-1	chr1:81001439-81001627	NONHSAT004118
5	lnc-LPHN2-1	chr1:81001440-81001627	XLOC_000268
6	lnc-LPHN2-10	chr1:80884836-80885061	NONHSAT004110
7	lnc-LPHN2-1	chr1:81112245-81112908	NONHSAT004118
8	lnc-LPHN2-1	chr1:81112248-81112473	XLOC_000268
9	lnc-LPHN2-1	chr1:81106969-81107086	XLOC_000268
10	lnc-LPHN2-10	chr1:80882498-80882626	l_76_chr1:80879560-80885114_adrenal
11	lnc-LPHN2-10	chr1:80778862-80778909	NONHSAT004109
12	lnc-LPHN2-1	chr1:81109910-81110038	XLOC_000268
13	lnc-LPHN2-1	chr1:81112248-81112473	XLOC_000268
14	lnc-LPHN2-1	chr1:81112248-81112473	XLOC_000268
15	lnc-LPHN2-1	chr1:81006274-81006321	XLOC_000268
16	lnc-LPHN2-10	chr1:80774028-80774215	NONHSAT004109
17	lnc-LPHN2-1	chr1:81006273-81006321	NONHSAT004118
18	lnc-LPHN2-10	chr1:80884836-80885061	NONHSAT004113
19	lnc-ELTD1-14	chr1:80929986-80930403	NONHSAT004115
20	lnc-ELTD1-13	chr1:80822563-80822636	NONHSAT004108
21	lnc-LPHN2-10	chr1:80882498-80882626	NONHSAT004110
22	lnc-LPHN2-1	chr1:81119760-81119893	NONHSAT004118
23	lnc-LPHN2-10	chr1:80882498-80882626	NONHSAT004113
24	lnc-LPHN2-1	chr1:81106968-81107086	NONHSAT004118
25	lnc-LPHN2-10	chr1:80884836-80885114	l_76_chr1:80879560-80885114_adrenal
26	lnc-LPHN2-1	chr1:81112248-81112458	NONHSAT004123
27	lnc-LPHN2-1	chr1:81109862-81110038	NONHSAT004123
28	lnc-LPHN2-1	chr1:81109910-81110038	XLOC_000268
29	lnc-LPHN2-10	chr1:80879557-80879674	NONHSAT004113
30	lnc-ELTD1-8	chr1:81049975-81050048	XLOC_000883
31	lnc-LPHN2-10	chr1:80774028-80774215	NONHSAT004110
32	lnc-ELTD1-7	chr1:80839049-80839443	XLOC_000882
33	lnc-LPHN2-1	chr1:81001424-81001627	NONHSAT004117
34	lnc-ELTD1-13	chr1:80773251-80773525	NONHSAT004108
35	lnc-LPHN2-11	chr1:80749037-80749655	NONHSAT004107
36	lnc-LPHN2-1	chr1:81109639-81110052	NONHSAT004118
37	lnc-ELTD1-7	chr1:80840122-80840306	XLOC_000882
38	lnc-LPHN2-1	chr1:81001445-81001627	XLOC_000268
39	lnc-LPHN2-1	chr1:81001440-81001627	XLOC_000268
40	lnc-LPHN2-10	chr1:80879561-80879674	l_76_chr1:80879560-80885114_adrenal
41	lnc-LPHN2-1	chr1:81109910-81110038	XLOC_000268
42	lnc-LPHN2-10	chr1:80882498-80882626	NONHSAT004109
43	lnc-LPHN2-1	chr1:81112248-81112834	XLOC_000268
44	lnc-LPHN2-1	chr1:81109910-81110038	NONHSAT004117
45	lnc-LPHN2-10	chr1:80884836-80885061	NONHSAT004109
46	lnc-LPHN2-1	chr1:81106973-81107086	XLOC_000268

No data

Variant related genes	Relation type
ENSG00000234184	TF binding region
ENSG00000227062	TF binding region
HNRNPA1P64	TF binding region
HMGB1P18	TF binding region
ENSG00000234108	TF binding region
ENSG00000224326	TF binding region
ENSG00000266033	TF binding region
ENSG00000225598	TF binding region
ENSG00000234184	CpG island
ENSG00000227062	CpG island
HNRNPA1P64	CpG island
HMGB1P18	CpG island
ENSG00000234108	CpG island
ENSG00000224326	CpG island
ENSG00000266033	CpG island
ENSG00000225598	CpG island
ENSG00000204256	chromatin interactions
ENSG00000263756	chromatin interactions
ENSG00000174744	chromatin interactions
NUFIP2	miRNA target sites

Extended variants
information (count: 7909 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:7909 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4310401	chr1:80656114-80656115	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536495053	chr1:80656140-80656141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530922621	chr1:80656141-80656142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184715402	chr1:80656156-80656157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs116741907	chr1:80656180-80656181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530273157	chr1:80656181-80656182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546888423	chr1:80656204-80656205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs199754615	chr1:80656260-80656261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79917264	chr1:80656282-80656283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146719877	chr1:80656284-80656285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs78275276	chr1:80656306-80656307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571293396	chr1:80656345-80656346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529350246	chr1:80661270-80661271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181001671	chr1:80661289-80661290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539250182	chr1:80661330-80661331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200829377	chr1:80661333-80661334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575801203	chr1:80661396-80661397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559621126	chr1:80661407-80661408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184244872	chr1:80661439-80661440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551696916	chr1:80661457-80661458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571880241	chr1:80661459-80661460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116289606	chr1:80661460-80661461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs372147733	chr1:80661491-80661492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs375174357	chr1:80661492-80661493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs33927560	chr1:80661493-80661494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs200676605	chr1:80661495-80661496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112890791	chr1:80661497-80661498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs112466229	chr1:80661498-80661499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567270063	chr1:80661518-80661519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549322492	chr1:80661529-80661530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547666546	chr1:80661549-80661550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555861579	chr1:80661553-80661554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115010724	chr1:80661555-80661556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs397779370	chr1:80665003-80665004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs201762154	chr1:80665004-80665005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs190946699	chr1:80665009-80665010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs182296111	chr1:80665088-80665089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576614181	chr1:80665101-80665102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185820091	chr1:80665240-80665241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562417037	chr1:80665289-80665290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576795911	chr1:80665355-80665356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs75370814	chr1:80665462-80665463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548250492	chr1:80665596-80665597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374522715	chr1:80665607-80665608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562102797	chr1:80665612-80665613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs371952713	chr1:80665650-80665651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs527728229	chr1:80665651-80665652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs547845702	chr1:80665663-80665664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs111741156	chr1:80665689-80665690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs12141290	chr1:80665753-80665754	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:106)

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
Ewing''s sarcoma	17952124	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
Colorectal cancer	16774939	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:533 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:80655800-80656200	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr1:80655800-80656200	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr1:80655800-80656400	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr1:80656000-80656400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr1:80661200-80661600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:80665000-80666000	Enhancers	Fetal Heart	heart
7	chr1:80668200-80668600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr1:80674600-80674800	Enhancers	Fetal Lung	lung
9	chr1:80674600-80675000	Enhancers	Ovary	ovary
10	chr1:80674800-80677200	Weak transcription	Fetal Lung	lung
11	chr1:80677200-80677800	Enhancers	Fetal Stomach	stomach
12	chr1:80677200-80678200	Enhancers	Fetal Lung	lung
13	chr1:80677400-80677800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr1:80677400-80678200	Enhancers	Fetal Kidney	kidney
15	chr1:80677400-80678400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr1:80677600-80678000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr1:80677600-80678000	Active TSS	NHDF-Ad	bronchial
18	chr1:80678200-80683000	Weak transcription	Fetal Kidney	kidney
19	chr1:80680800-80681200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr1:80681800-80682000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr1:80681800-80682600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:80682200-80683200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr1:80682600-80683000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr1:80682800-80683600	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr1:80683000-80683200	Enhancers	Fetal Kidney	kidney
26	chr1:80683000-80683800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr1:80683000-80683800	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr1:80683200-80683400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr1:80683200-80683600	Enhancers	Liver	Liver
30	chr1:80683200-80683600	Enhancers	Fetal Heart	heart
31	chr1:80683200-80683800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr1:80683200-80683800	Enhancers	Brain Angular Gyrus	brain
33	chr1:80683200-80684000	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr1:80683400-80683800	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr1:80683400-80683800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr1:80683400-80683800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr1:80683400-80683800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:80683400-80683800	Enhancers	Adipose Nuclei	Adipose
39	chr1:80683400-80683800	Enhancers	Fetal Intestine Large	intestine
40	chr1:80683400-80683800	Enhancers	Fetal Intestine Small	intestine
41	chr1:80683400-80683800	Enhancers	HMEC	breast
42	chr1:80683400-80684000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr1:80683800-80684800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr1:80683800-80684800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr1:80684000-80684200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr1:80685000-80685200	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr1:80685000-80685200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:80706600-80707000	Enhancers	Fetal Intestine Small	intestine
49	chr1:80707000-80707400	Weak transcription	Fetal Intestine Small	intestine
50	chr1:80707200-80708400	Enhancers	Fetal Intestine Large	intestine

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