Variant report

Variant	nsv1007092
Chromosome Location	chr1:221883491-221958279
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2877)
CpG islands
(count:1649)
Chromatin interactive
region (count:82)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2877 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:221934181-221934683	K562	blood:	n/a	n/a
2	ARID3A	chr1:221896474-221897430	K562	blood:	n/a	n/a
3	ARID3A	chr1:221915240-221915875	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:221949949-221950242	K562	blood:	n/a	n/a
5	ARID3A	chr1:221938966-221939099	K562	blood:	n/a	n/a
6	ARID3A	chr1:221890136-221890559	K562	blood:	n/a	n/a
7	ARID3A	chr1:221885446-221885985	K562	blood:	n/a	n/a
8	ARID3A	chr1:221916658-221917130	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:221890589-221891014	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:221884985-221884988	K562	blood:	n/a	n/a
11	ARID3A	chr1:221915692-221915921	K562	blood:	n/a	n/a
12	ARID3A	chr1:221887571-221888160	K562	blood:	n/a	n/a
13	ARID3A	chr1:221891624-221892654	HepG2	liver:	n/a	n/a
14	ARID3A	chr1:221886604-221886642	K562	blood:	n/a	n/a
15	ARID3A	chr1:221899157-221899511	K562	blood:	n/a	n/a
16	ARID3A	chr1:221912453-221912494	K562	blood:	n/a	n/a
17	ARID3A	chr1:221911312-221911334	K562	blood:	n/a	n/a
18	ARID3A	chr1:221888590-221889216	HepG2	liver:	n/a	n/a
19	ATF1	chr1:221888872-221889114	K562	blood:	n/a	n/a
20	ATF1	chr1:221914850-221915930	K562	blood:	n/a	n/a
21	ATF1	chr1:221890834-221891148	K562	blood:	n/a	n/a
22	ATF1	chr1:221896377-221897230	K562	blood:	n/a	n/a
23	ATF1	chr1:221890207-221890591	K562	blood:	n/a	n/a
24	ATF1	chr1:221949896-221950640	K562	blood:	n/a	n/a
25	ATF1	chr1:221885565-221885994	K562	blood:	n/a	n/a
26	ATF1	chr1:221934923-221935123	K562	blood:	n/a	n/a
27	ATF1	chr1:221887541-221888069	K562	blood:	n/a	n/a
28	ATF1	chr1:221910121-221910432	K562	blood:	n/a	n/a
29	ATF1	chr1:221899179-221899461	K562	blood:	n/a	n/a
30	ATF2	chr1:221927182-221927987	GM12878	blood:	n/a	n/a
31	ATF2	chr1:221915018-221916198	GM12878	blood:	n/a	n/a
32	ATF2	chr1:221948427-221948987	GM12878	blood:	n/a	n/a
33	ATF2	chr1:221899435-221900243	GM12878	blood:	n/a	n/a
34	ATF2	chr1:221899192-221900068	GM12878	blood:	n/a	n/a
35	ATF2	chr1:221914976-221917478	GM12878	blood:	n/a	n/a
36	ATF2	chr1:221916842-221917469	GM12878	blood:	n/a	n/a
37	ATF2	chr1:221929999-221931385	GM12878	blood:	n/a	n/a
38	ATF2	chr1:221927118-221927989	GM12878	blood:	n/a	n/a
39	ATF2	chr1:221915107-221916133	H1-hESC	embryonic stem cell:	n/a	n/a
40	ATF2	chr1:221930051-221931015	GM12878	blood:	n/a	n/a
41	ATF2	chr1:221934597-221935496	GM12878	blood:	n/a	n/a
42	ATF2	chr1:221934367-221935524	GM12878	blood:	n/a	n/a
43	ATF2	chr1:221885459-221886132	GM12878	blood:	n/a	n/a
44	ATF2	chr1:221948420-221948894	GM12878	blood:	n/a	n/a
45	ATF2	chr1:221915381-221916174	H1-hESC	embryonic stem cell:	n/a	n/a
46	ATF2	chr1:221888758-221889406	H1-hESC	embryonic stem cell:	n/a	n/a
47	ATF2	chr1:221885427-221886084	GM12878	blood:	n/a	n/a
48	ATF2	chr1:221950026-221951593	GM12878	blood:	n/a	n/a
49	ATF2	chr1:221886378-221886930	GM12878	blood:	n/a	n/a
50	ATF2	chr1:221949851-221952368	GM12878	blood:	n/a	n/a

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:221908735-221908785	H1-hESC	embryonic stem cell:	embryo
2	chr1:221908735-221908785	RPTEC	kidney:	n/a
3	chr1:221908735-221908785	H1-hESC	embryonic stem cell:	embryo
4	chr1:221908735-221908785	RPTEC	kidney:	n/a
5	chr1:221916686-221916736	BJ	skin:	n/a
6	chr1:221915794-221915844	HCPEpiC	choroid plexus:	n/a
7	chr1:221945814-221945864	HRCEpiC	kidney:	n/a
8	chr1:221915286-221915336	NT2-D1	testis:	n/a
9	chr1:221890431-221890481	HCM	heart:	n/a
10	chr1:221891307-221891357	H1-hESC	embryonic stem cell:	embryo
11	chr1:221916686-221916736	RPTEC	kidney:	n/a
12	chr1:221933302-221933352	HCT-116	colon:	n/a
13	chr1:221890431-221890481	PrEC	prostate:	n/a
14	chr1:221916303-221916353	Hela-S3	cervix:	n/a
15	chr1:221891307-221891357	GM19239	blood:	n/a
16	chr1:221916107-221916157	ovcar-3	ovarian:	n/a
17	chr1:221913576-221913626	ovcar-3	ovarian:	n/a
18	chr1:221916662-221916712	PrEC	prostate:	n/a
19	chr1:221886639-221886689	HUVEC	blood vessel:	n/a
20	chr1:221920271-221920321	Hepatocyte	liver:	n/a
21	chr1:221910211-221910261	AG09319	gingival:	n/a
22	chr1:221916662-221916712	H1-hESC	embryonic stem cell:	embryo
23	chr1:221886639-221886689	K562	blood:	n/a
24	chr1:221915739-221915789	HMEC	breast:	n/a
25	chr1:221910211-221910261	Hela-S3	cervix:	n/a
26	chr1:221910211-221910261	ProgFib	skin:	n/a
27	chr1:221915518-221915568	Hepatocyte	liver:	n/a
28	chr1:221915286-221915336	ECC-1	luminal epithelium:	n/a
29	chr1:221915475-221915525	HEK293	kidney:	embryo
30	chr1:221915650-221915700	AoSMC	blood vessel:	n/a
31	chr1:221920271-221920321	SKMC	muscle:	n/a
32	chr1:221915650-221915700	K562	blood:	n/a
33	chr1:221886639-221886689	GM06990	blood:	n/a
34	chr1:221890431-221890481	SKMC	muscle:	n/a
35	chr1:221916662-221916712	NHDF-neo	bronchial:	n/a
36	chr1:221916686-221916736	HIPEpiC	eye:	n/a
37	chr1:221915739-221915789	T-47D	breast:	n/a
38	chr1:221916861-221916911	A549	lung:	n/a
39	chr1:221915575-221915625	ovcar-3	ovarian:	n/a
40	chr1:221886639-221886689	HMEC	breast:	n/a
41	chr1:221912247-221912297	PANC-1	pancreas:	n/a
42	chr1:221890431-221890481	HMEC	breast:	n/a
43	chr1:221910211-221910261	SKMC	muscle:	n/a
44	chr1:221915286-221915336	HMEC	breast:	n/a
45	chr1:221920271-221920321	GM06990	blood:	n/a
46	chr1:221916861-221916911	LNCaP	prostate:	n/a
47	chr1:221915475-221915525	T-47D	breast:	n/a
48	chr1:221915355-221915405	HRE	kidney:	n/a
49	chr1:221915739-221915789	ProgFib	skin:	n/a
50	chr1:221945814-221945864	PFSK-1	brain:	n/a

(count:82 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:221915404..221918764-chr1:221918770..221924277,11	K562	blood:
2	chr1:221914930..221915875-chr7:54826862..54827555,2	Hela-S3	cervix:
3	chr1:221886064..221888475-chr1:221888570..221891136,3	K562	blood:
4	chr1:221916288..221917841-chr1:221930894..221932532,2	MCF-7	breast:
5	chr1:221887523..221889150-chr1:221891043..221892989,2	MCF-7	breast:
6	chr1:221915763..221917609-chr1:221970690..221972444,2	MCF-7	breast:
7	chr1:221886657..221890286-chr1:221915663..221918002,3	MCF-7	breast:
8	chr1:221859186..221861053-chr1:221907223..221909990,3	K562	blood:
9	chr1:221896601..221898804-chr1:221901497..221903460,2	K562	blood:
10	chr1:221950355..221953290-chr1:221957212..221959262,2	K562	blood:
11	chr1:221915140..221918678-chr1:221951678..221954670,3	K562	blood:
12	chr1:221946788..221948739-chr1:221949122..221950675,2	K562	blood:
13	chr1:221900620..221902911-chr1:221912175..221914927,2	MCF-7	breast:
14	chr1:221891993..221895094-chr1:221895705..221898533,3	K562	blood:
15	chr1:221886064..221888475-chr1:221888570..221891136,3	K562	blood:
16	chr1:221915958..221917862-chr1:221982281..221984311,2	MCF-7	breast:
17	chr1:210546811..210547476-chr1:221915732..221916703,2	Hela-S3	cervix:
18	chr1:221895265..221897996-chr1:222013655..222015689,2	K562	blood:
19	chr1:221902783..221905534-chr1:221906000..221908483,2	K562	blood:
20	chr1:221915737..221916640-chr7:100463746..100464357,2	Hela-S3	cervix:
21	chr1:221887523..221889150-chr1:221891043..221892989,2	MCF-7	breast:
22	chr1:221891993..221895094-chr1:221895705..221898533,3	K562	blood:
23	chr1:221883604..221886254-chr1:221893154..221895130,3	K562	blood:
24	chr1:221916305..221918049-chr1:221927008..221929788,2	K562	blood:
25	chr1:221921858..221923373-chr1:221925190..221928141,2	K562	blood:
26	chr1:221915847..221918268-chr1:222049176..222051061,2	K562	blood:
27	chr1:221943490..221945963-chr1:221951979..221954121,2	MCF-7	breast:
28	chr1:221915260..221918211-chr1:221931815..221934483,3	MCF-7	breast:
29	chr1:221915932..221916628-chr1:222182306..222183086,2	MCF-7	breast:
30	chr1:221882652..221891989-chr1:221912814..221917285,15	K562	blood:
31	chr1:221882812..221884320-chr1:221889796..221891918,2	MCF-7	breast:
32	chr1:221899643..221902280-chr1:221903912..221907018,3	K562	blood:
33	chr1:221856937..221858911-chr1:221881533..221884084,2	K562	blood:
34	chr1:221887650..221891571-chr1:221892438..221898117,9	K562	blood:
35	chr1:221915687..221916241-chr15:75931897..75932605,2	Hela-S3	cervix:
36	chr1:221897172..221898775-chr1:222217988..222220740,2	K562	blood:
37	chr1:221900354..221903760-chr1:221903849..221908437,4	MCF-7	breast:
38	chr1:221912612..221914842-chr1:222041850..222044308,2	MCF-7	breast:
39	chr1:221828900..221831688-chr1:221913117..221915245,2	K562	blood:
40	chr1:221915785..221917176-chr1:222059774..222060678,4	MCF-7	breast:
41	chr1:221902184..221910150-chr1:221912477..221917248,16	K562	blood:
42	chr1:221900354..221903760-chr1:221903849..221908437,4	MCF-7	breast:
43	chr1:221908849..221910394-chr1:221921201..221922958,2	K562	blood:
44	chr1:221863269..221865954-chr1:221885528..221887146,2	K562	blood:
45	chr1:221900620..221902911-chr1:221912175..221914927,2	MCF-7	breast:
46	chr1:221915773..221917564-chr1:221920253..221922492,3	MCF-7	breast:
47	chr1:221943490..221945963-chr1:221951979..221954121,2	MCF-7	breast:
48	chr1:221899643..221902280-chr1:221903912..221907018,3	K562	blood:
49	chr1:221889093..221891683-chr1:222160866..222163448,2	K562	blood:
50	chr1:221913498..221916410-chr1:221950188..221951845,2	K562	blood:

No data

Variant related genes	Relation type
DUSP10	TF binding region
DUSP10	CpG island
ENSG00000132432	chromatin interactions
ENSG00000143507	chromatin interactions
ENSG00000238042	chromatin interactions
ENSG00000234707	chromatin interactions
ENSG00000177971	chromatin interactions
ENSG00000227925	chromatin interactions

Extended variants
information (count: 2828 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2828 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12749729	chr1:221883496-221883497	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187015727	chr1:221883498-221883499	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs546008988	chr1:221883507-221883508	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs376252963	chr1:221883509-221883510	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs563513528	chr1:221883565-221883566	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs573516544	chr1:221883576-221883577	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs553028938	chr1:221883596-221883597	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs113375804	chr1:221883615-221883616	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs146319335	chr1:221883617-221883618	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs34102319	chr1:221883619-221883620	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs397863441	chr1:221883653-221883654	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs141301164	chr1:221883706-221883707	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs562378127	chr1:221883728-221883729	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371398884	chr1:221883873-221883874	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs57370939	chr1:221883885-221883886	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs529578969	chr1:221883887-221883888	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs541831244	chr1:221883896-221883897	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs563165853	chr1:221884026-221884027	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs190304530	chr1:221884208-221884209	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs145035389	chr1:221884211-221884212	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs530981743	chr1:221884239-221884240	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs528275416	chr1:221884248-221884249	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs112243227	chr1:221884249-221884250	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs555374409	chr1:221884255-221884256	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577584047	chr1:221884294-221884295	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs377324230	chr1:221884300-221884301	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs148987755	chr1:221884357-221884358	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs11118832	chr1:221884371-221884372	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs182937297	chr1:221884380-221884381	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs550827813	chr1:221884426-221884427	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs569191165	chr1:221884438-221884439	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs187611405	chr1:221884453-221884454	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs78744221	chr1:221884477-221884478	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs143753759	chr1:221884492-221884493	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs534409962	chr1:221884499-221884500	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs148177894	chr1:221884538-221884539	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs144092226	chr1:221884541-221884542	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs111549273	chr1:221884546-221884547	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs544615190	chr1:221884602-221884603	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs12068699	chr1:221884655-221884656	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs193239364	chr1:221884711-221884712	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs545738870	chr1:221884794-221884795	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs79494114	chr1:221884807-221884808	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs528138968	chr1:221884824-221884825	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs546408592	chr1:221884913-221884914	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs187862921	chr1:221884916-221884917	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs529068101	chr1:221884926-221884927	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs77054345	chr1:221884995-221884996	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs10746413	chr1:221885140-221885141	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs539451934	chr1:221885165-221885166	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	20808228	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2750 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221863800-221888600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr1:221870000-221885400	Weak transcription	NHEK	skin
3	chr1:221871200-221885800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr1:221873200-221885200	Weak transcription	NH-A	brain
5	chr1:221873800-221885200	Weak transcription	Hela-S3	cervix
6	chr1:221875400-221889600	Weak transcription	Fetal Kidney	kidney
7	chr1:221877400-221889200	Weak transcription	Colonic Mucosa	Colon
8	chr1:221878000-221885400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr1:221879400-221884600	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr1:221879400-221885000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:221879600-221886200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr1:221879600-221891000	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr1:221879600-221891800	Enhancers	Fetal Thymus	thymus
14	chr1:221879600-221902400	Enhancers	Brain Substantia Nigra	brain
15	chr1:221879800-221885200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr1:221879800-221886200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
17	chr1:221879800-221886400	Weak transcription	Spleen	Spleen
18	chr1:221879800-221887000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr1:221879800-221889000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr1:221879800-221889600	Weak transcription	Esophagus	oesophagus
21	chr1:221879800-221890200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr1:221879800-221890200	Weak transcription	Fetal Muscle Trunk	muscle
23	chr1:221879800-221896800	Enhancers	Colon Smooth Muscle	Colon
24	chr1:221880000-221886200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr1:221880000-221886200	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr1:221880000-221889600	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr1:221880200-221885400	Enhancers	Fetal Muscle Leg	muscle
28	chr1:221880200-221885600	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr1:221880200-221886400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr1:221880200-221886400	Weak transcription	Aorta	Aorta
31	chr1:221880200-221889200	Weak transcription	Right Atrium	heart
32	chr1:221880400-221885800	Enhancers	Primary T cells from cord blood	blood
33	chr1:221880400-221886000	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr1:221880400-221886200	Enhancers	Dnd41	blood
35	chr1:221880400-221886600	Enhancers	Brain Anterior Caudate	brain
36	chr1:221880400-221893200	Enhancers	Primary hematopoietic stem cells	blood
37	chr1:221880600-221883600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr1:221880800-221884200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr1:221880800-221884800	Weak transcription	NHDF-Ad	bronchial
40	chr1:221880800-221887600	Enhancers	Liver	Liver
41	chr1:221881000-221888600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:221881400-221884400	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr1:221881400-221885800	Enhancers	Stomach Mucosa	stomach
44	chr1:221881400-221886600	Enhancers	Duodenum Smooth Muscle	Duodenum
45	chr1:221881400-221886800	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr1:221881400-221887400	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr1:221881400-221888200	Enhancers	HepG2	liver
48	chr1:221881600-221884200	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr1:221881600-221884600	Enhancers	Brain Germinal Matrix	brain
50	chr1:221881600-221885400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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