Variant report

Variant	nsv1042550
Chromosome Location	chr12:123532028-123659500
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2758)
CpG islands
(count:2319)
Chromatin interactive
region (count:287)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:2758 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:123547002-123547854	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:123576824-123577183	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:123576962-123577116	K562	blood:	n/a	n/a
4	ARID3A	chr12:123611130-123611552	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:123625448-123625929	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:123634019-123634327	K562	blood:	n/a	n/a
7	ARID3A	chr12:123626226-123626861	HepG2	liver:	n/a	n/a
8	ARID3A	chr12:123579275-123579660	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:123574297-123574716	HepG2	liver:	n/a	n/a
10	ARID3A	chr12:123610933-123611537	K562	blood:	n/a	n/a
11	ARID3A	chr12:123574392-123574918	K562	blood:	n/a	n/a
12	ATF1	chr12:123576955-123577039	K562	blood:	n/a	n/a
13	ATF1	chr12:123611055-123611488	K562	blood:	n/a	n/a
14	ATF1	chr12:123579303-123579533	K562	blood:	n/a	n/a
15	ATF1	chr12:123574279-123574896	K562	blood:	n/a	n/a
16	ATF1	chr12:123600183-123600663	K562	blood:	n/a	n/a
17	ATF2	chr12:123604315-123604780	GM12878	blood:	n/a	n/a
18	ATF2	chr12:123599870-123600506	GM12878	blood:	n/a	n/a
19	ATF2	chr12:123648444-123649206	GM12878	blood:	n/a	n/a
20	ATF3	chr12:123574295-123574499	K562	blood:	n/a	n/a
21	ATF3	chr12:123626151-123627053	A549	lung:	n/a	n/a
22	ATF3	chr12:123626506-123626822	K562	blood:	n/a	n/a
23	ATF3	chr12:123574148-123574565	K562	blood:	n/a	n/a
24	ATF3	chr12:123611037-123611446	K562	blood:	n/a	n/a
25	BACH1	chr12:123577090-123577103	K562	blood:	n/a	n/a
26	BACH1	chr12:123610847-123611525	K562	blood:	n/a	n/a
27	BACH1	chr12:123634748-123634916	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr12:123610988-123611789	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr12:123540704-123540780	K562	blood:	n/a	chr12:123540714-123540728
30	BATF	chr12:123604415-123604682	GM12878	blood:	n/a	n/a
31	BATF	chr12:123604384-123604758	GM12878	blood:	n/a	n/a
32	BCL3	chr12:123579077-123579780	A549	lung:	n/a	n/a
33	BCL3	chr12:123635804-123636673	A549	lung:	n/a	chr12:123635880-123635893 chr12:123635879-123635888 chr12:123635882-123635891
34	BCL3	chr12:123635853-123636704	A549	lung:	n/a	chr12:123635880-123635893 chr12:123635879-123635888 chr12:123635882-123635891
35	BCL3	chr12:123626139-123627079	A549	lung:	n/a	n/a
36	BCL3	chr12:123626118-123627170	A549	lung:	n/a	n/a
37	BCL3	chr12:123570170-123570834	A549	lung:	n/a	n/a
38	BCL3	chr12:123578929-123579736	A549	lung:	n/a	n/a
39	BCL3	chr12:123635797-123636581	GM12878	blood:	n/a	chr12:123635880-123635893 chr12:123635879-123635888 chr12:123635882-123635891
40	BCLAF1	chr12:123604394-123604768	GM12878	blood:	n/a	n/a
41	BCLAF1	chr12:123636108-123636415	GM12878	blood:	n/a	n/a
42	BHLHE40	chr12:123634019-123634309	K562	blood:	n/a	n/a
43	BHLHE40	chr12:123579297-123579664	K562	blood:	n/a	n/a
44	BHLHE40	chr12:123635332-123635746	K562	blood:	n/a	chr12:123635487-123635503
45	BHLHE40	chr12:123635350-123635686	HepG2	liver:	n/a	chr12:123635487-123635503
46	BHLHE40	chr12:123633179-123633276	K562	blood:	n/a	n/a
47	BHLHE40	chr12:123540738-123540901	K562	blood:	n/a	n/a
48	BHLHE40	chr12:123611076-123611582	K562	blood:	n/a	n/a
49	BHLHE40	chr12:123570409-123570469	A549	lung:	n/a	n/a
50	BHLHE40	chr12:123561828-123562145	K562	blood:	n/a	n/a

(count:2319 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:123595122-123595172	GM12892	blood:	n/a
2	chr12:123595122-123595172	GM12892	blood:	n/a
3	chr12:123636175-123636225	RPTEC	kidney:	n/a
4	chr12:123579358-123579408	ProgFib	skin:	n/a
5	chr12:123636279-123636329	AG09319	gingival:	n/a
6	chr12:123595122-123595172	HCF	heart:	n/a
7	chr12:123596413-123596463	ProgFib	skin:	n/a
8	chr12:123582277-123582327	NB4	blood:	n/a
9	chr12:123596413-123596463	HRPEpiC	eye:	n/a
10	chr12:123637556-123637606	SK-N-SH_RA	brain:	n/a
11	chr12:123560479-123560529	HepG2	liver:	n/a
12	chr12:123569118-123569168	U87	brain:	n/a
13	chr12:123636175-123636225	HepG2	liver:	n/a
14	chr12:123601893-123601943	HEK293	kidney:	embryo
15	chr12:123616817-123616867	AG09309	skin:	n/a
16	chr12:123626132-123626182	T-47D	breast:	n/a
17	chr12:123636279-123636329	HL-60	blood:	n/a
18	chr12:123637556-123637606	CMK	blood:	n/a
19	chr12:123599873-123599923	GM12891	blood:	n/a
20	chr12:123599873-123599923	MCF10A-Er-Src	breast:	n/a
21	chr12:123636505-123636555	GM19239	blood:	n/a
22	chr12:123636505-123636555	NH-A	brain:	n/a
23	chr12:123634957-123635007	ECC-1	luminal epithelium:	n/a
24	chr12:123616817-123616867	A549	lung:	n/a
25	chr12:123595647-123595697	BE2_C	brain:	n/a
26	chr12:123634957-123635007	ovcar-3	ovarian:	n/a
27	chr12:123634159-123634209	HNPCEpiC	eye:	n/a
28	chr12:123633142-123633192	Hela-S3	cervix:	n/a
29	chr12:123587316-123587366	SK-N-SH	brain:	n/a
30	chr12:123632825-123632875	HL-60	blood:	n/a
31	chr12:123636480-123636530	H1-hESC	embryonic stem cell:	embryo
32	chr12:123636505-123636555	GM12892	blood:	n/a
33	chr12:123626132-123626182	NHDF-neo	bronchial:	n/a
34	chr12:123633142-123633192	HCM	heart:	n/a
35	chr12:123587316-123587366	HCF	heart:	n/a
36	chr12:123636480-123636530	HEEpiC	esophagus:	n/a
37	chr12:123639610-123639660	PFSK-1	brain:	n/a
38	chr12:123634957-123635007	K562	blood:	n/a
39	chr12:123634384-123634434	SAEC	small airway:	n/a
40	chr12:123616817-123616867	RPTEC	kidney:	n/a
41	chr12:123610989-123611039	HEEpiC	esophagus:	n/a
42	chr12:123596413-123596463	SAEC	small airway:	n/a
43	chr12:123634159-123634209	RPTEC	kidney:	n/a
44	chr12:123635215-123635265	PFSK-1	brain:	n/a
45	chr12:123595024-123595074	H1-hESC	embryonic stem cell:	embryo
46	chr12:123610989-123611039	NHDF-neo	bronchial:	n/a
47	chr12:123587316-123587366	GM19239	blood:	n/a
48	chr12:123548027-123548077	LNCaP	prostate:	n/a
49	chr12:123636480-123636530	PANC-1	pancreas:	n/a
50	chr12:123634159-123634209	GM19239	blood:	n/a

(count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr12:123609922..123611870-chr12:123629946..123632018,2	K562	blood:
2	chr12:123633130..123634910-chr12:123716201..123717715,2	K562	blood:
3	chr12:123458168..123460396-chr12:123636633..123638279,2	K562	blood:
4	chr12:123634522..123637208-chr12:123639726..123642249,4	K562	blood:
5	chr12:123626633..123628310-chr12:123628394..123630305,2	MCF-7	breast:
6	chr12:123553938..123556177-chr12:123569244..123571363,2	MCF-7	breast:
7	chr12:123588003..123590511-chr12:123634129..123636612,2	MCF-7	breast:
8	chr12:123582057..123584351-chr12:123601284..123603250,2	MCF-7	breast:
9	chr12:123583370..123585384-chr12:123598007..123600028,3	K562	blood:
10	chr12:123635735..123637727-chr12:123641892..123644139,3	MCF-7	breast:
11	chr12:123596283..123598515-chr17:56735298..56737640,2	MCF-7	breast:
12	chr12:123588003..123590511-chr12:123634129..123636612,2	MCF-7	breast:
13	chr12:123518174..123520749-chr12:123540012..123542472,2	MCF-7	breast:
14	chr12:123564490..123568285-chr12:123569418..123571923,3	MCF-7	breast:
15	chr12:123554110..123555021-chr12:123590854..123591747,3	MCF-7	breast:
16	chr12:123616507..123619286-chr12:123631305..123632986,2	K562	blood:
17	chr12:123572033..123574243-chr12:123627306..123629802,2	MCF-7	breast:
18	chr12:123574636..123576162-chr12:123864283..123866660,2	K562	blood:
19	chr12:123574271..123575945-chr12:123599295..123601794,2	MCF-7	breast:
20	chr12:123575945..123576658-chr12:123634764..123635731,2	K562	blood:
21	chr12:123574271..123575945-chr12:123599295..123601794,2	MCF-7	breast:
22	chr12:123546470..123548882-chr12:123596558..123599374,2	MCF-7	breast:
23	chr12:123527736..123529546-chr12:123540101..123542162,2	K562	blood:
24	chr12:123568355..123570038-chr12:123635637..123637696,2	MCF-7	breast:
25	chr12:123634064..123637299-chr12:123639365..123644376,5	K562	blood:
26	chr12:123544510..123545444-chr12:123554166..123554840,5	MCF-7	breast:
27	chr12:123538667..123541322-chr12:123544543..123546513,3	K562	blood:
28	chr12:123544559..123546655-chr12:123548613..123551754,3	K562	blood:
29	chr12:123604029..123607309-chr12:123609256..123611485,3	K562	blood:
30	chr12:123517171..123520609-chr12:123634791..123638617,3	K562	blood:
31	chr12:123578771..123581154-chr12:123581766..123585014,3	MCF-7	breast:
32	chr12:123547606..123549243-chr12:123635108..123637286,2	MCF-7	breast:
33	chr12:123550533..123552152-chr12:123560273..123563222,2	MCF-7	breast:
34	chr12:123558968..123563276-chr12:123716606..123719909,6	MCF-7	breast:
35	chr12:123583370..123585384-chr12:123598007..123600028,3	K562	blood:
36	chr12:123597677..123600543-chr12:123624922..123626506,2	K562	blood:
37	chr12:123601823..123603521-chr12:123605557..123608187,2	K562	blood:
38	chr12:123603321..123605934-chr12:123608527..123611657,3	K562	blood:
39	chr12:123574871..123577625-chr12:123635000..123637260,3	MCF-7	breast:
40	chr12:123583688..123586086-chr12:123633435..123635135,2	K562	blood:
41	chr12:123557220..123559958-chr12:123582515..123585405,2	MCF-7	breast:
42	chr12:123547184..123547743-chr12:123557921..123558809,2	MCF-7	breast:
43	chr12:123597677..123600543-chr12:123624922..123626506,2	K562	blood:
44	chr12:123555442..123558076-chr12:123754275..123756423,2	MCF-7	breast:
45	chr12:123574363..123577127-chr12:123716097..123719008,3	K562	blood:
46	chr12:123594098..123598804-chr12:123600213..123604964,5	K562	blood:
47	chr12:123628455..123632767-chr12:123632779..123636840,7	MCF-7	breast:
48	chr12:123582057..123584351-chr12:123601284..123603250,2	MCF-7	breast:
49	chr12:123500117..123502770-chr12:123590126..123592827,2	K562	blood:
50	chr12:123592814..123595580-chr12:123611489..123613555,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARL6IP4-1	chr12:123568171-123568369	NONHSAT031564
2	lnc-ARL6IP4-1	chr12:123567265-123567506	NONHSAT031562
3	lnc-MPHOSPH9-1	chr12:123638929-123638977	NONHSAT031566
4	lnc-C12orf65-2	chr12:123611829-123612163	NONHSAT031565
5	lnc-ARL6IP4-1	chr12:123567755-123568067	NONHSAT031562
6	lnc-ARL6IP4-1	chr12:123567337-123567506	ENSG00000251497
7	lnc-ARL6IP4-1	chr12:123568859-123569285	NONHSAT031564
8	lnc-ARL6IP4-1	chr12:123567782-123568676	ENSG00000251497
9	lnc-MPHOSPH9-1	chr12:123636867-123637172	NONHSAT031566
10	lnc-MPHOSPH9-1	chr12:123640235-123640363	NONHSAT031566

No data

(count:8 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	MPHOSPH9	hsa-miR-340-5p	chr12:123641008-123641030
2	MPHOSPH9	hsa-miR-340-5p	chr12:123641208-123641229
3	MPHOSPH9	hsa-miR-130b-3p	chr12:123641318-123641311
4	MPHOSPH9	hsa-miR-130b-3p	chr12:123641312-123641331
5	MPHOSPH9	hsa-miR-340-5p	chr12:123641098-123641117
6	MPHOSPH9	hsa-miR-19b-3p	chr12:123641319-123641313
7	MPHOSPH9	hsa-miR-19b-3p	chr12:123641313-123641340
8	MPHOSPH9	hsa-miR-340-5p	chr12:123641262-123641283

Variant related genes	Relation type
PITPNM2	TF binding region
ENSG00000251497	TF binding region
MPHOSPH9	TF binding region
PITPNM2	CpG island
ENSG00000251497	CpG island
MPHOSPH9	CpG island
ENSG00000104147	chromatin interactions
ENSG00000111325	chromatin interactions
ENSG00000130921	chromatin interactions
ENSG00000265603	chromatin interactions
ENSG00000150967	chromatin interactions
ENSG00000111666	chromatin interactions
ENSG00000111364	chromatin interactions
ENSG00000130787	chromatin interactions
ENSG00000090975	chromatin interactions
ENSG00000256028	chromatin interactions
ENSG00000111328	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000182196	chromatin interactions
ENSG00000051825	chromatin interactions
ENSG00000137804	chromatin interactions
ENSG00000251497	chromatin interactions
SETD1B	miRNA target sites
KATNAL1	miRNA target sites

Extended variants
information (count: 4073 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:4073 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563638961	chr12:123532053-123532054	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs80326885	chr12:123532142-123532143	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs542561780	chr12:123532147-123532148	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs560742461	chr12:123532162-123532163	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs528153752	chr12:123532190-123532191	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs117801578	chr12:123532260-123532261	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs145507864	chr12:123532304-123532305	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs565134359	chr12:123532321-123532322	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs35228599	chr12:123532324-123532325	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs76401309	chr12:123532419-123532420	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs532609610	chr12:123532460-123532461	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs575163343	chr12:123532475-123532476	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs550771824	chr12:123532494-123532495	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs12305187	chr12:123532507-123532508	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs536568176	chr12:123532569-123532570	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs150231543	chr12:123532583-123532584	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566790284	chr12:123532591-123532592	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534261575	chr12:123532615-123532616	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371231711	chr12:123532675-123532676	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184896843	chr12:123532680-123532681	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529289498	chr12:123532733-123532734	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190189653	chr12:123532738-123532739	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs75377581	chr12:123532770-123532771	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538795718	chr12:123532857-123532858	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs138887780	chr12:123532917-123532918	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537573133	chr12:123532921-123532922	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs556879877	chr12:123532948-123532949	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529808841	chr12:123532959-123532960	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374814911	chr12:123532982-123532983	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554648346	chr12:123532984-123532985	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11061549	chr12:123532991-123532992	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs367724804	chr12:123533001-123533002	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560922767	chr12:123533004-123533005	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572550127	chr12:123533045-123533046	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574727801	chr12:123533051-123533052	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539930917	chr12:123533054-123533055	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564597845	chr12:123533057-123533058	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs372149289	chr12:123533058-123533059	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs532083272	chr12:123533062-123533063	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540438613	chr12:123533070-123533071	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562958509	chr12:123533104-123533105	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530408535	chr12:123533105-123533106	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548626896	chr12:123533108-123533109	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566853733	chr12:123533180-123533181	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs527725486	chr12:123533181-123533182	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552611893	chr12:123533200-123533201	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs12819217	chr12:123533202-123533203	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs192271576	chr12:123533213-123533214	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs71444568	chr12:123533239-123533240	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs577232678	chr12:123533246-123533247	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Ependymoma	20639864	CNVD
head and neck squamous cell carcinoma	24351288	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:5642 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123504400-123540200	Weak transcription	Hela-S3	cervix
2	chr12:123518200-123535600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:123518400-123533600	Weak transcription	Aorta	Aorta
4	chr12:123518800-123540600	Weak transcription	HepG2	liver
5	chr12:123519000-123540400	Weak transcription	Gastric	stomach
6	chr12:123519000-123543400	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr12:123528200-123542400	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr12:123528400-123534000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr12:123528600-123534000	Weak transcription	Fetal Brain Female	brain
10	chr12:123528600-123534000	Weak transcription	Pancreas	Pancrea
11	chr12:123528600-123545800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr12:123528800-123533800	Weak transcription	HSMMtube	muscle
13	chr12:123528800-123535200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr12:123528800-123541400	Weak transcription	Primary B cells from peripheral blood	blood
15	chr12:123529000-123533800	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr12:123529000-123534200	Weak transcription	Osteobl	bone
17	chr12:123529000-123534800	Weak transcription	A549	lung
18	chr12:123529000-123535400	Weak transcription	Fetal Intestine Small	intestine
19	chr12:123529000-123540400	Weak transcription	Duodenum Mucosa	Duodenum
20	chr12:123529200-123533800	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr12:123529200-123533800	Weak transcription	NHDF-Ad	bronchial
22	chr12:123529200-123534000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr12:123529200-123534200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr12:123529200-123534400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr12:123529200-123534400	Weak transcription	NHLF	lung
26	chr12:123529200-123534600	Weak transcription	Adipose Nuclei	Adipose
27	chr12:123529400-123538800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr12:123529400-123544600	Weak transcription	Small Intestine	intestine
29	chr12:123529600-123533800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr12:123529600-123534000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr12:123529600-123546200	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr12:123529800-123535000	Weak transcription	Spleen	Spleen
33	chr12:123529800-123537800	Genic enhancers	Fetal Thymus	thymus
34	chr12:123529800-123548200	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr12:123530000-123534000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr12:123530200-123532200	Enhancers	Brain Substantia Nigra	brain
37	chr12:123530200-123533800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr12:123530200-123538800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr12:123530400-123532200	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr12:123530400-123533200	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr12:123530600-123533400	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr12:123530600-123533600	Weak transcription	HSMM	muscle
43	chr12:123530600-123533800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr12:123530800-123532200	Weak transcription	Left Ventricle	heart
45	chr12:123530800-123533600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr12:123530800-123533800	Weak transcription	Fetal Muscle Leg	muscle
47	chr12:123530800-123533800	Weak transcription	Lung	lung
48	chr12:123530800-123533800	Weak transcription	Psoas Muscle	Psoas
49	chr12:123530800-123540600	Weak transcription	Colonic Mucosa	Colon
50	chr12:123530800-123544600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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