Variant report

Variant	nsv524737
Chromosome Location	chr12:31399901-31464663
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1221)
CpG islands
(count:611)
Chromatin interactive
region (count:68)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:31424813-31425127	HepG2	liver:	n/a	n/a
2	ATF1	chr12:31424834-31425154	K562	blood:	n/a	n/a
3	ATF1	chr12:31459821-31460139	K562	blood:	n/a	n/a
4	ATF2	chr12:31432337-31432818	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr12:31450683-31451065	GM12878	blood:	n/a	n/a
6	BACH1	chr12:31456606-31456794	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr12:31464252-31464443	K562	blood:	n/a	n/a
8	BACH1	chr12:31457232-31457259	K562	blood:	n/a	n/a
9	BATF	chr12:31424868-31425107	GM12878	blood:	n/a	n/a
10	BATF	chr12:31434747-31435076	GM12878	blood:	n/a	n/a
11	BATF	chr12:31453298-31453548	GM12878	blood:	n/a	n/a
12	BATF	chr12:31453296-31453675	GM12878	blood:	n/a	n/a
13	BATF	chr12:31434733-31435004	GM12878	blood:	n/a	n/a
14	BHLHE40	chr12:31430083-31430222	K562	blood:	n/a	n/a
15	BHLHE40	chr12:31418855-31418967	K562	blood:	n/a	n/a
16	BHLHE40	chr12:31450670-31451865	GM12878	blood:	n/a	n/a
17	BHLHE40	chr12:31424468-31424644	K562	blood:	n/a	n/a
18	BRCA1	chr12:31457627-31458118	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr12:31427493-31427774	A549	lung:	n/a	n/a
20	CEBPB	chr12:31414835-31414948	K562	blood:	n/a	n/a
21	CEBPB	chr12:31458243-31458606	K562	blood:	n/a	chr12:31458424-31458435
22	CEBPB	chr12:31401755-31402127	A549	lung:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
23	CEBPB	chr12:31458289-31458607	A549	lung:	n/a	chr12:31458424-31458435
24	CEBPB	chr12:31458270-31458536	HepG2	liver:	n/a	chr12:31458424-31458435
25	CEBPB	chr12:31458256-31458534	Hela-S3	cervix:	n/a	chr12:31458424-31458435
26	CEBPB	chr12:31401830-31402026	HepG2	liver:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
27	CEBPB	chr12:31427540-31427765	HepG2	liver:	n/a	n/a
28	CEBPB	chr12:31401823-31402021	Hela-S3	cervix:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
29	CEBPB	chr12:31424820-31425080	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr12:31459997-31460027	K562	blood:	n/a	n/a
31	CEBPB	chr12:31458255-31458574	K562	blood:	n/a	chr12:31458424-31458435
32	CHD2	chr12:31432406-31433417	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr12:31436720-31436759	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr12:31459650-31459734	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr12:31424765-31425200	H1-hESC	embryonic stem cell:	n/a	chr12:31424980-31424993
36	CREB1	chr12:31424733-31425219	H1-hESC	embryonic stem cell:	n/a	chr12:31424980-31424993
37	CTCF	chr12:31425274-31425327	GM19240	blood:	n/a	n/a
38	CTCF	chr12:31405360-31405510	GM12867	blood:	n/a	n/a
39	CTCF	chr12:31404726-31404837	K562	blood:	n/a	chr12:31404806-31404827 chr12:31404804-31404822 chr12:31404809-31404817
40	CTCF	chr12:31424920-31425070	GM12865	blood:	n/a	chr12:31424995-31425011 chr12:31425001-31425008 chr12:31424989-31425010 chr12:31424996-31425009 chr12:31424994-31425012
41	CTCF	chr12:31424880-31425030	NHLF	lung:	n/a	chr12:31424995-31425011 chr12:31425001-31425008 chr12:31424989-31425010 chr12:31424996-31425009 chr12:31424994-31425012
42	CTCF	chr12:31404780-31404930	GM12873	blood:	n/a	chr12:31404806-31404827 chr12:31404804-31404822 chr12:31404809-31404817
43	CTCF	chr12:31424940-31425090	NB4	blood:	n/a	chr12:31424995-31425011 chr12:31425001-31425008 chr12:31424989-31425010 chr12:31424996-31425009 chr12:31424994-31425012
44	CTCF	chr12:31404720-31404870	HCPEpiC	choroid plexus:	n/a	chr12:31404806-31404827 chr12:31404804-31404822 chr12:31404809-31404817
45	CTCF	chr12:31405300-31405450	GM12869	blood:	n/a	n/a
46	CTCF	chr12:31424940-31425090	MCF-7	breast:	n/a	chr12:31424995-31425011 chr12:31425001-31425008 chr12:31424989-31425010 chr12:31424996-31425009 chr12:31424994-31425012
47	CTCF	chr12:31405338-31405586	MCF-7	breast:	n/a	n/a
48	CTCF	chr12:31405011-31405013	Gliobla	brain:	n/a	n/a
49	CTCF	chr12:31424944-31425124	MCF-7	breast:	n/a	chr12:31424995-31425011 chr12:31425001-31425008 chr12:31424989-31425010 chr12:31424996-31425009 chr12:31424994-31425012
50	CTCF	chr12:31425020-31425170	A549	lung:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31406441-31406491	HAEpiC	amniotic membrane:	n/a
2	chr12:31406441-31406491	HAEpiC	amniotic membrane:	n/a
3	chr12:31405369-31405419	HUVEC	blood vessel:	n/a
4	chr12:31405369-31405419	CMK	blood:	n/a
5	chr12:31412980-31413030	GM12891	blood:	n/a
6	chr12:31405359-31405409	PrEC	prostate:	n/a
7	chr12:31456880-31456930	HIPEpiC	eye:	n/a
8	chr12:31405369-31405419	PANC-1	pancreas:	n/a
9	chr12:31405369-31405419	HNPCEpiC	eye:	n/a
10	chr12:31432493-31432543	MCF-7	breast:	n/a
11	chr12:31412980-31413030	HCT-116	colon:	n/a
12	chr12:31456880-31456930	HEEpiC	esophagus:	n/a
13	chr12:31453901-31453951	SK-N-SH	brain:	n/a
14	chr12:31405359-31405409	HRE	kidney:	n/a
15	chr12:31405499-31405549	HAEpiC	amniotic membrane:	n/a
16	chr12:31405359-31405409	HEEpiC	esophagus:	n/a
17	chr12:31406441-31406491	HPAEpiC	pulmonary alveolar:	n/a
18	chr12:31432493-31432543	NHBE	bronchial:	n/a
19	chr12:31412980-31413030	MCF-7	breast:	n/a
20	chr12:31456880-31456930	BJ	skin:	n/a
21	chr12:31412980-31413030	HRCEpiC	kidney:	n/a
22	chr12:31412980-31413030	HRE	kidney:	n/a
23	chr12:31453901-31453951	GM06990	blood:	n/a
24	chr12:31423331-31423381	GM12892	blood:	n/a
25	chr12:31402470-31402520	SAEC	small airway:	n/a
26	chr12:31412980-31413030	NT2-D1	testis:	n/a
27	chr12:31412980-31413030	ECC-1	luminal epithelium:	n/a
28	chr12:31405369-31405419	HepG2	liver:	n/a
29	chr12:31406441-31406491	PANC-1	pancreas:	n/a
30	chr12:31423331-31423381	AG04450	lung:	fetal
31	chr12:31453901-31453951	NHDF-neo	bronchial:	n/a
32	chr12:31412980-31413030	HIPEpiC	eye:	n/a
33	chr12:31405359-31405409	HCPEpiC	choroid plexus:	n/a
34	chr12:31405499-31405549	AoSMC	blood vessel:	n/a
35	chr12:31412980-31413030	Hela-S3	cervix:	n/a
36	chr12:31405369-31405419	Jurkat	blood:	n/a
37	chr12:31402470-31402520	K562	blood:	n/a
38	chr12:31456880-31456930	HMEC	breast:	n/a
39	chr12:31423331-31423381	PFSK-1	brain:	n/a
40	chr12:31432493-31432543	ECC-1	luminal epithelium:	n/a
41	chr12:31405499-31405549	T-47D	breast:	n/a
42	chr12:31405359-31405409	ovcar-3	ovarian:	n/a
43	chr12:31405369-31405419	NB4	blood:	n/a
44	chr12:31406441-31406491	HCM	heart:	n/a
45	chr12:31412980-31413030	Jurkat	blood:	n/a
46	chr12:31405359-31405409	BE2_C	brain:	n/a
47	chr12:31405499-31405549	GM12878	blood:	n/a
48	chr12:31432493-31432543	ovcar-3	ovarian:	n/a
49	chr12:31402470-31402520	HCF	heart:	n/a
50	chr12:31432493-31432543	HMEC	breast:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:31458676..31462198-chr12:31475765..31478520,3	MCF-7	breast:
2	chr12:31424677..31426502-chr12:31428387..31431315,2	MCF-7	breast:
3	chr12:31440764..31443611-chr12:31446917..31448867,2	MCF-7	breast:
4	chr12:31450718..31452727-chr12:31455647..31457589,2	K562	blood:
5	chr12:31446277..31448012-chr12:31451966..31453945,2	K562	blood:
6	chr12:31420076..31422123-chr12:31458375..31460920,2	K562	blood:
7	chr12:31426550..31428867-chr8:91672656..91674769,2	MCF-7	breast:
8	chr12:31449988..31452418-chr12:31453015..31455328,4	K562	blood:
9	chr12:31431180..31432893-chr12:31435348..31438237,2	K562	blood:
10	chr12:31399094..31400618-chr12:31401527..31404209,2	K562	blood:
11	chr12:31399111..31400912-chr12:31476871..31479529,2	MCF-7	breast:
12	chr12:31456079..31458429-chr12:31476738..31479053,3	MCF-7	breast:
13	chr12:31402402..31404809-chr12:31411238..31413851,2	K562	blood:
14	chr12:31442106..31444745-chr12:31447754..31449545,2	K562	blood:
15	chr12:31403415..31403922-chr12:31424976..31425527,2	MCF-7	breast:
16	chr12:31444404..31449296-chr12:31476824..31481020,5	K562	blood:
17	chr12:31433746..31435306-chr12:31477957..31479847,2	MCF-7	breast:
18	chr12:31442106..31444745-chr12:31447754..31449545,2	K562	blood:
19	chr12:31269688..31270486-chr12:31404974..31405959,2	K562	blood:
20	chr12:31431407..31434228-chr12:31440191..31441794,2	MCF-7	breast:
21	chr12:31442055..31443948-chr12:31476343..31479106,2	MCF-7	breast:
22	chr12:31406545..31409230-chr12:31409522..31411986,2	MCF-7	breast:
23	chr12:31444617..31448853-chr12:31477609..31479787,4	MCF-7	breast:
24	chr12:31453022..31454953-chr12:31477543..31481718,3	K562	blood:
25	chr12:31455579..31460655-chr12:31474962..31479501,11	K562	blood:
26	chr12:31441936..31444471-chr12:31461300..31463621,2	K562	blood:
27	chr12:31451753..31453567-chr12:31463488..31465030,2	MCF-7	breast:
28	chr12:31431393..31434433-chr12:31435348..31438398,4	K562	blood:
29	chr12:31436681..31438944-chr12:31454544..31456802,2	K562	blood:
30	chr12:31447793..31455081-chr12:31455286..31461328,11	K562	blood:
31	chr12:31424984..31425698-chr12:31516137..31516810,2	MCF-7	breast:
32	chr12:31452762..31457432-chr12:31476482..31479243,5	MCF-7	breast:
33	chr12:31427531..31430100-chr12:31477192..31479203,2	K562	blood:
34	chr12:31445698..31447861-chr12:31473678..31476194,2	K562	blood:
35	chr12:31447880..31450711-chr12:31459405..31461625,2	K562	blood:
36	chr12:31437269..31440946-chr12:31476584..31478708,4	K562	blood:
37	chr12:31431393..31434433-chr12:31435348..31438398,4	K562	blood:
38	chr12:31402332..31404405-chr12:31413108..31415272,2	MCF-7	breast:
39	chr12:31399094..31400618-chr12:31401527..31404209,2	K562	blood:
40	chr12:31402402..31404809-chr12:31411238..31413851,2	K562	blood:
41	chr12:31402332..31404405-chr12:31413108..31415272,2	MCF-7	breast:
42	chr12:31438960..31441635-chr12:31476120..31479078,4	MCF-7	breast:
43	chr12:31403415..31403922-chr12:31424976..31425527,2	MCF-7	breast:
44	chr12:31447880..31450711-chr12:31459405..31461625,2	K562	blood:
45	chr12:31429753..31431642-chr12:31477161..31479179,2	MCF-7	breast:
46	chr12:31449879..31452217-chr12:31476391..31478263,2	MCF-7	breast:
47	chr12:31412613..31414977-chr12:31423446..31425840,2	K562	blood:
48	chr12:31424677..31426502-chr12:31428387..31431315,2	MCF-7	breast:
49	chr12:31420076..31422123-chr12:31458375..31460920,2	K562	blood:
50	chr12:31452911..31456081-chr12:31461692..31465766,4	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DENND5B-3	chr12:31456429-31458057	NONHSAT027543
2	lnc-AC024940.1-2	chr12:31464551-31464763	NONHSAT027545
3	lnc-FAM60A-2	chr12:31407684-31407996	ucscGeneNc_uc001rkg_2
4	lnc-FAM60A-2	chr12:31412950-31413502	ucscGeneNc_uc001rkg_2

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	FAM60A	hsa-miR-320a	chr12:31433853-31433872
2	FAM60A	hsa-miR-320a	chr12:31434102-31434124

Variant related genes	Relation type
ENSG00000238661	TF binding region
ENSG00000270395	TF binding region
FAM60A	TF binding region
ENSG00000243517	TF binding region
ENSG00000256176	TF binding region
ENSG00000238661	CpG island
ENSG00000270395	CpG island
FAM60A	CpG island
ENSG00000243517	CpG island
ENSG00000256176	CpG island
ENSG00000177340	chromatin interactions
ENSG00000256176	chromatin interactions
ENSG00000177359	chromatin interactions
ENSG00000139146	chromatin interactions
ENSG00000270395	chromatin interactions
ENSG00000243517	chromatin interactions
ENSG00000238661	chromatin interactions

Extended variants
information (count: 2547 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2547 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs713334	chr12:31399901-31399902	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531833077	chr12:31399936-31399937	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs180688483	chr12:31399939-31399940	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs571766767	chr12:31399967-31399968	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs78558703	chr12:31399992-31399993	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs116477894	chr12:31399993-31399994	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs563380257	chr12:31400008-31400009	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs536592030	chr12:31400026-31400027	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs554931906	chr12:31400049-31400050	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs530567528	chr12:31400061-31400062	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs574900941	chr12:31400118-31400119	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs550511795	chr12:31400126-31400127	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs186360477	chr12:31400148-31400149	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs727437	chr12:31400171-31400172	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs540038053	chr12:31400218-31400219	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs560322907	chr12:31400245-31400246	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs12321108	chr12:31400268-31400269	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs542984680	chr12:31400278-31400279	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs562831804	chr12:31400284-31400285	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs531742118	chr12:31400295-31400296	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs190760947	chr12:31400331-31400332	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs565253345	chr12:31400334-31400335	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs527823152	chr12:31400377-31400378	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs34136827	chr12:31400395-31400396	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs199545598	chr12:31400396-31400397	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs200991023	chr12:31400397-31400398	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs397850523	chr12:31400398-31400399	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs201909916	chr12:31400399-31400400	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs547668830	chr12:31400478-31400479	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs567557565	chr12:31400512-31400513	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs536504697	chr12:31400513-31400514	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs550062061	chr12:31400620-31400621	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs372473985	chr12:31400690-31400691	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs7315309	chr12:31400708-31400709	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
35	rs551482198	chr12:31400725-31400726	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs183807678	chr12:31400727-31400728	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs187098799	chr12:31400750-31400751	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs577642543	chr12:31400753-31400754	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs191577982	chr12:31400754-31400755	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs534155671	chr12:31400756-31400757	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs4931474	chr12:31400813-31400814	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs146733292	chr12:31400845-31400846	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs139287836	chr12:31400848-31400849	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs34818047	chr12:31400867-31400868	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs4931475	chr12:31400868-31400869	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs538517340	chr12:31400918-31400919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545061610	chr12:31400929-31400930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565311749	chr12:31400934-31400935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374427591	chr12:31400976-31400977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374423753	chr12:31400994-31400995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
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
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1311 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31395200-31405200	Weak transcription	Right Atrium	heart
2	chr12:31398600-31400400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr12:31398600-31400400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:31398800-31400000	Enhancers	Fetal Heart	heart
5	chr12:31399200-31400000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr12:31399200-31405000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr12:31399400-31400000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr12:31399400-31400200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr12:31399400-31400200	Enhancers	HSMMtube	muscle
10	chr12:31399800-31400000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr12:31399800-31400200	Enhancers	HepG2	liver
12	chr12:31399800-31400200	Enhancers	NHEK	skin
13	chr12:31399800-31400400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr12:31399800-31400400	Enhancers	HMEC	breast
15	chr12:31399800-31405200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr12:31399800-31412600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr12:31400400-31404800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr12:31401600-31403000	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr12:31402000-31403200	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr12:31402200-31403000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr12:31402400-31403400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr12:31402600-31402800	Enhancers	Lung	lung
23	chr12:31403000-31404800	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr12:31403200-31404800	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr12:31404400-31404600	Bivalent Enhancer	A549	lung
26	chr12:31404400-31404800	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr12:31404800-31405000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr12:31404800-31405000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
29	chr12:31404800-31405200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr12:31404800-31405200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr12:31404800-31405200	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr12:31404800-31405200	Active TSS	Primary B cells from cord blood	blood
33	chr12:31404800-31405200	Active TSS	Primary T cells from cord blood	blood
34	chr12:31404800-31405200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr12:31404800-31405200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr12:31404800-31405200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr12:31404800-31405200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
38	chr12:31404800-31405200	Active TSS	NHDF-Ad	bronchial
39	chr12:31404800-31405200	Active TSS	Osteobl	bone
40	chr12:31404800-31405400	Active TSS	Primary monocytes fromperipheralblood	blood
41	chr12:31404800-31405400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr12:31404800-31405400	Active TSS	Fetal Intestine Small	intestine
43	chr12:31404800-31405400	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr12:31404800-31405400	Active TSS	Placenta	Placenta
45	chr12:31404800-31405400	Active TSS	Ovary	ovary
46	chr12:31404800-31405400	Active TSS	Thymus	Thymus
47	chr12:31404800-31405400	Active TSS	Monocytes-CD14+_RO01746	blood
48	chr12:31404800-31405600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr12:31404800-31405600	Active TSS	A549	lung
50	chr12:31405000-31405200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung

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