Variant report

Variant	nsv899314
Chromosome Location	chr12:76079814-76110751
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:640)
CpG islands
(count:428)
Chromatin interactive
region (count:61)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:640 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:76108328-76108617	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:76100268-76101068	K562	blood:	n/a	n/a
3	ARID3A	chr12:76102531-76103057	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:76106004-76106501	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:76093747-76093899	K562	blood:	n/a	n/a
6	ATF1	chr12:76093562-76093892	K562	blood:	n/a	n/a
7	ATF1	chr12:76084388-76084626	K562	blood:	n/a	n/a
8	ATF1	chr12:76100180-76100978	K562	blood:	n/a	n/a
9	ATF1	chr12:76088834-76089049	K562	blood:	n/a	n/a
10	ATF3	chr12:76084341-76084703	K562	blood:	n/a	n/a
11	BCL3	chr12:76084337-76084864	A549	lung:	n/a	n/a
12	BHLHE40	chr12:76100319-76100352	K562	blood:	n/a	n/a
13	BHLHE40	chr12:76084418-76084464	K562	blood:	n/a	n/a
14	BHLHE40	chr12:76100577-76100866	K562	blood:	n/a	chr12:76100600-76100621 chr12:76100604-76100617
15	BHLHE40	chr12:76093544-76093687	K562	blood:	n/a	n/a
16	CBX3	chr12:76100533-76101041	K562	blood:	n/a	n/a
17	CBX3	chr12:76105806-76106573	HCT-116	colon:	n/a	n/a
18	CBX3	chr12:76088255-76089184	HCT-116	colon:	n/a	n/a
19	CBX3	chr12:76105871-76106552	HCT-116	colon:	n/a	n/a
20	CBX3	chr12:76084207-76084761	HCT-116	colon:	n/a	n/a
21	CBX3	chr12:76084319-76084682	K562	blood:	n/a	n/a
22	CCNT2	chr12:76100307-76100984	K562	blood:	n/a	n/a
23	CEBPB	chr12:76104910-76105252	MCF-7	breast:	n/a	n/a
24	CEBPB	chr12:76099897-76100190	A549	lung:	n/a	n/a
25	CEBPB	chr12:76105857-76106616	HCT-116	colon:	n/a	n/a
26	CEBPB	chr12:76108002-76110123	HCT-116	colon:	n/a	chr12:76110064-76110076 chr12:76108991-76109002
27	CEBPB	chr12:76084221-76084870	IMR90	lung:	n/a	n/a
28	CEBPB	chr12:76084233-76084981	A549	lung:	n/a	n/a
29	CEBPB	chr12:76108182-76109241	A549	lung:	n/a	chr12:76108991-76109002
30	CEBPB	chr12:76108210-76109434	HCT-116	colon:	n/a	chr12:76108991-76109002
31	CEBPB	chr12:76108837-76109155	A549	lung:	n/a	chr12:76108991-76109002
32	CEBPB	chr12:76094952-76096095	HCT-116	colon:	n/a	n/a
33	CEBPB	chr12:76098211-76099009	HCT-116	colon:	n/a	chr12:76098644-76098657
34	CEBPB	chr12:76106095-76106324	HepG2	liver:	n/a	n/a
35	CEBPB	chr12:76108848-76109161	HepG2	liver:	n/a	chr12:76108991-76109002
36	CEBPB	chr12:76098514-76098815	K562	blood:	n/a	chr12:76098644-76098657
37	CEBPB	chr12:76105330-76107194	HCT-116	colon:	n/a	chr12:76105433-76105444
38	CEBPB	chr12:76099798-76100239	IMR90	lung:	n/a	n/a
39	CEBPB	chr12:76108220-76109152	Hela-S3	cervix:	n/a	chr12:76108991-76109002
40	CEBPB	chr12:76098469-76098819	ECC-1	luminal epithelium:	n/a	chr12:76098644-76098657
41	CEBPB	chr12:76106157-76106333	HepG2	liver:	n/a	n/a
42	CEBPB	chr12:76108322-76108501	HepG2	liver:	n/a	n/a
43	CEBPB	chr12:76084438-76084841	A549	lung:	n/a	n/a
44	CEBPB	chr12:76097693-76099171	HCT-116	colon:	n/a	chr12:76098644-76098657
45	CEBPB	chr12:76100307-76100972	K562	blood:	n/a	chr12:76100811-76100822
46	CEBPB	chr12:76100565-76100986	K562	blood:	n/a	chr12:76100811-76100822
47	CEBPB	chr12:76108200-76108547	IMR90	lung:	n/a	n/a
48	CEBPB	chr12:76104237-76104425	HepG2	liver:	n/a	n/a
49	CEBPB	chr12:76108842-76109070	IMR90	lung:	n/a	chr12:76108991-76109002
50	CEBPB	chr12:76100141-76100555	MCF-7	breast:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:76107548-76107598	Jurkat	blood:	n/a
2	chr12:76107548-76107598	Jurkat	blood:	n/a
3	chr12:76107548-76107598	H1-hESC	embryonic stem cell:	embryo
4	chr12:76100610-76100660	A549	lung:	n/a
5	chr12:76100610-76100660	HRCEpiC	kidney:	n/a
6	chr12:76084549-76084599	HNPCEpiC	eye:	n/a
7	chr12:76105953-76106003	K562	blood:	n/a
8	chr12:76100610-76100660	NT2-D1	testis:	n/a
9	chr12:76099426-76099476	MCF10A-Er-Src	breast:	n/a
10	chr12:76099426-76099476	K562	blood:	n/a
11	chr12:76107548-76107598	ECC-1	luminal epithelium:	n/a
12	chr12:76105953-76106003	BJ	skin:	n/a
13	chr12:76105953-76106003	SK-N-MC	brain:	n/a
14	chr12:76102490-76102540	HEK293	kidney:	embryo
15	chr12:76099426-76099476	NT2-D1	testis:	n/a
16	chr12:76102490-76102540	PrEC	prostate:	n/a
17	chr12:76105953-76106003	HEK293	kidney:	embryo
18	chr12:76099426-76099476	HEK293	kidney:	embryo
19	chr12:76102490-76102540	HRE	kidney:	n/a
20	chr12:76107548-76107598	BJ	skin:	n/a
21	chr12:76099426-76099476	HEEpiC	esophagus:	n/a
22	chr12:76102490-76102540	AG04450	lung:	fetal
23	chr12:76084549-76084599	PFSK-1	brain:	n/a
24	chr12:76084549-76084599	Jurkat	blood:	n/a
25	chr12:76084549-76084599	HPAEpiC	pulmonary alveolar:	n/a
26	chr12:76100610-76100660	ProgFib	skin:	n/a
27	chr12:76098020-76098070	Caco-2	colon:	n/a
28	chr12:76102490-76102540	HCF	heart:	n/a
29	chr12:76100610-76100660	AG09309	skin:	n/a
30	chr12:76098020-76098070	GM12892	blood:	n/a
31	chr12:76098020-76098070	Hepatocyte	liver:	n/a
32	chr12:76105953-76106003	SAEC	small airway:	n/a
33	chr12:76098020-76098070	ovcar-3	ovarian:	n/a
34	chr12:76098020-76098070	NHBE	bronchial:	n/a
35	chr12:76105953-76106003	HAEpiC	amniotic membrane:	n/a
36	chr12:76107548-76107598	HAEpiC	amniotic membrane:	n/a
37	chr12:76100610-76100660	HepG2	liver:	n/a
38	chr12:76105953-76106003	AG09319	gingival:	n/a
39	chr12:76105953-76106003	Hepatocyte	liver:	n/a
40	chr12:76084549-76084599	BJ	skin:	n/a
41	chr12:76102490-76102540	SK-N-SH	brain:	n/a
42	chr12:76105953-76106003	HepG2	liver:	n/a
43	chr12:76100610-76100660	PrEC	prostate:	n/a
44	chr12:76100610-76100660	HPAEpiC	pulmonary alveolar:	n/a
45	chr12:76105953-76106003	HCF	heart:	n/a
46	chr12:76107548-76107598	AoSMC	blood vessel:	n/a
47	chr12:76107548-76107598	NHDF-neo	bronchial:	n/a
48	chr12:76107548-76107598	MCF-7	breast:	n/a
49	chr12:76099426-76099476	GM12891	blood:	n/a
50	chr12:76105953-76106003	PFSK-1	brain:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:76102037..76104133-chr12:76105458..76107815,2	K562	blood:
2	chr12:76028709..76030372-chr12:76096874..76098526,2	MCF-7	breast:
3	chr12:76108187..76109868-chr12:76423934..76425528,2	MCF-7	breast:
4	chr12:76100797..76102905-chr12:76103958..76106069,2	K562	blood:
5	chr12:76102097..76104624-chr12:76369876..76371857,2	MCF-7	breast:
6	chr12:76088110..76090693-chr12:76091900..76094765,3	K562	blood:
7	chr12:75919171..75922679-chr12:76098756..76100488,3	MCF-7	breast:
8	chr12:76095482..76097484-chr12:76476603..76478364,2	MCF-7	breast:
9	chr12:76097832..76100387-chr8:102502894..102505190,2	MCF-7	breast:
10	chr12:76098446..76100265-chr12:76101330..76104359,3	K562	blood:
11	chr12:76015495..76018360-chr12:76104509..76107219,2	MCF-7	breast:
12	chr12:76098673..76101455-chr12:76339304..76341951,2	MCF-7	breast:
13	chr12:76104622..76106937-chr12:76111729..76114237,3	K562	blood:
14	chr12:76101934..76108267-chr12:76336185..76339499,5	MCF-7	breast:
15	chr12:76098481..76102086-chr12:76423023..76426874,6	MCF-7	breast:
16	chr12:76098446..76100870-chr12:76101330..76106018,5	K562	blood:
17	chr12:76088271..76091093-chr12:76092388..76094453,2	MCF-7	breast:
18	chr12:76032329..76032994-chr12:76099843..76100643,3	MCF-7	breast:
19	chr12:76097180..76098838-chr12:76099370..76102152,2	MCF-7	breast:
20	chr12:76015734..76021626-chr12:76097256..76101818,9	MCF-7	breast:
21	chr12:76104879..76106449-chr12:76425488..76427132,2	MCF-7	breast:
22	chr12:76098446..76100265-chr12:76101330..76104359,3	K562	blood:
23	chr12:76098531..76101496-chr12:76371674..76373378,2	MCF-7	breast:
24	chr12:76105978..76108451-chr12:76281373..76283047,2	MCF-7	breast:
25	chr12:76109388..76110074-chr4:26322104..26322794,2	HCT-116	colon:
26	chr12:76083117..76087359-chr12:76087852..76091604,4	MCF-7	breast:
27	chr12:76099220..76100944-chr12:76739445..76741568,2	MCF-7	breast:
28	chr12:76100050..76100750-chr14:90910076..90910761,2	MCF-7	breast:
29	chr12:76100797..76102905-chr12:76103958..76106069,2	K562	blood:
30	chr12:76077618..76079261-chr12:76083300..76084983,2	MCF-7	breast:
31	chr12:76096760..76101934-chr12:76112737..76117926,8	MCF-7	breast:
32	chr12:76098571..76100662-chr12:76382454..76384688,2	MCF-7	breast:
33	chr12:76091616..76093150-chr12:76098574..76100894,2	MCF-7	breast:
34	chr12:76023357..76025100-chr12:76099295..76101249,2	MCF-7	breast:
35	chr12:76099898..76100434-chr12:76424775..76425728,2	MCF-7	breast:
36	chr12:76101957..76104575-chr12:76208488..76210993,2	MCF-7	breast:
37	chr12:76098446..76100870-chr12:76101330..76106018,5	K562	blood:
38	chr12:76102346..76108137-chr12:76108362..76111472,5	MCF-7	breast:
39	chr12:76089100..76090003-chr4:100920586..100921561,2	MCF-7	breast:
40	chr12:76101462..76103628-chr12:76173013..76174692,2	MCF-7	breast:
41	chr12:76082441..76084342-chr12:76093010..76095736,2	K562	blood:
42	chr12:76089791..76091590-chr12:76423370..76427266,4	MCF-7	breast:
43	chr12:76094900..76097140-chr12:76097176..76099734,2	K562	blood:
44	chr12:76084027..76086553-chr12:76090188..76092212,2	MCF-7	breast:
45	chr12:76088110..76089922-chr12:76091900..76094708,2	K562	blood:
46	chr12:76092093..76110851-chr12:76415034..76433496,122	MCF-7	breast:
47	chr12:76084534..76087387-chr12:76088110..76091100,3	K562	blood:
48	chr12:76102346..76108137-chr12:76108362..76111472,5	MCF-7	breast:
49	chr12:76099926..76101874-chr12:76365799..76367689,2	MCF-7	breast:
50	chr12:76098765..76099591-chr6:26123921..26124473,2	HCT-116	colon:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KRR1-2	chr12:76085885-76086138	ENSG00000258077.1
2	lnc-KRR1-2	chr12:76083248-76083387	ENSG00000258077.1
3	lnc-KRR1-3	chr12:76092487-76092596	ENSG00000258088.1
4	lnc-KRR1-2	chr12:76085885-76085959	ENSG00000258077.1
5	lnc-KRR1-2	chr12:76083275-76083387	ENSG00000258077.2
6	lnc-KRR1-2	chr12:76084425-76084611	XLOC_010132
7	lnc-KRR1-3	chr12:76087790-76088131	ENSG00000258088.1
8	lnc-GLIPR1-6	chr12:76084295-76084639	NONHSAT029538
9	lnc-KRR1-2	chr12:76084295-76084639	ENSG00000258077.2
10	lnc-KRR1-3	chr12:76088637-76088755	ENSG00000258088.1
11	lnc-KRR1-2	chr12:76084537-76084639	ENSG00000258077.1
12	lnc-KRR1-2	chr12:76083364-76083387	XLOC_010132
13	lnc-GLIPR1-6	chr12:76082509-76082551	NONHSAT029538
14	lnc-KRR1-2	chr12:76085885-76086138	ENSG00000258077.2
15	lnc-KRR1-3	chr12:76088380-76088550	ENSG00000258088.1
16	lnc-KRR1-2	chr12:76084295-76084615	ENSG00000258077.1

No data

Variant related genes	Relation type
ENSG00000258088	TF binding region
ENSG00000258077	TF binding region
ENSG00000251893	TF binding region
ENSG00000258245	TF binding region
ENSG00000258088	CpG island
ENSG00000258077	CpG island
ENSG00000251893	CpG island
ENSG00000258245	CpG island
ENSG00000254024	chromatin interactions
ENSG00000264062	chromatin interactions
ENSG00000257839	chromatin interactions
ENSG00000187109	chromatin interactions
ENSG00000180596	chromatin interactions
ENSG00000258077	chromatin interactions
ENSG00000083307	chromatin interactions
ENSG00000257453	chromatin interactions
ENSG00000168214	chromatin interactions
ENSG00000258245	chromatin interactions
ENSG00000139289	chromatin interactions
ENSG00000258088	chromatin interactions
ENSG00000180573	chromatin interactions
ENSG00000251893	chromatin interactions

Extended variants
information (count: 1170 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1170 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1882020	chr12:76079814-76079815	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563523515	chr12:76079842-76079843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147868706	chr12:76079879-76079880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566345632	chr12:76079906-76079907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369555091	chr12:76079926-76079927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559527666	chr12:76079960-76079961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148537574	chr12:76079969-76079970	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535490589	chr12:76080014-76080015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373773200	chr12:76080028-76080029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545253059	chr12:76080046-76080047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551458098	chr12:76080058-76080059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187795905	chr12:76080097-76080098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530894737	chr12:76080117-76080118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs567264235	chr12:76080118-76080119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550030575	chr12:76080141-76080142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs569864652	chr12:76080163-76080164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535790318	chr12:76080174-76080175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142861715	chr12:76080183-76080184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565792008	chr12:76080230-76080231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs10879960	chr12:76080231-76080232	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs557431575	chr12:76080232-76080233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577700128	chr12:76080246-76080247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs12578249	chr12:76080262-76080263	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs140828094	chr12:76080284-76080285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573885581	chr12:76080301-76080302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537678182	chr12:76080303-76080304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563535260	chr12:76080304-76080305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542772222	chr12:76080328-76080329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559997438	chr12:76080355-76080356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528745606	chr12:76080397-76080398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs10785205	chr12:76080417-76080418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565113061	chr12:76080480-76080481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192600100	chr12:76080511-76080512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551086970	chr12:76080562-76080563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567723057	chr12:76080568-76080569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs74799671	chr12:76080595-76080596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548873872	chr12:76080653-76080654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565978378	chr12:76080676-76080677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534596353	chr12:76080683-76080684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561114255	chr12:76080691-76080692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs35504036	chr12:76080783-76080784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs183273848	chr12:76080794-76080795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551382877	chr12:76080818-76080819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs17223072	chr12:76080856-76080857	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs187554655	chr12:76080865-76080866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140370438	chr12:76080921-76080922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573354323	chr12:76080992-76080993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs536464939	chr12:76081012-76081013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553276868	chr12:76081052-76081053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573510175	chr12:76081081-76081082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Wilms tumour	21544195	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
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
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	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
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
craniofacial dysmorphism	21918468	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	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
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21364760	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:545 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:76076200-76098400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:76076800-76080000	Enhancers	NHEK	skin
3	chr12:76077000-76081800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr12:76078200-76080000	Enhancers	Muscle Satellite Cultured Cells	--
5	chr12:76079000-76081000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr12:76079000-76081000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:76079000-76093600	Weak transcription	Psoas Muscle	Psoas
8	chr12:76079200-76080000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr12:76079200-76080000	Enhancers	NHDF-Ad	bronchial
10	chr12:76079200-76083800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr12:76079200-76084200	Weak transcription	K562	blood
12	chr12:76079400-76083800	Weak transcription	HSMM	muscle
13	chr12:76079400-76084000	Weak transcription	Fetal Stomach	stomach
14	chr12:76079400-76099800	Weak transcription	Right Atrium	heart
15	chr12:76079600-76083200	Weak transcription	HMEC	breast
16	chr12:76079600-76083800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr12:76079600-76083800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr12:76079800-76080800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr12:76079800-76083200	Weak transcription	NHLF	lung
20	chr12:76079800-76083800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr12:76079800-76083800	Weak transcription	NH-A	brain
22	chr12:76079800-76083800	Weak transcription	Osteobl	bone
23	chr12:76080000-76080400	Weak transcription	NHDF-Ad	bronchial
24	chr12:76080000-76083600	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr12:76080000-76083600	Weak transcription	NHEK	skin
26	chr12:76080000-76084200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr12:76080400-76081800	Enhancers	NHDF-Ad	bronchial
28	chr12:76080800-76081200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr12:76081000-76082200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr12:76081000-76083200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr12:76081000-76083200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr12:76081200-76083800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr12:76081400-76082000	Enhancers	Aorta	Aorta
34	chr12:76081800-76083000	Weak transcription	NHDF-Ad	bronchial
35	chr12:76081800-76083800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr12:76082600-76083200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr12:76083000-76084400	Enhancers	NHDF-Ad	bronchial
38	chr12:76083200-76084400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr12:76083200-76084400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr12:76083200-76084400	Enhancers	NHLF	lung
41	chr12:76083200-76084600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr12:76083200-76085000	Enhancers	HMEC	breast
43	chr12:76083600-76085000	Enhancers	NHEK	skin
44	chr12:76083600-76087400	Enhancers	Muscle Satellite Cultured Cells	--
45	chr12:76083800-76084200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr12:76083800-76084400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr12:76083800-76084600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr12:76083800-76085000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr12:76083800-76085000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr12:76083800-76085000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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