Variant report

Variant	esv3439887
Chromosome Location	chr12:46337377-46370366
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:93)
CpG islands
(count:61)
Chromatin interactive
region (count:57)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:93 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:46367648-46367797	HepG2	liver:	n/a	n/a
2	BATF	chr12:46367223-46367492	GM12878	blood:	n/a	n/a
3	CEBPB	chr12:46338675-46338855	A549	lung:	n/a	n/a
4	CEBPB	chr12:46361251-46361309	HepG2	liver:	n/a	n/a
5	CTCF	chr12:46369041-46369139	GM13977	blood:	n/a	n/a
6	CTCF	chr12:46347215-46347312	GM10266	blood:	n/a	n/a
7	CTCF	chr12:46347176-46347272	Fibrobl	skin:	n/a	n/a
8	E2F4	chr12:46367672-46367763	MCF10A-Er-Src	breast:	n/a	n/a
9	FOXA1	chr12:46367447-46367882	HepG2	liver:	n/a	n/a
10	FOXA1	chr12:46360310-46360560	T-47D	breast:	n/a	n/a
11	FOXA1	chr12:46360323-46360651	T-47D	breast:	n/a	n/a
12	FOXA1	chr12:46367530-46367884	T-47D	breast:	n/a	n/a
13	GATA2	chr12:46367229-46367622	HUVEC	blood vessel:	n/a	chr12:46367430-46367444
14	GATA3	chr12:46367171-46367904	SK-N-SH	brain:	n/a	n/a
15	GATA3	chr12:46354127-46354361	SH-SY5Y	brain:	n/a	chr12:46354244-46354254
16	GATA3	chr12:46360230-46360670	T-47D	breast:	n/a	n/a
17	GATA3	chr12:46360136-46360750	SK-N-SH	brain:	n/a	n/a
18	GATA3	chr12:46370271-46370805	SH-SY5Y	brain:	n/a	n/a
19	GATA3	chr12:46367222-46367891	SK-N-SH	brain:	n/a	n/a
20	GATA3	chr12:46357627-46357762	SH-SY5Y	brain:	n/a	chr12:46357669-46357680
21	GATA3	chr12:46347154-46347225	SH-SY5Y	brain:	n/a	n/a
22	GTF2F1	chr12:46346720-46346857	H1-hESC	embryonic stem cell:	n/a	n/a
23	IRF1	chr12:46353978-46354090	K562	blood:	n/a	n/a
24	JUND	chr12:46367330-46367525	K562	blood:	n/a	n/a
25	KAP1	chr12:46340781-46340974	K562	blood:	n/a	n/a
26	MAFF	chr12:46342383-46342684	HepG2	liver:	n/a	n/a
27	MAFK	chr12:46342386-46342653	IMR90	lung:	n/a	n/a
28	MAFK	chr12:46342373-46342661	HepG2	liver:	n/a	n/a
29	MAFK	chr12:46342366-46342699	HepG2	liver:	n/a	n/a
30	MAFK	chr12:46342453-46342643	Hela-S3	cervix:	n/a	n/a
31	MAFK	chr12:46356667-46356914	HepG2	liver:	n/a	chr12:46356794-46356809
32	MAX	chr12:46342645-46342676	A549	lung:	n/a	n/a
33	MXI1	chr12:46360384-46360426	GM12878	blood:	n/a	n/a
34	NFIC	chr12:46360268-46360724	ECC-1	luminal epithelium:	n/a	n/a
35	NFIC	chr12:46360164-46360709	SK-N-SH	brain:	n/a	n/a
36	NFYA	chr12:46337337-46337529	Hela-S3	cervix:	n/a	n/a
37	NFYB	chr12:46344400-46344616	GM12878	blood:	n/a	n/a
38	PBX3	chr12:46360219-46360677	SK-N-SH	brain:	n/a	n/a
39	POLR2A	chr12:46364163-46364511	HepG2	liver:	n/a	n/a
40	POLR2A	chr12:46339012-46339211	K562	blood:	n/a	n/a
41	POLR2A	chr12:46361192-46361209	MCF-7	breast:	n/a	n/a
42	POLR2A	chr12:46348951-46349074	ProgFib	skin:	n/a	n/a
43	POLR2A	chr12:46356612-46357239	HUVEC	blood vessel:	n/a	n/a
44	POLR2A	chr12:46337447-46337626	GM12878	blood:	n/a	n/a
45	POLR2A	chr12:46338580-46338692	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr12:46365065-46365149	MCF-7	breast:	n/a	n/a
47	POLR2A	chr12:46368670-46368773	ProgFib	skin:	n/a	n/a
48	POLR2A	chr12:46360349-46360418	ProgFib	skin:	n/a	n/a
49	POLR2A	chr12:46366523-46366541	GM12878	blood:	n/a	n/a
50	POLR2A	chr12:46362582-46362637	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:46361154-46361204	HEK293	kidney:	embryo
2	chr12:46361154-46361204	HPAEpiC	pulmonary alveolar:	n/a
3	chr12:46361154-46361204	Hepatocyte	liver:	n/a
4	chr12:46361154-46361204	ECC-1	luminal epithelium:	n/a
5	chr12:46361154-46361204	NHBE	bronchial:	n/a
6	chr12:46361154-46361204	HNPCEpiC	eye:	n/a
7	chr12:46361154-46361204	HCT-116	colon:	n/a
8	chr12:46361154-46361204	AG09309	skin:	n/a
9	chr12:46361154-46361204	BJ	skin:	n/a
10	chr12:46361154-46361204	H1-hESC	embryonic stem cell:	embryo
11	chr12:46361154-46361204	GM06990	blood:	n/a
12	chr12:46361154-46361204	RPTEC	kidney:	n/a
13	chr12:46361154-46361204	GM19239	blood:	n/a
14	chr12:46361154-46361204	NHDF-neo	bronchial:	n/a
15	chr12:46361154-46361204	AG04450	lung:	fetal
16	chr12:46361154-46361204	SK-N-MC	brain:	n/a
17	chr12:46361154-46361204	SK-N-SH_RA	brain:	n/a
18	chr12:46361154-46361204	SKMC	muscle:	n/a
19	chr12:46361154-46361204	AG09319	gingival:	n/a
20	chr12:46361154-46361204	ovcar-3	ovarian:	n/a
21	chr12:46361154-46361204	MCF-7	breast:	n/a
22	chr12:46361154-46361204	A549	lung:	n/a
23	chr12:46361154-46361204	HCM	heart:	n/a
24	chr12:46361154-46361204	PFSK-1	brain:	n/a
25	chr12:46361154-46361204	HUVEC	blood vessel:	n/a
26	chr12:46361154-46361204	GM12892	blood:	n/a
27	chr12:46361154-46361204	HL-60	blood:	n/a
28	chr12:46361154-46361204	T-47D	breast:	n/a
29	chr12:46361154-46361204	Caco-2	colon:	n/a
30	chr12:46361154-46361204	AG10803	skin:	n/a
31	chr12:46361154-46361204	HepG2	liver:	n/a
32	chr12:46361154-46361204	HCF	heart:	n/a
33	chr12:46361154-46361204	NB4	blood:	n/a
34	chr12:46361154-46361204	NT2-D1	testis:	n/a
35	chr12:46361154-46361204	PrEC	prostate:	n/a
36	chr12:46361154-46361204	K562	blood:	n/a
37	chr12:46361154-46361204	IMR90	lung:	fetal
38	chr12:46361154-46361204	HRCEpiC	kidney:	n/a
39	chr12:46361154-46361204	BE2_C	brain:	n/a
40	chr12:46361154-46361204	LNCaP	prostate:	n/a
41	chr12:46361154-46361204	HEEpiC	esophagus:	n/a
42	chr12:46361154-46361204	CMK	blood:	n/a
43	chr12:46361154-46361204	GM12891	blood:	n/a
44	chr12:46361154-46361204	HMEC	breast:	n/a
45	chr12:46361154-46361204	SAEC	small airway:	n/a
46	chr12:46361154-46361204	Hela-S3	cervix:	n/a
47	chr12:46361154-46361204	AG04449	skin:	fetal
48	chr12:46361154-46361204	HRPEpiC	eye:	n/a
49	chr12:46361154-46361204	PANC-1	pancreas:	n/a
50	chr12:46361154-46361204	Jurkat	blood:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:46344593..46346817-chr12:46380170..46382084,2	MCF-7	breast:
2	chr12:46353562..46359244-chr12:46361441..46367398,6	K562	blood:
3	chr12:46324666..46326347-chr12:46354736..46356489,2	K562	blood:
4	chr12:46345408..46347235-chr12:46357374..46359996,2	K562	blood:
5	chr12:46355803..46357871-chr12:46364503..46366164,2	K562	blood:
6	chr12:46368053..46370956-chr12:46373061..46376584,4	K562	blood:
7	chr12:46359781..46361331-chr12:46365330..46366912,2	K562	blood:
8	chr12:46348001..46351847-chr12:46352857..46355917,3	K562	blood:
9	chr11:10562281..10562799-chr12:46352551..46353071,2	Hela-S3	cervix:
10	chr12:46361732..46364124-chr12:46370348..46372099,2	K562	blood:
11	chr12:46359781..46361331-chr12:46365330..46366912,2	K562	blood:
12	chr12:46345408..46347235-chr12:46357374..46359996,2	K562	blood:
13	chr12:46354572..46357649-chr12:46367674..46371210,4	K562	blood:
14	chr12:46344313..46347392-chr12:46347500..46350157,3	MCF-7	breast:
15	chr12:46334355..46336055-chr12:46368531..46370108,2	MCF-7	breast:
16	chr12:46354837..46356506-chr12:46359246..46361993,2	MCF-7	breast:
17	chr12:46359963..46361845-chr12:46363690..46365645,2	K562	blood:
18	chr12:46338501..46342141-chr12:46348337..46351677,3	K562	blood:
19	chr12:46340522..46343768-chr12:46347527..46351157,4	K562	blood:
20	chr12:46351854..46356298-chr12:46382487..46386006,5	MCF-7	breast:
21	chr12:46365096..46367931-chr12:46383554..46385987,4	MCF-7	breast:
22	chr12:46364964..46367591-chr12:46368004..46369858,2	K562	blood:
23	chr12:46331019..46334796-chr12:46336326..46339137,4	K562	blood:
24	chr12:46336885..46339233-chr12:46356510..46359026,2	K562	blood:
25	chr12:46366328..46369312-chr12:46369671..46371966,2	K562	blood:
26	chr12:46360643..46362650-chr12:46363534..46365705,2	MCF-7	breast:
27	chr12:46361732..46364124-chr12:46370348..46372099,2	K562	blood:
28	chr12:46348656..46350244-chr12:46353257..46355450,2	MCF-7	breast:
29	chr12:46366328..46369312-chr12:46369671..46371966,2	K562	blood:
30	chr12:46119486..46122994-chr12:46354867..46358336,5	K562	blood:
31	chr12:46365772..46368016-chr12:46375925..46378868,2	K562	blood:
32	chr12:46354572..46357649-chr12:46367674..46371210,4	K562	blood:
33	chr12:46367766..46370474-chr12:46662022..46664572,2	K562	blood:
34	chr12:46331019..46333836-chr12:46336326..46339137,3	K562	blood:
35	chr12:46329633..46332497-chr12:46335135..46337573,2	MCF-7	breast:
36	chr12:46338501..46342141-chr12:46348337..46351677,3	K562	blood:
37	chr12:46364964..46367591-chr12:46368004..46369858,2	K562	blood:
38	chr12:46370168..46377627-chr12:46379598..46386227,22	MCF-7	breast:
39	chr12:46348389..46350985-chr12:46373470..46376418,2	K562	blood:
40	chr12:46369343..46373226-chr12:46374858..46377675,3	K562	blood:
41	chr12:46348656..46350244-chr12:46353257..46355450,2	MCF-7	breast:
42	chr12:46348001..46351847-chr12:46352857..46355917,3	K562	blood:
43	chr12:46344313..46347392-chr12:46347500..46350157,3	MCF-7	breast:
44	chr12:46341596..46343310-chr12:46343404..46346172,2	K562	blood:
45	chr12:46361472..46363562-chr12:46382349..46384332,2	K562	blood:
46	chr12:46361324..46363006-chr12:46372617..46375436,2	MCF-7	breast:
47	chr12:46336885..46339233-chr12:46356510..46359026,2	K562	blood:
48	chr12:46354837..46356506-chr12:46359246..46361993,2	MCF-7	breast:
49	chr12:46337598..46339287-chr12:46345137..46347327,2	K562	blood:
50	chr12:46353562..46359244-chr12:46361441..46367398,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC38A1-8	chr12:46338867-46339096	NONHSAT027845
2	lnc-SLC38A1-8	chr12:46342220-46342313	NONHSAT027845

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SFRS2IP	hsa-miR-124-3p	chr12:46349755-46349774

Variant related genes	Relation type
SCAF11	TF binding region
SCAF11	CpG island
ENSG00000111371	chromatin interactions
ENSG00000273015	chromatin interactions
ENSG00000139218	chromatin interactions
ENSG00000110315	chromatin interactions

Extended variants
information (count: 1118 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1118 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535462003	chr12:46337378-46337379	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs541160211	chr12:46337393-46337394	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs564110047	chr12:46337402-46337403	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs577795883	chr12:46337413-46337414	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs543323257	chr12:46337431-46337432	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs563587622	chr12:46337443-46337444	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs73292573	chr12:46337683-46337684	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs559435980	chr12:46337728-46337729	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs543045572	chr12:46337804-46337805	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs551206370	chr12:46337898-46337899	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559829715	chr12:46337944-46337945	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528582158	chr12:46338012-46338013	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551881337	chr12:46338014-46338015	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185480584	chr12:46338049-46338050	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs10880870	chr12:46338080-46338081	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs568001841	chr12:46338081-46338082	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115568419	chr12:46338113-46338114	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567623545	chr12:46338115-46338116	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536596122	chr12:46338189-46338190	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554932390	chr12:46338229-46338230	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147603901	chr12:46338317-46338318	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs17096346	chr12:46338374-46338375	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs74695797	chr12:46338419-46338420	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577727001	chr12:46338444-46338445	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs180746761	chr12:46338504-46338505	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557244808	chr12:46338536-46338537	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573977377	chr12:46338564-46338565	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs377343046	chr12:46338569-46338570	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs34591032	chr12:46338570-46338571	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs397720602	chr12:46338573-46338574	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542980380	chr12:46338609-46338610	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559762871	chr12:46338684-46338685	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79688489	chr12:46338693-46338694	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545139594	chr12:46338707-46338708	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11183244	chr12:46338759-46338760	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs530961136	chr12:46338809-46338810	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140509615	chr12:46338844-46338845	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567562483	chr12:46338913-46338914	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs375954137	chr12:46338951-46338952	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs532800329	chr12:46338993-46338994	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs374268135	chr12:46338995-46338996	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs374357737	chr12:46338998-46338999	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs376183351	chr12:46338999-46339000	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs397850789	chr12:46339001-46339002	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs546915251	chr12:46339005-46339006	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs370633652	chr12:46339008-46339009	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs11183245	chr12:46339033-46339034	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs534626567	chr12:46339083-46339084	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs116828610	chr12:46339183-46339184	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571319100	chr12:46339196-46339197	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
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
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
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Gastric cancer	18160780	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:1253 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:46299000-46381000	Weak transcription	Brain Germinal Matrix	brain
2	chr12:46312200-46348600	Strong transcription	Dnd41	blood
3	chr12:46314600-46345600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr12:46316600-46343400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr12:46317000-46341400	Weak transcription	Gastric	stomach
6	chr12:46318800-46338600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr12:46318800-46339200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr12:46319200-46341400	Weak transcription	Lung	lung
9	chr12:46319200-46362800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr12:46322400-46337400	Weak transcription	Fetal Brain Female	brain
11	chr12:46322600-46338600	Weak transcription	Stomach Smooth Muscle	stomach
12	chr12:46322600-46340000	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr12:46322600-46341400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr12:46322600-46341400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr12:46322600-46341400	Weak transcription	Pancreas	Pancrea
16	chr12:46322600-46360200	Weak transcription	Fetal Brain Male	brain
17	chr12:46322800-46338600	Weak transcription	Esophagus	oesophagus
18	chr12:46323200-46341400	Weak transcription	Colonic Mucosa	Colon
19	chr12:46323200-46341400	Weak transcription	Fetal Stomach	stomach
20	chr12:46323200-46341400	Weak transcription	Spleen	Spleen
21	chr12:46324400-46351600	Weak transcription	Psoas Muscle	Psoas
22	chr12:46325000-46341400	Weak transcription	Left Ventricle	heart
23	chr12:46325200-46343400	Weak transcription	Right Ventricle	heart
24	chr12:46326600-46338400	Weak transcription	Colon Smooth Muscle	Colon
25	chr12:46326600-46339400	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr12:46326600-46360400	Weak transcription	Small Intestine	intestine
27	chr12:46327200-46340600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr12:46327800-46338600	Weak transcription	Rectal Smooth Muscle	rectum
29	chr12:46327800-46340000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr12:46328800-46345200	Strong transcription	HSMM	muscle
31	chr12:46329200-46338400	Weak transcription	Brain Angular Gyrus	brain
32	chr12:46329200-46351800	Weak transcription	Fetal Heart	heart
33	chr12:46329400-46337600	Weak transcription	Brain Hippocampus Middle	brain
34	chr12:46329400-46338000	Weak transcription	Brain Anterior Caudate	brain
35	chr12:46329400-46338400	Weak transcription	Brain Substantia Nigra	brain
36	chr12:46329400-46344400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr12:46329600-46341400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr12:46329600-46342600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr12:46329600-46348800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr12:46329800-46371000	Weak transcription	Brain Cingulate Gyrus	brain
41	chr12:46330400-46344800	Strong transcription	Primary monocytes fromperipheralblood	blood
42	chr12:46330400-46358800	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr12:46331000-46338400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr12:46331000-46344600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr12:46331000-46347000	Strong transcription	Primary B cells from peripheral blood	blood
46	chr12:46331200-46337400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr12:46331200-46338400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr12:46331200-46338600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr12:46331200-46339600	Strong transcription	Hela-S3	cervix
50	chr12:46331200-46343000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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