Variant report

Variant	esv33583
Chromosome Location	chr12:12665776-12679108
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr12:12669084-12669195	K562	blood:	n/a	chr12:12669129-12669140
2	CEBPB	chr12:12668923-12669350	MCF-7	breast:	n/a	chr12:12669129-12669140
3	CEBPB	chr12:12669034-12669281	A549	lung:	n/a	chr12:12669129-12669140
4	CEBPB	chr12:12669008-12669298	HepG2	liver:	n/a	chr12:12669129-12669140
5	CEBPB	chr12:12669114-12669224	Hela-S3	cervix:	n/a	chr12:12669129-12669140
6	CEBPB	chr12:12674060-12674368	HepG2	liver:	n/a	chr12:12674334-12674351
7	CTCF	chr12:12666520-12666670	SK-N-SH_RA	brain:	n/a	n/a
8	CTCF	chr12:12676375-12676409	Lung_OC	lung:	n/a	n/a
9	E2F4	chr12:12678787-12678814	MCF10A-Er-Src	breast:	n/a	n/a
10	EP300	chr12:12666388-12666743	SK-N-SH_RA	brain:	n/a	n/a
11	EP300	chr12:12661255-12667747	SK-N-SH	brain:	n/a	chr12:12661260-12661274 chr12:12662415-12662429 chr12:12667385-12667399 chr12:12661255-12661269 chr12:12661301-12661311
12	ESR1	chr12:12670729-12670903	T-47D	breast:	n/a	chr12:12670802-12670817
13	ESR1	chr12:12670655-12670908	T-47D	breast:	n/a	chr12:12670802-12670817
14	GATA3	chr12:12663811-12665886	SK-N-SH	brain:	n/a	chr12:12664562-12664578
15	GATA3	chr12:12663757-12665942	SK-N-SH	brain:	n/a	chr12:12664562-12664578
16	GATA3	chr12:12673107-12673221	SH-SY5Y	brain:	n/a	n/a
17	GATA3	chr12:12676173-12676326	SH-SY5Y	brain:	n/a	n/a
18	GATA3	chr12:12675714-12676244	MCF-7	breast:	n/a	n/a
19	JUN	chr12:12674034-12674216	HepG2	liver:	n/a	chr12:12674076-12674089
20	JUND	chr12:12673923-12674521	HepG2	liver:	n/a	chr12:12674276-12674288
21	MAFF	chr12:12666557-12666900	HepG2	liver:	n/a	chr12:12666735-12666753
22	MAFF	chr12:12666586-12666893	K562	blood:	n/a	chr12:12666735-12666753
23	MAFK	chr12:12666564-12666920	IMR90	lung:	n/a	chr12:12666732-12666749 chr12:12666741-12666752 chr12:12666736-12666752 chr12:12666741-12666752 chr12:12666736-12666751 chr12:12666740-12666751
24	MAFK	chr12:12666557-12666921	HepG2	liver:	n/a	chr12:12666732-12666749 chr12:12666741-12666752 chr12:12666736-12666752 chr12:12666741-12666752 chr12:12666736-12666751 chr12:12666740-12666751
25	MAFK	chr12:12666599-12666901	HepG2	liver:	n/a	chr12:12666732-12666749 chr12:12666741-12666752 chr12:12666736-12666752 chr12:12666741-12666752 chr12:12666736-12666751 chr12:12666740-12666751
26	MAFK	chr12:12666572-12666897	K562	blood:	n/a	chr12:12666732-12666749 chr12:12666741-12666752 chr12:12666736-12666752 chr12:12666741-12666752 chr12:12666736-12666751 chr12:12666740-12666751
27	MAFK	chr12:12666646-12666847	Hela-S3	cervix:	n/a	chr12:12666732-12666749 chr12:12666741-12666752 chr12:12666736-12666752 chr12:12666741-12666752 chr12:12666736-12666751 chr12:12666740-12666751
28	MXI1	chr12:12662618-12666979	SK-N-SH	brain:	n/a	n/a
29	NR2F2	chr12:12675703-12676291	MCF-7	breast:	n/a	n/a
30	NR2F2	chr12:12675738-12676178	MCF-7	breast:	n/a	n/a
31	POLR2A	chr12:12673881-12673936	HepG2	liver:	n/a	n/a
32	POLR2A	chr12:12676308-12676321	MCF-7	breast:	n/a	n/a
33	POLR2A	chr12:12670125-12670137	HepG2	liver:	n/a	n/a
34	POLR2A	chr12:12676325-12676458	HepG2	liver:	n/a	n/a
35	POLR2A	chr12:12670130-12670177	MCF-7	breast:	n/a	n/a
36	POLR2A	chr12:12676748-12676754	MCF-7	breast:	n/a	n/a
37	POLR2A	chr12:12667686-12667704	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr12:12676769-12677400	HepG2	liver:	n/a	n/a
39	POLR2A	chr12:12672454-12672629	MCF-7	breast:	n/a	n/a
40	POLR2A	chr12:12674702-12675171	H1-neurons	neurons:	n/a	n/a
41	POLR2A	chr12:12673950-12673984	HepG2	liver:	n/a	n/a
42	POLR2A	chr12:12673636-12674660	H1-neurons	neurons:	n/a	n/a
43	POLR2A	chr12:12667748-12667896	HepG2	liver:	n/a	n/a
44	POLR2A	chr12:12677222-12677234	MCF-7	breast:	n/a	n/a
45	POLR2A	chr12:12674936-12675332	HepG2	liver:	n/a	n/a
46	POLR2A	chr12:12666485-12666616	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr12:12678849-12679032	GM12878	blood:	n/a	n/a
48	POLR2A	chr12:12673993-12674213	MCF-7	breast:	n/a	n/a
49	POLR2A	chr12:12677235-12677307	MCF-7	breast:	n/a	n/a
50	POLR2A	chr12:12675050-12675329	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:12673150-12673200	MCF10A-Er-Src	breast:	n/a
2	chr12:12673150-12673200	MCF10A-Er-Src	breast:	n/a
3	chr12:12673025-12673075	SK-N-SH	brain:	n/a
4	chr12:12673025-12673075	NHDF-neo	bronchial:	n/a
5	chr12:12673150-12673200	Hepatocyte	liver:	n/a
6	chr12:12673025-12673075	ProgFib	skin:	n/a
7	chr12:12673025-12673075	A549	lung:	n/a
8	chr12:12673150-12673200	U87	brain:	n/a
9	chr12:12673025-12673075	IMR90	lung:	fetal
10	chr12:12673150-12673200	NH-A	brain:	n/a
11	chr12:12673150-12673200	HNPCEpiC	eye:	n/a
12	chr12:12673025-12673075	AoSMC	blood vessel:	n/a
13	chr12:12673150-12673200	H1-hESC	embryonic stem cell:	embryo
14	chr12:12673025-12673075	MCF-7	breast:	n/a
15	chr12:12673025-12673075	Jurkat	blood:	n/a
16	chr12:12673150-12673200	AG04450	lung:	fetal
17	chr12:12673150-12673200	SKMC	muscle:	n/a
18	chr12:12673150-12673200	GM12878	blood:	n/a
19	chr12:12673025-12673075	PANC-1	pancreas:	n/a
20	chr12:12673025-12673075	HCF	heart:	n/a
21	chr12:12673025-12673075	HepG2	liver:	n/a
22	chr12:12673150-12673200	SK-N-MC	brain:	n/a
23	chr12:12673150-12673200	BE2_C	brain:	n/a
24	chr12:12673025-12673075	GM06990	blood:	n/a
25	chr12:12673025-12673075	ECC-1	luminal epithelium:	n/a
26	chr12:12673150-12673200	BJ	skin:	n/a
27	chr12:12673150-12673200	HEEpiC	esophagus:	n/a
28	chr12:12673025-12673075	HRPEpiC	eye:	n/a
29	chr12:12673150-12673200	MCF-7	breast:	n/a
30	chr12:12673025-12673075	AG09309	skin:	n/a
31	chr12:12673150-12673200	GM06990	blood:	n/a
32	chr12:12673150-12673200	NB4	blood:	n/a
33	chr12:12673025-12673075	LNCaP	prostate:	n/a
34	chr12:12673025-12673075	HCT-116	colon:	n/a
35	chr12:12673025-12673075	HL-60	blood:	n/a
36	chr12:12673150-12673200	NHBE	bronchial:	n/a
37	chr12:12673150-12673200	CMK	blood:	n/a
38	chr12:12673150-12673200	A549	lung:	n/a
39	chr12:12673150-12673200	AG04449	skin:	fetal
40	chr12:12673150-12673200	PrEC	prostate:	n/a
41	chr12:12673025-12673075	U87	brain:	n/a
42	chr12:12673025-12673075	AG09319	gingival:	n/a
43	chr12:12673025-12673075	SK-N-MC	brain:	n/a
44	chr12:12673025-12673075	NH-A	brain:	n/a
45	chr12:12673150-12673200	PANC-1	pancreas:	n/a
46	chr12:12673025-12673075	T-47D	breast:	n/a
47	chr12:12673025-12673075	CMK	blood:	n/a
48	chr12:12673150-12673200	RPTEC	kidney:	n/a
49	chr12:12673150-12673200	AoSMC	blood vessel:	n/a
50	chr12:12673150-12673200	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:12672602..12674761-chr12:12714230..12715790,2	MCF-7	breast:
2	chr12:12672692..12674511-chr12:12674724..12676812,2	MCF-7	breast:
3	chr12:12676963..12678914-chr12:12679102..12682035,2	MCF-7	breast:
4	chr12:12676963..12678914-chr12:12679102..12682035,2	MCF-7	breast:
5	chr12:12651288..12653412-chr12:12663902..12666446,2	MCF-7	breast:
6	chr12:12670175..12672490-chr12:12673979..12676406,2	MCF-7	breast:
7	chr12:12677909..12679570-chr12:12685352..12687736,2	MCF-7	breast:
8	chr12:12663586..12666811-chr12:12669278..12673958,4	MCF-7	breast:
9	chr12:12672595..12674438-chr12:12675513..12677632,2	MCF-7	breast:
10	chr12:12669443..12671401-chr12:12739772..12741382,2	MCF-7	breast:
11	chr12:12657662..12660778-chr12:12669355..12673750,5	MCF-7	breast:
12	chr12:12679007..12681498-chr12:12683733..12686607,2	K562	blood:
13	chr12:12676154..12677988-chr12:12685954..12688802,2	MCF-7	breast:
14	chr12:12672853..12675163-chr12:12712393..12714277,2	K562	blood:
15	chr12:12663586..12666811-chr12:12669278..12673958,4	MCF-7	breast:
16	chr12:12675003..12677370-chr12:12678643..12681429,2	K562	blood:
17	chr12:12673839..12677511-chr12:12678935..12682743,3	MCF-7	breast:
18	chr12:12551031..12553032-chr12:12674320..12676066,2	MCF-7	breast:
19	chr12:12676702..12679662-chr12:12711991..12714895,3	MCF-7	breast:
20	chr12:12673127..12675193-chr12:12712366..12713939,3	MCF-7	breast:
21	chr12:12669920..12672358-chr12:12713747..12715597,2	MCF-7	breast:
22	chr12:12675003..12677370-chr12:12678643..12681429,2	K562	blood:
23	chr12:12664441..12668310-chr12:12713996..12715655,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR19-3	chr12:12674261-12674397	NONHSAT026985

Variant related genes	Relation type
DUSP16	TF binding region
DUSP16	CpG island
ENSG00000111266	chromatin interactions

Extended variants
information (count: 504 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:504 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369091521	chr12:12665865-12665866	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs534255924	chr12:12665882-12665883	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs554043255	chr12:12665900-12665901	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs532071551	chr12:12665908-12665909	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150016639	chr12:12665962-12665963	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs527703895	chr12:12665976-12665977	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs577209455	chr12:12665979-12665980	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs77931688	chr12:12665980-12665981	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs576868097	chr12:12666018-12666019	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs11054945	chr12:12666130-12666131	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs191074142	chr12:12666138-12666139	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs11054946	chr12:12666142-12666143	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs550204286	chr12:12666186-12666187	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs73063430	chr12:12666209-12666210	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs114776322	chr12:12666221-12666222	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs182739244	chr12:12666246-12666247	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs566542717	chr12:12666315-12666316	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs533782476	chr12:12666316-12666317	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs534382960	chr12:12666336-12666337	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs145556584	chr12:12666440-12666441	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs188256009	chr12:12666457-12666458	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs76997454	chr12:12666521-12666522	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs115138919	chr12:12666544-12666545	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs77696186	chr12:12666571-12666572	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs574571423	chr12:12666616-12666617	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs199813486	chr12:12666651-12666652	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs546492866	chr12:12666762-12666763	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs374016059	chr12:12666764-12666765	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs541632672	chr12:12666810-12666811	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs79856228	chr12:12666811-12666812	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs527738972	chr12:12666872-12666873	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs545796942	chr12:12666906-12666907	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs536268901	chr12:12666944-12666945	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs560467601	chr12:12666963-12666964	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs532399706	chr12:12666983-12666984	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs564186299	chr12:12667031-12667032	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs531598479	chr12:12667046-12667047	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs550482974	chr12:12667055-12667056	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs562222422	chr12:12667066-12667067	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs145556179	chr12:12667150-12667151	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs564816661	chr12:12667158-12667159	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs373862779	chr12:12667162-12667163	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs138089081	chr12:12667199-12667200	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs566578878	chr12:12667272-12667273	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs141130608	chr12:12667346-12667347	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs144586869	chr12:12667361-12667362	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs531947459	chr12:12667402-12667403	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs550127818	chr12:12667410-12667411	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs570497852	chr12:12667415-12667416	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs148201477	chr12:12667418-12667419	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	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
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:12630800-12681000	Weak transcription	Colonic Mucosa	Colon
2	chr12:12634400-12685200	Weak transcription	Hela-S3	cervix
3	chr12:12639400-12679600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr12:12641600-12686200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr12:12653800-12669000	Weak transcription	Fetal Muscle Trunk	muscle
6	chr12:12654400-12667200	Weak transcription	Primary T cells from cord blood	blood
7	chr12:12656000-12666400	Weak transcription	Spleen	Spleen
8	chr12:12656800-12670800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr12:12659000-12667000	Weak transcription	Fetal Thymus	thymus
10	chr12:12659000-12669200	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr12:12659600-12665800	Enhancers	Brain Cingulate Gyrus	brain
12	chr12:12659800-12667800	Enhancers	Brain Hippocampus Middle	brain
13	chr12:12659800-12669000	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr12:12659800-12669800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr12:12659800-12670800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr12:12659800-12674200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr12:12659800-12678600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr12:12660000-12668600	Enhancers	Brain Substantia Nigra	brain
19	chr12:12660000-12670200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr12:12660000-12681800	Weak transcription	Fetal Kidney	kidney
21	chr12:12660200-12670000	Weak transcription	Fetal Lung	lung
22	chr12:12660400-12666000	Weak transcription	Placenta	Placenta
23	chr12:12660400-12666400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr12:12660400-12666400	Weak transcription	Aorta	Aorta
25	chr12:12660400-12667000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr12:12660400-12669600	Weak transcription	Stomach Smooth Muscle	stomach
27	chr12:12660400-12670000	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr12:12660400-12670000	Weak transcription	HUVEC	blood vessel
29	chr12:12660400-12670600	Weak transcription	Fetal Stomach	stomach
30	chr12:12660400-12672200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr12:12660400-12672400	Weak transcription	Right Ventricle	heart
32	chr12:12660400-12672600	Weak transcription	Esophagus	oesophagus
33	chr12:12660400-12672800	Weak transcription	K562	blood
34	chr12:12660400-12686200	Weak transcription	Rectal Smooth Muscle	rectum
35	chr12:12660600-12667200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr12:12660800-12665800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr12:12660800-12667200	Weak transcription	Right Atrium	heart
38	chr12:12660800-12670800	Weak transcription	Left Ventricle	heart
39	chr12:12660800-12672400	Weak transcription	Ovary	ovary
40	chr12:12660800-12676600	Weak transcription	Pancreas	Pancrea
41	chr12:12660800-12679800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr12:12661200-12665800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr12:12661800-12669200	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr12:12662000-12665800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr12:12662000-12668200	Strong transcription	HepG2	liver
46	chr12:12662000-12668600	Enhancers	Brain Anterior Caudate	brain
47	chr12:12662200-12669000	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr12:12662200-12669800	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr12:12662200-12672400	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr12:12662400-12669200	Weak transcription	Adipose Nuclei	Adipose

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