Variant report

Variant	nsv516421
Chromosome Location	chr12:30309076-30411299
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	BACH1	chr12:30350425-30350895	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr12:30322887-30323245	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr12:30392480-30392665	GM12878	blood:	n/a	chr12:30392574-30392585
4	CEBPB	chr12:30319021-30319366	HepG2	liver:	n/a	chr12:30319192-30319201 chr12:30319192-30319201 chr12:30319192-30319201 chr12:30319190-30319203 chr12:30319192-30319201 chr12:30319190-30319203 chr12:30319192-30319203 chr12:30319190-30319201
5	CEBPB	chr12:30361704-30361917	A549	lung:	n/a	chr12:30361791-30361802
6	CEBPB	chr12:30377310-30377513	A549	lung:	n/a	chr12:30377386-30377397
7	CEBPB	chr12:30360483-30360805	HepG2	liver:	n/a	chr12:30360641-30360652
8	CEBPB	chr12:30355896-30356101	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:30361676-30361926	HepG2	liver:	n/a	chr12:30361791-30361802
10	CEBPB	chr12:30363864-30364111	HepG2	liver:	n/a	chr12:30363953-30363964
11	CEBPB	chr12:30319056-30319342	K562	blood:	n/a	chr12:30319192-30319201 chr12:30319192-30319201 chr12:30319192-30319201 chr12:30319190-30319203 chr12:30319192-30319201 chr12:30319190-30319203 chr12:30319192-30319203 chr12:30319190-30319201
12	CEBPB	chr12:30361651-30361976	IMR90	lung:	n/a	chr12:30361791-30361802
13	CEBPB	chr12:30390833-30391122	HepG2	liver:	n/a	chr12:30390970-30390981
14	CEBPB	chr12:30318553-30318692	K562	blood:	n/a	n/a
15	CEBPB	chr12:30319007-30319367	IMR90	lung:	n/a	chr12:30319192-30319201 chr12:30319192-30319201 chr12:30319192-30319201 chr12:30319190-30319203 chr12:30319192-30319201 chr12:30319190-30319203 chr12:30319192-30319203 chr12:30319190-30319201
16	CEBPB	chr12:30363917-30364012	A549	lung:	n/a	chr12:30363953-30363964
17	CEBPB	chr12:30361766-30361910	K562	blood:	n/a	chr12:30361791-30361802
18	CEBPB	chr12:30351134-30351189	HepG2	liver:	n/a	n/a
19	CEBPB	chr12:30377254-30377495	HepG2	liver:	n/a	chr12:30377386-30377397
20	CEBPB	chr12:30363875-30364075	K562	blood:	n/a	chr12:30363953-30363964
21	CEBPB	chr12:30314014-30314075	A549	lung:	n/a	n/a
22	CHD2	chr12:30323346-30323475	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr12:30410503-30410598	Hela-S3	cervix:	n/a	n/a
24	CTBP2	chr12:30322662-30323667	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr12:30391737-30391853	K562	blood:	n/a	chr12:30391781-30391799
26	CTCF	chr12:30391700-30391850	HPAF	blood vessel:	n/a	chr12:30391781-30391799
27	CTCF	chr12:30377109-30377202	GM20000	blood:	n/a	n/a
28	CTCF	chr12:30361917-30361939	LNCaP	prostate:	n/a	n/a
29	CTCF	chr12:30330749-30330916	Medullo	brain:	n/a	n/a
30	CTCF	chr12:30354401-30354473	K562	blood:	n/a	n/a
31	CTCF	chr12:30330780-30330930	BE2_C	brain:	n/a	n/a
32	CTCF	chr12:30391700-30391850	HCPEpiC	choroid plexus:	n/a	chr12:30391781-30391799
33	CTCF	chr12:30391700-30391850	HMF	breast:	n/a	chr12:30391781-30391799
34	CTCF	chr12:30391660-30391810	AG04450	lung:	n/a	chr12:30391781-30391799
35	CTCF	chr12:30381550-30381652	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr12:30335849-30335887	ProgFib	skin:	n/a	n/a
37	CTCF	chr12:30354410-30354459	GM19240	blood:	n/a	n/a
38	CTCF	chr12:30354340-30354490	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr12:30330740-30330890	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr12:30354300-30354450	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr12:30391720-30391870	HPAF	blood vessel:	n/a	chr12:30391781-30391799
42	CTCF	chr12:30354480-30354630	GM12873	blood:	n/a	n/a
43	CTCF	chr12:30354340-30354490	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr12:30354380-30354530	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr12:30354320-30354470	HAc	cerebellar:	n/a	n/a
46	CTCF	chr12:30354340-30354490	AG04449	skin:	n/a	n/a
47	CTCF	chr12:30380614-30380652	ProgFib	skin:	n/a	n/a
48	CTCF	chr12:30354393-30354479	A549	lung:	n/a	n/a
49	CTCF	chr12:30354340-30354490	NHEK	skin:	n/a	n/a
50	CTCF	chr12:30391720-30391870	NB4	blood:	n/a	chr12:30391781-30391799

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:30353957-30354007	GM06990	blood:	n/a
2	chr12:30323251-30323301	PFSK-1	brain:	n/a
3	chr12:30353957-30354007	GM06990	blood:	n/a
4	chr12:30323251-30323301	PFSK-1	brain:	n/a
5	chr12:30354142-30354192	HUVEC	blood vessel:	n/a
6	chr12:30354142-30354192	AG04450	lung:	fetal
7	chr12:30354663-30354713	GM12892	blood:	n/a
8	chr12:30351139-30351189	ProgFib	skin:	n/a
9	chr12:30354611-30354661	HAEpiC	amniotic membrane:	n/a
10	chr12:30354246-30354296	HEK293	kidney:	embryo
11	chr12:30354663-30354713	PFSK-1	brain:	n/a
12	chr12:30354663-30354713	BJ	skin:	n/a
13	chr12:30353957-30354007	HMEC	breast:	n/a
14	chr12:30322864-30322914	SK-N-SH_RA	brain:	n/a
15	chr12:30325938-30325988	MCF10A-Er-Src	breast:	n/a
16	chr12:30357109-30357159	IMR90	lung:	fetal
17	chr12:30322730-30322780	HEEpiC	esophagus:	n/a
18	chr12:30354246-30354296	T-47D	breast:	n/a
19	chr12:30357109-30357159	AG09309	skin:	n/a
20	chr12:30354663-30354713	ProgFib	skin:	n/a
21	chr12:30322864-30322914	SK-N-MC	brain:	n/a
22	chr12:30354663-30354713	Jurkat	blood:	n/a
23	chr12:30354142-30354192	Jurkat	blood:	n/a
24	chr12:30354142-30354192	AoSMC	blood vessel:	n/a
25	chr12:30323676-30323726	SAEC	small airway:	n/a
26	chr12:30354663-30354713	SK-N-MC	brain:	n/a
27	chr12:30322730-30322780	MCF-7	breast:	n/a
28	chr12:30354246-30354296	GM19239	blood:	n/a
29	chr12:30354611-30354661	HEEpiC	esophagus:	n/a
30	chr12:30354663-30354713	NB4	blood:	n/a
31	chr12:30357109-30357159	NT2-D1	testis:	n/a
32	chr12:30323251-30323301	CMK	blood:	n/a
33	chr12:30351139-30351189	NHDF-neo	bronchial:	n/a
34	chr12:30323676-30323726	GM06990	blood:	n/a
35	chr12:30357109-30357159	HRE	kidney:	n/a
36	chr12:30320269-30320319	CMK	blood:	n/a
37	chr12:30320269-30320319	HCPEpiC	choroid plexus:	n/a
38	chr12:30353957-30354007	HL-60	blood:	n/a
39	chr12:30323251-30323301	U87	brain:	n/a
40	chr12:30322730-30322780	HCT-116	colon:	n/a
41	chr12:30322730-30322780	ProgFib	skin:	n/a
42	chr12:30357109-30357159	Hepatocyte	liver:	n/a
43	chr12:30354663-30354713	SK-N-SH_RA	brain:	n/a
44	chr12:30354142-30354192	NB4	blood:	n/a
45	chr12:30354142-30354192	SK-N-SH	brain:	n/a
46	chr12:30354663-30354713	GM12878	blood:	n/a
47	chr12:30354142-30354192	MCF10A-Er-Src	breast:	n/a
48	chr12:30354142-30354192	MCF-7	breast:	n/a
49	chr12:30357109-30357159	HepG2	liver:	n/a
50	chr12:30351139-30351189	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:30394846..30396422-chr12:30402248..30404623,2	K562	blood:
2	chr12:30345156..30347893-chr12:30349576..30351701,2	MCF-7	breast:
3	chr12:30375754..30378220-chr12:30379404..30381460,2	K562	blood:
4	chr12:30351001..30353432-chr12:30354481..30356033,2	MCF-7	breast:
5	chr12:30375754..30378220-chr12:30379404..30381460,2	K562	blood:
6	chr12:30307525..30310508-chr12:30315898..30318662,2	K562	blood:
7	chr12:30388256..30390909-chr12:30391939..30394799,2	K562	blood:
8	chr12:30354231..30355981-chr12:30359354..30362210,2	K562	blood:
9	chr12:30345156..30347893-chr12:30349576..30351701,2	MCF-7	breast:
10	chr12:30351001..30353432-chr12:30354481..30356033,2	MCF-7	breast:
11	chr12:30307525..30310508-chr12:30315898..30318662,2	K562	blood:
12	chr12:30354231..30355981-chr12:30359354..30362210,2	K562	blood:
13	chr12:30388256..30390909-chr12:30391939..30394799,2	K562	blood:
14	chr12:30394846..30396422-chr12:30402248..30404623,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IPO8-1	chr12:30385709-30385793	ENSG00000257756
2	lnc-IPO8-1	chr12:30383718-30383968	ENSG00000257756
3	lnc-TSPAN11-5	chr12:30361375-30361505	ENSG00000257262
4	lnc-TSPAN11-5	chr12:30353916-30354041	ENSG00000257262
5	lnc-IPO8-1	chr12:30397268-30397338	ENSG00000257756
6	lnc-TSPAN11-5	chr12:30370536-30370849	ENSG00000257262

Variant related genes	Relation type
ENSG00000257262	TF binding region
ENSG00000257262	CpG island

Extended variants
information (count: 1731 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1731 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10843627	chr12:30309076-30309077	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs548526185	chr12:30311201-30311202	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs565305517	chr12:30311215-30311216	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs532370642	chr12:30311226-30311227	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs547880516	chr12:30311236-30311237	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs559416675	chr12:30311258-30311259	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs529876758	chr12:30311260-30311261	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs116620643	chr12:30311320-30311321	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs569641959	chr12:30311326-30311327	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs563603690	chr12:30311373-30311374	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs114238747	chr12:30311374-30311375	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs192538050	chr12:30311382-30311383	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs570435683	chr12:30311384-30311385	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs75748277	chr12:30311400-30311401	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs572138776	chr12:30311404-30311405	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs553079830	chr12:30311410-30311411	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs574575243	chr12:30311431-30311432	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs139759306	chr12:30311447-30311448	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs536881992	chr12:30311449-30311450	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs184211408	chr12:30311454-30311455	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs576684462	chr12:30311457-30311458	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs115796888	chr12:30311515-30311516	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs565400481	chr12:30311544-30311545	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs35523551	chr12:30311545-30311546	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs138779966	chr12:30311569-30311570	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs541056231	chr12:30311571-30311572	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs140409338	chr12:30311711-30311712	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs77947645	chr12:30311792-30311793	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs541892031	chr12:30311793-30311794	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs563343713	chr12:30311800-30311801	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs61922908	chr12:30311840-30311841	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs563158226	chr12:30311854-30311855	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs529720769	chr12:30311876-30311877	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs530577881	chr12:30311901-30311902	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs74856099	chr12:30311902-30311903	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs200262467	chr12:30311917-30311918	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs143681092	chr12:30311919-30311920	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs201654041	chr12:30311920-30311921	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs199984846	chr12:30311921-30311922	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs199554496	chr12:30311922-30311923	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs72512288	chr12:30311923-30311924	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs199532350	chr12:30311924-30311925	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs570652807	chr12:30311951-30311952	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs7133761	chr12:30311977-30311978	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs113477576	chr12:30311986-30311987	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs199579742	chr12:30311987-30311988	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs546603446	chr12:30312016-30312017	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs566613162	chr12:30312067-30312068	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs186663064	chr12:30312079-30312080	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs7306389	chr12:30312107-30312108	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Melanoma	18172304	CNVD
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
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	17133270	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:323 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:30307600-30309200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr12:30307800-30309200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr12:30311200-30312000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr12:30312000-30312200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr12:30312200-30312400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr12:30312400-30313200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr12:30313200-30313600	ZNF genes & repeats	Left Ventricle	heart
8	chr12:30313200-30313800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr12:30313600-30313800	ZNF genes & repeats	Aorta	Aorta
10	chr12:30313600-30313800	ZNF genes & repeats	Pancreas	Pancrea
11	chr12:30315600-30316400	Enhancers	Brain Germinal Matrix	brain
12	chr12:30316400-30316600	Enhancers	HSMMtube	muscle
13	chr12:30316600-30317200	Weak transcription	HSMMtube	muscle
14	chr12:30316800-30319200	Enhancers	Fetal Lung	lung
15	chr12:30317200-30317600	Enhancers	HSMMtube	muscle
16	chr12:30317400-30318000	Enhancers	Spleen	Spleen
17	chr12:30317400-30318200	Enhancers	Fetal Stomach	stomach
18	chr12:30317600-30317800	Flanking Active TSS	HSMMtube	muscle
19	chr12:30318800-30320200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr12:30319000-30319200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr12:30319000-30319200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr12:30319000-30320200	Enhancers	NHDF-Ad	bronchial
23	chr12:30319200-30320000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr12:30319800-30320000	Enhancers	NH-A	brain
25	chr12:30320000-30320200	Bivalent/Poised TSS	Fetal Lung	lung
26	chr12:30321400-30322000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr12:30321600-30322200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
28	chr12:30321800-30322000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
29	chr12:30322000-30322400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
30	chr12:30322000-30322400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr12:30322000-30322600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
32	chr12:30322000-30322600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
33	chr12:30322000-30322800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
34	chr12:30322200-30322400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
35	chr12:30322200-30322400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr12:30322200-30322400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr12:30322200-30322800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
38	chr12:30322400-30323000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr12:30322400-30323600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
40	chr12:30322400-30323800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
41	chr12:30322600-30322800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
42	chr12:30322600-30323200	Bivalent/Poised TSS	Right Ventricle	heart
43	chr12:30322600-30323600	Active TSS	H9 Cell Line	embryonic stem cell
44	chr12:30322600-30323600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
45	chr12:30322600-30323800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
46	chr12:30322600-30323800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
47	chr12:30322800-30323000	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr12:30322800-30323200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
49	chr12:30322800-30323200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
50	chr12:30322800-30323200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin

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