Variant report

Variant	nsv1044929
Chromosome Location	chr12:30318488-30409475
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	chr12:30360483-30360805	HepG2	liver:	n/a	chr12:30360641-30360652
6	CEBPB	chr12:30361704-30361917	A549	lung:	n/a	chr12:30361791-30361802
7	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
8	CEBPB	chr12:30363917-30364012	A549	lung:	n/a	chr12:30363953-30363964
9	CEBPB	chr12:30363875-30364075	K562	blood:	n/a	chr12:30363953-30363964
10	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
11	CEBPB	chr12:30377310-30377513	A549	lung:	n/a	chr12:30377386-30377397
12	CEBPB	chr12:30361676-30361926	HepG2	liver:	n/a	chr12:30361791-30361802
13	CEBPB	chr12:30390833-30391122	HepG2	liver:	n/a	chr12:30390970-30390981
14	CEBPB	chr12:30351134-30351189	HepG2	liver:	n/a	n/a
15	CEBPB	chr12:30361766-30361910	K562	blood:	n/a	chr12:30361791-30361802
16	CEBPB	chr12:30363864-30364111	HepG2	liver:	n/a	chr12:30363953-30363964
17	CEBPB	chr12:30377254-30377495	HepG2	liver:	n/a	chr12:30377386-30377397
18	CEBPB	chr12:30318553-30318692	K562	blood:	n/a	n/a
19	CEBPB	chr12:30355896-30356101	HepG2	liver:	n/a	n/a
20	CEBPB	chr12:30361651-30361976	IMR90	lung:	n/a	chr12:30361791-30361802
21	CHD2	chr12:30323346-30323475	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr12:30322662-30323667	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr12:30391705-30391861	HUVEC	blood vessel:	n/a	chr12:30391781-30391799
24	CTCF	chr12:30330740-30330890	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr12:30330560-30330710	AG09319	gingival:	n/a	n/a
26	CTCF	chr12:30391660-30391810	AG04450	lung:	n/a	chr12:30391781-30391799
27	CTCF	chr12:30391640-30391790	BJ	skin:	n/a	n/a
28	CTCF	chr12:30391720-30391870	HRPEpiC	eye:	n/a	chr12:30391781-30391799
29	CTCF	chr12:30354380-30354530	HPF	lung:	n/a	n/a
30	CTCF	chr12:30354340-30354490	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr12:30391580-30391730	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr12:30391660-30391810	Hela-S3	cervix:	n/a	chr12:30391781-30391799
33	CTCF	chr12:30391700-30391850	HPF	lung:	n/a	chr12:30391781-30391799
34	CTCF	chr12:30391620-30391770	HCFaa	heart:	n/a	n/a
35	CTCF	chr12:30335557-30335599	Fibrobl	skin:	n/a	n/a
36	CTCF	chr12:30361881-30361911	LNCaP	prostate:	n/a	n/a
37	CTCF	chr12:30330780-30330930	HPF	lung:	n/a	n/a
38	CTCF	chr12:30330740-30330890	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr12:30354375-30354507	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr12:30354340-30354490	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr12:30354340-30354490	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr12:30377109-30377202	GM20000	blood:	n/a	n/a
43	CTCF	chr12:30330740-30330890	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr12:30354410-30354459	GM19240	blood:	n/a	n/a
45	CTCF	chr12:30354395-30354479	GM19239	blood:	n/a	n/a
46	CTCF	chr12:30391800-30391950	AG09319	gingival:	n/a	n/a
47	CTCF	chr12:30354340-30354490	NHEK	skin:	n/a	n/a
48	CTCF	chr12:30354420-30354570	HCFaa	heart:	n/a	n/a
49	CTCF	chr12:30354400-30354550	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr12:30391740-30391890	A549	lung:	n/a	chr12:30391781-30391799

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:30354142-30354192	HCPEpiC	choroid plexus:	n/a
2	chr12:30320269-30320319	T-47D	breast:	n/a
3	chr12:30354246-30354296	AG04449	skin:	fetal
4	chr12:30354142-30354192	HCPEpiC	choroid plexus:	n/a
5	chr12:30320269-30320319	T-47D	breast:	n/a
6	chr12:30354246-30354296	AG04449	skin:	fetal
7	chr12:30354663-30354713	HEK293	kidney:	embryo
8	chr12:30323251-30323301	PFSK-1	brain:	n/a
9	chr12:30325938-30325988	U87	brain:	n/a
10	chr12:30354142-30354192	BE2_C	brain:	n/a
11	chr12:30323676-30323726	AoSMC	blood vessel:	n/a
12	chr12:30354611-30354661	HNPCEpiC	eye:	n/a
13	chr12:30357109-30357159	HUVEC	blood vessel:	n/a
14	chr12:30322730-30322780	Jurkat	blood:	n/a
15	chr12:30354663-30354713	HIPEpiC	eye:	n/a
16	chr12:30320269-30320319	NB4	blood:	n/a
17	chr12:30354611-30354661	MCF10A-Er-Src	breast:	n/a
18	chr12:30323251-30323301	SK-N-SH	brain:	n/a
19	chr12:30354246-30354296	Caco-2	colon:	n/a
20	chr12:30323251-30323301	HRE	kidney:	n/a
21	chr12:30354246-30354296	HL-60	blood:	n/a
22	chr12:30322730-30322780	ovcar-3	ovarian:	n/a
23	chr12:30320269-30320319	HRPEpiC	eye:	n/a
24	chr12:30357109-30357159	AG10803	skin:	n/a
25	chr12:30354142-30354192	SAEC	small airway:	n/a
26	chr12:30322730-30322780	PFSK-1	brain:	n/a
27	chr12:30353957-30354007	HPAEpiC	pulmonary alveolar:	n/a
28	chr12:30354246-30354296	ovcar-3	ovarian:	n/a
29	chr12:30320269-30320319	HPAEpiC	pulmonary alveolar:	n/a
30	chr12:30323676-30323726	HCT-116	colon:	n/a
31	chr12:30353957-30354007	AG09309	skin:	n/a
32	chr12:30323676-30323726	NT2-D1	testis:	n/a
33	chr12:30354663-30354713	Hela-S3	cervix:	n/a
34	chr12:30354246-30354296	CMK	blood:	n/a
35	chr12:30354246-30354296	HAEpiC	amniotic membrane:	n/a
36	chr12:30354246-30354296	ECC-1	luminal epithelium:	n/a
37	chr12:30354611-30354661	HCT-116	colon:	n/a
38	chr12:30322730-30322780	HCM	heart:	n/a
39	chr12:30354611-30354661	HRE	kidney:	n/a
40	chr12:30354142-30354192	NHBE	bronchial:	n/a
41	chr12:30351139-30351189	HEK293	kidney:	embryo
42	chr12:30322730-30322780	GM12878	blood:	n/a
43	chr12:30353957-30354007	SK-N-SH	brain:	n/a
44	chr12:30322730-30322780	LNCaP	prostate:	n/a
45	chr12:30354246-30354296	K562	blood:	n/a
46	chr12:30353957-30354007	BJ	skin:	n/a
47	chr12:30354663-30354713	NB4	blood:	n/a
48	chr12:30354142-30354192	AG04449	skin:	fetal
49	chr12:30351139-30351189	HAEpiC	amniotic membrane:	n/a
50	chr12:30322730-30322780	SK-N-MC	brain:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IPO8-1	chr12:30385709-30385793	ENSG00000257756
2	lnc-TSPAN11-5	chr12:30361375-30361505	ENSG00000257262
3	lnc-TSPAN11-5	chr12:30353916-30354041	ENSG00000257262
4	lnc-IPO8-1	chr12:30397268-30397338	ENSG00000257756
5	lnc-IPO8-1	chr12:30383718-30383968	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: 1412 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1412 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2139745	chr12:30318488-30318489	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546605387	chr12:30318567-30318568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567742646	chr12:30318629-30318630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561796847	chr12:30318674-30318675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529003205	chr12:30318803-30318804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78404994	chr12:30318806-30318807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs35239024	chr12:30318811-30318812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570149839	chr12:30318842-30318843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs143649585	chr12:30318873-30318874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148179041	chr12:30318892-30318893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs75361584	chr12:30318967-30318968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552586368	chr12:30319006-30319007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs180835334	chr12:30319050-30319051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs16935498	chr12:30319118-30319119	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs535586710	chr12:30319120-30319121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528000708	chr12:30319126-30319127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs11050697	chr12:30319128-30319129	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs376945886	chr12:30319145-30319146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575397000	chr12:30319180-30319181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79948729	chr12:30319208-30319209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185779218	chr12:30319262-30319263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189495248	chr12:30319271-30319272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540507205	chr12:30319310-30319311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561685061	chr12:30319338-30319339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs370550915	chr12:30319344-30319345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181970155	chr12:30319353-30319354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550533805	chr12:30319361-30319362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2351219	chr12:30319380-30319381	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs35355013	chr12:30319395-30319396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112723995	chr12:30319397-30319398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs55685924	chr12:30319402-30319403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs398098100	chr12:30319403-30319404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370732531	chr12:30319452-30319453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570683030	chr12:30319465-30319466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs142009921	chr12:30319466-30319467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546849474	chr12:30319473-30319474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75234214	chr12:30319495-30319496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561492527	chr12:30319529-30319530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573390694	chr12:30319599-30319600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs187568076	chr12:30319661-30319662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs376596478	chr12:30319701-30319702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs116164084	chr12:30319735-30319736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs557674084	chr12:30319741-30319742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs199549947	chr12:30319756-30319757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs34367539	chr12:30319757-30319758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150684437	chr12:30319764-30319765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559525002	chr12:30319766-30319767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs138703767	chr12:30319794-30319795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs34735287	chr12:30319795-30319796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs67122428	chr12:30319796-30319797	Enhancers	n/a	n/a	Overlapped CNVs	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:298 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:30316800-30319200	Enhancers	Fetal Lung	lung
2	chr12:30318800-30320200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr12:30319000-30319200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr12:30319000-30319200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:30319000-30320200	Enhancers	NHDF-Ad	bronchial
6	chr12:30319200-30320000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr12:30319800-30320000	Enhancers	NH-A	brain
8	chr12:30320000-30320200	Bivalent/Poised TSS	Fetal Lung	lung
9	chr12:30321400-30322000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr12:30321600-30322200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
11	chr12:30321800-30322000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
12	chr12:30322000-30322400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
13	chr12:30322000-30322400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr12:30322000-30322600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
15	chr12:30322000-30322600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
16	chr12:30322000-30322800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
17	chr12:30322200-30322400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
18	chr12:30322200-30322400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr12:30322200-30322400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr12:30322200-30322800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
21	chr12:30322400-30323000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr12:30322400-30323600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
23	chr12:30322400-30323800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
24	chr12:30322600-30322800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
25	chr12:30322600-30323200	Bivalent/Poised TSS	Right Ventricle	heart
26	chr12:30322600-30323600	Active TSS	H9 Cell Line	embryonic stem cell
27	chr12:30322600-30323600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
28	chr12:30322600-30323800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
29	chr12:30322600-30323800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
30	chr12:30322800-30323000	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr12:30322800-30323200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
32	chr12:30322800-30323200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
33	chr12:30322800-30323200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr12:30322800-30323200	Bivalent Enhancer	Left Ventricle	heart
35	chr12:30322800-30323400	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr12:30322800-30323600	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
37	chr12:30322800-30323600	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr12:30322800-30323600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr12:30322800-30323600	Bivalent Enhancer	Lung	lung
40	chr12:30322800-30323600	Enhancers	Pancreas	Pancrea
41	chr12:30322800-30323800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
42	chr12:30322800-30323800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
43	chr12:30323000-30323200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr12:30323000-30323200	Bivalent/Poised TSS	Fetal Brain Female	brain
45	chr12:30323000-30323200	Bivalent/Poised TSS	Fetal Stomach	stomach
46	chr12:30323000-30323200	Bivalent/Poised TSS	Psoas Muscle	Psoas
47	chr12:30323000-30323400	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr12:30323000-30323400	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr12:30323000-30323400	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
50	chr12:30323000-30323400	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain

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