Variant report

Variant	esv2758302
Chromosome Location	chr12:30023167-30175232
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	ATF1	chr12:30074366-30074532	K562	blood:	n/a	n/a
2	ATF1	chr12:30169213-30169273	K562	blood:	n/a	n/a
3	ATF2	chr12:30037909-30038322	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr12:30037896-30038293	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr12:30037174-30037384	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr12:30037980-30038278	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr12:30037917-30038252	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr12:30083094-30083126	GM12878	blood:	n/a	n/a
9	BRCA1	chr12:30042695-30042991	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr12:30035579-30035745	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr12:30153435-30153826	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr12:30109117-30109423	HepG2	liver:	n/a	chr12:30109282-30109293
13	CEBPB	chr12:30113018-30113238	A549	lung:	n/a	chr12:30113192-30113203
14	CEBPB	chr12:30037981-30038350	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr12:30073678-30073947	IMR90	lung:	n/a	chr12:30073815-30073826 chr12:30073817-30073826
16	CEBPB	chr12:30114701-30115153	HepG2	liver:	n/a	chr12:30114798-30114809 chr12:30114796-30114807 chr12:30114796-30114809 chr12:30114796-30114809 chr12:30114921-30114934
17	CEBPB	chr12:30097586-30097898	IMR90	lung:	n/a	n/a
18	CEBPB	chr12:30042693-30042986	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr12:30073337-30073369	HepG2	liver:	n/a	chr12:30073350-30073361
20	CEBPB	chr12:30146138-30146480	HepG2	liver:	n/a	chr12:30146302-30146311 chr12:30146302-30146311 chr12:30146300-30146313 chr12:30146302-30146311
21	CEBPB	chr12:30134002-30134161	K562	blood:	n/a	chr12:30134097-30134108
22	CEBPB	chr12:30133909-30134272	H1-hESC	embryonic stem cell:	n/a	chr12:30134097-30134108
23	CEBPB	chr12:30109122-30109385	A549	lung:	n/a	chr12:30109282-30109293
24	CEBPB	chr12:30134001-30134216	Hela-S3	cervix:	n/a	chr12:30134097-30134108
25	CEBPB	chr12:30146167-30146385	A549	lung:	n/a	chr12:30146302-30146311 chr12:30146302-30146311 chr12:30146300-30146313 chr12:30146302-30146311
26	CEBPB	chr12:30097592-30097854	HepG2	liver:	n/a	n/a
27	CEBPB	chr12:30073708-30073951	HepG2	liver:	n/a	chr12:30073815-30073826 chr12:30073817-30073826
28	CEBPB	chr12:30134021-30134244	HepG2	liver:	n/a	chr12:30134097-30134108
29	CEBPB	chr12:30146134-30146446	IMR90	lung:	n/a	chr12:30146302-30146311 chr12:30146302-30146311 chr12:30146300-30146313 chr12:30146302-30146311
30	CEBPB	chr12:30133979-30134265	K562	blood:	n/a	chr12:30134097-30134108
31	CEBPB	chr12:30113155-30113253	HepG2	liver:	n/a	chr12:30113192-30113203
32	CEBPB	chr12:30097554-30097899	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr12:30134025-30134220	IMR90	lung:	n/a	chr12:30134097-30134108
34	CEBPB	chr12:30030003-30030203	HepG2	liver:	n/a	chr12:30030066-30030077
35	CEBPB	chr12:30146170-30146393	H1-hESC	embryonic stem cell:	n/a	chr12:30146302-30146311 chr12:30146302-30146311 chr12:30146300-30146313 chr12:30146302-30146311
36	CEBPB	chr12:30097575-30097889	A549	lung:	n/a	n/a
37	CEBPB	chr12:30134005-30134274	A549	lung:	n/a	chr12:30134097-30134108
38	CHD2	chr12:30037916-30038373	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr12:30042718-30043019	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr12:30032183-30032581	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr12:30054600-30054750	AG09309	skin:	n/a	n/a
42	CTCF	chr12:30042800-30042950	BE2_C	brain:	n/a	n/a
43	CTCF	chr12:30042800-30042950	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr12:30156680-30156830	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr12:30054623-30054850	MCF-7	breast:	n/a	chr12:30054741-30054757 chr12:30054735-30054756
46	CTCF	chr12:30054660-30054810	HepG2	liver:	n/a	chr12:30054741-30054757 chr12:30054735-30054756
47	CTCF	chr12:30042760-30042910	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr12:30042769-30042969	LNCaP	prostate:	n/a	n/a
49	CTCF	chr12:30155566-30155666	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:30156760-30156910	AG10803	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:30032232-30032282	HL-60	blood:	n/a
2	chr12:30032232-30032282	H1-hESC	embryonic stem cell:	embryo
3	chr12:30032232-30032282	HRPEpiC	eye:	n/a
4	chr12:30032232-30032282	SK-N-SH	brain:	n/a
5	chr12:30032232-30032282	NHBE	bronchial:	n/a
6	chr12:30032232-30032282	NHDF-neo	bronchial:	n/a
7	chr12:30032232-30032282	HepG2	liver:	n/a
8	chr12:30032232-30032282	PFSK-1	brain:	n/a
9	chr12:30032232-30032282	RPTEC	kidney:	n/a
10	chr12:30032232-30032282	GM19239	blood:	n/a
11	chr12:30032232-30032282	AG04449	skin:	fetal
12	chr12:30032232-30032282	HCF	heart:	n/a
13	chr12:30032232-30032282	HNPCEpiC	eye:	n/a
14	chr12:30032232-30032282	AG10803	skin:	n/a
15	chr12:30032232-30032282	ECC-1	luminal epithelium:	n/a
16	chr12:30032232-30032282	GM12891	blood:	n/a
17	chr12:30032232-30032282	HCT-116	colon:	n/a
18	chr12:30032232-30032282	GM12892	blood:	n/a
19	chr12:30032232-30032282	SKMC	muscle:	n/a
20	chr12:30032232-30032282	HEK293	kidney:	embryo
21	chr12:30032232-30032282	A549	lung:	n/a
22	chr12:30032232-30032282	AG04450	lung:	fetal
23	chr12:30032232-30032282	HRCEpiC	kidney:	n/a
24	chr12:30032232-30032282	NH-A	brain:	n/a
25	chr12:30032232-30032282	HMEC	breast:	n/a
26	chr12:30032232-30032282	Caco-2	colon:	n/a
27	chr12:30032232-30032282	PANC-1	pancreas:	n/a
28	chr12:30032232-30032282	NT2-D1	testis:	n/a
29	chr12:30032232-30032282	HEEpiC	esophagus:	n/a
30	chr12:30032232-30032282	Jurkat	blood:	n/a
31	chr12:30032232-30032282	IMR90	lung:	fetal
32	chr12:30032232-30032282	K562	blood:	n/a
33	chr12:30032232-30032282	U87	brain:	n/a
34	chr12:30032232-30032282	ovcar-3	ovarian:	n/a
35	chr12:30032232-30032282	SK-N-MC	brain:	n/a
36	chr12:30032232-30032282	PrEC	prostate:	n/a
37	chr12:30032232-30032282	T-47D	breast:	n/a
38	chr12:30032232-30032282	MCF-7	breast:	n/a
39	chr12:30032232-30032282	HPAEpiC	pulmonary alveolar:	n/a
40	chr12:30032232-30032282	HIPEpiC	eye:	n/a
41	chr12:30032232-30032282	HRE	kidney:	n/a
42	chr12:30032232-30032282	AG09319	gingival:	n/a
43	chr12:30032232-30032282	HCM	heart:	n/a
44	chr12:30032232-30032282	GM12878	blood:	n/a
45	chr12:30032232-30032282	Hepatocyte	liver:	n/a
46	chr12:30032232-30032282	AoSMC	blood vessel:	n/a
47	chr12:30032232-30032282	BE2_C	brain:	n/a
48	chr12:30032232-30032282	NB4	blood:	n/a
49	chr12:30032232-30032282	ProgFib	skin:	n/a
50	chr12:30032232-30032282	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:30048962..30051425-chr12:30054034..30055862,2	MCF-7	breast:
2	chr12:30161244..30163502-chr12:30164390..30167375,2	K562	blood:
3	chr12:30012273..30014244-chr12:30025832..30028070,2	MCF-7	breast:
4	chr12:30107931..30110000-chr12:30112088..30114969,2	K562	blood:
5	chr12:30107931..30110000-chr12:30112088..30114969,2	K562	blood:
6	chr12:30161244..30163502-chr12:30164390..30167375,2	K562	blood:
7	chr12:30093971..30096199-chr12:30100888..30102830,2	MCF-7	breast:
8	chr12:30093971..30096199-chr12:30100888..30102830,2	MCF-7	breast:
9	chr12:30130967..30132688-chr12:30459870..30462012,2	MCF-7	breast:
10	chr12:30029795..30032959-chr12:30033915..30036859,3	K562	blood:
11	chr12:30029795..30032959-chr12:30033915..30036859,3	K562	blood:
12	chr12:30048962..30051425-chr12:30054034..30055862,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000253052	TF binding region
ENSG00000253052	CpG island

Extended variants
information (count: 4221 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:4221 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552051979	chr12:30023192-30023193	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs529012847	chr12:30023253-30023254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143995364	chr12:30023326-30023327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549705036	chr12:30023334-30023335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35723679	chr12:30023373-30023374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191589114	chr12:30023401-30023402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184149744	chr12:30023451-30023452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549983267	chr12:30023463-30023464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571758182	chr12:30023475-30023476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12813154	chr12:30023539-30023540	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs535939887	chr12:30023554-30023555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs77366831	chr12:30023555-30023556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10431276	chr12:30023678-30023679	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs536113854	chr12:30023688-30023689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554457944	chr12:30023745-30023746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12811985	chr12:30023784-30023785	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs74472588	chr12:30023827-30023828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78647777	chr12:30023836-30023837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576912739	chr12:30023899-30023900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186620104	chr12:30023921-30023922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560625522	chr12:30023989-30023990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558461696	chr12:30023991-30023992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370925660	chr12:30024043-30024044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576913815	chr12:30024045-30024046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549666242	chr12:30024100-30024101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191119335	chr12:30024193-30024194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148534292	chr12:30024203-30024204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2101263	chr12:30024232-30024233	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs571558379	chr12:30024234-30024235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532420859	chr12:30024248-30024249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142854813	chr12:30024300-30024301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565504057	chr12:30024306-30024307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574496346	chr12:30024374-30024375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577100467	chr12:30024404-30024405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554420996	chr12:30024414-30024415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569981733	chr12:30024459-30024460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555463773	chr12:30024479-30024480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201323243	chr12:30024545-30024546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2351035	chr12:30024546-30024547	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs6487853	chr12:30024547-30024548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs6487854	chr12:30024568-30024569	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs576766949	chr12:30024583-30024584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs374112461	chr12:30024584-30024585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541102452	chr12:30024606-30024607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535225272	chr12:30024648-30024649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs367694932	chr12:30024701-30024702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182450354	chr12:30024705-30024706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552187807	chr12:30024706-30024707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185108361	chr12:30024714-30024715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563998427	chr12:30024718-30024719	Weak transcription	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:315 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:30018200-30023600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr12:30020200-30027000	Weak transcription	Fetal Kidney	kidney
3	chr12:30022800-30024000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr12:30022800-30024200	Enhancers	Fetal Lung	lung
5	chr12:30023000-30023800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:30023000-30024200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr12:30023000-30024400	Enhancers	Fetal Stomach	stomach
8	chr12:30023000-30032400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr12:30023600-30024200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr12:30023600-30024400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr12:30023600-30024400	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr12:30024200-30026400	Weak transcription	Fetal Lung	lung
13	chr12:30024200-30032400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr12:30024400-30027000	Weak transcription	Fetal Stomach	stomach
15	chr12:30026400-30027800	Enhancers	Fetal Lung	lung
16	chr12:30027000-30027200	Enhancers	Fetal Stomach	stomach
17	chr12:30027000-30027600	Enhancers	Fetal Kidney	kidney
18	chr12:30031000-30031200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr12:30031200-30032400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr12:30031400-30031600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr12:30031600-30032200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr12:30032200-30033200	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr12:30032200-30033400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr12:30032200-30033400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr12:30032200-30033400	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr12:30032400-30032800	Enhancers	H9 Cell Line	embryonic stem cell
27	chr12:30032400-30032800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:30032400-30033000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr12:30032400-30033200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr12:30032400-30033200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr12:30032400-30033400	Enhancers	H1 Cell Line	embryonic stem cell
32	chr12:30032400-30033400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr12:30032400-30033400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr12:30032400-30033400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr12:30032400-30033400	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr12:30032400-30033600	Enhancers	Fetal Heart	heart
37	chr12:30032800-30036800	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr12:30033200-30036800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr12:30033200-30036800	Weak transcription	Aorta	Aorta
40	chr12:30033400-30035000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr12:30033400-30035800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr12:30033400-30036000	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr12:30033400-30036200	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr12:30033400-30036600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr12:30033400-30036800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr12:30033400-30036800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr12:30033600-30034800	Weak transcription	Fetal Heart	heart
48	chr12:30034800-30037000	Enhancers	Fetal Heart	heart
49	chr12:30035000-30035200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr12:30035000-30035200	Enhancers	Fetal Muscle Leg	muscle

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