Variant report

Variant	nsv1050233
Chromosome Location	chr12:30590071-30670919
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:730)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:730 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:30610510-30611017	K562	blood:	n/a	n/a
2	ARID3A	chr12:30610643-30610992	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:30590673-30590940	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:30660618-30662061	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:30603569-30604106	K562	blood:	n/a	n/a
6	ARID3A	chr12:30590316-30590317	HepG2	liver:	n/a	n/a
7	ATF1	chr12:30610626-30610862	K562	blood:	n/a	n/a
8	ATF1	chr12:30651495-30651661	K562	blood:	n/a	n/a
9	ATF1	chr12:30603751-30604058	K562	blood:	n/a	n/a
10	ATF3	chr12:30610527-30610879	K562	blood:	n/a	n/a
11	BCL11A	chr12:30652693-30652850	GM12878	blood:	n/a	n/a
12	BHLHE40	chr12:30661452-30661610	K562	blood:	n/a	n/a
13	BHLHE40	chr12:30603732-30604120	K562	blood:	n/a	n/a
14	BHLHE40	chr12:30661416-30661829	HepG2	liver:	n/a	n/a
15	BHLHE40	chr12:30661416-30661885	HepG2	liver:	n/a	n/a
16	CBX3	chr12:30610474-30611013	HCT-116	colon:	n/a	n/a
17	CCNT2	chr12:30603407-30604027	K562	blood:	n/a	n/a
18	CEBPB	chr12:30661266-30661916	HepG2	liver:	n/a	n/a
19	CEBPB	chr12:30610566-30611106	Hela-S3	cervix:	n/a	chr12:30611021-30611032
20	CEBPB	chr12:30600990-30601270	Hela-S3	cervix:	n/a	chr12:30601098-30601109 chr12:30601130-30601141
21	CEBPB	chr12:30663192-30663437	HepG2	liver:	n/a	chr12:30663267-30663278
22	CEBPB	chr12:30640201-30640505	K562	blood:	n/a	chr12:30640367-30640378 chr12:30640281-30640294 chr12:30640282-30640293 chr12:30640367-30640380
23	CEBPB	chr12:30640161-30640481	HepG2	liver:	n/a	chr12:30640367-30640378 chr12:30640281-30640294 chr12:30640282-30640293 chr12:30640367-30640380
24	CEBPB	chr12:30610735-30611110	K562	blood:	n/a	chr12:30611021-30611032
25	CEBPB	chr12:30590637-30591005	HepG2	liver:	n/a	n/a
26	CEBPB	chr12:30640248-30640461	Hela-S3	cervix:	n/a	chr12:30640367-30640378 chr12:30640281-30640294 chr12:30640282-30640293 chr12:30640367-30640380
27	CEBPB	chr12:30590798-30590863	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr12:30590623-30590904	HepG2	liver:	n/a	n/a
29	CEBPB	chr12:30663140-30663397	A549	lung:	n/a	chr12:30663267-30663278
30	CEBPB	chr12:30661522-30661844	HepG2	liver:	n/a	n/a
31	CEBPB	chr12:30603830-30604199	K562	blood:	n/a	chr12:30604105-30604116
32	CEBPB	chr12:30610869-30611135	A549	lung:	n/a	chr12:30611021-30611032
33	CEBPB	chr12:30600954-30601319	K562	blood:	n/a	chr12:30601098-30601109 chr12:30601130-30601141
34	CEBPB	chr12:30663214-30663380	K562	blood:	n/a	chr12:30663267-30663278
35	CEBPB	chr12:30603904-30604298	K562	blood:	n/a	chr12:30604105-30604116
36	CEBPB	chr12:30661285-30661711	K562	blood:	n/a	n/a
37	CEBPB	chr12:30600963-30601324	IMR90	lung:	n/a	chr12:30601098-30601109 chr12:30601130-30601141
38	CEBPB	chr12:30603961-30604255	HepG2	liver:	n/a	chr12:30604105-30604116
39	CEBPB	chr12:30610850-30611163	HepG2	liver:	n/a	chr12:30611021-30611032
40	CEBPB	chr12:30603918-30604266	Hela-S3	cervix:	n/a	chr12:30604105-30604116
41	CEBPB	chr12:30640229-30640462	A549	lung:	n/a	chr12:30640367-30640378 chr12:30640281-30640294 chr12:30640282-30640293 chr12:30640367-30640380
42	CEBPB	chr12:30590691-30590906	HepG2	liver:	n/a	n/a
43	CEBPB	chr12:30590642-30591030	HepG2	liver:	n/a	n/a
44	CEBPB	chr12:30668466-30668696	HepG2	liver:	n/a	n/a
45	CEBPB	chr12:30661198-30662021	HepG2	liver:	n/a	n/a
46	CEBPB	chr12:30661041-30661981	HepG2	liver:	n/a	n/a
47	CEBPB	chr12:30603933-30604174	K562	blood:	n/a	chr12:30604105-30604116
48	CEBPB	chr12:30635726-30635985	HepG2	liver:	n/a	n/a
49	CEBPB	chr12:30610857-30611152	IMR90	lung:	n/a	chr12:30611021-30611032
50	CEBPB	chr12:30635640-30635891	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:30591384-30591434	AoSMC	blood vessel:	n/a
2	chr12:30591384-30591434	NHBE	bronchial:	n/a
3	chr12:30591384-30591434	Hepatocyte	liver:	n/a
4	chr12:30591384-30591434	HCF	heart:	n/a
5	chr12:30591384-30591434	HepG2	liver:	n/a
6	chr12:30591384-30591434	GM12878	blood:	n/a
7	chr12:30591384-30591434	H1-hESC	embryonic stem cell:	embryo
8	chr12:30591384-30591434	HCM	heart:	n/a
9	chr12:30591384-30591434	HEK293	kidney:	embryo
10	chr12:30591384-30591434	HL-60	blood:	n/a
11	chr12:30591384-30591434	BJ	skin:	n/a
12	chr12:30591384-30591434	PrEC	prostate:	n/a
13	chr12:30591384-30591434	ovcar-3	ovarian:	n/a
14	chr12:30591384-30591434	GM12891	blood:	n/a
15	chr12:30591384-30591434	HCT-116	colon:	n/a
16	chr12:30591384-30591434	HCPEpiC	choroid plexus:	n/a
17	chr12:30591384-30591434	Jurkat	blood:	n/a
18	chr12:30591384-30591434	SAEC	small airway:	n/a
19	chr12:30591384-30591434	HMEC	breast:	n/a
20	chr12:30591384-30591434	PFSK-1	brain:	n/a
21	chr12:30591384-30591434	MCF-7	breast:	n/a
22	chr12:30591384-30591434	LNCaP	prostate:	n/a
23	chr12:30591384-30591434	SK-N-SH	brain:	n/a
24	chr12:30591384-30591434	CMK	blood:	n/a
25	chr12:30591384-30591434	A549	lung:	n/a
26	chr12:30591384-30591434	ECC-1	luminal epithelium:	n/a
27	chr12:30591384-30591434	PANC-1	pancreas:	n/a
28	chr12:30591384-30591434	T-47D	breast:	n/a
29	chr12:30591384-30591434	HPAEpiC	pulmonary alveolar:	n/a
30	chr12:30591384-30591434	HIPEpiC	eye:	n/a
31	chr12:30591384-30591434	K562	blood:	n/a
32	chr12:30591384-30591434	RPTEC	kidney:	n/a
33	chr12:30591384-30591434	Caco-2	colon:	n/a
34	chr12:30591384-30591434	HRPEpiC	eye:	n/a
35	chr12:30591384-30591434	HEEpiC	esophagus:	n/a
36	chr12:30591384-30591434	HRE	kidney:	n/a
37	chr12:30591384-30591434	AG04450	lung:	fetal
38	chr12:30591384-30591434	GM12892	blood:	n/a
39	chr12:30591384-30591434	AG09319	gingival:	n/a
40	chr12:30591384-30591434	NHDF-neo	bronchial:	n/a
41	chr12:30591384-30591434	U87	brain:	n/a
42	chr12:30591384-30591434	AG10803	skin:	n/a
43	chr12:30591384-30591434	GM19239	blood:	n/a
44	chr12:30591384-30591434	NB4	blood:	n/a
45	chr12:30591384-30591434	IMR90	lung:	fetal
46	chr12:30591384-30591434	ProgFib	skin:	n/a
47	chr12:30591384-30591434	AG09309	skin:	n/a
48	chr12:30591384-30591434	NT2-D1	testis:	n/a
49	chr12:30591384-30591434	NH-A	brain:	n/a
50	chr12:30591384-30591434	MCF10A-Er-Src	breast:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:30600424..30602317-chr12:30605382..30607677,2	MCF-7	breast:
2	chr12:30630764..30632719-chr12:30642693..30644832,2	K562	blood:
3	chr12:30608258..30610479-chr12:30611137..30614676,3	MCF-7	breast:
4	chr12:30589442..30591891-chr12:30596596..30598208,2	K562	blood:
5	chr12:30589442..30591891-chr12:30596596..30598208,2	K562	blood:
6	chr12:29705381..29705928-chr12:30610654..30611317,2	MCF-7	breast:
7	chr12:30646656..30649637-chr12:30912418..30914854,2	K562	blood:
8	chr12:30603545..30605417-chr12:30948228..30949913,2	K562	blood:
9	chr12:30600424..30602317-chr12:30605382..30607677,2	MCF-7	breast:
10	chr12:30630764..30632719-chr12:30642693..30644832,2	K562	blood:
11	chr12:30635980..30637562-chr12:30640681..30642219,2	K562	blood:
12	chr12:30594497..30597214-chr12:30599271..30601913,3	K562	blood:
13	chr12:30659100..30661387-chr12:30684901..30687709,2	K562	blood:
14	chr12:30608258..30610479-chr12:30611137..30614676,3	MCF-7	breast:
15	chr12:30635980..30637562-chr12:30640681..30642219,2	K562	blood:
16	chr12:30594497..30597214-chr12:30599271..30601913,3	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IPO8-2	chr12:30619400-30619509	NONHSAT027511
2	lnc-TSPAN11-11	chr12:30607852-30608017	NONHSAT027510
3	lnc-IPO8-2	chr12:30656171-30656754	NONHSAT027511
4	lnc-TSPAN11-11	chr12:30645097-30645235	NONHSAT027510
5	lnc-TSPAN11-11	chr12:30632109-30632222	NONHSAT027510

No data

Variant related genes	Relation type
ENSG00000258202	TF binding region
ENSG00000258202	CpG island
ENSG00000235884	chromatin interactions

Extended variants
information (count: 2810 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2810 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188797486	chr12:30590107-30590108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs143576027	chr12:30590139-30590140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192596626	chr12:30590142-30590143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114508772	chr12:30590143-30590144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs10771719	chr12:30590175-30590176	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs78066323	chr12:30590244-30590245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533659009	chr12:30590299-30590300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375495142	chr12:30590311-30590312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555307498	chr12:30590313-30590314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79384591	chr12:30590333-30590334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs147085871	chr12:30590350-30590351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs138291296	chr12:30590376-30590377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575572497	chr12:30590385-30590386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10843753	chr12:30590426-30590427	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs555584919	chr12:30590461-30590462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573254773	chr12:30590495-30590496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540393312	chr12:30590509-30590510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574039814	chr12:30590517-30590518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149635394	chr12:30590549-30590550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144403857	chr12:30590566-30590567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551037857	chr12:30590610-30590611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184528183	chr12:30590662-30590663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs534469300	chr12:30590665-30590666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372364175	chr12:30590694-30590695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551562846	chr12:30590726-30590727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148708638	chr12:30590753-30590754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs74084310	chr12:30590778-30590779	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs548779691	chr12:30590784-30590785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10771720	chr12:30590796-30590797	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs537438092	chr12:30590814-30590815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368122975	chr12:30590833-30590834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189003990	chr12:30590938-30590939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560737700	chr12:30590960-30590961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4514511	chr12:30591044-30591045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4450239	chr12:30591046-30591047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182402405	chr12:30591051-30591052	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371377074	chr12:30591087-30591088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539761167	chr12:30591150-30591151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187406050	chr12:30591164-30591165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573335544	chr12:30591179-30591180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540855894	chr12:30591183-30591184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77361934	chr12:30591269-30591270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189283480	chr12:30591306-30591307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540185117	chr12:30591342-30591343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561670143	chr12:30591343-30591344	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562036413	chr12:30591363-30591364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528977718	chr12:30591370-30591371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550528791	chr12:30591386-30591387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544573098	chr12:30591387-30591388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2062999	chr12:30591428-30591429	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:58)

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
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	22037309	CNVD
microdeletion syndrome	16199537	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:30589400-30591600	Enhancers	HepG2	liver
2	chr12:30589800-30595000	Enhancers	Fetal Stomach	stomach
3	chr12:30590000-30590800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr12:30590000-30591800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr12:30590000-30592600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr12:30590000-30592600	Enhancers	Fetal Lung	lung
7	chr12:30590000-30593000	Enhancers	Liver	Liver
8	chr12:30590200-30590800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr12:30590200-30590800	Enhancers	NHDF-Ad	bronchial
10	chr12:30590200-30591000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr12:30590400-30590600	Enhancers	Lung	lung
12	chr12:30590400-30590800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr12:30590400-30590800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr12:30590400-30590800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr12:30590400-30590800	Enhancers	Fetal Muscle Leg	muscle
16	chr12:30590400-30590800	Enhancers	Pancreas	Pancrea
17	chr12:30590400-30590800	Enhancers	Right Atrium	heart
18	chr12:30590400-30591000	Enhancers	Fetal Kidney	kidney
19	chr12:30590400-30591400	Enhancers	Adipose Nuclei	Adipose
20	chr12:30590400-30592600	Enhancers	Stomach Mucosa	stomach
21	chr12:30590400-30593000	Enhancers	Fetal Brain Male	brain
22	chr12:30590400-30593000	Enhancers	Fetal Brain Female	brain
23	chr12:30590800-30592400	Weak transcription	Pancreas	Pancrea
24	chr12:30590800-30596400	Weak transcription	Right Atrium	heart
25	chr12:30591000-30591400	Weak transcription	Fetal Kidney	kidney
26	chr12:30591200-30594000	Enhancers	Fetal Heart	heart
27	chr12:30591400-30591800	Enhancers	Fetal Kidney	kidney
28	chr12:30591600-30594000	Weak transcription	HepG2	liver
29	chr12:30592400-30592600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr12:30592400-30592800	Enhancers	Left Ventricle	heart
31	chr12:30592400-30592800	Enhancers	Lung	lung
32	chr12:30592400-30592800	Enhancers	Pancreas	Pancrea
33	chr12:30592400-30593000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr12:30592400-30593600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr12:30592600-30594600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr12:30592600-30600000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr12:30592800-30594600	Weak transcription	Pancreas	Pancrea
38	chr12:30593000-30594200	Weak transcription	Fetal Brain Male	brain
39	chr12:30593000-30602400	Weak transcription	Liver	Liver
40	chr12:30594000-30594400	Enhancers	HepG2	liver
41	chr12:30594000-30596200	Weak transcription	Fetal Heart	heart
42	chr12:30594200-30595000	Enhancers	Fetal Brain Male	brain
43	chr12:30594600-30594800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr12:30594600-30594800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr12:30594600-30594800	Flanking Active TSS	Lung	lung
46	chr12:30594600-30594800	Enhancers	Pancreas	Pancrea
47	chr12:30594600-30594800	Enhancers	Spleen	Spleen
48	chr12:30594800-30596800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr12:30594800-30600200	Weak transcription	Spleen	Spleen
50	chr12:30595000-30596200	Weak transcription	Fetal Stomach	stomach

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