Variant report

Variant	nsv1046251
Chromosome Location	chr12:119353064-119467301
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:803)
CpG islands
(count:1406)
Chromatin interactive
region (count:21)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:803 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:119458462-119458894	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr12:119419234-119419779	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr12:119418338-119418558	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr12:119423914-119424114	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr12:119449965-119450392	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr12:119378130-119378354	GM12878	blood:	n/a	n/a
7	BHLHE40	chr12:119417687-119417852	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:119458590-119458813	K562	blood:	n/a	n/a
9	BRCA1	chr12:119418635-119418640	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr12:119446139-119446425	K562	blood:	n/a	n/a
11	CEBPB	chr12:119399113-119399430	A549	lung:	n/a	chr12:119399255-119399268 chr12:119399255-119399266
12	CEBPB	chr12:119446167-119446427	HepG2	liver:	n/a	n/a
13	CEBPB	chr12:119379763-119379825	HepG2	liver:	n/a	chr12:119379810-119379821
14	CEBPB	chr12:119399103-119399445	HepG2	liver:	n/a	chr12:119399255-119399268 chr12:119399255-119399266
15	CEBPB	chr12:119400911-119401106	H1-hESC	embryonic stem cell:	n/a	chr12:119400972-119400983
16	CEBPB	chr12:119400818-119401128	K562	blood:	n/a	chr12:119400972-119400983
17	CEBPB	chr12:119399124-119399442	K562	blood:	n/a	chr12:119399255-119399268 chr12:119399255-119399266
18	CEBPB	chr12:119446173-119446422	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr12:119446179-119446430	IMR90	lung:	n/a	n/a
20	CEBPB	chr12:119446190-119446422	K562	blood:	n/a	n/a
21	CEBPB	chr12:119433371-119433626	HepG2	liver:	n/a	chr12:119433518-119433529 chr12:119433517-119433530
22	CEBPB	chr12:119353554-119353742	HepG2	liver:	n/a	chr12:119353691-119353702
23	CEBPB	chr12:119356878-119357070	HepG2	liver:	n/a	chr12:119356952-119356963 chr12:119356951-119356964
24	CEBPB	chr12:119400799-119401160	IMR90	lung:	n/a	chr12:119400972-119400983
25	CEBPB	chr12:119445310-119445577	K562	blood:	n/a	n/a
26	CEBPB	chr12:119400797-119401108	A549	lung:	n/a	chr12:119400972-119400983
27	CEBPB	chr12:119392210-119392494	HepG2	liver:	n/a	chr12:119392333-119392344
28	CEBPB	chr12:119446192-119446403	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr12:119400791-119401141	HepG2	liver:	n/a	chr12:119400972-119400983
30	CEBPB	chr12:119458884-119459040	K562	blood:	n/a	n/a
31	CEBPB	chr12:119446168-119446444	A549	lung:	n/a	n/a
32	CHD1	chr12:119418298-119418447	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr12:119446434-119446670	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr12:119419032-119419832	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr12:119418587-119418685	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr12:119418918-119420181	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr12:119418927-119420130	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTBP2	chr12:119446458-119447300	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTBP2	chr12:119418218-119419923	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr12:119417680-119417830	BE2_C	brain:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
41	CTCF	chr12:119417595-119417907	A549	lung:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
42	CTCF	chr12:119417680-119417830	HCPEpiC	choroid plexus:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
43	CTCF	chr12:119417621-119417884	LNCaP	prostate:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
44	CTCF	chr12:119417609-119417892	A549	lung:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
45	CTCF	chr12:119417423-119418085	HCT-116	colon:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
46	CTCF	chr12:119417640-119417790	RPTEC	kidney:	n/a	chr12:119417751-119417772 chr12:119417749-119417767 chr12:119417750-119417766
47	CTCF	chr12:119421080-119421230	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr12:119458629-119458900	Gliobla	brain:	n/a	chr12:119458736-119458757 chr12:119458734-119458752
49	CTCF	chr12:119417413-119417475	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr12:119458640-119458790	GM12868	blood:	n/a	chr12:119458736-119458757 chr12:119458734-119458752

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:119416585-119416635	HRE	kidney:	n/a
2	chr12:119418004-119418054	BE2_C	brain:	n/a
3	chr12:119418804-119418854	IMR90	lung:	fetal
4	chr12:119416585-119416635	HRE	kidney:	n/a
5	chr12:119418004-119418054	BE2_C	brain:	n/a
6	chr12:119418804-119418854	IMR90	lung:	fetal
7	chr12:119417806-119417856	RPTEC	kidney:	n/a
8	chr12:119420927-119420977	NH-A	brain:	n/a
9	chr12:119419635-119419685	ECC-1	luminal epithelium:	n/a
10	chr12:119418676-119418726	NHDF-neo	bronchial:	n/a
11	chr12:119457146-119457196	HNPCEpiC	eye:	n/a
12	chr12:119423402-119423452	HCT-116	colon:	n/a
13	chr12:119446985-119447035	AG09309	skin:	n/a
14	chr12:119450600-119450650	HAEpiC	amniotic membrane:	n/a
15	chr12:119419143-119419193	HCPEpiC	choroid plexus:	n/a
16	chr12:119416585-119416635	SKMC	muscle:	n/a
17	chr12:119446891-119446941	AoSMC	blood vessel:	n/a
18	chr12:119457146-119457196	HRE	kidney:	n/a
19	chr12:119423402-119423452	Caco-2	colon:	n/a
20	chr12:119419786-119419836	A549	lung:	n/a
21	chr12:119446891-119446941	NH-A	brain:	n/a
22	chr12:119417743-119417793	HRPEpiC	eye:	n/a
23	chr12:119417743-119417793	Hepatocyte	liver:	n/a
24	chr12:119418004-119418054	Jurkat	blood:	n/a
25	chr12:119416585-119416635	LNCaP	prostate:	n/a
26	chr12:119419635-119419685	AG04450	lung:	fetal
27	chr12:119447476-119447526	HRE	kidney:	n/a
28	chr12:119419635-119419685	AG10803	skin:	n/a
29	chr12:119420927-119420977	NB4	blood:	n/a
30	chr12:119419786-119419836	HRCEpiC	kidney:	n/a
31	chr12:119419331-119419381	PrEC	prostate:	n/a
32	chr12:119417806-119417856	Jurkat	blood:	n/a
33	chr12:119418804-119418854	K562	blood:	n/a
34	chr12:119423402-119423452	PFSK-1	brain:	n/a
35	chr12:119418110-119418160	CMK	blood:	n/a
36	chr12:119418676-119418726	HRCEpiC	kidney:	n/a
37	chr12:119450600-119450650	BE2_C	brain:	n/a
38	chr12:119423402-119423452	NHBE	bronchial:	n/a
39	chr12:119450600-119450650	H1-hESC	embryonic stem cell:	embryo
40	chr12:119419635-119419685	GM12891	blood:	n/a
41	chr12:119419635-119419685	HMEC	breast:	n/a
42	chr12:119418804-119418854	NB4	blood:	n/a
43	chr12:119419635-119419685	BJ	skin:	n/a
44	chr12:119418110-119418160	NHBE	bronchial:	n/a
45	chr12:119417743-119417793	ovcar-3	ovarian:	n/a
46	chr12:119418622-119418672	HIPEpiC	eye:	n/a
47	chr12:119418110-119418160	GM06990	blood:	n/a
48	chr12:119417743-119417793	NHBE	bronchial:	n/a
49	chr12:119446985-119447035	AG10803	skin:	n/a
50	chr12:119450600-119450650	A549	lung:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:119417707..119418245-chr12:119474754..119475351,2	MCF-7	breast:
2	chr12:119458483..119459134-chr12:119850426..119851166,2	MCF-7	breast:
3	chr12:119427403..119431135-chr12:119431729..119434900,3	K562	blood:
4	chr12:119391322..119393259-chr12:119419157..119421683,2	MCF-7	breast:
5	chr12:119418300..119419905-chr12:119423300..119425735,2	K562	blood:
6	chr12:119458269..119459265-chr12:119850713..119851633,4	K562	blood:
7	chr12:119375176..119376854-chr12:119378459..119381025,3	K562	blood:
8	chr12:119457435..119458229-chr12:119552906..119553464,2	MCF-7	breast:
9	chr12:119417235..119417851-chr12:119850790..119851632,2	K562	blood:
10	chr12:119427403..119431135-chr12:119431729..119434900,3	K562	blood:
11	chr12:119391457..119393836-chr12:119397133..119400298,3	K562	blood:
12	chr12:119375176..119376854-chr12:119378459..119381025,3	K562	blood:
13	chr12:119458654..119459221-chr12:119982551..119983369,2	MCF-7	breast:
14	chr12:119391457..119394278-chr12:119398798..119400575,2	K562	blood:
15	chr12:119391457..119393836-chr12:119397133..119400298,3	K562	blood:
16	chr12:119449958..119452455-chr12:119456708..119459020,2	K562	blood:
17	chr12:119417365..119417869-chr12:120086788..120087682,2	MCF-7	breast:
18	chr12:119391457..119394278-chr12:119398798..119400575,2	K562	blood:
19	chr12:118842874..118843382-chr12:119458257..119458788,2	K562	blood:
20	chr12:119411792..119414282-chr12:119618328..119620117,2	MCF-7	breast:
21	chr12:119449958..119452455-chr12:119456708..119459020,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HSPB8-6	chr12:119431662-119431956	NONHSAT031062
2	lnc-TAOK3-12	chr12:119386525-119387370	expReg_chr12_10652_-
3	lnc-HSPB8-2	chr12:119439456-119439647	ENSG00000256031.1
4	lnc-TAOK3-7	chr12:119392577-119392919	XLOC_010216
5	lnc-TAOK3-7	chr12:119393388-119393428	NONHSAT031060
6	lnc-HSPB8-2	chr12:119438932-119439126	ENSG00000256031.1
7	lnc-TAOK3-13	chr12:119413206-119414296	ucscGeneNc_uc001tyk_1
8	lnc-TAOK3-13	chr12:119418009-119418111	ucscGeneNc_uc001tyk_1
9	lnc-TAOK3-7	chr12:119393388-119393419	XLOC_010216
10	lnc-HSPB8-2	chr12:119438581-119438648	ENSG00000256031.1
11	lnc-TAOK3-7	chr12:119393611-119393699	NONHSAT031059
12	lnc-TAOK3-7	chr12:119393794-119394018	NONHSAT031059
13	lnc-TAOK3-7	chr12:119392576-119392919	NONHSAT031060
14	lnc-TAOK3-7	chr12:119392576-119392919	NONHSAT031059

No data

Variant related genes	Relation type
ENSG00000256031	TF binding region
RN7SL508P	TF binding region
SRRM4	TF binding region
ENSG00000256031	CpG island
RN7SL508P	CpG island
SRRM4	CpG island
ENSG00000139767	chromatin interactions
FSCN1	miRNA target sites
MCL1	miRNA target sites

Extended variants
information (count: 2524 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2524 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371302633	chr12:119353064-119353065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs184304835	chr12:119353065-119353066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs74509701	chr12:119353105-119353106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187206598	chr12:119353166-119353167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532712943	chr12:119353175-119353176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562388878	chr12:119353176-119353177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529235316	chr12:119362405-119362406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542826834	chr12:119362488-119362489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79902143	chr12:119362496-119362497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531020079	chr12:119362578-119362579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577780201	chr12:119362590-119362591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543519799	chr12:119362595-119362596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs112880361	chr12:119362647-119362648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562998443	chr12:119362686-119362687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576965520	chr12:119362707-119362708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533140900	chr12:119362729-119362730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546993036	chr12:119362778-119362779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112540486	chr12:119362820-119362821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372801246	chr12:119362918-119362919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181598242	chr12:119362935-119362936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555539286	chr12:119362966-119362967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs146591563	chr12:119362995-119362996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538443686	chr12:119363048-119363049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138984560	chr12:119363086-119363087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527817062	chr12:119363099-119363100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376399108	chr12:119363104-119363105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs143009086	chr12:119363138-119363139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539828063	chr12:119363148-119363149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs56702662	chr12:119363161-119363162	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs147428337	chr12:119363196-119363197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs115258250	chr12:119363254-119363255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs562772414	chr12:119363265-119363266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531490733	chr12:119363304-119363305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs61425628	chr12:119363352-119363353	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs576387370	chr12:119363356-119363357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs9668696	chr12:119363411-119363412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs377215603	chr12:119363416-119363417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs57644345	chr12:119363426-119363427	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs531497110	chr12:119363428-119363429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs138112589	chr12:119363456-119363457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs566573381	chr12:119363470-119363471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529254567	chr12:119363613-119363614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186377425	chr12:119363623-119363624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs73403691	chr12:119363627-119363628	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs569228210	chr12:119363638-119363639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190894441	chr12:119363646-119363647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551981719	chr12:119363647-119363648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73403692	chr12:119363663-119363664	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs56839763	chr12:119363747-119363748	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs553797190	chr12:119363801-119363802	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:526 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119352400-119353200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:119362400-119364600	Enhancers	Adipose Nuclei	Adipose
3	chr12:119363000-119363400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr12:119363000-119363800	Enhancers	Fetal Lung	lung
5	chr12:119363400-119364200	Enhancers	Fetal Brain Male	brain
6	chr12:119363600-119364000	Enhancers	Fetal Brain Female	brain
7	chr12:119380200-119381400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr12:119380600-119381400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr12:119381000-119381400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr12:119381400-119382400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr12:119382400-119383400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr12:119383400-119384800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr12:119384000-119384200	Bivalent Enhancer	Left Ventricle	heart
14	chr12:119396000-119397200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr12:119396200-119396800	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr12:119396200-119397000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr12:119396200-119397000	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr12:119396200-119397200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr12:119396200-119397200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr12:119396200-119397200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr12:119396400-119396600	Enhancers	Lung	lung
22	chr12:119396400-119396800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr12:119396600-119397000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr12:119397000-119397200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
25	chr12:119407800-119409600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:119408200-119409600	Enhancers	H9 Cell Line	embryonic stem cell
27	chr12:119408400-119409600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr12:119408600-119409400	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr12:119408600-119409600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr12:119408800-119409400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr12:119408800-119409400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr12:119409000-119410000	Bivalent Enhancer	Fetal Brain Male	brain
33	chr12:119414000-119417400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr12:119417400-119417600	Enhancers	H1 Cell Line	embryonic stem cell
35	chr12:119417400-119417600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr12:119417400-119417600	Enhancers	Fetal Brain Female	brain
37	chr12:119417400-119417800	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr12:119417400-119417800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr12:119417600-119417800	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr12:119417600-119417800	Flanking Active TSS	Brain Germinal Matrix	brain
41	chr12:119417600-119418000	Flanking Active TSS	Fetal Brain Female	brain
42	chr12:119417600-119418000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
43	chr12:119417600-119418200	Enhancers	Fetal Brain Male	brain
44	chr12:119417600-119419800	Active TSS	H1 Cell Line	embryonic stem cell
45	chr12:119417600-119420200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr12:119417800-119418000	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr12:119417800-119418000	Enhancers	Placenta	Placenta
48	chr12:119417800-119418200	Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr12:119417800-119418200	Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr12:119417800-119418200	Active TSS	Cortex derived primary cultured neurospheres	brain

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