Variant report

Variant	esv2758314
Chromosome Location	chr12:72990707-73251109
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:524)
CpG islands
(count:246)
Chromatin interactive
region (count:10)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:524 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:72996821-72996840	K562	blood:	n/a	n/a
2	ATF1	chr12:73071729-73071865	K562	blood:	n/a	n/a
3	ATF2	chr12:73040903-73041319	GM12878	blood:	n/a	n/a
4	ATF2	chr12:73067526-73068137	GM12878	blood:	n/a	n/a
5	BACH1	chr12:73085107-73085586	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr12:73208970-73209323	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr12:73074983-73075111	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr12:73212115-73212362	GM12878	blood:	n/a	n/a
9	BATF	chr12:73040940-73041214	GM12878	blood:	n/a	n/a
10	BCL11A	chr12:73249185-73249390	GM12878	blood:	n/a	n/a
11	BCLAF1	chr12:73067501-73068061	GM12878	blood:	n/a	n/a
12	BHLHE40	chr12:73069299-73069320	GM12878	blood:	n/a	n/a
13	BHLHE40	chr12:73066581-73066626	GM12878	blood:	n/a	n/a
14	BHLHE40	chr12:73067799-73068001	GM12878	blood:	n/a	n/a
15	BHLHE40	chr12:73085142-73085302	GM12878	blood:	n/a	n/a
16	BRCA1	chr12:73184254-73184360	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr12:73036607-73036730	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr12:73153067-73153380	HCT-116	colon:	n/a	n/a
19	CEBPB	chr12:73200677-73201003	A549	lung:	n/a	chr12:73200811-73200822
20	CEBPB	chr12:73017088-73017288	HepG2	liver:	n/a	chr12:73017175-73017186
21	CEBPB	chr12:73200612-73201101	H1-hESC	embryonic stem cell:	n/a	chr12:73200811-73200822
22	CEBPB	chr12:73152789-73152830	K562	blood:	n/a	n/a
23	CEBPB	chr12:73200699-73200856	HepG2	liver:	n/a	chr12:73200811-73200822
24	CEBPB	chr12:73184092-73184484	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr12:73184115-73184468	MCF-7	breast:	n/a	n/a
26	CEBPB	chr12:73026095-73026405	IMR90	lung:	n/a	chr12:73026256-73026269
27	CEBPB	chr12:73196692-73196836	HepG2	liver:	n/a	n/a
28	CEBPB	chr12:73020979-73021186	HepG2	liver:	n/a	chr12:73021076-73021087
29	CEBPB	chr12:73193897-73194188	HepG2	liver:	n/a	chr12:73194021-73194032
30	CEBPB	chr12:73230494-73230590	A549	lung:	n/a	chr12:73230521-73230532 chr12:73230519-73230532
31	CEBPB	chr12:73058184-73058384	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr12:73074666-73074866	A549	lung:	n/a	chr12:73074782-73074795 chr12:73074779-73074796
33	CEBPB	chr12:73157951-73158107	A549	lung:	n/a	n/a
34	CEBPB	chr12:73193952-73194101	K562	blood:	n/a	chr12:73194021-73194032
35	CEBPB	chr12:73063480-73063680	HepG2	liver:	n/a	chr12:73063547-73063560 chr12:73063601-73063618
36	CEBPB	chr12:73217928-73217981	HepG2	liver:	n/a	chr12:73217954-73217965
37	CEBPB	chr12:73121205-73121535	IMR90	lung:	n/a	chr12:73121373-73121386 chr12:73121375-73121386 chr12:73121373-73121386 chr12:73121373-73121386 chr12:73121375-73121386
38	CEBPB	chr12:73005979-73006406	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr12:73222605-73222617	GM12878	blood:	n/a	n/a
40	CHD2	chr12:73067777-73067994	GM12878	blood:	n/a	n/a
41	CTCF	chr12:73212285-73212364	LNCaP	prostate:	n/a	n/a
42	CTCF	chr12:73076254-73076328	GM20000	blood:	n/a	n/a
43	CTCF	chr12:73093260-73093410	GM12873	blood:	n/a	n/a
44	CTCF	chr12:73004800-73004950	A549	lung:	n/a	n/a
45	CTCF	chr12:73093180-73093330	AG04449	skin:	n/a	n/a
46	CTCF	chr12:73093240-73093390	GM12867	blood:	n/a	n/a
47	CTCF	chr12:73093260-73093410	GM12867	blood:	n/a	n/a
48	CTCF	chr12:73093292-73093294	A549	lung:	n/a	n/a
49	CTCF	chr12:73167560-73167710	RPTEC	kidney:	n/a	n/a
50	CTCF	chr12:73093280-73093430	GM12873	blood:	n/a	n/a

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:73085225-73085275	U87	brain:	n/a
2	chr12:73057369-73057419	SK-N-SH_RA	brain:	n/a
3	chr12:73085225-73085275	U87	brain:	n/a
4	chr12:73057369-73057419	SK-N-SH_RA	brain:	n/a
5	chr12:73057369-73057419	AG04449	skin:	fetal
6	chr12:73034008-73034058	PFSK-1	brain:	n/a
7	chr12:73057369-73057419	AG04450	lung:	fetal
8	chr12:73085225-73085275	NT2-D1	testis:	n/a
9	chr12:73085225-73085275	PANC-1	pancreas:	n/a
10	chr12:73005050-73005100	ProgFib	skin:	n/a
11	chr12:73057369-73057419	HMEC	breast:	n/a
12	chr12:73085225-73085275	A549	lung:	n/a
13	chr12:73057369-73057419	U87	brain:	n/a
14	chr12:73005050-73005100	AG09319	gingival:	n/a
15	chr12:73034008-73034058	HMEC	breast:	n/a
16	chr12:73005050-73005100	SKMC	muscle:	n/a
17	chr12:73057369-73057419	HCPEpiC	choroid plexus:	n/a
18	chr12:73085225-73085275	IMR90	lung:	fetal
19	chr12:73057369-73057419	RPTEC	kidney:	n/a
20	chr12:73057369-73057419	MCF-7	breast:	n/a
21	chr12:73085225-73085275	AoSMC	blood vessel:	n/a
22	chr12:73057369-73057419	AoSMC	blood vessel:	n/a
23	chr12:73034008-73034058	GM06990	blood:	n/a
24	chr12:73005050-73005100	NHBE	bronchial:	n/a
25	chr12:73034008-73034058	Jurkat	blood:	n/a
26	chr12:73057369-73057419	HRPEpiC	eye:	n/a
27	chr12:73034008-73034058	ECC-1	luminal epithelium:	n/a
28	chr12:73057369-73057419	PANC-1	pancreas:	n/a
29	chr12:73034008-73034058	GM12892	blood:	n/a
30	chr12:73085225-73085275	SKMC	muscle:	n/a
31	chr12:73085225-73085275	HMEC	breast:	n/a
32	chr12:73085225-73085275	SK-N-MC	brain:	n/a
33	chr12:73085225-73085275	Hela-S3	cervix:	n/a
34	chr12:73057369-73057419	CMK	blood:	n/a
35	chr12:73005050-73005100	RPTEC	kidney:	n/a
36	chr12:73005050-73005100	HCT-116	colon:	n/a
37	chr12:73005050-73005100	LNCaP	prostate:	n/a
38	chr12:73005050-73005100	AG09309	skin:	n/a
39	chr12:73034008-73034058	NT2-D1	testis:	n/a
40	chr12:73085225-73085275	AG04450	lung:	fetal
41	chr12:73034008-73034058	NHDF-neo	bronchial:	n/a
42	chr12:73034008-73034058	HCPEpiC	choroid plexus:	n/a
43	chr12:73034008-73034058	AG10803	skin:	n/a
44	chr12:73057369-73057419	GM12878	blood:	n/a
45	chr12:73034008-73034058	HUVEC	blood vessel:	n/a
46	chr12:73034008-73034058	AG09319	gingival:	n/a
47	chr12:73057369-73057419	HepG2	liver:	n/a
48	chr12:73085225-73085275	NB4	blood:	n/a
49	chr12:73057369-73057419	HNPCEpiC	eye:	n/a
50	chr12:73085225-73085275	Caco-2	colon:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:73177952..73180851-chr12:73182448..73184176,2	K562	blood:
2	chr12:73162846..73164376-chr12:73166429..73169138,2	MCF-7	breast:
3	chr12:73066407..73068991-chr12:73070185..73072919,2	K562	blood:
4	chr12:73177952..73180851-chr12:73182448..73184176,2	K562	blood:
5	chr1:53191543..53194375-chr12:73227297..73229475,2	MCF-7	breast:
6	chr1:110863042..110863616-chr12:73109953..73110460,2	MCF-7	breast:
7	chr12:73003659..73006224-chr12:73008245..73010751,2	K562	blood:
8	chr12:73066407..73068991-chr12:73070185..73072919,2	K562	blood:
9	chr12:73050089..73050693-chr4:90478139..90478639,2	MCF-7	breast:
10	chr12:73162846..73164376-chr12:73166429..73169138,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFC3H1-15	chr12:73065223-73065430	NONHSAT029475
2	lnc-ZFC3H1-14	chr12:73061098-73061371	NONHSAT029474
3	lnc-ZFC3H1-7	chr12:73122565-73122624	ENSG00000258235.1
4	lnc-TPH2-5	chr12:73004458-73005096	NONHSAT029473
5	lnc-ZFC3H1-7	chr12:73121703-73122023	ENSG00000258235.1

No data

Variant related genes	Relation type
CHCHD3P2	TF binding region
ENSG00000216084	TF binding region
ENSG00000258235	TF binding region
CHCHD3P2	CpG island
ENSG00000216084	CpG island
ENSG00000258235	CpG island
ENSG00000162378	chromatin interactions
ENSG00000257723	chromatin interactions

Extended variants
information (count: 6155 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:6155 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184918680	chr12:72995469-72995470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs61926613	chr12:72995488-72995489	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs73336722	chr12:72995491-72995492	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs556506791	chr12:72995509-72995510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562535300	chr12:72995555-72995556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568537530	chr12:72995598-72995599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535613190	chr12:72995618-72995619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187792407	chr12:72995641-72995642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572109824	chr12:72995675-72995676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139727430	chr12:72995709-72995710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545260308	chr12:72995751-72995752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557648907	chr12:72995766-72995767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200664843	chr12:72995808-72995809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374238863	chr12:72995821-72995822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561781181	chr12:72995862-72995863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6582093	chr12:72995946-72995947	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs554599733	chr12:72995983-72995984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371610738	chr12:72996013-72996014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559346689	chr12:72996022-72996023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192192409	chr12:72996048-72996049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144826960	chr12:72996051-72996052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374842708	chr12:72996070-72996071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551430541	chr12:72996099-72996100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571103578	chr12:72996105-72996106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143058232	chr12:72996149-72996150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550337240	chr12:72996150-72996151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527444255	chr12:72996186-72996187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547654356	chr12:72996231-72996232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565157711	chr12:72996251-72996252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568566915	chr12:72996281-72996282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535508315	chr12:72996323-72996324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547505353	chr12:72996335-72996336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560565522	chr12:72996343-72996344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529435832	chr12:72996418-72996419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184223413	chr12:72996419-72996420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549385749	chr12:72996550-72996551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557897478	chr12:72996558-72996559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146161898	chr12:72996574-72996575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs58509346	chr12:72996585-72996586	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs370903655	chr12:72996634-72996635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189459918	chr12:72996686-72996687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573758395	chr12:72996701-72996702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371323074	chr12:72996736-72996737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140017355	chr12:72996743-72996744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs58687032	chr12:72996759-72996760	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs571885239	chr12:72996816-72996817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545018228	chr12:72996887-72996888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561931320	chr12:72996904-72996905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563177931	chr12:72996944-72996945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs181812391	chr12:72996964-72996965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Wilms tumour	21544195	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
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
Neurodevelopmental disorder	22521361	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
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Autism	20685689	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	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
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:72995400-73002200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:73001000-73001400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
3	chr12:73001400-73002000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr12:73001800-73002400	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr12:73001800-73002400	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr12:73002000-73002600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr12:73002200-73002400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr12:73002200-73002600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr12:73002200-73006000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr12:73002200-73006800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:73002400-73003600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr12:73002400-73003600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr12:73002400-73004200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr12:73002400-73004200	Weak transcription	Fetal Intestine Large	intestine
15	chr12:73002600-73004000	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr12:73002600-73004000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr12:73002600-73004600	Weak transcription	Ovary	ovary
18	chr12:73002800-73003000	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr12:73002800-73003000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr12:73002800-73004000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr12:73003000-73003600	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr12:73003000-73004200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr12:73003600-73005600	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr12:73003600-73007800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr12:73003600-73008800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr12:73004000-73005600	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr12:73004000-73005800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr12:73004000-73008000	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr12:73004200-73005000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr12:73004200-73005000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr12:73004200-73005000	Strong transcription	Fetal Intestine Large	intestine
32	chr12:73004200-73005200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr12:73004200-73005200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr12:73004200-73005600	Enhancers	H1 Cell Line	embryonic stem cell
35	chr12:73004200-73006200	Enhancers	H9 Cell Line	embryonic stem cell
36	chr12:73004200-73008000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr12:73004400-73005200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr12:73004600-73005200	Strong transcription	Ovary	ovary
39	chr12:73004600-73005600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr12:73004800-73005000	Enhancers	Pancreas	Pancrea
41	chr12:73004800-73005200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr12:73005000-73006000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr12:73005000-73051600	Weak transcription	Fetal Intestine Large	intestine
44	chr12:73005200-73005600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr12:73005200-73006200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr12:73005200-73009200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr12:73005200-73038000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr12:73005200-73053200	Weak transcription	Ovary	ovary
49	chr12:73005600-73005800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
50	chr12:73005600-73006200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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