Variant report

Variant	esv34457
Chromosome Location	chr12:73082433-73232340
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:294)
CpG islands
(count:62)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:294 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr12:73085107-73085586	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr12:73208970-73209323	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr12:73212115-73212362	GM12878	blood:	n/a	n/a
4	BHLHE40	chr12:73085142-73085302	GM12878	blood:	n/a	n/a
5	BRCA1	chr12:73184254-73184360	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr12:73153067-73153380	HCT-116	colon:	n/a	n/a
7	CEBPB	chr12:73193897-73194188	HepG2	liver:	n/a	chr12:73194021-73194032
8	CEBPB	chr12:73200612-73201101	H1-hESC	embryonic stem cell:	n/a	chr12:73200811-73200822
9	CEBPB	chr12:73157951-73158107	A549	lung:	n/a	n/a
10	CEBPB	chr12:73121205-73121535	IMR90	lung:	n/a	chr12:73121373-73121386 chr12:73121375-73121386 chr12:73121373-73121386 chr12:73121373-73121386 chr12:73121375-73121386
11	CEBPB	chr12:73230494-73230590	A549	lung:	n/a	chr12:73230521-73230532 chr12:73230519-73230532
12	CEBPB	chr12:73193952-73194101	K562	blood:	n/a	chr12:73194021-73194032
13	CEBPB	chr12:73184115-73184468	MCF-7	breast:	n/a	n/a
14	CEBPB	chr12:73217928-73217981	HepG2	liver:	n/a	chr12:73217954-73217965
15	CEBPB	chr12:73184092-73184484	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:73152789-73152830	K562	blood:	n/a	n/a
17	CEBPB	chr12:73200699-73200856	HepG2	liver:	n/a	chr12:73200811-73200822
18	CEBPB	chr12:73196692-73196836	HepG2	liver:	n/a	n/a
19	CEBPB	chr12:73200677-73201003	A549	lung:	n/a	chr12:73200811-73200822
20	CHD2	chr12:73222605-73222617	GM12878	blood:	n/a	n/a
21	CTCF	chr12:73093260-73093410	MCF-7	breast:	n/a	n/a
22	CTCF	chr12:73093180-73093330	AG04449	skin:	n/a	n/a
23	CTCF	chr12:73093180-73093330	NHEK	skin:	n/a	n/a
24	CTCF	chr12:73093220-73093370	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr12:73093180-73093330	BJ	skin:	n/a	n/a
26	CTCF	chr12:73093200-73093350	GM12875	blood:	n/a	n/a
27	CTCF	chr12:73091100-73091250	NHLF	lung:	n/a	n/a
28	CTCF	chr12:73093300-73093450	AG04449	skin:	n/a	n/a
29	CTCF	chr12:73093268-73093434	MCF-7	breast:	n/a	n/a
30	CTCF	chr12:73093316-73093376	MCF-7	breast:	n/a	n/a
31	CTCF	chr12:73093240-73093390	GM12868	blood:	n/a	n/a
32	CTCF	chr12:73093273-73093424	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr12:73093240-73093390	GM12869	blood:	n/a	n/a
34	CTCF	chr12:73093240-73093390	GM12867	blood:	n/a	n/a
35	CTCF	chr12:73167440-73167590	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr12:73093220-73093370	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr12:73104269-73104292	GM20000	blood:	n/a	n/a
38	CTCF	chr12:73093220-73093370	HFF	foreskin:	n/a	n/a
39	CTCF	chr12:73093260-73093410	Caco-2	colon:	n/a	n/a
40	CTCF	chr12:73093300-73093450	GM12875	blood:	n/a	n/a
41	CTCF	chr12:73093280-73093430	HL-60	blood:	n/a	n/a
42	CTCF	chr12:73093280-73093430	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr12:73093293-73093362	Gliobla	brain:	n/a	n/a
44	CTCF	chr12:73212285-73212364	LNCaP	prostate:	n/a	n/a
45	CTCF	chr12:73093200-73093350	GM12864	blood:	n/a	n/a
46	CTCF	chr12:73093300-73093450	HRE	kidney:	n/a	n/a
47	CTCF	chr12:73093300-73093450	GM12864	blood:	n/a	n/a
48	CTCF	chr12:73093301-73093403	A549	lung:	n/a	n/a
49	CTCF	chr12:73093300-73093450	HCT-116	colon:	n/a	n/a
50	CTCF	chr12:73093300-73093450	BE2_C	brain:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:73085225-73085275	H1-hESC	embryonic stem cell:	embryo
2	chr12:73085225-73085275	H1-hESC	embryonic stem cell:	embryo
3	chr12:73085225-73085275	CMK	blood:	n/a
4	chr12:73085225-73085275	HCF	heart:	n/a
5	chr12:73085225-73085275	HUVEC	blood vessel:	n/a
6	chr12:73085225-73085275	GM19239	blood:	n/a
7	chr12:73085225-73085275	Jurkat	blood:	n/a
8	chr12:73085225-73085275	GM12892	blood:	n/a
9	chr12:73085225-73085275	SK-N-SH	brain:	n/a
10	chr12:73085225-73085275	Hela-S3	cervix:	n/a
11	chr12:73085225-73085275	K562	blood:	n/a
12	chr12:73085225-73085275	NHDF-neo	bronchial:	n/a
13	chr12:73085225-73085275	HCM	heart:	n/a
14	chr12:73085225-73085275	HMEC	breast:	n/a
15	chr12:73085225-73085275	PrEC	prostate:	n/a
16	chr12:73085225-73085275	NT2-D1	testis:	n/a
17	chr12:73085225-73085275	ovcar-3	ovarian:	n/a
18	chr12:73085225-73085275	PANC-1	pancreas:	n/a
19	chr12:73085225-73085275	AoSMC	blood vessel:	n/a
20	chr12:73085225-73085275	HRPEpiC	eye:	n/a
21	chr12:73085225-73085275	SK-N-MC	brain:	n/a
22	chr12:73085225-73085275	HEK293	kidney:	embryo
23	chr12:73085225-73085275	BJ	skin:	n/a
24	chr12:73085225-73085275	HRE	kidney:	n/a
25	chr12:73085225-73085275	HepG2	liver:	n/a
26	chr12:73085225-73085275	GM12878	blood:	n/a
27	chr12:73085225-73085275	GM06990	blood:	n/a
28	chr12:73085225-73085275	IMR90	lung:	fetal
29	chr12:73085225-73085275	AG09319	gingival:	n/a
30	chr12:73085225-73085275	AG04449	skin:	fetal
31	chr12:73085225-73085275	HAEpiC	amniotic membrane:	n/a
32	chr12:73085225-73085275	HL-60	blood:	n/a
33	chr12:73085225-73085275	AG10803	skin:	n/a
34	chr12:73085225-73085275	U87	brain:	n/a
35	chr12:73085225-73085275	LNCaP	prostate:	n/a
36	chr12:73085225-73085275	HPAEpiC	pulmonary alveolar:	n/a
37	chr12:73085225-73085275	SAEC	small airway:	n/a
38	chr12:73085225-73085275	A549	lung:	n/a
39	chr12:73085225-73085275	Hepatocyte	liver:	n/a
40	chr12:73085225-73085275	ECC-1	luminal epithelium:	n/a
41	chr12:73085225-73085275	SK-N-SH_RA	brain:	n/a
42	chr12:73085225-73085275	PFSK-1	brain:	n/a
43	chr12:73085225-73085275	RPTEC	kidney:	n/a
44	chr12:73085225-73085275	NB4	blood:	n/a
45	chr12:73085225-73085275	NHBE	bronchial:	n/a
46	chr12:73085225-73085275	HEEpiC	esophagus:	n/a
47	chr12:73085225-73085275	GM12891	blood:	n/a
48	chr12:73085225-73085275	NH-A	brain:	n/a
49	chr12:73085225-73085275	AG09309	skin:	n/a
50	chr12:73085225-73085275	ProgFib	skin:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:73162846..73164376-chr12:73166429..73169138,2	MCF-7	breast:
2	chr12:73177952..73180851-chr12:73182448..73184176,2	K562	blood:
3	chr1:53191543..53194375-chr12:73227297..73229475,2	MCF-7	breast:
4	chr12:73162846..73164376-chr12:73166429..73169138,2	MCF-7	breast:
5	chr12:73177952..73180851-chr12:73182448..73184176,2	K562	blood:
6	chr1:110863042..110863616-chr12:73109953..73110460,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFC3H1-7	chr12:73122565-73122624	ENSG00000258235.1
2	lnc-ZFC3H1-7	chr12:73121703-73122023	ENSG00000258235.1

No data

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

Extended variants
information (count: 3462 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:3462 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530032993	chr12:73083601-73083602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs7980056	chr12:73083602-73083603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7315768	chr12:73083604-73083605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577567768	chr12:73083615-73083616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558878718	chr12:73083627-73083628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540125090	chr12:73083637-73083638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577405856	chr12:73083681-73083682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544361865	chr12:73083700-73083701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562973419	chr12:73083707-73083708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375159114	chr12:73083775-73083776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190938640	chr12:73083810-73083811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183021843	chr12:73083826-73083827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560491947	chr12:73083834-73083835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527305172	chr12:73083941-73083942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573861882	chr12:73084068-73084069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552485619	chr12:73084128-73084129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570540059	chr12:73084143-73084144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146302554	chr12:73084155-73084156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558791934	chr12:73084199-73084200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542892498	chr12:73084200-73084201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567780803	chr12:73084225-73084226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535185355	chr12:73084247-73084248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185951705	chr12:73084293-73084294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547445592	chr12:73084300-73084301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570444665	chr12:73084333-73084334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369516362	chr12:73084340-73084341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559235560	chr12:73084342-73084343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577343547	chr12:73084352-73084353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190856883	chr12:73084364-73084365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183051358	chr12:73084387-73084388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139285748	chr12:73084392-73084393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186885677	chr12:73084447-73084448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs60426623	chr12:73084486-73084487	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs113107922	chr12:73084498-73084499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545757919	chr12:73084516-73084517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564379431	chr12:73084571-73084572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531522207	chr12:73084635-73084636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549906164	chr12:73084637-73084638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567917579	chr12:73084660-73084661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528950252	chr12:73084710-73084711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115041022	chr12:73084716-73084717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565319230	chr12:73084718-73084719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7958689	chr12:73084755-73084756	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs557486501	chr12:73084770-73084771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571087691	chr12:73084811-73084812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538161877	chr12:73084841-73084842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556795665	chr12:73084849-73084850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575127201	chr12:73084851-73084852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535937394	chr12:73084863-73084864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554336405	chr12:73084930-73084931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:73083600-73085400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr12:73085000-73085600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr12:73085000-73085600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr12:73085200-73085400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:73085200-73086000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr12:73085400-73085800	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr12:73085400-73086200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr12:73086000-73086200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:73093400-73093600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr12:73093400-73094000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
11	chr12:73093800-73094000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr12:73094000-73094400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:73096600-73097000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
14	chr12:73096800-73097400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
15	chr12:73097400-73100000	Active TSS	HUES6 Cell Line	embryonic stem cell
16	chr12:73099400-73099800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr12:73100000-73100800	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr12:73100800-73102000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
19	chr12:73102000-73104600	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr12:73104600-73105800	Strong transcription	HUES6 Cell Line	embryonic stem cell
21	chr12:73105000-73106600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr12:73105800-73108000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr12:73105800-73113200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr12:73106600-73106800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr12:73106800-73110400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:73108000-73112400	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr12:73109800-73112200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:73109800-73113000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr12:73110000-73111400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr12:73110000-73111400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr12:73110200-73110400	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr12:73110400-73110600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr12:73110600-73111000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr12:73110800-73111200	Enhancers	Fetal Brain Male	brain
35	chr12:73111000-73111200	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr12:73111000-73111200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr12:73111200-73114000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr12:73111400-73113000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr12:73112400-73112800	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr12:73112800-73116000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
41	chr12:73114000-73115800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chr12:73115800-73117200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr12:73122600-73122800	ZNF genes & repeats	Psoas Muscle	Psoas
44	chr12:73122600-73123400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr12:73122800-73124800	Weak transcription	Psoas Muscle	Psoas
46	chr12:73123000-73123400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr12:73131400-73131600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr12:73131400-73131800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr12:73131600-73132800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr12:73132000-73132600	Enhancers	Primary hematopoietic stem cells	blood

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