Variant report

Variant	nsv899271
Chromosome Location	chr12:73448714-73595395
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:243)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:243 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:73553885-73554028	K562	blood:	n/a	n/a
2	ATF1	chr12:73555580-73555738	K562	blood:	n/a	n/a
3	BACH1	chr12:73490226-73490228	K562	blood:	n/a	n/a
4	CEBPB	chr12:73462556-73462819	HepG2	liver:	n/a	chr12:73462682-73462693
5	CEBPB	chr12:73557988-73558252	H1-hESC	embryonic stem cell:	n/a	chr12:73558141-73558152
6	CEBPB	chr12:73563337-73563670	H1-hESC	embryonic stem cell:	n/a	chr12:73563465-73563476
7	CEBPB	chr12:73563369-73563618	K562	blood:	n/a	chr12:73563465-73563476
8	CEBPB	chr12:73505936-73506210	HepG2	liver:	n/a	chr12:73506085-73506096 chr12:73506085-73506098
9	CEBPB	chr12:73555545-73555788	IMR90	lung:	n/a	n/a
10	CEBPB	chr12:73493465-73493768	A549	lung:	n/a	chr12:73493579-73493592 chr12:73493579-73493590
11	CEBPB	chr12:73558041-73558226	HepG2	liver:	n/a	chr12:73558141-73558152
12	CEBPB	chr12:73587091-73587347	HepG2	liver:	n/a	chr12:73587246-73587257 chr12:73587244-73587257 chr12:73587244-73587257 chr12:73587244-73587255 chr12:73587246-73587257
13	CEBPB	chr12:73575421-73575579	K562	blood:	n/a	n/a
14	CEBPB	chr12:73555583-73555718	A549	lung:	n/a	n/a
15	CEBPB	chr12:73493411-73493732	HepG2	liver:	n/a	chr12:73493579-73493592 chr12:73493579-73493590
16	CEBPB	chr12:73563303-73563632	HepG2	liver:	n/a	chr12:73563465-73563476
17	CEBPB	chr12:73462627-73462775	H1-hESC	embryonic stem cell:	n/a	chr12:73462682-73462693
18	CEBPB	chr12:73453380-73453538	HepG2	liver:	n/a	chr12:73453482-73453493
19	CEBPB	chr12:73563316-73563637	IMR90	lung:	n/a	chr12:73563465-73563476
20	CEBPB	chr12:73575333-73575533	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:73493413-73493714	IMR90	lung:	n/a	chr12:73493579-73493592 chr12:73493579-73493590
22	CEBPB	chr12:73563344-73563632	A549	lung:	n/a	chr12:73563465-73563476
23	CEBPB	chr12:73505928-73506138	IMR90	lung:	n/a	chr12:73506085-73506096 chr12:73506085-73506098
24	CEBPB	chr12:73494777-73495229	HepG2	liver:	n/a	chr12:73494791-73494808 chr12:73495041-73495052
25	CTCF	chr12:73451290-73451485	MCF-7	breast:	n/a	n/a
26	CTCF	chr12:73451260-73451410	Caco-2	colon:	n/a	n/a
27	CTCF	chr12:73475860-73476010	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:73481355-73481433	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:73481340-73481490	NB4	blood:	n/a	n/a
30	CTCF	chr12:73451340-73451490	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr12:73519800-73519950	AG10803	skin:	n/a	n/a
32	CTCF	chr12:73557190-73557197	GM20000	blood:	n/a	n/a
33	CTCF	chr12:73451220-73451370	HCT-116	colon:	n/a	n/a
34	CTCF	chr12:73481300-73481450	HEK293	kidney:	n/a	n/a
35	CTCF	chr12:73481646-73481735	MCF-7	breast:	n/a	n/a
36	CTCF	chr12:73567852-73567898	GM13977	blood:	n/a	n/a
37	CTCF	chr12:73476828-73476872	GM10248	blood:	n/a	n/a
38	CTCF	chr12:73451260-73451410	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr12:73481371-73481427	HepG2	liver:	n/a	n/a
40	CTCF	chr12:73451282-73451470	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr12:73466354-73466413	Fibrobl	skin:	n/a	n/a
42	CTCF	chr12:73451296-73451487	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:73481280-73481430	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr12:73481686-73481692	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr12:73451342-73451393	Gliobla	brain:	n/a	n/a
46	CTCF	chr12:73451282-73451498	MCF-7	breast:	n/a	n/a
47	CTCF	chr12:73451336-73451450	MCF-7	breast:	n/a	n/a
48	CTCF	chr12:73451320-73451470	HEK293	kidney:	n/a	n/a
49	CTCF	chr12:73451223-73451542	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr12:73451260-73451410	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:73547253-73547303	ovcar-3	ovarian:	n/a
2	chr12:73547253-73547303	HEEpiC	esophagus:	n/a
3	chr12:73547253-73547303	GM12892	blood:	n/a
4	chr12:73547253-73547303	PANC-1	pancreas:	n/a
5	chr12:73547253-73547303	SK-N-SH_RA	brain:	n/a
6	chr12:73547253-73547303	HEK293	kidney:	embryo
7	chr12:73547253-73547303	HepG2	liver:	n/a
8	chr12:73547253-73547303	NT2-D1	testis:	n/a
9	chr12:73547253-73547303	PrEC	prostate:	n/a
10	chr12:73547253-73547303	AG10803	skin:	n/a
11	chr12:73547253-73547303	NHBE	bronchial:	n/a
12	chr12:73547253-73547303	A549	lung:	n/a
13	chr12:73547253-73547303	Hela-S3	cervix:	n/a
14	chr12:73547253-73547303	MCF-7	breast:	n/a
15	chr12:73547253-73547303	ECC-1	luminal epithelium:	n/a
16	chr12:73547253-73547303	HCT-116	colon:	n/a
17	chr12:73547253-73547303	NB4	blood:	n/a
18	chr12:73547253-73547303	ProgFib	skin:	n/a
19	chr12:73547253-73547303	HMEC	breast:	n/a
20	chr12:73547253-73547303	HL-60	blood:	n/a
21	chr12:73547253-73547303	IMR90	lung:	fetal
22	chr12:73547253-73547303	Caco-2	colon:	n/a
23	chr12:73547253-73547303	HPAEpiC	pulmonary alveolar:	n/a
24	chr12:73547253-73547303	GM19239	blood:	n/a
25	chr12:73547253-73547303	H1-hESC	embryonic stem cell:	embryo
26	chr12:73547253-73547303	T-47D	breast:	n/a
27	chr12:73547253-73547303	SK-N-MC	brain:	n/a
28	chr12:73547253-73547303	U87	brain:	n/a
29	chr12:73547253-73547303	SK-N-SH	brain:	n/a
30	chr12:73547253-73547303	NHDF-neo	bronchial:	n/a
31	chr12:73547253-73547303	AG09309	skin:	n/a
32	chr12:73547253-73547303	HIPEpiC	eye:	n/a
33	chr12:73547253-73547303	NH-A	brain:	n/a
34	chr12:73547253-73547303	HRPEpiC	eye:	n/a
35	chr12:73547253-73547303	SKMC	muscle:	n/a
36	chr12:73547253-73547303	MCF10A-Er-Src	breast:	n/a
37	chr12:73547253-73547303	HRCEpiC	kidney:	n/a
38	chr12:73547253-73547303	AG09319	gingival:	n/a
39	chr12:73547253-73547303	RPTEC	kidney:	n/a
40	chr12:73547253-73547303	AG04449	skin:	fetal
41	chr12:73547253-73547303	AoSMC	blood vessel:	n/a
42	chr12:73547253-73547303	GM12891	blood:	n/a
43	chr12:73547253-73547303	PFSK-1	brain:	n/a
44	chr12:73547253-73547303	HUVEC	blood vessel:	n/a
45	chr12:73547253-73547303	Jurkat	blood:	n/a
46	chr12:73547253-73547303	Hepatocyte	liver:	n/a
47	chr12:73547253-73547303	BE2_C	brain:	n/a
48	chr12:73547253-73547303	GM12878	blood:	n/a
49	chr12:73547253-73547303	HCM	heart:	n/a
50	chr12:73547253-73547303	HRE	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:73540711..73542844-chr12:73545220..73547293,2	MCF-7	breast:
2	chr12:73461127..73463632-chr9:103114692..103116309,2	MCF-7	breast:
3	chr12:73469631..73472442-chr12:73473148..73475503,2	K562	blood:
4	chr12:73469631..73472442-chr12:73473148..73475503,2	K562	blood:
5	chr12:73540711..73542844-chr12:73545220..73547293,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFC3H1-8	chr12:73537533-73537636	ENSG00000258294
2	lnc-ZFC3H1-8	chr12:73537533-73537634	ENSG00000258294
3	lnc-ZFC3H1-8	chr12:73521670-73521796	ENSG00000258294
4	lnc-ZFC3H1-8	chr12:73509737-73510416	ENSG00000258294
5	lnc-ZFC3H1-8	chr12:73522765-73522941	ENSG00000258294
6	lnc-ZFC3H1-8	chr12:73510275-73510416	ENSG00000258294
7	lnc-TRHDE-2	chr12:73556974-73557013	ENSG00000258123
8	lnc-ZFC3H1-8	chr12:73522872-73522942	ENSG00000258294
9	lnc-ZFC3H1-8	chr12:73521670-73521796	ENSG00000258294
10	lnc-TRHDE-2	chr12:73552970-73553223	ENSG00000258123
11	lnc-ZFC3H1-8	chr12:73537533-73537638	ENSG00000258294
12	lnc-ZFC3H1-8	chr12:73522872-73522941	ENSG00000258294
13	lnc-ZFC3H1-8	chr12:73522872-73522941	ENSG00000258294
14	lnc-ZFC3H1-8	chr12:73509789-73510351	ENSG00000258294

No data

Variant related genes	Relation type
ENSG00000258294	TF binding region
ENSG00000258123	TF binding region
ENSG00000258294	CpG island
ENSG00000258123	CpG island
ENSG00000136891	chromatin interactions
SUV420H1	miRNA target sites
DDX5	miRNA target sites
FIZ1	miRNA target sites
PPP2R5A	miRNA target sites
C20orf177	miRNA target sites
FOXO1	miRNA target sites
ATP11B	miRNA target sites
ANP32B	miRNA target sites
TIMP3	miRNA target sites

Extended variants
information (count: 1450 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1450 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117968174	chr12:73460030-73460031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs535738417	chr12:73460090-73460091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184813140	chr12:73460093-73460094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143837879	chr12:73460097-73460098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545647206	chr12:73460128-73460129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12296138	chr12:73460190-73460191	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs576007573	chr12:73460224-73460225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543451702	chr12:73460248-73460249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561340985	chr12:73460278-73460279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530363165	chr12:73460279-73460280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548453623	chr12:73460304-73460305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560387931	chr12:73460334-73460335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527899821	chr12:73460340-73460341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187286947	chr12:73460342-73460343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200633614	chr12:73460370-73460371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12316852	chr12:73460415-73460416	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs4384435	chr12:73460431-73460432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550238810	chr12:73460454-73460455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568448315	chr12:73460470-73460471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148084608	chr12:73460504-73460505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554129730	chr12:73460509-73460510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12296330	chr12:73460558-73460559	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs539625014	chr12:73460559-73460560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143264021	chr12:73460563-73460564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184744859	chr12:73460564-73460565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375038174	chr12:73460565-73460566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576127593	chr12:73460612-73460613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369567158	chr12:73460621-73460622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543101406	chr12:73460674-73460675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549782886	chr12:73460729-73460730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554974824	chr12:73460736-73460737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189607195	chr12:73460744-73460745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540591575	chr12:73460801-73460802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs180678789	chr12:73460803-73460804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73161463	chr12:73460822-73460823	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs546422278	chr12:73460858-73460859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553387272	chr12:73460879-73460880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564510717	chr12:73460882-73460883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs73161466	chr12:73460887-73460888	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs372743858	chr12:73460895-73460896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542480035	chr12:73460924-73460925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550275449	chr12:73460930-73460931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143884113	chr12:73460941-73460942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529316534	chr12:73460978-73460979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562159014	chr12:73460982-73460983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547768307	chr12:73460995-73460996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566012992	chr12:73461056-73461057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs58965457	chr12:73461066-73461067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372700519	chr12:73461109-73461110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539343497	chr12:73461139-73461140	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
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
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:73460000-73466200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:73466200-73466400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr12:73466200-73466400	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr12:73466400-73467200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr12:73469200-73471200	Enhancers	Liver	Liver
6	chr12:73473400-73473800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:73481600-73482400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
8	chr12:73487800-73488400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr12:73490600-73492200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr12:73490800-73492200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr12:73491000-73491400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr12:73491000-73491600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr12:73500000-73500400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr12:73500000-73500400	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr12:73500000-73500400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr12:73500000-73500600	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr12:73500000-73500600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr12:73500000-73500600	Enhancers	H1 Cell Line	embryonic stem cell
19	chr12:73500000-73500600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr12:73505400-73506600	Enhancers	Liver	Liver
21	chr12:73516600-73516800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr12:73516800-73518400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:73518200-73518600	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr12:73518400-73518800	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr12:73518400-73518800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr12:73518400-73519200	Enhancers	Liver	Liver
27	chr12:73529400-73530200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:73529600-73531000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr12:73530200-73530400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr12:73530400-73530600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr12:73530400-73530600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr12:73530600-73530800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr12:73530800-73531000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr12:73547000-73547400	Active TSS	HepG2	liver
35	chr12:73549200-73549400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr12:73551000-73555600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr12:73551600-73554800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr12:73553800-73554400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr12:73554000-73554200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr12:73554400-73558600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr12:73554800-73555600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr12:73555600-73556600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr12:73555800-73556400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr12:73556400-73556800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr12:73556600-73559800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr12:73556800-73559200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr12:73557000-73557800	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr12:73557000-73559200	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr12:73557800-73558200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr12:73558000-73559400	Enhancers	HUES64 Cell Line	embryonic stem cell

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