Variant report

Variant	nsv832458
Chromosome Location	chr12:73885329-74075491
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:398)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:74010248-74010400	K562	blood:	n/a	n/a
2	BACH1	chr12:74053673-74053952	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr12:73993330-73993343	GM12878	blood:	n/a	n/a
4	CEBPB	chr12:73885830-73886062	HepG2	liver:	n/a	chr12:73885902-73885913
5	CEBPB	chr12:74022772-74023062	HepG2	liver:	n/a	chr12:74022915-74022926
6	CEBPB	chr12:73946799-73947119	HepG2	liver:	n/a	chr12:73946977-73946988 chr12:73946976-73946989
7	CEBPB	chr12:74021361-74021622	IMR90	lung:	n/a	n/a
8	CEBPB	chr12:73946819-73947102	IMR90	lung:	n/a	chr12:73946977-73946988 chr12:73946976-73946989
9	CEBPB	chr12:74035798-74036052	A549	lung:	n/a	n/a
10	CEBPB	chr12:74021381-74021691	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr12:74028246-74028499	A549	lung:	n/a	chr12:74028348-74028359
12	CEBPB	chr12:73925716-73925796	HepG2	liver:	n/a	n/a
13	CEBPB	chr12:73946800-73947082	A549	lung:	n/a	chr12:73946977-73946988 chr12:73946976-73946989
14	CEBPB	chr12:74031940-74031970	A549	lung:	n/a	n/a
15	CEBPB	chr12:74028234-74028479	HepG2	liver:	n/a	chr12:74028348-74028359
16	CEBPB	chr12:74021476-74021558	A549	lung:	n/a	n/a
17	CEBPB	chr12:73913630-73913710	HepG2	liver:	n/a	chr12:73913651-73913664 chr12:73913652-73913663
18	CHD2	chr12:73995941-73995952	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr12:73908540-73908690	GM12866	blood:	n/a	n/a
20	CTCF	chr12:74050280-74050430	MCF-7	breast:	n/a	n/a
21	CTCF	chr12:74050240-74050390	HEK293	kidney:	n/a	n/a
22	CTCF	chr12:73908600-73908750	GM12866	blood:	n/a	n/a
23	CTCF	chr12:73908480-73908630	HL-60	blood:	n/a	n/a
24	CTCF	chr12:74023820-74023970	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr12:73908640-73908790	MCF-7	breast:	n/a	n/a
26	CTCF	chr12:73966080-73966230	GM12869	blood:	n/a	n/a
27	CTCF	chr12:73908545-73908744	Gliobla	brain:	n/a	n/a
28	CTCF	chr12:73961280-73961430	GM12866	blood:	n/a	n/a
29	CTCF	chr12:73908520-73908670	HepG2	liver:	n/a	n/a
30	CTCF	chr12:73923224-73923280	GM20000	blood:	n/a	n/a
31	CTCF	chr12:74023840-74023990	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr12:74050296-74050469	MCF-7	breast:	n/a	n/a
33	CTCF	chr12:74023740-74023890	HCT-116	colon:	n/a	n/a
34	CTCF	chr12:73908540-73908690	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr12:73908580-73908730	HEK293	kidney:	n/a	n/a
36	CTCF	chr12:73908540-73908690	GM12874	blood:	n/a	n/a
37	CTCF	chr12:73908540-73908690	GM12873	blood:	n/a	n/a
38	CTCF	chr12:73908451-73908782	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr12:73908553-73908734	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr12:74050317-74050438	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr12:74023780-74023930	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr12:73908560-73908710	GM12865	blood:	n/a	n/a
43	CTCF	chr12:73908600-73908750	MCF-7	breast:	n/a	n/a
44	CTCF	chr12:73908560-73908710	SAEC	small airway:	n/a	n/a
45	CTCF	chr12:73908560-73908710	A549	lung:	n/a	n/a
46	CTCF	chr12:74023700-74023850	RPTEC	kidney:	n/a	n/a
47	CTCF	chr12:73908585-73908663	K562	blood:	n/a	n/a
48	CTCF	chr12:74050275-74050479	MCF-7	breast:	n/a	n/a
49	CTCF	chr12:73908519-73908764	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:73891885-73891942	LNCaP	prostate:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:74072114-74072164	ovcar-3	ovarian:	n/a
2	chr12:74072114-74072164	T-47D	breast:	n/a
3	chr12:74072114-74072164	HAEpiC	amniotic membrane:	n/a
4	chr12:74072114-74072164	GM12892	blood:	n/a
5	chr12:74072114-74072164	HUVEC	blood vessel:	n/a
6	chr12:74072114-74072164	AG09309	skin:	n/a
7	chr12:74072114-74072164	HIPEpiC	eye:	n/a
8	chr12:74072114-74072164	HNPCEpiC	eye:	n/a
9	chr12:74072114-74072164	GM12878	blood:	n/a
10	chr12:74072114-74072164	PANC-1	pancreas:	n/a
11	chr12:74072114-74072164	HCT-116	colon:	n/a
12	chr12:74072114-74072164	SKMC	muscle:	n/a
13	chr12:74072114-74072164	AG09319	gingival:	n/a
14	chr12:74072114-74072164	H1-hESC	embryonic stem cell:	embryo
15	chr12:74072114-74072164	GM06990	blood:	n/a
16	chr12:74072114-74072164	HRCEpiC	kidney:	n/a
17	chr12:74072114-74072164	HEEpiC	esophagus:	n/a
18	chr12:74072114-74072164	A549	lung:	n/a
19	chr12:74072114-74072164	BJ	skin:	n/a
20	chr12:74072114-74072164	HCF	heart:	n/a
21	chr12:74072114-74072164	IMR90	lung:	fetal
22	chr12:74072114-74072164	Caco-2	colon:	n/a
23	chr12:74072114-74072164	SK-N-MC	brain:	n/a
24	chr12:74072114-74072164	AG10803	skin:	n/a
25	chr12:74072114-74072164	RPTEC	kidney:	n/a
26	chr12:74072114-74072164	MCF-7	breast:	n/a
27	chr12:74072114-74072164	HEK293	kidney:	embryo
28	chr12:74072114-74072164	PFSK-1	brain:	n/a
29	chr12:74072114-74072164	NH-A	brain:	n/a
30	chr12:74072114-74072164	NT2-D1	testis:	n/a
31	chr12:74072114-74072164	BE2_C	brain:	n/a
32	chr12:74072114-74072164	HL-60	blood:	n/a
33	chr12:74072114-74072164	NHDF-neo	bronchial:	n/a
34	chr12:74072114-74072164	NHBE	bronchial:	n/a
35	chr12:74072114-74072164	GM12891	blood:	n/a
36	chr12:74072114-74072164	HPAEpiC	pulmonary alveolar:	n/a
37	chr12:74072114-74072164	HRE	kidney:	n/a
38	chr12:74072114-74072164	ECC-1	luminal epithelium:	n/a
39	chr12:74072114-74072164	GM19239	blood:	n/a
40	chr12:74072114-74072164	AG04450	lung:	fetal
41	chr12:74072114-74072164	Hepatocyte	liver:	n/a
42	chr12:74072114-74072164	NB4	blood:	n/a
43	chr12:74072114-74072164	MCF10A-Er-Src	breast:	n/a
44	chr12:74072114-74072164	LNCaP	prostate:	n/a
45	chr12:74072114-74072164	K562	blood:	n/a
46	chr12:74072114-74072164	SAEC	small airway:	n/a
47	chr12:74072114-74072164	ProgFib	skin:	n/a
48	chr12:74072114-74072164	PrEC	prostate:	n/a
49	chr12:74072114-74072164	Hela-S3	cervix:	n/a
50	chr12:74072114-74072164	U87	brain:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:73941837..73944242-chr9:86536650..86538183,2	MCF-7	breast:
2	chr12:74035671..74038050-chr12:74931309..74933975,2	K562	blood:
3	chr12:73946481..73947983-chr12:73948607..73951513,2	K562	blood:
4	chr12:73908195..73908905-chr12:74049929..74050461,2	MCF-7	breast:
5	chr12:74008618..74010272-chr12:74013442..74015238,2	K562	blood:
6	chr12:73924250..73927148-chr12:73929034..73931250,2	K562	blood:
7	chr12:73924250..73927148-chr12:73929034..73931250,2	K562	blood:
8	chr12:74013871..74015768-chr12:74016739..74019231,2	MCF-7	breast:
9	chr12:74008618..74010272-chr12:74013442..74015238,2	K562	blood:
10	chr12:73908195..73908905-chr12:74049929..74050461,2	MCF-7	breast:
11	chr12:74013871..74015768-chr12:74016739..74019231,2	MCF-7	breast:
12	chr12:73946481..73947983-chr12:73948607..73951513,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRHDE-4	chr12:73914766-73915164	l_679_chr12:73914765-73931279_testes
2	lnc-TRHDE-4	chr12:73930540-73931332	l_679_chr12:73914765-73931279_testes

No data

Variant related genes	Relation type
RNU6-1012P	TF binding region
ENSG00000243164	TF binding region
RNU6-1012P	CpG island
ENSG00000243164	CpG island
ENSG00000253719	chromatin interactions
ENSG00000257386	chromatin interactions

Extended variants
information (count: 2486 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2486 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111878435	chr12:73896231-73896232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552525045	chr12:73896233-73896234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569081166	chr12:73896308-73896309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532113775	chr12:73896313-73896314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs7306348	chr12:73896324-73896325	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs115121546	chr12:73896376-73896377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553937383	chr12:73896377-73896378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534799792	chr12:73896399-73896400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs2197289	chr12:73896458-73896459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184864204	chr12:73896466-73896467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563161353	chr12:73896539-73896540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs6582165	chr12:73896578-73896579	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs544148320	chr12:73896609-73896610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560765929	chr12:73896618-73896619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529801393	chr12:73896622-73896623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2197288	chr12:73896626-73896627	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs547938394	chr12:73896647-73896648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150274348	chr12:73896660-73896661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532319573	chr12:73896662-73896663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188848308	chr12:73896748-73896749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375927619	chr12:73896772-73896773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7953263	chr12:73896773-73896774	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs531513840	chr12:73896778-73896779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548561388	chr12:73896794-73896795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149430686	chr12:73896827-73896828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182114264	chr12:73896835-73896836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372959693	chr12:73896838-73896839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570627357	chr12:73896856-73896857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184601016	chr12:73896861-73896862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189922482	chr12:73896874-73896875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576670619	chr12:73896875-73896876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542196591	chr12:73896877-73896878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536309877	chr12:73896879-73896880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372888004	chr12:73896948-73896949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs180671867	chr12:73896964-73896965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560257736	chr12:73897001-73897002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532256436	chr12:73897020-73897021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545939205	chr12:73897059-73897060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556221792	chr12:73897086-73897087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531624637	chr12:73897092-73897093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185363234	chr12:73897093-73897094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568093754	chr12:73897125-73897126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527644608	chr12:73897138-73897139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547395401	chr12:73897147-73897148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190019129	chr12:73897177-73897178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539591328	chr12:73897194-73897195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181919901	chr12:73897200-73897201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs556705368	chr12:73897202-73897203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113608634	chr12:73897205-73897206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536122484	chr12:73897226-73897227	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
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
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:73896200-73901400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr12:73897400-73898200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:73897800-73898200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr12:73898000-73898400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
5	chr12:73898200-73900400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:73898400-73900200	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr12:73900200-73901000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr12:73900200-73901200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr12:73900200-73901400	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr12:73900200-73901400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr12:73900200-73901600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr12:73900400-73900600	Enhancers	H1 Cell Line	embryonic stem cell
13	chr12:73900400-73901000	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr12:73900400-73901400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr12:73900600-73901000	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr12:73901200-73901400	Enhancers	H1 Cell Line	embryonic stem cell
17	chr12:73901400-73901600	Enhancers	H9 Cell Line	embryonic stem cell
18	chr12:73901400-73902600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:73902600-73902800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:73923600-73926000	Enhancers	Liver	Liver
21	chr12:73925800-73926400	Enhancers	Primary B cells from cord blood	blood
22	chr12:73926000-73926400	Flanking Active TSS	Liver	Liver
23	chr12:73926400-73926800	Enhancers	Liver	Liver
24	chr12:73927600-73928200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr12:73928400-73929800	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr12:73928400-73931000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr12:73928800-73929600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:73928800-73929600	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr12:73941800-73942200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr12:73941800-73943000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr12:73965000-73966000	Enhancers	Muscle Satellite Cultured Cells	--
32	chr12:73991000-73991200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr12:73991200-73991400	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr12:73991200-73992000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr12:73991200-73994000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr12:73991400-73992000	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr12:73991600-73991800	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr12:73991600-73993800	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr12:73991800-73992800	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr12:73992000-73992800	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr12:73992000-73993600	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr12:73992000-73994000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr12:73992000-73994200	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr12:73992800-73993800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr12:73993600-73999600	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr12:73999600-73999800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr12:73999600-74000000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr12:73999600-74000000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr12:73999600-74000000	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr12:73999600-74000000	Enhancers	HUES6 Cell Line	embryonic stem cell

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