Variant report

Variant	esv2759906
Chromosome Location	chr12:66905405-66980180
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:336)
CpG islands
(count:122)
Chromatin interactive
region (count:15)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:66944481-66944665	K562	blood:	n/a	n/a
2	ATF1	chr12:66956774-66956900	K562	blood:	n/a	n/a
3	ATF1	chr12:66948999-66949199	K562	blood:	n/a	n/a
4	ATF1	chr12:66944465-66944726	K562	blood:	n/a	n/a
5	BACH1	chr12:66909973-66910269	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr12:66927501-66927946	GM12878	blood:	n/a	n/a
7	CEBPB	chr12:66944454-66944708	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr12:66944409-66944714	K562	blood:	n/a	n/a
9	CEBPB	chr12:66908491-66908956	IMR90	lung:	n/a	chr12:66908612-66908625 chr12:66908941-66908952
10	CTCF	chr12:66942620-66942770	WERI-Rb-1	eye:	n/a	n/a
11	CTCF	chr12:66942720-66942870	HFF	foreskin:	n/a	n/a
12	CTCF	chr12:66942700-66942850	HFF-Myc	foreskin:	n/a	n/a
13	CTCF	chr12:66942660-66942810	HepG2	liver:	n/a	n/a
14	CTCF	chr12:66942840-66942990	GM12873	blood:	n/a	n/a
15	CTCF	chr12:66909420-66909570	BE2_C	brain:	n/a	n/a
16	CTCF	chr12:66942360-66942510	HEK293	kidney:	n/a	n/a
17	CTCF	chr12:66949005-66949258	GM12878	blood:	n/a	n/a
18	CTCF	chr12:66942640-66942790	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr12:66942680-66942830	A549	lung:	n/a	n/a
20	CTCF	chr12:66953845-66953890	Pancreas_OC	pancreas:	n/a	n/a
21	CTCF	chr12:66942531-66942929	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr12:66942600-66942750	HRPEpiC	eye:	n/a	n/a
23	CTCF	chr12:66942680-66942770	MCF-7	breast:	n/a	n/a
24	CTCF	chr12:66942640-66942790	HepG2	liver:	n/a	n/a
25	CTCF	chr12:66942680-66942830	GM12871	blood:	n/a	n/a
26	CTCF	chr12:66942670-66942792	GM20000	blood:	n/a	n/a
27	CTCF	chr12:66942640-66942790	AG04449	skin:	n/a	n/a
28	CTCF	chr12:66942700-66942850	AG10803	skin:	n/a	n/a
29	CTCF	chr12:66942720-66942870	GM12864	blood:	n/a	n/a
30	CTCF	chr12:66942660-66942910	GM12801	blood:	n/a	n/a
31	CTCF	chr12:66942920-66943070	GM12875	blood:	n/a	n/a
32	CTCF	chr12:66949055-66949247	NHEK	skin:	n/a	n/a
33	CTCF	chr12:66942473-66942915	MCF-7	breast:	n/a	n/a
34	CTCF	chr12:66942640-66942790	RPTEC	kidney:	n/a	n/a
35	CTCF	chr12:66942700-66942850	GM12865	blood:	n/a	n/a
36	CTCF	chr12:66942660-66942810	HCT-116	colon:	n/a	n/a
37	CTCF	chr12:66938180-66938330	GM12874	blood:	n/a	n/a
38	CTCF	chr12:66942658-66942803	GM13977	blood:	n/a	n/a
39	CTCF	chr12:66942660-66942810	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr12:66942680-66942830	GM12866	blood:	n/a	n/a
41	CTCF	chr12:66942640-66942790	AG10803	skin:	n/a	n/a
42	CTCF	chr12:66942680-66942830	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr12:66949112-66949212	MCF-7	breast:	n/a	n/a
44	CTCF	chr12:66942640-66942790	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr12:66949116-66949159	HepG2	liver:	n/a	n/a
46	CTCF	chr12:66942700-66942850	GM12878	blood:	n/a	n/a
47	CTCF	chr12:66942540-66942690	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr12:66942680-66942830	HMEC	breast:	n/a	n/a
49	CTCF	chr12:66942680-66942805	GM10266	blood:	n/a	n/a
50	CTCF	chr12:66942600-66942750	HCM	heart:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:66965641-66965691	HMEC	breast:	n/a
2	chr12:66965991-66966041	SK-N-SH	brain:	n/a
3	chr12:66965991-66966041	AG04450	lung:	fetal
4	chr12:66965991-66966041	AG04449	skin:	fetal
5	chr12:66965991-66966041	SKMC	muscle:	n/a
6	chr12:66965991-66966041	BE2_C	brain:	n/a
7	chr12:66965991-66966041	HRE	kidney:	n/a
8	chr12:66965641-66965691	H1-hESC	embryonic stem cell:	embryo
9	chr12:66965641-66965691	HepG2	liver:	n/a
10	chr12:66965991-66966041	HepG2	liver:	n/a
11	chr12:66965991-66966041	NHDF-neo	bronchial:	n/a
12	chr12:66965991-66966041	HCT-116	colon:	n/a
13	chr12:66965991-66966041	HMEC	breast:	n/a
14	chr12:66965991-66966041	U87	brain:	n/a
15	chr12:66965641-66965691	ProgFib	skin:	n/a
16	chr12:66965991-66966041	GM12892	blood:	n/a
17	chr12:66965991-66966041	HNPCEpiC	eye:	n/a
18	chr12:66965641-66965691	HL-60	blood:	n/a
19	chr12:66965991-66966041	GM06990	blood:	n/a
20	chr12:66965641-66965691	HAEpiC	amniotic membrane:	n/a
21	chr12:66965641-66965691	NT2-D1	testis:	n/a
22	chr12:66965641-66965691	NHDF-neo	bronchial:	n/a
23	chr12:66965641-66965691	NH-A	brain:	n/a
24	chr12:66965641-66965691	ECC-1	luminal epithelium:	n/a
25	chr12:66965991-66966041	NHBE	bronchial:	n/a
26	chr12:66965991-66966041	HL-60	blood:	n/a
27	chr12:66965991-66966041	NB4	blood:	n/a
28	chr12:66965641-66965691	NB4	blood:	n/a
29	chr12:66965641-66965691	GM12892	blood:	n/a
30	chr12:66965991-66966041	HCF	heart:	n/a
31	chr12:66965991-66966041	HRCEpiC	kidney:	n/a
32	chr12:66965641-66965691	HCM	heart:	n/a
33	chr12:66965991-66966041	GM12878	blood:	n/a
34	chr12:66965641-66965691	BJ	skin:	n/a
35	chr12:66965641-66965691	Hepatocyte	liver:	n/a
36	chr12:66965641-66965691	AG04449	skin:	fetal
37	chr12:66965991-66966041	PFSK-1	brain:	n/a
38	chr12:66965641-66965691	PANC-1	pancreas:	n/a
39	chr12:66965991-66966041	Jurkat	blood:	n/a
40	chr12:66965991-66966041	HRPEpiC	eye:	n/a
41	chr12:66965991-66966041	LNCaP	prostate:	n/a
42	chr12:66965641-66965691	IMR90	lung:	fetal
43	chr12:66965991-66966041	ovcar-3	ovarian:	n/a
44	chr12:66965641-66965691	PrEC	prostate:	n/a
45	chr12:66965991-66966041	IMR90	lung:	fetal
46	chr12:66965991-66966041	HEEpiC	esophagus:	n/a
47	chr12:66965641-66965691	SKMC	muscle:	n/a
48	chr12:66965991-66966041	SK-N-MC	brain:	n/a
49	chr12:66965641-66965691	GM12891	blood:	n/a
50	chr12:66965991-66966041	CMK	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:17014602..17017113-chr12:66936746..66938540,2	MCF-7	breast:
2	chr12:66938952..66941584-chr12:66945034..66947261,2	K562	blood:
3	chr12:66908461..66910349-chr12:66910423..66912141,2	MCF-7	breast:
4	chr12:66934881..66936462-chr12:66943891..66946152,2	MCF-7	breast:
5	chr12:66940803..66943368-chr12:66944201..66946459,3	MCF-7	breast:
6	chr12:66942264..66943151-chr12:67082787..67083333,2	MCF-7	breast:
7	chr12:66940803..66943368-chr12:66944201..66946459,3	MCF-7	breast:
8	chr12:66934881..66936462-chr12:66943891..66946152,2	MCF-7	breast:
9	chr12:66932403..66936111-chr12:66940757..66944323,3	K562	blood:
10	chr12:66938952..66941584-chr12:66945034..66947261,2	K562	blood:
11	chr12:66905511..66907339-chr12:66908597..66911172,2	K562	blood:
12	chr12:66905511..66907339-chr12:66908597..66911172,2	K562	blood:
13	chr12:66924711..66926666-chr12:67101075..67103092,2	MCF-7	breast:
14	chr12:66908495..66911478-chr9:73033466..73036076,2	MCF-7	breast:
15	chr12:66930710..66933060-chr12:66933973..66935708,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMBIM4-2	chr12:66957747-66957916	NONHSAT029232
2	lnc-TMBIM4-2	chr12:66961345-66962974	NONHSAT029232

No data

Variant related genes	Relation type
GRIP1	TF binding region
OSBPL9P4	TF binding region
OSBPL9P5	TF binding region
GRIP1	CpG island
OSBPL9P4	CpG island
OSBPL9P5	CpG island
ENSG00000155974	chromatin interactions

Extended variants
information (count: 2954 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2954 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7973654	chr12:66905405-66905406	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187526315	chr12:66905466-66905467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148665335	chr12:66905554-66905555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143807290	chr12:66905579-66905580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146684611	chr12:66905639-66905640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536220024	chr12:66905664-66905665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs28513666	chr12:66905678-66905679	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs557594309	chr12:66905703-66905704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140216861	chr12:66905716-66905717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543228058	chr12:66905786-66905787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7976952	chr12:66905792-66905793	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs144883575	chr12:66905809-66905810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540985620	chr12:66905820-66905821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs116526318	chr12:66905835-66905836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149045791	chr12:66905858-66905859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567766670	chr12:66905978-66905979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551832047	chr12:66906016-66906017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146069476	chr12:66906035-66906036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531095312	chr12:66906041-66906042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138941691	chr12:66906061-66906062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs61925952	chr12:66906063-66906064	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs61925953	chr12:66906094-66906095	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs576788692	chr12:66906107-66906108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535323620	chr12:66906125-66906126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs1813738	chr12:66906145-66906146	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs2009924	chr12:66906170-66906171	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs7488693	chr12:66906183-66906184	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs556159618	chr12:66906186-66906187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553426699	chr12:66906260-66906261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12099548	chr12:66906276-66906277	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs7977592	chr12:66906325-66906326	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs192638119	chr12:66906339-66906340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146989472	chr12:66906352-66906353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540924231	chr12:66906357-66906358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369117380	chr12:66906474-66906475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184755901	chr12:66906514-66906515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372632167	chr12:66906551-66906552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577956563	chr12:66906578-66906579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7977856	chr12:66906586-66906587	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs75614362	chr12:66906610-66906611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531032263	chr12:66906628-66906629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543206099	chr12:66906668-66906669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187632439	chr12:66906681-66906682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs148041899	chr12:66906744-66906745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547254080	chr12:66906767-66906768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564483675	chr12:66906801-66906802	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs141460766	chr12:66906828-66906829	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs61925954	chr12:66906901-66906902	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs551092027	chr12:66906958-66906959	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs192093896	chr12:66906963-66906964	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Renal cell carcinoma	18194544	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
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21364760	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	22048815	CNVD
Congenital anomalies of the kidney and urinary tract	21113617	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Myxofibrosarcoma	16751306	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Lung cancer	17925434	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:66890600-66909200	Weak transcription	Pancreas	Pancrea
2	chr12:66897600-66912600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr12:66900400-66908800	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr12:66900600-66909800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr12:66902200-66910200	Weak transcription	HMEC	breast
6	chr12:66902600-66909600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:66906800-66907000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr12:66907000-66909200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr12:66907000-66910000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr12:66907200-66910000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:66907400-66910000	Weak transcription	Aorta	Aorta
12	chr12:66907800-66908200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr12:66908200-66908800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr12:66908200-66910200	Enhancers	Hela-S3	cervix
15	chr12:66908600-66909400	Enhancers	HSMMtube	muscle
16	chr12:66908800-66909000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr12:66908800-66910000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr12:66909000-66909400	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr12:66909200-66909400	Enhancers	H9 Cell Line	embryonic stem cell
20	chr12:66909200-66911400	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr12:66909200-66911400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr12:66909200-66911400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr12:66909400-66910200	Enhancers	H1 Cell Line	embryonic stem cell
24	chr12:66909400-66911000	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr12:66909400-66911400	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr12:66909600-66910000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr12:66909600-66910200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr12:66909600-66911400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr12:66909600-66911600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr12:66909800-66911400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr12:66909800-66911400	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr12:66909800-66911600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr12:66910000-66910200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr12:66910000-66910600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr12:66910000-66910800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr12:66910000-66910800	Enhancers	HUVEC	blood vessel
37	chr12:66910000-66911400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr12:66910000-66911600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr12:66910200-66911200	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr12:66910200-66932800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr12:66910600-66911400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr12:66911000-66911400	Enhancers	H9 Cell Line	embryonic stem cell
43	chr12:66911000-66911800	Enhancers	Fetal Heart	heart
44	chr12:66911200-66911400	Enhancers	H1 Cell Line	embryonic stem cell
45	chr12:66911400-66911600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr12:66911400-66913600	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr12:66911400-66914200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr12:66911400-66914200	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr12:66911400-66914200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr12:66911400-66914800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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