Variant report

Variant	esv3325978
Chromosome Location	chr12:66920993-67016708
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:457)
CpG islands
(count:306)
Chromatin interactive
region (count:16)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:457 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	chr12:66948999-66949199	K562	blood:	n/a	n/a
3	ATF1	chr12:66956774-66956900	K562	blood:	n/a	n/a
4	ATF1	chr12:66944465-66944726	K562	blood:	n/a	n/a
5	ATF2	chr12:66982816-66983294	GM12878	blood:	n/a	n/a
6	ATF2	chr12:67010047-67011107	GM12878	blood:	n/a	n/a
7	BATF	chr12:67010582-67010897	GM12878	blood:	n/a	n/a
8	BCL3	chr12:67010669-67010952	GM12878	blood:	n/a	n/a
9	BCL3	chr12:67010215-67010866	GM12878	blood:	n/a	n/a
10	BCLAF1	chr12:67010067-67010990	GM12878	blood:	n/a	n/a
11	BCLAF1	chr12:66927501-66927946	GM12878	blood:	n/a	n/a
12	BHLHE40	chr12:67010139-67011127	GM12878	blood:	n/a	n/a
13	CEBPB	chr12:66944409-66944714	K562	blood:	n/a	n/a
14	CEBPB	chr12:66944454-66944708	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr12:66997287-66997589	MCF-7	breast:	n/a	n/a
16	CTCF	chr12:66942620-66942770	NB4	blood:	n/a	n/a
17	CTCF	chr12:66942660-66942810	GM12864	blood:	n/a	n/a
18	CTCF	chr12:66942680-66942830	HMEC	breast:	n/a	n/a
19	CTCF	chr12:66942700-66942850	K562	blood:	n/a	n/a
20	CTCF	chr12:66942260-66942410	GM12864	blood:	n/a	n/a
21	CTCF	chr12:66942640-66942790	GM12878	blood:	n/a	n/a
22	CTCF	chr12:66942640-66942790	RPTEC	kidney:	n/a	n/a
23	CTCF	chr12:66942580-66942730	HAc	cerebellar:	n/a	n/a
24	CTCF	chr12:66949005-66949258	GM12878	blood:	n/a	n/a
25	CTCF	chr12:66942820-66942970	GM12870	blood:	n/a	n/a
26	CTCF	chr12:66949116-66949159	HepG2	liver:	n/a	n/a
27	CTCF	chr12:66942600-66942750	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr12:66942700-66942850	HMF	breast:	n/a	n/a
29	CTCF	chr12:66949069-66949199	GM12878	blood:	n/a	n/a
30	CTCF	chr12:66942100-66942250	GM12873	blood:	n/a	n/a
31	CTCF	chr12:66942660-66942810	HepG2	liver:	n/a	n/a
32	CTCF	chr12:66942700-66942850	GM12871	blood:	n/a	n/a
33	CTCF	chr12:66942680-66942830	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr12:66949136-66949155	GM13976	blood:	n/a	n/a
35	CTCF	chr12:66942680-66942830	GM06990	blood:	n/a	n/a
36	CTCF	chr12:66942640-66942790	HCT-116	colon:	n/a	n/a
37	CTCF	chr12:66949180-66949330	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr12:66942589-66942946	K562	blood:	n/a	n/a
39	CTCF	chr12:66942660-66942810	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:66942669-66942756	GM13976	blood:	n/a	n/a
41	CTCF	chr12:66942680-66942830	AG09309	skin:	n/a	n/a
42	CTCF	chr12:66942640-66942790	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr12:66942720-66942870	AG04450	lung:	n/a	n/a
44	CTCF	chr12:66942660-66942810	A549	lung:	n/a	n/a
45	CTCF	chr12:66942680-66942805	GM10266	blood:	n/a	n/a
46	CTCF	chr12:66942360-66942510	HEK293	kidney:	n/a	n/a
47	CTCF	chr12:66942660-66942910	GM12801	blood:	n/a	n/a
48	CTCF	chr12:66942680-66942830	GM12869	blood:	n/a	n/a
49	CTCF	chr12:66942500-66942650	RPTEC	kidney:	n/a	n/a
50	CTCF	chr12:66942680-66942830	AG09319	gingival:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:66996175-66996225	BE2_C	brain:	n/a
2	chr12:66996175-66996225	BE2_C	brain:	n/a
3	chr12:66965991-66966041	HRE	kidney:	n/a
4	chr12:66983908-66983958	GM06990	blood:	n/a
5	chr12:66965991-66966041	HCF	heart:	n/a
6	chr12:67009135-67009185	NT2-D1	testis:	n/a
7	chr12:66965991-66966041	HRCEpiC	kidney:	n/a
8	chr12:66965641-66965691	GM12892	blood:	n/a
9	chr12:66983908-66983958	H1-hESC	embryonic stem cell:	embryo
10	chr12:67009135-67009185	Hela-S3	cervix:	n/a
11	chr12:67009135-67009185	AoSMC	blood vessel:	n/a
12	chr12:66965991-66966041	Jurkat	blood:	n/a
13	chr12:66983908-66983958	ProgFib	skin:	n/a
14	chr12:66965641-66965691	K562	blood:	n/a
15	chr12:66983908-66983958	HNPCEpiC	eye:	n/a
16	chr12:66965991-66966041	PrEC	prostate:	n/a
17	chr12:66996175-66996225	AG09319	gingival:	n/a
18	chr12:66983908-66983958	SK-N-MC	brain:	n/a
19	chr12:66983908-66983958	SKMC	muscle:	n/a
20	chr12:66996175-66996225	BJ	skin:	n/a
21	chr12:66983908-66983958	SK-N-SH	brain:	n/a
22	chr12:66965641-66965691	AG10803	skin:	n/a
23	chr12:66965641-66965691	BE2_C	brain:	n/a
24	chr12:66965641-66965691	Hepatocyte	liver:	n/a
25	chr12:66996175-66996225	AG09309	skin:	n/a
26	chr12:67009135-67009185	U87	brain:	n/a
27	chr12:66965991-66966041	HEEpiC	esophagus:	n/a
28	chr12:66965991-66966041	ECC-1	luminal epithelium:	n/a
29	chr12:67009135-67009185	HepG2	liver:	n/a
30	chr12:67009135-67009185	HEK293	kidney:	embryo
31	chr12:67009135-67009185	PANC-1	pancreas:	n/a
32	chr12:66983908-66983958	HRCEpiC	kidney:	n/a
33	chr12:66965991-66966041	AG09309	skin:	n/a
34	chr12:66983908-66983958	U87	brain:	n/a
35	chr12:66965991-66966041	NT2-D1	testis:	n/a
36	chr12:66996175-66996225	SK-N-SH	brain:	n/a
37	chr12:66965641-66965691	AG04450	lung:	fetal
38	chr12:66965641-66965691	HCPEpiC	choroid plexus:	n/a
39	chr12:67009135-67009185	Jurkat	blood:	n/a
40	chr12:66965991-66966041	AG04449	skin:	fetal
41	chr12:67009135-67009185	HCT-116	colon:	n/a
42	chr12:66965991-66966041	MCF10A-Er-Src	breast:	n/a
43	chr12:66983908-66983958	HCPEpiC	choroid plexus:	n/a
44	chr12:66965641-66965691	HNPCEpiC	eye:	n/a
45	chr12:66996175-66996225	Hepatocyte	liver:	n/a
46	chr12:67009135-67009185	RPTEC	kidney:	n/a
47	chr12:66996175-66996225	HNPCEpiC	eye:	n/a
48	chr12:66983908-66983958	PrEC	prostate:	n/a
49	chr12:66996175-66996225	IMR90	lung:	fetal
50	chr12:66965991-66966041	U87	brain:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:66934881..66936462-chr12:66943891..66946152,2	MCF-7	breast:
2	chr12:67001163..67003119-chr12:67003939..67006619,2	MCF-7	breast:
3	chr12:66940803..66943368-chr12:66944201..66946459,3	MCF-7	breast:
4	chr12:66938952..66941584-chr12:66945034..66947261,2	K562	blood:
5	chr12:66942264..66943151-chr12:67082787..67083333,2	MCF-7	breast:
6	chr12:66997569..67000508-chr12:67003857..67006793,2	K562	blood:
7	chr12:67014224..67016972-chr12:67017944..67019515,2	K562	blood:
8	chr12:66930710..66933060-chr12:66933973..66935708,2	MCF-7	breast:
9	chr12:66940803..66943368-chr12:66944201..66946459,3	MCF-7	breast:
10	chr12:67001163..67003119-chr12:67003939..67006619,2	MCF-7	breast:
11	chr12:66997569..67000508-chr12:67003857..67006793,2	K562	blood:
12	chr12:66924711..66926666-chr12:67101075..67103092,2	MCF-7	breast:
13	chr1:17014602..17017113-chr12:66936746..66938540,2	MCF-7	breast:
14	chr12:66934881..66936462-chr12:66943891..66946152,2	MCF-7	breast:
15	chr12:66932403..66936111-chr12:66940757..66944323,3	K562	blood:
16	chr12:66938952..66941584-chr12:66945034..66947261,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMBIM4-2	chr12:66957747-66957916	NONHSAT029232
2	lnc-TMBIM4-3	chr12:67012839-67013711	l_670_chr12:67012838-67028694_prostate
3	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: 3715 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3715 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201559050	chr12:66920998-66920999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs529610178	chr12:66921006-66921007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548150980	chr12:66921011-66921012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373147137	chr12:66921020-66921021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376249093	chr12:66921032-66921033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533776271	chr12:66921054-66921055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374634996	chr12:66921065-66921066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558660756	chr12:66921069-66921070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570471647	chr12:66921080-66921081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146262690	chr12:66921098-66921099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs111868415	chr12:66921104-66921105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562644856	chr12:66921128-66921129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577396700	chr12:66921137-66921138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186076497	chr12:66921200-66921201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140262592	chr12:66921205-66921206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541709797	chr12:66921207-66921208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138935995	chr12:66921219-66921220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373991883	chr12:66921222-66921223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147270734	chr12:66921227-66921228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs367962008	chr12:66921262-66921263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192049883	chr12:66921290-66921291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553659400	chr12:66921292-66921293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181874472	chr12:66921293-66921294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546308908	chr12:66921307-66921308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12579342	chr12:66921315-66921316	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs186323805	chr12:66921318-66921319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531691729	chr12:66921330-66921331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190721065	chr12:66921360-66921361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528602668	chr12:66921368-66921369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182852515	chr12:66921371-66921372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200459795	chr12:66921417-66921418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188006198	chr12:66921420-66921421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548066694	chr12:66921423-66921424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191378157	chr12:66921435-66921436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527246800	chr12:66921457-66921458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200612514	chr12:66921465-66921466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs117464210	chr12:66921466-66921467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10784550	chr12:66921478-66921479	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs537538819	chr12:66921494-66921495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374500960	chr12:66921500-66921501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567870391	chr12:66921502-66921503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144165648	chr12:66921513-66921514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146482600	chr12:66921558-66921559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572023240	chr12:66921568-66921569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182748123	chr12:66921592-66921593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557864988	chr12:66921599-66921600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114293676	chr12:66921606-66921607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187813194	chr12:66921637-66921638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191151088	chr12:66921643-66921644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574260483	chr12:66921675-66921676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Melanoma	20877625	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:66910200-66932800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:66911400-66938200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:66921000-66933000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr12:66921600-66926200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr12:66922800-66923200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr12:66923200-66926000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr12:66923600-66924400	Enhancers	HUVEC	blood vessel
8	chr12:66923800-66924000	Enhancers	Fetal Brain Female	brain
9	chr12:66924200-66925400	Weak transcription	Fetal Brain Female	brain
10	chr12:66924600-66925000	Enhancers	Fetal Brain Male	brain
11	chr12:66925000-66925200	Weak transcription	Fetal Brain Male	brain
12	chr12:66925200-66925600	Enhancers	Fetal Brain Male	brain
13	chr12:66925200-66926600	Enhancers	Brain Germinal Matrix	brain
14	chr12:66925400-66926600	Enhancers	Fetal Brain Female	brain
15	chr12:66925600-66932200	Weak transcription	Fetal Brain Male	brain
16	chr12:66926000-66926400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr12:66926000-66926600	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr12:66926000-66926600	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr12:66926200-66926400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr12:66926200-66926600	Enhancers	H1 Cell Line	embryonic stem cell
21	chr12:66926200-66926600	Enhancers	H9 Cell Line	embryonic stem cell
22	chr12:66926200-66926600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr12:66926200-66926600	Enhancers	Gastric	stomach
24	chr12:66926200-66926800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr12:66926400-66926600	Enhancers	Pancreas	Pancrea
26	chr12:66926400-66929600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr12:66926600-66929800	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr12:66926600-66931000	Weak transcription	Fetal Brain Female	brain
29	chr12:66926600-66932800	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr12:66926600-66933000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr12:66926800-66930200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr12:66928800-66930000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr12:66928800-66933000	Weak transcription	Pancreas	Pancrea
34	chr12:66929400-66930200	Enhancers	Fetal Intestine Small	intestine
35	chr12:66929600-66930400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr12:66929800-66930400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr12:66929800-66930400	Enhancers	H9 Cell Line	embryonic stem cell
38	chr12:66930000-66930400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr12:66930200-66930600	Weak transcription	Fetal Intestine Small	intestine
40	chr12:66930400-66933000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr12:66930400-66933000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr12:66930400-66938000	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr12:66930600-66930800	Enhancers	Fetal Intestine Small	intestine
44	chr12:66930800-66932800	Weak transcription	Fetal Intestine Small	intestine
45	chr12:66931000-66933600	Enhancers	Fetal Brain Female	brain
46	chr12:66932200-66934200	Enhancers	Fetal Brain Male	brain
47	chr12:66932800-66933200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr12:66932800-66933200	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr12:66932800-66933200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr12:66932800-66933200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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