Variant report

Variant	nsv559206
Chromosome Location	chr12:66854354-66950289
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:419)
CpG islands
(count:428)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr12:66868458-66868657	K562	blood:	n/a	n/a
3	ATF1	chr12:66944465-66944726	K562	blood:	n/a	n/a
4	ATF1	chr12:66948999-66949199	K562	blood:	n/a	n/a
5	ATF2	chr12:66894404-66895118	GM12878	blood:	n/a	n/a
6	BACH1	chr12:66909973-66910269	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr12:66868545-66868695	GM12878	blood:	n/a	n/a
8	BCL3	chr12:66894604-66894980	GM12878	blood:	n/a	n/a
9	BCLAF1	chr12:66927501-66927946	GM12878	blood:	n/a	n/a
10	BRCA1	chr12:66891157-66891313	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr12:66901893-66902021	K562	blood:	n/a	chr12:66901923-66901932 chr12:66901921-66901934 chr12:66901921-66901932 chr12:66901923-66901932 chr12:66901923-66901932 chr12:66901923-66901932 chr12:66901922-66901933
12	CEBPB	chr12:66944409-66944714	K562	blood:	n/a	n/a
13	CEBPB	chr12:66891025-66891338	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr12:66944454-66944708	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr12:66908491-66908956	IMR90	lung:	n/a	chr12:66908612-66908625 chr12:66908941-66908952
16	CEBPB	chr12:66894718-66894992	HepG2	liver:	n/a	chr12:66894813-66894824
17	CEBPB	chr12:66901819-66902057	HepG2	liver:	n/a	chr12:66901923-66901932 chr12:66901921-66901934 chr12:66901921-66901932 chr12:66901923-66901932 chr12:66901923-66901932 chr12:66901923-66901932 chr12:66901922-66901933
18	CHD1	chr12:66891257-66891381	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr12:66890400-66890560	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr12:66891306-66891495	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr12:66894619-66895053	GM12878	blood:	n/a	n/a
22	CTCF	chr12:66942940-66943090	NHEK	skin:	n/a	n/a
23	CTCF	chr12:66942100-66942250	GM12873	blood:	n/a	n/a
24	CTCF	chr12:66949124-66949209	GM19240	blood:	n/a	n/a
25	CTCF	chr12:66949060-66949210	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr12:66942480-66942630	NHLF	lung:	n/a	n/a
27	CTCF	chr12:66942200-66942350	HPF	lung:	n/a	n/a
28	CTCF	chr12:66942972-66943011	A549	lung:	n/a	n/a
29	CTCF	chr12:66942620-66942770	GM12867	blood:	n/a	n/a
30	CTCF	chr12:66909420-66909570	BE2_C	brain:	n/a	n/a
31	CTCF	chr12:66942665-66942774	GM10248	blood:	n/a	n/a
32	CTCF	chr12:66942320-66942345	MCF-7	breast:	n/a	n/a
33	CTCF	chr12:66942712-66942777	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr12:66942620-66942770	GM12875	blood:	n/a	n/a
35	CTCF	chr12:66942660-66942810	GM12870	blood:	n/a	n/a
36	CTCF	chr12:66942640-66942790	HEK293	kidney:	n/a	n/a
37	CTCF	chr12:66942700-66942850	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr12:66949008-66949356	HCT-116	colon:	n/a	n/a
39	CTCF	chr12:66942640-66942790	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr12:66949063-66949214	K562	blood:	n/a	n/a
41	CTCF	chr12:66867292-66867316	GM19240	blood:	n/a	n/a
42	CTCF	chr12:66942620-66942770	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr12:66882247-66882353	GM13976	blood:	n/a	n/a
44	CTCF	chr12:66942920-66943070	GM12875	blood:	n/a	n/a
45	CTCF	chr12:66942640-66942790	GM12878	blood:	n/a	n/a
46	CTCF	chr12:66942820-66942970	HAc	cerebellar:	n/a	n/a
47	CTCF	chr12:66942660-66942810	HepG2	liver:	n/a	n/a
48	CTCF	chr12:66942680-66942830	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr12:66867295-66867374	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:66942720-66942870	AG04450	lung:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:66889730-66889780	MCF10A-Er-Src	breast:	n/a
2	chr12:66889730-66889780	MCF10A-Er-Src	breast:	n/a
3	chr12:66889730-66889780	HNPCEpiC	eye:	n/a
4	chr12:66889730-66889780	SK-N-SH	brain:	n/a
5	chr12:66889655-66889705	HepG2	liver:	n/a
6	chr12:66890229-66890279	SK-N-MC	brain:	n/a
7	chr12:66890229-66890279	Caco-2	colon:	n/a
8	chr12:66889730-66889780	PrEC	prostate:	n/a
9	chr12:66889098-66889148	AG10803	skin:	n/a
10	chr12:66889730-66889780	HRCEpiC	kidney:	n/a
11	chr12:66876894-66876944	HepG2	liver:	n/a
12	chr12:66890229-66890279	HL-60	blood:	n/a
13	chr12:66889098-66889148	RPTEC	kidney:	n/a
14	chr12:66859938-66859988	T-47D	breast:	n/a
15	chr12:66889730-66889780	K562	blood:	n/a
16	chr12:66890229-66890279	SK-N-SH_RA	brain:	n/a
17	chr12:66889655-66889705	GM12878	blood:	n/a
18	chr12:66889655-66889705	CMK	blood:	n/a
19	chr12:66890229-66890279	Jurkat	blood:	n/a
20	chr12:66889655-66889705	ECC-1	luminal epithelium:	n/a
21	chr12:66889098-66889148	U87	brain:	n/a
22	chr12:66860050-66860100	HUVEC	blood vessel:	n/a
23	chr12:66860050-66860100	PANC-1	pancreas:	n/a
24	chr12:66860050-66860100	SAEC	small airway:	n/a
25	chr12:66889655-66889705	NH-A	brain:	n/a
26	chr12:66890229-66890279	SKMC	muscle:	n/a
27	chr12:66890229-66890279	BJ	skin:	n/a
28	chr12:66859938-66859988	GM12878	blood:	n/a
29	chr12:66889730-66889780	HAEpiC	amniotic membrane:	n/a
30	chr12:66890229-66890279	AG04449	skin:	fetal
31	chr12:66890229-66890279	HUVEC	blood vessel:	n/a
32	chr12:66859938-66859988	SK-N-SH_RA	brain:	n/a
33	chr12:66860050-66860100	HCT-116	colon:	n/a
34	chr12:66889655-66889705	IMR90	lung:	fetal
35	chr12:66889098-66889148	HEEpiC	esophagus:	n/a
36	chr12:66889655-66889705	AG09309	skin:	n/a
37	chr12:66860050-66860100	K562	blood:	n/a
38	chr12:66859938-66859988	PFSK-1	brain:	n/a
39	chr12:66860050-66860100	SK-N-SH	brain:	n/a
40	chr12:66876894-66876944	T-47D	breast:	n/a
41	chr12:66889730-66889780	T-47D	breast:	n/a
42	chr12:66876894-66876944	ProgFib	skin:	n/a
43	chr12:66889655-66889705	PFSK-1	brain:	n/a
44	chr12:66889655-66889705	AG04450	lung:	fetal
45	chr12:66890229-66890279	BE2_C	brain:	n/a
46	chr12:66860050-66860100	ECC-1	luminal epithelium:	n/a
47	chr12:66889098-66889148	GM06990	blood:	n/a
48	chr12:66876894-66876944	GM12878	blood:	n/a
49	chr12:66890229-66890279	HIPEpiC	eye:	n/a
50	chr12:66889098-66889148	NT2-D1	testis:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:66908461..66910349-chr12:66910423..66912141,2	MCF-7	breast:
2	chr12:66893673..66895856-chr12:66898880..66900612,2	MCF-7	breast:
3	chr12:66932403..66936111-chr12:66940757..66944323,3	K562	blood:
4	chr12:66938952..66941584-chr12:66945034..66947261,2	K562	blood:
5	chr12:66934881..66936462-chr12:66943891..66946152,2	MCF-7	breast:
6	chr12:66893673..66895856-chr12:66898880..66900612,2	MCF-7	breast:
7	chr12:66905511..66907339-chr12:66908597..66911172,2	K562	blood:
8	chr12:66924711..66926666-chr12:67101075..67103092,2	MCF-7	breast:
9	chr1:17014602..17017113-chr12:66936746..66938540,2	MCF-7	breast:
10	chr12:66934881..66936462-chr12:66943891..66946152,2	MCF-7	breast:
11	chr12:66905511..66907339-chr12:66908597..66911172,2	K562	blood:
12	chr12:66930710..66933060-chr12:66933973..66935708,2	MCF-7	breast:
13	chr12:66940803..66943368-chr12:66944201..66946459,3	MCF-7	breast:
14	chr12:66850566..66853464-chr12:66854684..66856904,2	MCF-7	breast:
15	chr12:66942264..66943151-chr12:67082787..67083333,2	MCF-7	breast:
16	chr12:66940803..66943368-chr12:66944201..66946459,3	MCF-7	breast:
17	chr12:66938952..66941584-chr12:66945034..66947261,2	K562	blood:
18	chr12:66908495..66911478-chr9:73033466..73036076,2	MCF-7	breast:
19	chr11:77849195..77850765-chr12:66898775..66901373,2	MCF-7	breast:

No data

Variant related genes	Relation type
GRIP1	TF binding region
GRIP1	CpG island
ENSG00000159063	chromatin interactions
ENSG00000155974	chromatin interactions

Extended variants
information (count: 3766 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3766 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7952846	chr12:66854354-66854355	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535169812	chr12:66854370-66854371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558056721	chr12:66854374-66854375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186757741	chr12:66854409-66854410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576607516	chr12:66854415-66854416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138021659	chr12:66854461-66854462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562411720	chr12:66854479-66854480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12809616	chr12:66854521-66854522	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs56060111	chr12:66854526-66854527	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs373431691	chr12:66854578-66854579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141273596	chr12:66854629-66854630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372328330	chr12:66854636-66854637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs116927428	chr12:66854704-66854705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182100719	chr12:66854744-66854745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527367944	chr12:66854746-66854747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552276672	chr12:66854749-66854750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12366637	chr12:66854780-66854781	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs531550710	chr12:66854835-66854836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566712766	chr12:66854839-66854840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12366651	chr12:66854849-66854850	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs535798574	chr12:66854874-66854875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149522018	chr12:66854882-66854883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369662647	chr12:66854907-66854908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188823670	chr12:66854917-66854918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558245446	chr12:66854935-66854936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145126803	chr12:66854976-66854977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369648959	chr12:66854977-66854978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs193210048	chr12:66855069-66855070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538980766	chr12:66855107-66855108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185317935	chr12:66855133-66855134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11176199	chr12:66855136-66855137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368078843	chr12:66855146-66855147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573985078	chr12:66855173-66855174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541357650	chr12:66855222-66855223	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540932773	chr12:66855252-66855253	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145685284	chr12:66855265-66855266	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs10219463	chr12:66855280-66855281	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs564217655	chr12:66855281-66855282	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531361104	chr12:66855291-66855292	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543602072	chr12:66855296-66855297	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561906472	chr12:66855306-66855307	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188588689	chr12:66855420-66855421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10219465	chr12:66855519-66855520	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs566054434	chr12:66855520-66855521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533370267	chr12:66855547-66855548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78520873	chr12:66855580-66855581	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570130265	chr12:66855594-66855595	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35960191	chr12:66855609-66855610	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376432695	chr12:66855632-66855633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10219665	chr12:66855700-66855701	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Osteosarcoma	21215367	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:66823200-66859000	Weak transcription	Brain Germinal Matrix	brain
2	chr12:66836200-66856600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr12:66836400-66855200	Weak transcription	Placenta	Placenta
4	chr12:66838800-66858400	Weak transcription	Fetal Brain Female	brain
5	chr12:66843800-66857200	Weak transcription	HMEC	breast
6	chr12:66844000-66861600	Weak transcription	Primary T cells from cord blood	blood
7	chr12:66846800-66860200	Weak transcription	Colon Smooth Muscle	Colon
8	chr12:66849400-66866400	Weak transcription	Pancreas	Pancrea
9	chr12:66849600-66860000	Weak transcription	Esophagus	oesophagus
10	chr12:66851600-66857600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:66853000-66876200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr12:66855200-66855400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr12:66855200-66856200	Strong transcription	Placenta	Placenta
14	chr12:66855400-66857600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr12:66856200-66857800	Weak transcription	Placenta	Placenta
16	chr12:66856600-66856800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr12:66856800-66859600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr12:66856800-66868400	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr12:66857600-66858000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr12:66858000-66860000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr12:66860000-66860200	Enhancers	Esophagus	oesophagus
22	chr12:66860200-66868400	Weak transcription	Esophagus	oesophagus
23	chr12:66860400-66861200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr12:66866400-66866600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr12:66866400-66866600	Enhancers	Gastric	stomach
26	chr12:66866400-66867200	ZNF genes & repeats	Pancreas	Pancrea
27	chr12:66866600-66868400	Weak transcription	Gastric	stomach
28	chr12:66867000-66867200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr12:66867000-66868400	Weak transcription	Right Atrium	heart
30	chr12:66867200-66868400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr12:66867200-66868400	Weak transcription	Pancreas	Pancrea
32	chr12:66867800-66868200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr12:66868400-66868600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr12:66868400-66868600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
35	chr12:66868400-66868600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr12:66868400-66868600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
37	chr12:66868400-66868600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
38	chr12:66868400-66868600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
39	chr12:66868400-66868600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr12:66868400-66868600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
41	chr12:66868400-66868600	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
42	chr12:66868400-66868600	Flanking Bivalent TSS/Enh	Primary T helper 17 cells PMA-I stimulated	--
43	chr12:66868400-66868600	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
44	chr12:66868400-66868600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
45	chr12:66868400-66868600	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr12:66868400-66868600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr12:66868400-66868600	ZNF genes & repeats	Adipose Nuclei	Adipose
48	chr12:66868400-66868600	Flanking Bivalent TSS/Enh	Liver	Liver
49	chr12:66868400-66868600	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
50	chr12:66868400-66868600	ZNF genes & repeats	Brain Hippocampus Middle	brain

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