Variant report

Variant	nsv1054961
Chromosome Location	chr12:59516659-59764209
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1255)
CpG islands
(count:244)
Chromatin interactive
region (count:29)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1255 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:59558954-59559259	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:59543814-59544172	HepG2	liver:	n/a	n/a
3	ATF2	chr12:59711326-59712140	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr12:59712703-59713078	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr12:59715232-59716577	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr12:59596104-59596133	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr12:59580337-59580620	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr12:59584739-59584963	H1-hESC	embryonic stem cell:	n/a	chr12:59584811-59584825
9	BACH1	chr12:59676806-59677328	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr12:59688446-59688498	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr12:59523675-59523784	GM12878	blood:	n/a	n/a
12	BRCA1	chr12:59543796-59544135	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr12:59543816-59544153	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr12:59543727-59544292	HCT-116	colon:	n/a	n/a
15	CEBPB	chr12:59630023-59630360	HepG2	liver:	n/a	chr12:59630176-59630187
16	CEBPB	chr12:59630024-59630326	A549	lung:	n/a	chr12:59630176-59630187
17	CEBPB	chr12:59607913-59608112	HepG2	liver:	n/a	chr12:59608059-59608070
18	CEBPB	chr12:59527138-59527472	HepG2	liver:	n/a	chr12:59527311-59527322
19	CEBPB	chr12:59714782-59714836	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr12:59527201-59527419	K562	blood:	n/a	chr12:59527311-59527322
21	CEBPB	chr12:59630066-59630325	IMR90	lung:	n/a	chr12:59630176-59630187
22	CEBPB	chr12:59630081-59630280	K562	blood:	n/a	chr12:59630176-59630187
23	CEBPB	chr12:59558699-59559115	MCF-7	breast:	n/a	chr12:59558938-59558949
24	CEBPB	chr12:59601814-59602057	A549	lung:	n/a	chr12:59601915-59601926 chr12:59601947-59601958
25	CEBPB	chr12:59601870-59602048	K562	blood:	n/a	chr12:59601915-59601926 chr12:59601947-59601958
26	CEBPB	chr12:59601766-59602100	HepG2	liver:	n/a	chr12:59601915-59601926 chr12:59601947-59601958
27	CEBPB	chr12:59556826-59557109	IMR90	lung:	n/a	n/a
28	CEBPB	chr12:59551959-59552180	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr12:59527189-59527469	IMR90	lung:	n/a	chr12:59527311-59527322
30	CEBPB	chr12:59549372-59549509	A549	lung:	n/a	chr12:59549411-59549422 chr12:59549409-59549422
31	CEBPB	chr12:59545018-59545359	IMR90	lung:	n/a	n/a
32	CEBPB	chr12:59651136-59651360	HepG2	liver:	n/a	chr12:59651173-59651184 chr12:59651172-59651183 chr12:59651302-59651314
33	CEBPB	chr12:59588614-59588899	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr12:59590775-59591118	MCF-7	breast:	n/a	n/a
35	CEBPB	chr12:59711472-59711762	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr12:59676742-59677102	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr12:59601830-59602056	IMR90	lung:	n/a	chr12:59601915-59601926 chr12:59601947-59601958
38	CEBPB	chr12:59522205-59522280	K562	blood:	n/a	n/a
39	CEBPB	chr12:59528560-59528870	HepG2	liver:	n/a	n/a
40	CEBPB	chr12:59629083-59629271	H1-hESC	embryonic stem cell:	n/a	chr12:59629222-59629233
41	CEBPB	chr12:59629154-59629354	HepG2	liver:	n/a	chr12:59629222-59629233
42	CEBPB	chr12:59715106-59715383	HepG2	liver:	n/a	chr12:59715258-59715269 chr12:59715259-59715270
43	CEBPB	chr12:59626577-59626940	Hela-S3	cervix:	n/a	chr12:59626734-59626745
44	CEBPB	chr12:59626604-59626900	A549	lung:	n/a	chr12:59626734-59626745
45	CEBPB	chr12:59556889-59557091	A549	lung:	n/a	n/a
46	CEBPB	chr12:59626627-59626941	HepG2	liver:	n/a	chr12:59626734-59626745
47	CEBPB	chr12:59558547-59559201	MCF-7	breast:	n/a	chr12:59558938-59558949
48	CEBPB	chr12:59676821-59677075	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr12:59715120-59715444	H1-hESC	embryonic stem cell:	n/a	chr12:59715258-59715269 chr12:59715259-59715270
50	CHD1	chr12:59721521-59721835	H1-hESC	embryonic stem cell:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:59676888-59676938	HEK293	kidney:	embryo
2	chr12:59730539-59730589	Jurkat	blood:	n/a
3	chr12:59730539-59730589	HNPCEpiC	eye:	n/a
4	chr12:59715992-59716042	HNPCEpiC	eye:	n/a
5	chr12:59715992-59716042	Caco-2	colon:	n/a
6	chr12:59676888-59676938	K562	blood:	n/a
7	chr12:59715992-59716042	BE2_C	brain:	n/a
8	chr12:59721694-59721744	HEEpiC	esophagus:	n/a
9	chr12:59715992-59716042	BJ	skin:	n/a
10	chr12:59730539-59730589	HIPEpiC	eye:	n/a
11	chr12:59715992-59716042	HIPEpiC	eye:	n/a
12	chr12:59721694-59721744	AG04449	skin:	fetal
13	chr12:59715992-59716042	IMR90	lung:	fetal
14	chr12:59715992-59716042	H1-hESC	embryonic stem cell:	embryo
15	chr12:59715992-59716042	PFSK-1	brain:	n/a
16	chr12:59721694-59721744	HPAEpiC	pulmonary alveolar:	n/a
17	chr12:59676888-59676938	NT2-D1	testis:	n/a
18	chr12:59676888-59676938	Jurkat	blood:	n/a
19	chr12:59721694-59721744	NB4	blood:	n/a
20	chr12:59715992-59716042	U87	brain:	n/a
21	chr12:59715992-59716042	ECC-1	luminal epithelium:	n/a
22	chr12:59676888-59676938	IMR90	lung:	fetal
23	chr12:59721694-59721744	AG10803	skin:	n/a
24	chr12:59676888-59676938	HUVEC	blood vessel:	n/a
25	chr12:59715992-59716042	K562	blood:	n/a
26	chr12:59676888-59676938	HMEC	breast:	n/a
27	chr12:59730539-59730589	GM12892	blood:	n/a
28	chr12:59721694-59721744	HAEpiC	amniotic membrane:	n/a
29	chr12:59715992-59716042	HEK293	kidney:	embryo
30	chr12:59676888-59676938	LNCaP	prostate:	n/a
31	chr12:59676888-59676938	A549	lung:	n/a
32	chr12:59721694-59721744	NH-A	brain:	n/a
33	chr12:59730539-59730589	Caco-2	colon:	n/a
34	chr12:59730539-59730589	HMEC	breast:	n/a
35	chr12:59676888-59676938	HEEpiC	esophagus:	n/a
36	chr12:59721694-59721744	HepG2	liver:	n/a
37	chr12:59721694-59721744	K562	blood:	n/a
38	chr12:59730539-59730589	A549	lung:	n/a
39	chr12:59730539-59730589	H1-hESC	embryonic stem cell:	embryo
40	chr12:59721694-59721744	HIPEpiC	eye:	n/a
41	chr12:59730539-59730589	SK-N-SH_RA	brain:	n/a
42	chr12:59715992-59716042	AG04449	skin:	fetal
43	chr12:59676888-59676938	AG04449	skin:	fetal
44	chr12:59721694-59721744	HCM	heart:	n/a
45	chr12:59676888-59676938	BJ	skin:	n/a
46	chr12:59721694-59721744	HNPCEpiC	eye:	n/a
47	chr12:59676888-59676938	HepG2	liver:	n/a
48	chr12:59715992-59716042	Hela-S3	cervix:	n/a
49	chr12:59715992-59716042	HCF	heart:	n/a
50	chr12:59730539-59730589	NH-A	brain:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:59653805..59656189-chr12:59672943..59675327,2	MCF-7	breast:
2	chr12:59692138..59694777-chr12:59713415..59715358,2	MCF-7	breast:
3	chr12:59586597..59588701-chr12:59589774..59591287,2	MCF-7	breast:
4	chr12:59567506..59568224-chr12:59739584..59740478,2	MCF-7	breast:
5	chr12:59543592..59544432-chr12:59558545..59559537,3	MCF-7	breast:
6	chr12:58934331..58934849-chr12:59544859..59545828,2	MCF-7	breast:
7	chr12:59507135..59508358-chr12:59543262..59544671,18	MCF-7	breast:
8	chr12:59673431..59675592-chr12:59677210..59679968,2	MCF-7	breast:
9	chr12:59227394..59228307-chr12:59543616..59544500,4	MCF-7	breast:
10	chr12:59653805..59656189-chr12:59672943..59675327,2	MCF-7	breast:
11	chr12:58809849..58810654-chr12:59543572..59544140,2	MCF-7	breast:
12	chr12:59655684..59657205-chr12:59659679..59661187,2	MCF-7	breast:
13	chr12:59577181..59579768-chr12:59589219..59591001,2	MCF-7	breast:
14	chr12:59692138..59694777-chr12:59713415..59715358,2	MCF-7	breast:
15	chr12:59543700..59544432-chr20:52816306..52816814,2	MCF-7	breast:
16	chr12:58739581..58740441-chr12:59543579..59544208,2	MCF-7	breast:
17	chr12:59673431..59675592-chr12:59677210..59679968,2	MCF-7	breast:
18	chr12:59567506..59568224-chr12:59739584..59740478,2	MCF-7	breast:
19	chr12:59567188..59568180-chr12:59766489..59767406,3	MCF-7	breast:
20	chr12:59577181..59579768-chr12:59589219..59591001,2	MCF-7	breast:
21	chr12:59507415..59508147-chr12:59543545..59544473,6	MCF-7	breast:
22	chr12:59543592..59544432-chr12:59558545..59559537,3	MCF-7	breast:
23	chr12:59655684..59657205-chr12:59659679..59661187,2	MCF-7	breast:
24	chr12:58934010..58934928-chr12:59543596..59544503,6	MCF-7	breast:
25	chr12:58739967..58740565-chr12:59543543..59544432,2	K562	blood:
26	chr12:59537940..59539473-chr12:59543587..59545089,2	MCF-7	breast:
27	chr12:59586597..59588701-chr12:59589774..59591287,2	MCF-7	breast:
28	chr12:59537940..59539473-chr12:59543587..59545089,2	MCF-7	breast:
29	chr12:59506527..59507272-chr12:59543925..59544447,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-362K2.2.1-2	chr12:59523275-59523600	XLOC_009782
2	lnc-SLC16A7-4	chr12:59712962-59714552	NONHSAT029042
3	lnc-RP11-272B17.2.1-1	chr12:59759999-59760050	ENSG00000258214
4	lnc-SLC16A7-4	chr12:59714688-59717255	NONHSAT029042
5	lnc-RP11-362K2.2.1-2	chr12:59524433-59524642	XLOC_009782

No data

Variant related genes	Relation type
RNU6-279P	TF binding region
RNU6-279P	CpG island

Extended variants
information (count: 5494 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:5494 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560899902	chr12:59516671-59516672	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs567506684	chr12:59516674-59516675	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs529715323	chr12:59516726-59516727	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs35008231	chr12:59516754-59516755	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs145831409	chr12:59516787-59516788	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs574398929	chr12:59516915-59516916	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs74696145	chr12:59516927-59516928	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs563589285	chr12:59516958-59516959	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs115603866	chr12:59516962-59516963	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs79929143	chr12:59516984-59516985	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs187478374	chr12:59517002-59517003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565166770	chr12:59517022-59517023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575380138	chr12:59517027-59517028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192486481	chr12:59517034-59517035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566062202	chr12:59517044-59517045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529995543	chr12:59517086-59517087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs371455649	chr12:59517099-59517100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183888843	chr12:59517101-59517102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566857298	chr12:59517102-59517103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs75711989	chr12:59517109-59517110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145739916	chr12:59517178-59517179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558761190	chr12:59517183-59517184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570585333	chr12:59517213-59517214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534704081	chr12:59517228-59517229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552749628	chr12:59517379-59517380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574487487	chr12:59517426-59517427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528579461	chr12:59517460-59517461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1846624	chr12:59517503-59517504	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs188780848	chr12:59517539-59517540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78619118	chr12:59517554-59517555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565128260	chr12:59517579-59517580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537071042	chr12:59517582-59517583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532643333	chr12:59517599-59517600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541615683	chr12:59517636-59517637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559546727	chr12:59517666-59517667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371971782	chr12:59517716-59517717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs10877205	chr12:59517725-59517726	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs192616340	chr12:59517753-59517754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570092408	chr12:59517789-59517790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138269272	chr12:59517794-59517795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552542871	chr12:59517795-59517796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373533226	chr12:59517818-59517819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141226991	chr12:59517828-59517829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534479600	chr12:59517865-59517866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184407864	chr12:59517902-59517903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568036316	chr12:59517907-59517908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187094310	chr12:59517928-59517929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs556524100	chr12:59518021-59518022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574936077	chr12:59518035-59518036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191861845	chr12:59518044-59518045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Thoracic aortic aneurysm	21092924	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:527 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:59506000-59517400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:59513000-59517000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr12:59513200-59516800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr12:59515400-59517000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr12:59516000-59516800	Enhancers	Ovary	ovary
6	chr12:59516000-59517000	Enhancers	Adipose Nuclei	Adipose
7	chr12:59516000-59517200	Enhancers	HUVEC	blood vessel
8	chr12:59516400-59517000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr12:59516400-59517000	Enhancers	NH-A	brain
10	chr12:59516600-59516800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr12:59516600-59516800	Enhancers	NHDF-Ad	bronchial
12	chr12:59516600-59517000	Active TSS	Stomach Smooth Muscle	stomach
13	chr12:59516600-59517000	Enhancers	Osteobl	bone
14	chr12:59516800-59520800	Weak transcription	Ovary	ovary
15	chr12:59517000-59518200	Weak transcription	Pancreas	Pancrea
16	chr12:59518200-59518600	Enhancers	Pancreas	Pancrea
17	chr12:59518800-59519000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr12:59523000-59523600	Enhancers	Gastric	stomach
19	chr12:59523600-59524600	Weak transcription	Gastric	stomach
20	chr12:59524600-59524800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr12:59524600-59524800	Enhancers	Gastric	stomach
22	chr12:59524600-59525600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr12:59524600-59525800	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr12:59524800-59525000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr12:59524800-59525200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:59524800-59525600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr12:59524800-59525600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr12:59524800-59525600	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr12:59524800-59525800	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr12:59524800-59525800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr12:59525000-59525400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr12:59525000-59525400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr12:59525000-59525400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr12:59525400-59525600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr12:59525600-59525800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr12:59525600-59527000	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr12:59525800-59526400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr12:59526400-59527000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr12:59527000-59527800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
40	chr12:59528400-59528600	Enhancers	Aorta	Aorta
41	chr12:59528600-59528800	Weak transcription	Aorta	Aorta
42	chr12:59529000-59529400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr12:59534400-59534600	Enhancers	Fetal Lung	lung
44	chr12:59534800-59535800	Weak transcription	Fetal Lung	lung
45	chr12:59535400-59536600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr12:59535800-59536600	Enhancers	Fetal Lung	lung
47	chr12:59536000-59537200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr12:59536000-59537600	Enhancers	NHDF-Ad	bronchial
49	chr12:59536200-59536600	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr12:59536200-59536600	Enhancers	Brain Anterior Caudate	brain

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