Variant report

Variant	esv2754127
Chromosome Location	chr12:86723232-87576932
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2629)
CpG islands
(count:671)
Chromatin interactive
region (count:33)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2629 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:87328246-87328300	K562	blood:	n/a	n/a
2	ARID3A	chr12:87402568-87403105	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:87403863-87404208	HepG2	liver:	n/a	n/a
4	ATF1	chr12:87371930-87371953	K562	blood:	n/a	n/a
5	ATF1	chr12:87283289-87283337	K562	blood:	n/a	n/a
6	ATF2	chr12:87129495-87130047	GM12878	blood:	n/a	n/a
7	ATF2	chr12:87129390-87130163	GM12878	blood:	n/a	n/a
8	ATF3	chr12:87106001-87106627	HCT-116	colon:	n/a	chr12:87106339-87106352
9	ATF3	chr12:87054387-87055009	A549	lung:	n/a	n/a
10	ATF3	chr12:87106039-87106609	A549	lung:	n/a	chr12:87106339-87106352
11	ATF3	chr12:87054371-87054987	A549	lung:	n/a	n/a
12	ATF3	chr12:87106056-87106583	A549	lung:	n/a	chr12:87106339-87106352
13	ATF3	chr12:87054428-87054989	HCT-116	colon:	n/a	n/a
14	ATF3	chr12:87551480-87552148	A549	lung:	n/a	n/a
15	ATF3	chr12:87551512-87551937	A549	lung:	n/a	n/a
16	ATF3	chr12:87054426-87055001	HCT-116	colon:	n/a	n/a
17	BACH1	chr12:87530120-87530610	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr12:87530180-87530435	K562	blood:	n/a	n/a
19	BACH1	chr12:87545070-87545339	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr12:87077208-87077425	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr12:87106192-87106389	GM12878	blood:	n/a	chr12:87106276-87106287 chr12:87106273-87106283 chr12:87106277-87106287
22	BATF	chr12:87545111-87545295	GM12878	blood:	n/a	n/a
23	BATF	chr12:87128924-87129189	GM12878	blood:	n/a	chr12:87129029-87129040 chr12:87129124-87129137
24	BATF	chr12:87129616-87130068	GM12878	blood:	n/a	n/a
25	BATF	chr12:87128909-87129147	GM12878	blood:	n/a	chr12:87129029-87129040 chr12:87129124-87129137
26	BATF	chr12:87507875-87508091	GM12878	blood:	n/a	n/a
27	BATF	chr12:87545017-87545298	GM12878	blood:	n/a	n/a
28	BATF	chr12:87129654-87130011	GM12878	blood:	n/a	n/a
29	BCL11A	chr12:87129719-87130045	GM12878	blood:	n/a	n/a
30	BCL3	chr12:87053492-87055044	A549	lung:	n/a	chr12:87053948-87053957
31	BCL3	chr12:87129614-87129994	GM12878	blood:	n/a	n/a
32	BCL3	chr12:87105926-87106732	A549	lung:	n/a	chr12:87106275-87106284 chr12:87106276-87106285
33	BCL3	chr12:87106135-87106543	A549	lung:	n/a	chr12:87106275-87106284 chr12:87106276-87106285
34	BCL3	chr12:87220989-87221712	A549	lung:	n/a	n/a
35	BDP1	chr12:87551645-87551965	Hela-S3	cervix:	n/a	n/a
36	BHLHE40	chr12:87507928-87508017	GM12878	blood:	n/a	n/a
37	BHLHE40	chr12:86907623-86907945	GM12878	blood:	n/a	n/a
38	BHLHE40	chr12:87545104-87545452	GM12878	blood:	n/a	n/a
39	BHLHE40	chr12:87219939-87220108	A549	lung:	n/a	n/a
40	BHLHE40	chr12:87222440-87222493	GM12878	blood:	n/a	n/a
41	BRCA1	chr12:87120957-87121494	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr12:87343121-87343160	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr12:87297594-87297609	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr12:87551557-87551893	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr12:87106043-87106541	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr12:87280525-87280594	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr12:87562905-87562963	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr12:87340632-87340744	GM12878	blood:	n/a	n/a
49	BRCA1	chr12:87054526-87054996	Hela-S3	cervix:	n/a	n/a
50	CBX3	chr12:87106000-87106729	HCT-116	colon:	n/a	chr12:87106072-87106083

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:86727874-86727924	HCF	heart:	n/a
2	chr12:86995758-86995808	MCF-7	breast:	n/a
3	chr12:87232511-87232561	H1-hESC	embryonic stem cell:	embryo
4	chr12:87119199-87119249	HCT-116	colon:	n/a
5	chr12:87119199-87119249	PANC-1	pancreas:	n/a
6	chr12:86995819-86995869	HCF	heart:	n/a
7	chr12:87232821-87232871	BJ	skin:	n/a
8	chr12:86995819-86995869	HepG2	liver:	n/a
9	chr12:86727874-86727924	U87	brain:	n/a
10	chr12:87106229-87106279	SKMC	muscle:	n/a
11	chr12:86994755-86994805	ProgFib	skin:	n/a
12	chr12:87119199-87119249	NHBE	bronchial:	n/a
13	chr12:86995758-86995808	HIPEpiC	eye:	n/a
14	chr12:86994815-86994865	AG09319	gingival:	n/a
15	chr12:87232511-87232561	ECC-1	luminal epithelium:	n/a
16	chr12:87232511-87232561	Jurkat	blood:	n/a
17	chr12:87119199-87119249	ovcar-3	ovarian:	n/a
18	chr12:86995819-86995869	HEK293	kidney:	embryo
19	chr12:86994755-86994805	HRCEpiC	kidney:	n/a
20	chr12:87232821-87232871	HIPEpiC	eye:	n/a
21	chr12:87119199-87119249	BJ	skin:	n/a
22	chr12:87106229-87106279	HPAEpiC	pulmonary alveolar:	n/a
23	chr12:87232692-87232742	Hepatocyte	liver:	n/a
24	chr12:87119199-87119249	NH-A	brain:	n/a
25	chr12:87106229-87106279	Hela-S3	cervix:	n/a
26	chr12:87119199-87119249	HRE	kidney:	n/a
27	chr12:86995758-86995808	Caco-2	colon:	n/a
28	chr12:87232511-87232561	SKMC	muscle:	n/a
29	chr12:86727874-86727924	HCT-116	colon:	n/a
30	chr12:86995819-86995869	GM06990	blood:	n/a
31	chr12:87232511-87232561	NB4	blood:	n/a
32	chr12:86995758-86995808	SK-N-SH	brain:	n/a
33	chr12:87106229-87106279	GM12878	blood:	n/a
34	chr12:87119199-87119249	MCF-7	breast:	n/a
35	chr12:87232692-87232742	PrEC	prostate:	n/a
36	chr12:87106229-87106279	MCF-7	breast:	n/a
37	chr12:87119199-87119249	AoSMC	blood vessel:	n/a
38	chr12:86995758-86995808	AG04449	skin:	fetal
39	chr12:87232511-87232561	NT2-D1	testis:	n/a
40	chr12:86994815-86994865	HNPCEpiC	eye:	n/a
41	chr12:87232821-87232871	Hela-S3	cervix:	n/a
42	chr12:86994755-86994805	HAEpiC	amniotic membrane:	n/a
43	chr12:87232692-87232742	HEK293	kidney:	embryo
44	chr12:86995758-86995808	K562	blood:	n/a
45	chr12:87510712-87510762	HCPEpiC	choroid plexus:	n/a
46	chr12:86727874-86727924	AG09319	gingival:	n/a
47	chr12:87232821-87232871	H1-hESC	embryonic stem cell:	embryo
48	chr12:87119199-87119249	NT2-D1	testis:	n/a
49	chr12:87232511-87232561	CMK	blood:	n/a
50	chr12:86995758-86995808	GM12878	blood:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:86873477..86875774-chr12:86880255..86882982,2	K562	blood:
2	chr12:87507574..87509719-chr12:87517143..87519195,2	MCF-7	breast:
3	chr12:87132936..87135299-chr12:87145575..87148336,2	K562	blood:
4	chr12:87190903..87192895-chr12:87193374..87195934,2	K562	blood:
5	chr12:87237467..87238342-chr7:40961627..40962369,2	MCF-7	breast:
6	chr12:87512190..87514558-chr12:87523597..87525941,2	K562	blood:
7	chr12:86873477..86875774-chr12:86880255..86882982,2	K562	blood:
8	chr12:87148253..87150354-chr12:87164115..87166023,2	MCF-7	breast:
9	chr12:87190903..87192895-chr12:87193374..87195934,2	K562	blood:
10	chr12:87071567..87073233-chr12:87073299..87075080,2	MCF-7	breast:
11	chr12:87386481..87388359-chr12:87403399..87406210,2	MCF-7	breast:
12	chr12:87513960..87515515-chr12:87520858..87523427,2	MCF-7	breast:
13	chr12:87071567..87073233-chr12:87073299..87075080,2	MCF-7	breast:
14	chr12:87039292..87041386-chr12:87052095..87053649,2	MCF-7	breast:
15	chr12:87523604..87525877-chr12:87529351..87531918,2	MCF-7	breast:
16	chr12:87513960..87515515-chr12:87520858..87523427,2	MCF-7	breast:
17	chr12:87039292..87041386-chr12:87052095..87053649,2	MCF-7	breast:
18	chr12:87512654..87515691-chr12:87528653..87530382,3	MCF-7	breast:
19	chr12:87559731..87562438-chr12:87594241..87595999,2	K562	blood:
20	chr12:87512654..87515691-chr12:87528653..87530382,3	MCF-7	breast:
21	chr12:87386481..87388359-chr12:87403399..87406210,2	MCF-7	breast:
22	chr12:87523604..87525877-chr12:87529351..87531918,2	MCF-7	breast:
23	chr12:87376736..87379148-chr12:87408006..87409813,2	K562	blood:
24	chr12:86723150..86725256-chr12:86785265..86787177,2	MCF-7	breast:
25	chr12:87148253..87150354-chr12:87164115..87166023,2	MCF-7	breast:
26	chr12:87132936..87135299-chr12:87145575..87148336,2	K562	blood:
27	chr12:87507574..87509719-chr12:87517143..87519195,2	MCF-7	breast:
28	chr12:86723150..86725256-chr12:86785265..86787177,2	MCF-7	breast:
29	chr12:87572443..87573395-chr3:190629682..190630453,2	MCF-7	breast:
30	chr12:86783284..86785651-chr14:104583194..104586028,2	MCF-7	breast:
31	chr12:87039746..87040275-chr20:55849330..55849889,2	MCF-7	breast:
32	chr12:87376736..87379148-chr12:87408006..87409813,2	K562	blood:
33	chr12:87512190..87514558-chr12:87523597..87525941,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MGAT4C-3	chr12:87335669-87335818	NONHSAT029768
2	lnc-MGAT4C-1	chr12:86993355-86993438	NONHSAT029759
3	lnc-MGAT4C-2	chr12:86953025-86953268	l_687_chr12:86951511-86953159_testes
4	lnc-MGAT4C-1	chr12:86828934-86829042	NONHSAT029759
5	lnc-MGAT4C-1	chr12:87120986-87121018	ENSG00000258185
6	lnc-MGAT4C-2	chr12:86951512-86952255	l_687_chr12:86951511-86953159_testes
7	lnc-MGAT4C-1	chr12:86727843-86727905	NONHSAT029762
8	lnc-MGAT4C-1	chr12:86993355-86993438	ENSG00000258185
9	lnc-MGAT4C-1	chr12:86828934-86829042	NONHSAT029762
10	lnc-MGAT4C-1	chr12:87232443-87232905	ENSG00000258185
11	lnc-MGAT4C-1	chr12:87120982-87121018	ENSG00000258185
12	lnc-MGAT4C-1	chr12:86727843-86727905	NONHSAT029759
13	lnc-MGAT4C-4	chr12:87563762-87564206	NONHSAT029769
14	lnc-MGAT4C-1	chr12:86889028-86889092	NONHSAT029762
15	lnc-MGAT4C-3	chr12:87345415-87345519	NONHSAT029768
16	lnc-MGAT4C-1	chr12:87120986-87121018	NONHSAT029762
17	lnc-MGAT4C-1	chr12:86995005-86995081	NONHSAT029759
18	lnc-MGAT4C-1	chr12:87232443-87232775	ENSG00000258185
19	lnc-MGAT4C-1	chr12:87232443-87232681	NONHSAT029762

No data

Variant related genes	Relation type
MGAT4C	TF binding region
ENSG00000258185	TF binding region
ENSG00000264077	TF binding region
RPL23AP68	TF binding region
MGAT4C	CpG island
ENSG00000258185	CpG island
ENSG00000264077	CpG island
RPL23AP68	CpG island
ENSG00000207568	chromatin interactions

Extended variants
information (count: 12727 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:12727 , 50 per page) page: 1 2 3 4 5 6 7 ... 255

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530875987	chr12:86723235-86723236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551589883	chr12:86723352-86723353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534086986	chr12:86723434-86723435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12303046	chr12:86723435-86723436	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs569511414	chr12:86723443-86723444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139886789	chr12:86723462-86723463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs35063969	chr12:86723466-86723467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143262780	chr12:86723571-86723572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs535086841	chr12:86723588-86723589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577979321	chr12:86723591-86723592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545282852	chr12:86723623-86723624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368273089	chr12:86723650-86723651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560475179	chr12:86723655-86723656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527591608	chr12:86723665-86723666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542817045	chr12:86723717-86723718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561084478	chr12:86723718-86723719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550576181	chr12:86723721-86723722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12581912	chr12:86723728-86723729	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs181680998	chr12:86723812-86723813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571219641	chr12:86723830-86723831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs186021244	chr12:86723856-86723857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374138976	chr12:86723871-86723872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11103931	chr12:86723878-86723879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191475803	chr12:86723920-86723921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549433405	chr12:86723930-86723931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566778588	chr12:86723994-86723995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534243077	chr12:86724052-86724053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570497824	chr12:86724066-86724067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs369889046	chr12:86724069-86724070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs4526834	chr12:86724156-86724157	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs567553384	chr12:86724184-86724185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs371449456	chr12:86724216-86724217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146680596	chr12:86724262-86724263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181169369	chr12:86724325-86724326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577958707	chr12:86724331-86724332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148878713	chr12:86724332-86724333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs373461500	chr12:86724410-86724411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs535388090	chr12:86724455-86724456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs186130679	chr12:86724482-86724483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs376909756	chr12:86724535-86724536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542980329	chr12:86724552-86724553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs373155536	chr12:86724609-86724610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561045200	chr12:86724624-86724625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs2405931	chr12:86724678-86724679	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs4616111	chr12:86724690-86724691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs543495910	chr12:86724729-86724730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564788820	chr12:86724758-86724759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190946600	chr12:86724782-86724783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs546959932	chr12:86724820-86724821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs578116008	chr12:86724829-86724830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
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
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
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	22522925	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Urothelial cell carcinoma	18451213	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute lymphoblastic leukemia	17443227	CNVD

Chromatin state (count:983 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86721600-86724600	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr12:86723800-86725400	Enhancers	Fetal Kidney	kidney
3	chr12:86723800-86726000	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr12:86724600-86724800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr12:86724600-86725200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr12:86724600-86726000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr12:86724600-86726400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr12:86724800-86725200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr12:86724800-86725400	Enhancers	Small Intestine	intestine
10	chr12:86724800-86725600	Enhancers	H1 Cell Line	embryonic stem cell
11	chr12:86724800-86725600	Enhancers	Fetal Muscle Leg	muscle
12	chr12:86724800-86725800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr12:86724800-86725800	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr12:86724800-86726400	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr12:86724800-86727600	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr12:86725000-86725200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr12:86725000-86725200	Enhancers	Fetal Brain Male	brain
18	chr12:86725000-86725400	Enhancers	H9 Cell Line	embryonic stem cell
19	chr12:86725000-86725400	Enhancers	Adipose Nuclei	Adipose
20	chr12:86725000-86725400	Enhancers	Brain Germinal Matrix	brain
21	chr12:86725000-86725400	Enhancers	Fetal Lung	lung
22	chr12:86725000-86725600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr12:86725000-86725600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr12:86725000-86726000	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr12:86725000-86726000	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr12:86725200-86726000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr12:86725400-86725600	Flanking Active TSS	Brain Germinal Matrix	brain
28	chr12:86725400-86726800	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr12:86725600-86726400	Active TSS	Brain Germinal Matrix	brain
30	chr12:86725600-86726800	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr12:86725800-86726200	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr12:86725800-86727600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr12:86726000-86726200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr12:86726000-86726400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr12:86726000-86726400	Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr12:86726000-86726800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr12:86726000-86728200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr12:86726200-86726600	Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr12:86726200-86726600	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr12:86726200-86727000	Active TSS	Fetal Brain Female	brain
41	chr12:86726400-86726600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr12:86726400-86727000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr12:86726400-86727000	Flanking Active TSS	Brain Germinal Matrix	brain
44	chr12:86726400-86727200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
45	chr12:86726400-86728400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
46	chr12:86726400-86729600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr12:86726600-86726800	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr12:86726600-86727000	Enhancers	Fetal Brain Male	brain
49	chr12:86726600-86727200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
50	chr12:86726600-86727400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell

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