Variant report

Variant	nsv468683
Chromosome Location	chr1:242739083-243141099
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1579)
CpG islands
(count:915)
Chromatin interactive
region (count:29)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1579 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:243088083-243088303	K562	blood:	n/a	n/a
2	ATF2	chr1:242976778-242977056	GM12878	blood:	n/a	n/a
3	ATF2	chr1:242749196-242749772	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:242765415-242765554	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:242907415-242907671	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:242802067-242802078	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:242848092-242848258	K562	blood:	n/a	n/a
8	BACH1	chr1:243122482-243122506	K562	blood:	n/a	n/a
9	BACH1	chr1:242996994-242996997	K562	blood:	n/a	n/a
10	BACH1	chr1:242918799-242919176	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:242908535-242908689	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr1:242976721-242977165	GM12878	blood:	n/a	chr1:242976959-242976968
13	BCL11A	chr1:242749309-242749565	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr1:242976760-242977140	GM12878	blood:	n/a	chr1:242976959-242976968
15	BCL3	chr1:242843343-242843676	GM12878	blood:	n/a	n/a
16	BCL3	chr1:242843399-242843681	GM12878	blood:	n/a	n/a
17	BHLHE40	chr1:242976782-242977230	GM12878	blood:	n/a	n/a
18	BHLHE40	chr1:243031757-243031938	GM12878	blood:	n/a	n/a
19	BHLHE40	chr1:243087986-243088483	K562	blood:	n/a	n/a
20	BRCA1	chr1:242997383-242997489	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr1:242798548-242798608	HepG2	liver:	n/a	n/a
22	BRCA1	chr1:242749358-242749729	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr1:242954012-242954043	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr1:243053418-243053739	K562	blood:	n/a	n/a
25	CBX3	chr1:243100093-243100300	K562	blood:	n/a	n/a
26	CBX3	chr1:243087941-243088379	K562	blood:	n/a	n/a
27	CBX3	chr1:243130209-243130606	K562	blood:	n/a	n/a
28	CCNT2	chr1:243129321-243129526	K562	blood:	n/a	n/a
29	CCNT2	chr1:243087975-243088306	K562	blood:	n/a	n/a
30	CEBPB	chr1:243118300-243118585	A549	lung:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
31	CEBPB	chr1:243118288-243118578	Hela-S3	cervix:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
32	CEBPB	chr1:242774541-242774804	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr1:242749263-242749763	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr1:242861497-242861649	HepG2	liver:	n/a	n/a
35	CEBPB	chr1:242899993-242900287	HepG2	liver:	n/a	chr1:242900141-242900152
36	CEBPB	chr1:242933698-242934016	A549	lung:	n/a	n/a
37	CEBPB	chr1:243118280-243118602	IMR90	lung:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
38	CEBPB	chr1:243105243-243105313	A549	lung:	n/a	chr1:243105272-243105283
39	CEBPB	chr1:242766634-242766975	HepG2	liver:	n/a	n/a
40	CEBPB	chr1:243072543-243072743	K562	blood:	n/a	chr1:243072592-243072603
41	CEBPB	chr1:242998320-242998357	HepG2	liver:	n/a	chr1:242998327-242998338
42	CEBPB	chr1:242998985-242999533	A549	lung:	n/a	n/a
43	CEBPB	chr1:242774611-242774728	A549	lung:	n/a	n/a
44	CEBPB	chr1:242774529-242774815	HepG2	liver:	n/a	n/a
45	CEBPB	chr1:242766610-242766982	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr1:242791286-242791544	HepG2	liver:	n/a	chr1:242791427-242791436 chr1:242791479-242791490 chr1:242791479-242791492 chr1:242791425-242791436 chr1:242791480-242791491 chr1:242791479-242791492 chr1:242791479-242791490
47	CEBPB	chr1:242742398-242742616	HepG2	liver:	n/a	chr1:242742505-242742516
48	CEBPB	chr1:242933600-242934106	A549	lung:	n/a	n/a
49	CEBPB	chr1:243105260-243105310	HepG2	liver:	n/a	chr1:243105272-243105283
50	CEBPB	chr1:243072507-243072681	IMR90	lung:	n/a	chr1:243072592-243072603

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:242767727-242767777	AG10803	skin:	n/a
2	chr1:242767942-242767992	HCF	heart:	n/a
3	chr1:242937866-242937916	NHBE	bronchial:	n/a
4	chr1:242937866-242937916	SK-N-SH_RA	brain:	n/a
5	chr1:243139525-243139575	HMEC	breast:	n/a
6	chr1:243053673-243053723	HEEpiC	esophagus:	n/a
7	chr1:242749065-242749115	SK-N-SH_RA	brain:	n/a
8	chr1:243053673-243053723	HRPEpiC	eye:	n/a
9	chr1:242749065-242749115	PANC-1	pancreas:	n/a
10	chr1:243139525-243139575	NB4	blood:	n/a
11	chr1:242767942-242767992	HCM	heart:	n/a
12	chr1:243053425-243053475	HCF	heart:	n/a
13	chr1:243053934-243053984	LNCaP	prostate:	n/a
14	chr1:242767727-242767777	HEK293	kidney:	embryo
15	chr1:242767727-242767777	HCPEpiC	choroid plexus:	n/a
16	chr1:242874219-242874269	HCT-116	colon:	n/a
17	chr1:243050875-243050925	LNCaP	prostate:	n/a
18	chr1:242767942-242767992	SKMC	muscle:	n/a
19	chr1:243054071-243054121	HEEpiC	esophagus:	n/a
20	chr1:243053934-243053984	ProgFib	skin:	n/a
21	chr1:243139525-243139575	PANC-1	pancreas:	n/a
22	chr1:243053865-243053915	ovcar-3	ovarian:	n/a
23	chr1:243053673-243053723	HPAEpiC	pulmonary alveolar:	n/a
24	chr1:242937866-242937916	GM12891	blood:	n/a
25	chr1:242767942-242767992	GM19239	blood:	n/a
26	chr1:243050875-243050925	HIPEpiC	eye:	n/a
27	chr1:243057080-243057130	GM12878	blood:	n/a
28	chr1:243053425-243053475	T-47D	breast:	n/a
29	chr1:243053865-243053915	GM12892	blood:	n/a
30	chr1:242936925-242936975	HRE	kidney:	n/a
31	chr1:243053673-243053723	HCM	heart:	n/a
32	chr1:243053865-243053915	CMK	blood:	n/a
33	chr1:242767727-242767777	SK-N-SH	brain:	n/a
34	chr1:243053425-243053475	ECC-1	luminal epithelium:	n/a
35	chr1:242937866-242937916	IMR90	lung:	fetal
36	chr1:242874219-242874269	K562	blood:	n/a
37	chr1:242749065-242749115	Caco-2	colon:	n/a
38	chr1:243053865-243053915	HCPEpiC	choroid plexus:	n/a
39	chr1:242767942-242767992	HNPCEpiC	eye:	n/a
40	chr1:243050875-243050925	GM06990	blood:	n/a
41	chr1:243053425-243053475	AG04449	skin:	fetal
42	chr1:242767727-242767777	SK-N-MC	brain:	n/a
43	chr1:243054071-243054121	PANC-1	pancreas:	n/a
44	chr1:243053934-243053984	Jurkat	blood:	n/a
45	chr1:243054071-243054121	SK-N-SH	brain:	n/a
46	chr1:243057080-243057130	HCPEpiC	choroid plexus:	n/a
47	chr1:243139525-243139575	SK-N-SH_RA	brain:	n/a
48	chr1:243053934-243053984	HRCEpiC	kidney:	n/a
49	chr1:243053673-243053723	GM12878	blood:	n/a
50	chr1:242767942-242767992	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr1:242991254..242992220-chr1:243099841..243100636,3	MCF-7	breast:
2	chr1:243028092..243030417-chr1:243031884..243034309,2	K562	blood:
3	chr1:243003845..243005366-chr1:243007691..243009298,2	K562	blood:
4	chr1:242989477..242991101-chr1:242991941..242994002,2	K562	blood:
5	chr1:242867321..242869149-chr1:242869227..242872156,2	MCF-7	breast:
6	chr1:243028092..243030417-chr1:243031884..243034309,2	K562	blood:
7	chr1:242998388..243001295-chr1:243002456..243004745,2	K562	blood:
8	chr1:243019974..243021671-chr1:243028235..243030687,2	K562	blood:
9	chr1:242817323..242819787-chr1:242897350..242900264,2	K562	blood:
10	chr1:242991254..242992220-chr1:243099841..243100636,3	MCF-7	breast:
11	chr1:242867321..242869149-chr1:242869227..242872156,2	MCF-7	breast:
12	chr1:242868996..242871474-chr1:242872273..242874608,2	K562	blood:
13	chr1:243028922..243031643-chr1:243036505..243039074,2	K562	blood:
14	chr1:242725284..242727359-chr1:242740097..242742633,2	K562	blood:
15	chr1:242907367..242907987-chr1:242917774..242918489,2	MCF-7	breast:
16	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
17	chr1:243003845..243005366-chr1:243007691..243009298,2	K562	blood:
18	chr1:242938370..242940205-chr1:242949135..242951746,2	K562	blood:
19	chr1:242938370..242940205-chr1:242949135..242951746,2	K562	blood:
20	chr1:242617838..242618342-chr1:242955947..242956813,2	MCF-7	breast:
21	chr1:242817323..242819787-chr1:242897350..242900264,2	K562	blood:
22	chr1:242907367..242907987-chr1:242917774..242918489,2	MCF-7	breast:
23	chr1:242998388..243001295-chr1:243002456..243004745,2	K562	blood:
24	chr1:242868996..242871474-chr1:242872273..242874608,2	K562	blood:
25	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
26	chr1:243028922..243031643-chr1:243036505..243039074,2	K562	blood:
27	chr1:242731452..242733233-chr1:242737501..242739906,2	K562	blood:
28	chr1:242989477..242991101-chr1:242991941..242994002,2	K562	blood:
29	chr1:243019974..243021671-chr1:243028235..243030687,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP170-9	chr1:243070564-243075269	refGeneNc_994_NR_026778
2	lnc-CEP170-8	chr1:243077153-243077520	expReg_chr1_22679_-
3	lnc-CEP170-7	chr1:243078426-243078834	expReg_chr1_22680_-
4	lnc-SDCCAG8-4	chr1:242834442-242834878	NONHSAT010573
5	lnc-CEP170-9	chr1:243076529-243076866	refGeneNc_994_NR_026778
6	lnc-CEP170-9	chr1:243076807-243077141	expReg_chr1_22678_-

No data

Variant related genes	Relation type
ENSG00000230199	TF binding region
ENSG00000270859	TF binding region
ENSG00000270818	TF binding region
RSL24D1P4	TF binding region
ENSG00000264972	TF binding region
ENSG00000230199	CpG island
ENSG00000270859	CpG island
ENSG00000270818	CpG island
RSL24D1P4	CpG island
ENSG00000264972	CpG island

Extended variants
information (count: 9862 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:9862 , 50 per page) page: 1 2 3 4 5 6 7 ... 198

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10926773	chr1:242739083-242739084	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530059046	chr1:242739165-242739166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74648510	chr1:242739208-242739209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560198965	chr1:242739319-242739320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184019525	chr1:242739359-242739360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10926774	chr1:242739397-242739398	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs190101332	chr1:242739410-242739411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530789694	chr1:242739413-242739414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs10926775	chr1:242739424-242739425	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs546796835	chr1:242739452-242739453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568656066	chr1:242739476-242739477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567241165	chr1:242739556-242739557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs57860392	chr1:242739570-242739571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181808128	chr1:242739583-242739584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185597055	chr1:242739593-242739594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538403123	chr1:242739690-242739691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371129389	chr1:242739742-242739743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116355306	chr1:242739925-242739926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73136401	chr1:242739967-242739968	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs149902405	chr1:242740035-242740036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112279872	chr1:242740116-242740117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374342978	chr1:242740150-242740151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190525636	chr1:242740151-242740152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144077136	chr1:242740157-242740158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558900522	chr1:242740179-242740180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73136402	chr1:242740195-242740196	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs538845120	chr1:242740212-242740213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs180846904	chr1:242740234-242740235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368231684	chr1:242740238-242740239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535820499	chr1:242740301-242740302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148659322	chr1:242740304-242740305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185502426	chr1:242740310-242740311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558757815	chr1:242740397-242740398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs56843485	chr1:242740405-242740406	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs550857934	chr1:242740440-242740441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77216592	chr1:242740498-242740499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530043844	chr1:242740563-242740564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537836365	chr1:242740578-242740579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566384813	chr1:242740594-242740595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556498435	chr1:242740607-242740608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143348772	chr1:242740627-242740628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs61386118	chr1:242740631-242740632	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs77847475	chr1:242740640-242740641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115135831	chr1:242740649-242740650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188302109	chr1:242740657-242740658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547545439	chr1:242740658-242740659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574791179	chr1:242740686-242740687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534264691	chr1:242740738-242740739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6658662	chr1:242740810-242740811	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs577170200	chr1:242740931-242740932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:624 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242734000-242747800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:242742600-242742800	Enhancers	A549	lung
3	chr1:242742800-242743200	Flanking Active TSS	A549	lung
4	chr1:242743200-242743600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr1:242743200-242744200	Enhancers	A549	lung
6	chr1:242744200-242746000	Weak transcription	A549	lung
7	chr1:242745800-242747200	Enhancers	HepG2	liver
8	chr1:242746000-242746200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr1:242746000-242746400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr1:242746000-242747000	Enhancers	A549	lung
11	chr1:242746200-242746400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr1:242746400-242747800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr1:242746600-242748800	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr1:242747800-242748000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:242747800-242748000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
16	chr1:242747800-242748000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr1:242747800-242748000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:242748000-242748600	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr1:242748000-242749600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr1:242748400-242750000	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr1:242748400-242750200	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr1:242748600-242749000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr1:242748600-242750000	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr1:242748800-242749000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr1:242748800-242749000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr1:242748800-242749600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr1:242748800-242749800	Enhancers	Brain Germinal Matrix	brain
28	chr1:242748800-242750200	Enhancers	H9 Cell Line	embryonic stem cell
29	chr1:242748800-242750200	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr1:242748800-242750200	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr1:242748800-242750600	Enhancers	H1 Cell Line	embryonic stem cell
32	chr1:242749000-242749200	Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr1:242749000-242750600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr1:242749000-242750800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:242749200-242749400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr1:242749200-242749800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr1:242749200-242750200	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr1:242749200-242750600	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr1:242749400-242749800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr1:242749600-242750200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:242749600-242750200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr1:242749600-242750200	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr1:242749800-242750000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr1:242750200-242753000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr1:242750600-242751000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr1:242755600-242756200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr1:242756800-242757000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr1:242757000-242757200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:242757200-242757400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr1:242757400-242762000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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