Variant report

Variant	nsv1012319
Chromosome Location	chr1:73337418-73547086
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:380)
CpG islands
(count:488)
Chromatin interactive
region (count:12)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:73531195-73531578	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr1:73356817-73356845	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr1:73531255-73531557	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr1:73384626-73384992	IMR90	lung:	n/a	chr1:73384801-73384812 chr1:73384801-73384814
5	CEBPB	chr1:73357527-73357727	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr1:73357453-73357766	IMR90	lung:	n/a	n/a
7	CEBPB	chr1:73383624-73384000	H1-hESC	embryonic stem cell:	n/a	chr1:73383807-73383818
8	CEBPB	chr1:73469342-73469542	HepG2	liver:	n/a	chr1:73469391-73469402
9	CEBPB	chr1:73341844-73342044	HepG2	liver:	n/a	chr1:73341906-73341917
10	CEBPB	chr1:73468665-73468872	A549	lung:	n/a	chr1:73468696-73468707
11	CEBPB	chr1:73383718-73383960	Hela-S3	cervix:	n/a	chr1:73383807-73383818
12	CEBPB	chr1:73383621-73384014	K562	blood:	n/a	chr1:73383807-73383818
13	CEBPB	chr1:73359196-73359450	HepG2	liver:	n/a	chr1:73359288-73359299 chr1:73359288-73359301 chr1:73359289-73359300 chr1:73359288-73359301
14	CEBPB	chr1:73384639-73384972	K562	blood:	n/a	chr1:73384801-73384812 chr1:73384801-73384814
15	CEBPB	chr1:73384725-73384963	ECC-1	luminal epithelium:	n/a	chr1:73384801-73384812 chr1:73384801-73384814
16	CEBPB	chr1:73384623-73384986	Hela-S3	cervix:	n/a	chr1:73384801-73384812 chr1:73384801-73384814
17	CEBPB	chr1:73383621-73383994	ECC-1	luminal epithelium:	n/a	chr1:73383807-73383818
18	CEBPB	chr1:73495346-73495601	H1-hESC	embryonic stem cell:	n/a	chr1:73495466-73495477
19	CEBPB	chr1:73383650-73383996	HepG2	liver:	n/a	chr1:73383807-73383818
20	CEBPB	chr1:73383715-73383996	MCF-7	breast:	n/a	chr1:73383807-73383818
21	CEBPB	chr1:73495083-73495670	Hela-S3	cervix:	n/a	chr1:73495466-73495477
22	CEBPB	chr1:73384644-73384989	H1-hESC	embryonic stem cell:	n/a	chr1:73384801-73384812 chr1:73384801-73384814
23	CEBPB	chr1:73495397-73495572	A549	lung:	n/a	chr1:73495466-73495477
24	CEBPB	chr1:73383692-73383976	A549	lung:	n/a	chr1:73383807-73383818
25	CEBPB	chr1:73384632-73384976	HepG2	liver:	n/a	chr1:73384801-73384812 chr1:73384801-73384814
26	CEBPB	chr1:73445404-73445550	HepG2	liver:	n/a	chr1:73445492-73445503
27	CEBPB	chr1:73506591-73506863	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr1:73351498-73351837	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:73495334-73495618	HepG2	liver:	n/a	chr1:73495466-73495477
30	CEBPB	chr1:73383643-73384042	ECC-1	luminal epithelium:	n/a	chr1:73383807-73383818
31	CEBPB	chr1:73468568-73468768	H1-hESC	embryonic stem cell:	n/a	chr1:73468696-73468707
32	CEBPB	chr1:73383634-73383995	IMR90	lung:	n/a	chr1:73383807-73383818
33	CEBPB	chr1:73531272-73531677	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr1:73468505-73469059	HepG2	liver:	n/a	chr1:73468696-73468707
35	CTCF	chr1:73396800-73396950	GM12872	blood:	n/a	n/a
36	CTCF	chr1:73525257-73525335	GM10266	blood:	n/a	n/a
37	CTCF	chr1:73544840-73544990	HMEC	breast:	n/a	n/a
38	CTCF	chr1:73374983-73375044	LNCaP	prostate:	n/a	n/a
39	CTCF	chr1:73367572-73367640	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr1:73544959-73545007	LNCaP	prostate:	n/a	n/a
41	CTCF	chr1:73449120-73449134	GM13976	blood:	n/a	n/a
42	CTCF	chr1:73544923-73544961	LNCaP	prostate:	n/a	n/a
43	CTCF	chr1:73527050-73527084	GM10266	blood:	n/a	n/a
44	CTCF	chr1:73511620-73511770	HPF	lung:	n/a	n/a
45	CTCF	chr1:73544905-73545028	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr1:73471788-73471866	GM13976	blood:	n/a	n/a
47	CUX1	chr1:73402601-73402635	K562	blood:	n/a	n/a
48	E2F4	chr1:73358266-73358476	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr1:73466327-73466585	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr1:73503319-73503497	MCF10A-Er-Src	breast:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:73500111-73500161	A549	lung:	n/a
2	chr1:73531614-73531664	AG04450	lung:	fetal
3	chr1:73425038-73425088	AG09309	skin:	n/a
4	chr1:73500111-73500161	AoSMC	blood vessel:	n/a
5	chr1:73463170-73463220	HNPCEpiC	eye:	n/a
6	chr1:73364736-73364786	GM19239	blood:	n/a
7	chr1:73364736-73364786	U87	brain:	n/a
8	chr1:73500111-73500161	HRCEpiC	kidney:	n/a
9	chr1:73425038-73425088	GM12892	blood:	n/a
10	chr1:73531614-73531664	U87	brain:	n/a
11	chr1:73364736-73364786	AG09309	skin:	n/a
12	chr1:73500111-73500161	LNCaP	prostate:	n/a
13	chr1:73364736-73364786	IMR90	lung:	fetal
14	chr1:73463170-73463220	ProgFib	skin:	n/a
15	chr1:73500111-73500161	HRE	kidney:	n/a
16	chr1:73404526-73404576	SK-N-SH_RA	brain:	n/a
17	chr1:73531614-73531664	AG04449	skin:	fetal
18	chr1:73404526-73404576	SKMC	muscle:	n/a
19	chr1:73381117-73381167	U87	brain:	n/a
20	chr1:73463170-73463220	PrEC	prostate:	n/a
21	chr1:73404526-73404576	SK-N-SH	brain:	n/a
22	chr1:73531614-73531664	HRCEpiC	kidney:	n/a
23	chr1:73364736-73364786	HIPEpiC	eye:	n/a
24	chr1:73463170-73463220	MCF-7	breast:	n/a
25	chr1:73452800-73452850	AG09309	skin:	n/a
26	chr1:73404526-73404576	PANC-1	pancreas:	n/a
27	chr1:73452800-73452850	HRPEpiC	eye:	n/a
28	chr1:73364736-73364786	A549	lung:	n/a
29	chr1:73404526-73404576	NHDF-neo	bronchial:	n/a
30	chr1:73364736-73364786	RPTEC	kidney:	n/a
31	chr1:73381117-73381167	HEEpiC	esophagus:	n/a
32	chr1:73452800-73452850	BJ	skin:	n/a
33	chr1:73531614-73531664	SK-N-SH	brain:	n/a
34	chr1:73364736-73364786	Jurkat	blood:	n/a
35	chr1:73463170-73463220	LNCaP	prostate:	n/a
36	chr1:73425038-73425088	NHBE	bronchial:	n/a
37	chr1:73463170-73463220	HEEpiC	esophagus:	n/a
38	chr1:73364736-73364786	PrEC	prostate:	n/a
39	chr1:73364736-73364786	HCPEpiC	choroid plexus:	n/a
40	chr1:73381117-73381167	NHBE	bronchial:	n/a
41	chr1:73452800-73452850	NHDF-neo	bronchial:	n/a
42	chr1:73500111-73500161	HRPEpiC	eye:	n/a
43	chr1:73381117-73381167	HL-60	blood:	n/a
44	chr1:73463170-73463220	NHDF-neo	bronchial:	n/a
45	chr1:73381117-73381167	MCF-7	breast:	n/a
46	chr1:73500111-73500161	HNPCEpiC	eye:	n/a
47	chr1:73364736-73364786	AG10803	skin:	n/a
48	chr1:73364736-73364786	SK-N-MC	brain:	n/a
49	chr1:73381117-73381167	HCT-116	colon:	n/a
50	chr1:73463170-73463220	BJ	skin:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:73529446..73532358-chr1:73537897..73540448,2	K562	blood:
2	chr1:73349931..73352459-chr1:73352891..73354785,2	MCF-7	breast:
3	chr1:73349931..73352459-chr1:73352891..73354785,2	MCF-7	breast:
4	chr1:73529446..73532358-chr1:73537897..73540448,2	K562	blood:
5	chr1:73463171..73465472-chr1:73562170..73563672,2	K562	blood:
6	chr1:73518684..73521320-chr1:73523360..73524908,2	K562	blood:
7	chr1:73472905..73475418-chr1:73476553..73478531,2	K562	blood:
8	chr1:73472905..73475418-chr1:73476553..73478531,2	K562	blood:
9	chr1:73361210..73361731-chr8:33949907..33950427,2	MCF-7	breast:
10	chr1:73518684..73521320-chr1:73523360..73524908,2	K562	blood:
11	chr1:73354311..73356043-chr1:73358130..73359768,2	K562	blood:
12	chr1:73354311..73356043-chr1:73358130..73359768,2	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NEGR1-1	chr1:73364712-73364823	ENSG00000225087
2	lnc-FPGT-9	chr1:73545487-73545634	NONHSAT003931
3	lnc-NEGR1-5	chr1:73444697-73444997	NONHSAT003923
4	lnc-FPGT-9	chr1:73544505-73544545	NONHSAT003929
5	lnc-FPGT-11	chr1:73453059-73453073	NONHSAT003922
6	lnc-FPGT-10	chr1:73447761-73447828	FPKM1_group_852_transcript_3
7	lnc-FPGT-9	chr1:73544500-73544545	NONHSAT003928
8	lnc-FPGT-11	chr1:73448860-73448966	NONHSAT003922
9	lnc-FPGT-9	chr1:73545439-73545843	NONHSAT003930
10	lnc-FPGT-9	chr1:73545439-73545634	NONHSAT003927
11	lnc-FPGT-9	chr1:73544510-73544545	NONHSAT003930
12	lnc-FPGT-10	chr1:73450871-73451011	NONHSAT003925
13	lnc-FPGT-9	chr1:73544441-73544545	NONHSAT003927
14	lnc-FPGT-9	chr1:73544441-73544545	ucscGeneNc_uc001dfx_2
15	lnc-NEGR1-6	chr1:73454821-73455014	NONHSAT003926
16	lnc-FPGT-9	chr1:73545439-73545634	ucscGeneNc_uc001dfx_2
17	lnc-FPGT-11	chr1:73448295-73448360	NONHSAT003922
18	lnc-NEGR1-1	chr1:73364450-73364566	ENSG00000225087
19	lnc-FPGT-11	chr1:73439903-73440206	NONHSAT003922
20	lnc-FPGT-10	chr1:73447761-73447828	NONHSAT003925
21	lnc-NEGR1-6	chr1:73458736-73458746	NONHSAT003926
22	lnc-FPGT-10	chr1:73448072-73448212	FPKM1_group_852_transcript_3

No data

Variant related genes	Relation type
ENSG00000225087	TF binding region
ENSG00000225087	CpG island

Extended variants
information (count: 4236 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:4236 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12077316	chr1:73350817-73350818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs540067554	chr1:73350864-73350865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570595885	chr1:73350888-73350889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138404814	chr1:73350972-73350973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538732920	chr1:73350988-73350989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534542492	chr1:73350996-73350997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs61774085	chr1:73351002-73351003	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs572084222	chr1:73351069-73351070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs539427036	chr1:73351092-73351093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540898144	chr1:73351122-73351123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs143804052	chr1:73351140-73351141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs74092220	chr1:73351148-73351149	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs1358033	chr1:73351199-73351200	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs562995351	chr1:73351201-73351202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs74092221	chr1:73351211-73351212	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs535440176	chr1:73351212-73351213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs56386330	chr1:73351246-73351247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs184228643	chr1:73351279-73351280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551862944	chr1:73351342-73351343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs148728737	chr1:73351354-73351355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs527708281	chr1:73351358-73351359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556949321	chr1:73351379-73351380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543989097	chr1:73351408-73351409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs79062202	chr1:73351409-73351410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529897800	chr1:73351416-73351417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544096687	chr1:73351433-73351434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189654314	chr1:73351466-73351467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369082178	chr1:73351467-73351468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538318820	chr1:73351537-73351538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11587774	chr1:73351557-73351558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557968020	chr1:73351558-73351559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs75379787	chr1:73351559-73351560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558705682	chr1:73351568-73351569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs397831469	chr1:73351572-73351573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs565655125	chr1:73351599-73351600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534637564	chr1:73351617-73351618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs2692849	chr1:73351648-73351649	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs574298157	chr1:73351655-73351656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs200981213	chr1:73351663-73351664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs1525983	chr1:73351758-73351759	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs11799576	chr1:73351777-73351778	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs186305871	chr1:73351778-73351779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs12039928	chr1:73351791-73351792	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs141575703	chr1:73351795-73351796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150906197	chr1:73351832-73351833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs560777211	chr1:73351890-73351891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs560947743	chr1:73351894-73351895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529903095	chr1:73351921-73351922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550062274	chr1:73351940-73351941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs6689491	chr1:73352029-73352030	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:73350800-73352200	Enhancers	Hela-S3	cervix
2	chr1:73356600-73358600	Enhancers	HMEC	breast
3	chr1:73356600-73359400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:73357200-73358600	Enhancers	NHEK	skin
5	chr1:73357800-73358200	Enhancers	NHDF-Ad	bronchial
6	chr1:73357800-73358600	Enhancers	NH-A	brain
7	chr1:73358400-73358600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:73359400-73361800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:73360600-73360800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr1:73360800-73362800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr1:73361800-73362000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:73361800-73362200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:73361800-73362400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr1:73361800-73362400	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr1:73361800-73362400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr1:73362000-73362200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr1:73362800-73363000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr1:73362800-73363000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr1:73362800-73363000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr1:73362800-73365000	Active TSS	HUES6 Cell Line	embryonic stem cell
21	chr1:73363000-73363400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr1:73363000-73364000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr1:73363000-73365000	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr1:73363400-73364000	Active TSS	iPS-15b Cell Line	embryonic stem cell
25	chr1:73364000-73364400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
26	chr1:73364000-73364400	Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr1:73364000-73364400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr1:73364000-73364600	Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr1:73364000-73364800	Active TSS	HUES64 Cell Line	embryonic stem cell
30	chr1:73364000-73365000	Active TSS	H1 Cell Line	embryonic stem cell
31	chr1:73364000-73365000	Active TSS	Hela-S3	cervix
32	chr1:73364200-73365000	Active TSS	iPS-18 Cell Line	embryonic stem cell
33	chr1:73364400-73365000	Active TSS	iPS-15b Cell Line	embryonic stem cell
34	chr1:73364600-73365000	Active TSS	H9 Cell Line	embryonic stem cell
35	chr1:73376400-73377800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr1:73377800-73381000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr1:73378600-73382600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr1:73380200-73382000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr1:73381000-73381200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr1:73381000-73381200	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr1:73381000-73381200	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr1:73381000-73381400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr1:73381000-73381400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr1:73381000-73382000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr1:73381000-73382600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr1:73381200-73381400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
47	chr1:73381200-73381600	Enhancers	H1 Cell Line	embryonic stem cell
48	chr1:73381200-73381600	Enhancers	H9 Cell Line	embryonic stem cell
49	chr1:73381200-73381600	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr1:73381200-73381600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell

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