Variant report

Variant	nsv462184
Chromosome Location	chr1:80297950-80731568
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:80579439-80579499	K562	blood:	n/a	n/a
2	BACH1	chr1:80449701-80449938	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:80520012-80520093	K562	blood:	n/a	n/a
4	BACH1	chr1:80549615-80549808	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:80515843-80516159	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:80548886-80548916	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:80519821-80520165	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr1:80515876-80516018	K562	blood:	n/a	n/a
9	BHLHE40	chr1:80723225-80723289	K562	blood:	n/a	n/a
10	CBX3	chr1:80313986-80314397	HCT-116	colon:	n/a	n/a
11	CBX3	chr1:80576699-80576922	K562	blood:	n/a	n/a
12	CBX3	chr1:80621089-80621493	HCT-116	colon:	n/a	n/a
13	CBX3	chr1:80576645-80576941	K562	blood:	n/a	n/a
14	CCNT2	chr1:80678816-80679016	K562	blood:	n/a	n/a
15	CEBPB	chr1:80368117-80368491	K562	blood:	n/a	chr1:80368297-80368314 chr1:80368302-80368311 chr1:80368302-80368311 chr1:80368300-80368311 chr1:80368300-80368313 chr1:80368300-80368313 chr1:80368302-80368311
16	CEBPB	chr1:80363822-80364163	IMR90	lung:	n/a	chr1:80363999-80364008 chr1:80363999-80364008 chr1:80363999-80364008 chr1:80363999-80364008 chr1:80363998-80364009 chr1:80363997-80364008
17	CEBPB	chr1:80555874-80556156	IMR90	lung:	n/a	chr1:80555985-80555998 chr1:80555986-80555997
18	CEBPB	chr1:80641923-80642163	A549	lung:	n/a	chr1:80642050-80642061
19	CEBPB	chr1:80308938-80309182	IMR90	lung:	n/a	n/a
20	CEBPB	chr1:80578688-80579006	HepG2	liver:	n/a	n/a
21	CEBPB	chr1:80331672-80331958	IMR90	lung:	n/a	n/a
22	CEBPB	chr1:80555874-80556123	HepG2	liver:	n/a	chr1:80555985-80555998 chr1:80555986-80555997
23	CEBPB	chr1:80344218-80344283	HepG2	liver:	n/a	chr1:80344249-80344260
24	CEBPB	chr1:80368190-80368467	ECC-1	luminal epithelium:	n/a	chr1:80368297-80368314 chr1:80368302-80368311 chr1:80368302-80368311 chr1:80368300-80368311 chr1:80368300-80368313 chr1:80368300-80368313 chr1:80368302-80368311
25	CEBPB	chr1:80641904-80642221	IMR90	lung:	n/a	chr1:80642050-80642061
26	CEBPB	chr1:80368127-80368488	A549	lung:	n/a	chr1:80368297-80368314 chr1:80368302-80368311 chr1:80368302-80368311 chr1:80368300-80368311 chr1:80368300-80368313 chr1:80368300-80368313 chr1:80368302-80368311
27	CEBPB	chr1:80578699-80578996	IMR90	lung:	n/a	n/a
28	CEBPB	chr1:80301583-80301939	HepG2	liver:	n/a	n/a
29	CEBPB	chr1:80572688-80572902	IMR90	lung:	n/a	n/a
30	CEBPB	chr1:80548985-80549185	HepG2	liver:	n/a	n/a
31	CEBPB	chr1:80642006-80642206	H1-hESC	embryonic stem cell:	n/a	chr1:80642050-80642061
32	CEBPB	chr1:80368119-80368499	IMR90	lung:	n/a	chr1:80368297-80368314 chr1:80368302-80368311 chr1:80368302-80368311 chr1:80368300-80368311 chr1:80368300-80368313 chr1:80368300-80368313 chr1:80368302-80368311
33	CEBPB	chr1:80716920-80717073	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr1:80365601-80366058	IMR90	lung:	n/a	n/a
35	CEBPB	chr1:80578708-80578995	A549	lung:	n/a	n/a
36	CEBPB	chr1:80641901-80642226	HepG2	liver:	n/a	chr1:80642050-80642061
37	CEBPB	chr1:80368120-80368475	HepG2	liver:	n/a	chr1:80368297-80368314 chr1:80368302-80368311 chr1:80368302-80368311 chr1:80368300-80368311 chr1:80368300-80368313 chr1:80368300-80368313 chr1:80368302-80368311
38	CEBPB	chr1:80363833-80364134	HepG2	liver:	n/a	chr1:80363999-80364008 chr1:80363999-80364008 chr1:80363999-80364008 chr1:80363999-80364008 chr1:80363998-80364009 chr1:80363997-80364008
39	CEBPB	chr1:80445774-80446053	IMR90	lung:	n/a	chr1:80445872-80445881 chr1:80445872-80445881
40	CEBPB	chr1:80368149-80368463	H1-hESC	embryonic stem cell:	n/a	chr1:80368297-80368314 chr1:80368302-80368311 chr1:80368302-80368311 chr1:80368300-80368311 chr1:80368300-80368313 chr1:80368300-80368313 chr1:80368302-80368311
41	CEBPB	chr1:80368134-80368482	Hela-S3	cervix:	n/a	chr1:80368297-80368314 chr1:80368302-80368311 chr1:80368302-80368311 chr1:80368300-80368311 chr1:80368300-80368313 chr1:80368300-80368313 chr1:80368302-80368311
42	CEBPB	chr1:80578715-80578978	K562	blood:	n/a	n/a
43	CEBPB	chr1:80325230-80325605	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr1:80641938-80642153	Hela-S3	cervix:	n/a	chr1:80642050-80642061
45	CTCF	chr1:80683880-80684030	SK-N-SH_RA	brain:	n/a	chr1:80683980-80683998 chr1:80683982-80684003
46	CTCF	chr1:80317760-80317910	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr1:80448120-80448270	HPF	lung:	n/a	n/a
48	CTCF	chr1:80349728-80349797	ProgFib	skin:	n/a	n/a
49	CTCF	chr1:80461692-80461880	MCF-7	breast:	n/a	chr1:80461763-80461772
50	CTCF	chr1:80621200-80621350	HEEpiC	esophagus:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:80516486-80516536	SK-N-SH	brain:	n/a
2	chr1:80517010-80517060	GM12878	blood:	n/a
3	chr1:80516138-80516188	BE2_C	brain:	n/a
4	chr1:80516591-80516641	HRPEpiC	eye:	n/a
5	chr1:80516486-80516536	AG04450	lung:	fetal
6	chr1:80516486-80516536	HRCEpiC	kidney:	n/a
7	chr1:80603921-80603971	HRCEpiC	kidney:	n/a
8	chr1:80516591-80516641	NHBE	bronchial:	n/a
9	chr1:80516486-80516536	T-47D	breast:	n/a
10	chr1:80516591-80516641	HCT-116	colon:	n/a
11	chr1:80603921-80603971	A549	lung:	n/a
12	chr1:80516486-80516536	BE2_C	brain:	n/a
13	chr1:80516591-80516641	Hela-S3	cervix:	n/a
14	chr1:80516486-80516536	ECC-1	luminal epithelium:	n/a
15	chr1:80516486-80516536	HNPCEpiC	eye:	n/a
16	chr1:80516138-80516188	NT2-D1	testis:	n/a
17	chr1:80366403-80366453	NHBE	bronchial:	n/a
18	chr1:80517010-80517060	MCF-7	breast:	n/a
19	chr1:80516591-80516641	AG10803	skin:	n/a
20	chr1:80517098-80517148	HUVEC	blood vessel:	n/a
21	chr1:80517010-80517060	PrEC	prostate:	n/a
22	chr1:80517010-80517060	HEEpiC	esophagus:	n/a
23	chr1:80517010-80517060	U87	brain:	n/a
24	chr1:80447732-80447782	LNCaP	prostate:	n/a
25	chr1:80517098-80517148	IMR90	lung:	fetal
26	chr1:80517010-80517060	LNCaP	prostate:	n/a
27	chr1:80516591-80516641	NH-A	brain:	n/a
28	chr1:80516486-80516536	K562	blood:	n/a
29	chr1:80517098-80517148	AoSMC	blood vessel:	n/a
30	chr1:80517098-80517148	GM12892	blood:	n/a
31	chr1:80516591-80516641	HAEpiC	amniotic membrane:	n/a
32	chr1:80517010-80517060	RPTEC	kidney:	n/a
33	chr1:80516486-80516536	NH-A	brain:	n/a
34	chr1:80517010-80517060	ovcar-3	ovarian:	n/a
35	chr1:80517010-80517060	A549	lung:	n/a
36	chr1:80516138-80516188	Caco-2	colon:	n/a
37	chr1:80517010-80517060	ECC-1	luminal epithelium:	n/a
38	chr1:80516486-80516536	HIPEpiC	eye:	n/a
39	chr1:80603921-80603971	HNPCEpiC	eye:	n/a
40	chr1:80447732-80447782	HCT-116	colon:	n/a
41	chr1:80366403-80366453	H1-hESC	embryonic stem cell:	embryo
42	chr1:80366403-80366453	BJ	skin:	n/a
43	chr1:80516138-80516188	T-47D	breast:	n/a
44	chr1:80516591-80516641	ovcar-3	ovarian:	n/a
45	chr1:80366403-80366453	BE2_C	brain:	n/a
46	chr1:80517010-80517060	SK-N-SH_RA	brain:	n/a
47	chr1:80603921-80603971	AoSMC	blood vessel:	n/a
48	chr1:80447732-80447782	HRE	kidney:	n/a
49	chr1:80366403-80366453	HRPEpiC	eye:	n/a
50	chr1:80517010-80517060	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:80375215..80377919-chr1:80380333..80383065,2	K562	blood:
2	chr1:80624318..80626596-chr1:80627891..80630503,3	MCF-7	breast:
3	chr1:80568623..80571326-chr1:80577304..80579523,2	K562	blood:
4	chr1:80436532..80438165-chr1:80446885..80448789,2	K562	blood:
5	chr1:80380861..80381772-chr1:80785065..80785571,2	K562	blood:
6	chr1:80375215..80377919-chr1:80380333..80383065,2	K562	blood:
7	chr1:80678626..80682159-chr1:80682380..80685207,3	K562	blood:
8	chr1:80455740..80458353-chr1:80460069..80462983,2	MCF-7	breast:
9	chr1:80683192..80684047-chr1:82226087..82226734,2	MCF-7	breast:
10	chr1:80568623..80571326-chr1:80577304..80579523,2	K562	blood:
11	chr1:80678626..80682159-chr1:80682380..80685207,3	K562	blood:
12	chr1:80330992..80332492-chr17:59388398..59390197,2	MCF-7	breast:
13	chr1:79962962..79963539-chr1:80683583..80684326,2	MCF-7	breast:
14	chr1:80624318..80626596-chr1:80627891..80630503,3	MCF-7	breast:
15	chr1:80717061..80719964-chr1:80721747..80724139,2	K562	blood:
16	chr1:80656975..80659221-chr1:80663008..80665270,2	K562	blood:
17	chr1:80455740..80458353-chr1:80460069..80462983,2	MCF-7	breast:
18	chr1:80436532..80438165-chr1:80446885..80448789,2	K562	blood:
19	chr1:80717061..80719964-chr1:80721747..80724139,2	K562	blood:
20	chr1:80656975..80659221-chr1:80663008..80665270,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELTD1-12	chr1:80612710-80612894	NONHSAT004106
2	lnc-ELTD1-11	chr1:80557788-80558922	NONHSAT004104
3	lnc-LPHN2-3	chr1:80580628-80582603	ENSG00000260322.1
4	lnc-ELTD1-12	chr1:80611637-80612031	NONHSAT004106

Variant related genes	Relation type
ENSG00000235756	TF binding region
ENSG00000260322	TF binding region
ENSG00000235756	CpG island
ENSG00000260322	CpG island

Extended variants
information (count: 6549 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:6549 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12125467	chr1:80297950-80297951	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567950931	chr1:80298040-80298041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185182039	chr1:80298061-80298062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547195530	chr1:80298177-80298178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190420391	chr1:80298220-80298221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10874091	chr1:80298246-80298247	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs557349620	chr1:80298253-80298254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556957030	chr1:80298273-80298274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569113795	chr1:80298290-80298291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192879809	chr1:80298317-80298318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185811730	chr1:80298346-80298347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201360238	chr1:80298347-80298348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370025705	chr1:80298381-80298382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572777298	chr1:80298388-80298389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371551633	chr1:80298577-80298578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs61091480	chr1:80298578-80298579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200342974	chr1:80298579-80298580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74096872	chr1:80298583-80298584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs56202314	chr1:80298586-80298587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs57309760	chr1:80298587-80298588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540068860	chr1:80298606-80298607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189374627	chr1:80298651-80298652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1524175	chr1:80298706-80298707	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs576551012	chr1:80298727-80298728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs180942600	chr1:80298739-80298740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550155666	chr1:80298761-80298762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376885919	chr1:80298766-80298767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78067529	chr1:80298781-80298782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529697306	chr1:80298800-80298801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541806609	chr1:80298801-80298802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561597472	chr1:80298803-80298804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12145936	chr1:80298833-80298834	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs539305434	chr1:80298897-80298898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185159347	chr1:80298957-80298958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547232574	chr1:80298985-80298986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571843348	chr1:80298989-80298990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368818128	chr1:80298999-80299000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532644455	chr1:80299001-80299002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550760639	chr1:80299018-80299019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1524176	chr1:80299020-80299021	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs12118861	chr1:80299024-80299025	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs200352183	chr1:80299120-80299121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140580922	chr1:80299122-80299123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201035219	chr1:80299123-80299124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35818988	chr1:80299124-80299125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10671981	chr1:80299125-80299126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115036703	chr1:80299146-80299147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566443539	chr1:80299205-80299206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533807458	chr1:80299271-80299272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535961234	chr1:80299289-80299290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Ewing''s sarcoma	17952124	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
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:392 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:80297400-80298000	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr1:80297400-80298200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr1:80297800-80300200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr1:80306600-80307000	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr1:80306800-80307200	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr1:80306800-80307200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr1:80306800-80307200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr1:80306800-80307200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr1:80307200-80313600	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr1:80308800-80309400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr1:80311600-80314400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr1:80312200-80314400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:80312800-80313600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:80312800-80314000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr1:80312800-80314200	Enhancers	Ovary	ovary
16	chr1:80313400-80313800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr1:80313400-80314200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr1:80313400-80314600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr1:80313600-80314000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr1:80313600-80314200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr1:80313600-80318800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:80313800-80314400	Enhancers	HMEC	breast
23	chr1:80313800-80314600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr1:80313800-80318600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr1:80314400-80318400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:80314600-80318200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr1:80318200-80318600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr1:80318400-80320200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:80318400-80320400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr1:80318600-80318800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr1:80318600-80319000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr1:80318600-80319000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr1:80318600-80319000	Active TSS	Brain Angular Gyrus	brain
34	chr1:80318800-80320200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:80319000-80319200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr1:80319000-80320000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr1:80319200-80319600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr1:80319400-80319600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr1:80319600-80319800	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr1:80323400-80324600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr1:80323800-80324200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr1:80324000-80327000	Enhancers	HUVEC	blood vessel
43	chr1:80324200-80324600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr1:80324600-80324800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr1:80324600-80324800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr1:80324600-80324800	Bivalent Enhancer	Stomach Mucosa	stomach
47	chr1:80324600-80325000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr1:80324600-80325000	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr1:80324600-80325200	Enhancers	Gastric	stomach
50	chr1:80324600-80325200	Enhancers	Ovary	ovary

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