Variant report

Variant	nsv546658
Chromosome Location	chr1:80536798-80683606
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	chr1:80548886-80548916	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:80549615-80549808	H1-hESC	embryonic stem cell:	n/a	n/a
4	CBX3	chr1:80576645-80576941	K562	blood:	n/a	n/a
5	CBX3	chr1:80576699-80576922	K562	blood:	n/a	n/a
6	CBX3	chr1:80621089-80621493	HCT-116	colon:	n/a	n/a
7	CCNT2	chr1:80678816-80679016	K562	blood:	n/a	n/a
8	CEBPB	chr1:80578688-80579006	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:80555874-80556123	HepG2	liver:	n/a	chr1:80555985-80555998 chr1:80555986-80555997
10	CEBPB	chr1:80555874-80556156	IMR90	lung:	n/a	chr1:80555985-80555998 chr1:80555986-80555997
11	CEBPB	chr1:80578699-80578996	IMR90	lung:	n/a	n/a
12	CEBPB	chr1:80578708-80578995	A549	lung:	n/a	n/a
13	CEBPB	chr1:80572688-80572902	IMR90	lung:	n/a	n/a
14	CEBPB	chr1:80642006-80642206	H1-hESC	embryonic stem cell:	n/a	chr1:80642050-80642061
15	CEBPB	chr1:80578715-80578978	K562	blood:	n/a	n/a
16	CEBPB	chr1:80641901-80642226	HepG2	liver:	n/a	chr1:80642050-80642061
17	CEBPB	chr1:80641923-80642163	A549	lung:	n/a	chr1:80642050-80642061
18	CEBPB	chr1:80548985-80549185	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:80641904-80642221	IMR90	lung:	n/a	chr1:80642050-80642061
20	CEBPB	chr1:80641938-80642153	Hela-S3	cervix:	n/a	chr1:80642050-80642061
21	CTCF	chr1:80621155-80621338	LNCaP	prostate:	n/a	n/a
22	CTCF	chr1:80683160-80683310	HAc	cerebellar:	n/a	chr1:80683228-80683246 chr1:80683230-80683251 chr1:80683233-80683241
23	CTCF	chr1:80621220-80621370	HAc	cerebellar:	n/a	n/a
24	CTCF	chr1:80621129-80621359	IMR90	lung:	n/a	n/a
25	CTCF	chr1:80621133-80621361	MCF-7	breast:	n/a	n/a
26	CTCF	chr1:80683200-80683350	GM12874	blood:	n/a	chr1:80683228-80683246 chr1:80683230-80683251 chr1:80683233-80683241
27	CTCF	chr1:80683120-80683270	AG04450	lung:	n/a	chr1:80683228-80683246 chr1:80683230-80683251 chr1:80683233-80683241
28	CTCF	chr1:80683180-80683330	GM06990	blood:	n/a	chr1:80683228-80683246 chr1:80683230-80683251 chr1:80683233-80683241
29	CTCF	chr1:80683150-80683350	Kidney_OC	kidney:	n/a	chr1:80683228-80683246 chr1:80683230-80683251 chr1:80683233-80683241
30	CTCF	chr1:80621180-80621330	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr1:80619613-80619671	MCF-7	breast:	n/a	n/a
32	CTCF	chr1:80621200-80621350	GM12872	blood:	n/a	n/a
33	CTCF	chr1:80683160-80683303	GM13977	blood:	n/a	chr1:80683228-80683246 chr1:80683230-80683251 chr1:80683233-80683241
34	CTCF	chr1:80629920-80630070	AG10803	skin:	n/a	chr1:80630021-80630042
35	CTCF	chr1:80683092-80683405	HUVEC	blood vessel:	n/a	chr1:80683228-80683246 chr1:80683230-80683251 chr1:80683233-80683241
36	CTCF	chr1:80683160-80683310	MCF-7	breast:	n/a	chr1:80683228-80683246 chr1:80683230-80683251 chr1:80683233-80683241
37	CTCF	chr1:80683160-80683310	SAEC	small airway:	n/a	chr1:80683228-80683246 chr1:80683230-80683251 chr1:80683233-80683241
38	CTCF	chr1:80593060-80593210	RPTEC	kidney:	n/a	n/a
39	CTCF	chr1:80683140-80683290	AG09309	skin:	n/a	chr1:80683228-80683246 chr1:80683230-80683251 chr1:80683233-80683241
40	CTCF	chr1:80629940-80630090	MCF-7	breast:	n/a	chr1:80630021-80630042
41	CTCF	chr1:80683180-80683330	HBMEC	blood vessel:	n/a	chr1:80683228-80683246 chr1:80683230-80683251 chr1:80683233-80683241
42	CTCF	chr1:80683140-80683290	HRPEpiC	eye:	n/a	chr1:80683228-80683246 chr1:80683230-80683251 chr1:80683233-80683241
43	CTCF	chr1:80621100-80621250	HPF	lung:	n/a	n/a
44	CTCF	chr1:80570240-80570390	GM12869	blood:	n/a	n/a
45	CTCF	chr1:80683180-80683330	GM12874	blood:	n/a	chr1:80683228-80683246 chr1:80683230-80683251 chr1:80683233-80683241
46	CTCF	chr1:80549600-80549750	MCF-7	breast:	n/a	n/a
47	CTCF	chr1:80619527-80619746	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr1:80683220-80683370	MCF-7	breast:	n/a	chr1:80683228-80683246 chr1:80683230-80683251 chr1:80683233-80683241
49	CTCF	chr1:80619480-80619630	GM12871	blood:	n/a	n/a
50	CTCF	chr1:80683160-80683310	HCPEpiC	choroid plexus:	n/a	chr1:80683228-80683246 chr1:80683230-80683251 chr1:80683233-80683241

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:80603921-80603971	H1-hESC	embryonic stem cell:	embryo
2	chr1:80603921-80603971	H1-hESC	embryonic stem cell:	embryo
3	chr1:80603921-80603971	IMR90	lung:	fetal
4	chr1:80603921-80603971	ProgFib	skin:	n/a
5	chr1:80603921-80603971	Hela-S3	cervix:	n/a
6	chr1:80603921-80603971	NHBE	bronchial:	n/a
7	chr1:80603921-80603971	SK-N-SH	brain:	n/a
8	chr1:80603921-80603971	SAEC	small airway:	n/a
9	chr1:80603921-80603971	HCM	heart:	n/a
10	chr1:80603921-80603971	PANC-1	pancreas:	n/a
11	chr1:80603921-80603971	AG04449	skin:	fetal
12	chr1:80603921-80603971	HMEC	breast:	n/a
13	chr1:80603921-80603971	AG10803	skin:	n/a
14	chr1:80603921-80603971	U87	brain:	n/a
15	chr1:80603921-80603971	GM12878	blood:	n/a
16	chr1:80603921-80603971	MCF10A-Er-Src	breast:	n/a
17	chr1:80603921-80603971	HUVEC	blood vessel:	n/a
18	chr1:80603921-80603971	HepG2	liver:	n/a
19	chr1:80603921-80603971	AoSMC	blood vessel:	n/a
20	chr1:80603921-80603971	SK-N-SH_RA	brain:	n/a
21	chr1:80603921-80603971	A549	lung:	n/a
22	chr1:80603921-80603971	GM12891	blood:	n/a
23	chr1:80603921-80603971	NHDF-neo	bronchial:	n/a
24	chr1:80603921-80603971	GM12892	blood:	n/a
25	chr1:80603921-80603971	RPTEC	kidney:	n/a
26	chr1:80603921-80603971	AG04450	lung:	fetal
27	chr1:80603921-80603971	NT2-D1	testis:	n/a
28	chr1:80603921-80603971	Hepatocyte	liver:	n/a
29	chr1:80603921-80603971	AG09309	skin:	n/a
30	chr1:80603921-80603971	NH-A	brain:	n/a
31	chr1:80603921-80603971	PrEC	prostate:	n/a
32	chr1:80603921-80603971	HRE	kidney:	n/a
33	chr1:80603921-80603971	GM19239	blood:	n/a
34	chr1:80603921-80603971	AG09319	gingival:	n/a
35	chr1:80603921-80603971	MCF-7	breast:	n/a
36	chr1:80603921-80603971	T-47D	breast:	n/a
37	chr1:80603921-80603971	HL-60	blood:	n/a
38	chr1:80603921-80603971	SKMC	muscle:	n/a
39	chr1:80603921-80603971	HCF	heart:	n/a
40	chr1:80603921-80603971	BE2_C	brain:	n/a
41	chr1:80603921-80603971	HAEpiC	amniotic membrane:	n/a
42	chr1:80603921-80603971	LNCaP	prostate:	n/a
43	chr1:80603921-80603971	ECC-1	luminal epithelium:	n/a
44	chr1:80603921-80603971	CMK	blood:	n/a
45	chr1:80603921-80603971	K562	blood:	n/a
46	chr1:80603921-80603971	NB4	blood:	n/a
47	chr1:80603921-80603971	HEK293	kidney:	embryo
48	chr1:80603921-80603971	HCPEpiC	choroid plexus:	n/a
49	chr1:80603921-80603971	HNPCEpiC	eye:	n/a
50	chr1:80603921-80603971	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:80678626..80682159-chr1:80682380..80685207,3	K562	blood:
2	chr1:80624318..80626596-chr1:80627891..80630503,3	MCF-7	breast:
3	chr1:79962962..79963539-chr1:80683583..80684326,2	MCF-7	breast:
4	chr1:80656975..80659221-chr1:80663008..80665270,2	K562	blood:
5	chr1:80678626..80682159-chr1:80682380..80685207,3	K562	blood:
6	chr1:80624318..80626596-chr1:80627891..80630503,3	MCF-7	breast:
7	chr1:80683192..80684047-chr1:82226087..82226734,2	MCF-7	breast:
8	chr1:80568623..80571326-chr1:80577304..80579523,2	K562	blood:
9	chr1:80656975..80659221-chr1:80663008..80665270,2	K562	blood:
10	chr1:80568623..80571326-chr1:80577304..80579523,2	K562	blood:

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

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

Extended variants
information (count: 2952 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2952 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114802941	chr1:80537617-80537618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs184638366	chr1:80537631-80537632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547979730	chr1:80537674-80537675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188958967	chr1:80537700-80537701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545536615	chr1:80537742-80537743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs976106	chr1:80537798-80537799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563654688	chr1:80537826-80537827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566585098	chr1:80537862-80537863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531001103	chr1:80537877-80537878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549145012	chr1:80537894-80537895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535499492	chr1:80537908-80537909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs141648866	chr1:80537952-80537953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528410048	chr1:80537985-80537986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181969499	chr1:80537987-80537988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs186305111	chr1:80538001-80538002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs201875074	chr1:80538002-80538003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs111524949	chr1:80538004-80538005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538177767	chr1:80538014-80538015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550714696	chr1:80538059-80538060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs190798675	chr1:80538083-80538084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs377727865	chr1:80538126-80538127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181081216	chr1:80538136-80538137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576830725	chr1:80538166-80538167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1414410	chr1:80538172-80538173	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs1414411	chr1:80538189-80538190	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs533732092	chr1:80538255-80538256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs367830158	chr1:80538260-80538261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs574057210	chr1:80538277-80538278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540055331	chr1:80538320-80538321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs116802728	chr1:80538331-80538332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs578243025	chr1:80538334-80538335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545288603	chr1:80538339-80538340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557515908	chr1:80538369-80538370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs575678318	chr1:80538400-80538401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543097666	chr1:80538470-80538471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs370202807	chr1:80538515-80538516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375606601	chr1:80538527-80538528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185924734	chr1:80538528-80538529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs540205737	chr1:80538539-80538540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs74097162	chr1:80538553-80538554	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs543019696	chr1:80538559-80538560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532418958	chr1:80538610-80538611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs573799873	chr1:80538611-80538612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550528813	chr1:80538667-80538668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs114899210	chr1:80538782-80538783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112683663	chr1:80538798-80538799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529793638	chr1:80538852-80538853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs74097164	chr1:80538874-80538875	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs566528501	chr1:80538877-80538878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs533792522	chr1:80538920-80538921	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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

Chromatin state (count:133 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:80537600-80539800	Enhancers	Fetal Brain Male	brain
2	chr1:80539200-80540200	Enhancers	Fetal Brain Female	brain
3	chr1:80540200-80540800	Weak transcription	Fetal Brain Female	brain
4	chr1:80540800-80541000	Enhancers	Fetal Brain Female	brain
5	chr1:80541000-80541400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:80545200-80545600	Enhancers	Fetal Heart	heart
7	chr1:80545600-80554000	Weak transcription	Fetal Heart	heart
8	chr1:80551000-80553000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:80552000-80552600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:80563600-80568800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr1:80564600-80565600	Enhancers	Liver	Liver
12	chr1:80565600-80566000	Flanking Active TSS	Liver	Liver
13	chr1:80566000-80566200	Enhancers	Liver	Liver
14	chr1:80577800-80578400	Weak transcription	Liver	Liver
15	chr1:80578600-80579000	Enhancers	Liver	Liver
16	chr1:80579000-80579200	Flanking Active TSS	Liver	Liver
17	chr1:80579200-80579400	Enhancers	Liver	Liver
18	chr1:80579400-80579600	Flanking Active TSS	Liver	Liver
19	chr1:80579600-80580200	Enhancers	Liver	Liver
20	chr1:80604800-80608800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr1:80608800-80609200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr1:80609000-80609400	ZNF genes & repeats	Esophagus	oesophagus
23	chr1:80619400-80620200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr1:80619800-80620000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr1:80620200-80626600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr1:80621000-80621800	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr1:80621000-80621800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr1:80621200-80621600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr1:80621400-80621600	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr1:80621400-80622000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr1:80621400-80622200	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr1:80621600-80623000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr1:80621800-80623000	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr1:80621800-80623000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr1:80621800-80623000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr1:80622000-80623400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr1:80622200-80623200	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr1:80623000-80624200	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr1:80623000-80624200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr1:80623000-80624200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr1:80623000-80624600	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr1:80623000-80624600	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr1:80623200-80624200	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr1:80623400-80624800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr1:80623600-80625200	Enhancers	Fetal Brain Male	brain
46	chr1:80623800-80624200	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr1:80623800-80624200	Enhancers	Placenta Amnion	Placenta Amnion
48	chr1:80624200-80626000	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr1:80624600-80624800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr1:80624600-80624800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin

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