Variant report

Variant	nsv872719
Chromosome Location	chr1:189602917-189731048
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	ARID3A	chr1:189655218-189655237	K562	blood:	n/a	n/a
2	ATF1	chr1:189692607-189692756	K562	blood:	n/a	n/a
3	ATF1	chr1:189645110-189645131	K562	blood:	n/a	n/a
4	ATF3	chr1:189624065-189624449	HCT-116	colon:	n/a	n/a
5	BACH1	chr1:189660033-189660067	K562	blood:	n/a	n/a
6	BCL3	chr1:189650561-189651101	A549	lung:	n/a	n/a
7	BRCA1	chr1:189640354-189640407	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr1:189626762-189627309	HCT-116	colon:	n/a	n/a
9	CBX3	chr1:189631288-189631734	HCT-116	colon:	n/a	n/a
10	CBX3	chr1:189627431-189627982	HCT-116	colon:	n/a	n/a
11	CBX3	chr1:189631264-189631803	HCT-116	colon:	n/a	n/a
12	CEBPB	chr1:189624035-189624369	K562	blood:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
13	CEBPB	chr1:189672613-189673256	IMR90	lung:	n/a	n/a
14	CEBPB	chr1:189626736-189627414	HCT-116	colon:	n/a	chr1:189627200-189627217
15	CEBPB	chr1:189688196-189688361	H1-hESC	embryonic stem cell:	n/a	chr1:189688274-189688285 chr1:189688275-189688286
16	CEBPB	chr1:189650548-189650953	A549	lung:	n/a	n/a
17	CEBPB	chr1:189624089-189624306	MCF-7	breast:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
18	CEBPB	chr1:189675215-189675438	HepG2	liver:	n/a	chr1:189675255-189675266
19	CEBPB	chr1:189718405-189718652	A549	lung:	n/a	chr1:189718486-189718497
20	CEBPB	chr1:189624086-189624348	ECC-1	luminal epithelium:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
21	CEBPB	chr1:189624014-189624396	IMR90	lung:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
22	CEBPB	chr1:189689001-189689131	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:189688098-189688417	A549	lung:	n/a	chr1:189688274-189688285 chr1:189688275-189688286
24	CEBPB	chr1:189606177-189606515	Hela-S3	cervix:	n/a	chr1:189606323-189606334
25	CEBPB	chr1:189624017-189624416	A549	lung:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
26	CEBPB	chr1:189651781-189651981	A549	lung:	n/a	n/a
27	CEBPB	chr1:189623967-189624524	HCT-116	colon:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
28	CEBPB	chr1:189606191-189606464	HepG2	liver:	n/a	chr1:189606323-189606334
29	CEBPB	chr1:189623938-189624460	HCT-116	colon:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
30	CEBPB	chr1:189624011-189624388	Hela-S3	cervix:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
31	CEBPB	chr1:189626703-189627383	HCT-116	colon:	n/a	chr1:189627200-189627217
32	CEBPB	chr1:189688107-189688436	HepG2	liver:	n/a	chr1:189688274-189688285 chr1:189688275-189688286
33	CEBPB	chr1:189646472-189646806	HepG2	liver:	n/a	n/a
34	CEBPB	chr1:189718442-189718647	HepG2	liver:	n/a	chr1:189718486-189718497
35	CEBPB	chr1:189626976-189627210	IMR90	lung:	n/a	n/a
36	CEBPB	chr1:189675218-189675345	A549	lung:	n/a	chr1:189675255-189675266
37	CEBPB	chr1:189604468-189604766	A549	lung:	n/a	n/a
38	CEBPB	chr1:189631180-189631818	HCT-116	colon:	n/a	n/a
39	CEBPB	chr1:189626761-189627411	A549	lung:	n/a	chr1:189627200-189627217
40	CEBPB	chr1:189688106-189688428	IMR90	lung:	n/a	chr1:189688274-189688285 chr1:189688275-189688286
41	CEBPB	chr1:189626896-189627281	A549	lung:	n/a	chr1:189627200-189627217
42	CEBPB	chr1:189624053-189624347	H1-hESC	embryonic stem cell:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
43	CEBPB	chr1:189624021-189624372	A549	lung:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
44	CEBPB	chr1:189626830-189627327	MCF-7	breast:	n/a	chr1:189627200-189627217
45	CEBPB	chr1:189626895-189627312	Hela-S3	cervix:	n/a	chr1:189627200-189627217
46	CEBPB	chr1:189626911-189627214	MCF-7	breast:	n/a	n/a
47	CEBPB	chr1:189623953-189624457	MCF-7	breast:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
48	CEBPB	chr1:189626898-189627277	HepG2	liver:	n/a	chr1:189627200-189627217
49	CEBPB	chr1:189623883-189624474	A549	lung:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
50	CEBPB	chr1:189624041-189624385	HepG2	liver:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:189722103-189722153	HMEC	breast:	n/a
2	chr1:189722103-189722153	ovcar-3	ovarian:	n/a
3	chr1:189722103-189722153	HRE	kidney:	n/a
4	chr1:189722103-189722153	HPAEpiC	pulmonary alveolar:	n/a
5	chr1:189722103-189722153	CMK	blood:	n/a
6	chr1:189722103-189722153	HRPEpiC	eye:	n/a
7	chr1:189722103-189722153	HCPEpiC	choroid plexus:	n/a
8	chr1:189722103-189722153	AG10803	skin:	n/a
9	chr1:189722103-189722153	LNCaP	prostate:	n/a
10	chr1:189722103-189722153	U87	brain:	n/a
11	chr1:189722103-189722153	SAEC	small airway:	n/a
12	chr1:189722103-189722153	HRCEpiC	kidney:	n/a
13	chr1:189722103-189722153	PANC-1	pancreas:	n/a
14	chr1:189722103-189722153	ProgFib	skin:	n/a
15	chr1:189722103-189722153	NHDF-neo	bronchial:	n/a
16	chr1:189722103-189722153	Jurkat	blood:	n/a
17	chr1:189722103-189722153	GM19239	blood:	n/a
18	chr1:189722103-189722153	HIPEpiC	eye:	n/a
19	chr1:189722103-189722153	A549	lung:	n/a
20	chr1:189722103-189722153	NH-A	brain:	n/a
21	chr1:189722103-189722153	IMR90	lung:	fetal
22	chr1:189722103-189722153	AG09309	skin:	n/a
23	chr1:189722103-189722153	NT2-D1	testis:	n/a
24	chr1:189722103-189722153	HNPCEpiC	eye:	n/a
25	chr1:189722103-189722153	HepG2	liver:	n/a
26	chr1:189722103-189722153	AG09319	gingival:	n/a
27	chr1:189722103-189722153	GM12878	blood:	n/a
28	chr1:189722103-189722153	ECC-1	luminal epithelium:	n/a
29	chr1:189722103-189722153	HAEpiC	amniotic membrane:	n/a
30	chr1:189722103-189722153	PrEC	prostate:	n/a
31	chr1:189722103-189722153	HCM	heart:	n/a
32	chr1:189722103-189722153	HEK293	kidney:	embryo
33	chr1:189722103-189722153	AG04450	lung:	fetal
34	chr1:189722103-189722153	HEEpiC	esophagus:	n/a
35	chr1:189722103-189722153	RPTEC	kidney:	n/a
36	chr1:189722103-189722153	T-47D	breast:	n/a
37	chr1:189722103-189722153	SK-N-MC	brain:	n/a
38	chr1:189722103-189722153	SK-N-SH	brain:	n/a
39	chr1:189722103-189722153	BJ	skin:	n/a
40	chr1:189722103-189722153	PFSK-1	brain:	n/a
41	chr1:189722103-189722153	H1-hESC	embryonic stem cell:	embryo
42	chr1:189722103-189722153	Caco-2	colon:	n/a
43	chr1:189722103-189722153	Hela-S3	cervix:	n/a
44	chr1:189722103-189722153	Hepatocyte	liver:	n/a
45	chr1:189722103-189722153	AG04449	skin:	fetal
46	chr1:189722103-189722153	GM12891	blood:	n/a
47	chr1:189722103-189722153	HCT-116	colon:	n/a
48	chr1:189722103-189722153	GM12892	blood:	n/a
49	chr1:189722103-189722153	GM06990	blood:	n/a
50	chr1:189722103-189722153	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:189705345..189707314-chr1:189708117..189710746,3	MCF-7	breast:
2	chr1:189617058..189619904-chr1:189621793..189623517,2	MCF-7	breast:
3	chr1:189624367..189627091-chr1:189650312..189652304,2	MCF-7	breast:
4	chr1:189705156..189706947-chr1:189708552..189710958,2	K562	blood:
5	chr1:189627826..189630498-chr1:189636599..189639267,2	MCF-7	breast:
6	chr1:189709848..189710556-chr1:189743646..189744501,3	MCF-7	breast:
7	chr1:189627801..189630516-chr1:189640573..189642596,2	MCF-7	breast:
8	chr1:189625524..189628069-chr1:189701890..189703665,2	MCF-7	breast:
9	chr1:189627801..189630516-chr1:189640573..189642596,2	MCF-7	breast:
10	chr1:189398509..189399144-chr1:189660311..189661261,2	MCF-7	breast:
11	chr1:189589226..189590045-chr1:189662088..189662866,2	MCF-7	breast:
12	chr1:189625524..189628069-chr1:189701890..189703665,2	MCF-7	breast:
13	chr1:189398408..189399387-chr1:189661985..189662829,2	MCF-7	breast:
14	chr1:189705156..189706947-chr1:189708552..189710958,2	K562	blood:
15	chr1:189398440..189399083-chr1:189642226..189643036,4	MCF-7	breast:
16	chr1:189677420..189678491-chr1:190289916..190290952,3	MCF-7	breast:
17	chr1:189630297..189631878-chr1:189633078..189635794,2	K562	blood:
18	chr1:189608651..189610421-chr1:189613616..189615684,2	K562	blood:
19	chr1:189677502..189678569-chr1:190053452..190054228,3	MCF-7	breast:
20	chr1:189608651..189610421-chr1:189613616..189615684,2	K562	blood:
21	chr1:189672702..189674835-chr1:189679900..189682761,2	MCF-7	breast:
22	chr1:189646033..189647879-chr5:175874488..175876371,2	MCF-7	breast:
23	chr1:189624367..189627091-chr1:189650312..189652304,2	MCF-7	breast:
24	chr1:189705345..189707314-chr1:189708117..189710746,3	MCF-7	breast:
25	chr1:189627826..189630498-chr1:189636599..189639267,2	MCF-7	breast:
26	chr1:189617058..189619904-chr1:189621793..189623517,2	MCF-7	breast:
27	chr1:189672702..189674835-chr1:189679900..189682761,2	MCF-7	breast:

Variant related genes	Relation type
RNA5SP73	TF binding region
RNA5SP73	CpG island
ENSG00000113194	chromatin interactions
ENSG00000252553	chromatin interactions

Extended variants
information (count: 1252 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1252 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575190338	chr1:189606005-189606006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532451721	chr1:189606007-189606008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567455703	chr1:189606030-189606031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545576281	chr1:189606045-189606046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73049597	chr1:189606114-189606115	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs12239738	chr1:189606141-189606142	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs534772946	chr1:189606150-189606151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558086637	chr1:189606177-189606178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577996431	chr1:189606279-189606280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs59409561	chr1:189606285-189606286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs115560937	chr1:189606306-189606307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs78592386	chr1:189606349-189606350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542376608	chr1:189606365-189606366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs73049600	chr1:189606407-189606408	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs374094372	chr1:189606426-189606427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528684256	chr1:189606458-189606459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs545583364	chr1:189606462-189606463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114904496	chr1:189606483-189606484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531094540	chr1:189606552-189606553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188430773	chr1:189606554-189606555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567345443	chr1:189606616-189606617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530069986	chr1:189606639-189606640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138618483	chr1:189606658-189606659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566910452	chr1:189606665-189606666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551188049	chr1:189606685-189606686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73049602	chr1:189606686-189606687	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs551267772	chr1:189606687-189606688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192897539	chr1:189606706-189606707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs571597385	chr1:189606710-189606711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112791839	chr1:189606723-189606724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557263219	chr1:189606736-189606737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs112231748	chr1:189606753-189606754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189273541	chr1:189606757-189606758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs552841819	chr1:189606763-189606764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572888031	chr1:189606797-189606798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148564279	chr1:189606828-189606829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79492758	chr1:189606867-189606868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530982589	chr1:189606872-189606873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192369043	chr1:189606882-189606883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141924018	chr1:189606885-189606886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147326714	chr1:189606920-189606921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141011973	chr1:189606932-189606933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184784930	chr1:189606936-189606937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74138451	chr1:189606973-189606974	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs551626732	chr1:189606981-189606982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555800263	chr1:189607006-189607007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571487394	chr1:189607029-189607030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144652410	chr1:189607054-189607055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189006037	chr1:189607072-189607073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533704538	chr1:189607078-189607079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	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
Prostate cancer	18632612	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
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17899364	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:189606000-189606800	Enhancers	A549	lung
2	chr1:189606200-189606600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:189606400-189606800	Enhancers	Fetal Intestine Small	intestine
4	chr1:189606800-189610400	Weak transcription	Fetal Intestine Small	intestine
5	chr1:189610400-189611000	Enhancers	Fetal Intestine Small	intestine
6	chr1:189624000-189624200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr1:189624000-189624200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:189624000-189624400	Enhancers	HMEC	breast
9	chr1:189624200-189624600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:189624200-189625000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr1:189624200-189626000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr1:189624400-189626000	Weak transcription	HMEC	breast
13	chr1:189624600-189626200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:189625000-189626000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:189626000-189626200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:189626000-189626200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr1:189626000-189626400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr1:189626000-189629200	Enhancers	HMEC	breast
19	chr1:189626200-189626800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:189626200-189627000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr1:189626200-189629400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr1:189626400-189628200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr1:189626600-189626800	Enhancers	A549	lung
24	chr1:189626800-189627200	Flanking Active TSS	A549	lung
25	chr1:189626800-189628800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr1:189627000-189628000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr1:189627000-189628000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:189627000-189628000	Enhancers	NHEK	skin
29	chr1:189627200-189628200	Enhancers	A549	lung
30	chr1:189627600-189628000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:189628200-189628600	Weak transcription	A549	lung
32	chr1:189628200-189628800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr1:189628600-189629200	Enhancers	A549	lung
34	chr1:189628800-189629000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr1:189629400-189641400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr1:189636400-189636600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr1:189639200-189639400	Enhancers	A549	lung
38	chr1:189640400-189640600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr1:189640800-189641000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr1:189645000-189645400	Enhancers	Fetal Heart	heart
41	chr1:189649600-189650400	Enhancers	A549	lung
42	chr1:189650200-189651200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr1:189650400-189650600	Flanking Active TSS	A549	lung
44	chr1:189650400-189651000	Enhancers	HepG2	liver
45	chr1:189650600-189651000	Active TSS	A549	lung
46	chr1:189651200-189651600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr1:189651600-189652000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr1:189665400-189666400	Active TSS	Placenta	Placenta
49	chr1:189666400-189666600	Flanking Active TSS	Placenta	Placenta
50	chr1:189675200-189676200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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