Variant report

Variant	esv3411228
Chromosome Location	chr1:215704606-215742745
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:771)
CpG islands
(count:549)
Chromatin interactive
region (count:26)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:215731313-215731767	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:215740376-215740690	K562	blood:	n/a	n/a
3	ARID3A	chr1:215740265-215740878	HepG2	liver:	n/a	n/a
4	ATF1	chr1:215716679-215716899	K562	blood:	n/a	n/a
5	BACH1	chr1:215740321-215740761	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:215740222-215740685	K562	blood:	n/a	n/a
7	BACH1	chr1:215741172-215741269	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr1:215740317-215740899	A549	lung:	n/a	chr1:215740719-215740732 chr1:215740865-215740878 chr1:215740885-215740894
9	BCLAF1	chr1:215740366-215741262	GM12878	blood:	n/a	chr1:215740719-215740732 chr1:215740865-215740878 chr1:215741130-215741143 chr1:215740885-215740894
10	BCLAF1	chr1:215740328-215740960	K562	blood:	n/a	chr1:215740719-215740732 chr1:215740865-215740878 chr1:215740885-215740894
11	BHLHE40	chr1:215740502-215741201	GM12878	blood:	n/a	chr1:215740964-215740980
12	BHLHE40	chr1:215740115-215741532	K562	blood:	n/a	chr1:215740964-215740980
13	BRCA1	chr1:215740073-215740146	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr1:215721111-215721310	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr1:215740296-215740719	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr1:215740383-215740558	H1-hESC	embryonic stem cell:	n/a	n/a
17	CBX3	chr1:215728884-215729225	K562	blood:	n/a	n/a
18	CBX3	chr1:215733994-215734308	K562	blood:	n/a	n/a
19	CBX3	chr1:215728870-215729255	K562	blood:	n/a	n/a
20	CBX3	chr1:215741077-215741619	K562	blood:	n/a	n/a
21	CBX3	chr1:215740281-215740949	K562	blood:	n/a	n/a
22	CBX3	chr1:215742181-215743187	K562	blood:	n/a	n/a
23	CCNT2	chr1:215740373-215741290	K562	blood:	n/a	n/a
24	CEBPB	chr1:215741235-215741591	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr1:215716565-215716809	K562	blood:	n/a	n/a
26	CEBPB	chr1:215716442-215716859	MCF-7	breast:	n/a	n/a
27	CEBPB	chr1:215716505-215716831	A549	lung:	n/a	n/a
28	CEBPB	chr1:215716500-215716856	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:215741018-215741094	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr1:215740527-215740802	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr1:215716473-215716875	IMR90	lung:	n/a	n/a
32	CEBPB	chr1:215725518-215725587	A549	lung:	n/a	n/a
33	CEBPB	chr1:215716476-215716854	HepG2	liver:	n/a	n/a
34	CEBPB	chr1:215716610-215716770	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr1:215740197-215740562	A549	lung:	n/a	n/a
36	CEBPB	chr1:215740060-215740887	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr1:215732852-215733011	K562	blood:	n/a	n/a
38	CEBPB	chr1:215716522-215716806	HepG2	liver:	n/a	n/a
39	CEBPB	chr1:215740367-215740700	K562	blood:	n/a	n/a
40	CEBPB	chr1:215741097-215741591	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr1:215740158-215740868	MCF-7	breast:	n/a	n/a
42	CEBPB	chr1:215716505-215716972	HepG2	liver:	n/a	n/a
43	CEBPB	chr1:215714287-215714400	K562	blood:	n/a	chr1:215714357-215714368 chr1:215714357-215714370 chr1:215714359-215714368 chr1:215714359-215714368 chr1:215714357-215714368 chr1:215714359-215714368 chr1:215714359-215714368
44	CEBPD	chr1:215716532-215716765	HepG2	liver:	n/a	n/a
45	CEBPD	chr1:215740378-215741077	HepG2	liver:	n/a	n/a
46	CHD1	chr1:215742064-215742237	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr1:215741048-215741499	GM12878	blood:	n/a	n/a
48	CHD1	chr1:215739972-215741689	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr1:215741123-215741327	HepG2	liver:	n/a	n/a
50	CHD2	chr1:215740378-215741620	K562	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:215740424-215740474	ECC-1	luminal epithelium:	n/a
2	chr1:215737048-215737098	Hela-S3	cervix:	n/a
3	chr1:215741318-215741368	HepG2	liver:	n/a
4	chr1:215741182-215741232	A549	lung:	n/a
5	chr1:215741182-215741232	HepG2	liver:	n/a
6	chr1:215741843-215741893	LNCaP	prostate:	n/a
7	chr1:215737048-215737098	SKMC	muscle:	n/a
8	chr1:215740071-215740121	PFSK-1	brain:	n/a
9	chr1:215741182-215741232	SAEC	small airway:	n/a
10	chr1:215741843-215741893	Hepatocyte	liver:	n/a
11	chr1:215740071-215740121	HEEpiC	esophagus:	n/a
12	chr1:215737048-215737098	AG09309	skin:	n/a
13	chr1:215740071-215740121	HEK293	kidney:	embryo
14	chr1:215737048-215737098	A549	lung:	n/a
15	chr1:215741318-215741368	GM12892	blood:	n/a
16	chr1:215740701-215740751	HIPEpiC	eye:	n/a
17	chr1:215737048-215737098	HCPEpiC	choroid plexus:	n/a
18	chr1:215740424-215740474	GM06990	blood:	n/a
19	chr1:215740697-215740747	Caco-2	colon:	n/a
20	chr1:215740424-215740474	NHDF-neo	bronchial:	n/a
21	chr1:215740697-215740747	PFSK-1	brain:	n/a
22	chr1:215741182-215741232	LNCaP	prostate:	n/a
23	chr1:215740701-215740751	PANC-1	pancreas:	n/a
24	chr1:215741318-215741368	ovcar-3	ovarian:	n/a
25	chr1:215740701-215740751	SK-N-SH	brain:	n/a
26	chr1:215737048-215737098	GM06990	blood:	n/a
27	chr1:215740424-215740474	T-47D	breast:	n/a
28	chr1:215737048-215737098	ProgFib	skin:	n/a
29	chr1:215740697-215740747	HEK293	kidney:	embryo
30	chr1:215740424-215740474	HAEpiC	amniotic membrane:	n/a
31	chr1:215740697-215740747	HRCEpiC	kidney:	n/a
32	chr1:215741843-215741893	Caco-2	colon:	n/a
33	chr1:215741182-215741232	MCF-7	breast:	n/a
34	chr1:215741318-215741368	Caco-2	colon:	n/a
35	chr1:215741843-215741893	ECC-1	luminal epithelium:	n/a
36	chr1:215740424-215740474	HEEpiC	esophagus:	n/a
37	chr1:215741258-215741308	Jurkat	blood:	n/a
38	chr1:215740071-215740121	U87	brain:	n/a
39	chr1:215740424-215740474	K562	blood:	n/a
40	chr1:215740071-215740121	T-47D	breast:	n/a
41	chr1:215741318-215741368	T-47D	breast:	n/a
42	chr1:215741182-215741232	HPAEpiC	pulmonary alveolar:	n/a
43	chr1:215740071-215740121	Hepatocyte	liver:	n/a
44	chr1:215740071-215740121	H1-hESC	embryonic stem cell:	embryo
45	chr1:215740071-215740121	HIPEpiC	eye:	n/a
46	chr1:215737048-215737098	U87	brain:	n/a
47	chr1:215741318-215741368	BE2_C	brain:	n/a
48	chr1:215740424-215740474	IMR90	lung:	fetal
49	chr1:215740424-215740474	H1-hESC	embryonic stem cell:	embryo
50	chr1:215740697-215740747	GM12891	blood:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:215732968..215735499-chr1:215739364..215742165,4	MCF-7	breast:
2	chr1:215731051..215732589-chr1:215739123..215741939,2	MCF-7	breast:
3	chr1:215740857..215741766-chr12:7052939..7053914,2	Hela-S3	cervix:
4	chr1:215727802..215730014-chr1:215737556..215740283,2	K562	blood:
5	chr1:215727863..215730220-chr1:215736025..215738063,2	K562	blood:
6	chr1:215741634..215744285-chr1:215769987..215771958,3	K562	blood:
7	chr1:215739388..215743068-chr1:215745972..215749293,5	MCF-7	breast:
8	chr1:215727863..215730220-chr1:215736025..215738063,2	K562	blood:
9	chr1:215740395..215741072-chr11:62608879..62609640,2	Hela-S3	cervix:
10	chr1:215728975..215731835-chr1:215739008..215743111,5	MCF-7	breast:
11	chr1:215728115..215729776-chr1:215731286..215732796,2	MCF-7	breast:
12	chr1:215729059..215730729-chr1:215736109..215738919,2	MCF-7	breast:
13	chr1:215655508..215656065-chr1:215718108..215718963,2	MCF-7	breast:
14	chr1:215728115..215729776-chr1:215731286..215732796,2	MCF-7	breast:
15	chr1:215727846..215730896-chr1:215740314..215742858,4	K562	blood:
16	chr1:215740294..215741084-chr19:3985081..3985884,2	Hela-S3	cervix:
17	chr1:215727802..215730014-chr1:215737556..215740283,2	K562	blood:
18	chr1:215742124..215744108-chr1:215859791..215861523,2	K562	blood:
19	chr1:215722423..215724891-chr1:215740211..215742928,2	K562	blood:
20	chr1:215735916..215738873-chr1:215738967..215741974,4	MCF-7	breast:
21	chr1:215718496..215720254-chr1:215739655..215742103,3	MCF-7	breast:
22	chr1:215729059..215730729-chr1:215736109..215738919,2	MCF-7	breast:
23	chr1:215712013..215714709-chr1:215738982..215741822,3	MCF-7	breast:
24	chr1:215726004..215728201-chr1:215739965..215741596,2	MCF-7	breast:
25	chr1:215722423..215725926-chr1:215740211..215742928,3	K562	blood:
26	chr1:215711625..215715065-chr1:215739611..215743991,7	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USH2A-1	chr1:215740146-215740734	NONHSAT009473

No data

Variant related genes	Relation type
KCTD3	TF binding region
KCTD3	CpG island
ENSG00000238923	chromatin interactions
ENSG00000272173	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000136636	chromatin interactions
ENSG00000167658	chromatin interactions

Extended variants
information (count: 974 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:974 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138805649	chr1:215704675-215704676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs556481558	chr1:215704733-215704734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs74141274	chr1:215704759-215704760	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs192223160	chr1:215704835-215704836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555503246	chr1:215704864-215704865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572154461	chr1:215704902-215704903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77995738	chr1:215704918-215704919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564284962	chr1:215704930-215704931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577601879	chr1:215704935-215704936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs372538796	chr1:215704940-215704941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543442326	chr1:215704945-215704946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149365922	chr1:215704995-215704996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546713536	chr1:215711638-215711639	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs182102770	chr1:215711643-215711644	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs72739253	chr1:215711666-215711667	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs202083882	chr1:215711692-215711693	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs58682085	chr1:215711698-215711699	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs377467346	chr1:215711789-215711790	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs192493801	chr1:215711841-215711842	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs148041672	chr1:215711881-215711882	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs573525822	chr1:215711951-215711952	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs185056129	chr1:215711952-215711953	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs550594161	chr1:215711960-215711961	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs532919740	chr1:215711963-215711964	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs549482059	chr1:215711970-215711971	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs188297606	chr1:215712041-215712042	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs529132671	chr1:215712096-215712097	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs193058208	chr1:215712136-215712137	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs549715530	chr1:215712174-215712175	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs569423714	chr1:215712188-215712189	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs565533326	chr1:215712196-215712197	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs141726962	chr1:215712202-215712203	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs551442289	chr1:215712233-215712234	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs571625470	chr1:215712257-215712258	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs558028401	chr1:215712309-215712310	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs537570115	chr1:215712332-215712333	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs373319796	chr1:215712339-215712340	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs150540183	chr1:215712342-215712343	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs370258263	chr1:215712345-215712346	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs185242781	chr1:215712441-215712442	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs542127427	chr1:215712466-215712467	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs536542526	chr1:215712519-215712520	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs189679605	chr1:215712558-215712559	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs573458506	chr1:215712574-215712575	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs545644299	chr1:215712576-215712577	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs139500387	chr1:215712594-215712595	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs2797387	chr1:215712638-215712639	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs543510513	chr1:215712683-215712684	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs563088778	chr1:215712688-215712689	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs368466025	chr1:215712772-215712773	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	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
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
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:508 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215703000-215705000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr1:215704200-215704800	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr1:215712600-215716600	Enhancers	Rectal Smooth Muscle	rectum
4	chr1:215712600-215717000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr1:215712800-215714000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:215712800-215714000	Enhancers	Colon Smooth Muscle	Colon
7	chr1:215713000-215713800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:215713000-215713800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr1:215713000-215714000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr1:215713000-215714000	Enhancers	Muscle Satellite Cultured Cells	--
11	chr1:215713200-215713400	Bivalent Enhancer	HUVEC	blood vessel
12	chr1:215713200-215713600	Enhancers	Adipose Nuclei	Adipose
13	chr1:215713200-215713600	Enhancers	NHDF-Ad	bronchial
14	chr1:215713200-215713800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr1:215713200-215713800	Enhancers	Ovary	ovary
16	chr1:215713200-215713800	Enhancers	Pancreas	Pancrea
17	chr1:215713200-215713800	Enhancers	Psoas Muscle	Psoas
18	chr1:215713200-215714000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr1:215713200-215714000	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr1:215713200-215714000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr1:215713200-215714000	Enhancers	Spleen	Spleen
22	chr1:215713200-215714000	Enhancers	Osteobl	bone
23	chr1:215713400-215714000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:215713400-215714400	Enhancers	Fetal Brain Male	brain
25	chr1:215713600-215713800	Enhancers	Duodenum Smooth Muscle	Duodenum
26	chr1:215713600-215713800	Bivalent Enhancer	NHLF	lung
27	chr1:215713600-215716200	Weak transcription	Adipose Nuclei	Adipose
28	chr1:215713800-215716400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr1:215713800-215716400	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr1:215714000-215715000	Weak transcription	Colon Smooth Muscle	Colon
31	chr1:215714000-215716200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:215714000-215716200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr1:215714000-215716200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr1:215714000-215716200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr1:215714000-215716200	Weak transcription	Osteobl	bone
36	chr1:215714000-215716400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr1:215714200-215714400	Enhancers	Liver	Liver
38	chr1:215714600-215716000	Weak transcription	Liver	Liver
39	chr1:215715000-215715200	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr1:215715000-215715600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr1:215715000-215719600	Enhancers	Colon Smooth Muscle	Colon
42	chr1:215715200-215716600	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr1:215715800-215717200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:215716000-215717400	Enhancers	Liver	Liver
45	chr1:215716200-215716400	Enhancers	Fetal Intestine Small	intestine
46	chr1:215716200-215716400	Enhancers	GM12878-XiMat	blood
47	chr1:215716200-215716400	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr1:215716200-215716600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr1:215716200-215716800	Enhancers	Adipose Nuclei	Adipose
50	chr1:215716200-215717000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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