Variant report

Variant	nsv4766
Chromosome Location	chr1:227025954-227070961
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:773)
CpG islands
(count:855)
Chromatin interactive
region (count:25)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:773 , 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	ATF1	chr1:227063668-227063972	K562	blood:	n/a	n/a
2	ATF1	chr1:227057940-227058295	K562	blood:	n/a	n/a
3	ATF2	chr1:227070159-227070797	GM12878	blood:	n/a	n/a
4	ATF3	chr1:227057988-227058398	K562	blood:	n/a	chr1:227058187-227058196
5	ATF3	chr1:227063633-227064029	K562	blood:	n/a	n/a
6	BACH1	chr1:227057909-227058331	K562	blood:	n/a	n/a
7	BACH1	chr1:227057896-227058744	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr1:227063473-227063904	H1-hESC	embryonic stem cell:	n/a	chr1:227063806-227063820
9	BCL3	chr1:227068065-227068475	GM12878	blood:	n/a	n/a
10	BCL3	chr1:227068008-227068477	GM12878	blood:	n/a	n/a
11	BCLAF1	chr1:227070402-227070883	GM12878	blood:	n/a	chr1:227070558-227070567
12	BHLHE40	chr1:227060145-227060526	K562	blood:	n/a	n/a
13	BHLHE40	chr1:227057895-227059083	GM12878	blood:	n/a	chr1:227058884-227058897 chr1:227058689-227058705 chr1:227058385-227058401 chr1:227058559-227058575
14	BHLHE40	chr1:227058700-227059037	A549	lung:	n/a	chr1:227058884-227058897
15	BHLHE40	chr1:227070119-227070914	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:227063546-227064039	K562	blood:	n/a	n/a
17	BHLHE40	chr1:227058301-227059310	HepG2	liver:	n/a	chr1:227058884-227058897 chr1:227058689-227058705 chr1:227058385-227058401 chr1:227058559-227058575
18	BHLHE40	chr1:227057896-227059411	K562	blood:	n/a	chr1:227058884-227058897 chr1:227058689-227058705 chr1:227058385-227058401 chr1:227058559-227058575
19	BRCA1	chr1:227057790-227058505	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr1:227058551-227058644	GM12878	blood:	n/a	n/a
21	BRCA1	chr1:227058745-227058914	HepG2	liver:	n/a	n/a
22	CBX3	chr1:227057693-227058352	K562	blood:	n/a	n/a
23	CBX3	chr1:227063466-227064059	K562	blood:	n/a	n/a
24	CBX3	chr1:227058402-227058887	K562	blood:	n/a	n/a
25	CBX3	chr1:227057889-227058213	K562	blood:	n/a	n/a
26	CCNT2	chr1:227058077-227058973	K562	blood:	n/a	n/a
27	CEBPB	chr1:227053349-227054015	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:227063752-227063871	K562	blood:	n/a	n/a
29	CEBPB	chr1:227026411-227026732	HepG2	liver:	n/a	chr1:227026552-227026563
30	CEBPB	chr1:227026528-227026623	H1-hESC	embryonic stem cell:	n/a	chr1:227026552-227026563
31	CEBPB	chr1:227026215-227026729	Hela-S3	cervix:	n/a	chr1:227026552-227026563
32	CEBPB	chr1:227070369-227071147	GM12878	blood:	n/a	n/a
33	CEBPB	chr1:227058084-227058275	K562	blood:	n/a	n/a
34	CEBPB	chr1:227026476-227026701	K562	blood:	n/a	chr1:227026552-227026563
35	CEBPB	chr1:227057947-227058601	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:227039012-227039016	K562	blood:	n/a	n/a
37	CEBPB	chr1:227026391-227026746	A549	lung:	n/a	chr1:227026552-227026563
38	CEBPB	chr1:227052080-227052366	HepG2	liver:	n/a	n/a
39	CEBPB	chr1:227025751-227025957	Hela-S3	cervix:	n/a	n/a
40	CHD1	chr1:227033611-227033639	GM12878	blood:	n/a	n/a
41	CHD2	chr1:227057876-227058813	Hela-S3	cervix:	n/a	chr1:227058695-227058705
42	CHD2	chr1:227058322-227058624	GM12878	blood:	n/a	n/a
43	CHD2	chr1:227063866-227063870	HepG2	liver:	n/a	n/a
44	CHD2	chr1:227063676-227063978	K562	blood:	n/a	n/a
45	CHD2	chr1:227069840-227070874	GM12878	blood:	n/a	n/a
46	CHD2	chr1:227057977-227058825	K562	blood:	n/a	chr1:227058695-227058705
47	CREB1	chr1:227057900-227058698	HepG2	liver:	n/a	n/a
48	CREB1	chr1:227057793-227058578	K562	blood:	n/a	n/a
49	CREB1	chr1:227063606-227064014	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr1:227057896-227058709	A549	lung:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:227058070-227058120	T-47D	breast:	n/a
2	chr1:227058070-227058120	T-47D	breast:	n/a
3	chr1:227058905-227058955	GM12891	blood:	n/a
4	chr1:227058070-227058120	HRE	kidney:	n/a
5	chr1:227051345-227051395	Caco-2	colon:	n/a
6	chr1:227058595-227058645	Hela-S3	cervix:	n/a
7	chr1:227059109-227059159	GM12878	blood:	n/a
8	chr1:227058941-227058991	U87	brain:	n/a
9	chr1:227059463-227059513	Hela-S3	cervix:	n/a
10	chr1:227051345-227051395	HEEpiC	esophagus:	n/a
11	chr1:227061009-227061059	HCF	heart:	n/a
12	chr1:227051345-227051395	Jurkat	blood:	n/a
13	chr1:227059109-227059159	HUVEC	blood vessel:	n/a
14	chr1:227056896-227056946	U87	brain:	n/a
15	chr1:227058905-227058955	NH-A	brain:	n/a
16	chr1:227058426-227058476	NT2-D1	testis:	n/a
17	chr1:227058905-227058955	PANC-1	pancreas:	n/a
18	chr1:227058941-227058991	GM19239	blood:	n/a
19	chr1:227058754-227058804	HEK293	kidney:	embryo
20	chr1:227058070-227058120	AG09309	skin:	n/a
21	chr1:227058754-227058804	PrEC	prostate:	n/a
22	chr1:227056896-227056946	K562	blood:	n/a
23	chr1:227051345-227051395	NT2-D1	testis:	n/a
24	chr1:227061009-227061059	GM06990	blood:	n/a
25	chr1:227061009-227061059	BE2_C	brain:	n/a
26	chr1:227051345-227051395	HRPEpiC	eye:	n/a
27	chr1:227058070-227058120	HEEpiC	esophagus:	n/a
28	chr1:227061009-227061059	HRE	kidney:	n/a
29	chr1:227058070-227058120	ovcar-3	ovarian:	n/a
30	chr1:227058046-227058096	GM06990	blood:	n/a
31	chr1:227056896-227056946	Caco-2	colon:	n/a
32	chr1:227059109-227059159	MCF10A-Er-Src	breast:	n/a
33	chr1:227058046-227058096	HEK293	kidney:	embryo
34	chr1:227056896-227056946	SK-N-SH	brain:	n/a
35	chr1:227070630-227070680	AG04450	lung:	fetal
36	chr1:227058070-227058120	GM12891	blood:	n/a
37	chr1:227058426-227058476	ovcar-3	ovarian:	n/a
38	chr1:227056896-227056946	PFSK-1	brain:	n/a
39	chr1:227058046-227058096	Jurkat	blood:	n/a
40	chr1:227058426-227058476	PrEC	prostate:	n/a
41	chr1:227059109-227059159	GM19239	blood:	n/a
42	chr1:227061009-227061059	ovcar-3	ovarian:	n/a
43	chr1:227058426-227058476	GM06990	blood:	n/a
44	chr1:227054129-227054179	BE2_C	brain:	n/a
45	chr1:227058595-227058645	PFSK-1	brain:	n/a
46	chr1:227058046-227058096	H1-hESC	embryonic stem cell:	embryo
47	chr1:227059109-227059159	PFSK-1	brain:	n/a
48	chr1:227058426-227058476	BE2_C	brain:	n/a
49	chr1:227058941-227058991	NH-A	brain:	n/a
50	chr1:227070630-227070680	AG09319	gingival:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:227062873..227064895-chr1:227127991..227129793,2	K562	blood:
2	chr1:227063913..227065661-chr1:227075217..227077074,2	MCF-7	breast:
3	chr1:227063385..227063950-chr11:76463692..76464295,2	Hela-S3	cervix:
4	chr1:227044580..227047261-chr1:227056474..227058125,2	MCF-7	breast:
5	chr1:226830168..226832886-chr1:227064468..227067080,2	K562	blood:
6	chr1:227031005..227032884-chr1:227503623..227506611,2	MCF-7	breast:
7	chr1:227058393..227060106-chr1:227070481..227073137,2	MCF-7	breast:
8	chr1:227022576..227024779-chr1:227029976..227031514,2	K562	blood:
9	chr1:227061527..227064235-chr1:227072734..227074353,2	K562	blood:
10	chr1:227044512..227048863-chr1:227049496..227051817,3	K562	blood:
11	chr1:227057812..227060402-chr1:227061799..227065310,4	MCF-7	breast:
12	chr1:227051915..227054203-chr1:227056473..227058361,2	K562	blood:
13	chr1:227045661..227048469-chr1:227054532..227056179,2	K562	blood:
14	chr1:227063874..227066086-chr1:227080166..227082122,2	K562	blood:
15	chr1:227056972..227060781-chr1:227061022..227064648,10	MCF-7	breast:
16	chr1:227068805..227071011-chr1:227076122..227078773,2	K562	blood:
17	chr1:227045661..227048469-chr1:227054532..227056179,2	K562	blood:
18	chr1:227060695..227062412-chr1:227077367..227078940,2	MCF-7	breast:
19	chr1:227058010..227060717-chr1:227127922..227130467,2	K562	blood:
20	chr1:227067713..227070080-chr1:227071671..227073358,2	K562	blood:
21	chr1:227044512..227048863-chr1:227049496..227051817,3	K562	blood:
22	chr1:227045661..227050211-chr1:227053920..227059739,5	K562	blood:
23	chr1:227064075..227066855-chr1:227067871..227070259,4	MCF-7	breast:
24	chr1:227058393..227060106-chr1:227070481..227073137,2	MCF-7	breast:
25	chr1:227063887..227066680-chr1:227122260..227124831,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADCK3-4	chr1:227063066-227063253	NONHSAT009905
2	lnc-CDC42BPA-3	chr1:227049124-227049418	NONHSAT009904
3	lnc-ADCK3-4	chr1:227058564-227059105	NONHSAT009905
4	lnc-CDC42BPA-3	chr1:227058063-227058176	NONHSAT009904

No data

Variant related genes	Relation type
PSEN2	TF binding region
PSEN2	CpG island
ENSG00000163050	chromatin interactions
ENSG00000143801	chromatin interactions
ENSG00000143776	chromatin interactions

Extended variants
information (count: 1681 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1681 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548833912	chr1:227025968-227025969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs552586683	chr1:227025971-227025972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs562018313	chr1:227025988-227025989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184335706	chr1:227026091-227026092	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs370385329	chr1:227026096-227026097	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs528457178	chr1:227026098-227026099	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs547095182	chr1:227026100-227026101	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs568183108	chr1:227026121-227026122	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs529064955	chr1:227026122-227026123	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs527843991	chr1:227026129-227026130	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs116345057	chr1:227026130-227026131	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs188714830	chr1:227026200-227026201	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs539759468	chr1:227026211-227026212	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs531078878	chr1:227026226-227026227	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs114243238	chr1:227026227-227026228	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs566491316	chr1:227026229-227026230	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs143564481	chr1:227026297-227026298	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs372977735	chr1:227026367-227026368	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs555516632	chr1:227026447-227026448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573736157	chr1:227026476-227026477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs180684948	chr1:227026500-227026501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377307054	chr1:227026509-227026510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs557630025	chr1:227026568-227026569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575733564	chr1:227026577-227026578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs546504402	chr1:227026644-227026645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185402993	chr1:227026672-227026673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528505124	chr1:227026739-227026740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138108778	chr1:227026755-227026756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190503004	chr1:227026833-227026834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182263821	chr1:227026856-227026857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550649049	chr1:227026877-227026878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs74139838	chr1:227026893-227026894	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs532958549	chr1:227026982-227026983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551675965	chr1:227026989-227026990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142474726	chr1:227026993-227026994	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533791964	chr1:227027036-227027037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375250694	chr1:227027110-227027111	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs66867464	chr1:227027159-227027160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs58062683	chr1:227027166-227027167	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs146468072	chr1:227027173-227027174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556273380	chr1:227027219-227027220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575818942	chr1:227027286-227027287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139061730	chr1:227027295-227027296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12733650	chr1:227027304-227027305	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs573412570	chr1:227027313-227027314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs71179176	chr1:227027346-227027347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186886485	chr1:227027422-227027423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs375110790	chr1:227027436-227027437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561784334	chr1:227027444-227027445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191784560	chr1:227027473-227027474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
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
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
Breast cancer	17603634	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
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1314 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227024600-227026000	Enhancers	Hela-S3	cervix
2	chr1:227025400-227026800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
3	chr1:227025600-227027200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr1:227025800-227026600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr1:227025800-227026800	Enhancers	HMEC	breast
6	chr1:227025800-227027400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr1:227026000-227026400	Enhancers	H9 Cell Line	embryonic stem cell
8	chr1:227026000-227026400	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr1:227026000-227026400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:227026000-227026400	Flanking Active TSS	Hela-S3	cervix
11	chr1:227026000-227026600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr1:227026000-227026600	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr1:227026000-227026800	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr1:227026000-227027000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr1:227026200-227026600	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr1:227026200-227026600	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr1:227026200-227026600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr1:227026200-227026800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr1:227026400-227026800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr1:227026400-227027000	Enhancers	Hela-S3	cervix
21	chr1:227026600-227028000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr1:227026800-227034200	Weak transcription	HMEC	breast
23	chr1:227026800-227043800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr1:227027000-227034400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr1:227028000-227034200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:227033000-227034800	Enhancers	GM12878-XiMat	blood
27	chr1:227034200-227034800	Enhancers	Thymus	Thymus
28	chr1:227034200-227035000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr1:227034200-227035000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:227034200-227035000	Enhancers	HMEC	breast
31	chr1:227034200-227035200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:227034200-227035400	Enhancers	NHEK	skin
33	chr1:227034400-227034800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:227034400-227035200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr1:227034600-227035000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr1:227034800-227035000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr1:227034800-227035200	Enhancers	NHDF-Ad	bronchial
38	chr1:227035000-227036600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr1:227035000-227039800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr1:227035800-227036000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr1:227035800-227036200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr1:227035800-227036600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr1:227035800-227037600	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr1:227035800-227037600	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr1:227036000-227037000	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr1:227036000-227037200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr1:227036200-227037200	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr1:227036400-227037200	Enhancers	H1 Cell Line	embryonic stem cell
49	chr1:227036600-227036800	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr1:227036600-227037000	Weak transcription	HUES64 Cell Line	embryonic stem cell

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