Variant report

Variant	nsv1061762
Chromosome Location	chr16:70960990-71025438
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:996)
CpG islands
(count:427)
Chromatin interactive
region (count:79)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:996 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:70961655-70961897	K562	blood:	n/a	n/a
2	ARID3A	chr16:71021049-71021536	K562	blood:	n/a	n/a
3	ARID3A	chr16:70971786-70971832	HepG2	liver:	n/a	n/a
4	ATF1	chr16:70980043-70980287	K562	blood:	n/a	n/a
5	ATF1	chr16:70987738-70988064	K562	blood:	n/a	n/a
6	ATF1	chr16:70992165-70992287	K562	blood:	n/a	n/a
7	ATF1	chr16:71021180-71021685	K562	blood:	n/a	n/a
8	ATF1	chr16:70977109-70977159	K562	blood:	n/a	n/a
9	ATF1	chr16:70990674-70991056	K562	blood:	n/a	n/a
10	ATF2	chr16:70987603-70988175	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr16:71021188-71021575	K562	blood:	n/a	n/a
12	BACH1	chr16:71021074-71021564	K562	blood:	n/a	n/a
13	BACH1	chr16:71020996-71021702	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr16:70969729-70969731	K562	blood:	n/a	n/a
15	BATF	chr16:70963263-70963562	GM12878	blood:	n/a	n/a
16	BCL3	chr16:70973768-70974260	GM12878	blood:	n/a	chr16:70974079-70974088
17	BCL3	chr16:70973830-70974232	GM12878	blood:	n/a	chr16:70974079-70974088
18	BCL3	chr16:70976321-70976732	GM12878	blood:	n/a	n/a
19	BCL3	chr16:70983386-70983627	GM12878	blood:	n/a	n/a
20	BCL3	chr16:70976273-70976645	GM12878	blood:	n/a	n/a
21	BHLHE40	chr16:71002389-71002555	K562	blood:	n/a	n/a
22	BHLHE40	chr16:70976497-70976604	K562	blood:	n/a	n/a
23	BHLHE40	chr16:71019095-71019184	GM12878	blood:	n/a	n/a
24	BHLHE40	chr16:70997563-70997637	K562	blood:	n/a	n/a
25	BRCA1	chr16:70969309-70969497	HepG2	liver:	n/a	n/a
26	BRCA1	chr16:70961522-70961526	GM12878	blood:	n/a	n/a
27	BRCA1	chr16:70969488-70969516	GM12878	blood:	n/a	n/a
28	BRCA1	chr16:71018809-71018825	GM12878	blood:	n/a	n/a
29	BRCA1	chr16:70992799-70992823	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr16:71020905-71021711	HCT-116	colon:	n/a	n/a
31	CBX3	chr16:71020755-71021807	HCT-116	colon:	n/a	n/a
32	CEBPB	chr16:71024636-71024962	A549	lung:	n/a	chr16:71024787-71024800 chr16:71024787-71024798
33	CEBPB	chr16:70991449-70991788	MCF-7	breast:	n/a	chr16:70991555-70991566
34	CEBPB	chr16:71021170-71021547	Hela-S3	cervix:	n/a	chr16:71021201-71021212
35	CEBPB	chr16:70991397-70991750	A549	lung:	n/a	chr16:70991555-70991566
36	CEBPB	chr16:70991479-70991717	H1-hESC	embryonic stem cell:	n/a	chr16:70991555-70991566
37	CEBPB	chr16:71024779-71024825	H1-hESC	embryonic stem cell:	n/a	chr16:71024787-71024800 chr16:71024787-71024798
38	CEBPB	chr16:70967927-70967947	A549	lung:	n/a	n/a
39	CEBPB	chr16:71024603-71024953	K562	blood:	n/a	chr16:71024787-71024800 chr16:71024787-71024798
40	CEBPB	chr16:71024619-71024968	HepG2	liver:	n/a	chr16:71024787-71024800 chr16:71024787-71024798
41	CEBPB	chr16:70991389-70991726	K562	blood:	n/a	chr16:70991555-70991566
42	CEBPB	chr16:70991383-70991727	IMR90	lung:	n/a	chr16:70991555-70991566
43	CEBPB	chr16:70991383-70991750	Hela-S3	cervix:	n/a	chr16:70991555-70991566
44	CEBPB	chr16:70991380-70991739	HepG2	liver:	n/a	chr16:70991555-70991566
45	CEBPB	chr16:71024619-71024968	IMR90	lung:	n/a	chr16:71024787-71024800 chr16:71024787-71024798
46	CEBPB	chr16:71012868-71013089	A549	lung:	n/a	n/a
47	CHD2	chr16:70976345-70976351	K562	blood:	n/a	n/a
48	CHD2	chr16:71019239-71019275	K562	blood:	n/a	n/a
49	CHD2	chr16:70973978-70974178	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr16:71020911-71021155	K562	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:71011407-71011457	AG04450	lung:	fetal
2	chr16:71009778-71009828	PANC-1	pancreas:	n/a
3	chr16:71008732-71008782	HCT-116	colon:	n/a
4	chr16:71011407-71011457	HEK293	kidney:	embryo
5	chr16:70967321-70967371	GM12878	blood:	n/a
6	chr16:71008063-71008113	HCPEpiC	choroid plexus:	n/a
7	chr16:71008063-71008113	HAEpiC	amniotic membrane:	n/a
8	chr16:71008063-71008113	HCT-116	colon:	n/a
9	chr16:71011407-71011457	HCT-116	colon:	n/a
10	chr16:70967321-70967371	IMR90	lung:	fetal
11	chr16:71008050-71008100	SK-N-MC	brain:	n/a
12	chr16:71008454-71008504	PFSK-1	brain:	n/a
13	chr16:71008732-71008782	K562	blood:	n/a
14	chr16:70967321-70967371	AoSMC	blood vessel:	n/a
15	chr16:71008454-71008504	H1-hESC	embryonic stem cell:	embryo
16	chr16:71009778-71009828	PrEC	prostate:	n/a
17	chr16:71009778-71009828	K562	blood:	n/a
18	chr16:71009778-71009828	ovcar-3	ovarian:	n/a
19	chr16:71008050-71008100	HNPCEpiC	eye:	n/a
20	chr16:71011407-71011457	K562	blood:	n/a
21	chr16:71011407-71011457	GM12892	blood:	n/a
22	chr16:71008732-71008782	ECC-1	luminal epithelium:	n/a
23	chr16:71009778-71009828	NH-A	brain:	n/a
24	chr16:70967321-70967371	HAEpiC	amniotic membrane:	n/a
25	chr16:70967321-70967371	AG09309	skin:	n/a
26	chr16:71008454-71008504	HMEC	breast:	n/a
27	chr16:71008732-71008782	GM12891	blood:	n/a
28	chr16:70967321-70967371	ProgFib	skin:	n/a
29	chr16:71008063-71008113	HUVEC	blood vessel:	n/a
30	chr16:71008050-71008100	ProgFib	skin:	n/a
31	chr16:71008050-71008100	HCM	heart:	n/a
32	chr16:70967321-70967371	HRE	kidney:	n/a
33	chr16:71008454-71008504	NB4	blood:	n/a
34	chr16:71008454-71008504	AG09319	gingival:	n/a
35	chr16:71008732-71008782	PFSK-1	brain:	n/a
36	chr16:71009778-71009828	HEEpiC	esophagus:	n/a
37	chr16:71011407-71011457	HepG2	liver:	n/a
38	chr16:71008732-71008782	MCF-7	breast:	n/a
39	chr16:70967321-70967371	A549	lung:	n/a
40	chr16:71008050-71008100	CMK	blood:	n/a
41	chr16:71011407-71011457	HMEC	breast:	n/a
42	chr16:71008454-71008504	NH-A	brain:	n/a
43	chr16:71008732-71008782	HRCEpiC	kidney:	n/a
44	chr16:70967321-70967371	PANC-1	pancreas:	n/a
45	chr16:71008732-71008782	HPAEpiC	pulmonary alveolar:	n/a
46	chr16:71008050-71008100	GM19239	blood:	n/a
47	chr16:71008454-71008504	HCF	heart:	n/a
48	chr16:70967321-70967371	AG09319	gingival:	n/a
49	chr16:70967321-70967371	Caco-2	colon:	n/a
50	chr16:71011407-71011457	Caco-2	colon:	n/a

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:71018662..71021748-chr16:71021953..71025067,5	MCF-7	breast:
2	chr1:146551738..146553728-chr16:71003126..71004713,2	K562	blood:
3	chr1:146554622..146556451-chr16:70987348..70989369,2	K562	blood:
4	chr16:70961723..70963824-chr16:70975853..70978413,2	K562	blood:
5	chr16:70988936..70990480-chr16:71001097..71003483,2	MCF-7	breast:
6	chr1:146712973..146714848-chr16:71024751..71027232,2	K562	blood:
7	chr16:70988936..70990480-chr16:71001097..71003483,2	MCF-7	breast:
8	chr16:71021881..71024065-chr16:71024703..71026242,2	MCF-7	breast:
9	chr16:71016847..71019528-chr16:71019803..71022593,2	K562	blood:
10	chr16:71015461..71020683-chr16:71023504..71027533,5	K562	blood:
11	chr16:71001935..71005265-chr16:71019285..71021480,3	MCF-7	breast:
12	chr16:71016144..71018459-chr16:71020187..71022011,2	MCF-7	breast:
13	chr16:70998254..71000264-chr16:71012369..71014034,2	MCF-7	breast:
14	chr16:70984290..70985826-chr16:70990032..70992588,2	K562	blood:
15	chr16:70975629..70978329-chr16:70983065..70987137,4	MCF-7	breast:
16	chr16:70987273..70988975-chr16:70994599..70997050,2	K562	blood:
17	chr16:70984290..70985826-chr16:70990032..70992588,2	K562	blood:
18	chr1:146553166..146555205-chr16:71012392..71014067,2	K562	blood:
19	chr16:70969502..70971128-chr16:70977170..70980144,2	K562	blood:
20	chr16:71015461..71020683-chr16:71023504..71027533,5	K562	blood:
21	chr16:70993038..70996024-chr16:70999635..71003501,3	MCF-7	breast:
22	chr16:70975629..70978329-chr16:70983065..70987137,4	MCF-7	breast:
23	chr16:71016144..71018459-chr16:71020187..71022011,2	MCF-7	breast:
24	chr16:70973640..70974283-chr16:71001999..71002517,2	MCF-7	breast:
25	chr16:70975665..70976544-chr16:71002234..71002996,4	MCF-7	breast:
26	chr16:70974977..70976783-chr16:70983975..70986129,4	K562	blood:
27	chr16:71022061..71023931-chr16:71025665..71027702,2	K562	blood:
28	chr16:70969502..70971128-chr16:70977170..70980144,2	K562	blood:
29	chr1:146555062..146557093-chr16:71013791..71016169,2	K562	blood:
30	chr16:70974977..70976783-chr16:70984340..70986129,3	K562	blood:
31	chr16:71016847..71019528-chr16:71019803..71022593,2	K562	blood:
32	chr16:71012994..71015519-chr16:71016139..71019048,3	K562	blood:
33	chr16:70964598..70966450-chr16:70970669..70972869,2	K562	blood:
34	chr16:70973270..70974820-chr16:70975145..70976849,2	K562	blood:
35	chr16:70989001..70991561-chr16:71001327..71004060,2	K562	blood:
36	chr16:71012907..71014525-chr16:71017910..71020041,2	MCF-7	breast:
37	chr16:71018902..71020683-chr16:71024263..71026975,2	K562	blood:
38	chr16:71004902..71006542-chr16:71008221..71010075,2	MCF-7	breast:
39	chr16:71001861..71002521-chr4:43883310..43883810,2	MCF-7	breast:
40	chr16:70939686..70942468-chr16:70993534..70995760,3	MCF-7	breast:
41	chr16:70988681..70989466-chr16:71391903..71392654,2	MCF-7	breast:
42	chr16:70978242..70980847-chr16:70987111..70991166,3	MCF-7	breast:
43	chr16:70998731..71000452-chr16:71002285..71005126,2	K562	blood:
44	chr16:71021881..71024065-chr16:71024703..71026242,2	MCF-7	breast:
45	chr1:146553932..146556565-chr16:70965325..70968195,2	K562	blood:
46	chr16:70961723..70963824-chr16:70975853..70978413,2	K562	blood:
47	chr16:70988569..70989071-chr16:71392095..71392758,2	MCF-7	breast:
48	chr1:121484930..121485886-chr16:70961464..70962432,2	MCF-7	breast:
49	chr16:71019839..71022639-chr16:71314110..71316674,2	K562	blood:
50	chr16:71009810..71011533-chr16:71011886..71014440,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL34-4	chr16:71017348-71020288	ucscGeneNc_uc002fch_1
2	lnc-CALB2-4	chr16:71020753-71021463	ucscGeneNc_uc002fci_1

No data

Variant related genes	Relation type
HYDIN	TF binding region
HYDIN	CpG island
ENSG00000260593	chromatin interactions
ENSG00000131781	chromatin interactions
ENSG00000230832	chromatin interactions
ENSG00000131778	chromatin interactions
ENSG00000172137	chromatin interactions
ENSG00000157423	chromatin interactions
ENSG00000140832	chromatin interactions

Extended variants
information (count: 2480 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2480 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2502714	chr16:70960990-70960991	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs534457644	chr16:70961029-70961030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552843869	chr16:70961118-70961119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369253652	chr16:70961171-70961172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544938169	chr16:70961173-70961174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1798414	chr16:70961182-70961183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557242033	chr16:70961215-70961216	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575634897	chr16:70961228-70961229	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543821357	chr16:70961232-70961233	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562113766	chr16:70961288-70961289	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529362717	chr16:70961301-70961302	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541548985	chr16:70961336-70961337	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372690742	chr16:70961406-70961407	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112258350	chr16:70961417-70961418	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574652685	chr16:70961463-70961464	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs59757138	chr16:70961510-70961511	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2135004	chr16:70961545-70961546	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs1798412	chr16:70961557-70961558	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs1798411	chr16:70961595-70961596	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1819724	chr16:70961631-70961632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1818199	chr16:70961664-70961665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184674961	chr16:70961671-70961672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533597190	chr16:70961679-70961680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551716142	chr16:70961681-70961682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570313402	chr16:70961713-70961714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs1798410	chr16:70961747-70961748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs61482142	chr16:70961756-70961757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188119790	chr16:70961770-70961771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369874778	chr16:70961771-70961772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1798409	chr16:70961778-70961779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112904817	chr16:70961808-70961809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548565998	chr16:70961831-70961832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543719982	chr16:70961844-70961845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201801378	chr16:70961856-70961857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566925495	chr16:70961858-70961859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560282012	chr16:70961864-70961865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201070029	chr16:70961865-70961866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200907681	chr16:70961872-70961873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112363132	chr16:70961873-70961874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546688324	chr16:70961880-70961881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2968371	chr16:70961883-70961884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs57186604	chr16:70961911-70961912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571324155	chr16:70962023-70962024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538802414	chr16:70962081-70962082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556908762	chr16:70962095-70962096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373200229	chr16:70962112-70962113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575610133	chr16:70962155-70962156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536557382	chr16:70962158-70962159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs11075822	chr16:70962179-70962180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs60027628	chr16:70962185-70962186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
small cell lung cancer	20016488	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	18923524	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:898 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70952600-70973000	Weak transcription	Fetal Intestine Small	intestine
2	chr16:70956200-70961200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:70956200-70969200	Weak transcription	Fetal Brain Female	brain
4	chr16:70956400-70964800	Weak transcription	Brain Substantia Nigra	brain
5	chr16:70956400-70970600	Weak transcription	Brain Cingulate Gyrus	brain
6	chr16:70956600-70961200	Weak transcription	Colon Smooth Muscle	Colon
7	chr16:70956600-70970600	Weak transcription	Brain Angular Gyrus	brain
8	chr16:70956600-70970800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr16:70956800-70966800	Weak transcription	Brain Anterior Caudate	brain
10	chr16:70957000-70971800	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr16:70958800-70966600	Weak transcription	Brain Germinal Matrix	brain
12	chr16:70961200-70961600	Enhancers	H1 Cell Line	embryonic stem cell
13	chr16:70961200-70961600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr16:70961400-70961600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr16:70961400-70961600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr16:70961600-70965200	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr16:70961800-70967200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr16:70963200-70963400	Enhancers	GM12878-XiMat	blood
19	chr16:70963200-70965400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr16:70963200-70966200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr16:70963400-70963600	Bivalent Enhancer	Colonic Mucosa	Colon
22	chr16:70963400-70963600	Flanking Active TSS	GM12878-XiMat	blood
23	chr16:70963400-70963800	Enhancers	Esophagus	oesophagus
24	chr16:70963600-70963800	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr16:70963600-70963800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr16:70963600-70963800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
27	chr16:70963600-70964600	Enhancers	GM12878-XiMat	blood
28	chr16:70963800-70965400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr16:70963800-70967000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr16:70963800-70967000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr16:70963800-70970400	Weak transcription	Fetal Brain Male	brain
32	chr16:70964600-70965000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr16:70964600-70965200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr16:70964600-70965200	Enhancers	NHDF-Ad	bronchial
35	chr16:70964600-70965400	Enhancers	Osteobl	bone
36	chr16:70965200-70965400	Enhancers	H9 Cell Line	embryonic stem cell
37	chr16:70965200-70965400	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr16:70965200-70965600	Enhancers	H1 Cell Line	embryonic stem cell
39	chr16:70965400-70966000	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr16:70965400-70966000	Weak transcription	NHDF-Ad	bronchial
41	chr16:70965600-70966400	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr16:70965600-70966400	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr16:70966000-70968200	Enhancers	H9 Cell Line	embryonic stem cell
44	chr16:70966200-70967400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr16:70966200-70968000	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr16:70966200-70968200	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr16:70966200-70968200	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr16:70966200-70968200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr16:70966200-70968400	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr16:70966400-70966800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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