Variant report

Variant	nsv829781
Chromosome Location	chr3:163600633-163761895
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:640)
CpG islands
(count:429)
Chromatin interactive
region (count:32)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:640 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr3:163722192-163722316	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr3:163637042-163637289	K562	blood:	n/a	chr3:163637142-163637153
3	CEBPB	chr3:163637008-163637304	A549	lung:	n/a	chr3:163637142-163637153
4	CEBPB	chr3:163742739-163742774	A549	lung:	n/a	n/a
5	CEBPB	chr3:163636968-163637322	IMR90	lung:	n/a	chr3:163637142-163637153
6	CEBPB	chr3:163637047-163637323	H1-hESC	embryonic stem cell:	n/a	chr3:163637142-163637153
7	CEBPB	chr3:163636953-163637335	Hela-S3	cervix:	n/a	chr3:163637142-163637153
8	CEBPB	chr3:163636925-163637363	MCF-7	breast:	n/a	chr3:163637142-163637153
9	CEBPB	chr3:163636991-163637415	MCF-7	breast:	n/a	chr3:163637142-163637153
10	CEBPB	chr3:163651011-163651032	K562	blood:	n/a	n/a
11	CEBPB	chr3:163636959-163637331	HepG2	liver:	n/a	chr3:163637142-163637153
12	CEBPB	chr3:163632505-163632852	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr3:163657645-163657992	MCF-7	breast:	n/a	n/a
14	CEBPB	chr3:163650778-163651258	MCF-7	breast:	n/a	n/a
15	CEBPB	chr3:163722123-163722274	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr3:163722101-163722388	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr3:163669400-163669550	HMEC	breast:	n/a	n/a
18	CTCF	chr3:163722178-163722338	K562	blood:	n/a	chr3:163722244-163722257
19	CTCF	chr3:163634719-163634927	T-47D	breast:	n/a	n/a
20	CTCF	chr3:163669180-163669330	HAc	cerebellar:	n/a	n/a
21	CTCF	chr3:163669300-163669450	SK-N-SH_RA	brain:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
22	CTCF	chr3:163634660-163634810	GM12872	blood:	n/a	n/a
23	CTCF	chr3:163722126-163722337	K562	blood:	n/a	chr3:163722244-163722257
24	CTCF	chr3:163722180-163722330	Hela-S3	cervix:	n/a	chr3:163722244-163722257
25	CTCF	chr3:163669340-163669490	NB4	blood:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
26	CTCF	chr3:163669371-163669443	GM13976	blood:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
27	CTCF	chr3:163669284-163669503	Hela-S3	cervix:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
28	CTCF	chr3:163669256-163669535	Medullo	brain:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
29	CTCF	chr3:163657982-163658038	HepG2	liver:	n/a	n/a
30	CTCF	chr3:163669274-163669549	HCT-116	colon:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
31	CTCF	chr3:163609680-163609830	Caco-2	colon:	n/a	n/a
32	CTCF	chr3:163669300-163669450	Hela-S3	cervix:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
33	CTCF	chr3:163634760-163634910	GM06990	blood:	n/a	n/a
34	CTCF	chr3:163657900-163658050	RPTEC	kidney:	n/a	n/a
35	CTCF	chr3:163722140-163722290	GM12865	blood:	n/a	chr3:163722244-163722257
36	CTCF	chr3:163686000-163686150	GM12867	blood:	n/a	n/a
37	CTCF	chr3:163722200-163722350	K562	blood:	n/a	chr3:163722244-163722257
38	CTCF	chr3:163634700-163634850	GM12878	blood:	n/a	n/a
39	CTCF	chr3:163634700-163634850	HEK293	kidney:	n/a	n/a
40	CTCF	chr3:163609700-163609850	MCF-7	breast:	n/a	n/a
41	CTCF	chr3:163669320-163669470	GM12871	blood:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
42	CTCF	chr3:163657940-163658090	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:163634680-163634830	HepG2	liver:	n/a	n/a
44	CTCF	chr3:163657920-163658070	HCT-116	colon:	n/a	n/a
45	CTCF	chr3:163674920-163675175	Medullo	brain:	n/a	n/a
46	CTCF	chr3:163669305-163669483	GM12878	blood:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
47	CTCF	chr3:163634760-163634910	HCT-116	colon:	n/a	n/a
48	CTCF	chr3:163722040-163722190	HCT-116	colon:	n/a	n/a
49	CTCF	chr3:163669289-163669498	LNCaP	prostate:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
50	CTCF	chr3:163634519-163634968	HCT-116	colon:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:163719428-163719478	GM06990	blood:	n/a
2	chr3:163608814-163608864	GM06990	blood:	n/a
3	chr3:163719428-163719478	GM06990	blood:	n/a
4	chr3:163608814-163608864	GM06990	blood:	n/a
5	chr3:163719236-163719286	PrEC	prostate:	n/a
6	chr3:163722208-163722258	GM12891	blood:	n/a
7	chr3:163722294-163722344	PANC-1	pancreas:	n/a
8	chr3:163719428-163719478	HNPCEpiC	eye:	n/a
9	chr3:163722294-163722344	HL-60	blood:	n/a
10	chr3:163632090-163632140	BJ	skin:	n/a
11	chr3:163722208-163722258	HCT-116	colon:	n/a
12	chr3:163719236-163719286	U87	brain:	n/a
13	chr3:163719428-163719478	ovcar-3	ovarian:	n/a
14	chr3:163719428-163719478	NT2-D1	testis:	n/a
15	chr3:163719236-163719286	Hepatocyte	liver:	n/a
16	chr3:163632090-163632140	MCF-7	breast:	n/a
17	chr3:163719428-163719478	HEEpiC	esophagus:	n/a
18	chr3:163719428-163719478	Jurkat	blood:	n/a
19	chr3:163722051-163722101	HL-60	blood:	n/a
20	chr3:163719236-163719286	PANC-1	pancreas:	n/a
21	chr3:163722208-163722258	GM12878	blood:	n/a
22	chr3:163719428-163719478	K562	blood:	n/a
23	chr3:163608814-163608864	HUVEC	blood vessel:	n/a
24	chr3:163719236-163719286	RPTEC	kidney:	n/a
25	chr3:163632090-163632140	NB4	blood:	n/a
26	chr3:163719428-163719478	AG09319	gingival:	n/a
27	chr3:163719236-163719286	LNCaP	prostate:	n/a
28	chr3:163722208-163722258	A549	lung:	n/a
29	chr3:163608814-163608864	HCM	heart:	n/a
30	chr3:163719236-163719286	GM19239	blood:	n/a
31	chr3:163719428-163719478	ProgFib	skin:	n/a
32	chr3:163632090-163632140	GM06990	blood:	n/a
33	chr3:163722208-163722258	BE2_C	brain:	n/a
34	chr3:163722208-163722258	AG09309	skin:	n/a
35	chr3:163722051-163722101	U87	brain:	n/a
36	chr3:163632090-163632140	HNPCEpiC	eye:	n/a
37	chr3:163608814-163608864	BE2_C	brain:	n/a
38	chr3:163719428-163719478	A549	lung:	n/a
39	chr3:163632090-163632140	HEEpiC	esophagus:	n/a
40	chr3:163722051-163722101	CMK	blood:	n/a
41	chr3:163608814-163608864	SK-N-SH	brain:	n/a
42	chr3:163608814-163608864	ECC-1	luminal epithelium:	n/a
43	chr3:163719236-163719286	GM12892	blood:	n/a
44	chr3:163722051-163722101	HEEpiC	esophagus:	n/a
45	chr3:163722051-163722101	AG09319	gingival:	n/a
46	chr3:163632090-163632140	HPAEpiC	pulmonary alveolar:	n/a
47	chr3:163722208-163722258	AG04449	skin:	fetal
48	chr3:163722051-163722101	AG04449	skin:	fetal
49	chr3:163722294-163722344	CMK	blood:	n/a
50	chr3:163722051-163722101	SK-N-MC	brain:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:163639924..163641654-chr3:163663861..163665823,2	MCF-7	breast:
2	chr3:163639118..163640834-chr3:163641183..163642713,2	MCF-7	breast:
3	chr3:163660440..163662829-chr3:163666000..163668542,2	K562	blood:
4	chr3:163611385..163613477-chr3:163617466..163620081,2	K562	blood:
5	chr3:163741470..163744256-chr3:163747090..163749437,2	K562	blood:
6	chr3:163219408..163221189-chr3:163663438..163665910,2	K562	blood:
7	chr3:163669046..163669790-chr3:164903266..164903861,2	MCF-7	breast:
8	chr3:163660440..163662829-chr3:163666000..163668542,2	K562	blood:
9	chr3:163634067..163635345-chr3:163668973..163669822,4	MCF-7	breast:
10	chr3:163741470..163744256-chr3:163747090..163749437,2	K562	blood:
11	chr1:219388883..219389633-chr3:163652052..163652630,2	MCF-7	breast:
12	chr3:163689823..163692046-chr3:163703767..163706359,2	K562	blood:
13	chr3:163756511..163759205-chr3:163797731..163799263,2	MCF-7	breast:
14	chr3:163639118..163640834-chr3:163641183..163642713,2	MCF-7	breast:
15	chr3:163611385..163613477-chr3:163617466..163620081,2	K562	blood:
16	chr3:163759624..163761925-chr3:163765313..163767072,2	MCF-7	breast:
17	chr3:163674728..163675758-chr3:164903457..164904093,3	MCF-7	breast:
18	chr3:163664276..163666199-chr3:163667456..163669439,2	MCF-7	breast:
19	chr3:163664276..163666199-chr3:163667456..163669439,2	MCF-7	breast:
20	chr3:163738641..163741233-chr3:163742705..163744722,2	MCF-7	breast:
21	chr3:163676571..163679360-chr3:163699055..163700602,2	MCF-7	breast:
22	chr3:163497409..163497997-chr3:163668939..163669921,2	MCF-7	breast:
23	chr3:163503157..163504078-chr3:163634240..163634926,2	MCF-7	breast:
24	chr3:163738641..163741233-chr3:163742705..163744722,2	MCF-7	breast:
25	chr20:46012245..46013152-chr3:163614507..163615347,2	MCF-7	breast:
26	chr3:163674674..163675466-chr3:164524045..164524647,3	MCF-7	breast:
27	chr3:163676571..163679360-chr3:163699055..163700602,2	MCF-7	breast:
28	chr3:163639924..163641654-chr3:163663861..163665823,2	MCF-7	breast:
29	chr3:163647521..163649115-chr3:163652164..163654381,2	MCF-7	breast:
30	chr3:163689823..163692046-chr3:163703767..163706359,2	K562	blood:
31	chr3:163647521..163649115-chr3:163652164..163654381,2	MCF-7	breast:
32	chr3:163634067..163635345-chr3:163668973..163669822,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SI-6	chr3:163719394-163720253	NONHSAT093045

No data

Variant related genes	Relation type
ENSG00000214210	TF binding region
ENSG00000214210	CpG island

Extended variants
information (count: 3112 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3112 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375782825	chr3:163606666-163606667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574112905	chr3:163606667-163606668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs13095962	chr3:163606682-163606683	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs1881967	chr3:163606708-163606709	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs1907861	chr3:163606756-163606757	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs140068300	chr3:163606774-163606775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564063562	chr3:163606820-163606821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533036692	chr3:163606827-163606828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184690609	chr3:163606845-163606846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560083343	chr3:163606849-163606850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150308829	chr3:163606867-163606868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548810230	chr3:163606877-163606878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190074183	chr3:163606915-163606916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561041944	chr3:163606930-163606931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs377092630	chr3:163606966-163606967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568895485	chr3:163607008-163607009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1881968	chr3:163607022-163607023	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs551365595	chr3:163607072-163607073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561462270	chr3:163607094-163607095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144941218	chr3:163607129-163607130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191944544	chr3:163607156-163607157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs7648396	chr3:163607202-163607203	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs560840985	chr3:163607234-163607235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs16847343	chr3:163607266-163607267	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs556399134	chr3:163607296-163607297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34867972	chr3:163607453-163607454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs397991537	chr3:163607455-163607456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374078563	chr3:163607456-163607457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs367953383	chr3:163607457-163607458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149048096	chr3:163607513-163607514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs74988986	chr3:163607591-163607592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533861805	chr3:163607596-163607597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558513267	chr3:163607623-163607624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532334083	chr3:163607654-163607655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577558786	chr3:163607674-163607675	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540155671	chr3:163607702-163607703	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560350678	chr3:163607729-163607730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73876499	chr3:163607759-163607760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7626120	chr3:163607772-163607773	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs184273179	chr3:163607876-163607877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111757255	chr3:163607909-163607910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs4632546	chr3:163607960-163607961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368761205	chr3:163608041-163608042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553636958	chr3:163608045-163608046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569324983	chr3:163608138-163608139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536092015	chr3:163608139-163608140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372099731	chr3:163608177-163608178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531410921	chr3:163608188-163608189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201063504	chr3:163608291-163608292	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs375356306	chr3:163608319-163608320	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Sudden cardiac death	19188705	CNVD
Mantle cell lymphoma	19029149	CNVD
Malformation	19546859	CNVD
Schizophrenia	19546859	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Bladder cancer	21909424	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164919	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:163606600-163608400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:163606800-163607200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr3:163607200-163608200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr3:163608200-163608800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr3:163608200-163609000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr3:163608200-163609600	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr3:163608200-163610000	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr3:163608400-163609000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr3:163608400-163609000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr3:163608400-163609600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr3:163608600-163609000	Enhancers	H1 Cell Line	embryonic stem cell
12	chr3:163608800-163609000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:163610000-163611600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr3:163611600-163611800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr3:163615400-163615800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr3:163622000-163622200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr3:163622200-163623400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr3:163623400-163624600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr3:163623600-163624200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr3:163623800-163624400	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr3:163623800-163624600	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr3:163624200-163625200	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr3:163624400-163625800	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr3:163624600-163625200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr3:163625200-163625400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr3:163625200-163628400	Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr3:163625800-163626600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
28	chr3:163626200-163627000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
29	chr3:163626600-163627600	Active TSS	HUES6 Cell Line	embryonic stem cell
30	chr3:163627000-163631800	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr3:163627600-163631800	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr3:163627800-163631800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr3:163628200-163628400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
34	chr3:163628400-163629800	Transcr. at gene 5' and 3'	iPS-18 Cell Line	embryonic stem cell
35	chr3:163628400-163631800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr3:163629400-163629600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr3:163629600-163630200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr3:163629800-163631000	Active TSS	iPS-18 Cell Line	embryonic stem cell
39	chr3:163630200-163630800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr3:163630400-163630800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:163630600-163630800	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr3:163630800-163631800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:163630800-163631800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr3:163631000-163631800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr3:163631800-163632000	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr3:163631800-163632000	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr3:163631800-163632200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr3:163631800-163632200	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr3:163631800-163632200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr3:163631800-163632800	Enhancers	HUES6 Cell Line	embryonic stem cell

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