Variant report

Variant	nsv470439
Chromosome Location	chr3:17394615-17538921
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1191)
CpG islands
(count:0)
Chromatin interactive
region (count:76)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1191 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:17472416-17472770	K562	blood:	n/a	n/a
2	ARID3A	chr3:17506407-17506512	K562	blood:	n/a	n/a
3	ARID3A	chr3:17414297-17414619	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:17484122-17484922	K562	blood:	n/a	n/a
5	ARID3A	chr3:17486399-17486776	K562	blood:	n/a	n/a
6	ARID3A	chr3:17462080-17462754	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:17454500-17454738	HepG2	liver:	n/a	n/a
8	ATF1	chr3:17520229-17520516	K562	blood:	n/a	n/a
9	ATF1	chr3:17486434-17486698	K562	blood:	n/a	n/a
10	ATF1	chr3:17472550-17472822	K562	blood:	n/a	n/a
11	ATF1	chr3:17484669-17484932	K562	blood:	n/a	n/a
12	ATF1	chr3:17410725-17410748	K562	blood:	n/a	n/a
13	ATF1	chr3:17484018-17484387	K562	blood:	n/a	n/a
14	ATF2	chr3:17440604-17441083	GM12878	blood:	n/a	n/a
15	ATF2	chr3:17440529-17441152	GM12878	blood:	n/a	n/a
16	ATF3	chr3:17520058-17520526	A549	lung:	n/a	n/a
17	ATF3	chr3:17484191-17484365	K562	blood:	n/a	n/a
18	ATF3	chr3:17486331-17486754	K562	blood:	n/a	n/a
19	ATF3	chr3:17520011-17520619	A549	lung:	n/a	n/a
20	ATF3	chr3:17484214-17484440	K562	blood:	n/a	n/a
21	BACH1	chr3:17473755-17474077	H1-hESC	embryonic stem cell:	n/a	chr3:17473906-17473920
22	BACH1	chr3:17473751-17474065	K562	blood:	n/a	chr3:17473906-17473920
23	BACH1	chr3:17474299-17474445	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr3:17440687-17441050	GM12878	blood:	n/a	n/a
25	BATF	chr3:17440584-17441027	GM12878	blood:	n/a	n/a
26	BCL11A	chr3:17440655-17441034	GM12878	blood:	n/a	chr3:17440792-17440801
27	BCL11A	chr3:17440636-17441099	GM12878	blood:	n/a	chr3:17440792-17440801
28	BCL3	chr3:17520027-17520714	A549	lung:	n/a	n/a
29	BCLAF1	chr3:17440619-17441234	GM12878	blood:	n/a	chr3:17440792-17440801
30	BCLAF1	chr3:17440538-17441322	GM12878	blood:	n/a	chr3:17440792-17440801
31	BHLHE40	chr3:17428087-17428202	K562	blood:	n/a	n/a
32	BHLHE40	chr3:17484668-17485011	K562	blood:	n/a	n/a
33	BHLHE40	chr3:17462222-17462436	K562	blood:	n/a	n/a
34	BHLHE40	chr3:17440644-17441042	GM12878	blood:	n/a	n/a
35	BHLHE40	chr3:17462223-17462521	HepG2	liver:	n/a	n/a
36	BHLHE40	chr3:17520199-17520344	HepG2	liver:	n/a	n/a
37	BRCA1	chr3:17454624-17454755	HepG2	liver:	n/a	n/a
38	BRCA1	chr3:17519940-17520632	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr3:17484048-17484463	K562	blood:	n/a	n/a
40	CBX3	chr3:17484569-17485167	K562	blood:	n/a	n/a
41	CCNT2	chr3:17472494-17472658	K562	blood:	n/a	n/a
42	CCNT2	chr3:17410588-17410779	K562	blood:	n/a	n/a
43	CEBPB	chr3:17426439-17426703	H1-hESC	embryonic stem cell:	n/a	chr3:17426557-17426568 chr3:17426594-17426605 chr3:17426573-17426584
44	CEBPB	chr3:17514883-17514974	A549	lung:	n/a	chr3:17514942-17514953
45	CEBPB	chr3:17449089-17449511	ECC-1	luminal epithelium:	n/a	chr3:17449123-17449136 chr3:17449300-17449313
46	CEBPB	chr3:17486337-17486646	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr3:17426333-17426879	A549	lung:	n/a	chr3:17426557-17426568 chr3:17426594-17426605 chr3:17426573-17426584
48	CEBPB	chr3:17449812-17449950	K562	blood:	n/a	chr3:17449856-17449867
49	CEBPB	chr3:17520038-17520681	A549	lung:	n/a	n/a
50	CEBPB	chr3:17426381-17426797	A549	lung:	n/a	chr3:17426557-17426568 chr3:17426594-17426605 chr3:17426573-17426584

No data

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:17322980..17323870-chr3:17472180..17472688,2	K562	blood:
2	chr3:17472134..17473149-chr3:17882441..17883393,5	K562	blood:
3	chr3:17415575..17418642-chr3:17419331..17422264,3	MCF-7	breast:
4	chr3:17497521..17499126-chr3:17503539..17506247,2	MCF-7	breast:
5	chr3:17299444..17301149-chr3:17449495..17452150,2	K562	blood:
6	chr3:17507187..17509434-chr3:17516355..17517975,2	MCF-7	breast:
7	chr3:17299624..17302842-chr3:17453304..17456180,3	MCF-7	breast:
8	chr3:17415575..17418642-chr3:17419331..17422264,3	MCF-7	breast:
9	chr3:17468044..17471008-chr3:17472912..17474863,2	MCF-7	breast:
10	chr3:17444293..17446289-chr3:17447323..17449518,2	K562	blood:
11	chr3:17422120..17423958-chr3:17425722..17427286,2	MCF-7	breast:
12	chr3:17472374..17472992-chr3:18020408..18021268,3	MCF-7	breast:
13	chr3:17515055..17515929-chr3:17882561..17883391,3	MCF-7	breast:
14	chr3:17396587..17398372-chr3:17401849..17403635,2	K562	blood:
15	chr3:17454593..17456440-chr3:17885577..17887079,2	MCF-7	breast:
16	chr3:17419146..17421913-chr3:17422228..17424571,2	K562	blood:
17	chr3:17464487..17468576-chr3:17470106..17473767,3	K562	blood:
18	chr3:17455901..17458583-chr3:17462176..17465120,2	K562	blood:
19	chr3:17518313..17520629-chr3:17521648..17524012,2	MCF-7	breast:
20	chr3:17444789..17447315-chr3:17447509..17449518,2	K562	blood:
21	chr3:17497865..17499392-chr3:17503466..17506313,2	K562	blood:
22	chr3:17352641..17354178-chr3:17468928..17471565,2	MCF-7	breast:
23	chr3:17300330..17301004-chr3:17455425..17455933,2	K562	blood:
24	chr3:17459732..17461276-chr3:17463158..17466015,2	MCF-7	breast:
25	chr3:17419146..17421913-chr3:17422228..17424571,2	K562	blood:
26	chr3:17485709..17487231-chr3:17783472..17786007,2	MCF-7	breast:
27	chr3:17472682..17474282-chr3:17477579..17479223,2	K562	blood:
28	chr3:17396023..17398371-chr3:17401669..17406284,4	K562	blood:
29	chr3:17348477..17349876-chr3:17454198..17455145,8	MCF-7	breast:
30	chr3:17300011..17301671-chr3:17454009..17455084,9	MCF-7	breast:
31	chr3:17460223..17462241-chr3:17894481..17896425,2	K562	blood:
32	chr3:17300074..17301498-chr3:17454119..17455081,6	K562	blood:
33	chr3:17463709..17467146-chr3:17467192..17469844,3	K562	blood:
34	chr3:17484535..17486940-chr3:17491207..17493318,2	MCF-7	breast:
35	chr3:17520321..17522399-chr3:17522640..17525341,2	K562	blood:
36	chr3:17472331..17474427-chr3:17733760..17736029,2	MCF-7	breast:
37	chr3:17518313..17520629-chr3:17521648..17524012,2	MCF-7	breast:
38	chr3:17463498..17465841-chr3:17880192..17882882,2	MCF-7	breast:
39	chr3:17472510..17474069-chr3:17729758..17732549,2	K562	blood:
40	chr3:17463709..17467146-chr3:17467192..17469844,3	K562	blood:
41	chr3:17472273..17475803-chr3:17482384..17484152,3	K562	blood:
42	chr3:17484535..17486940-chr3:17491207..17493318,2	MCF-7	breast:
43	chr3:17466006..17468780-chr3:17782780..17784383,2	MCF-7	breast:
44	chr3:17515336..17515883-chr3:17728199..17729050,2	MCF-7	breast:
45	chr3:17471748..17472727-chr3:18430698..18431277,2	MCF-7	breast:
46	chr3:17348679..17349303-chr3:17454556..17455118,3	MCF-7	breast:
47	chr3:17426084..17429101-chr3:17432439..17434660,3	MCF-7	breast:
48	chr3:17454330..17455065-chr3:17882486..17883391,2	K562	blood:
49	chr3:17497865..17499392-chr3:17503466..17506313,2	K562	blood:
50	chr3:17455901..17458583-chr3:17462176..17465120,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DAZL-5	chr3:17413567-17413626	NONHSAT088543
2	lnc-PLCL2-8	chr3:17506642-17507002	NONHSAT088548

No data

Variant related genes	Relation type
TBC1D5	TF binding region
ENSG00000227309	TF binding region
ENSG00000131374	chromatin interactions

Extended variants
information (count: 5188 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:5188 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1374197	chr3:17394615-17394616	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551090197	chr3:17394652-17394653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571333527	chr3:17394695-17394696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76784056	chr3:17394699-17394700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138698440	chr3:17394728-17394729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557124345	chr3:17394738-17394739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190215626	chr3:17394743-17394744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535710992	chr3:17394808-17394809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1374198	chr3:17394843-17394844	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs142765229	chr3:17394852-17394853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541388744	chr3:17394912-17394913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185744392	chr3:17394965-17394966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs112705531	chr3:17395034-17395035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs117859431	chr3:17395085-17395086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563486877	chr3:17395106-17395107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529074303	chr3:17395116-17395117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531218531	chr3:17395138-17395139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190409717	chr3:17395145-17395146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146836363	chr3:17395208-17395209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559550978	chr3:17395214-17395215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs528395563	chr3:17395251-17395252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181306346	chr3:17395279-17395280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186313684	chr3:17395307-17395308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531921470	chr3:17395317-17395318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs13318609	chr3:17395320-17395321	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs567379498	chr3:17395344-17395345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139058197	chr3:17395402-17395403	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs373153233	chr3:17395442-17395443	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs17272978	chr3:17395446-17395447	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs565429895	chr3:17395464-17395465	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191209113	chr3:17395492-17395493	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs149425293	chr3:17395530-17395531	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533471564	chr3:17395539-17395540	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs74737040	chr3:17395563-17395564	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112426316	chr3:17395654-17395655	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148587823	chr3:17395700-17395701	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs144349709	chr3:17395710-17395711	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554321223	chr3:17395781-17395782	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574051742	chr3:17395801-17395802	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542777038	chr3:17395810-17395811	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1867773	chr3:17395838-17395839	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112428490	chr3:17395850-17395851	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536963635	chr3:17395892-17395893	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182365288	chr3:17395894-17395895	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545321419	chr3:17395898-17395899	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565220377	chr3:17395900-17395901	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146613225	chr3:17395916-17395917	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550598746	chr3:17395921-17395922	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189096295	chr3:17395947-17395948	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140058242	chr3:17395972-17395973	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	21364760	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:17339400-17442200	Weak transcription	Fetal Intestine Small	intestine
2	chr3:17344400-17439000	Weak transcription	Aorta	Aorta
3	chr3:17356200-17412800	Weak transcription	Left Ventricle	heart
4	chr3:17365600-17413000	Weak transcription	Primary hematopoietic stem cells	blood
5	chr3:17370000-17406200	Weak transcription	Primary B cells from peripheral blood	blood
6	chr3:17370800-17411000	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr3:17372400-17410600	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr3:17379800-17414400	Weak transcription	HSMM	muscle
9	chr3:17390200-17412600	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr3:17390800-17411600	Weak transcription	GM12878-XiMat	blood
11	chr3:17391000-17411000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr3:17391800-17398200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr3:17393800-17396000	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr3:17393800-17410800	Weak transcription	Dnd41	blood
15	chr3:17394000-17396000	Weak transcription	Small Intestine	intestine
16	chr3:17394600-17395400	Weak transcription	Primary B cells from cord blood	blood
17	chr3:17394600-17395600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr3:17395000-17411800	Weak transcription	Primary T cells from cord blood	blood
19	chr3:17395400-17398800	Strong transcription	Primary B cells from cord blood	blood
20	chr3:17395600-17396000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr3:17395600-17397000	Enhancers	Fetal Heart	heart
22	chr3:17395800-17396200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:17396000-17396200	Enhancers	Small Intestine	intestine
24	chr3:17396000-17396800	Enhancers	HSMMtube	muscle
25	chr3:17396000-17406600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr3:17396200-17412200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:17396400-17398400	Enhancers	NHDF-Ad	bronchial
28	chr3:17396400-17398800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr3:17396400-17399000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr3:17396600-17396800	Enhancers	Adipose Nuclei	Adipose
31	chr3:17396800-17412400	Weak transcription	Adipose Nuclei	Adipose
32	chr3:17397000-17398600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr3:17397800-17399000	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr3:17398200-17398800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr3:17398200-17398800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr3:17398200-17398800	Enhancers	H9 Cell Line	embryonic stem cell
37	chr3:17398200-17398800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr3:17398200-17398800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr3:17398200-17398800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr3:17398200-17398800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr3:17398200-17398800	Enhancers	Ovary	ovary
42	chr3:17398200-17399000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr3:17398200-17399000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr3:17398200-17399000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr3:17398200-17399200	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr3:17398400-17398800	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr3:17398400-17398800	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr3:17398400-17399000	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr3:17398400-17414600	Weak transcription	NHDF-Ad	bronchial
50	chr3:17398600-17398800	Enhancers	Pancreas	Pancrea

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