Variant report

Variant	nsv461122
Chromosome Location	chr3:191499500-191741781
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:658)
CpG islands
(count:733)
Chromatin interactive
region (count:19)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:658 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:191527176-191527375	HepG2	liver:	n/a	n/a
2	ATF2	chr3:191645728-191646232	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr3:191645274-191646194	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:191581715-191581880	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr3:191681014-191681263	GM12878	blood:	n/a	chr3:191681142-191681153
6	BATF	chr3:191680972-191681345	GM12878	blood:	n/a	chr3:191681142-191681153
7	BCL11A	chr3:191715522-191715941	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr3:191681123-191681282	H1-hESC	embryonic stem cell:	n/a	n/a
9	CCNT2	chr3:191670465-191670665	K562	blood:	n/a	n/a
10	CEBPB	chr3:191600038-191600479	MCF-7	breast:	n/a	chr3:191600048-191600057
11	CEBPB	chr3:191512929-191513417	ECC-1	luminal epithelium:	n/a	chr3:191513150-191513161
12	CEBPB	chr3:191600171-191600371	HepG2	liver:	n/a	n/a
13	CEBPB	chr3:191546390-191546626	A549	lung:	n/a	chr3:191546571-191546582
14	CEBPB	chr3:191645863-191646174	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr3:191600116-191600457	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr3:191601788-191602458	Hela-S3	cervix:	n/a	chr3:191602068-191602081 chr3:191602068-191602081
17	CEBPB	chr3:191601936-191602235	MCF-7	breast:	n/a	chr3:191602068-191602081 chr3:191602068-191602081
18	CEBPB	chr3:191691865-191692065	HepG2	liver:	n/a	chr3:191692008-191692019
19	CEBPB	chr3:191600152-191600461	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr3:191602484-191602548	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr3:191675948-191676126	HepG2	liver:	n/a	chr3:191676012-191676023
22	CEBPB	chr3:191513126-191513332	A549	lung:	n/a	chr3:191513150-191513161
23	CEBPB	chr3:191543987-191544290	IMR90	lung:	n/a	n/a
24	CEBPB	chr3:191600062-191600482	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr3:191546443-191546721	HepG2	liver:	n/a	chr3:191546571-191546582
26	CEBPB	chr3:191512943-191513393	ECC-1	luminal epithelium:	n/a	chr3:191513150-191513161
27	CEBPB	chr3:191644969-191645326	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr3:191681654-191681823	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr3:191632254-191632572	HepG2	liver:	n/a	chr3:191632399-191632410
30	CEBPB	chr3:191527205-191527258	HepG2	liver:	n/a	n/a
31	CEBPB	chr3:191513019-191513296	HepG2	liver:	n/a	chr3:191513150-191513161
32	CEBPB	chr3:191500786-191501305	Hela-S3	cervix:	n/a	chr3:191500951-191500962
33	CEBPB	chr3:191662659-191662901	HepG2	liver:	n/a	chr3:191662724-191662735
34	CEBPB	chr3:191586547-191586833	HepG2	liver:	n/a	chr3:191586706-191586717
35	CEBPB	chr3:191502362-191502464	H1-hESC	embryonic stem cell:	n/a	chr3:191502435-191502446
36	CEBPB	chr3:191680827-191681243	HCT-116	colon:	n/a	n/a
37	CEBPB	chr3:191662605-191662823	H1-hESC	embryonic stem cell:	n/a	chr3:191662724-191662735
38	CEBPB	chr3:191502284-191502484	HepG2	liver:	n/a	chr3:191502435-191502446
39	CEBPB	chr3:191643948-191644172	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr3:191602062-191602066	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr3:191567964-191568164	HepG2	liver:	n/a	chr3:191568037-191568050 chr3:191568037-191568048
42	CEBPB	chr3:191632244-191632538	H1-hESC	embryonic stem cell:	n/a	chr3:191632399-191632410
43	CEBPB	chr3:191546520-191546623	H1-hESC	embryonic stem cell:	n/a	chr3:191546571-191546582
44	CEBPB	chr3:191512799-191513399	Hela-S3	cervix:	n/a	chr3:191513150-191513161
45	CEBPB	chr3:191600120-191600419	MCF-7	breast:	n/a	n/a
46	CEBPB	chr3:191632247-191632587	IMR90	lung:	n/a	chr3:191632399-191632410
47	CEBPB	chr3:191500819-191501411	HepG2	liver:	n/a	chr3:191500951-191500962
48	CEBPB	chr3:191600078-191600526	ECC-1	luminal epithelium:	n/a	n/a
49	CHD1	chr3:191646279-191646309	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr3:191640164-191640215	H1-hESC	embryonic stem cell:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:191670165-191670215	SK-N-SH_RA	brain:	n/a
2	chr3:191670165-191670215	SK-N-SH_RA	brain:	n/a
3	chr3:191578720-191578770	AG04449	skin:	fetal
4	chr3:191578720-191578770	SK-N-MC	brain:	n/a
5	chr3:191670642-191670692	ProgFib	skin:	n/a
6	chr3:191581259-191581309	GM19239	blood:	n/a
7	chr3:191581259-191581309	MCF-7	breast:	n/a
8	chr3:191670642-191670692	PrEC	prostate:	n/a
9	chr3:191578720-191578770	Jurkat	blood:	n/a
10	chr3:191581259-191581309	GM12892	blood:	n/a
11	chr3:191585219-191585269	SKMC	muscle:	n/a
12	chr3:191670637-191670687	Caco-2	colon:	n/a
13	chr3:191670637-191670687	Jurkat	blood:	n/a
14	chr3:191670165-191670215	MCF10A-Er-Src	breast:	n/a
15	chr3:191588392-191588442	MCF10A-Er-Src	breast:	n/a
16	chr3:191588392-191588442	HRPEpiC	eye:	n/a
17	chr3:191680064-191680114	AG10803	skin:	n/a
18	chr3:191670485-191670535	HCM	heart:	n/a
19	chr3:191715823-191715873	AoSMC	blood vessel:	n/a
20	chr3:191670642-191670692	AoSMC	blood vessel:	n/a
21	chr3:191670637-191670687	PrEC	prostate:	n/a
22	chr3:191670257-191670307	MCF10A-Er-Src	breast:	n/a
23	chr3:191670642-191670692	IMR90	lung:	fetal
24	chr3:191585219-191585269	GM12878	blood:	n/a
25	chr3:191680064-191680114	PFSK-1	brain:	n/a
26	chr3:191588392-191588442	MCF-7	breast:	n/a
27	chr3:191585219-191585269	K562	blood:	n/a
28	chr3:191578720-191578770	HCM	heart:	n/a
29	chr3:191670165-191670215	BE2_C	brain:	n/a
30	chr3:191578720-191578770	HCPEpiC	choroid plexus:	n/a
31	chr3:191670165-191670215	AG09319	gingival:	n/a
32	chr3:191680064-191680114	GM12891	blood:	n/a
33	chr3:191579258-191579308	IMR90	lung:	fetal
34	chr3:191670165-191670215	NHBE	bronchial:	n/a
35	chr3:191670485-191670535	PrEC	prostate:	n/a
36	chr3:191579258-191579308	MCF10A-Er-Src	breast:	n/a
37	chr3:191680064-191680114	K562	blood:	n/a
38	chr3:191581259-191581309	T-47D	breast:	n/a
39	chr3:191670642-191670692	ECC-1	luminal epithelium:	n/a
40	chr3:191670257-191670307	GM19239	blood:	n/a
41	chr3:191670165-191670215	T-47D	breast:	n/a
42	chr3:191670642-191670692	Hepatocyte	liver:	n/a
43	chr3:191578720-191578770	PrEC	prostate:	n/a
44	chr3:191670257-191670307	CMK	blood:	n/a
45	chr3:191579258-191579308	HMEC	breast:	n/a
46	chr3:191578720-191578770	GM12878	blood:	n/a
47	chr3:191585219-191585269	IMR90	lung:	fetal
48	chr3:191588392-191588442	NH-A	brain:	n/a
49	chr3:191715823-191715873	NT2-D1	testis:	n/a
50	chr3:191715823-191715873	BJ	skin:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:191543102..191545359-chr3:191547187..191548804,2	K562	blood:
2	chr3:191642414..191643940-chr3:191650422..191652499,2	K562	blood:
3	chr3:191666453..191669153-chr3:191669731..191672462,2	K562	blood:
4	chr3:191673185..191674856-chr3:191675139..191678048,2	MCF-7	breast:
5	chr3:191586534..191587250-chr3:191604791..191605375,2	MCF-7	breast:
6	chr3:191586534..191587250-chr3:191604791..191605375,2	MCF-7	breast:
7	chr12:14927202..14927710-chr3:191649972..191650753,2	MCF-7	breast:
8	chr3:191699997..191702549-chr3:191705897..191708844,2	K562	blood:
9	chr3:191220103..191221050-chr3:191527147..191528017,3	MCF-7	breast:
10	chr3:191673185..191674856-chr3:191675139..191678048,2	MCF-7	breast:
11	chr3:191699562..191701581-chr3:191755371..191757226,2	MCF-7	breast:
12	chr3:191699997..191702549-chr3:191705897..191708844,2	K562	blood:
13	chr15:71423988..71424731-chr3:191581561..191582555,2	MCF-7	breast:
14	chr3:191655366..191657510-chr3:191658751..191661236,3	MCF-7	breast:
15	chr3:191642414..191643940-chr3:191650422..191652499,2	K562	blood:
16	chr3:191134537..191135165-chr3:191527181..191527753,2	MCF-7	breast:
17	chr3:191655366..191657510-chr3:191658751..191661236,3	MCF-7	breast:
18	chr3:191543102..191545359-chr3:191547187..191548804,2	K562	blood:
19	chr3:191636417..191637147-chr9:139422447..139423366,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGF12-3	chr3:191634462-191635275	NONHSAT093987
2	lnc-FGF12-3	chr3:191632977-191633333	NONHSAT093987
3	lnc-FGF12-3	chr3:191644766-191645225	NONHSAT093987
4	lnc-FGF12-1	chr3:191500507-191500590	XLOC_003375
5	lnc-FGF12-1	chr3:191500506-191500590	NONHSAT093983

No data

Variant related genes	Relation type
ENSG00000216020	TF binding region
ENSG00000237653	TF binding region
ENSG00000216020	CpG island
ENSG00000237653	CpG island
ENSG00000246705	chromatin interactions
ENSG00000237653	chromatin interactions

Extended variants
information (count: 7015 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:7015 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1516496	chr3:191499500-191499501	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368525334	chr3:191499503-191499504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144842955	chr3:191499510-191499511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560836403	chr3:191499511-191499512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528590023	chr3:191499563-191499564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs529727953	chr3:191499564-191499565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548330618	chr3:191499577-191499578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569827705	chr3:191499646-191499647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532483487	chr3:191499652-191499653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138715216	chr3:191499671-191499672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs76989688	chr3:191499725-191499726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141746712	chr3:191499733-191499734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6782617	chr3:191499735-191499736	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs73062864	chr3:191499749-191499750	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs531755753	chr3:191499769-191499770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369081903	chr3:191499793-191499794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556570322	chr3:191499815-191499816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs1400245	chr3:191499816-191499817	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs545695937	chr3:191499856-191499857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192542109	chr3:191499874-191499875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183877907	chr3:191499883-191499884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541092039	chr3:191499901-191499902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs74840161	chr3:191499967-191499968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574611792	chr3:191499987-191499988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543438621	chr3:191499990-191499991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138206708	chr3:191499993-191499994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188160939	chr3:191500001-191500002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78389938	chr3:191500007-191500008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559248715	chr3:191500055-191500056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149580471	chr3:191500058-191500059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79492663	chr3:191500071-191500072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144234124	chr3:191500109-191500110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140668848	chr3:191500170-191500171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192630130	chr3:191500216-191500217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144965212	chr3:191500255-191500256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147535076	chr3:191500259-191500260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35093202	chr3:191500322-191500323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78746077	chr3:191500343-191500344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs117546120	chr3:191500362-191500363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535207043	chr3:191500416-191500417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555247089	chr3:191500420-191500421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574574860	chr3:191500427-191500428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543514190	chr3:191500431-191500432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563110528	chr3:191500465-191500466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576789065	chr3:191500473-191500474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11331237	chr3:191500486-191500487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs386669645	chr3:191500488-191500489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs56308539	chr3:191500490-191500491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559578465	chr3:191500492-191500493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528418370	chr3:191500519-191500520	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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	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
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Lung cancer	19547694	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Optic atrophy	21457585	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-small cell lung cancer	21829676	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	16397240	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD

Chromatin state (count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:191498000-191501600	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr3:191501600-191502200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
3	chr3:191502200-191506000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr3:191505800-191506400	Enhancers	Stomach Mucosa	stomach
5	chr3:191506000-191510800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
6	chr3:191508000-191510000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr3:191508400-191509000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr3:191510000-191511400	Enhancers	HUVEC	blood vessel
9	chr3:191511600-191511800	Enhancers	Liver	Liver
10	chr3:191511800-191512800	Weak transcription	Liver	Liver
11	chr3:191511800-191523200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr3:191512800-191513000	Enhancers	Liver	Liver
13	chr3:191513000-191513600	Flanking Active TSS	Liver	Liver
14	chr3:191513200-191513600	Enhancers	Hela-S3	cervix
15	chr3:191518600-191519600	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr3:191519000-191519800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr3:191519200-191520000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
18	chr3:191519600-191519800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
19	chr3:191519800-191522200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr3:191520000-191521000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:191522200-191523400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr3:191523400-191525800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr3:191525800-191526000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr3:191525800-191526400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr3:191526000-191526200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr3:191526000-191527000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
27	chr3:191526400-191527800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr3:191526600-191527400	Enhancers	Liver	Liver
29	chr3:191527000-191527600	Enhancers	HepG2	liver
30	chr3:191527000-191528800	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr3:191530800-191532200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr3:191534200-191534400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
33	chr3:191534400-191542600	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr3:191536600-191537800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:191537600-191537800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr3:191537800-191539200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:191537800-191545400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr3:191539200-191540400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr3:191540400-191540800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:191542600-191542800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
41	chr3:191545400-191545600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr3:191564000-191565200	Enhancers	Fetal Heart	heart
43	chr3:191564000-191565600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr3:191564000-191566400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:191564800-191565600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr3:191568400-191573200	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr3:191573200-191574600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
48	chr3:191574600-191579000	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr3:191576000-191576800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr3:191576400-191577000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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