Variant report

Variant	nsv592440
Chromosome Location	chr3:163951886-164114553
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr3:164065590-164065659	K562	blood:	n/a	n/a
2	CEBPB	chr3:163961632-163962275	MCF-7	breast:	n/a	chr3:163961848-163961865
3	CEBPB	chr3:164107081-164107356	A549	lung:	n/a	chr3:164107227-164107236 chr3:164107225-164107238 chr3:164107227-164107236 chr3:164107227-164107236 chr3:164107226-164107237 chr3:164107225-164107238 chr3:164107225-164107236 chr3:164107227-164107236
4	CEBPB	chr3:164085608-164085831	IMR90	lung:	n/a	chr3:164085753-164085766
5	CEBPB	chr3:164093370-164093659	Hela-S3	cervix:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
6	CEBPB	chr3:164093357-164093663	A549	lung:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
7	CEBPB	chr3:164097994-164098357	MCF-7	breast:	n/a	n/a
8	CEBPB	chr3:163980076-163980312	A549	lung:	n/a	chr3:163980184-163980195
9	CEBPB	chr3:164077961-164078328	HepG2	liver:	n/a	chr3:164078134-164078145
10	CEBPB	chr3:164078064-164078196	HepG2	liver:	n/a	chr3:164078134-164078145
11	CEBPB	chr3:163961690-163962327	MCF-7	breast:	n/a	chr3:163961848-163961865
12	CEBPB	chr3:164093320-164093640	HepG2	liver:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
13	CEBPB	chr3:164077996-164078260	A549	lung:	n/a	chr3:164078134-164078145
14	CEBPB	chr3:164077987-164078333	Hela-S3	cervix:	n/a	chr3:164078134-164078145
15	CEBPB	chr3:164093408-164093523	K562	blood:	n/a	chr3:164093476-164093487
16	CEBPB	chr3:164107093-164107343	IMR90	lung:	n/a	chr3:164107227-164107236 chr3:164107225-164107238 chr3:164107227-164107236 chr3:164107227-164107236 chr3:164107226-164107237 chr3:164107225-164107238 chr3:164107225-164107236 chr3:164107227-164107236
17	CEBPB	chr3:164085628-164085750	K562	blood:	n/a	n/a
18	CEBPB	chr3:164066095-164066166	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:164107072-164107346	HepG2	liver:	n/a	chr3:164107227-164107236 chr3:164107225-164107238 chr3:164107227-164107236 chr3:164107227-164107236 chr3:164107226-164107237 chr3:164107225-164107238 chr3:164107225-164107236 chr3:164107227-164107236
20	CEBPB	chr3:164078036-164078173	H1-hESC	embryonic stem cell:	n/a	chr3:164078134-164078145
21	CEBPB	chr3:164078081-164078324	MCF-7	breast:	n/a	chr3:164078134-164078145
22	CEBPB	chr3:163980067-163980373	HepG2	liver:	n/a	chr3:163980184-163980195
23	CEBPB	chr3:163980107-163980307	H1-hESC	embryonic stem cell:	n/a	chr3:163980184-163980195
24	CEBPB	chr3:163980083-163980289	Hela-S3	cervix:	n/a	chr3:163980184-163980195
25	CTBP2	chr3:164038799-164039115	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr3:164050680-164050830	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr3:164111120-164111270	AG09319	gingival:	n/a	n/a
28	CTCF	chr3:164107880-164108030	HCT-116	colon:	n/a	n/a
29	CTCF	chr3:163968839-163968974	MCF-7	breast:	n/a	chr3:163968895-163968916 chr3:163968905-163968913 chr3:163968901-163968917
30	CTCF	chr3:164107960-164108110	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr3:164107920-164108070	HAc	cerebellar:	n/a	n/a
32	CTCF	chr3:164050680-164050830	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr3:164108016-164108176	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr3:164108000-164108150	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr3:163979232-163979359	K562	blood:	n/a	n/a
36	CTCF	chr3:164066300-164066450	MCF-7	breast:	n/a	n/a
37	CTCF	chr3:164093880-164094030	RPTEC	kidney:	n/a	n/a
38	CTCF	chr3:164050640-164050790	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr3:164050700-164050850	AG09319	gingival:	n/a	n/a
40	CTCF	chr3:164108000-164108150	AG10803	skin:	n/a	n/a
41	CTCF	chr3:164107980-164108130	GM12878	blood:	n/a	n/a
42	CTCF	chr3:164054702-164054778	GM13976	blood:	n/a	n/a
43	CTCF	chr3:164111120-164111270	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr3:164111040-164111190	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr3:164108040-164108190	HMEC	breast:	n/a	n/a
46	CTCF	chr3:163968800-163968950	MCF-7	breast:	n/a	chr3:163968895-163968916 chr3:163968905-163968913 chr3:163968901-163968917
47	CTCF	chr3:163968800-163968950	RPTEC	kidney:	n/a	chr3:163968895-163968916 chr3:163968905-163968913 chr3:163968901-163968917
48	CTCF	chr3:164111040-164111190	AG09319	gingival:	n/a	n/a
49	CTCF	chr3:164107998-164108113	K562	blood:	n/a	n/a
50	CTCF	chr3:164093920-164094070	AG09319	gingival:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:164059124-164059174	AG10803	skin:	n/a
2	chr3:164059255-164059305	PFSK-1	brain:	n/a
3	chr3:164056463-164056513	PrEC	prostate:	n/a
4	chr3:164059011-164059061	HEEpiC	esophagus:	n/a
5	chr3:164009569-164009619	Jurkat	blood:	n/a
6	chr3:164059124-164059174	A549	lung:	n/a
7	chr3:164059255-164059305	HepG2	liver:	n/a
8	chr3:164059124-164059174	HNPCEpiC	eye:	n/a
9	chr3:164059011-164059061	HMEC	breast:	n/a
10	chr3:164050953-164051003	ProgFib	skin:	n/a
11	chr3:164056463-164056513	HCT-116	colon:	n/a
12	chr3:164056753-164056803	HNPCEpiC	eye:	n/a
13	chr3:164059255-164059305	HUVEC	blood vessel:	n/a
14	chr3:164050953-164051003	MCF10A-Er-Src	breast:	n/a
15	chr3:164050953-164051003	HCF	heart:	n/a
16	chr3:164059011-164059061	A549	lung:	n/a
17	chr3:164056753-164056803	Jurkat	blood:	n/a
18	chr3:164009569-164009619	PrEC	prostate:	n/a
19	chr3:164050953-164051003	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:164009569-164009619	SAEC	small airway:	n/a
21	chr3:164059011-164059061	PANC-1	pancreas:	n/a
22	chr3:164059011-164059061	RPTEC	kidney:	n/a
23	chr3:164059011-164059061	SK-N-SH_RA	brain:	n/a
24	chr3:164009569-164009619	HEEpiC	esophagus:	n/a
25	chr3:164056463-164056513	AG04449	skin:	fetal
26	chr3:164056463-164056513	SK-N-SH_RA	brain:	n/a
27	chr3:164050953-164051003	HMEC	breast:	n/a
28	chr3:164050953-164051003	IMR90	lung:	fetal
29	chr3:164050953-164051003	SAEC	small airway:	n/a
30	chr3:164059255-164059305	AG10803	skin:	n/a
31	chr3:164059011-164059061	AG04449	skin:	fetal
32	chr3:164059124-164059174	HUVEC	blood vessel:	n/a
33	chr3:164056753-164056803	BE2_C	brain:	n/a
34	chr3:164059011-164059061	T-47D	breast:	n/a
35	chr3:164009569-164009619	AG10803	skin:	n/a
36	chr3:164059011-164059061	Jurkat	blood:	n/a
37	chr3:164050953-164051003	HCT-116	colon:	n/a
38	chr3:164059124-164059174	PFSK-1	brain:	n/a
39	chr3:164009569-164009619	HCF	heart:	n/a
40	chr3:164059011-164059061	HIPEpiC	eye:	n/a
41	chr3:164059011-164059061	HUVEC	blood vessel:	n/a
42	chr3:164056463-164056513	NHBE	bronchial:	n/a
43	chr3:164059124-164059174	MCF-7	breast:	n/a
44	chr3:164009569-164009619	GM06990	blood:	n/a
45	chr3:164056463-164056513	SAEC	small airway:	n/a
46	chr3:164009569-164009619	GM12878	blood:	n/a
47	chr3:164009569-164009619	ProgFib	skin:	n/a
48	chr3:164056753-164056803	ProgFib	skin:	n/a
49	chr3:164059255-164059305	NH-A	brain:	n/a
50	chr3:164009569-164009619	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:164033562..164036466-chr3:164041623..164043945,2	MCF-7	breast:
2	chr3:164033562..164036466-chr3:164041623..164043945,2	MCF-7	breast:
3	chr3:163968485..163970197-chr3:163971709..163973734,2	MCF-7	breast:
4	chr3:164097708..164098703-chr3:164352353..164353241,9	MCF-7	breast:
5	chr3:163988892..163990964-chr3:163991912..163993953,2	K562	blood:
6	chr3:163988892..163990964-chr3:163991912..163993953,2	K562	blood:
7	chr3:164097709..164098424-chr3:164241494..164242452,3	MCF-7	breast:
8	chr3:164032173..164034796-chr3:164095339..164097722,2	K562	blood:
9	chr3:164097711..164098324-chr3:164241488..164242187,2	MCF-7	breast:
10	chr3:164097731..164098551-chr3:164154660..164155422,4	MCF-7	breast:
11	chr3:164097659..164099012-chr3:164352282..164353331,34	MCF-7	breast:
12	chr3:164072695..164075481-chr3:164078791..164081086,2	MCF-7	breast:
13	chr3:164097647..164098715-chr3:164154502..164155534,19	MCF-7	breast:
14	chr3:164032173..164034796-chr3:164095339..164097722,2	K562	blood:
15	chr3:163995585..163997750-chr3:164093655..164096327,2	K562	blood:
16	chr3:164072695..164075481-chr3:164078791..164081086,2	MCF-7	breast:
17	chr3:164097647..164098678-chr3:164154502..164155534,10	MCF-7	breast:
18	chr3:164097711..164099012-chr3:164352332..164353250,14	MCF-7	breast:
19	chr3:163995585..163997750-chr3:164093655..164096327,2	K562	blood:
20	chr3:164097711..164098324-chr3:164241488..164242482,3	MCF-7	breast:
21	chr3:164050649..164051226-chr3:164523700..164524566,2	MCF-7	breast:
22	chr3:164093244..164094225-chr3:164903325..164904113,2	MCF-7	breast:
23	chr3:163968485..163970197-chr3:163971709..163973734,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OTOL1-4	chr3:164078868-164078917	XLOC_002899
2	lnc-OTOL1-4	chr3:164088402-164088464	XLOC_002899

Variant related genes	Relation type
MIR720	TF binding region
MIR720	CpG island

Extended variants
information (count: 5512 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:5512 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1667783	chr3:163951886-163951887	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568665507	chr3:163951926-163951927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs377555007	chr3:163951929-163951930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138433875	chr3:163951935-163951936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557599957	chr3:163951956-163951957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116801932	chr3:163951978-163951979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545772726	chr3:163951982-163951983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1796596	chr3:163951991-163951992	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs573280968	chr3:163952015-163952016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376034065	chr3:163952098-163952099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562216745	chr3:163952114-163952115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531099575	chr3:163952270-163952271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192360173	chr3:163952328-163952329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142772670	chr3:163952375-163952376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs13068525	chr3:163952379-163952380	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs549926102	chr3:163952399-163952400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546565521	chr3:163952422-163952423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373927486	chr3:163952423-163952424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528884209	chr3:163952428-163952429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548773634	chr3:163952445-163952446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568624553	chr3:163952449-163952450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536241871	chr3:163952459-163952460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537631728	chr3:163952460-163952461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557563131	chr3:163952476-163952477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568431869	chr3:163952478-163952479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73154457	chr3:163952510-163952511	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs533885096	chr3:163952544-163952545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs367953377	chr3:163952569-163952570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182102326	chr3:163952627-163952628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs146982435	chr3:163952661-163952662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138064675	chr3:163952662-163952663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573668356	chr3:163952711-163952712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs575842400	chr3:163952725-163952726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs374245002	chr3:163952788-163952789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547893075	chr3:163952815-163952816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187099447	chr3:163952843-163952844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191807898	chr3:163953033-163953034	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539247626	chr3:163953040-163953041	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183939634	chr3:163953071-163953072	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540522799	chr3:163953078-163953079	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190166767	chr3:163953147-163953148	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143636597	chr3:163953161-163953162	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567006713	chr3:163953162-163953163	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144103809	chr3:163953213-163953214	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371137599	chr3:163953260-163953261	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562219524	chr3:163953262-163953263	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148697220	chr3:163953266-163953267	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368963190	chr3:163953280-163953281	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539232184	chr3:163953421-163953422	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558693317	chr3:163953442-163953443	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Alcoholism	21790672	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute myeloid leukemia	19651600	CNVD
Autism	19287141	CNVD
Incontinentia Pigmenti	22033527	CNVD
Rett syndrome	21593744	CNVD
Urothelial carcinoma	21177765	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Recurrent pregnancy loss	19789632	CNVD

Chromatin state (count:251 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:163948800-163953000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr3:163948800-163953000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:163952400-163953600	Enhancers	Fetal Kidney	kidney
4	chr3:163953000-163953600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr3:163953000-163959200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:163953600-163954800	Weak transcription	Fetal Kidney	kidney
7	chr3:163954800-163955600	Enhancers	Fetal Kidney	kidney
8	chr3:163959200-163962000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr3:163962000-163962600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:163962600-163963200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:163963200-163995200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:163979000-163996200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr3:163982400-163983200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr3:163990800-163993200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr3:163994400-163995200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
16	chr3:163995200-164000600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:163996200-163997000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
18	chr3:164000600-164002200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:164002200-164003000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:164003000-164005600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:164005600-164006800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:164006800-164007200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:164007200-164007600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:164007600-164009400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr3:164009400-164009800	Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr3:164009400-164009800	Active TSS	H9 Cell Line	embryonic stem cell
27	chr3:164009400-164009800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr3:164009800-164014200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:164014200-164015400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr3:164015400-164017000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr3:164017000-164017400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr3:164017400-164019800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:164018200-164019000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr3:164019800-164020400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:164020400-164023200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr3:164023200-164025000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:164025000-164026000	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr3:164026000-164026600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr3:164026600-164031400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:164027000-164027200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
41	chr3:164027400-164028200	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr3:164031400-164033800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:164033800-164034800	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr3:164034800-164035400	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:164035400-164035600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr3:164035600-164036200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr3:164036200-164038400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr3:164038400-164038600	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr3:164038400-164039400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr3:164038400-164042400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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