Variant report

Variant	nsv877891
Chromosome Location	chr3:163989075-164126802
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	chr3:164121454-164121666	H1-hESC	embryonic stem cell:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
3	CEBPB	chr3:164066095-164066166	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr3:164085608-164085831	IMR90	lung:	n/a	chr3:164085753-164085766
5	CEBPB	chr3:164078064-164078196	HepG2	liver:	n/a	chr3:164078134-164078145
6	CEBPB	chr3:164093357-164093663	A549	lung:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
7	CEBPB	chr3:164121373-164121695	HepG2	liver:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
8	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
9	CEBPB	chr3:164078081-164078324	MCF-7	breast:	n/a	chr3:164078134-164078145
10	CEBPB	chr3:164077996-164078260	A549	lung:	n/a	chr3:164078134-164078145
11	CEBPB	chr3:164093370-164093659	Hela-S3	cervix:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
12	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
13	CEBPB	chr3:164093320-164093640	HepG2	liver:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
14	CEBPB	chr3:164077987-164078333	Hela-S3	cervix:	n/a	chr3:164078134-164078145
15	CEBPB	chr3:164077961-164078328	HepG2	liver:	n/a	chr3:164078134-164078145
16	CEBPB	chr3:164085628-164085750	K562	blood:	n/a	n/a
17	CEBPB	chr3:164121369-164121693	A549	lung:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
18	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
19	CEBPB	chr3:164121359-164121699	IMR90	lung:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
20	CEBPB	chr3:164078036-164078173	H1-hESC	embryonic stem cell:	n/a	chr3:164078134-164078145
21	CEBPB	chr3:164093408-164093523	K562	blood:	n/a	chr3:164093476-164093487
22	CEBPB	chr3:164121426-164121694	K562	blood:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
23	CEBPB	chr3:164097994-164098357	MCF-7	breast:	n/a	n/a
24	CTBP2	chr3:164038799-164039115	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr3:164093976-164094009	LNCaP	prostate:	n/a	n/a
26	CTCF	chr3:164111120-164111270	AG09319	gingival:	n/a	n/a
27	CTCF	chr3:164107820-164107970	RPTEC	kidney:	n/a	n/a
28	CTCF	chr3:164093860-164094010	RPTEC	kidney:	n/a	n/a
29	CTCF	chr3:164108116-164108119	K562	blood:	n/a	n/a
30	CTCF	chr3:164093900-164094050	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr3:164050720-164050870	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr3:164111100-164111250	HCT-116	colon:	n/a	n/a
33	CTCF	chr3:164093900-164094050	HCT-116	colon:	n/a	n/a
34	CTCF	chr3:164111060-164111210	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr3:164108000-164108150	GM12864	blood:	n/a	n/a
36	CTCF	chr3:164111040-164111190	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr3:164111040-164111190	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr3:164108060-164108210	GM12873	blood:	n/a	n/a
39	CTCF	chr3:164050700-164050850	AG09319	gingival:	n/a	n/a
40	CTCF	chr3:164107920-164108070	HAc	cerebellar:	n/a	n/a
41	CTCF	chr3:164108016-164108176	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr3:164108020-164108170	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr3:164111080-164111230	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr3:164108000-164108150	SAEC	small airway:	n/a	n/a
45	CTCF	chr3:164108060-164108210	HRE	kidney:	n/a	n/a
46	CTCF	chr3:164108020-164108170	HMF	breast:	n/a	n/a
47	CTCF	chr3:164050700-164050850	GM12864	blood:	n/a	n/a
48	CTCF	chr3:164050640-164050790	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr3:164093920-164094070	AG09319	gingival:	n/a	n/a
50	CTCF	chr3:164111127-164111216	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:164056753-164056803	HUVEC	blood vessel:	n/a
2	chr3:164059011-164059061	HepG2	liver:	n/a
3	chr3:164119020-164119070	Jurkat	blood:	n/a
4	chr3:164059124-164059174	SAEC	small airway:	n/a
5	chr3:164059011-164059061	AG09319	gingival:	n/a
6	chr3:164059124-164059174	PrEC	prostate:	n/a
7	chr3:164119020-164119070	NH-A	brain:	n/a
8	chr3:164059124-164059174	HEK293	kidney:	embryo
9	chr3:164119020-164119070	BE2_C	brain:	n/a
10	chr3:164119737-164119787	ovcar-3	ovarian:	n/a
11	chr3:164009569-164009619	AG10803	skin:	n/a
12	chr3:164009569-164009619	AoSMC	blood vessel:	n/a
13	chr3:164119959-164120009	Caco-2	colon:	n/a
14	chr3:164009569-164009619	NB4	blood:	n/a
15	chr3:164119020-164119070	SK-N-MC	brain:	n/a
16	chr3:164050953-164051003	Caco-2	colon:	n/a
17	chr3:164059124-164059174	GM19239	blood:	n/a
18	chr3:164119737-164119787	HCT-116	colon:	n/a
19	chr3:164119959-164120009	SK-N-SH_RA	brain:	n/a
20	chr3:164059255-164059305	RPTEC	kidney:	n/a
21	chr3:164056463-164056513	HCM	heart:	n/a
22	chr3:164059011-164059061	ovcar-3	ovarian:	n/a
23	chr3:164059011-164059061	AG10803	skin:	n/a
24	chr3:164056463-164056513	NB4	blood:	n/a
25	chr3:164050953-164051003	AoSMC	blood vessel:	n/a
26	chr3:164059011-164059061	SK-N-SH_RA	brain:	n/a
27	chr3:164059011-164059061	NB4	blood:	n/a
28	chr3:164009569-164009619	HCT-116	colon:	n/a
29	chr3:164056463-164056513	HRE	kidney:	n/a
30	chr3:164056753-164056803	SK-N-SH	brain:	n/a
31	chr3:164009569-164009619	AG09319	gingival:	n/a
32	chr3:164059011-164059061	HMEC	breast:	n/a
33	chr3:164050953-164051003	GM06990	blood:	n/a
34	chr3:164056753-164056803	NT2-D1	testis:	n/a
35	chr3:164119959-164120009	HCF	heart:	n/a
36	chr3:164059255-164059305	BJ	skin:	n/a
37	chr3:164119959-164120009	GM12892	blood:	n/a
38	chr3:164059124-164059174	HCM	heart:	n/a
39	chr3:164119959-164120009	IMR90	lung:	fetal
40	chr3:164059124-164059174	HRPEpiC	eye:	n/a
41	chr3:164056753-164056803	AG10803	skin:	n/a
42	chr3:164056463-164056513	HIPEpiC	eye:	n/a
43	chr3:164119959-164120009	AG09319	gingival:	n/a
44	chr3:164119020-164119070	HEEpiC	esophagus:	n/a
45	chr3:164056463-164056513	HCF	heart:	n/a
46	chr3:164056463-164056513	NT2-D1	testis:	n/a
47	chr3:164119737-164119787	HRCEpiC	kidney:	n/a
48	chr3:164059011-164059061	AG09309	skin:	n/a
49	chr3:164056463-164056513	HUVEC	blood vessel:	n/a
50	chr3:164056463-164056513	HEK293	kidney:	embryo

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

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

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

Extended variants
information (count: 4404 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:4404 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9863717	chr3:163989075-163989076	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538565048	chr3:163989078-163989079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558096190	chr3:163989101-163989102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372166654	chr3:163989155-163989156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540136929	chr3:163989172-163989173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs146619814	chr3:163989191-163989192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78579509	chr3:163989213-163989214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370963336	chr3:163989230-163989231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181422540	chr3:163989298-163989299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573894010	chr3:163989321-163989322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573550770	chr3:163989328-163989329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185510239	chr3:163989329-163989330	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs13078662	chr3:163989345-163989346	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs376137616	chr3:163989381-163989382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141353244	chr3:163989382-163989383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190670694	chr3:163989422-163989423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145141679	chr3:163989434-163989435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568979640	chr3:163989455-163989456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146883781	chr3:163989459-163989460	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547504405	chr3:163989473-163989474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567414507	chr3:163989479-163989480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529817362	chr3:163989496-163989497	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549961583	chr3:163989516-163989517	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181650866	chr3:163989524-163989525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538894566	chr3:163989586-163989587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558605079	chr3:163989610-163989611	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571599736	chr3:163989655-163989656	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533979297	chr3:163989662-163989663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553755331	chr3:163989668-163989669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370872465	chr3:163989683-163989684	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140068069	chr3:163989687-163989688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549572543	chr3:163989695-163989696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542731497	chr3:163989699-163989700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573124183	chr3:163989714-163989715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187303297	chr3:163989719-163989720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576589675	chr3:163989745-163989746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192413225	chr3:163989779-163989780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150304714	chr3:163989783-163989784	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572065617	chr3:163989785-163989786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567734770	chr3:163989793-163989794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs137974431	chr3:163989825-163989826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149494956	chr3:163989837-163989838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535373127	chr3:163989857-163989858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529780545	chr3:163989866-163989867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116058579	chr3:163989933-163989934	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563473929	chr3:163989964-163989965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145952764	chr3:163989981-163989982	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552435957	chr3:163989995-163989996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138783862	chr3:163990022-163990023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142812915	chr3:163990112-163990113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
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
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
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Alcoholism	21790672	CNVD
Schizophrenia	20967226	CNVD
small cell lung cancer	20016488	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:250 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:163963200-163995200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:163979000-163996200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr3:163990800-163993200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr3:163994400-163995200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
5	chr3:163995200-164000600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:163996200-163997000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
7	chr3:164000600-164002200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:164002200-164003000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr3:164003000-164005600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:164005600-164006800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:164006800-164007200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:164007200-164007600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:164007600-164009400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:164009400-164009800	Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr3:164009400-164009800	Active TSS	H9 Cell Line	embryonic stem cell
16	chr3:164009400-164009800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:164009800-164014200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr3:164014200-164015400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:164015400-164017000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:164017000-164017400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:164017400-164019800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:164018200-164019000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr3:164019800-164020400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:164020400-164023200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr3:164023200-164025000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:164025000-164026000	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:164026000-164026600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr3:164026600-164031400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:164027000-164027200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
30	chr3:164027400-164028200	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr3:164031400-164033800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr3:164033800-164034800	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:164034800-164035400	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:164035400-164035600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:164035600-164036200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr3:164036200-164038400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:164038400-164038600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr3:164038400-164039400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr3:164038400-164042400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:164038600-164038800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chr3:164038600-164039200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr3:164038600-164039200	Enhancers	H9 Cell Line	embryonic stem cell
43	chr3:164038600-164039200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr3:164038600-164039400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr3:164038600-164039400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr3:164038600-164039400	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr3:164038600-164039600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr3:164038600-164039800	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr3:164038800-164039000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr3:164038800-164039400	Enhancers	H1 Cell Line	embryonic stem cell

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