Variant report

Variant	nsv592437
Chromosome Location	chr3:163885473-164095655
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	BACH1	chr3:163946376-163946549	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr3:164065590-164065659	K562	blood:	n/a	n/a
3	CEBPB	chr3:164085628-164085750	K562	blood:	n/a	n/a
4	CEBPB	chr3:163912738-163913096	MCF-7	breast:	n/a	n/a
5	CEBPB	chr3:163886053-163886253	HepG2	liver:	n/a	chr3:163886110-163886119 chr3:163886110-163886119 chr3:163886110-163886119 chr3:163886109-163886120 chr3:163886108-163886121 chr3:163886108-163886119 chr3:163886110-163886119
6	CEBPB	chr3:164077996-164078260	A549	lung:	n/a	chr3:164078134-164078145
7	CEBPB	chr3:164078036-164078173	H1-hESC	embryonic stem cell:	n/a	chr3:164078134-164078145
8	CEBPB	chr3:163980076-163980312	A549	lung:	n/a	chr3:163980184-163980195
9	CEBPB	chr3:163961632-163962275	MCF-7	breast:	n/a	chr3:163961848-163961865
10	CEBPB	chr3:163917743-163918240	MCF-7	breast:	n/a	n/a
11	CEBPB	chr3:163912780-163912994	A549	lung:	n/a	n/a
12	CEBPB	chr3:163937041-163937366	HepG2	liver:	n/a	chr3:163937193-163937204
13	CEBPB	chr3:164077987-164078333	Hela-S3	cervix:	n/a	chr3:164078134-164078145
14	CEBPB	chr3:164078081-164078324	MCF-7	breast:	n/a	chr3:164078134-164078145
15	CEBPB	chr3:163937023-163937362	A549	lung:	n/a	chr3:163937193-163937204
16	CEBPB	chr3:163890801-163890962	H1-hESC	embryonic stem cell:	n/a	chr3:163890911-163890922
17	CEBPB	chr3:164078064-164078196	HepG2	liver:	n/a	chr3:164078134-164078145
18	CEBPB	chr3:164093357-164093663	A549	lung:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
19	CEBPB	chr3:164093320-164093640	HepG2	liver:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
20	CEBPB	chr3:164093408-164093523	K562	blood:	n/a	chr3:164093476-164093487
21	CEBPB	chr3:164077961-164078328	HepG2	liver:	n/a	chr3:164078134-164078145
22	CEBPB	chr3:163937048-163937294	Hela-S3	cervix:	n/a	chr3:163937193-163937204
23	CEBPB	chr3:163980083-163980289	Hela-S3	cervix:	n/a	chr3:163980184-163980195
24	CEBPB	chr3:164066095-164066166	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr3:163912779-163913052	HepG2	liver:	n/a	n/a
26	CEBPB	chr3:163980107-163980307	H1-hESC	embryonic stem cell:	n/a	chr3:163980184-163980195
27	CEBPB	chr3:164085608-164085831	IMR90	lung:	n/a	chr3:164085753-164085766
28	CEBPB	chr3:163980067-163980373	HepG2	liver:	n/a	chr3:163980184-163980195
29	CEBPB	chr3:163961690-163962327	MCF-7	breast:	n/a	chr3:163961848-163961865
30	CEBPB	chr3:163890818-163891012	HepG2	liver:	n/a	chr3:163890911-163890922
31	CEBPB	chr3:163925893-163926208	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr3:163937094-163937307	K562	blood:	n/a	chr3:163937193-163937204
33	CEBPB	chr3:164093370-164093659	Hela-S3	cervix:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
34	CEBPB	chr3:163885974-163886233	A549	lung:	n/a	chr3:163886110-163886119 chr3:163886110-163886119 chr3:163886110-163886119 chr3:163886109-163886120 chr3:163886108-163886121 chr3:163886108-163886119 chr3:163886110-163886119
35	CEBPB	chr3:163917764-163918192	MCF-7	breast:	n/a	n/a
36	CEBPB	chr3:163917760-163918155	Hela-S3	cervix:	n/a	n/a
37	CTBP2	chr3:164038799-164039115	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr3:164050700-164050850	HAc	cerebellar:	n/a	n/a
39	CTCF	chr3:163926841-163927193	MCF-7	breast:	n/a	n/a
40	CTCF	chr3:163926920-163927070	MCF-7	breast:	n/a	n/a
41	CTCF	chr3:163912760-163912910	HEK293	kidney:	n/a	n/a
42	CTCF	chr3:163928466-163928600	GM10248	blood:	n/a	n/a
43	CTCF	chr3:163912765-163912878	GM13977	blood:	n/a	n/a
44	CTCF	chr3:163912740-163912890	RPTEC	kidney:	n/a	n/a
45	CTCF	chr3:163968644-163969167	MCF-7	breast:	n/a	chr3:163968895-163968916 chr3:163968905-163968913 chr3:163968901-163968917
46	CTCF	chr3:163968860-163969010	Caco-2	colon:	n/a	chr3:163968895-163968916 chr3:163968905-163968913 chr3:163968901-163968917
47	CTCF	chr3:164050660-164050810	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr3:164093932-164094044	MCF-7	breast:	n/a	n/a
49	CTCF	chr3:164093900-164094050	AG09319	gingival:	n/a	n/a
50	CTCF	chr3:164093903-164094094	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:164009569-164009619	NH-A	brain:	n/a
2	chr3:164059255-164059305	HAEpiC	amniotic membrane:	n/a
3	chr3:164056463-164056513	HCF	heart:	n/a
4	chr3:164059011-164059061	HRPEpiC	eye:	n/a
5	chr3:164059255-164059305	GM12891	blood:	n/a
6	chr3:164059011-164059061	Jurkat	blood:	n/a
7	chr3:164050953-164051003	GM12891	blood:	n/a
8	chr3:164009569-164009619	SK-N-SH_RA	brain:	n/a
9	chr3:164009569-164009619	BJ	skin:	n/a
10	chr3:164059011-164059061	HPAEpiC	pulmonary alveolar:	n/a
11	chr3:164059124-164059174	HRCEpiC	kidney:	n/a
12	chr3:164059011-164059061	GM12878	blood:	n/a
13	chr3:164009569-164009619	Hela-S3	cervix:	n/a
14	chr3:164050953-164051003	HEEpiC	esophagus:	n/a
15	chr3:164050953-164051003	H1-hESC	embryonic stem cell:	embryo
16	chr3:164050953-164051003	HNPCEpiC	eye:	n/a
17	chr3:164050953-164051003	NH-A	brain:	n/a
18	chr3:164056753-164056803	H1-hESC	embryonic stem cell:	embryo
19	chr3:164056463-164056513	Hela-S3	cervix:	n/a
20	chr3:164050953-164051003	HCM	heart:	n/a
21	chr3:164059255-164059305	HUVEC	blood vessel:	n/a
22	chr3:164050953-164051003	GM19239	blood:	n/a
23	chr3:164059124-164059174	HCM	heart:	n/a
24	chr3:164056463-164056513	AG10803	skin:	n/a
25	chr3:164009569-164009619	HRCEpiC	kidney:	n/a
26	chr3:164059011-164059061	U87	brain:	n/a
27	chr3:164059255-164059305	AG09319	gingival:	n/a
28	chr3:164059255-164059305	AG04450	lung:	fetal
29	chr3:164059255-164059305	ovcar-3	ovarian:	n/a
30	chr3:164059011-164059061	SKMC	muscle:	n/a
31	chr3:164059124-164059174	HNPCEpiC	eye:	n/a
32	chr3:164056753-164056803	HL-60	blood:	n/a
33	chr3:164050953-164051003	HUVEC	blood vessel:	n/a
34	chr3:164056753-164056803	NT2-D1	testis:	n/a
35	chr3:164056753-164056803	BJ	skin:	n/a
36	chr3:164056463-164056513	AG09309	skin:	n/a
37	chr3:164050953-164051003	BJ	skin:	n/a
38	chr3:164009569-164009619	IMR90	lung:	fetal
39	chr3:164059011-164059061	AG04450	lung:	fetal
40	chr3:164059124-164059174	NHDF-neo	bronchial:	n/a
41	chr3:164009569-164009619	HRE	kidney:	n/a
42	chr3:164056463-164056513	HRE	kidney:	n/a
43	chr3:164050953-164051003	Jurkat	blood:	n/a
44	chr3:164056463-164056513	AG09319	gingival:	n/a
45	chr3:164056753-164056803	HCF	heart:	n/a
46	chr3:164056753-164056803	MCF-7	breast:	n/a
47	chr3:164056753-164056803	CMK	blood:	n/a
48	chr3:164059124-164059174	Caco-2	colon:	n/a
49	chr3:164059255-164059305	NT2-D1	testis:	n/a
50	chr3:164056463-164056513	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:163919977..163922257-chr3:163923536..163925910,2	MCF-7	breast:
2	chr17:57914661..57917089-chr3:163901184..163903192,2	MCF-7	breast:
3	chr3:163916797..163919508-chr3:163924219..163927520,3	MCF-7	breast:
4	chr3:163916797..163919508-chr3:163924219..163927520,3	MCF-7	breast:
5	chr3:163919977..163922257-chr3:163923536..163925910,2	MCF-7	breast:
6	chr3:163995585..163997750-chr3:164093655..164096327,2	K562	blood:
7	chr3:163995585..163997750-chr3:164093655..164096327,2	K562	blood:
8	chr3:164072695..164075481-chr3:164078791..164081086,2	MCF-7	breast:
9	chr3:164033562..164036466-chr3:164041623..164043945,2	MCF-7	breast:
10	chr3:164033562..164036466-chr3:164041623..164043945,2	MCF-7	breast:
11	chr3:163968485..163970197-chr3:163971709..163973734,2	MCF-7	breast:
12	chr10:36759743..36761957-chr3:163916939..163919179,2	K562	blood:
13	chr3:164032173..164034796-chr3:164095339..164097722,2	K562	blood:
14	chr3:164032173..164034796-chr3:164095339..164097722,2	K562	blood:
15	chr3:164072695..164075481-chr3:164078791..164081086,2	MCF-7	breast:
16	chr3:163988892..163990964-chr3:163991912..163993953,2	K562	blood:
17	chr3:164093244..164094225-chr3:164903325..164904113,2	MCF-7	breast:
18	chr3:164050649..164051226-chr3:164523700..164524566,2	MCF-7	breast:
19	chr3:163968485..163970197-chr3:163971709..163973734,2	MCF-7	breast:
20	chr3:163988892..163990964-chr3:163991912..163993953,2	K562	blood:

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

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1263	chr3:163889311-163889332	MIMAT0005915

Variant related genes	Relation type
MIR1263	TF binding region
MIR720	TF binding region
MIR1263	CpG island
MIR720	CpG island
ENSG00000062716	chromatin interactions

Extended variants
information (count: 7946 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:7946 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2218935	chr3:163885473-163885474	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537441434	chr3:163885474-163885475	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145117225	chr3:163885514-163885515	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148370232	chr3:163885515-163885516	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559431512	chr3:163885524-163885525	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141592291	chr3:163885544-163885545	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577881471	chr3:163885608-163885609	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs114346438	chr3:163885612-163885613	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553453888	chr3:163885622-163885623	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573308693	chr3:163885664-163885665	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150293635	chr3:163885691-163885692	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531898821	chr3:163885694-163885695	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6548333	chr3:163885704-163885705	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs137953194	chr3:163885731-163885732	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373551947	chr3:163885751-163885752	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543781390	chr3:163885768-163885769	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563770912	chr3:163885794-163885795	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369581192	chr3:163885799-163885800	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149482573	chr3:163885822-163885823	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539905094	chr3:163885835-163885836	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73876562	chr3:163885897-163885898	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147153638	chr3:163885922-163885923	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570736114	chr3:163885954-163885955	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549208778	chr3:163885963-163885964	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562751151	chr3:163886013-163886014	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148879204	chr3:163886088-163886089	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs10936411	chr3:163886113-163886114	Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs548700252	chr3:163886148-163886149	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs570967278	chr3:163886152-163886153	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs138730791	chr3:163886197-163886198	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570830883	chr3:163886297-163886298	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185105809	chr3:163886349-163886350	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560625982	chr3:163886371-163886372	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs115277726	chr3:163886427-163886428	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566994699	chr3:163886459-163886460	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs6548334	chr3:163886462-163886463	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs555567756	chr3:163886499-163886500	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372001100	chr3:163886510-163886511	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142785457	chr3:163886569-163886570	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538113384	chr3:163886577-163886578	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558035868	chr3:163886635-163886636	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577179458	chr3:163886637-163886638	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540265136	chr3:163886679-163886680	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559988652	chr3:163886698-163886699	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs28588722	chr3:163886700-163886701	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375132598	chr3:163886708-163886709	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369969483	chr3:163886711-163886712	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147410520	chr3:163886717-163886718	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542441936	chr3:163886737-163886738	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562638665	chr3:163886744-163886745	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	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	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
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:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:163879600-163898800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:163885200-163886000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:163886000-163886200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:163890800-163892800	Enhancers	Dnd41	blood
5	chr3:163892600-163892800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr3:163896800-163897400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:163898800-163904200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:163904200-163912800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr3:163911000-163911600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr3:163912400-163912800	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr3:163912800-163913000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:163912800-163918400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr3:163913000-163914000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:163914000-163914600	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:163914600-163915800	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:163915800-163916400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:163916400-163917200	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr3:163917200-163918000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:163918000-163918600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:163918200-163918600	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr3:163918400-163918600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr3:163918600-163919400	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:163919400-163925600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:163925600-163926000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr3:163925600-163926600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:163925800-163927800	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr3:163926200-163927400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr3:163926400-163926800	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr3:163926600-163927400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr3:163926600-163927600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr3:163926600-163927600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr3:163926600-163927800	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:163926800-163927200	Enhancers	Fetal Brain Male	brain
34	chr3:163926800-163927800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr3:163927800-163929200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr3:163929200-163931000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:163931000-163931400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr3:163931400-163932000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr3:163932000-163932600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:163932600-163933200	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:163933200-163934600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr3:163934600-163948600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:163938600-163940400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr3:163939200-163940000	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr3:163939200-163940400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr3:163939200-163940400	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr3:163939600-163940800	Enhancers	Dnd41	blood
48	chr3:163940000-163940400	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr3:163940000-163940400	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr3:163940000-163940400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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