Variant report

Variant	nsv877833
Chromosome Location	chr3:163761825-164109377
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	BRCA1	chr3:163881866-163881882	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr3:163805104-163805270	HepG2	liver:	n/a	chr3:163805134-163805145
5	CEBPB	chr3:163776828-163777158	HepG2	liver:	n/a	chr3:163777001-163777012
6	CEBPB	chr3:163811718-163811889	H1-hESC	embryonic stem cell:	n/a	chr3:163811787-163811796 chr3:163811785-163811796
7	CEBPB	chr3:163766254-163766629	IMR90	lung:	n/a	chr3:163766435-163766446
8	CEBPB	chr3:164085628-164085750	K562	blood:	n/a	n/a
9	CEBPB	chr3:163765442-163765609	A549	lung:	n/a	chr3:163765471-163765482
10	CEBPB	chr3:163776930-163777140	H1-hESC	embryonic stem cell:	n/a	chr3:163777001-163777012
11	CEBPB	chr3:163912780-163912994	A549	lung:	n/a	n/a
12	CEBPB	chr3:163980107-163980307	H1-hESC	embryonic stem cell:	n/a	chr3:163980184-163980195
13	CEBPB	chr3:164077996-164078260	A549	lung:	n/a	chr3:164078134-164078145
14	CEBPB	chr3:164097994-164098357	MCF-7	breast:	n/a	n/a
15	CEBPB	chr3:163811663-163811965	MCF-7	breast:	n/a	chr3:163811787-163811796 chr3:163811785-163811796
16	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
17	CEBPB	chr3:163980076-163980312	A549	lung:	n/a	chr3:163980184-163980195
18	CEBPB	chr3:164093370-164093659	Hela-S3	cervix:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
19	CEBPB	chr3:163890801-163890962	H1-hESC	embryonic stem cell:	n/a	chr3:163890911-163890922
20	CEBPB	chr3:163766257-163766618	HepG2	liver:	n/a	chr3:163766435-163766446
21	CEBPB	chr3:164085608-164085831	IMR90	lung:	n/a	chr3:164085753-164085766
22	CEBPB	chr3:164093320-164093640	HepG2	liver:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
23	CEBPB	chr3:163859641-163859926	HepG2	liver:	n/a	n/a
24	CEBPB	chr3:164066095-164066166	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr3:164078036-164078173	H1-hESC	embryonic stem cell:	n/a	chr3:164078134-164078145
26	CEBPB	chr3:163766262-163766585	K562	blood:	n/a	chr3:163766435-163766446
27	CEBPB	chr3:163766249-163766626	A549	lung:	n/a	chr3:163766435-163766446
28	CEBPB	chr3:164093357-164093663	A549	lung:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
29	CEBPB	chr3:163917743-163918240	MCF-7	breast:	n/a	n/a
30	CEBPB	chr3:163961690-163962327	MCF-7	breast:	n/a	chr3:163961848-163961865
31	CEBPB	chr3:163766342-163766605	ECC-1	luminal epithelium:	n/a	chr3:163766435-163766446
32	CEBPB	chr3:164077961-164078328	HepG2	liver:	n/a	chr3:164078134-164078145
33	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
34	CEBPB	chr3:163912779-163913052	HepG2	liver:	n/a	n/a
35	CEBPB	chr3:163961632-163962275	MCF-7	breast:	n/a	chr3:163961848-163961865
36	CEBPB	chr3:163925893-163926208	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr3:164077987-164078333	Hela-S3	cervix:	n/a	chr3:164078134-164078145
38	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
39	CEBPB	chr3:163917760-163918155	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr3:163937023-163937362	A549	lung:	n/a	chr3:163937193-163937204
41	CEBPB	chr3:163776822-163777172	IMR90	lung:	n/a	chr3:163777001-163777012
42	CEBPB	chr3:163937041-163937366	HepG2	liver:	n/a	chr3:163937193-163937204
43	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
44	CEBPB	chr3:163776817-163777197	A549	lung:	n/a	chr3:163777001-163777012
45	CEBPB	chr3:163980083-163980289	Hela-S3	cervix:	n/a	chr3:163980184-163980195
46	CEBPB	chr3:163860167-163860485	HepG2	liver:	n/a	chr3:163860323-163860334
47	CEBPB	chr3:164093408-164093523	K562	blood:	n/a	chr3:164093476-164093487
48	CEBPB	chr3:163766280-163766585	Hela-S3	cervix:	n/a	chr3:163766435-163766446
49	CEBPB	chr3:163767676-163768024	Hela-S3	cervix:	n/a	chr3:163767891-163767904
50	CEBPB	chr3:163767753-163767980	HepG2	liver:	n/a	chr3:163767891-163767904

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:164059011-164059061	GM19239	blood:	n/a
2	chr3:164059124-164059174	MCF10A-Er-Src	breast:	n/a
3	chr3:164050953-164051003	SAEC	small airway:	n/a
4	chr3:164056463-164056513	ECC-1	luminal epithelium:	n/a
5	chr3:164009569-164009619	NH-A	brain:	n/a
6	chr3:164009569-164009619	AG09319	gingival:	n/a
7	chr3:164059255-164059305	BE2_C	brain:	n/a
8	chr3:164056753-164056803	Hela-S3	cervix:	n/a
9	chr3:164056753-164056803	T-47D	breast:	n/a
10	chr3:164059255-164059305	HL-60	blood:	n/a
11	chr3:164009569-164009619	HRE	kidney:	n/a
12	chr3:164009569-164009619	HMEC	breast:	n/a
13	chr3:164050953-164051003	HIPEpiC	eye:	n/a
14	chr3:164056753-164056803	NHBE	bronchial:	n/a
15	chr3:164059124-164059174	ECC-1	luminal epithelium:	n/a
16	chr3:164056463-164056513	HRE	kidney:	n/a
17	chr3:164059011-164059061	HMEC	breast:	n/a
18	chr3:164059255-164059305	HEK293	kidney:	embryo
19	chr3:164056463-164056513	NHBE	bronchial:	n/a
20	chr3:164059255-164059305	Jurkat	blood:	n/a
21	chr3:164056753-164056803	PFSK-1	brain:	n/a
22	chr3:164050953-164051003	HCT-116	colon:	n/a
23	chr3:164009569-164009619	PANC-1	pancreas:	n/a
24	chr3:164059124-164059174	PFSK-1	brain:	n/a
25	chr3:164059255-164059305	PrEC	prostate:	n/a
26	chr3:164056463-164056513	AG04450	lung:	fetal
27	chr3:164050953-164051003	NH-A	brain:	n/a
28	chr3:164056463-164056513	AG04449	skin:	fetal
29	chr3:164059255-164059305	RPTEC	kidney:	n/a
30	chr3:164056463-164056513	HRCEpiC	kidney:	n/a
31	chr3:164009569-164009619	HIPEpiC	eye:	n/a
32	chr3:164059124-164059174	SK-N-MC	brain:	n/a
33	chr3:164059011-164059061	MCF10A-Er-Src	breast:	n/a
34	chr3:164059124-164059174	GM12892	blood:	n/a
35	chr3:164009569-164009619	MCF10A-Er-Src	breast:	n/a
36	chr3:164009569-164009619	MCF-7	breast:	n/a
37	chr3:164059255-164059305	HPAEpiC	pulmonary alveolar:	n/a
38	chr3:164059255-164059305	GM19239	blood:	n/a
39	chr3:164059255-164059305	HEEpiC	esophagus:	n/a
40	chr3:164059011-164059061	ovcar-3	ovarian:	n/a
41	chr3:164059255-164059305	HRE	kidney:	n/a
42	chr3:164056753-164056803	HCM	heart:	n/a
43	chr3:164009569-164009619	AG04450	lung:	fetal
44	chr3:164056463-164056513	Jurkat	blood:	n/a
45	chr3:164059011-164059061	SK-N-MC	brain:	n/a
46	chr3:164009569-164009619	K562	blood:	n/a
47	chr3:164059255-164059305	A549	lung:	n/a
48	chr3:164056753-164056803	GM12878	blood:	n/a
49	chr3:164050953-164051003	GM12878	blood:	n/a
50	chr3:164056753-164056803	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:36759743..36761957-chr3:163916939..163919179,2	K562	blood:
2	chr3:164097659..164099012-chr3:164352282..164353331,34	MCF-7	breast:
3	chr3:163759624..163761925-chr3:163765313..163767072,2	MCF-7	breast:
4	chr3:164097647..164098678-chr3:164154502..164155534,10	MCF-7	breast:
5	chr3:164050649..164051226-chr3:164523700..164524566,2	MCF-7	breast:
6	chr3:164097711..164098324-chr3:164241488..164242187,2	MCF-7	breast:
7	chr3:164097731..164098551-chr3:164154660..164155422,4	MCF-7	breast:
8	chr3:164072695..164075481-chr3:164078791..164081086,2	MCF-7	breast:
9	chr3:163916797..163919508-chr3:163924219..163927520,3	MCF-7	breast:
10	chr3:164097709..164098424-chr3:164241494..164242452,3	MCF-7	breast:
11	chr3:163919977..163922257-chr3:163923536..163925910,2	MCF-7	breast:
12	chr3:163968485..163970197-chr3:163971709..163973734,2	MCF-7	breast:
13	chr3:164032173..164034796-chr3:164095339..164097722,2	K562	blood:
14	chr3:163831824..163833454-chr3:163836559..163838959,2	K562	blood:
15	chr3:163816031..163818067-chr3:163819325..163821288,2	MCF-7	breast:
16	chr3:163995585..163997750-chr3:164093655..164096327,2	K562	blood:
17	chr3:164097647..164098715-chr3:164154502..164155534,19	MCF-7	breast:
18	chr3:163988892..163990964-chr3:163991912..163993953,2	K562	blood:
19	chr3:163968485..163970197-chr3:163971709..163973734,2	MCF-7	breast:
20	chr17:57914661..57917089-chr3:163901184..163903192,2	MCF-7	breast:
21	chr3:164097711..164099012-chr3:164352332..164353250,14	MCF-7	breast:
22	chr3:163759624..163761925-chr3:163765313..163767072,2	MCF-7	breast:
23	chr14:86195432..86196215-chr3:163793960..163794780,2	MCF-7	breast:
24	chr3:163756511..163759205-chr3:163797731..163799263,2	MCF-7	breast:
25	chr3:164072695..164075481-chr3:164078791..164081086,2	MCF-7	breast:
26	chr3:164032173..164034796-chr3:164095339..164097722,2	K562	blood:
27	chr3:163916797..163919508-chr3:163924219..163927520,3	MCF-7	breast:
28	chr3:164093244..164094225-chr3:164903325..164904113,2	MCF-7	breast:
29	chr3:163995585..163997750-chr3:164093655..164096327,2	K562	blood:
30	chr3:163919977..163922257-chr3:163923536..163925910,2	MCF-7	breast:
31	chr3:163831824..163833454-chr3:163836559..163838959,2	K562	blood:
32	chr3:164033562..164036466-chr3:164041623..164043945,2	MCF-7	breast:
33	chr3:163988892..163990964-chr3:163991912..163993953,2	K562	blood:
34	chr15:52587462..52588981-chr3:163831086..163833177,2	MCF-7	breast:
35	chr3:164033562..164036466-chr3:164041623..164043945,2	MCF-7	breast:
36	chr3:164097708..164098703-chr3:164352353..164353241,9	MCF-7	breast:
37	chr3:163816031..163818067-chr3:163819325..163821288,2	MCF-7	breast:
38	chr3:164097711..164098324-chr3:164241488..164242482,3	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

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

Variant related genes	Relation type
MIR720	TF binding region
MIR1263	TF binding region
MIR720	CpG island
MIR1263	CpG island
ENSG00000062716	chromatin interactions
ENSG00000128833	chromatin interactions

Extended variants
information (count: 13087 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:13087 , 50 per page) page: 1 2 3 4 5 6 7 ... 262

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13095640	chr3:163761825-163761826	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573342134	chr3:163761844-163761845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542318891	chr3:163761932-163761933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs7427021	chr3:163761964-163761965	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
5	rs187937112	chr3:163761986-163761987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545170716	chr3:163762005-163762006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546111065	chr3:163762043-163762044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78851654	chr3:163762166-163762167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527579207	chr3:163762193-163762194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376581199	chr3:163762231-163762232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529053009	chr3:163762287-163762288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs377582339	chr3:163762440-163762441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541375493	chr3:163762442-163762443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192305221	chr3:163762500-163762501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529289506	chr3:163762529-163762530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs58463603	chr3:163762541-163762542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs57704722	chr3:163762542-163762543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539822082	chr3:163762587-163762588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549183785	chr3:163762660-163762661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571741009	chr3:163762683-163762684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs151144430	chr3:163762703-163762704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139079431	chr3:163762727-163762728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531748640	chr3:163762808-163762809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183647441	chr3:163762810-163762811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532348873	chr3:163762869-163762870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550708696	chr3:163762909-163762910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149909543	chr3:163762912-163762913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs116489178	chr3:163762924-163762925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147608501	chr3:163762984-163762985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78712818	chr3:163763008-163763009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569095346	chr3:163763017-163763018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189032343	chr3:163763022-163763023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142213945	chr3:163763063-163763064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192950835	chr3:163763091-163763092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146125429	chr3:163763112-163763113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184876237	chr3:163763113-163763114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189777248	chr3:163763209-163763210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541278263	chr3:163763216-163763217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147839131	chr3:163763238-163763239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114510729	chr3:163763251-163763252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542993833	chr3:163763296-163763297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534784676	chr3:163763328-163763329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73876546	chr3:163763369-163763370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531831302	chr3:163763406-163763407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554299841	chr3:163763412-163763413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551502306	chr3:163763416-163763417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568468047	chr3:163763566-163763567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148903482	chr3:163763568-163763569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368537039	chr3:163763705-163763706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143222413	chr3:163763712-163763713	Weak 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	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	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:339 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:163758400-163771800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:163763800-163764000	Enhancers	Placenta	Placenta
3	chr3:163764000-163768000	Weak transcription	Placenta	Placenta
4	chr3:163765800-163766000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr3:163766000-163766200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr3:163768000-163768200	Enhancers	Placenta	Placenta
7	chr3:163771800-163795600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:163795600-163796000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr3:163796000-163797400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:163797400-163798800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:163798800-163803400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:163803400-163804400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:163804400-163805400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:163805400-163806800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:163806800-163811400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:163811400-163814400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:163811800-163814400	Enhancers	Dnd41	blood
18	chr3:163814400-163832200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:163831200-163831600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr3:163831200-163831600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr3:163831200-163832000	Enhancers	Dnd41	blood
22	chr3:163832200-163833000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:163833000-163837800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:163837800-163839200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr3:163839200-163852000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:163841400-163841800	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr3:163841400-163841800	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr3:163841400-163841800	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr3:163841800-163842200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr3:163848600-163849800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr3:163852000-163854600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr3:163854600-163862000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:163860000-163861400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr3:163862000-163870200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:163863200-163866400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
36	chr3:163865800-163867600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
37	chr3:163868200-163870200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr3:163870200-163874600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr3:163873400-163873800	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr3:163874600-163879600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:163875800-163876200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr3:163879600-163898800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:163881400-163881600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr3:163883600-163885200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr3:163885200-163886000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr3:163886000-163886200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr3:163890800-163892800	Enhancers	Dnd41	blood
48	chr3:163892600-163892800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr3:163896800-163897400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr3:163898800-163904200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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