Variant report

Variant	nsv877843
Chromosome Location	chr3:163835270-164126802
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	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	chr3:163980083-163980289	Hela-S3	cervix:	n/a	chr3:163980184-163980195
5	CEBPB	chr3:164077987-164078333	Hela-S3	cervix:	n/a	chr3:164078134-164078145
6	CEBPB	chr3:164121373-164121695	HepG2	liver:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
7	CEBPB	chr3:164093357-164093663	A549	lung:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
8	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
9	CEBPB	chr3:164121454-164121666	H1-hESC	embryonic stem cell:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
10	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
11	CEBPB	chr3:164078036-164078173	H1-hESC	embryonic stem cell:	n/a	chr3:164078134-164078145
12	CEBPB	chr3:163860167-163860485	HepG2	liver:	n/a	chr3:163860323-163860334
13	CEBPB	chr3:164085608-164085831	IMR90	lung:	n/a	chr3:164085753-164085766
14	CEBPB	chr3:163917760-163918155	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr3:163961632-163962275	MCF-7	breast:	n/a	chr3:163961848-163961865
16	CEBPB	chr3:164093320-164093640	HepG2	liver:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
17	CEBPB	chr3:164077996-164078260	A549	lung:	n/a	chr3:164078134-164078145
18	CEBPB	chr3:163912779-163913052	HepG2	liver:	n/a	n/a
19	CEBPB	chr3:163917764-163918192	MCF-7	breast:	n/a	n/a
20	CEBPB	chr3:163937048-163937294	Hela-S3	cervix:	n/a	chr3:163937193-163937204
21	CEBPB	chr3:164121369-164121693	A549	lung:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
22	CEBPB	chr3:163890801-163890962	H1-hESC	embryonic stem cell:	n/a	chr3:163890911-163890922
23	CEBPB	chr3:164097994-164098357	MCF-7	breast:	n/a	n/a
24	CEBPB	chr3:163925893-163926208	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr3:163917743-163918240	MCF-7	breast:	n/a	n/a
26	CEBPB	chr3:163912780-163912994	A549	lung:	n/a	n/a
27	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
28	CEBPB	chr3:164121426-164121694	K562	blood:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
29	CEBPB	chr3:163937023-163937362	A549	lung:	n/a	chr3:163937193-163937204
30	CEBPB	chr3:163980067-163980373	HepG2	liver:	n/a	chr3:163980184-163980195
31	CEBPB	chr3:163859641-163859926	HepG2	liver:	n/a	n/a
32	CEBPB	chr3:163890818-163891012	HepG2	liver:	n/a	chr3:163890911-163890922
33	CEBPB	chr3:163937094-163937307	K562	blood:	n/a	chr3:163937193-163937204
34	CEBPB	chr3:163937041-163937366	HepG2	liver:	n/a	chr3:163937193-163937204
35	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
36	CEBPB	chr3:164121359-164121699	IMR90	lung:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
37	CEBPB	chr3:164085628-164085750	K562	blood:	n/a	n/a
38	CEBPB	chr3:163980107-163980307	H1-hESC	embryonic stem cell:	n/a	chr3:163980184-163980195
39	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
40	CEBPB	chr3:164066095-164066166	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr3:164078081-164078324	MCF-7	breast:	n/a	chr3:164078134-164078145
42	CEBPB	chr3:164093370-164093659	Hela-S3	cervix:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
43	CEBPB	chr3:163980076-163980312	A549	lung:	n/a	chr3:163980184-163980195
44	CEBPB	chr3:163961690-163962327	MCF-7	breast:	n/a	chr3:163961848-163961865
45	CEBPB	chr3:163912738-163913096	MCF-7	breast:	n/a	n/a
46	CEBPB	chr3:164077961-164078328	HepG2	liver:	n/a	chr3:164078134-164078145
47	CEBPB	chr3:164078064-164078196	HepG2	liver:	n/a	chr3:164078134-164078145
48	CEBPB	chr3:164093408-164093523	K562	blood:	n/a	chr3:164093476-164093487
49	CEBPB	chr3:163855035-163855235	HepG2	liver:	n/a	chr3:163855103-163855114
50	CTBP2	chr3:164038799-164039115	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:164059011-164059061	BJ	skin:	n/a
2	chr3:164119959-164120009	LNCaP	prostate:	n/a
3	chr3:164056463-164056513	HNPCEpiC	eye:	n/a
4	chr3:164119737-164119787	Hela-S3	cervix:	n/a
5	chr3:164056753-164056803	Jurkat	blood:	n/a
6	chr3:164056463-164056513	SAEC	small airway:	n/a
7	chr3:164119959-164120009	HAEpiC	amniotic membrane:	n/a
8	chr3:164056753-164056803	NB4	blood:	n/a
9	chr3:164059124-164059174	HUVEC	blood vessel:	n/a
10	chr3:164119959-164120009	HUVEC	blood vessel:	n/a
11	chr3:164059124-164059174	MCF10A-Er-Src	breast:	n/a
12	chr3:164119959-164120009	SK-N-MC	brain:	n/a
13	chr3:164059255-164059305	AG04450	lung:	fetal
14	chr3:164009569-164009619	BE2_C	brain:	n/a
15	chr3:164059011-164059061	NT2-D1	testis:	n/a
16	chr3:164119959-164120009	A549	lung:	n/a
17	chr3:164059124-164059174	GM12891	blood:	n/a
18	chr3:164119737-164119787	HL-60	blood:	n/a
19	chr3:164119737-164119787	PrEC	prostate:	n/a
20	chr3:164119959-164120009	NB4	blood:	n/a
21	chr3:164119020-164119070	SK-N-MC	brain:	n/a
22	chr3:164119959-164120009	NH-A	brain:	n/a
23	chr3:164009569-164009619	CMK	blood:	n/a
24	chr3:164056753-164056803	SAEC	small airway:	n/a
25	chr3:164059255-164059305	T-47D	breast:	n/a
26	chr3:164009569-164009619	MCF10A-Er-Src	breast:	n/a
27	chr3:164059255-164059305	NB4	blood:	n/a
28	chr3:164059255-164059305	HIPEpiC	eye:	n/a
29	chr3:164050953-164051003	Caco-2	colon:	n/a
30	chr3:164050953-164051003	HUVEC	blood vessel:	n/a
31	chr3:164059255-164059305	HCPEpiC	choroid plexus:	n/a
32	chr3:164056463-164056513	K562	blood:	n/a
33	chr3:164119959-164120009	T-47D	breast:	n/a
34	chr3:164009569-164009619	GM19239	blood:	n/a
35	chr3:164059255-164059305	HCT-116	colon:	n/a
36	chr3:164059124-164059174	GM12892	blood:	n/a
37	chr3:164059124-164059174	LNCaP	prostate:	n/a
38	chr3:164056753-164056803	HEK293	kidney:	embryo
39	chr3:164119020-164119070	AG09309	skin:	n/a
40	chr3:164056753-164056803	SKMC	muscle:	n/a
41	chr3:164059011-164059061	PANC-1	pancreas:	n/a
42	chr3:164119959-164120009	ovcar-3	ovarian:	n/a
43	chr3:164059011-164059061	NH-A	brain:	n/a
44	chr3:164050953-164051003	AG04449	skin:	fetal
45	chr3:164056753-164056803	GM12892	blood:	n/a
46	chr3:164119020-164119070	GM12891	blood:	n/a
47	chr3:164059011-164059061	Hela-S3	cervix:	n/a
48	chr3:164056463-164056513	GM12892	blood:	n/a
49	chr3:164059124-164059174	HCF	heart:	n/a
50	chr3:164119020-164119070	SKMC	muscle:	n/a

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

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: 10624 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:10624 , 50 per page) page: 1 2 3 4 5 6 7 ... 213

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2122377	chr3:163835270-163835271	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368616366	chr3:163835304-163835305	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527714085	chr3:163835349-163835350	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76751663	chr3:163835362-163835363	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552130694	chr3:163835365-163835366	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143536342	chr3:163835388-163835389	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1449920	chr3:163835442-163835443	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531680856	chr3:163835496-163835497	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574529173	chr3:163835507-163835508	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1449921	chr3:163835511-163835512	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs77454717	chr3:163835541-163835542	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs1449922	chr3:163835546-163835547	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs1449923	chr3:163835591-163835592	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs191474428	chr3:163835593-163835594	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565278962	chr3:163835756-163835757	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566512097	chr3:163835765-163835766	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs527729670	chr3:163835821-163835822	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150991268	chr3:163835870-163835871	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567777182	chr3:163835890-163835891	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565960219	chr3:163835895-163835896	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536369795	chr3:163835915-163835916	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550315010	chr3:163835999-163836000	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570164961	chr3:163836079-163836080	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs56322923	chr3:163836108-163836109	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs558868589	chr3:163836124-163836125	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184269240	chr3:163836130-163836131	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10155028	chr3:163836131-163836132	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs371289330	chr3:163836153-163836154	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs397778515	chr3:163836164-163836165	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575793186	chr3:163836168-163836169	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576068527	chr3:163836173-163836174	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544665035	chr3:163836214-163836215	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114629170	chr3:163836229-163836230	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543165976	chr3:163836280-163836281	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563453787	chr3:163836311-163836312	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577159502	chr3:163836336-163836337	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546113250	chr3:163836353-163836354	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559721091	chr3:163836357-163836358	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200159709	chr3:163836409-163836410	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148463977	chr3:163836425-163836426	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs55986997	chr3:163836426-163836427	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7427031	chr3:163836427-163836428	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs116492424	chr3:163836462-163836463	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34989619	chr3:163836476-163836477	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1375832	chr3:163836487-163836488	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs188028848	chr3:163836529-163836530	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530169550	chr3:163836571-163836572	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1375833	chr3:163836581-163836582	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs540537466	chr3:163836588-163836589	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368365993	chr3:163836601-163836602	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:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:163833000-163837800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:163837800-163839200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:163839200-163852000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:163841400-163841800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr3:163841400-163841800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr3:163841400-163841800	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr3:163841800-163842200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr3:163848600-163849800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr3:163852000-163854600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:163854600-163862000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:163860000-163861400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr3:163862000-163870200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:163863200-163866400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
14	chr3:163865800-163867600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
15	chr3:163868200-163870200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr3:163870200-163874600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:163873400-163873800	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr3:163874600-163879600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:163875800-163876200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr3:163879600-163898800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:163881400-163881600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr3:163883600-163885200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr3:163885200-163886000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr3:163886000-163886200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr3:163890800-163892800	Enhancers	Dnd41	blood
26	chr3:163892600-163892800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr3:163896800-163897400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr3:163898800-163904200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:163904200-163912800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr3:163911000-163911600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr3:163912400-163912800	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr3:163912800-163913000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:163912800-163918400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr3:163913000-163914000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:163914000-163914600	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr3:163914600-163915800	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:163915800-163916400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr3:163916400-163917200	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr3:163917200-163918000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:163918000-163918600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:163918200-163918600	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr3:163918400-163918600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr3:163918600-163919400	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr3:163919400-163925600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:163925600-163926000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr3:163925600-163926600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr3:163925800-163927800	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr3:163926200-163927400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr3:163926400-163926800	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr3:163926600-163927400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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