Variant report

Variant	nsv877839
Chromosome Location	chr3:163823186-164126802
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	chr3:164107093-164107343	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
5	CEBPB	chr3:163980107-163980307	H1-hESC	embryonic stem cell:	n/a	chr3:163980184-163980195
6	CEBPB	chr3:164077996-164078260	A549	lung:	n/a	chr3:164078134-164078145
7	CEBPB	chr3:164077961-164078328	HepG2	liver:	n/a	chr3:164078134-164078145
8	CEBPB	chr3:164097994-164098357	MCF-7	breast:	n/a	n/a
9	CEBPB	chr3:164121369-164121693	A549	lung:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
10	CEBPB	chr3:163859641-163859926	HepG2	liver:	n/a	n/a
11	CEBPB	chr3:164121359-164121699	IMR90	lung:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
12	CEBPB	chr3:164093408-164093523	K562	blood:	n/a	chr3:164093476-164093487
13	CEBPB	chr3:163855035-163855235	HepG2	liver:	n/a	chr3:163855103-163855114
14	CEBPB	chr3:163917760-163918155	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr3:164093320-164093640	HepG2	liver:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
16	CEBPB	chr3:163937048-163937294	Hela-S3	cervix:	n/a	chr3:163937193-163937204
17	CEBPB	chr3:163961632-163962275	MCF-7	breast:	n/a	chr3:163961848-163961865
18	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
19	CEBPB	chr3:163961690-163962327	MCF-7	breast:	n/a	chr3:163961848-163961865
20	CEBPB	chr3:163860167-163860485	HepG2	liver:	n/a	chr3:163860323-163860334
21	CEBPB	chr3:164078064-164078196	HepG2	liver:	n/a	chr3:164078134-164078145
22	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
23	CEBPB	chr3:164085608-164085831	IMR90	lung:	n/a	chr3:164085753-164085766
24	CEBPB	chr3:163937023-163937362	A549	lung:	n/a	chr3:163937193-163937204
25	CEBPB	chr3:163937094-163937307	K562	blood:	n/a	chr3:163937193-163937204
26	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
27	CEBPB	chr3:164077987-164078333	Hela-S3	cervix:	n/a	chr3:164078134-164078145
28	CEBPB	chr3:163937041-163937366	HepG2	liver:	n/a	chr3:163937193-163937204
29	CEBPB	chr3:164078081-164078324	MCF-7	breast:	n/a	chr3:164078134-164078145
30	CEBPB	chr3:163925893-163926208	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr3:163890818-163891012	HepG2	liver:	n/a	chr3:163890911-163890922
32	CEBPB	chr3:164121454-164121666	H1-hESC	embryonic stem cell:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
33	CEBPB	chr3:164121426-164121694	K562	blood:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
34	CEBPB	chr3:164078036-164078173	H1-hESC	embryonic stem cell:	n/a	chr3:164078134-164078145
35	CEBPB	chr3:164093370-164093659	Hela-S3	cervix:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
36	CEBPB	chr3:163980083-163980289	Hela-S3	cervix:	n/a	chr3:163980184-163980195
37	CEBPB	chr3:163912780-163912994	A549	lung:	n/a	n/a
38	CEBPB	chr3:163912779-163913052	HepG2	liver:	n/a	n/a
39	CEBPB	chr3:163917764-163918192	MCF-7	breast:	n/a	n/a
40	CEBPB	chr3:163912738-163913096	MCF-7	breast:	n/a	n/a
41	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
42	CEBPB	chr3:164093357-164093663	A549	lung:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
43	CEBPB	chr3:163980076-163980312	A549	lung:	n/a	chr3:163980184-163980195
44	CEBPB	chr3:163980067-163980373	HepG2	liver:	n/a	chr3:163980184-163980195
45	CEBPB	chr3:163917743-163918240	MCF-7	breast:	n/a	n/a
46	CEBPB	chr3:164066095-164066166	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr3:164121373-164121695	HepG2	liver:	n/a	chr3:164121533-164121544 chr3:164121535-164121544
48	CEBPB	chr3:163890801-163890962	H1-hESC	embryonic stem cell:	n/a	chr3:163890911-163890922
49	CEBPB	chr3:164085628-164085750	K562	blood:	n/a	n/a
50	CTBP2	chr3:164038799-164039115	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:164119737-164119787	K562	blood:	n/a
2	chr3:164119737-164119787	K562	blood:	n/a
3	chr3:164059255-164059305	GM12878	blood:	n/a
4	chr3:164119020-164119070	HIPEpiC	eye:	n/a
5	chr3:164056753-164056803	GM06990	blood:	n/a
6	chr3:164059255-164059305	HL-60	blood:	n/a
7	chr3:164119959-164120009	HCT-116	colon:	n/a
8	chr3:164050953-164051003	HUVEC	blood vessel:	n/a
9	chr3:164119737-164119787	Caco-2	colon:	n/a
10	chr3:164059255-164059305	GM06990	blood:	n/a
11	chr3:164050953-164051003	AG04450	lung:	fetal
12	chr3:164119737-164119787	CMK	blood:	n/a
13	chr3:164119020-164119070	K562	blood:	n/a
14	chr3:164050953-164051003	GM19239	blood:	n/a
15	chr3:164050953-164051003	Hepatocyte	liver:	n/a
16	chr3:164059124-164059174	Hela-S3	cervix:	n/a
17	chr3:164056753-164056803	HL-60	blood:	n/a
18	chr3:164056753-164056803	AG09319	gingival:	n/a
19	chr3:164056463-164056513	HCF	heart:	n/a
20	chr3:164119737-164119787	HIPEpiC	eye:	n/a
21	chr3:164059255-164059305	GM19239	blood:	n/a
22	chr3:164059124-164059174	NB4	blood:	n/a
23	chr3:164056463-164056513	HIPEpiC	eye:	n/a
24	chr3:164119737-164119787	ECC-1	luminal epithelium:	n/a
25	chr3:164056463-164056513	AG04449	skin:	fetal
26	chr3:164119959-164120009	T-47D	breast:	n/a
27	chr3:164059011-164059061	Hepatocyte	liver:	n/a
28	chr3:164059124-164059174	HNPCEpiC	eye:	n/a
29	chr3:164119020-164119070	H1-hESC	embryonic stem cell:	embryo
30	chr3:164050953-164051003	ovcar-3	ovarian:	n/a
31	chr3:164059255-164059305	SKMC	muscle:	n/a
32	chr3:164059124-164059174	HepG2	liver:	n/a
33	chr3:164059255-164059305	MCF-7	breast:	n/a
34	chr3:164119020-164119070	HRCEpiC	kidney:	n/a
35	chr3:164119737-164119787	HCF	heart:	n/a
36	chr3:164059011-164059061	HCF	heart:	n/a
37	chr3:164050953-164051003	RPTEC	kidney:	n/a
38	chr3:164119737-164119787	AoSMC	blood vessel:	n/a
39	chr3:164059011-164059061	PANC-1	pancreas:	n/a
40	chr3:164119020-164119070	HPAEpiC	pulmonary alveolar:	n/a
41	chr3:164119737-164119787	NH-A	brain:	n/a
42	chr3:164056753-164056803	NHDF-neo	bronchial:	n/a
43	chr3:164059255-164059305	PANC-1	pancreas:	n/a
44	chr3:164119737-164119787	HRPEpiC	eye:	n/a
45	chr3:164050953-164051003	BJ	skin:	n/a
46	chr3:164056753-164056803	A549	lung:	n/a
47	chr3:164056463-164056513	HPAEpiC	pulmonary alveolar:	n/a
48	chr3:164119020-164119070	ECC-1	luminal epithelium:	n/a
49	chr3:164119020-164119070	ProgFib	skin:	n/a
50	chr3:164056753-164056803	ECC-1	luminal epithelium:	n/a

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

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
MIR1263	TF binding region
MIR720	TF binding region
MIR1263	CpG island
MIR720	CpG island
ENSG00000128833	chromatin interactions
ENSG00000062716	chromatin interactions

Extended variants
information (count: 11094 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:11094 , 50 per page) page: 1 2 3 4 5 6 7 ... 222

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1901552	chr3:163823186-163823187	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115005251	chr3:163823279-163823280	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs139716854	chr3:163823281-163823282	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs116692005	chr3:163823282-163823283	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540915225	chr3:163823309-163823310	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537206422	chr3:163823343-163823344	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs193027021	chr3:163823370-163823371	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184554027	chr3:163823394-163823395	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189276058	chr3:163823395-163823396	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543025846	chr3:163823396-163823397	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs180827246	chr3:163823403-163823404	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532054625	chr3:163823413-163823414	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545916463	chr3:163823456-163823457	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556065005	chr3:163823462-163823463	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574246152	chr3:163823504-163823505	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559271077	chr3:163823524-163823525	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376167331	chr3:163823572-163823573	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149798470	chr3:163823581-163823582	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144708349	chr3:163823611-163823612	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568371637	chr3:163823656-163823657	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530080706	chr3:163823675-163823676	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550218404	chr3:163823717-163823718	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570094110	chr3:163823727-163823728	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185627292	chr3:163823791-163823792	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559049398	chr3:163823792-163823793	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146572534	chr3:163823796-163823797	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113966203	chr3:163823808-163823809	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564258879	chr3:163823850-163823851	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs34454664	chr3:163823899-163823900	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371115764	chr3:163823991-163823992	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566139352	chr3:163823997-163823998	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373404894	chr3:163824044-163824045	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148537133	chr3:163824051-163824052	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554803642	chr3:163824052-163824053	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574810645	chr3:163824067-163824068	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114565960	chr3:163824078-163824079	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556521901	chr3:163824133-163824134	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576811464	chr3:163824136-163824137	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545575502	chr3:163824209-163824210	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372270631	chr3:163824222-163824223	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544858265	chr3:163824267-163824268	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377089384	chr3:163824274-163824275	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533275928	chr3:163824282-163824283	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199545141	chr3:163824297-163824298	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542060625	chr3:163824306-163824307	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188533083	chr3:163824320-163824321	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573722948	chr3:163824356-163824357	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs80143441	chr3:163824357-163824358	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145518358	chr3:163824380-163824381	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550929494	chr3:163824419-163824420	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:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:163814400-163832200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:163831200-163831600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:163831200-163831600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr3:163831200-163832000	Enhancers	Dnd41	blood
5	chr3:163832200-163833000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:163833000-163837800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr3:163837800-163839200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:163839200-163852000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr3:163841400-163841800	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr3:163841400-163841800	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr3:163841400-163841800	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr3:163841800-163842200	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr3:163848600-163849800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr3:163852000-163854600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:163854600-163862000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:163860000-163861400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr3:163862000-163870200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr3:163863200-163866400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
19	chr3:163865800-163867600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
20	chr3:163868200-163870200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr3:163870200-163874600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:163873400-163873800	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr3:163874600-163879600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:163875800-163876200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr3:163879600-163898800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:163881400-163881600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr3:163883600-163885200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr3:163885200-163886000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr3:163886000-163886200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr3:163890800-163892800	Enhancers	Dnd41	blood
31	chr3:163892600-163892800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr3:163896800-163897400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr3:163898800-163904200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:163904200-163912800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:163911000-163911600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr3:163912400-163912800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr3:163912800-163913000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr3:163912800-163918400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr3:163913000-163914000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:163914000-163914600	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:163914600-163915800	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr3:163915800-163916400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:163916400-163917200	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr3:163917200-163918000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:163918000-163918600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr3:163918200-163918600	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr3:163918400-163918600	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr3:163918600-163919400	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:163919400-163925600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr3:163925600-163926000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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