Variant report

Variant	nsv511924
Chromosome Location	chr6:164762179-165077399
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:925)
CpG islands
(count:488)
Chromatin interactive
region (count:61)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:925 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:164767622-164767980	K562	blood:	n/a	n/a
2	ARID3A	chr6:164798491-164798683	K562	blood:	n/a	n/a
3	ATF1	chr6:164918144-164918284	K562	blood:	n/a	n/a
4	ATF1	chr6:164767707-164768041	K562	blood:	n/a	n/a
5	ATF2	chr6:164928321-164929043	GM12878	blood:	n/a	n/a
6	ATF2	chr6:164928270-164929113	GM12878	blood:	n/a	n/a
7	ATF2	chr6:164765756-164766224	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr6:164926459-164926870	GM12878	blood:	n/a	n/a
9	ATF3	chr6:164768570-164768730	K562	blood:	n/a	n/a
10	BATF	chr6:164928549-164928927	GM12878	blood:	n/a	n/a
11	BATF	chr6:164952830-164953115	GM12878	blood:	n/a	chr6:164952982-164952993
12	BATF	chr6:164898891-164899123	GM12878	blood:	n/a	n/a
13	BATF	chr6:164926445-164926910	GM12878	blood:	n/a	n/a
14	BATF	chr6:164928521-164929021	GM12878	blood:	n/a	n/a
15	BATF	chr6:164952872-164953114	GM12878	blood:	n/a	chr6:164952982-164952993
16	BATF	chr6:164898863-164899130	GM12878	blood:	n/a	n/a
17	BCL11A	chr6:164928408-164928949	GM12878	blood:	n/a	n/a
18	BCL11A	chr6:164765922-164766293	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL11A	chr6:164926483-164926915	GM12878	blood:	n/a	n/a
20	BCL11A	chr6:164928320-164929011	GM12878	blood:	n/a	n/a
21	BCL3	chr6:164928630-164929027	GM12878	blood:	n/a	n/a
22	BCL3	chr6:164926405-164926609	GM12878	blood:	n/a	n/a
23	BCLAF1	chr6:164928453-164929082	GM12878	blood:	n/a	n/a
24	BCLAF1	chr6:164928419-164929054	GM12878	blood:	n/a	n/a
25	BHLHE40	chr6:164952948-164953079	GM12878	blood:	n/a	n/a
26	BHLHE40	chr6:164826224-164826542	K562	blood:	n/a	n/a
27	BHLHE40	chr6:164953286-164953312	GM12878	blood:	n/a	n/a
28	BHLHE40	chr6:164926462-164926801	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:164928355-164929088	GM12878	blood:	n/a	n/a
30	CBX3	chr6:164777916-164778190	K562	blood:	n/a	n/a
31	CBX3	chr6:165055640-165055827	K562	blood:	n/a	n/a
32	CBX3	chr6:164825821-164826135	K562	blood:	n/a	n/a
33	CBX3	chr6:164767637-164768036	K562	blood:	n/a	n/a
34	CBX3	chr6:164947063-164947378	K562	blood:	n/a	n/a
35	CBX3	chr6:164768484-164768814	K562	blood:	n/a	n/a
36	CBX3	chr6:164802633-164802852	K562	blood:	n/a	n/a
37	CCNT2	chr6:164767714-164768074	K562	blood:	n/a	n/a
38	CCNT2	chr6:164889314-164889407	K562	blood:	n/a	n/a
39	CCNT2	chr6:164858191-164858336	K562	blood:	n/a	n/a
40	CEBPB	chr6:164767777-164767926	K562	blood:	n/a	n/a
41	CEBPB	chr6:164798384-164798726	K562	blood:	n/a	n/a
42	CEBPB	chr6:164798376-164798710	K562	blood:	n/a	n/a
43	CEBPB	chr6:164928530-164929093	GM12878	blood:	n/a	n/a
44	CEBPB	chr6:164996421-164996674	HepG2	liver:	n/a	chr6:164996578-164996589
45	CEBPB	chr6:164899513-164899619	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr6:165054168-165054395	HepG2	liver:	n/a	chr6:165054256-165054267
47	CEBPB	chr6:164955364-164955598	HepG2	liver:	n/a	chr6:164955492-164955503
48	CEBPB	chr6:164765798-164766625	H1-hESC	embryonic stem cell:	n/a	chr6:164766519-164766530
49	CEBPB	chr6:164767547-164768187	K562	blood:	n/a	n/a
50	CEBPB	chr6:164920704-164920887	K562	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:164975487-164975537	HEK293	kidney:	embryo
2	chr6:164767056-164767106	Jurkat	blood:	n/a
3	chr6:165062070-165062120	SK-N-SH_RA	brain:	n/a
4	chr6:164975487-164975537	MCF-7	breast:	n/a
5	chr6:164767056-164767106	IMR90	lung:	fetal
6	chr6:165032072-165032122	AG09309	skin:	n/a
7	chr6:164990879-164990929	NHBE	bronchial:	n/a
8	chr6:165032124-165032174	GM06990	blood:	n/a
9	chr6:164817337-164817387	RPTEC	kidney:	n/a
10	chr6:164767056-164767106	Hepatocyte	liver:	n/a
11	chr6:165032072-165032122	SKMC	muscle:	n/a
12	chr6:164817337-164817387	T-47D	breast:	n/a
13	chr6:165032068-165032118	MCF-7	breast:	n/a
14	chr6:165032072-165032122	PFSK-1	brain:	n/a
15	chr6:164817337-164817387	HRPEpiC	eye:	n/a
16	chr6:165062070-165062120	NHBE	bronchial:	n/a
17	chr6:164990879-164990929	K562	blood:	n/a
18	chr6:164767056-164767106	HEEpiC	esophagus:	n/a
19	chr6:165062070-165062120	NHDF-neo	bronchial:	n/a
20	chr6:165032072-165032122	NH-A	brain:	n/a
21	chr6:165032124-165032174	Hela-S3	cervix:	n/a
22	chr6:164975487-164975537	Hepatocyte	liver:	n/a
23	chr6:165062070-165062120	MCF-7	breast:	n/a
24	chr6:164990879-164990929	NHDF-neo	bronchial:	n/a
25	chr6:165062070-165062120	NT2-D1	testis:	n/a
26	chr6:165032124-165032174	MCF-7	breast:	n/a
27	chr6:165032072-165032122	AG04450	lung:	fetal
28	chr6:165032072-165032122	MCF10A-Er-Src	breast:	n/a
29	chr6:164817337-164817387	AG04449	skin:	fetal
30	chr6:164975487-164975537	HCF	heart:	n/a
31	chr6:165032072-165032122	BE2_C	brain:	n/a
32	chr6:165032124-165032174	Jurkat	blood:	n/a
33	chr6:164817337-164817387	HEEpiC	esophagus:	n/a
34	chr6:165062070-165062120	A549	lung:	n/a
35	chr6:165032124-165032174	HCM	heart:	n/a
36	chr6:165032072-165032122	HMEC	breast:	n/a
37	chr6:164990879-164990929	ECC-1	luminal epithelium:	n/a
38	chr6:165062070-165062120	PANC-1	pancreas:	n/a
39	chr6:165032072-165032122	NT2-D1	testis:	n/a
40	chr6:164975487-164975537	GM12891	blood:	n/a
41	chr6:165032068-165032118	MCF10A-Er-Src	breast:	n/a
42	chr6:164975487-164975537	Caco-2	colon:	n/a
43	chr6:164767056-164767106	PANC-1	pancreas:	n/a
44	chr6:164990879-164990929	HPAEpiC	pulmonary alveolar:	n/a
45	chr6:165032124-165032174	Hepatocyte	liver:	n/a
46	chr6:165032124-165032174	HMEC	breast:	n/a
47	chr6:164767056-164767106	HPAEpiC	pulmonary alveolar:	n/a
48	chr6:164975487-164975537	MCF10A-Er-Src	breast:	n/a
49	chr6:164990879-164990929	AoSMC	blood vessel:	n/a
50	chr6:164817337-164817387	GM12878	blood:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:164974094..164976654-chr6:164987580..164991765,3	K562	blood:
2	chr6:164686752..164688649-chr6:164926400..164929069,2	K562	blood:
3	chr6:164767365..164769035-chr6:164822554..164824204,2	K562	blood:
4	chr6:165029398..165031412-chr6:165033183..165034759,2	K562	blood:
5	chr6:164767711..164769131-chr6:165340232..165341669,7	MCF-7	breast:
6	chr6:164860412..164863160-chr6:164883552..164885284,2	K562	blood:
7	chr6:164798125..164802014-chr6:164802831..164806274,3	K562	blood:
8	chr6:164797286..164799479-chr6:164818764..164821424,2	K562	blood:
9	chr6:164862673..164864670-chr6:164866180..164868156,2	K562	blood:
10	chr6:164767365..164769035-chr6:164822554..164824204,2	K562	blood:
11	chr6:164814459..164817291-chr6:164821398..164824476,3	K562	blood:
12	chr6:164826913..164829845-chr6:164834931..164836483,2	MCF-7	breast:
13	chr6:164563456..164565737-chr6:164880821..164882711,2	K562	blood:
14	chr6:164781175..164783778-chr6:164784737..164786491,2	K562	blood:
15	chr6:164862673..164864670-chr6:164866180..164868156,2	K562	blood:
16	chr6:164752242..164755007-chr6:164766257..164769251,2	K562	blood:
17	chr6:164921896..164924065-chr6:164926926..164929032,3	K562	blood:
18	chr6:164796151..164797865-chr6:164799819..164802680,2	K562	blood:
19	chr6:164815480..164817452-chr6:164823900..164826799,2	K562	blood:
20	chr6:164754441..164757188-chr6:164816379..164818209,2	K562	blood:
21	chr6:165050032..165051589-chr6:165053797..165056474,2	K562	blood:
22	chr6:164757750..164761032-chr6:164766105..164769189,4	K562	blood:
23	chr6:164876917..164879487-chr6:164880579..164883020,3	K562	blood:
24	chr6:164860906..164865070-chr6:164865678..164869874,4	K562	blood:
25	chr6:164752284..164754596-chr6:164826369..164828641,2	K562	blood:
26	chr6:164880581..164883038-chr6:164888427..164890046,2	K562	blood:
27	chr6:164925048..164927475-chr6:164929518..164932281,2	K562	blood:
28	chr6:164876917..164879487-chr6:164880579..164883020,3	K562	blood:
29	chr6:164814585..164816801-chr6:164819045..164822898,3	K562	blood:
30	chr6:164943103..164945490-chr6:164951248..164953495,2	K562	blood:
31	chr6:164974094..164976654-chr6:164987580..164991765,3	K562	blood:
32	chr6:164768200..164769032-chr6:165340931..165341635,2	MCF-7	breast:
33	chr6:164781175..164783778-chr6:164784737..164786491,2	K562	blood:
34	chr6:164798125..164802014-chr6:164802831..164806274,3	K562	blood:
35	chr6:164925048..164927475-chr6:164929518..164932281,2	K562	blood:
36	chr6:164768274..164768906-chr6:165033273..165034147,2	MCF-7	breast:
37	chr6:164826913..164829845-chr6:164834931..164836483,2	MCF-7	breast:
38	chr6:164860906..164865070-chr6:164865678..164869874,4	K562	blood:
39	chr6:165007452..165009387-chr6:165042540..165044932,2	K562	blood:
40	chr6:164798340..164800182-chr6:164837678..164840406,2	K562	blood:
41	chr6:164921896..164924065-chr6:164926926..164929032,3	K562	blood:
42	chr6:164877377..164879077-chr6:164881330..164883684,2	K562	blood:
43	chr6:164663964..164666886-chr6:164937813..164940222,2	K562	blood:
44	chr6:165050032..165051589-chr6:165053797..165056474,2	K562	blood:
45	chr6:164711353..164714302-chr6:164897118..164899591,2	K562	blood:
46	chr6:164880581..164883038-chr6:164888427..164890046,2	K562	blood:
47	chr6:164944443..164946258-chr6:164955428..164957824,2	K562	blood:
48	chr6:165029398..165031412-chr6:165033183..165034759,2	K562	blood:
49	chr6:164943103..164945490-chr6:164951248..164953495,2	K562	blood:
50	chr6:164815480..164817452-chr6:164823900..164826799,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf118-2	chr6:164769333-164769677	XLOC_005914
2	lnc-C6orf118-2	chr6:164767522-164767642	XLOC_005914

No data

Variant related genes	Relation type
ENSG00000226739	TF binding region
ENSG00000226739	CpG island
HIVEP2	miRNA target sites

Extended variants
information (count: 6061 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:6061 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201598126	chr6:164762182-164762183	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs188625800	chr6:164762184-164762185	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs147373829	chr6:164762187-164762188	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs536494258	chr6:164762205-164762206	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs553181188	chr6:164762206-164762207	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs573321838	chr6:164762209-164762210	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs139571774	chr6:164762214-164762215	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs200776454	chr6:164762224-164762225	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs4521561	chr6:164762249-164762250	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs181415624	chr6:164762263-164762264	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs113862124	chr6:164762289-164762290	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs544479238	chr6:164762292-164762293	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs561171133	chr6:164762295-164762296	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs200103950	chr6:164762304-164762305	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs183773237	chr6:164762314-164762315	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs201192356	chr6:164762317-164762318	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs201983030	chr6:164762325-164762326	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs11967037	chr6:164762329-164762330	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs9347004	chr6:164762363-164762364	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs368998898	chr6:164762386-164762387	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs140543321	chr6:164762407-164762408	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs562462618	chr6:164762410-164762411	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs189487228	chr6:164762432-164762433	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs550857686	chr6:164762438-164762439	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs567659440	chr6:164762465-164762466	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs536432018	chr6:164762468-164762469	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs145814253	chr6:164762478-164762479	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs11967082	chr6:164762480-164762481	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs181960576	chr6:164762500-164762501	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs187501592	chr6:164762539-164762540	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs141301303	chr6:164762563-164762564	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs149210557	chr6:164762636-164762637	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs554898305	chr6:164762652-164762653	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs553826881	chr6:164762689-164762690	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs540175650	chr6:164762707-164762708	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs551970980	chr6:164762728-164762729	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs560269416	chr6:164762740-164762741	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs192044294	chr6:164762761-164762762	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs545844981	chr6:164762821-164762822	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs562285268	chr6:164762852-164762853	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs531205276	chr6:164762864-164762865	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs541453466	chr6:164762873-164762874	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs561231605	chr6:164762931-164762932	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs562018033	chr6:164762981-164762982	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs529534202	chr6:164762984-164762985	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs138715966	chr6:164762985-164762986	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs149362566	chr6:164762988-164762989	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs535293080	chr6:164762999-164763000	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs552629950	chr6:164763000-164763001	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs569419016	chr6:164763014-164763015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:669 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:164758800-164762800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:164758800-164763800	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr6:164758800-164767000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:164761800-164766200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr6:164762000-164763000	Active TSS	H9 Cell Line	embryonic stem cell
6	chr6:164762000-164765600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr6:164763000-164763800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr6:164763000-164767800	Weak transcription	Right Atrium	heart
9	chr6:164763800-164764200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
10	chr6:164763800-164764600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
11	chr6:164764000-164765000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
12	chr6:164764000-164765800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
13	chr6:164764200-164764800	Strong transcription	H1 Cell Line	embryonic stem cell
14	chr6:164764200-164766200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr6:164764600-164765800	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr6:164764800-164765000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr6:164764800-164765600	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr6:164764800-164766200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr6:164764800-164766400	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr6:164765000-164765800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr6:164765000-164766200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr6:164765600-164765800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr6:164765600-164765800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr6:164765600-164766000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:164765600-164766200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:164765600-164766400	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr6:164765800-164766000	Enhancers	H9 Cell Line	embryonic stem cell
28	chr6:164765800-164766000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr6:164765800-164766200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr6:164765800-164766200	Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr6:164765800-164766200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr6:164765800-164766400	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr6:164765800-164767000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr6:164766000-164766200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr6:164766000-164766200	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr6:164766000-164766400	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr6:164766000-164766600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:164766000-164766800	Enhancers	Fetal Stomach	stomach
39	chr6:164766000-164767200	Enhancers	K562	blood
40	chr6:164766200-164766400	Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr6:164766200-164766400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr6:164766200-164766600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
43	chr6:164766200-164766600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
44	chr6:164766200-164766800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr6:164766200-164766800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:164766200-164766800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr6:164766200-164767000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:164766200-164767000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr6:164766200-164767000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr6:164766200-164767800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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