Variant report

Variant	nsv886919
Chromosome Location	chr6:164756364-165079834
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1008)
CpG islands
(count:856)
Chromatin interactive
region (count:66)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1008 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:164798491-164798683	K562	blood:	n/a	n/a
2	ARID3A	chr6:164767622-164767980	K562	blood:	n/a	n/a
3	ARID3A	chr6:164759033-164759408	K562	blood:	n/a	n/a
4	ATF1	chr6:164918144-164918284	K562	blood:	n/a	n/a
5	ATF1	chr6:164759070-164759314	K562	blood:	n/a	n/a
6	ATF1	chr6:164767707-164768041	K562	blood:	n/a	n/a
7	ATF2	chr6:164928270-164929113	GM12878	blood:	n/a	n/a
8	ATF2	chr6:164765756-164766224	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr6:164928321-164929043	GM12878	blood:	n/a	n/a
10	ATF2	chr6:164926459-164926870	GM12878	blood:	n/a	n/a
11	ATF3	chr6:164768570-164768730	K562	blood:	n/a	n/a
12	BACH1	chr6:164758290-164758363	K562	blood:	n/a	n/a
13	BATF	chr6:164898891-164899123	GM12878	blood:	n/a	n/a
14	BATF	chr6:164952830-164953115	GM12878	blood:	n/a	chr6:164952982-164952993
15	BATF	chr6:164928549-164928927	GM12878	blood:	n/a	n/a
16	BATF	chr6:164952872-164953114	GM12878	blood:	n/a	chr6:164952982-164952993
17	BATF	chr6:164926445-164926910	GM12878	blood:	n/a	n/a
18	BATF	chr6:164898863-164899130	GM12878	blood:	n/a	n/a
19	BATF	chr6:164928521-164929021	GM12878	blood:	n/a	n/a
20	BCL11A	chr6:164765922-164766293	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL11A	chr6:164926483-164926915	GM12878	blood:	n/a	n/a
22	BCL11A	chr6:164928320-164929011	GM12878	blood:	n/a	n/a
23	BCL11A	chr6:164928408-164928949	GM12878	blood:	n/a	n/a
24	BCL3	chr6:164926405-164926609	GM12878	blood:	n/a	n/a
25	BCL3	chr6:164928630-164929027	GM12878	blood:	n/a	n/a
26	BCLAF1	chr6:164928419-164929054	GM12878	blood:	n/a	n/a
27	BCLAF1	chr6:164928453-164929082	GM12878	blood:	n/a	n/a
28	BHLHE40	chr6:164928355-164929088	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:164952948-164953079	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:164826224-164826542	K562	blood:	n/a	n/a
31	BHLHE40	chr6:164953286-164953312	GM12878	blood:	n/a	n/a
32	BHLHE40	chr6:164926462-164926801	GM12878	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	chr6:164777916-164778190	K562	blood:	n/a	n/a
37	CBX3	chr6:165055640-165055827	K562	blood:	n/a	n/a
38	CBX3	chr6:164802633-164802852	K562	blood:	n/a	n/a
39	CBX3	chr6:164825821-164826135	K562	blood:	n/a	n/a
40	CCNT2	chr6:164858191-164858336	K562	blood:	n/a	n/a
41	CCNT2	chr6:164767714-164768074	K562	blood:	n/a	n/a
42	CCNT2	chr6:164889314-164889407	K562	blood:	n/a	n/a
43	CCNT2	chr6:164757991-164758662	K562	blood:	n/a	n/a
44	CEBPB	chr6:164920704-164920887	K562	blood:	n/a	n/a
45	CEBPB	chr6:164798394-164798659	K562	blood:	n/a	n/a
46	CEBPB	chr6:164996421-164996674	HepG2	liver:	n/a	chr6:164996578-164996589
47	CEBPB	chr6:164928530-164929093	GM12878	blood:	n/a	n/a
48	CEBPB	chr6:164765798-164766625	H1-hESC	embryonic stem cell:	n/a	chr6:164766519-164766530
49	CEBPB	chr6:164955364-164955598	HepG2	liver:	n/a	chr6:164955492-164955503
50	CEBPB	chr6:164996538-164996737	A549	lung:	n/a	chr6:164996578-164996589

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:165032124-165032174	SK-N-SH_RA	brain:	n/a
2	chr6:165032072-165032122	ECC-1	luminal epithelium:	n/a
3	chr6:165032124-165032174	SK-N-SH_RA	brain:	n/a
4	chr6:165032072-165032122	ECC-1	luminal epithelium:	n/a
5	chr6:165062070-165062120	AG04450	lung:	fetal
6	chr6:164758166-164758216	HCPEpiC	choroid plexus:	n/a
7	chr6:165032072-165032122	A549	lung:	n/a
8	chr6:164758166-164758216	SKMC	muscle:	n/a
9	chr6:164990879-164990929	BJ	skin:	n/a
10	chr6:164758166-164758216	HCT-116	colon:	n/a
11	chr6:165062070-165062120	ProgFib	skin:	n/a
12	chr6:164990879-164990929	U87	brain:	n/a
13	chr6:164760845-164760895	CMK	blood:	n/a
14	chr6:164758166-164758216	NB4	blood:	n/a
15	chr6:164758516-164758566	HCPEpiC	choroid plexus:	n/a
16	chr6:164990879-164990929	HMEC	breast:	n/a
17	chr6:164758166-164758216	HUVEC	blood vessel:	n/a
18	chr6:165032072-165032122	PFSK-1	brain:	n/a
19	chr6:164817337-164817387	HepG2	liver:	n/a
20	chr6:165062070-165062120	GM12878	blood:	n/a
21	chr6:164990879-164990929	MCF10A-Er-Src	breast:	n/a
22	chr6:164758166-164758216	K562	blood:	n/a
23	chr6:164758333-164758383	U87	brain:	n/a
24	chr6:164757735-164757785	AoSMC	blood vessel:	n/a
25	chr6:164758059-164758109	HUVEC	blood vessel:	n/a
26	chr6:165032068-165032118	A549	lung:	n/a
27	chr6:164767056-164767106	SK-N-MC	brain:	n/a
28	chr6:164758059-164758109	SK-N-SH	brain:	n/a
29	chr6:164990879-164990929	AoSMC	blood vessel:	n/a
30	chr6:165032072-165032122	HepG2	liver:	n/a
31	chr6:164758516-164758566	HMEC	breast:	n/a
32	chr6:164758333-164758383	HEEpiC	esophagus:	n/a
33	chr6:165032124-165032174	NT2-D1	testis:	n/a
34	chr6:164757735-164757785	GM12892	blood:	n/a
35	chr6:165032124-165032174	HRPEpiC	eye:	n/a
36	chr6:164758166-164758216	ProgFib	skin:	n/a
37	chr6:165032068-165032118	ECC-1	luminal epithelium:	n/a
38	chr6:164758516-164758566	GM12878	blood:	n/a
39	chr6:164758059-164758109	NB4	blood:	n/a
40	chr6:165032124-165032174	CMK	blood:	n/a
41	chr6:164758333-164758383	NHBE	bronchial:	n/a
42	chr6:165032124-165032174	SK-N-SH	brain:	n/a
43	chr6:165032072-165032122	HCT-116	colon:	n/a
44	chr6:164767056-164767106	GM12892	blood:	n/a
45	chr6:165032068-165032118	BE2_C	brain:	n/a
46	chr6:164758333-164758383	GM12891	blood:	n/a
47	chr6:164760845-164760895	AG10803	skin:	n/a
48	chr6:164758333-164758383	HCF	heart:	n/a
49	chr6:164758333-164758383	NB4	blood:	n/a
50	chr6:164758166-164758216	HRPEpiC	eye:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:164798340..164800182-chr6:164837678..164840406,2	K562	blood:
2	chr6:164768274..164768906-chr6:165033273..165034147,2	MCF-7	breast:
3	chr6:165050032..165051589-chr6:165053797..165056474,2	K562	blood:
4	chr6:164768200..164769032-chr6:165340931..165341635,2	MCF-7	breast:
5	chr6:164797286..164799479-chr6:164818764..164821424,2	K562	blood:
6	chr6:164757750..164761032-chr6:164766105..164769189,4	K562	blood:
7	chr6:164814459..164817291-chr6:164821398..164824476,3	K562	blood:
8	chr6:164711353..164714302-chr6:164897118..164899591,2	K562	blood:
9	chr6:164798125..164802014-chr6:164802831..164806274,3	K562	blood:
10	chr6:164719975..164721719-chr6:164755940..164758933,2	K562	blood:
11	chr6:164754441..164757188-chr6:164816379..164818209,2	K562	blood:
12	chr6:164862673..164864670-chr6:164866180..164868156,2	K562	blood:
13	chr6:164921896..164924065-chr6:164926926..164929032,3	K562	blood:
14	chr6:164943103..164945490-chr6:164951248..164953495,2	K562	blood:
15	chr6:164757750..164761032-chr6:164766105..164769189,4	K562	blood:
16	chr6:165007452..165009387-chr6:165042540..165044932,2	K562	blood:
17	chr6:164767365..164769035-chr6:164822554..164824204,2	K562	blood:
18	chr6:164686752..164688649-chr6:164926400..164929069,2	K562	blood:
19	chr6:164781175..164783778-chr6:164784737..164786491,2	K562	blood:
20	chr6:164925048..164927475-chr6:164929518..164932281,2	K562	blood:
21	chr6:164752242..164755007-chr6:164766257..164769251,2	K562	blood:
22	chr6:164815480..164817452-chr6:164823900..164826799,2	K562	blood:
23	chr6:164826913..164829845-chr6:164834931..164836483,2	MCF-7	breast:
24	chr20:49345923..49347705-chr6:164930864..164932942,2	MCF-7	breast:
25	chr6:164860906..164865070-chr6:164865678..164869874,4	K562	blood:
26	chr6:164860412..164863160-chr6:164883552..164885284,2	K562	blood:
27	chr6:164798125..164802014-chr6:164802831..164806274,3	K562	blood:
28	chr6:164768274..164768906-chr6:165033273..165034147,2	MCF-7	breast:
29	chr6:164974094..164976654-chr6:164987580..164991765,3	K562	blood:
30	chr6:165029398..165031412-chr6:165033183..165034759,2	K562	blood:
31	chr6:164974094..164976654-chr6:164987580..164991765,3	K562	blood:
32	chr6:164663964..164666886-chr6:164937813..164940222,2	K562	blood:
33	chr6:164798340..164800182-chr6:164837678..164840406,2	K562	blood:
34	chr6:164814585..164816801-chr6:164819045..164822898,3	K562	blood:
35	chr6:164796151..164797865-chr6:164799819..164802680,2	K562	blood:
36	chr6:164814459..164817291-chr6:164821398..164824476,3	K562	blood:
37	chr6:164797286..164799479-chr6:164818764..164821424,2	K562	blood:
38	chr6:164860906..164865070-chr6:164865678..164869874,4	K562	blood:
39	chr6:164747721..164749736-chr6:164756889..164759044,2	K562	blood:
40	chr6:165029398..165031412-chr6:165033183..165034759,2	K562	blood:
41	chr6:164796151..164797865-chr6:164799819..164802680,2	K562	blood:
42	chr6:164880581..164883038-chr6:164888427..164890046,2	K562	blood:
43	chr6:164752284..164754596-chr6:164826369..164828641,2	K562	blood:
44	chr6:164767365..164769035-chr6:164822554..164824204,2	K562	blood:
45	chr6:164880581..164883038-chr6:164888427..164890046,2	K562	blood:
46	chr6:164862673..164864670-chr6:164866180..164868156,2	K562	blood:
47	chr6:164754441..164757188-chr6:164816379..164818209,2	K562	blood:
48	chr6:164944443..164946258-chr6:164955428..164957824,2	K562	blood:
49	chr6:164876917..164879487-chr6:164880579..164883020,3	K562	blood:
50	chr6:164815480..164817452-chr6:164823900..164826799,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf118-2	chr6:164767522-164767642	XLOC_005914
2	lnc-C6orf118-2	chr6:164769333-164769677	XLOC_005914
3	lnc-C6orf118-6	chr6:164758746-164758836	NONHSAT115987

No data

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

Extended variants
information (count: 6337 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:6337 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1340079	chr6:164756364-164756365	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536460173	chr6:164756396-164756397	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs189525041	chr6:164756404-164756405	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs566620178	chr6:164756414-164756415	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs558209946	chr6:164756454-164756455	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs139554197	chr6:164756581-164756582	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs538630776	chr6:164756590-164756591	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs558306053	chr6:164756591-164756592	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs575216088	chr6:164756593-164756594	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs181598466	chr6:164756596-164756597	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs185775304	chr6:164756599-164756600	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs573846853	chr6:164756607-164756608	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs542860162	chr6:164756686-164756687	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs559410804	chr6:164756757-164756758	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs189893496	chr6:164756791-164756792	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs528095873	chr6:164756792-164756793	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs139943397	chr6:164756796-164756797	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs139283318	chr6:164756806-164756807	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs576663023	chr6:164756813-164756814	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs565106808	chr6:164756874-164756875	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs183272153	chr6:164756908-164756909	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs544138235	chr6:164756911-164756912	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs142634927	chr6:164756920-164756921	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs75164455	chr6:164756925-164756926	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs150949243	chr6:164757002-164757003	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs566559007	chr6:164757008-164757009	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs532275568	chr6:164757051-164757052	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs552262409	chr6:164757069-164757070	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs140789885	chr6:164757078-164757079	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs75444418	chr6:164757096-164757097	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs368238510	chr6:164757104-164757105	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs557364642	chr6:164757137-164757138	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs570270853	chr6:164757166-164757167	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs541717820	chr6:164757184-164757185	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs567659480	chr6:164757355-164757356	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs536432051	chr6:164757364-164757365	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs553178175	chr6:164757386-164757387	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs573121424	chr6:164757398-164757399	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs556194759	chr6:164757438-164757439	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs545139223	chr6:164757440-164757441	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs117500678	chr6:164757449-164757450	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs559020779	chr6:164757490-164757491	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs575502654	chr6:164757492-164757493	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs186507322	chr6:164757501-164757502	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs561160591	chr6:164757514-164757515	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs111720373	chr6:164757565-164757566	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs79254292	chr6:164757607-164757608	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs78393539	chr6:164757637-164757638	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs532354957	chr6:164757691-164757692	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs551936112	chr6:164757698-164757699	Enhancers Active TSS	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:683 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:164753600-164757400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:164754200-164759800	Active TSS	K562	blood
3	chr6:164757400-164757800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:164757800-164761400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr6:164758000-164758200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:164758000-164758200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr6:164758000-164758800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr6:164758200-164758800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
9	chr6:164758200-164758800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:164758200-164761200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr6:164758600-164759000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
12	chr6:164758800-164762800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:164758800-164763800	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr6:164758800-164767000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:164759200-164759600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr6:164759400-164759800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr6:164761400-164762000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr6:164761800-164766200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:164762000-164763000	Active TSS	H9 Cell Line	embryonic stem cell
20	chr6:164762000-164765600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr6:164763000-164763800	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr6:164763000-164767800	Weak transcription	Right Atrium	heart
23	chr6:164763800-164764200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
24	chr6:164763800-164764600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
25	chr6:164764000-164765000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
26	chr6:164764000-164765800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
27	chr6:164764200-164764800	Strong transcription	H1 Cell Line	embryonic stem cell
28	chr6:164764200-164766200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr6:164764600-164765800	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr6:164764800-164765000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr6:164764800-164765600	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr6:164764800-164766200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr6:164764800-164766400	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr6:164765000-164765800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr6:164765000-164766200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr6:164765600-164765800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr6:164765600-164765800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr6:164765600-164766000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:164765600-164766200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:164765600-164766400	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr6:164765800-164766000	Enhancers	H9 Cell Line	embryonic stem cell
42	chr6:164765800-164766000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr6:164765800-164766200	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr6:164765800-164766200	Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr6:164765800-164766200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr6:164765800-164766400	Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr6:164765800-164767000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr6:164766000-164766200	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr6:164766000-164766200	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr6:164766000-164766400	Weak transcription	H9 Cell Line	embryonic stem cell

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