Variant report

Variant	nsv464144
Chromosome Location	chr6:167647872-167687892
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	ARID3A	chr6:167652605-167653007	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167682223-167682912	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167651727-167651738	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167655013-167655211	HepG2	liver:	n/a	n/a
5	ATF2	chr6:167651500-167652487	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr6:167682232-167682824	HepG2	liver:	n/a	n/a
7	CBX3	chr6:167669429-167669771	K562	blood:	n/a	n/a
8	CEBPB	chr6:167682231-167682489	HepG2	liver:	n/a	n/a
9	CEBPB	chr6:167682158-167682752	HepG2	liver:	n/a	n/a
10	CEBPB	chr6:167652443-167653271	HepG2	liver:	n/a	n/a
11	CEBPB	chr6:167665707-167665869	HepG2	liver:	n/a	chr6:167665793-167665804
12	CEBPB	chr6:167682141-167682592	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:167682303-167682375	K562	blood:	n/a	n/a
14	CEBPB	chr6:167658239-167658916	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr6:167682160-167682788	HepG2	liver:	n/a	n/a
16	CEBPD	chr6:167682127-167682826	HepG2	liver:	n/a	n/a
17	CEBPD	chr6:167655889-167656224	K562	blood:	n/a	n/a
18	CHD2	chr6:167682229-167682772	HepG2	liver:	n/a	n/a
19	CHD2	chr6:167652674-167652844	HepG2	liver:	n/a	n/a
20	CHD2	chr6:167651731-167652357	HepG2	liver:	n/a	n/a
21	CHD2	chr6:167649919-167650108	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr6:167661782-167661982	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTBP2	chr6:167651694-167652850	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr6:167661760-167661910	HepG2	liver:	n/a	chr6:167661854-167661872
25	CTCF	chr6:167669520-167669670	HEK293	kidney:	n/a	chr6:167669607-167669617 chr6:167669602-167669620 chr6:167669604-167669625 chr6:167669603-167669619
26	CTCF	chr6:167649880-167650030	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr6:167669460-167669610	A549	lung:	n/a	n/a
28	CTCF	chr6:167669520-167669670	GM12873	blood:	n/a	chr6:167669607-167669617 chr6:167669602-167669620 chr6:167669604-167669625 chr6:167669603-167669619
29	CTCF	chr6:167648440-167648590	BE2_C	brain:	n/a	n/a
30	CTCF	chr6:167661782-167662019	K562	blood:	n/a	chr6:167661854-167661872
31	CTCF	chr6:167661785-167661956	K562	blood:	n/a	chr6:167661854-167661872
32	CTCF	chr6:167661340-167661490	HEK293	kidney:	n/a	n/a
33	CTCF	chr6:167669600-167669750	GM12872	blood:	n/a	chr6:167669607-167669617 chr6:167669602-167669620 chr6:167669604-167669625 chr6:167669603-167669619
34	CTCF	chr6:167669440-167669590	BE2_C	brain:	n/a	n/a
35	CTCF	chr6:167649935-167650015	K562	blood:	n/a	n/a
36	CTCF	chr6:167661860-167662010	K562	blood:	n/a	n/a
37	CTCF	chr6:167669380-167669530	RPTEC	kidney:	n/a	n/a
38	CTCF	chr6:167661780-167661930	BE2_C	brain:	n/a	chr6:167661854-167661872
39	CTCF	chr6:167669560-167669710	Hela-S3	cervix:	n/a	chr6:167669607-167669617 chr6:167669602-167669620 chr6:167669604-167669625 chr6:167669603-167669619
40	CTCF	chr6:167669480-167669630	GM12865	blood:	n/a	chr6:167669607-167669617 chr6:167669602-167669620 chr6:167669604-167669625 chr6:167669603-167669619
41	CTCF	chr6:167669620-167669770	Caco-2	colon:	n/a	n/a
42	CTCF	chr6:167661631-167662054	K562	blood:	n/a	chr6:167661854-167661872
43	CTCF	chr6:167661768-167661950	HepG2	liver:	n/a	chr6:167661854-167661872
44	CTCF	chr6:167669520-167669670	SK-N-SH_RA	brain:	n/a	chr6:167669607-167669617 chr6:167669602-167669620 chr6:167669604-167669625 chr6:167669603-167669619
45	CTCF	chr6:167669473-167669717	HepG2	liver:	n/a	chr6:167669607-167669617 chr6:167669602-167669620 chr6:167669604-167669625 chr6:167669603-167669619
46	CTCF	chr6:167669480-167669630	GM12873	blood:	n/a	chr6:167669607-167669617 chr6:167669602-167669620 chr6:167669604-167669625 chr6:167669603-167669619
47	CTCF	chr6:167669440-167669590	RPTEC	kidney:	n/a	n/a
48	CTCF	chr6:167669519-167669704	HepG2	liver:	n/a	chr6:167669607-167669617 chr6:167669602-167669620 chr6:167669604-167669625 chr6:167669603-167669619
49	CTCF	chr6:167686200-167686350	Caco-2	colon:	n/a	n/a
50	CTCF	chr6:167669860-167670010	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167652028-167652078	AG04449	skin:	fetal
2	chr6:167649539-167649589	NHDF-neo	bronchial:	n/a
3	chr6:167649631-167649681	AG04450	lung:	fetal
4	chr6:167652028-167652078	AG04449	skin:	fetal
5	chr6:167649539-167649589	NHDF-neo	bronchial:	n/a
6	chr6:167649631-167649681	AG04450	lung:	fetal
7	chr6:167653957-167654007	NHDF-neo	bronchial:	n/a
8	chr6:167649749-167649799	GM12891	blood:	n/a
9	chr6:167653982-167654032	GM12891	blood:	n/a
10	chr6:167652028-167652078	HL-60	blood:	n/a
11	chr6:167653957-167654007	RPTEC	kidney:	n/a
12	chr6:167655053-167655103	BJ	skin:	n/a
13	chr6:167652028-167652078	PrEC	prostate:	n/a
14	chr6:167661905-167661955	HepG2	liver:	n/a
15	chr6:167649631-167649681	ovcar-3	ovarian:	n/a
16	chr6:167649749-167649799	NH-A	brain:	n/a
17	chr6:167649539-167649589	HAEpiC	amniotic membrane:	n/a
18	chr6:167680447-167680497	AG09319	gingival:	n/a
19	chr6:167649336-167649386	Caco-2	colon:	n/a
20	chr6:167649256-167649306	BJ	skin:	n/a
21	chr6:167653982-167654032	HRE	kidney:	n/a
22	chr6:167655053-167655103	HRE	kidney:	n/a
23	chr6:167649631-167649681	SK-N-SH_RA	brain:	n/a
24	chr6:167653907-167653957	Jurkat	blood:	n/a
25	chr6:167655053-167655103	IMR90	lung:	fetal
26	chr6:167653982-167654032	SK-N-SH_RA	brain:	n/a
27	chr6:167680455-167680505	GM12878	blood:	n/a
28	chr6:167655290-167655340	SK-N-SH	brain:	n/a
29	chr6:167649539-167649589	GM19239	blood:	n/a
30	chr6:167649539-167649589	ovcar-3	ovarian:	n/a
31	chr6:167649539-167649589	SKMC	muscle:	n/a
32	chr6:167680447-167680497	U87	brain:	n/a
33	chr6:167655053-167655103	AG09309	skin:	n/a
34	chr6:167652028-167652078	SK-N-MC	brain:	n/a
35	chr6:167649384-167649434	T-47D	breast:	n/a
36	chr6:167653907-167653957	PFSK-1	brain:	n/a
37	chr6:167655290-167655340	ProgFib	skin:	n/a
38	chr6:167655053-167655103	HepG2	liver:	n/a
39	chr6:167649749-167649799	AG09319	gingival:	n/a
40	chr6:167655053-167655103	NT2-D1	testis:	n/a
41	chr6:167649384-167649434	HL-60	blood:	n/a
42	chr6:167655053-167655103	PrEC	prostate:	n/a
43	chr6:167649256-167649306	IMR90	lung:	fetal
44	chr6:167649384-167649434	AG09319	gingival:	n/a
45	chr6:167654977-167655027	A549	lung:	n/a
46	chr6:167649384-167649434	A549	lung:	n/a
47	chr6:167649539-167649589	HRE	kidney:	n/a
48	chr6:167680455-167680505	HRCEpiC	kidney:	n/a
49	chr6:167649256-167649306	GM12892	blood:	n/a
50	chr6:167655053-167655103	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
2	chr6:167668192..167671777-chr6:167684157..167687082,3	K562	blood:
3	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
4	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:
5	chr6:167669951..167671777-chr6:167683631..167687000,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR31-1	chr6:167650996-167651293	XLOC_005921
2	lnc-UNC93A-1	chr6:167655379-167655453	XLOC_005540
3	lnc-GPR31-1	chr6:167653688-167653968	XLOC_005921
4	lnc-GPR31-1	chr6:167653636-167653833	XLOC_005921
5	lnc-UNC93A-1	chr6:167659275-167659404	XLOC_005540
6	lnc-GPR31-1	chr6:167651156-167651293	XLOC_005921

Variant related genes	Relation type
UNC93A	TF binding region
ENSG00000228648	TF binding region
ENSG00000231720	TF binding region
UNC93A	CpG island
ENSG00000228648	CpG island
ENSG00000231720	CpG island
ENSG00000112494	chromatin interactions
CYBASC3	miRNA target sites
CYB5R4	miRNA target sites

Extended variants
information (count: 1940 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1940 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6927070	chr6:167647872-167647873	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs141645779	chr6:167647913-167647914	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186692971	chr6:167647921-167647922	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551342713	chr6:167647935-167647936	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191282282	chr6:167647969-167647970	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569427062	chr6:167647986-167647987	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540046696	chr6:167648014-167648015	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs35717062	chr6:167648031-167648032	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6456165	chr6:167648045-167648046	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs202192866	chr6:167648118-167648119	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs144596427	chr6:167648138-167648139	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553847235	chr6:167648142-167648143	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182424343	chr6:167648176-167648177	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555457948	chr6:167648196-167648197	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574029563	chr6:167648197-167648198	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541677858	chr6:167648205-167648206	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572247301	chr6:167648227-167648228	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139038380	chr6:167648237-167648238	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs6926514	chr6:167648276-167648277	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532410378	chr6:167648308-167648309	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545617078	chr6:167648339-167648340	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs146365764	chr6:167648350-167648351	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572837395	chr6:167648368-167648369	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs62437235	chr6:167648385-167648386	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs112920932	chr6:167648437-167648438	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs540363273	chr6:167648445-167648446	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs561523278	chr6:167648451-167648452	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs139340588	chr6:167648461-167648462	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs551253191	chr6:167648525-167648526	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs563189330	chr6:167648538-167648539	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs533534601	chr6:167648554-167648555	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs551980414	chr6:167648622-167648623	Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149594306	chr6:167648665-167648666	Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371329878	chr6:167648703-167648704	Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534034313	chr6:167648706-167648707	Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549462353	chr6:167648711-167648712	Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567513640	chr6:167648749-167648750	Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144299907	chr6:167648760-167648761	Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556811017	chr6:167648806-167648807	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs575175718	chr6:167648811-167648812	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs373000055	chr6:167648816-167648817	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs539382979	chr6:167648857-167648858	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs79629996	chr6:167648904-167648905	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs369409170	chr6:167648913-167648914	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs148739455	chr6:167648927-167648928	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs539901082	chr6:167649004-167649005	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561830461	chr6:167649037-167649038	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373577027	chr6:167649048-167649049	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544246105	chr6:167649049-167649050	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562493903	chr6:167649050-167649051	Genic enhancers Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	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	17122850	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167640000-167648600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr6:167643600-167648600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:167644200-167649800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr6:167645400-167652800	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr6:167645600-167648600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:167645600-167650600	Genic enhancers	H1 Cell Line	embryonic stem cell
7	chr6:167646200-167648800	Genic enhancers	HUES64 Cell Line	embryonic stem cell
8	chr6:167646200-167649000	Genic enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr6:167646200-167653000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:167647000-167648400	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr6:167647000-167648400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr6:167647000-167650000	Weak transcription	HepG2	liver
13	chr6:167647000-167651200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:167647000-167652600	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr6:167647200-167648600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr6:167647200-167648600	Weak transcription	Right Atrium	heart
17	chr6:167647200-167649400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr6:167647200-167650200	Enhancers	Fetal Brain Male	brain
19	chr6:167647200-167650400	Genic enhancers	HUES48 Cell Line	embryonic stem cell
20	chr6:167647200-167650600	Weak transcription	Fetal Intestine Small	intestine
21	chr6:167647400-167648400	Genic enhancers	HUES6 Cell Line	embryonic stem cell
22	chr6:167647400-167648600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr6:167647400-167653000	Genic enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr6:167647600-167648600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr6:167648400-167648800	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
26	chr6:167648400-167649000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr6:167648400-167649000	Enhancers	Fetal Thymus	thymus
28	chr6:167648400-167649000	Enhancers	Thymus	Thymus
29	chr6:167648400-167649200	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr6:167648400-167649200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr6:167648400-167649200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr6:167648600-167648800	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr6:167648600-167648800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr6:167648600-167648800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr6:167648600-167648800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
36	chr6:167648600-167649000	Genic enhancers	H9 Cell Line	embryonic stem cell
37	chr6:167648600-167649000	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr6:167648600-167649000	Enhancers	Primary hematopoietic stem cells	blood
39	chr6:167648600-167649200	Enhancers	Fetal Lung	lung
40	chr6:167648600-167649200	Enhancers	Placenta Amnion	Placenta Amnion
41	chr6:167648600-167649800	Strong transcription	Right Atrium	heart
42	chr6:167648600-167650000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr6:167648600-167650200	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr6:167648800-167649000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr6:167648800-167649000	Enhancers	Fetal Brain Female	brain
46	chr6:167648800-167649800	Strong transcription	HUES64 Cell Line	embryonic stem cell
47	chr6:167648800-167650200	Genic enhancers	HUES6 Cell Line	embryonic stem cell
48	chr6:167648800-167651600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr6:167649000-167649800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr6:167649000-167650200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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