Variant report

Variant	nsv886162
Chromosome Location	chr6:74903797-75006170
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:301)
CpG islands
(count:366)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr6:74915215-74915733	HCT-116	colon:	n/a	n/a
2	CEBPB	chr6:74941205-74941486	IMR90	lung:	n/a	chr6:74941335-74941346 chr6:74941333-74941344 chr6:74941333-74941346 chr6:74941335-74941346 chr6:74941333-74941346 chr6:74941333-74941346
3	CEBPB	chr6:74963070-74963400	MCF-7	breast:	n/a	n/a
4	CEBPB	chr6:74941255-74941384	A549	lung:	n/a	chr6:74941335-74941346 chr6:74941333-74941344 chr6:74941333-74941346 chr6:74941335-74941346 chr6:74941333-74941346 chr6:74941333-74941346
5	CEBPB	chr6:74923585-74923837	IMR90	lung:	n/a	n/a
6	CEBPB	chr6:74999604-75000012	IMR90	lung:	n/a	chr6:74999810-74999827
7	CEBPB	chr6:74941188-74941504	HepG2	liver:	n/a	chr6:74941335-74941346 chr6:74941333-74941344 chr6:74941333-74941346 chr6:74941335-74941346 chr6:74941333-74941346 chr6:74941333-74941346
8	CEBPB	chr6:74952171-74952349	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr6:74932618-74932709	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr6:74923542-74923816	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr6:74952095-74952381	IMR90	lung:	n/a	n/a
12	CEBPB	chr6:74973756-74973764	HepG2	liver:	n/a	n/a
13	CEBPZ	chr6:74985570-74985693	HepG2	liver:	n/a	n/a
14	CHD2	chr6:74932601-74932801	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr6:74990140-74990290	NHEK	skin:	n/a	n/a
16	CTCF	chr6:74990120-74990270	AG09319	gingival:	n/a	n/a
17	CTCF	chr6:74932595-74932709	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr6:74989540-74989690	GM12873	blood:	n/a	chr6:74989638-74989647
19	CTCF	chr6:74989620-74989770	GM12866	blood:	n/a	chr6:74989638-74989647
20	CTCF	chr6:74990107-74990249	HepG2	liver:	n/a	n/a
21	CTCF	chr6:74990160-74990310	GM06990	blood:	n/a	n/a
22	CTCF	chr6:74990120-74990270	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr6:74990120-74990270	HRE	kidney:	n/a	n/a
24	CTCF	chr6:74990157-74990244	A549	lung:	n/a	n/a
25	CTCF	chr6:74989560-74989710	RPTEC	kidney:	n/a	chr6:74989638-74989647
26	CTCF	chr6:74990160-74990310	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr6:74999160-74999310	NHDF-neo	bronchial:	n/a	chr6:74999245-74999258
28	CTCF	chr6:74990120-74990270	Caco-2	colon:	n/a	n/a
29	CTCF	chr6:74990040-74990190	MCF-7	breast:	n/a	n/a
30	CTCF	chr6:74990140-74990290	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr6:74990160-74990310	HEK293	kidney:	n/a	n/a
32	CTCF	chr6:74989840-74989990	RPTEC	kidney:	n/a	n/a
33	CTCF	chr6:74990068-74990326	MCF-7	breast:	n/a	n/a
34	CTCF	chr6:74990200-74990350	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr6:74990220-74990370	HCM	heart:	n/a	n/a
36	CTCF	chr6:74990080-74990230	AG04449	skin:	n/a	n/a
37	CTCF	chr6:74965404-74965419	Fibrobl	skin:	n/a	n/a
38	CTCF	chr6:74990080-74990230	HepG2	liver:	n/a	n/a
39	CTCF	chr6:74990120-74990270	AG10803	skin:	n/a	n/a
40	CTCF	chr6:74990080-74990230	A549	lung:	n/a	n/a
41	CTCF	chr6:74989660-74989810	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr6:74989994-74990386	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr6:74965660-74965810	AG09319	gingival:	n/a	n/a
44	CTCF	chr6:74965620-74965770	AG09319	gingival:	n/a	n/a
45	CTCF	chr6:74990040-74990190	RPTEC	kidney:	n/a	n/a
46	CTCF	chr6:74990100-74990250	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr6:74989680-74989830	HAc	cerebellar:	n/a	n/a
48	CTCF	chr6:74990107-74990282	HepG2	liver:	n/a	n/a
49	CTCF	chr6:74990220-74990370	AG04450	lung:	n/a	n/a
50	CTCF	chr6:74990120-74990270	NHDF-neo	bronchial:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:74965323-74965373	SKMC	muscle:	n/a
2	chr6:74960030-74960080	Jurkat	blood:	n/a
3	chr6:74960030-74960080	SK-N-MC	brain:	n/a
4	chr6:74909201-74909251	SK-N-SH_RA	brain:	n/a
5	chr6:74909201-74909251	GM12878	blood:	n/a
6	chr6:74998385-74998435	AoSMC	blood vessel:	n/a
7	chr6:74960030-74960080	CMK	blood:	n/a
8	chr6:74987753-74987803	HNPCEpiC	eye:	n/a
9	chr6:74909201-74909251	CMK	blood:	n/a
10	chr6:74998385-74998435	T-47D	breast:	n/a
11	chr6:74978996-74979046	Caco-2	colon:	n/a
12	chr6:74987753-74987803	CMK	blood:	n/a
13	chr6:74960030-74960080	NHBE	bronchial:	n/a
14	chr6:74960030-74960080	LNCaP	prostate:	n/a
15	chr6:74978996-74979046	AG09319	gingival:	n/a
16	chr6:74965323-74965373	Hepatocyte	liver:	n/a
17	chr6:74960030-74960080	GM06990	blood:	n/a
18	chr6:74998385-74998435	SKMC	muscle:	n/a
19	chr6:74987753-74987803	ProgFib	skin:	n/a
20	chr6:74960030-74960080	SK-N-SH_RA	brain:	n/a
21	chr6:74909201-74909251	AG10803	skin:	n/a
22	chr6:74978996-74979046	HRPEpiC	eye:	n/a
23	chr6:74965323-74965373	GM19239	blood:	n/a
24	chr6:74978996-74979046	HL-60	blood:	n/a
25	chr6:74909201-74909251	HEK293	kidney:	embryo
26	chr6:74987753-74987803	HCF	heart:	n/a
27	chr6:74998385-74998435	MCF-7	breast:	n/a
28	chr6:74960030-74960080	HL-60	blood:	n/a
29	chr6:74998385-74998435	Jurkat	blood:	n/a
30	chr6:74998385-74998435	AG09309	skin:	n/a
31	chr6:74965323-74965373	RPTEC	kidney:	n/a
32	chr6:74998385-74998435	PrEC	prostate:	n/a
33	chr6:74987753-74987803	HCT-116	colon:	n/a
34	chr6:74965323-74965373	AG04450	lung:	fetal
35	chr6:74987753-74987803	GM12878	blood:	n/a
36	chr6:74987753-74987803	Jurkat	blood:	n/a
37	chr6:74987753-74987803	GM12892	blood:	n/a
38	chr6:74960030-74960080	IMR90	lung:	fetal
39	chr6:74978996-74979046	GM12891	blood:	n/a
40	chr6:74965323-74965373	LNCaP	prostate:	n/a
41	chr6:74987753-74987803	MCF10A-Er-Src	breast:	n/a
42	chr6:74960030-74960080	HCM	heart:	n/a
43	chr6:74978996-74979046	NT2-D1	testis:	n/a
44	chr6:74987753-74987803	ECC-1	luminal epithelium:	n/a
45	chr6:74909201-74909251	HUVEC	blood vessel:	n/a
46	chr6:74965323-74965373	ovcar-3	ovarian:	n/a
47	chr6:74965323-74965373	HEK293	kidney:	embryo
48	chr6:74960030-74960080	U87	brain:	n/a
49	chr6:74965323-74965373	HL-60	blood:	n/a
50	chr6:74965323-74965373	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:74892709..74895952-chr6:74900506..74904423,4	K562	blood:
2	chr6:74912181..74915078-chr6:74916489..74918406,2	K562	blood:
3	chr6:74912181..74915078-chr6:74916489..74918406,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000217178	TF binding region
ENSG00000217178	CpG island

Extended variants
information (count: 1920 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1920 , 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	rs115555650	chr6:74906614-74906615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs555400540	chr6:74906624-74906625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114199522	chr6:74906640-74906641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541873173	chr6:74906659-74906660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560606213	chr6:74906669-74906670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs527793810	chr6:74906670-74906671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548187842	chr6:74906671-74906672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs546360355	chr6:74906732-74906733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564666830	chr6:74906755-74906756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531970802	chr6:74906763-74906764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138261386	chr6:74906791-74906792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568678415	chr6:74906806-74906807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528854889	chr6:74906807-74906808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs78422954	chr6:74906838-74906839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7451891	chr6:74906843-74906844	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs186098711	chr6:74906863-74906864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546570672	chr6:74906873-74906874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1931283	chr6:74906901-74906902	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs149201471	chr6:74907033-74907034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs74729800	chr6:74907034-74907035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374894483	chr6:74907085-74907086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566785172	chr6:74907100-74907101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550882631	chr6:74907113-74907114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs190681745	chr6:74907160-74907161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs368599112	chr6:74907182-74907183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs184118522	chr6:74907187-74907188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12209187	chr6:74907194-74907195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561602905	chr6:74907220-74907221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs72950543	chr6:74907232-74907233	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs531909160	chr6:74907269-74907270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs72950546	chr6:74907293-74907294	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs368914178	chr6:74907296-74907297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182843542	chr6:74908818-74908819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562935214	chr6:74908827-74908828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530556909	chr6:74908847-74908848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs548788133	chr6:74908848-74908849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561054165	chr6:74908854-74908855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528248169	chr6:74908857-74908858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs76743242	chr6:74908890-74908891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs569134970	chr6:74908916-74908917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs80350064	chr6:74908990-74908991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs187927224	chr6:74909033-74909034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192254081	chr6:74909064-74909065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570042024	chr6:74909079-74909080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs374343366	chr6:74909086-74909087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537484100	chr6:74909092-74909093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555541803	chr6:74909123-74909124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567768865	chr6:74909145-74909146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536849537	chr6:74909195-74909196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534859006	chr6:74909202-74909203	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	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
Ependymoma	16718352	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
Prostate cancer	16573809	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD

Chromatin state (count:176 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74906600-74907400	Enhancers	Placenta Amnion	Placenta Amnion
2	chr6:74908800-74909600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:74908800-74909600	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr6:74908800-74910000	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr6:74909000-74909400	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr6:74909000-74909400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr6:74909000-74909400	Enhancers	Fetal Muscle Trunk	muscle
8	chr6:74909000-74909400	Enhancers	Fetal Muscle Leg	muscle
9	chr6:74909000-74909800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr6:74909000-74909800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr6:74910200-74910400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr6:74923200-74923800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr6:74923400-74923800	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr6:74932200-74932400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr6:74932200-74932400	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr6:74932200-74932600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr6:74932200-74933200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr6:74932200-74933400	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr6:74932200-74933600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:74932400-74932600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
21	chr6:74932400-74932600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr6:74932400-74932600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:74932400-74932800	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr6:74932400-74933000	Enhancers	H1 Cell Line	embryonic stem cell
25	chr6:74932400-74933000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr6:74932400-74933000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr6:74932400-74933000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr6:74932400-74933000	Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr6:74932400-74933200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr6:74932600-74933000	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr6:74932600-74933000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr6:74932600-74933200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr6:74932800-74933000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
34	chr6:74932800-74933200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:74932800-74933400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr6:74933000-74933200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr6:74933000-74933200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr6:74933200-74933400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr6:74938800-74939200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:74939400-74939800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr6:74939800-74940000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:74940000-74940200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr6:74940200-74940400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr6:74958000-74958200	Enhancers	NHLF	lung
45	chr6:74958000-74959000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr6:74958000-74961400	Enhancers	HUVEC	blood vessel
47	chr6:74958800-74959600	Enhancers	HMEC	breast
48	chr6:74958800-74959800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr6:74958800-74960400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr6:74958800-74960800	Enhancers	NHEK	skin

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