Variant report

Variant	nsv886165
Chromosome Location	chr6:74981125-75070742
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	CBX3	chr6:75053493-75053926	HCT-116	colon:	n/a	n/a
2	CEBPB	chr6:75067143-75067433	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr6:74999604-75000012	IMR90	lung:	n/a	chr6:74999810-74999827
4	CEBPB	chr6:75056405-75056627	A549	lung:	n/a	chr6:75056490-75056501 chr6:75056489-75056502 chr6:75056489-75056502 chr6:75056489-75056502
5	CEBPB	chr6:75056246-75056651	HepG2	liver:	n/a	chr6:75056490-75056501 chr6:75056489-75056502 chr6:75056489-75056502 chr6:75056489-75056502
6	CEBPB	chr6:75056353-75056636	IMR90	lung:	n/a	chr6:75056490-75056501 chr6:75056489-75056502 chr6:75056489-75056502 chr6:75056489-75056502
7	CEBPZ	chr6:74985570-74985693	HepG2	liver:	n/a	n/a
8	CTCF	chr6:75053500-75053650	GM12867	blood:	n/a	n/a
9	CTCF	chr6:75053600-75053750	BJ	skin:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
10	CTCF	chr6:74990120-74990270	AG09319	gingival:	n/a	n/a
11	CTCF	chr6:74990096-74990307	MCF-7	breast:	n/a	n/a
12	CTCF	chr6:74989640-74989790	HMF	breast:	n/a	n/a
13	CTCF	chr6:75053600-75053750	Hela-S3	cervix:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
14	CTCF	chr6:75053640-75053790	AG10803	skin:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
15	CTCF	chr6:74989560-74989710	RPTEC	kidney:	n/a	chr6:74989638-74989647
16	CTCF	chr6:75019980-75020130	HMF	breast:	n/a	n/a
17	CTCF	chr6:75053627-75053817	HUVEC	blood vessel:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
18	CTCF	chr6:74990080-74990230	A549	lung:	n/a	n/a
19	CTCF	chr6:74990120-74990270	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr6:74990140-74990290	HRPEpiC	eye:	n/a	n/a
21	CTCF	chr6:75053600-75053750	GM12875	blood:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
22	CTCF	chr6:75053620-75053770	HEEpiC	esophagus:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
23	CTCF	chr6:74990100-74990250	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr6:74990080-74990230	HepG2	liver:	n/a	n/a
25	CTCF	chr6:74989540-74989690	Caco-2	colon:	n/a	chr6:74989638-74989647
26	CTCF	chr6:75053435-75053509	MCF-7	breast:	n/a	n/a
27	CTCF	chr6:74990120-74990270	Caco-2	colon:	n/a	n/a
28	CTCF	chr6:75053620-75053770	AG04449	skin:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
29	CTCF	chr6:74990100-74990250	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr6:75053686-75053729	Gliobla	brain:	n/a	chr6:75053717-75053726 chr6:75053719-75053729
31	CTCF	chr6:75020056-75020103	LNCaP	prostate:	n/a	n/a
32	CTCF	chr6:75053569-75053898	IMR90	lung:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
33	CTCF	chr6:74990040-74990190	GM12868	blood:	n/a	n/a
34	CTCF	chr6:75053580-75053730	AG04450	lung:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053719-75053729
35	CTCF	chr6:74990120-74990270	NHLF	lung:	n/a	n/a
36	CTCF	chr6:74989600-74989750	NHEK	skin:	n/a	chr6:74989638-74989647
37	CTCF	chr6:75053620-75053770	HVMF	connective:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
38	CTCF	chr6:74990080-74990230	HCT-116	colon:	n/a	n/a
39	CTCF	chr6:74990040-74990190	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:74990163-74990258	Medullo	brain:	n/a	n/a
41	CTCF	chr6:75053387-75053963	A549	lung:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
42	CTCF	chr6:74989840-74989990	NHEK	skin:	n/a	n/a
43	CTCF	chr6:74999200-74999350	RPTEC	kidney:	n/a	chr6:74999245-74999258
44	CTCF	chr6:74990100-74990250	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr6:75053440-75053590	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr6:75053433-75053501	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:75053609-75053783	LNCaP	prostate:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
48	CTCF	chr6:74989580-74989730	HCFaa	heart:	n/a	chr6:74989638-74989647
49	CTCF	chr6:75053526-75053818	HepG2	liver:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729
50	CTCF	chr6:75053620-75053770	HPF	lung:	n/a	chr6:75053717-75053726 chr6:75053717-75053730 chr6:75053714-75053732 chr6:75053716-75053737 chr6:75053715-75053731 chr6:75053719-75053729

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:74998385-74998435	Jurkat	blood:	n/a
2	chr6:74987753-74987803	HRCEpiC	kidney:	n/a
3	chr6:75061364-75061414	GM12891	blood:	n/a
4	chr6:74987753-74987803	AG04450	lung:	fetal
5	chr6:74987753-74987803	LNCaP	prostate:	n/a
6	chr6:75061364-75061414	NT2-D1	testis:	n/a
7	chr6:75061364-75061414	SK-N-SH	brain:	n/a
8	chr6:75061364-75061414	SK-N-MC	brain:	n/a
9	chr6:75061364-75061414	SK-N-SH_RA	brain:	n/a
10	chr6:74998385-74998435	HCT-116	colon:	n/a
11	chr6:74998385-74998435	HCF	heart:	n/a
12	chr6:75061364-75061414	Caco-2	colon:	n/a
13	chr6:74998385-74998435	T-47D	breast:	n/a
14	chr6:75061364-75061414	HMEC	breast:	n/a
15	chr6:74987753-74987803	NHDF-neo	bronchial:	n/a
16	chr6:74998385-74998435	PANC-1	pancreas:	n/a
17	chr6:75061364-75061414	MCF10A-Er-Src	breast:	n/a
18	chr6:75061364-75061414	NB4	blood:	n/a
19	chr6:75061364-75061414	HRCEpiC	kidney:	n/a
20	chr6:74998385-74998435	MCF-7	breast:	n/a
21	chr6:74998385-74998435	SKMC	muscle:	n/a
22	chr6:74987753-74987803	HL-60	blood:	n/a
23	chr6:74987753-74987803	GM06990	blood:	n/a
24	chr6:74987753-74987803	AG10803	skin:	n/a
25	chr6:75061364-75061414	GM12878	blood:	n/a
26	chr6:75061364-75061414	GM19239	blood:	n/a
27	chr6:74998385-74998435	AG10803	skin:	n/a
28	chr6:75061364-75061414	NH-A	brain:	n/a
29	chr6:74987753-74987803	SAEC	small airway:	n/a
30	chr6:74987753-74987803	AG09309	skin:	n/a
31	chr6:75061364-75061414	RPTEC	kidney:	n/a
32	chr6:75061364-75061414	U87	brain:	n/a
33	chr6:74998385-74998435	HRE	kidney:	n/a
34	chr6:74998385-74998435	K562	blood:	n/a
35	chr6:75061364-75061414	Jurkat	blood:	n/a
36	chr6:74987753-74987803	T-47D	breast:	n/a
37	chr6:75061364-75061414	HRPEpiC	eye:	n/a
38	chr6:74987753-74987803	HCF	heart:	n/a
39	chr6:74987753-74987803	HepG2	liver:	n/a
40	chr6:75061364-75061414	BE2_C	brain:	n/a
41	chr6:74998385-74998435	GM19239	blood:	n/a
42	chr6:74998385-74998435	GM12878	blood:	n/a
43	chr6:74998385-74998435	HCPEpiC	choroid plexus:	n/a
44	chr6:74987753-74987803	HNPCEpiC	eye:	n/a
45	chr6:74998385-74998435	ovcar-3	ovarian:	n/a
46	chr6:75061364-75061414	PFSK-1	brain:	n/a
47	chr6:74987753-74987803	NHBE	bronchial:	n/a
48	chr6:74998385-74998435	HUVEC	blood vessel:	n/a
49	chr6:74987753-74987803	HIPEpiC	eye:	n/a
50	chr6:75061364-75061414	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:18479342..18480148-chr6:75021400..75022173,2	MCF-7	breast:
2	chr6:75026464..75029067-chr6:75031297..75033184,2	K562	blood:
3	chr6:75053590..75054206-chr6:75918614..75919395,2	MCF-7	breast:
4	chr6:75012871..75015540-chr6:75027590..75030064,2	MCF-7	breast:
5	chr6:75007204..75009226-chr6:75014821..75017230,2	K562	blood:
6	chr6:75012871..75015540-chr6:75027590..75030064,2	MCF-7	breast:
7	chr6:75026464..75029067-chr6:75031297..75033184,2	K562	blood:
8	chr6:75053870..75055720-chr6:75913011..75915599,2	MCF-7	breast:
9	chr6:75007204..75009226-chr6:75014821..75017230,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD109-3	chr6:75056791-75056845	ENSG00000223786.1

Variant related genes	Relation type
ENSG00000217178	TF binding region
ENSG00000217178	CpG island
ENSG00000111799	chromatin interactions

Extended variants
information (count: 1865 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1865 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2029393	chr6:74981125-74981126	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183068918	chr6:74981126-74981127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188525734	chr6:74981128-74981129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560216315	chr6:74981142-74981143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553880520	chr6:74981231-74981232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192748223	chr6:74981287-74981288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375067791	chr6:74981296-74981297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549295120	chr6:74981308-74981309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs72953740	chr6:74981340-74981341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557733800	chr6:74981456-74981457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575953467	chr6:74981460-74981461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9360759	chr6:74981483-74981484	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs547870102	chr6:74981606-74981607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574531458	chr6:74981642-74981643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370781514	chr6:74981657-74981658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560635119	chr6:74981660-74981661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150521746	chr6:74981717-74981718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs13214343	chr6:74981760-74981761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527838872	chr6:74981763-74981764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147694818	chr6:74981792-74981793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533367319	chr6:74981799-74981800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564554726	chr6:74981808-74981809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142322007	chr6:74981825-74981826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551596766	chr6:74981837-74981838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550537364	chr6:74981858-74981859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs28478913	chr6:74981967-74981968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569895566	chr6:74982132-74982133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537397262	chr6:74982142-74982143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555776433	chr6:74982162-74982163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs9359077	chr6:74982166-74982167	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs146405531	chr6:74982180-74982181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373825678	chr6:74982198-74982199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376130988	chr6:74982242-74982243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376461666	chr6:74982332-74982333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536936674	chr6:74982506-74982507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77820779	chr6:74982511-74982512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534276704	chr6:74982515-74982516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574441823	chr6:74982544-74982545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs72953745	chr6:74982579-74982580	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs184803789	chr6:74982590-74982591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553949907	chr6:74982682-74982683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189304789	chr6:74982747-74982748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375472171	chr6:74982760-74982761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534636920	chr6:74982777-74982778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs118053369	chr6:74982847-74982848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs16884590	chr6:74982880-74982881	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs77164751	chr6:74982881-74982882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4708140	chr6:74982935-74982936	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs528849709	chr6:74982973-74982974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1489380	chr6:74982991-74982992	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:97)

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	17122850	CNVD
Myelodysplastic syndrome	18508791	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74979400-74987400	Weak transcription	Fetal Muscle Leg	muscle
2	chr6:74979600-74983800	Weak transcription	Fetal Stomach	stomach
3	chr6:74981200-74981600	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr6:74983800-74984200	Enhancers	Fetal Stomach	stomach
5	chr6:74987200-74987800	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr6:74987200-74988000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:74987200-74988000	Enhancers	Rectal Smooth Muscle	rectum
8	chr6:74987200-74988000	Enhancers	HSMMtube	muscle
9	chr6:74987200-74988400	Enhancers	Fetal Kidney	kidney
10	chr6:74987200-74988800	Enhancers	Placenta Amnion	Placenta Amnion
11	chr6:74987400-74987600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr6:74987400-74987600	Enhancers	NHDF-Ad	bronchial
13	chr6:74987400-74987800	Enhancers	Brain Hippocampus Middle	brain
14	chr6:74987400-74987800	Enhancers	Colon Smooth Muscle	Colon
15	chr6:74987400-74987800	Enhancers	Fetal Heart	heart
16	chr6:74987400-74988000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr6:74987400-74988000	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr6:74987400-74988000	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr6:74987400-74988000	Enhancers	Brain Germinal Matrix	brain
20	chr6:74987400-74988000	Enhancers	Duodenum Smooth Muscle	Duodenum
21	chr6:74987400-74988000	Enhancers	Fetal Lung	lung
22	chr6:74987400-74988000	Enhancers	Fetal Muscle Leg	muscle
23	chr6:74987400-74988000	Enhancers	Psoas Muscle	Psoas
24	chr6:74987400-74988000	Enhancers	Right Ventricle	heart
25	chr6:74987400-74988400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr6:74987400-74988600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr6:74987600-74989600	Weak transcription	NHDF-Ad	bronchial
28	chr6:74988000-74992600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr6:74989600-74990000	Enhancers	NHDF-Ad	bronchial
30	chr6:74992000-74992200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr6:74992000-74992200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr6:74992600-74994800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr6:74993000-74993600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr6:74993200-74994000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr6:74993400-74994200	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr6:74993800-74994400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr6:74994800-74996000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr6:74995600-74996400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr6:74996000-74996600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr6:74996000-74997200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr6:74996400-74998600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr6:74996600-74998400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr6:74997200-74998200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr6:74998200-74999800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr6:74998400-74999800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr6:74998600-75000600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr6:74999000-75001200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr6:74999800-75000800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr6:75001000-75001200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr6:75001400-75002000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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