Variant report

Variant	nsv886927
Chromosome Location	chr6:165368163-165644276
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:994)
CpG islands
(count:122)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:994 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:165501047-165501063	K562	blood:	n/a	n/a
2	ATF1	chr6:165441073-165441114	K562	blood:	n/a	n/a
3	BCL3	chr6:165426595-165426923	GM12878	blood:	n/a	n/a
4	BCL3	chr6:165426681-165426931	GM12878	blood:	n/a	n/a
5	BCL3	chr6:165418145-165418452	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:165639608-165639621	K562	blood:	n/a	n/a
7	CBX3	chr6:165462791-165463264	HCT-116	colon:	n/a	n/a
8	CBX3	chr6:165462829-165463232	K562	blood:	n/a	n/a
9	CBX3	chr6:165462768-165463242	K562	blood:	n/a	n/a
10	CEBPB	chr6:165568950-165569240	A549	lung:	n/a	chr6:165569062-165569073
11	CEBPB	chr6:165440862-165440891	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr6:165533080-165533415	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr6:165491383-165491633	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:165556474-165556739	IMR90	lung:	n/a	n/a
15	CEBPB	chr6:165556460-165556793	HepG2	liver:	n/a	n/a
16	CEBPB	chr6:165630086-165630271	HepG2	liver:	n/a	n/a
17	CEBPB	chr6:165641158-165641506	Hela-S3	cervix:	n/a	chr6:165641270-165641283 chr6:165641272-165641283 chr6:165641272-165641283 chr6:165641351-165641362
18	CEBPB	chr6:165533000-165533478	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr6:165595689-165595865	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr6:165595660-165595860	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr6:165641184-165641536	IMR90	lung:	n/a	chr6:165641270-165641283 chr6:165641272-165641283 chr6:165641272-165641283 chr6:165641351-165641362
22	CEBPB	chr6:165641184-165641505	A549	lung:	n/a	chr6:165641270-165641283 chr6:165641272-165641283 chr6:165641272-165641283 chr6:165641351-165641362
23	CEBPB	chr6:165641185-165641522	HepG2	liver:	n/a	chr6:165641270-165641283 chr6:165641272-165641283 chr6:165641272-165641283 chr6:165641351-165641362
24	CEBPB	chr6:165426733-165426862	A549	lung:	n/a	n/a
25	CEBPB	chr6:165511782-165511924	K562	blood:	n/a	n/a
26	CEBPB	chr6:165572815-165572909	H1-hESC	embryonic stem cell:	n/a	chr6:165572819-165572830 chr6:165572819-165572830 chr6:165572819-165572832 chr6:165572819-165572832
27	CEBPB	chr6:165630165-165630323	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr6:165568927-165569218	HepG2	liver:	n/a	chr6:165569062-165569073
29	CHD2	chr6:165463083-165463102	GM12878	blood:	n/a	n/a
30	CTCF	chr6:165463080-165463230	GM12864	blood:	n/a	n/a
31	CTCF	chr6:165642853-165642980	Fibrobl	skin:	n/a	chr6:165642923-165642941 chr6:165642907-165642920 chr6:165642925-165642938
32	CTCF	chr6:165463000-165463150	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr6:165468878-165468969	LNCaP	prostate:	n/a	n/a
34	CTCF	chr6:165468760-165468910	HAc	cerebellar:	n/a	n/a
35	CTCF	chr6:165511460-165511610	HEK293	kidney:	n/a	n/a
36	CTCF	chr6:165468860-165469060	GM12878	blood:	n/a	n/a
37	CTCF	chr6:165642860-165642988	MCF-7	breast:	n/a	chr6:165642923-165642941 chr6:165642907-165642920 chr6:165642925-165642938
38	CTCF	chr6:165468863-165468931	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:165462949-165463198	GM12878	blood:	n/a	n/a
40	CTCF	chr6:165511684-165512035	GM12878	blood:	n/a	n/a
41	CTCF	chr6:165462953-165463212	Gliobla	brain:	n/a	n/a
42	CTCF	chr6:165456483-165456654	MCF-7	breast:	n/a	n/a
43	CTCF	chr6:165572836-165572888	Lung_OC	lung:	n/a	n/a
44	CTCF	chr6:165463007-165463173	GM13976	blood:	n/a	n/a
45	CTCF	chr6:165511700-165511850	HVMF	connective:	n/a	n/a
46	CTCF	chr6:165511720-165511870	GM12878	blood:	n/a	n/a
47	CTCF	chr6:165462915-165463214	A549	lung:	n/a	n/a
48	CTCF	chr6:165463012-165463175	GM10248	blood:	n/a	n/a
49	CTCF	chr6:165511800-165511950	HepG2	liver:	n/a	n/a
50	CTCF	chr6:165463000-165463150	WERI-Rb-1	eye:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:165415258-165415308	HMEC	breast:	n/a
2	chr6:165415258-165415308	HEEpiC	esophagus:	n/a
3	chr6:165415258-165415308	GM06990	blood:	n/a
4	chr6:165384599-165384649	T-47D	breast:	n/a
5	chr6:165384599-165384649	H1-hESC	embryonic stem cell:	embryo
6	chr6:165415258-165415308	HEK293	kidney:	embryo
7	chr6:165415258-165415308	SK-N-MC	brain:	n/a
8	chr6:165384599-165384649	MCF10A-Er-Src	breast:	n/a
9	chr6:165384599-165384649	RPTEC	kidney:	n/a
10	chr6:165415258-165415308	RPTEC	kidney:	n/a
11	chr6:165384599-165384649	PrEC	prostate:	n/a
12	chr6:165384599-165384649	SK-N-SH_RA	brain:	n/a
13	chr6:165415258-165415308	CMK	blood:	n/a
14	chr6:165415258-165415308	GM12891	blood:	n/a
15	chr6:165384599-165384649	K562	blood:	n/a
16	chr6:165415258-165415308	A549	lung:	n/a
17	chr6:165384599-165384649	LNCaP	prostate:	n/a
18	chr6:165384599-165384649	IMR90	lung:	fetal
19	chr6:165415258-165415308	SKMC	muscle:	n/a
20	chr6:165384599-165384649	AG09309	skin:	n/a
21	chr6:165415258-165415308	IMR90	lung:	fetal
22	chr6:165384599-165384649	SKMC	muscle:	n/a
23	chr6:165384599-165384649	HMEC	breast:	n/a
24	chr6:165415258-165415308	BJ	skin:	n/a
25	chr6:165384599-165384649	Caco-2	colon:	n/a
26	chr6:165415258-165415308	AG04449	skin:	fetal
27	chr6:165415258-165415308	PFSK-1	brain:	n/a
28	chr6:165415258-165415308	Hela-S3	cervix:	n/a
29	chr6:165384599-165384649	ovcar-3	ovarian:	n/a
30	chr6:165384599-165384649	PANC-1	pancreas:	n/a
31	chr6:165415258-165415308	AG09309	skin:	n/a
32	chr6:165384599-165384649	NT2-D1	testis:	n/a
33	chr6:165384599-165384649	HIPEpiC	eye:	n/a
34	chr6:165415258-165415308	T-47D	breast:	n/a
35	chr6:165384599-165384649	ProgFib	skin:	n/a
36	chr6:165415258-165415308	HCF	heart:	n/a
37	chr6:165415258-165415308	SK-N-SH_RA	brain:	n/a
38	chr6:165415258-165415308	GM12892	blood:	n/a
39	chr6:165415258-165415308	GM19239	blood:	n/a
40	chr6:165384599-165384649	HPAEpiC	pulmonary alveolar:	n/a
41	chr6:165415258-165415308	HRE	kidney:	n/a
42	chr6:165415258-165415308	BE2_C	brain:	n/a
43	chr6:165384599-165384649	ECC-1	luminal epithelium:	n/a
44	chr6:165384599-165384649	SK-N-SH	brain:	n/a
45	chr6:165384599-165384649	GM19239	blood:	n/a
46	chr6:165384599-165384649	AG10803	skin:	n/a
47	chr6:165415258-165415308	NT2-D1	testis:	n/a
48	chr6:165415258-165415308	Caco-2	colon:	n/a
49	chr6:165384599-165384649	HRE	kidney:	n/a
50	chr6:165384599-165384649	Jurkat	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:165566946..165568457-chr6:165571126..165572931,2	K562	blood:
2	chr6:165632737..165634730-chr6:165637289..165639668,2	K562	blood:
3	chr6:165271396..165272279-chr6:165462865..165463466,2	MCF-7	breast:
4	chr6:165539543..165541848-chr6:165544518..165546207,2	K562	blood:
5	chr6:165577753..165580449-chr6:165583004..165584853,2	K562	blood:
6	chr6:165610948..165613240-chr6:165614979..165616709,2	K562	blood:
7	chr6:165610948..165613240-chr6:165614979..165616709,2	K562	blood:
8	chr6:165549550..165552338-chr6:165552859..165555355,2	K562	blood:
9	chr6:165539543..165541848-chr6:165544518..165546207,2	K562	blood:
10	chr6:165632737..165634730-chr6:165637289..165639668,2	K562	blood:
11	chr6:165549550..165552338-chr6:165552859..165555355,2	K562	blood:
12	chr6:165375696..165377875-chr6:165438259..165440436,2	K562	blood:
13	chr6:165375696..165377875-chr6:165438259..165440436,2	K562	blood:
14	chr6:165566946..165568457-chr6:165571126..165572931,2	K562	blood:
15	chr6:165447524..165449382-chr6:165456045..165457781,2	K562	blood:
16	chr6:165577753..165580449-chr6:165583004..165584853,2	K562	blood:
17	chr6:165447524..165449382-chr6:165456045..165457781,2	K562	blood:
18	chr6:165641887..165643835-chr6:165647824..165649680,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf118-4	chr6:165530684-165531013	NONHSAT115999

No data

Variant related genes	Relation type
ENSG00000217878	TF binding region
ENSG00000217878	CpG island

Extended variants
information (count: 7395 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:7395 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148043914	chr6:165374062-165374063	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs552381025	chr6:165374069-165374070	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs570618768	chr6:165374094-165374095	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs534941551	chr6:165374101-165374102	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs193299018	chr6:165374139-165374140	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs141678492	chr6:165374174-165374175	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs535500117	chr6:165374183-165374184	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs10455802	chr6:165374272-165374273	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs575721908	chr6:165374283-165374284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552837382	chr6:165374301-165374302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539629257	chr6:165374317-165374318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558346351	chr6:165374334-165374335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573410506	chr6:165374363-165374364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185082654	chr6:165374403-165374404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562408434	chr6:165374456-165374457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577701519	chr6:165374472-165374473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541872701	chr6:165374475-165374476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs9356317	chr6:165374482-165374483	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs9347050	chr6:165374508-165374509	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs552060854	chr6:165374516-165374517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575632827	chr6:165374551-165374552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375497902	chr6:165374555-165374556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564311989	chr6:165374564-165374565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs67252669	chr6:165374576-165374577	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs561121456	chr6:165374599-165374600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546482366	chr6:165374606-165374607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372824032	chr6:165374671-165374672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568061377	chr6:165374698-165374699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79347324	chr6:165374770-165374771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528303603	chr6:165374795-165374796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550987311	chr6:165374809-165374810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138598928	chr6:165374824-165374825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539924313	chr6:165374838-165374839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558028257	chr6:165374850-165374851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535740016	chr6:165374857-165374858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs9356318	chr6:165374882-165374883	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs34270884	chr6:165374896-165374897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9347962	chr6:165374914-165374915	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs199732898	chr6:165376251-165376252	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs386708313	chr6:165376252-165376253	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs58680076	chr6:165376253-165376254	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs552823996	chr6:165376294-165376295	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs571329675	chr6:165376320-165376321	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs573496298	chr6:165376353-165376354	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs375614158	chr6:165376382-165376383	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs376166577	chr6:165376421-165376422	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs12528648	chr6:165376441-165376442	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs544103717	chr6:165376451-165376452	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs60132705	chr6:165376460-165376461	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs112605698	chr6:165376467-165376468	ZNF genes & repeats	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
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD

Chromatin state (count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:165374000-165374200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:165374200-165375000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:165376200-165376600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:165377400-165377800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr6:165380400-165381000	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr6:165380600-165380800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr6:165380600-165381000	Enhancers	H1 Cell Line	embryonic stem cell
8	chr6:165381000-165384200	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr6:165384200-165385000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr6:165384400-165384800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr6:165384400-165385200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr6:165384400-165385400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr6:165384600-165385200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr6:165384600-165385200	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr6:165385000-165385200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr6:165404200-165406200	Enhancers	Placenta	Placenta
17	chr6:165405000-165406200	Enhancers	Placenta Amnion	Placenta Amnion
18	chr6:165408200-165408400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr6:165408400-165410200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr6:165410200-165410600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr6:165410400-165411000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr6:165420000-165420200	Enhancers	Spleen	Spleen
23	chr6:165420000-165420400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr6:165420400-165424200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr6:165422200-165425600	Enhancers	HSMM	muscle
26	chr6:165422400-165422800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr6:165422400-165423000	Enhancers	HSMMtube	muscle
28	chr6:165422400-165423000	Enhancers	NH-A	brain
29	chr6:165422400-165425800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr6:165422800-165426800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr6:165423000-165423400	Weak transcription	HSMMtube	muscle
32	chr6:165423000-165423400	Weak transcription	NH-A	brain
33	chr6:165423200-165425400	Enhancers	Fetal Heart	heart
34	chr6:165423400-165424000	Enhancers	HSMMtube	muscle
35	chr6:165423400-165425400	Enhancers	NH-A	brain
36	chr6:165423600-165425800	Enhancers	Placenta Amnion	Placenta Amnion
37	chr6:165423800-165425200	Enhancers	Muscle Satellite Cultured Cells	--
38	chr6:165424000-165424400	Flanking Active TSS	HSMMtube	muscle
39	chr6:165424000-165424800	Enhancers	Fetal Kidney	kidney
40	chr6:165424000-165425600	Enhancers	Osteobl	bone
41	chr6:165424200-165424400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr6:165424200-165424800	Enhancers	H1 Cell Line	embryonic stem cell
43	chr6:165424200-165424800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr6:165424200-165425000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:165424200-165425000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr6:165424200-165425200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr6:165424200-165425400	Enhancers	Placenta	Placenta
48	chr6:165424400-165424800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr6:165424400-165425000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr6:165424400-165425600	Enhancers	HSMMtube	muscle

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