Variant report

Variant	esv1004150
Chromosome Location	chr6:160493668-160499709
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	ATF2	chr6:160497001-160497492	GM12878	blood:	n/a	n/a
2	ATF2	chr6:160496963-160497414	GM12878	blood:	n/a	n/a
3	BATF	chr6:160496997-160497477	GM12878	blood:	n/a	n/a
4	BATF	chr6:160497113-160497369	GM12878	blood:	n/a	n/a
5	BCL3	chr6:160496940-160497402	GM12878	blood:	n/a	n/a
6	BCLAF1	chr6:160496992-160497459	GM12878	blood:	n/a	n/a
7	BHLHE40	chr6:160497215-160497370	GM12878	blood:	n/a	n/a
8	CEBPB	chr6:160495242-160495539	HepG2	liver:	n/a	n/a
9	CEBPB	chr6:160495351-160495408	A549	lung:	n/a	n/a
10	CEBPB	chr6:160495345-160495371	K562	blood:	n/a	n/a
11	CEBPB	chr6:160495314-160495434	IMR90	lung:	n/a	n/a
12	CEBPB	chr6:160495290-160495443	HepG2	liver:	n/a	n/a
13	CTCF	chr6:160496080-160496230	HMF	breast:	n/a	n/a
14	CTCF	chr6:160496050-160496170	GM19239	blood:	n/a	n/a
15	CTCF	chr6:160495940-160496090	HEK293	kidney:	n/a	n/a
16	CTCF	chr6:160494200-160494350	K562	blood:	n/a	n/a
17	CTCF	chr6:160496038-160496118	GM12892	blood:	n/a	n/a
18	CTCF	chr6:160496020-160496130	NHEK	skin:	n/a	n/a
19	CTCF	chr6:160495960-160496110	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr6:160493457-160493670	NHEK	skin:	n/a	chr6:160493557-160493578 chr6:160493558-160493571 chr6:160493555-160493573
21	CTCF	chr6:160493426-160493678	Fibrobl	skin:	n/a	chr6:160493557-160493578 chr6:160493558-160493571 chr6:160493555-160493573
22	CTCF	chr6:160493520-160493670	RPTEC	kidney:	n/a	chr6:160493557-160493578 chr6:160493558-160493571 chr6:160493555-160493573
23	CTCF	chr6:160493660-160493810	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr6:160493520-160493670	GM12874	blood:	n/a	chr6:160493557-160493578 chr6:160493558-160493571 chr6:160493555-160493573
25	CTCF	chr6:160493540-160493690	BJ	skin:	n/a	chr6:160493557-160493578 chr6:160493558-160493571 chr6:160493555-160493573
26	CTCF	chr6:160493560-160493710	HVMF	connective:	n/a	n/a
27	CTCF	chr6:160495980-160496130	HCM	heart:	n/a	n/a
28	CTCF	chr6:160493540-160493690	GM12864	blood:	n/a	chr6:160493557-160493578 chr6:160493558-160493571 chr6:160493555-160493573
29	CTCF	chr6:160493580-160493730	HAc	cerebellar:	n/a	n/a
30	CTCF	chr6:160496082-160496112	A549	lung:	n/a	n/a
31	CTCF	chr6:160496000-160496150	GM12875	blood:	n/a	n/a
32	CTCF	chr6:160493393-160493709	K562	blood:	n/a	chr6:160493557-160493578 chr6:160493558-160493571 chr6:160493555-160493573
33	CTCF	chr6:160496160-160496310	HVMF	connective:	n/a	n/a
34	CTCF	chr6:160493520-160493670	GM12872	blood:	n/a	chr6:160493557-160493578 chr6:160493558-160493571 chr6:160493555-160493573
35	CTCF	chr6:160497080-160497230	GM06990	blood:	n/a	n/a
36	CTCF	chr6:160493540-160493690	RPTEC	kidney:	n/a	chr6:160493557-160493578 chr6:160493558-160493571 chr6:160493555-160493573
37	CTCF	chr6:160493484-160493671	K562	blood:	n/a	chr6:160493557-160493578 chr6:160493558-160493571 chr6:160493555-160493573
38	CTCF	chr6:160493514-160493692	IMR90	lung:	n/a	chr6:160493557-160493578 chr6:160493558-160493571 chr6:160493555-160493573
39	CTCF	chr6:160493520-160493670	HFF	foreskin:	n/a	chr6:160493557-160493578 chr6:160493558-160493571 chr6:160493555-160493573
40	CTCF	chr6:160496072-160496089	GM13976	blood:	n/a	n/a
41	CTCF	chr6:160493540-160493690	MCF-7	breast:	n/a	chr6:160493557-160493578 chr6:160493558-160493571 chr6:160493555-160493573
42	CTCF	chr6:160493520-160493670	GM12864	blood:	n/a	chr6:160493557-160493578 chr6:160493558-160493571 chr6:160493555-160493573
43	CTCF	chr6:160493560-160493710	GM12869	blood:	n/a	n/a
44	CTCF	chr6:160496065-160496099	K562	blood:	n/a	n/a
45	CTCF	chr6:160493520-160493670	HBMEC	blood vessel:	n/a	chr6:160493557-160493578 chr6:160493558-160493571 chr6:160493555-160493573
46	CTCF	chr6:160495931-160496223	GM12878	blood:	n/a	n/a
47	CTCF	chr6:160493580-160493730	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr6:160493600-160493750	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr6:160493393-160493721	K562	blood:	n/a	chr6:160493557-160493578 chr6:160493558-160493571 chr6:160493555-160493573
50	CTCF	chr6:160493520-160493670	HRE	kidney:	n/a	chr6:160493557-160493578 chr6:160493558-160493571 chr6:160493555-160493573

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:160498383-160498433	HCM	heart:	n/a
2	chr6:160498383-160498433	AoSMC	blood vessel:	n/a
3	chr6:160498383-160498433	HAEpiC	amniotic membrane:	n/a
4	chr6:160498383-160498433	Hepatocyte	liver:	n/a
5	chr6:160498383-160498433	U87	brain:	n/a
6	chr6:160498383-160498433	BE2_C	brain:	n/a
7	chr6:160498383-160498433	HRE	kidney:	n/a
8	chr6:160498383-160498433	H1-hESC	embryonic stem cell:	embryo
9	chr6:160498383-160498433	ECC-1	luminal epithelium:	n/a
10	chr6:160498383-160498433	Caco-2	colon:	n/a
11	chr6:160498383-160498433	GM12891	blood:	n/a
12	chr6:160498383-160498433	HEK293	kidney:	embryo
13	chr6:160498383-160498433	ProgFib	skin:	n/a
14	chr6:160498383-160498433	SK-N-SH_RA	brain:	n/a
15	chr6:160498383-160498433	PFSK-1	brain:	n/a
16	chr6:160498383-160498433	HUVEC	blood vessel:	n/a
17	chr6:160498383-160498433	GM06990	blood:	n/a
18	chr6:160498383-160498433	NHBE	bronchial:	n/a
19	chr6:160498383-160498433	K562	blood:	n/a
20	chr6:160498383-160498433	GM12878	blood:	n/a
21	chr6:160498383-160498433	NT2-D1	testis:	n/a
22	chr6:160498383-160498433	HEEpiC	esophagus:	n/a
23	chr6:160498383-160498433	HepG2	liver:	n/a
24	chr6:160498383-160498433	LNCaP	prostate:	n/a
25	chr6:160498383-160498433	Jurkat	blood:	n/a
26	chr6:160498383-160498433	HMEC	breast:	n/a
27	chr6:160498383-160498433	NHDF-neo	bronchial:	n/a
28	chr6:160498383-160498433	AG04449	skin:	fetal
29	chr6:160498383-160498433	T-47D	breast:	n/a
30	chr6:160498383-160498433	AG04450	lung:	fetal
31	chr6:160498383-160498433	HL-60	blood:	n/a
32	chr6:160498383-160498433	HPAEpiC	pulmonary alveolar:	n/a
33	chr6:160498383-160498433	SAEC	small airway:	n/a
34	chr6:160498383-160498433	BJ	skin:	n/a
35	chr6:160498383-160498433	HIPEpiC	eye:	n/a
36	chr6:160498383-160498433	HRCEpiC	kidney:	n/a
37	chr6:160498383-160498433	MCF-7	breast:	n/a
38	chr6:160498383-160498433	AG09309	skin:	n/a
39	chr6:160498383-160498433	HNPCEpiC	eye:	n/a
40	chr6:160498383-160498433	Hela-S3	cervix:	n/a
41	chr6:160498383-160498433	NB4	blood:	n/a
42	chr6:160498383-160498433	RPTEC	kidney:	n/a
43	chr6:160498383-160498433	PrEC	prostate:	n/a
44	chr6:160498383-160498433	CMK	blood:	n/a
45	chr6:160498383-160498433	A549	lung:	n/a
46	chr6:160498383-160498433	SK-N-SH	brain:	n/a
47	chr6:160498383-160498433	PANC-1	pancreas:	n/a
48	chr6:160498383-160498433	GM19239	blood:	n/a
49	chr6:160498383-160498433	IMR90	lung:	fetal
50	chr6:160498383-160498433	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:160491211..160493153-chr6:160494849..160496655,2	K562	blood:
2	chr6:160495573..160497446-chr6:160542645..160544424,2	K562	blood:
3	chr6:160486955..160489342-chr6:160498753..160500327,2	K562	blood:
4	chr6:160496060..160498453-chr6:160518764..160521652,3	K562	blood:
5	chr6:160497364..160500238-chr6:160505047..160507278,2	K562	blood:
6	chr6:160488589..160490220-chr6:160491030..160493855,2	MCF-7	breast:

Variant related genes	Relation type
IGF2R	TF binding region
IGF2R	CpG island
ENSG00000175003	chromatin interactions
ENSG00000197081	chromatin interactions

Extended variants
information (count: 309 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565068137	chr6:160493671-160493672	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs111643050	chr6:160493697-160493698	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs116729773	chr6:160493728-160493729	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs551074781	chr6:160493730-160493731	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs8191885	chr6:160493734-160493735	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs376385502	chr6:160493802-160493803	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs140091632	chr6:160493827-160493828	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs2230044	chr6:160493834-160493835	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs546930435	chr6:160493855-160493856	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs199789899	chr6:160493860-160493861	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs371628678	chr6:160493864-160493865	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs137918443	chr6:160493874-160493875	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs576113617	chr6:160493925-160493926	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs539312629	chr6:160493926-160493927	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs201699013	chr6:160493934-160493935	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs374272747	chr6:160493935-160493936	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs17847649	chr6:160493936-160493937	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs200917457	chr6:160493944-160493945	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs558766744	chr6:160493954-160493955	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs569093775	chr6:160493955-160493956	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs368192536	chr6:160493966-160493967	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs8191887	chr6:160493968-160493969	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs573641589	chr6:160494028-160494029	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs76023313	chr6:160494055-160494056	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs8191888	chr6:160494068-160494069	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs573096016	chr6:160494090-160494091	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs141666676	chr6:160494106-160494107	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs545310630	chr6:160494109-160494110	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs376450558	chr6:160494110-160494111	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs142884365	chr6:160494118-160494119	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs530749274	chr6:160494166-160494167	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs544389084	chr6:160494173-160494174	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs8191889	chr6:160494174-160494175	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs561232930	chr6:160494201-160494202	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs181073665	chr6:160494203-160494204	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs374601410	chr6:160494239-160494240	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs151194150	chr6:160494241-160494242	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs140337762	chr6:160494258-160494259	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs546126471	chr6:160494281-160494282	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs140858283	chr6:160494304-160494305	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs144686841	chr6:160494315-160494316	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs376670792	chr6:160494318-160494319	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs369882295	chr6:160494336-160494337	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs201529415	chr6:160494362-160494363	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs201938520	chr6:160494390-160494391	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs375863720	chr6:160494391-160494392	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs629849	chr6:160494409-160494410	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs56029582	chr6:160494432-160494433	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs200330928	chr6:160494475-160494476	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369644129	chr6:160494479-160494480	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Follicular lymphoma	20505157	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
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Developmental delay	19459884	CNVD
Hearing loss	19459884	CNVD
Microcephaly	19459884	CNVD
Coronary artery disease	17160897	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:160444200-160521600	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr6:160453000-160534600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:160455800-160532000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr6:160459200-160501200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:160459600-160519200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr6:160460600-160500800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
7	chr6:160460800-160520200	Strong transcription	HUES6 Cell Line	embryonic stem cell
8	chr6:160460800-160520200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr6:160461000-160497400	Strong transcription	H1 Cell Line	embryonic stem cell
10	chr6:160461000-160500600	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chr6:160461200-160500800	Strong transcription	HUES64 Cell Line	embryonic stem cell
12	chr6:160464400-160519800	Strong transcription	Lung	lung
13	chr6:160464600-160531800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr6:160465600-160530800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr6:160466000-160521000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr6:160466200-160494800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:160474200-160501200	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr6:160474200-160519600	Strong transcription	Cortex derived primary cultured neurospheres	brain
19	chr6:160474200-160519800	Strong transcription	Fetal Stomach	stomach
20	chr6:160474400-160520600	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr6:160474800-160497400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr6:160474800-160509200	Strong transcription	Brain Inferior Temporal Lobe	brain
23	chr6:160474800-160509400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr6:160477200-160531200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr6:160477200-160531400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:160477600-160497600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr6:160479400-160499200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr6:160480200-160510600	Strong transcription	Fetal Intestine Large	intestine
29	chr6:160480600-160502800	Strong transcription	Rectal Mucosa Donor 31	rectum
30	chr6:160484800-160497800	Strong transcription	HSMM	muscle
31	chr6:160485000-160512600	Weak transcription	Right Atrium	heart
32	chr6:160485600-160501800	Strong transcription	Placenta	Placenta
33	chr6:160485800-160522800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr6:160487400-160498000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr6:160487600-160497200	Strong transcription	NHLF	lung
36	chr6:160487600-160497400	Strong transcription	Brain Cingulate Gyrus	brain
37	chr6:160487600-160498000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr6:160487600-160498200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr6:160487600-160498400	Strong transcription	Muscle Satellite Cultured Cells	--
40	chr6:160487600-160503000	Strong transcription	K562	blood
41	chr6:160487600-160503800	Strong transcription	Osteobl	bone
42	chr6:160487600-160509400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr6:160487600-160520000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:160487600-160530800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr6:160487800-160494800	Strong transcription	Colon Smooth Muscle	Colon
46	chr6:160487800-160495000	Strong transcription	Fetal Lung	lung
47	chr6:160487800-160495600	Strong transcription	Brain Substantia Nigra	brain
48	chr6:160487800-160496400	Strong transcription	HSMMtube	muscle
49	chr6:160487800-160496600	Strong transcription	Rectal Smooth Muscle	rectum
50	chr6:160487800-160497200	Strong transcription	H9 Cell Line	embryonic stem cell

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