Variant report

Variant	nsv427757
Chromosome Location	chr6:54296552-54507210
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:617)
CpG islands
(count:122)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:617 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:54356311-54356514	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr6:54432582-54432614	K562	blood:	n/a	n/a
3	BACH1	chr6:54461395-54461453	K562	blood:	n/a	n/a
4	BACH1	chr6:54402647-54402686	K562	blood:	n/a	n/a
5	BHLHE40	chr6:54453873-54453958	GM12878	blood:	n/a	n/a
6	BRCA1	chr6:54424810-54424911	H1-hESC	embryonic stem cell:	n/a	n/a
7	CBX3	chr6:54357824-54358432	HCT-116	colon:	n/a	n/a
8	CEBPB	chr6:54498429-54498779	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr6:54359429-54359584	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr6:54498459-54498670	HepG2	liver:	n/a	n/a
11	CEBPB	chr6:54410771-54410975	HepG2	liver:	n/a	chr6:54410877-54410888
12	CEBPB	chr6:54463785-54464134	Hela-S3	cervix:	n/a	chr6:54464011-54464028 chr6:54464012-54464023 chr6:54463956-54463967 chr6:54464012-54464025 chr6:54464012-54464025 chr6:54464012-54464023
13	CEBPB	chr6:54498398-54498757	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:54441221-54441514	A549	lung:	n/a	chr6:54441352-54441365
15	CEBPB	chr6:54316353-54316602	HepG2	liver:	n/a	chr6:54316433-54316444
16	CEBPB	chr6:54451109-54451413	HepG2	liver:	n/a	n/a
17	CEBPB	chr6:54443257-54443576	HepG2	liver:	n/a	chr6:54443403-54443416 chr6:54443403-54443416 chr6:54443404-54443415
18	CEBPB	chr6:54443238-54443586	H1-hESC	embryonic stem cell:	n/a	chr6:54443403-54443416 chr6:54443403-54443416 chr6:54443404-54443415
19	CEBPB	chr6:54460649-54461120	IMR90	lung:	n/a	chr6:54460918-54460929
20	CEBPB	chr6:54451121-54451385	A549	lung:	n/a	n/a
21	CEBPB	chr6:54463670-54464221	ECC-1	luminal epithelium:	n/a	chr6:54464011-54464028 chr6:54464012-54464023 chr6:54463956-54463967 chr6:54464012-54464025 chr6:54464012-54464025 chr6:54464012-54464023
22	CEBPB	chr6:54357925-54358248	IMR90	lung:	n/a	n/a
23	CEBPB	chr6:54303361-54303473	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr6:54451079-54451429	IMR90	lung:	n/a	n/a
25	CEBPB	chr6:54357794-54358385	HCT-116	colon:	n/a	n/a
26	CEBPB	chr6:54463695-54464200	ECC-1	luminal epithelium:	n/a	chr6:54464011-54464028 chr6:54464012-54464023 chr6:54463956-54463967 chr6:54464012-54464025 chr6:54464012-54464025 chr6:54464012-54464023
27	CEBPB	chr6:54381778-54382077	IMR90	lung:	n/a	n/a
28	CEBPB	chr6:54381710-54382048	HepG2	liver:	n/a	n/a
29	CEBPB	chr6:54410817-54410937	H1-hESC	embryonic stem cell:	n/a	chr6:54410877-54410888
30	CEBPB	chr6:54506445-54506621	A549	lung:	n/a	n/a
31	CEBPB	chr6:54381717-54381994	A549	lung:	n/a	n/a
32	CEBPB	chr6:54439558-54439892	MCF-7	breast:	n/a	chr6:54439734-54439745 chr6:54439734-54439745
33	CEBPB	chr6:54451104-54451434	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr6:54328670-54328680	GM12878	blood:	n/a	n/a
35	CTCF	chr6:54379940-54380090	Caco-2	colon:	n/a	n/a
36	CTCF	chr6:54485480-54485630	HMEC	breast:	n/a	n/a
37	CTCF	chr6:54486230-54486313	GM20000	blood:	n/a	n/a
38	CTCF	chr6:54482520-54482670	HAc	cerebellar:	n/a	n/a
39	CTCF	chr6:54486201-54486344	ProgFib	skin:	n/a	n/a
40	CTCF	chr6:54486180-54486330	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr6:54486180-54486330	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr6:54485959-54486589	A549	lung:	n/a	n/a
43	CTCF	chr6:54379954-54380077	MCF-7	breast:	n/a	n/a
44	CTCF	chr6:54486160-54486310	GM12878	blood:	n/a	n/a
45	CTCF	chr6:54486188-54486300	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr6:54305529-54305610	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:54486180-54486330	HRE	kidney:	n/a	n/a
48	CTCF	chr6:54486202-54486340	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr6:54486180-54486330	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr6:54482460-54482610	BJ	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:54328858-54328908	HCM	heart:	n/a
2	chr6:54460871-54460921	HPAEpiC	pulmonary alveolar:	n/a
3	chr6:54328858-54328908	HUVEC	blood vessel:	n/a
4	chr6:54460871-54460921	A549	lung:	n/a
5	chr6:54328858-54328908	ECC-1	luminal epithelium:	n/a
6	chr6:54460871-54460921	HMEC	breast:	n/a
7	chr6:54328858-54328908	AoSMC	blood vessel:	n/a
8	chr6:54460871-54460921	HCPEpiC	choroid plexus:	n/a
9	chr6:54460871-54460921	GM12891	blood:	n/a
10	chr6:54460871-54460921	LNCaP	prostate:	n/a
11	chr6:54328858-54328908	HIPEpiC	eye:	n/a
12	chr6:54460871-54460921	HCT-116	colon:	n/a
13	chr6:54328858-54328908	ovcar-3	ovarian:	n/a
14	chr6:54460871-54460921	ProgFib	skin:	n/a
15	chr6:54460871-54460921	AG10803	skin:	n/a
16	chr6:54460871-54460921	HepG2	liver:	n/a
17	chr6:54328858-54328908	NHBE	bronchial:	n/a
18	chr6:54460871-54460921	SK-N-SH_RA	brain:	n/a
19	chr6:54328858-54328908	NHDF-neo	bronchial:	n/a
20	chr6:54460871-54460921	HAEpiC	amniotic membrane:	n/a
21	chr6:54328858-54328908	RPTEC	kidney:	n/a
22	chr6:54460871-54460921	GM12878	blood:	n/a
23	chr6:54328858-54328908	SKMC	muscle:	n/a
24	chr6:54460871-54460921	Hepatocyte	liver:	n/a
25	chr6:54460871-54460921	AG09309	skin:	n/a
26	chr6:54460871-54460921	ovcar-3	ovarian:	n/a
27	chr6:54460871-54460921	HRE	kidney:	n/a
28	chr6:54328858-54328908	GM19239	blood:	n/a
29	chr6:54460871-54460921	NHDF-neo	bronchial:	n/a
30	chr6:54328858-54328908	NH-A	brain:	n/a
31	chr6:54460871-54460921	HRPEpiC	eye:	n/a
32	chr6:54328858-54328908	GM12892	blood:	n/a
33	chr6:54460871-54460921	NH-A	brain:	n/a
34	chr6:54328858-54328908	H1-hESC	embryonic stem cell:	embryo
35	chr6:54328858-54328908	HRPEpiC	eye:	n/a
36	chr6:54328858-54328908	BE2_C	brain:	n/a
37	chr6:54460871-54460921	BE2_C	brain:	n/a
38	chr6:54460871-54460921	H1-hESC	embryonic stem cell:	embryo
39	chr6:54460871-54460921	MCF-7	breast:	n/a
40	chr6:54328858-54328908	SK-N-SH_RA	brain:	n/a
41	chr6:54460871-54460921	IMR90	lung:	fetal
42	chr6:54460871-54460921	MCF10A-Er-Src	breast:	n/a
43	chr6:54460871-54460921	SK-N-MC	brain:	n/a
44	chr6:54460871-54460921	AG04449	skin:	fetal
45	chr6:54460871-54460921	Caco-2	colon:	n/a
46	chr6:54460871-54460921	T-47D	breast:	n/a
47	chr6:54460871-54460921	SK-N-SH	brain:	n/a
48	chr6:54328858-54328908	Caco-2	colon:	n/a
49	chr6:54328858-54328908	MCF-7	breast:	n/a
50	chr6:54460871-54460921	HEK293	kidney:	embryo

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:54337437..54340096-chr6:54340126..54342389,2	MCF-7	breast:
2	chr6:54383919..54385673-chr6:54387884..54389679,2	MCF-7	breast:
3	chr6:54445130..54447694-chr6:54452087..54454495,2	K562	blood:
4	chr6:54334351..54336130-chr6:54337919..54340373,2	MCF-7	breast:
5	chr6:54433346..54436074-chr6:54443412..54445005,2	MCF-7	breast:
6	chr6:54485033..54487186-chr6:54562620..54564688,2	MCF-7	breast:
7	chr6:54438796..54440751-chr6:54452137..54454145,2	MCF-7	breast:
8	chr6:54438796..54440751-chr6:54452137..54454145,2	MCF-7	breast:
9	chr6:54383919..54385673-chr6:54387884..54389679,2	MCF-7	breast:
10	chr6:54334351..54336130-chr6:54337919..54340373,2	MCF-7	breast:
11	chr6:54337437..54340096-chr6:54340126..54342389,2	MCF-7	breast:
12	chr6:54462717..54465444-chr6:54712732..54714446,2	MCF-7	breast:
13	chr6:54483454..54486448-chr6:54709404..54710933,2	MCF-7	breast:
14	chr6:54433346..54436074-chr6:54443412..54445005,2	MCF-7	breast:
15	chr6:54445130..54447694-chr6:54452087..54454495,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMGCLL1-3	chr6:54467285-54467948	NONHSAT113223

No data

Variant related genes	Relation type
ENSG00000220773	TF binding region
ENSG00000216347	TF binding region
CLNS1AP1	TF binding region
ENSG00000220773	CpG island
ENSG00000216347	CpG island
CLNS1AP1	CpG island

Extended variants
information (count: 4640 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4640 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535493960	chr6:54296558-54296559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs561154449	chr6:54296605-54296606	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs529930457	chr6:54296654-54296655	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs171492	chr6:54296664-54296665	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs559815550	chr6:54296666-54296667	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs243818	chr6:54296677-54296678	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs180749306	chr6:54296715-54296716	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs551756278	chr6:54296717-54296718	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs564985184	chr6:54296721-54296722	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs530805214	chr6:54296736-54296737	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs373422866	chr6:54296763-54296764	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs567590703	chr6:54296808-54296809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536867365	chr6:54296842-54296843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546836804	chr6:54296884-54296885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566563815	chr6:54296899-54296900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541556735	chr6:54296933-54296934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538380910	chr6:54296936-54296937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538399420	chr6:54296961-54296962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186184829	chr6:54297004-54297005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376800788	chr6:54297043-54297044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368958332	chr6:54297051-54297052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs78439347	chr6:54297125-54297126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537821876	chr6:54297128-54297129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs243817	chr6:54297158-54297159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141605782	chr6:54297160-54297161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540433921	chr6:54297181-54297182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs560045000	chr6:54297197-54297198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576965077	chr6:54297222-54297223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545138460	chr6:54297224-54297225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs513780	chr6:54297250-54297251	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs243816	chr6:54297293-54297294	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs243815	chr6:54297305-54297306	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs371284659	chr6:54297312-54297313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs79428542	chr6:54297355-54297356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573565287	chr6:54297369-54297370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561805275	chr6:54297401-54297402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535300381	chr6:54297466-54297467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2092413	chr6:54297501-54297502	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs9474868	chr6:54297513-54297514	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs552331811	chr6:54297534-54297535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568948634	chr6:54297565-54297566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs515020	chr6:54297588-54297589	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs140685542	chr6:54305216-54305217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564039356	chr6:54305249-54305250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533101689	chr6:54305265-54305266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549795302	chr6:54305279-54305280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs552488164	chr6:54305290-54305291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs374113944	chr6:54305304-54305305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182826100	chr6:54305307-54305308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548686448	chr6:54305371-54305372	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	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
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Osteosarcoma	16790693	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
Lung cancer	18438408	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:212 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:54292000-54297000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr6:54293800-54296600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr6:54295200-54297000	Enhancers	NHDF-Ad	bronchial
4	chr6:54295600-54296800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr6:54295600-54296800	Enhancers	NHLF	lung
6	chr6:54296000-54296800	Enhancers	Osteobl	bone
7	chr6:54296000-54297000	Enhancers	HUVEC	blood vessel
8	chr6:54296200-54296800	Enhancers	Muscle Satellite Cultured Cells	--
9	chr6:54296400-54296600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr6:54296400-54297000	Enhancers	GM12878-XiMat	blood
11	chr6:54296400-54297600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:54296600-54296800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:54296600-54297000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr6:54296800-54297200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr6:54305200-54305600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:54305200-54306000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr6:54305400-54305800	Enhancers	NHEK	skin
18	chr6:54305400-54306000	Enhancers	Esophagus	oesophagus
19	chr6:54305800-54306000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr6:54306000-54307200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr6:54307200-54307400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr6:54309600-54310200	Enhancers	Osteobl	bone
23	chr6:54309800-54310200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr6:54310600-54311200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr6:54327800-54329000	Enhancers	HSMMtube	muscle
26	chr6:54328200-54328800	Enhancers	H9 Cell Line	embryonic stem cell
27	chr6:54328200-54328800	Enhancers	NHEK	skin
28	chr6:54328200-54329000	Enhancers	HSMM	muscle
29	chr6:54328400-54328800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr6:54328400-54328800	Enhancers	H1 Cell Line	embryonic stem cell
31	chr6:54328400-54328800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr6:54328400-54328800	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr6:54328400-54328800	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr6:54328400-54328800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr6:54328400-54328800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr6:54328400-54329000	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr6:54328400-54329000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr6:54328800-54338200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr6:54329000-54338200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr6:54336400-54336600	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr6:54336400-54336600	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr6:54336600-54338400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr6:54336600-54338600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr6:54337000-54339800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr6:54338200-54338600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr6:54338200-54338800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr6:54338200-54338800	Enhancers	NHEK	skin
48	chr6:54338200-54339000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr6:54338400-54338800	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr6:54338600-54339200	Enhancers	H1 Cell Line	embryonic stem cell

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