Variant report

Variant	nsv1020208
Chromosome Location	chr6:55870429-55932120
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:416)
CpG islands
(count:184)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr6:55888699-55888722	HepG2	liver:	n/a	n/a
2	CBX3	chr6:55918563-55918866	HCT-116	colon:	n/a	n/a
3	CEBPB	chr6:55905081-55905419	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr6:55929895-55930181	HepG2	liver:	n/a	n/a
5	CEBPB	chr6:55884800-55885126	HepG2	liver:	n/a	chr6:55884963-55884974
6	CEBPB	chr6:55925803-55925911	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr6:55884861-55885013	H1-hESC	embryonic stem cell:	n/a	chr6:55884963-55884974
8	CEBPB	chr6:55929954-55930109	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr6:55905099-55905433	IMR90	lung:	n/a	n/a
10	CEBPB	chr6:55884808-55885065	A549	lung:	n/a	chr6:55884963-55884974
11	CEBPB	chr6:55929926-55930126	A549	lung:	n/a	n/a
12	CEBPB	chr6:55884782-55885131	IMR90	lung:	n/a	chr6:55884963-55884974
13	CEBPB	chr6:55884793-55885108	Hela-S3	cervix:	n/a	chr6:55884963-55884974
14	CTCF	chr6:55918700-55918850	HRPEpiC	eye:	n/a	chr6:55918717-55918730
15	CTCF	chr6:55918622-55918783	MCF-7	breast:	n/a	chr6:55918717-55918730
16	CTCF	chr6:55918700-55918850	RPTEC	kidney:	n/a	chr6:55918717-55918730
17	CTCF	chr6:55886840-55886990	RPTEC	kidney:	n/a	n/a
18	CTCF	chr6:55902500-55902650	AoAF	blood vessel:	n/a	n/a
19	CTCF	chr6:55918640-55918790	HEK293	kidney:	n/a	chr6:55918717-55918730
20	CTCF	chr6:55902540-55902690	AG09319	gingival:	n/a	n/a
21	CTCF	chr6:55918700-55918850	HRE	kidney:	n/a	chr6:55918717-55918730
22	CTCF	chr6:55918500-55918650	BE2_C	brain:	n/a	n/a
23	CTCF	chr6:55918673-55918767	GM19240	blood:	n/a	chr6:55918717-55918730
24	CTCF	chr6:55886820-55886970	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr6:55927800-55927950	AoAF	blood vessel:	n/a	chr6:55927903-55927912
26	CTCF	chr6:55927820-55927970	AoAF	blood vessel:	n/a	chr6:55927903-55927912
27	CTCF	chr6:55918680-55918830	AoAF	blood vessel:	n/a	chr6:55918717-55918730
28	CTCF	chr6:55918720-55918870	A549	lung:	n/a	n/a
29	CTCF	chr6:55916560-55916710	GM12872	blood:	n/a	n/a
30	CTCF	chr6:55902500-55902650	AG09319	gingival:	n/a	n/a
31	CTCF	chr6:55918640-55918790	GM12871	blood:	n/a	chr6:55918717-55918730
32	CTCF	chr6:55918680-55918830	GM12873	blood:	n/a	chr6:55918717-55918730
33	CTCF	chr6:55918720-55918870	HCM	heart:	n/a	n/a
34	CTCF	chr6:55918644-55918763	GM12892	blood:	n/a	chr6:55918717-55918730
35	CTCF	chr6:55886820-55886970	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr6:55902580-55902730	AG04449	skin:	n/a	n/a
37	CTCF	chr6:55918720-55918870	AG09309	skin:	n/a	n/a
38	CTCF	chr6:55886840-55886990	AG09319	gingival:	n/a	n/a
39	CTCF	chr6:55918657-55918783	Fibrobl	skin:	n/a	chr6:55918717-55918730
40	CTCF	chr6:55918685-55918738	GM12891	blood:	n/a	chr6:55918717-55918730
41	CTCF	chr6:55902540-55902690	HPF	lung:	n/a	n/a
42	CTCF	chr6:55886837-55886998	Gliobla	brain:	n/a	n/a
43	CTCF	chr6:55918651-55918778	GM13977	blood:	n/a	chr6:55918717-55918730
44	CTCF	chr6:55918659-55918817	Gliobla	brain:	n/a	chr6:55918717-55918730
45	CTCF	chr6:55918681-55918785	ProgFib	skin:	n/a	chr6:55918717-55918730
46	CTCF	chr6:55918740-55918890	HCM	heart:	n/a	n/a
47	CTCF	chr6:55918680-55918830	GM12866	blood:	n/a	chr6:55918717-55918730
48	CTCF	chr6:55886820-55886970	GM12874	blood:	n/a	n/a
49	CTCF	chr6:55918680-55918830	NHDF-neo	bronchial:	n/a	chr6:55918717-55918730
50	CTCF	chr6:55918720-55918870	HRPEpiC	eye:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:55921912-55921962	AoSMC	blood vessel:	n/a
2	chr6:55921912-55921962	AoSMC	blood vessel:	n/a
3	chr6:55887782-55887832	GM12892	blood:	n/a
4	chr6:55905409-55905459	ECC-1	luminal epithelium:	n/a
5	chr6:55905409-55905459	HL-60	blood:	n/a
6	chr6:55887782-55887832	ovcar-3	ovarian:	n/a
7	chr6:55905409-55905459	SAEC	small airway:	n/a
8	chr6:55905409-55905459	BJ	skin:	n/a
9	chr6:55921912-55921962	NHDF-neo	bronchial:	n/a
10	chr6:55887782-55887832	HCT-116	colon:	n/a
11	chr6:55887782-55887832	Caco-2	colon:	n/a
12	chr6:55887782-55887832	HCM	heart:	n/a
13	chr6:55921912-55921962	SK-N-SH_RA	brain:	n/a
14	chr6:55921912-55921962	AG04449	skin:	fetal
15	chr6:55905409-55905459	HUVEC	blood vessel:	n/a
16	chr6:55921912-55921962	Caco-2	colon:	n/a
17	chr6:55905409-55905459	NB4	blood:	n/a
18	chr6:55905409-55905459	HAEpiC	amniotic membrane:	n/a
19	chr6:55921912-55921962	LNCaP	prostate:	n/a
20	chr6:55887782-55887832	NHBE	bronchial:	n/a
21	chr6:55905409-55905459	ovcar-3	ovarian:	n/a
22	chr6:55905409-55905459	HMEC	breast:	n/a
23	chr6:55887782-55887832	MCF10A-Er-Src	breast:	n/a
24	chr6:55887782-55887832	HIPEpiC	eye:	n/a
25	chr6:55905409-55905459	GM06990	blood:	n/a
26	chr6:55887782-55887832	BE2_C	brain:	n/a
27	chr6:55887782-55887832	HCPEpiC	choroid plexus:	n/a
28	chr6:55905409-55905459	SKMC	muscle:	n/a
29	chr6:55887782-55887832	GM06990	blood:	n/a
30	chr6:55887782-55887832	AG04449	skin:	fetal
31	chr6:55921912-55921962	BE2_C	brain:	n/a
32	chr6:55905409-55905459	HIPEpiC	eye:	n/a
33	chr6:55887782-55887832	PrEC	prostate:	n/a
34	chr6:55887782-55887832	LNCaP	prostate:	n/a
35	chr6:55887782-55887832	NHDF-neo	bronchial:	n/a
36	chr6:55921912-55921962	MCF-7	breast:	n/a
37	chr6:55921912-55921962	HCF	heart:	n/a
38	chr6:55921912-55921962	SAEC	small airway:	n/a
39	chr6:55905409-55905459	A549	lung:	n/a
40	chr6:55921912-55921962	HRCEpiC	kidney:	n/a
41	chr6:55905409-55905459	MCF10A-Er-Src	breast:	n/a
42	chr6:55887782-55887832	SK-N-SH_RA	brain:	n/a
43	chr6:55905409-55905459	NHDF-neo	bronchial:	n/a
44	chr6:55921912-55921962	PFSK-1	brain:	n/a
45	chr6:55887782-55887832	HRPEpiC	eye:	n/a
46	chr6:55905409-55905459	U87	brain:	n/a
47	chr6:55905409-55905459	AG09319	gingival:	n/a
48	chr6:55905409-55905459	Caco-2	colon:	n/a
49	chr6:55905409-55905459	ProgFib	skin:	n/a
50	chr6:55887782-55887832	HPAEpiC	pulmonary alveolar:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:55904181..55905774-chr6:55908809..55911144,2	MCF-7	breast:
2	chr6:55904181..55905774-chr6:55908809..55911144,2	MCF-7	breast:
3	chr6:55886589..55887225-chr6:56157105..56157760,2	MCF-7	breast:
4	chr6:55865744..55868626-chr6:55870571..55872911,2	K562	blood:
5	chr6:55886603..55887384-chr6:55918244..55919071,2	MCF-7	breast:
6	chr6:55886745..55887604-chr6:56157130..56158002,2	MCF-7	breast:
7	chr6:55886603..55887384-chr6:55918244..55919071,2	MCF-7	breast:
8	chr6:55886493..55887163-chr6:56155410..56156320,2	MCF-7	breast:
9	chr6:55926997..55929020-chr6:55932279..55934927,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	COL21A1	hsa-miR-29c-3p	chr6:55922417-55922438
2	COL21A1	hsa-miR-29c-3p	chr6:55922423-55922417
3	COL21A1	hsa-miR-29c-3p	chr6:55921829-55921850

Variant related genes	Relation type
COL21A1	TF binding region
COL21A1	CpG island

Extended variants
information (count: 1816 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1816 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562169650	chr6:55870450-55870451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548619247	chr6:55870517-55870518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs578075015	chr6:55870522-55870523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556067155	chr6:55870603-55870604	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs572635593	chr6:55870612-55870613	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs541639939	chr6:55870617-55870618	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs397886084	chr6:55870724-55870725	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs138694767	chr6:55870735-55870736	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs577723363	chr6:55870814-55870815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577319864	chr6:55870841-55870842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370524035	chr6:55870843-55870844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs373589418	chr6:55870844-55870845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141695473	chr6:55870897-55870898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563436720	chr6:55870904-55870905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529287089	chr6:55870930-55870931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146103721	chr6:55870941-55870942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558159639	chr6:55870946-55870947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs714069	chr6:55870962-55870963	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs188948950	chr6:55870973-55870974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140075537	chr6:55871008-55871009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs199815028	chr6:55871051-55871052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530627187	chr6:55871076-55871077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550742214	chr6:55871097-55871098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141429471	chr6:55871107-55871108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs7449722	chr6:55871114-55871115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573903163	chr6:55871155-55871156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115232495	chr6:55871156-55871157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs193215114	chr6:55871253-55871254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182316267	chr6:55871263-55871264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558332029	chr6:55871271-55871272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs9475497	chr6:55871490-55871491	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs372159387	chr6:55871530-55871531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12110972	chr6:55871534-55871535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573773198	chr6:55871589-55871590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543028179	chr6:55871591-55871592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559455972	chr6:55871592-55871593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150820216	chr6:55871606-55871607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374809255	chr6:55871716-55871717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544931665	chr6:55871776-55871777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562557036	chr6:55871818-55871819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139234393	chr6:55871854-55871855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568567047	chr6:55871885-55871886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534333396	chr6:55871901-55871902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560995473	chr6:55871913-55871914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529727035	chr6:55871965-55871966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150066884	chr6:55871995-55871996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566296255	chr6:55872036-55872037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186671850	chr6:55872179-55872180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551826100	chr6:55872316-55872317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112592112	chr6:55872330-55872331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21509527	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:55868800-55870800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr6:55869000-55870600	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr6:55869600-55874200	Weak transcription	Osteobl	bone
4	chr6:55869800-55870800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr6:55869800-55874600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:55870000-55871000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:55870200-55871000	Enhancers	Primary hematopoietic stem cells	blood
8	chr6:55870400-55870600	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr6:55870600-55870800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
10	chr6:55870800-55871200	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr6:55874200-55874600	Enhancers	NHDF-Ad	bronchial
12	chr6:55874200-55875200	Enhancers	Osteobl	bone
13	chr6:55874800-55875000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr6:55886200-55887200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr6:55886400-55887000	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr6:55886400-55887200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr6:55886400-55887200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr6:55886600-55887200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr6:55886600-55887400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:55886600-55887400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr6:55886800-55887400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr6:55886800-55888000	Enhancers	HSMM	muscle
23	chr6:55887000-55887800	Enhancers	HSMMtube	muscle
24	chr6:55887200-55888400	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr6:55887400-55888400	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr6:55887600-55887800	Enhancers	Muscle Satellite Cultured Cells	--
27	chr6:55887600-55887800	Enhancers	Fetal Stomach	stomach
28	chr6:55887600-55887800	Enhancers	Osteobl	bone
29	chr6:55887600-55888400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr6:55887800-55890000	Weak transcription	Osteobl	bone
31	chr6:55887800-55891000	Weak transcription	Fetal Stomach	stomach
32	chr6:55888000-55889800	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr6:55888400-55888800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr6:55888400-55889400	Enhancers	HUVEC	blood vessel
35	chr6:55888600-55888800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr6:55888600-55888800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr6:55889200-55889400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr6:55889200-55890000	Active TSS	Ovary	ovary
39	chr6:55889400-55889800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr6:55889400-55890000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr6:55889400-55890000	Active TSS	Right Atrium	heart
42	chr6:55889400-55890000	Active TSS	Stomach Smooth Muscle	stomach
43	chr6:55889400-55890000	Enhancers	Hela-S3	cervix
44	chr6:55889400-55890200	Active TSS	Aorta	Aorta
45	chr6:55889400-55890400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr6:55889400-55891200	Flanking Active TSS	HUVEC	blood vessel
47	chr6:55889800-55890000	Enhancers	Fetal Muscle Leg	muscle
48	chr6:55889800-55890200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr6:55889800-55890200	Enhancers	Muscle Satellite Cultured Cells	--
50	chr6:55890000-55891000	Weak transcription	Fetal Muscle Leg	muscle

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