Variant report

Variant	nsv830821
Chromosome Location	chr6:140890955-141060220
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:897)
CpG islands
(count:122)
Chromatin interactive
region (count:28)
LncRNA
region (count:2)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:897 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:140905921-140905975	K562	blood:	n/a	n/a
2	ATF1	chr6:140893405-140893685	K562	blood:	n/a	n/a
3	ATF1	chr6:141032327-141032490	K562	blood:	n/a	n/a
4	ATF1	chr6:141057542-141057722	K562	blood:	n/a	n/a
5	ATF2	chr6:140907544-140908522	GM12878	blood:	n/a	n/a
6	ATF2	chr6:140907528-140908482	GM12878	blood:	n/a	n/a
7	ATF2	chr6:140962459-140962964	GM12878	blood:	n/a	n/a
8	ATF2	chr6:140893204-140893707	GM12878	blood:	n/a	n/a
9	BACH1	chr6:140931711-140931747	K562	blood:	n/a	n/a
10	BATF	chr6:140907813-140908309	GM12878	blood:	n/a	n/a
11	BATF	chr6:140962571-140962917	GM12878	blood:	n/a	n/a
12	BATF	chr6:140962532-140962960	GM12878	blood:	n/a	n/a
13	BATF	chr6:140957343-140957787	GM12878	blood:	n/a	n/a
14	BATF	chr6:140999274-140999525	GM12878	blood:	n/a	n/a
15	BATF	chr6:140893208-140893582	GM12878	blood:	n/a	chr6:140893374-140893385
16	BATF	chr6:140907543-140908374	GM12878	blood:	n/a	n/a
17	BCL11A	chr6:140907600-140908344	GM12878	blood:	n/a	n/a
18	BCL11A	chr6:140962665-140962965	GM12878	blood:	n/a	n/a
19	BCL11A	chr6:140962597-140962976	GM12878	blood:	n/a	n/a
20	BCL11A	chr6:140907738-140908243	GM12878	blood:	n/a	n/a
21	BCL11A	chr6:140957373-140957725	GM12878	blood:	n/a	n/a
22	BCL3	chr6:140907648-140908396	GM12878	blood:	n/a	n/a
23	BCL3	chr6:140923817-140924135	GM12878	blood:	n/a	n/a
24	BCL3	chr6:140907733-140908269	GM12878	blood:	n/a	n/a
25	BCLAF1	chr6:140907860-140908292	GM12878	blood:	n/a	n/a
26	BCLAF1	chr6:140957284-140957740	GM12878	blood:	n/a	n/a
27	BCLAF1	chr6:140907489-140908402	GM12878	blood:	n/a	n/a
28	BHLHE40	chr6:140962545-140962966	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:141032530-141032747	GM12878	blood:	n/a	n/a
30	CBX3	chr6:140948115-140948497	K562	blood:	n/a	n/a
31	CCNT2	chr6:141006502-141006618	K562	blood:	n/a	n/a
32	CEBPB	chr6:140992588-140992943	HepG2	liver:	n/a	chr6:140992865-140992876
33	CEBPB	chr6:140978793-140979003	K562	blood:	n/a	n/a
34	CEBPB	chr6:140944554-140945005	IMR90	lung:	n/a	chr6:140944736-140944747
35	CEBPB	chr6:140926256-140926456	HepG2	liver:	n/a	chr6:140926351-140926362 chr6:140926350-140926363
36	CEBPB	chr6:141046985-141047253	IMR90	lung:	n/a	chr6:141047121-141047132
37	CEBPB	chr6:141006378-141006630	IMR90	lung:	n/a	n/a
38	CEBPB	chr6:140928375-140928391	K562	blood:	n/a	n/a
39	CEBPB	chr6:140950718-140951059	HepG2	liver:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
40	CEBPB	chr6:140950735-140950999	A549	lung:	n/a	chr6:140950893-140950904 chr6:140950895-140950906
41	CEBPB	chr6:141046992-141047275	HepG2	liver:	n/a	chr6:141047121-141047132
42	CEBPB	chr6:140944453-140945069	HCT-116	colon:	n/a	chr6:140944736-140944747
43	CEBPB	chr6:140950521-140950534	K562	blood:	n/a	n/a
44	CEBPB	chr6:140978710-140979038	HepG2	liver:	n/a	n/a
45	CEBPB	chr6:140907389-140908537	GM12878	blood:	n/a	n/a
46	CEBPB	chr6:140944568-140944937	Hela-S3	cervix:	n/a	chr6:140944736-140944747
47	CEBPB	chr6:140944477-140945154	HCT-116	colon:	n/a	chr6:140944736-140944747
48	CEBPB	chr6:141006465-141006576	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:140911779-140912094	IMR90	lung:	n/a	chr6:140911918-140911929 chr6:140911918-140911931 chr6:140911917-140911934 chr6:140911918-140911931 chr6:140911918-140911929 chr6:140911918-140911931
50	CEBPB	chr6:140905206-140905380	HepG2	liver:	n/a	chr6:140905237-140905248

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:140957775-140957825	SAEC	small airway:	n/a
2	chr6:140923112-140923162	MCF-7	breast:	n/a
3	chr6:140923112-140923162	NHBE	bronchial:	n/a
4	chr6:140957775-140957825	NT2-D1	testis:	n/a
5	chr6:140957775-140957825	HCPEpiC	choroid plexus:	n/a
6	chr6:140957775-140957825	AG09319	gingival:	n/a
7	chr6:140957775-140957825	GM06990	blood:	n/a
8	chr6:140923112-140923162	LNCaP	prostate:	n/a
9	chr6:140957775-140957825	NHDF-neo	bronchial:	n/a
10	chr6:140957775-140957825	HRE	kidney:	n/a
11	chr6:140923112-140923162	HIPEpiC	eye:	n/a
12	chr6:140923112-140923162	HCPEpiC	choroid plexus:	n/a
13	chr6:140957775-140957825	HAEpiC	amniotic membrane:	n/a
14	chr6:140923112-140923162	SK-N-SH	brain:	n/a
15	chr6:140923112-140923162	GM19239	blood:	n/a
16	chr6:140957775-140957825	GM19239	blood:	n/a
17	chr6:140957775-140957825	HPAEpiC	pulmonary alveolar:	n/a
18	chr6:140957775-140957825	Caco-2	colon:	n/a
19	chr6:140923112-140923162	HCF	heart:	n/a
20	chr6:140923112-140923162	AG10803	skin:	n/a
21	chr6:140957775-140957825	RPTEC	kidney:	n/a
22	chr6:140923112-140923162	K562	blood:	n/a
23	chr6:140957775-140957825	Hepatocyte	liver:	n/a
24	chr6:140923112-140923162	AG04449	skin:	fetal
25	chr6:140957775-140957825	Hela-S3	cervix:	n/a
26	chr6:140923112-140923162	T-47D	breast:	n/a
27	chr6:140923112-140923162	HPAEpiC	pulmonary alveolar:	n/a
28	chr6:140957775-140957825	AG04449	skin:	fetal
29	chr6:140957775-140957825	NH-A	brain:	n/a
30	chr6:140957775-140957825	IMR90	lung:	fetal
31	chr6:140957775-140957825	A549	lung:	n/a
32	chr6:140923112-140923162	A549	lung:	n/a
33	chr6:140957775-140957825	ProgFib	skin:	n/a
34	chr6:140923112-140923162	RPTEC	kidney:	n/a
35	chr6:140957775-140957825	MCF10A-Er-Src	breast:	n/a
36	chr6:140923112-140923162	BE2_C	brain:	n/a
37	chr6:140957775-140957825	AG04450	lung:	fetal
38	chr6:140923112-140923162	HEK293	kidney:	embryo
39	chr6:140923112-140923162	HAEpiC	amniotic membrane:	n/a
40	chr6:140957775-140957825	HL-60	blood:	n/a
41	chr6:140923112-140923162	SK-N-MC	brain:	n/a
42	chr6:140923112-140923162	Hela-S3	cervix:	n/a
43	chr6:140957775-140957825	SKMC	muscle:	n/a
44	chr6:140923112-140923162	HRE	kidney:	n/a
45	chr6:140957775-140957825	BE2_C	brain:	n/a
46	chr6:140923112-140923162	Jurkat	blood:	n/a
47	chr6:140923112-140923162	PrEC	prostate:	n/a
48	chr6:140923112-140923162	PANC-1	pancreas:	n/a
49	chr6:140957775-140957825	GM12892	blood:	n/a
50	chr6:140923112-140923162	HCT-116	colon:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:140995862..140998424-chr6:141006767..141008386,2	K562	blood:
2	chr6:140919683..140922477-chr6:140922951..140925065,2	K562	blood:
3	chr6:140988668..140990726-chr6:140994294..140996979,2	K562	blood:
4	chr6:140976457..140978107-chr6:140978749..140981141,2	K562	blood:
5	chr6:140905860..140907615-chr6:140923172..140925767,2	K562	blood:
6	chr6:140988668..140990726-chr6:140994294..140996979,2	K562	blood:
7	chr6:139691177..139693399-chr6:140971784..140974474,2	MCF-7	breast:
8	chr6:140983001..140985814-chr6:140986473..140989700,3	K562	blood:
9	chr6:140974220..140975794-chr6:140989570..140992507,2	K562	blood:
10	chr6:141043491..141046275-chr6:141049561..141051082,2	MCF-7	breast:
11	chr6:140974220..140975794-chr6:140989570..140992507,2	K562	blood:
12	chr6:140912649..140915188-chr6:140915453..140918177,2	K562	blood:
13	chr6:140983001..140985814-chr6:140986473..140989700,3	K562	blood:
14	chr6:140919683..140922477-chr6:140922951..140925065,2	K562	blood:
15	chr6:140995862..140998424-chr6:141006767..141008386,2	K562	blood:
16	chr6:140781738..140784199-chr6:140901701..140903255,2	MCF-7	breast:
17	chr6:140973276..140976134-chr6:140976580..140978655,2	MCF-7	breast:
18	chr6:140905427..140908857-chr6:140910975..140913769,3	K562	blood:
19	chr6:140919169..140921783-chr6:140922844..140925130,2	MCF-7	breast:
20	chr6:140905427..140908857-chr6:140910975..140913769,3	K562	blood:
21	chr6:140973276..140976134-chr6:140976580..140978655,2	MCF-7	breast:
22	chr6:141041326..141043698-chr6:141051751..141054060,2	K562	blood:
23	chr6:141043491..141046275-chr6:141049561..141051082,2	MCF-7	breast:
24	chr6:140912649..140915188-chr6:140915453..140918177,2	K562	blood:
25	chr6:140976457..140978107-chr6:140978749..140981141,2	K562	blood:
26	chr6:141041326..141043698-chr6:141051751..141054060,2	K562	blood:
27	chr6:140919169..140921783-chr6:140922844..140925130,2	MCF-7	breast:
28	chr6:140905860..140907615-chr6:140923172..140925767,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HECA-10	chr6:140972927-140973185	l_3279_chr6:140928454-140973185_placenta
2	lnc-HECA-10	chr6:140928455-140928491	l_3279_chr6:140928454-140973185_placenta

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4465	chr6:141004992-141005013	MIMAT0018992

No data

Variant related genes	Relation type
ENSG00000221336	TF binding region
MIR4465	TF binding region
ENSG00000221336	CpG island
MIR4465	CpG island

Extended variants
information (count: 4854 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4854 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570839779	chr6:140890964-140890965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs565698667	chr6:140891021-140891022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138339992	chr6:140891083-140891084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112325574	chr6:140891100-140891101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548452529	chr6:140891126-140891127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569957931	chr6:140891152-140891153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs149550673	chr6:140891173-140891174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187805384	chr6:140891241-140891242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs117811823	chr6:140891287-140891288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs193166988	chr6:140891294-140891295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs116369417	chr6:140891296-140891297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76744434	chr6:140891361-140891362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369115755	chr6:140891381-140891382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183305582	chr6:140891388-140891389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527492321	chr6:140891395-140891396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199533360	chr6:140891406-140891407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539867100	chr6:140891408-140891409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189151093	chr6:140891483-140891484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192598497	chr6:140891506-140891507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527803733	chr6:140891528-140891529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs117286009	chr6:140891573-140891574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546108752	chr6:140891643-140891644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115983456	chr6:140891655-140891656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184842107	chr6:140891751-140891752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540325082	chr6:140891940-140891941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188431347	chr6:140891950-140891951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377341358	chr6:140891953-140891954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547736772	chr6:140891970-140891971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs9484409	chr6:140891975-140891976	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs59857340	chr6:140892007-140892008	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs563013104	chr6:140892030-140892031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs114134637	chr6:140892043-140892044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs530136431	chr6:140892057-140892058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs550204347	chr6:140892079-140892080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570372620	chr6:140892135-140892136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs552453032	chr6:140892138-140892139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539188635	chr6:140892147-140892148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs118102032	chr6:140892155-140892156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534608229	chr6:140892181-140892182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs552731378	chr6:140892188-140892189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs6912792	chr6:140892200-140892201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs72979900	chr6:140892211-140892212	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs557103347	chr6:140892215-140892216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs575451117	chr6:140892246-140892247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs546049515	chr6:140892308-140892309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558433900	chr6:140892358-140892359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191413385	chr6:140892369-140892370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs1414838	chr6:140892501-140892502	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs561974810	chr6:140892502-140892503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529385322	chr6:140892513-140892514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Autism	22495311	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
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	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
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
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	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
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:406 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:140888400-140892800	Weak transcription	NHEK	skin
2	chr6:140888400-140893200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr6:140888400-140893200	Weak transcription	HMEC	breast
4	chr6:140888400-140901000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:140888800-140892000	Weak transcription	NHDF-Ad	bronchial
6	chr6:140888800-140892400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr6:140888800-140892400	Weak transcription	NH-A	brain
8	chr6:140888800-140892800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr6:140888800-140892800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr6:140888800-140893200	Weak transcription	Colon Smooth Muscle	Colon
11	chr6:140888800-140893200	Weak transcription	Stomach Smooth Muscle	stomach
12	chr6:140888800-140893400	Weak transcription	Adipose Nuclei	Adipose
13	chr6:140889000-140892400	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr6:140889000-140892400	Weak transcription	HUVEC	blood vessel
15	chr6:140889000-140893200	Weak transcription	Rectal Smooth Muscle	rectum
16	chr6:140889200-140891800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr6:140889200-140892000	Weak transcription	Osteobl	bone
18	chr6:140889200-140892200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr6:140889200-140892200	Weak transcription	HSMM	muscle
20	chr6:140889200-140892800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr6:140889200-140892800	Weak transcription	Hela-S3	cervix
22	chr6:140889400-140891600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:140891600-140894400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr6:140891800-140892600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr6:140892000-140894400	Enhancers	NHDF-Ad	bronchial
26	chr6:140892000-140894400	Enhancers	Osteobl	bone
27	chr6:140892200-140892600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr6:140892200-140894400	Enhancers	HSMM	muscle
29	chr6:140892400-140893400	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr6:140892400-140894200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr6:140892400-140894200	Enhancers	NH-A	brain
32	chr6:140892400-140894400	Enhancers	Muscle Satellite Cultured Cells	--
33	chr6:140892400-140894600	Enhancers	HUVEC	blood vessel
34	chr6:140892600-140893400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr6:140892600-140893800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr6:140892600-140894000	Enhancers	HSMMtube	muscle
37	chr6:140892800-140893200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr6:140892800-140894000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr6:140892800-140894000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr6:140892800-140894000	Enhancers	Hela-S3	cervix
41	chr6:140892800-140894200	Enhancers	NHEK	skin
42	chr6:140892800-140894400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr6:140893000-140894000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr6:140893200-140893600	Enhancers	Primary hematopoietic stem cells	blood
45	chr6:140893200-140893600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr6:140893200-140893600	Enhancers	Small Intestine	intestine
47	chr6:140893200-140893600	Enhancers	Stomach Smooth Muscle	stomach
48	chr6:140893200-140894000	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr6:140893200-140894000	Enhancers	Rectal Smooth Muscle	rectum
50	chr6:140893200-140894200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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