Variant report

Variant	esv3430461
Chromosome Location	chr6:127727308-127754317
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	ARID3A	chr6:127741611-127742122	HepG2	liver:	n/a	n/a
2	ATF2	chr6:127741588-127742005	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr6:127741642-127741991	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr6:127741661-127742010	K562	blood:	n/a	n/a
5	BACH1	chr6:127741626-127742021	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr6:127741595-127741912	GM12878	blood:	n/a	chr6:127741772-127741782
7	BCL3	chr6:127741611-127741987	A549	lung:	n/a	n/a
8	BCL3	chr6:127741559-127742079	A549	lung:	n/a	n/a
9	BCL3	chr6:127741668-127741944	GM12878	blood:	n/a	n/a
10	BCLAF1	chr6:127741537-127742055	GM12878	blood:	n/a	n/a
11	BCLAF1	chr6:127741573-127741926	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:127741630-127742020	GM12878	blood:	n/a	n/a
13	BRCA1	chr6:127741663-127741968	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr6:127741607-127742014	K562	blood:	n/a	n/a
15	CBX3	chr6:127741673-127741952	K562	blood:	n/a	n/a
16	CHD2	chr6:127741675-127742107	GM12878	blood:	n/a	n/a
17	CHD2	chr6:127741646-127742065	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr6:127741571-127742043	GM12878	blood:	n/a	chr6:127741780-127741798
19	CTCF	chr6:127741680-127741830	RPTEC	kidney:	n/a	chr6:127741780-127741798
20	CTCF	chr6:127742100-127742250	HAc	cerebellar:	n/a	n/a
21	CTCF	chr6:127741646-127742030	MCF-7	breast:	n/a	chr6:127741780-127741798
22	CTCF	chr6:127741680-127741830	HAc	cerebellar:	n/a	chr6:127741780-127741798
23	CTCF	chr6:127741621-127741863	T-47D	breast:	n/a	chr6:127741780-127741798
24	CTCF	chr6:127741740-127741890	GM12871	blood:	n/a	chr6:127741780-127741798
25	CTCF	chr6:127741680-127741830	AoAF	blood vessel:	n/a	chr6:127741780-127741798
26	CTCF	chr6:127741680-127741830	GM12871	blood:	n/a	chr6:127741780-127741798
27	CTCF	chr6:127741700-127741850	HCPEpiC	choroid plexus:	n/a	chr6:127741780-127741798
28	CTCF	chr6:127741780-127741930	HCT-116	colon:	n/a	chr6:127741780-127741798
29	CTCF	chr6:127741740-127741890	WERI-Rb-1	eye:	n/a	chr6:127741780-127741798
30	CTCF	chr6:127741740-127741890	NHEK	skin:	n/a	chr6:127741780-127741798
31	CTCF	chr6:127741664-127741949	K562	blood:	n/a	chr6:127741780-127741798
32	CTCF	chr6:127741584-127741977	A549	lung:	n/a	chr6:127741780-127741798
33	CTCF	chr6:127741700-127741850	AG10803	skin:	n/a	chr6:127741780-127741798
34	CTCF	chr6:127741704-127741893	K562	blood:	n/a	chr6:127741780-127741798
35	CTCF	chr6:127741600-127742077	HCT-116	colon:	n/a	chr6:127741780-127741798
36	CTCF	chr6:127741497-127742390	A549	lung:	n/a	chr6:127741780-127741798
37	CTCF	chr6:127741581-127741940	A549	lung:	n/a	chr6:127741780-127741798
38	CTCF	chr6:127741720-127741870	GM12865	blood:	n/a	chr6:127741780-127741798
39	CTCF	chr6:127741720-127741870	HVMF	connective:	n/a	chr6:127741780-127741798
40	CTCF	chr6:127741700-127741850	GM12869	blood:	n/a	chr6:127741780-127741798
41	CTCF	chr6:127741740-127741890	HMF	breast:	n/a	chr6:127741780-127741798
42	CTCF	chr6:127741664-127741960	HepG2	liver:	n/a	chr6:127741780-127741798
43	CTCF	chr6:127741583-127742155	K562	blood:	n/a	chr6:127741780-127741798
44	CTCF	chr6:127741670-127741820	A549	lung:	n/a	chr6:127741780-127741798
45	CTCF	chr6:127741740-127741890	HCT-116	colon:	n/a	chr6:127741780-127741798
46	CTCF	chr6:127741700-127741850	GM12878	blood:	n/a	chr6:127741780-127741798
47	CTCF	chr6:127741611-127741942	SK-N-SH_RA	brain:	n/a	chr6:127741780-127741798
48	CTCF	chr6:127741720-127741870	AG04450	lung:	n/a	chr6:127741780-127741798
49	CTCF	chr6:127741720-127741870	HRPEpiC	eye:	n/a	chr6:127741780-127741798
50	CTCF	chr6:127741573-127742015	IMR90	lung:	n/a	chr6:127741780-127741798

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:127741813-127741863	NHDF-neo	bronchial:	n/a
2	chr6:127741813-127741863	PFSK-1	brain:	n/a
3	chr6:127741813-127741863	BE2_C	brain:	n/a
4	chr6:127741813-127741863	SK-N-SH	brain:	n/a
5	chr6:127741813-127741863	HRE	kidney:	n/a
6	chr6:127741813-127741863	HCF	heart:	n/a
7	chr6:127741813-127741863	HMEC	breast:	n/a
8	chr6:127741813-127741863	HNPCEpiC	eye:	n/a
9	chr6:127741813-127741863	T-47D	breast:	n/a
10	chr6:127741813-127741863	NHBE	bronchial:	n/a
11	chr6:127741813-127741863	IMR90	lung:	fetal
12	chr6:127741813-127741863	SK-N-MC	brain:	n/a
13	chr6:127741813-127741863	GM06990	blood:	n/a
14	chr6:127741813-127741863	HL-60	blood:	n/a
15	chr6:127741813-127741863	ProgFib	skin:	n/a
16	chr6:127741813-127741863	RPTEC	kidney:	n/a
17	chr6:127741813-127741863	GM12891	blood:	n/a
18	chr6:127741813-127741863	Hepatocyte	liver:	n/a
19	chr6:127741813-127741863	MCF10A-Er-Src	breast:	n/a
20	chr6:127741813-127741863	HRCEpiC	kidney:	n/a
21	chr6:127741813-127741863	GM12892	blood:	n/a
22	chr6:127741813-127741863	NT2-D1	testis:	n/a
23	chr6:127741813-127741863	ECC-1	luminal epithelium:	n/a
24	chr6:127741813-127741863	Caco-2	colon:	n/a
25	chr6:127741813-127741863	HAEpiC	amniotic membrane:	n/a
26	chr6:127741813-127741863	PANC-1	pancreas:	n/a
27	chr6:127741813-127741863	GM19239	blood:	n/a
28	chr6:127741813-127741863	HCM	heart:	n/a
29	chr6:127741813-127741863	PrEC	prostate:	n/a
30	chr6:127741813-127741863	GM12878	blood:	n/a
31	chr6:127741813-127741863	H1-hESC	embryonic stem cell:	embryo
32	chr6:127741813-127741863	HPAEpiC	pulmonary alveolar:	n/a
33	chr6:127741813-127741863	SK-N-SH_RA	brain:	n/a
34	chr6:127741813-127741863	AoSMC	blood vessel:	n/a
35	chr6:127741813-127741863	A549	lung:	n/a
36	chr6:127741813-127741863	NB4	blood:	n/a
37	chr6:127741813-127741863	AG10803	skin:	n/a
38	chr6:127741813-127741863	ovcar-3	ovarian:	n/a
39	chr6:127741813-127741863	BJ	skin:	n/a
40	chr6:127741813-127741863	Jurkat	blood:	n/a
41	chr6:127741813-127741863	NH-A	brain:	n/a
42	chr6:127741813-127741863	AG09309	skin:	n/a
43	chr6:127741813-127741863	AG04449	skin:	fetal
44	chr6:127741813-127741863	SKMC	muscle:	n/a
45	chr6:127741813-127741863	MCF-7	breast:	n/a
46	chr6:127741813-127741863	HCPEpiC	choroid plexus:	n/a
47	chr6:127741813-127741863	AG04450	lung:	fetal
48	chr6:127741813-127741863	AG09319	gingival:	n/a
49	chr6:127741813-127741863	HCT-116	colon:	n/a
50	chr6:127741813-127741863	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:127663086..127665527-chr6:127739757..127741393,2	K562	blood:
2	chr6:127623612..127624559-chr6:127741344..127742234,3	MCF-7	breast:
3	chr6:127665440..127667332-chr6:127741973..127744614,2	MCF-7	breast:
4	chr6:127623606..127624647-chr6:127741293..127742295,4	K562	blood:
5	chr6:127663380..127665925-chr6:127744349..127746965,2	K562	blood:
6	chr6:127623451..127624500-chr6:127741516..127742270,5	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf174-1	chr6:127737680-127738097	NONHSAT114853

Variant related genes	Relation type
ENSG00000220522	TF binding region
ENSG00000220694	TF binding region
ENSG00000220522	CpG island
ENSG00000220694	CpG island
ENSG00000093144	chromatin interactions

Extended variants
information (count: 658 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:658 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548843801	chr6:127727365-127727366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs141375772	chr6:127727395-127727396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544630087	chr6:127727402-127727403	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs6906003	chr6:127727406-127727407	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs199786886	chr6:127727407-127727408	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531500444	chr6:127727413-127727414	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548394240	chr6:127727426-127727427	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560706087	chr6:127727553-127727554	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs528285595	chr6:127727615-127727616	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546459876	chr6:127727639-127727640	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373192245	chr6:127727674-127727675	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370270170	chr6:127727675-127727676	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571234646	chr6:127727681-127727682	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538247523	chr6:127727684-127727685	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575133351	chr6:127727698-127727699	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568763420	chr6:127727709-127727710	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs143784880	chr6:127727725-127727726	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183975026	chr6:127727731-127727732	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146825948	chr6:127727742-127727743	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187196002	chr6:127727752-127727753	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559280314	chr6:127727754-127727755	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577504599	chr6:127727758-127727759	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs35409184	chr6:127727762-127727763	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs193042008	chr6:127727771-127727772	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556472122	chr6:127727799-127727800	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs113979223	chr6:127727828-127727829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112689708	chr6:127727851-127727852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150408007	chr6:127727861-127727862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528247862	chr6:127727888-127727889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35662306	chr6:127727900-127727901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs199572457	chr6:127727903-127727904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569292460	chr6:127727905-127727906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540070588	chr6:127727912-127727913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539929268	chr6:127727941-127727942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558329993	chr6:127727942-127727943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547846345	chr6:127727981-127727982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373347808	chr6:127728040-127728041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370624849	chr6:127728053-127728054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532390138	chr6:127728056-127728057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550610637	chr6:127728062-127728063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568801721	chr6:127728065-127728066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529681021	chr6:127728070-127728071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377416713	chr6:127728071-127728072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566848838	chr6:127728096-127728097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534386151	chr6:127728098-127728099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138122461	chr6:127728182-127728183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148905183	chr6:127728258-127728259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538488348	chr6:127728276-127728277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555988859	chr6:127728323-127728324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9321081	chr6:127728325-127728326	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:102)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	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
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
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Neurocytoma	17123091	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Ependymoma	18628472	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21958427	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Mental retardation	17847001	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:127720400-127729200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr6:127726800-127727400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:127727200-127727800	Enhancers	K562	blood
4	chr6:127727400-127727600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:127727600-127727800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr6:127733200-127734200	Enhancers	Fetal Lung	lung
7	chr6:127733800-127734000	Enhancers	Esophagus	oesophagus
8	chr6:127734000-127734800	Enhancers	K562	blood
9	chr6:127734000-127735000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr6:127734200-127734600	Enhancers	Lung	lung
11	chr6:127734200-127734800	Enhancers	H1 Cell Line	embryonic stem cell
12	chr6:127734200-127734800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr6:127734200-127734800	Active TSS	HepG2	liver
14	chr6:127734400-127734800	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr6:127734400-127734800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr6:127734400-127734800	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr6:127734400-127734800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:127734400-127734800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr6:127734600-127734800	Enhancers	Esophagus	oesophagus
20	chr6:127734600-127735400	Enhancers	Fetal Muscle Leg	muscle
21	chr6:127734800-127735000	Flanking Active TSS	HepG2	liver
22	chr6:127734800-127735400	Enhancers	NHEK	skin
23	chr6:127734800-127735800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr6:127734800-127737800	Weak transcription	K562	blood
25	chr6:127734800-127741800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr6:127735200-127735400	Enhancers	HSMMtube	muscle
27	chr6:127735400-127741200	Weak transcription	HSMMtube	muscle
28	chr6:127735800-127736600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr6:127736400-127736800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr6:127736400-127736800	Enhancers	Muscle Satellite Cultured Cells	--
31	chr6:127736400-127737000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr6:127736600-127737000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr6:127736800-127741000	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr6:127736800-127741200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr6:127737000-127737800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr6:127737800-127738000	Enhancers	K562	blood
37	chr6:127737800-127740600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr6:127738000-127741800	Weak transcription	K562	blood
39	chr6:127739400-127739800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:127739800-127740000	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr6:127739800-127741800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:127740600-127740800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr6:127740600-127741800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr6:127740600-127742200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr6:127740800-127741800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr6:127741000-127741800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr6:127741000-127741800	Enhancers	NHDF-Ad	bronchial
48	chr6:127741000-127742600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:127741200-127741400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr6:127741200-127741800	Enhancers	HSMM	muscle

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