Variant report

Variant	nsv1032687
Chromosome Location	chr6:133987372-134059728
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:267)
CpG islands
(count:367)
Chromatin interactive
region (count:24)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:134022318-134023459	K562	blood:	n/a	n/a
2	ATF1	chr6:134022564-134023237	K562	blood:	n/a	n/a
3	ATF2	chr6:134002906-134003434	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:134022796-134023117	K562	blood:	n/a	n/a
5	BCL3	chr6:134022550-134023171	K562	blood:	n/a	chr6:134023113-134023122 chr6:134022702-134022711
6	BCLAF1	chr6:134022619-134023278	K562	blood:	n/a	chr6:134023113-134023122 chr6:134022702-134022711
7	BHLHE40	chr6:134022595-134023258	K562	blood:	n/a	n/a
8	BHLHE40	chr6:134028755-134028812	K562	blood:	n/a	n/a
9	CBX3	chr6:134022715-134023221	K562	blood:	n/a	n/a
10	CBX3	chr6:134012895-134013266	K562	blood:	n/a	n/a
11	CBX3	chr6:134054462-134054819	HCT-116	colon:	n/a	n/a
12	CBX3	chr6:134022443-134023505	K562	blood:	n/a	n/a
13	CCNT2	chr6:134022691-134023140	K562	blood:	n/a	chr6:134022892-134022912
14	CEBPB	chr6:134028614-134029081	IMR90	lung:	n/a	n/a
15	CEBPB	chr6:134026220-134026608	IMR90	lung:	n/a	n/a
16	CEBPB	chr6:134009297-134009554	HepG2	liver:	n/a	chr6:134009430-134009441 chr6:134009429-134009442 chr6:134009429-134009440
17	CEBPB	chr6:134045969-134046170	IMR90	lung:	n/a	n/a
18	CEBPB	chr6:134044779-134044817	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr6:134052729-134052979	IMR90	lung:	n/a	chr6:134052875-134052886
20	CEBPB	chr6:134026240-134026606	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr6:134026312-134026568	A549	lung:	n/a	n/a
22	CEBPB	chr6:134009330-134009610	A549	lung:	n/a	chr6:134009430-134009441 chr6:134009429-134009442 chr6:134009429-134009440
23	CEBPB	chr6:134022768-134023258	K562	blood:	n/a	n/a
24	CEBPB	chr6:134052727-134052927	HepG2	liver:	n/a	chr6:134052875-134052886
25	CEBPB	chr6:134022671-134023288	K562	blood:	n/a	n/a
26	CEBPD	chr6:134022602-134023377	K562	blood:	n/a	n/a
27	CEBPD	chr6:134022687-134023292	K562	blood:	n/a	n/a
28	CHD2	chr6:134022811-134023177	K562	blood:	n/a	n/a
29	CREB1	chr6:134022625-134023226	K562	blood:	n/a	n/a
30	CREB1	chr6:134022630-134023316	K562	blood:	n/a	n/a
31	CTCF	chr6:134045081-134045180	GM20000	blood:	n/a	n/a
32	CTCF	chr6:134018940-134019090	AG04449	skin:	n/a	n/a
33	CTCF	chr6:134018940-134019090	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr6:134019080-134019230	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr6:134034077-134034153	K562	blood:	n/a	n/a
36	CTCF	chr6:134018980-134019130	AG10803	skin:	n/a	n/a
37	CTCF	chr6:134025660-134025810	AG10803	skin:	n/a	n/a
38	CTCF	chr6:134023202-134023205	K562	blood:	n/a	n/a
39	CTCF	chr6:133988052-133988124	Spleen_OC	spleen:	n/a	n/a
40	CUX1	chr6:134006774-134006792	GM12878	blood:	n/a	n/a
41	CUX1	chr6:134022743-134023167	K562	blood:	n/a	n/a
42	E2F4	chr6:134027006-134027282	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr6:134026279-134026738	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr6:134028782-134029443	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr6:134032421-134032621	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F6	chr6:134022750-134022998	K562	blood:	n/a	n/a
47	E2F6	chr6:134022649-134023160	K562	blood:	n/a	n/a
48	EGR1	chr6:134022743-134023091	K562	blood:	n/a	n/a
49	EGR1	chr6:134028634-134028891	K562	blood:	n/a	n/a
50	ELF1	chr6:134022767-134023247	K562	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:134022234-134022284	IMR90	lung:	fetal
2	chr6:134022234-134022284	IMR90	lung:	fetal
3	chr6:133988702-133988752	ProgFib	skin:	n/a
4	chr6:133995954-133996004	HCT-116	colon:	n/a
5	chr6:134052041-134052091	A549	lung:	n/a
6	chr6:134026410-134026460	HPAEpiC	pulmonary alveolar:	n/a
7	chr6:134052041-134052091	HIPEpiC	eye:	n/a
8	chr6:133995954-133996004	PFSK-1	brain:	n/a
9	chr6:133995954-133996004	NH-A	brain:	n/a
10	chr6:134052041-134052091	NHDF-neo	bronchial:	n/a
11	chr6:134052041-134052091	ECC-1	luminal epithelium:	n/a
12	chr6:134022234-134022284	HEK293	kidney:	embryo
13	chr6:133988702-133988752	NH-A	brain:	n/a
14	chr6:134052041-134052091	GM12878	blood:	n/a
15	chr6:134026410-134026460	GM12892	blood:	n/a
16	chr6:134026410-134026460	SK-N-SH_RA	brain:	n/a
17	chr6:134004505-134004555	HNPCEpiC	eye:	n/a
18	chr6:134026410-134026460	A549	lung:	n/a
19	chr6:134022234-134022284	PANC-1	pancreas:	n/a
20	chr6:134052041-134052091	PFSK-1	brain:	n/a
21	chr6:133988702-133988752	PFSK-1	brain:	n/a
22	chr6:134004505-134004555	A549	lung:	n/a
23	chr6:134004505-134004555	NT2-D1	testis:	n/a
24	chr6:134026410-134026460	Hepatocyte	liver:	n/a
25	chr6:134004505-134004555	Hela-S3	cervix:	n/a
26	chr6:133995954-133996004	HNPCEpiC	eye:	n/a
27	chr6:133995954-133996004	SK-N-MC	brain:	n/a
28	chr6:134052041-134052091	AG04449	skin:	fetal
29	chr6:134026410-134026460	AG10803	skin:	n/a
30	chr6:133988702-133988752	SKMC	muscle:	n/a
31	chr6:134022234-134022284	AG09309	skin:	n/a
32	chr6:133988702-133988752	ECC-1	luminal epithelium:	n/a
33	chr6:133995954-133996004	GM12878	blood:	n/a
34	chr6:134052041-134052091	SK-N-SH	brain:	n/a
35	chr6:134026410-134026460	PANC-1	pancreas:	n/a
36	chr6:134026410-134026460	LNCaP	prostate:	n/a
37	chr6:134022234-134022284	HCT-116	colon:	n/a
38	chr6:134026410-134026460	ProgFib	skin:	n/a
39	chr6:134004505-134004555	RPTEC	kidney:	n/a
40	chr6:133988702-133988752	GM12891	blood:	n/a
41	chr6:133988702-133988752	Hela-S3	cervix:	n/a
42	chr6:133995954-133996004	HL-60	blood:	n/a
43	chr6:134004505-134004555	AoSMC	blood vessel:	n/a
44	chr6:133988702-133988752	AG04449	skin:	fetal
45	chr6:134022234-134022284	AG04450	lung:	fetal
46	chr6:134022234-134022284	SK-N-SH_RA	brain:	n/a
47	chr6:134004505-134004555	T-47D	breast:	n/a
48	chr6:133988702-133988752	K562	blood:	n/a
49	chr6:133995954-133996004	NT2-D1	testis:	n/a
50	chr6:133988702-133988752	ovcar-3	ovarian:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:134011892..134014081-chr6:134020457..134023191,3	K562	blood:
2	chr3:124729941..124730621-chr6:134016953..134017515,2	MCF-7	breast:
3	chr6:134000236..134003025-chr6:134005182..134007868,2	K562	blood:
4	chr6:133135284..133137097-chr6:133999263..134001156,2	MCF-7	breast:
5	chr6:134033546..134036088-chr6:134038192..134040824,2	K562	blood:
6	chr6:134008546..134010265-chr6:134012956..134014855,2	K562	blood:
7	chr6:134000236..134003025-chr6:134005182..134007868,2	K562	blood:
8	chr6:134028426..134030950-chr6:134042269..134044112,2	K562	blood:
9	chr6:134020858..134023121-chr6:134025538..134028514,2	K562	blood:
10	chr6:134020858..134023121-chr6:134025538..134028514,2	K562	blood:
11	chr6:134015981..134018039-chr6:134018709..134021575,3	K562	blood:
12	chr6:134051702..134053602-chr6:134053874..134056406,2	K562	blood:
13	chr6:134033966..134036088-chr6:134039324..134041505,2	K562	blood:
14	chr6:134011870..134014344-chr6:134017659..134020361,3	K562	blood:
15	chr6:134033966..134036088-chr6:134039324..134041505,2	K562	blood:
16	chr6:134033546..134036088-chr6:134038192..134040824,2	K562	blood:
17	chr6:134051702..134053602-chr6:134053874..134056406,2	K562	blood:
18	chr6:134028426..134030950-chr6:134042269..134044112,2	K562	blood:
19	chr6:134053761..134056353-chr6:134057455..134059552,2	K562	blood:
20	chr6:134011870..134014344-chr6:134017659..134020361,3	K562	blood:
21	chr6:134053761..134056353-chr6:134057455..134059552,2	K562	blood:
22	chr6:134011892..134014081-chr6:134020457..134023191,3	K562	blood:
23	chr6:134008546..134010265-chr6:134012956..134014855,2	K562	blood:
24	chr6:134015981..134018039-chr6:134018709..134021575,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC2A12-10	chr6:133997867-133998567	NONHSAT115001

No data

Variant related genes	Relation type
FTH1P26	TF binding region
FTH1P26	CpG island
ENSG00000206754	chromatin interactions
ENSG00000112306	chromatin interactions

Extended variants
information (count: 2358 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2358 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577281397	chr6:133988626-133988627	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs6914525	chr6:133988652-133988653	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs187423964	chr6:133988673-133988674	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs561597589	chr6:133988712-133988713	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs530416725	chr6:133988765-133988766	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs540871523	chr6:133988770-133988771	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs6569892	chr6:133988802-133988803	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs192231222	chr6:133988829-133988830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532552643	chr6:133988834-133988835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551467163	chr6:133988895-133988896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs149045745	chr6:133988924-133988925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530552996	chr6:133988945-133988946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6569894	chr6:133989016-133989017	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs184111718	chr6:133989045-133989046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs73555389	chr6:133989142-133989143	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs552801719	chr6:133989162-133989163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7752751	chr6:133989262-133989263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559596089	chr6:133989310-133989311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538421700	chr6:133989330-133989331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371978364	chr6:133989369-133989370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529643608	chr6:133989402-133989403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559043879	chr6:133989405-133989406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189716227	chr6:133989474-133989475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143023794	chr6:133989486-133989487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113847720	chr6:133989503-133989504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551181344	chr6:133989511-133989512	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553354782	chr6:133989544-133989545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113636561	chr6:133989549-133989550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs28406462	chr6:133989573-133989574	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369322941	chr6:133989671-133989672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7738973	chr6:133989674-133989675	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs540934620	chr6:133989698-133989699	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560741909	chr6:133989703-133989704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76367255	chr6:133989714-133989715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372459795	chr6:133989740-133989741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs13218156	chr6:133989786-133989787	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs565036283	chr6:133989848-133989849	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568161279	chr6:133989854-133989855	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116147538	chr6:133989871-133989872	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7757690	chr6:133989896-133989897	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs566925379	chr6:133989926-133989927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs56244833	chr6:133989939-133989940	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs546504922	chr6:133989975-133989976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566639114	chr6:133990003-133990004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538855787	chr6:133990031-133990032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140176664	chr6:133990040-133990041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550814005	chr6:133990068-133990069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145318761	chr6:133990241-133990242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534194101	chr6:133990363-133990364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs180894183	chr6:133990375-133990376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Colorectal cancer	16272173	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
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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	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
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	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
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133988600-133988800	ZNF genes & repeats	Fetal Lung	lung
2	chr6:133988800-133995600	Weak transcription	Fetal Lung	lung
3	chr6:133989400-133990600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:133990400-133990600	Enhancers	NHDF-Ad	bronchial
5	chr6:133990600-133991600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr6:133990800-133991800	Weak transcription	NHDF-Ad	bronchial
7	chr6:133991600-133993200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr6:133991800-133993200	Enhancers	NHDF-Ad	bronchial
9	chr6:133992400-133993200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr6:133992400-133993200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr6:133994000-133994600	Enhancers	Fetal Kidney	kidney
12	chr6:133994200-133994400	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr6:133994200-133994600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:133994200-133994600	Enhancers	Ovary	ovary
15	chr6:133994400-133995000	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr6:133994400-134001600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr6:133994600-133995600	Weak transcription	Fetal Kidney	kidney
18	chr6:133994600-134000000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:133994600-134001800	Weak transcription	Ovary	ovary
20	chr6:133995000-133995400	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr6:133995200-133995400	Enhancers	H9 Cell Line	embryonic stem cell
22	chr6:133995400-133996000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr6:133995400-133996000	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr6:133995400-133996200	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr6:133995600-133996800	Enhancers	Fetal Kidney	kidney
26	chr6:133995600-133997400	Enhancers	Fetal Lung	lung
27	chr6:133995800-133996400	Enhancers	Fetal Stomach	stomach
28	chr6:133996000-133996200	Enhancers	H9 Cell Line	embryonic stem cell
29	chr6:133996000-133996200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr6:133996000-133996200	Bivalent/Poised TSS	Fetal Brain Male	brain
31	chr6:133996000-133996400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr6:133996000-133996800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr6:133996200-133996400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr6:133996200-134002400	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr6:133996200-134002400	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr6:133996400-134000800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr6:133996400-134002800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr6:133996800-134000000	Weak transcription	Fetal Kidney	kidney
39	chr6:133997400-134000800	Weak transcription	Fetal Lung	lung
40	chr6:133998200-133998600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr6:133998600-134002200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr6:134000000-134000600	Enhancers	Fetal Kidney	kidney
43	chr6:134000000-134001000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:134000600-134002400	Weak transcription	Fetal Kidney	kidney
45	chr6:134000800-134002400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr6:134000800-134005800	Enhancers	Fetal Lung	lung
47	chr6:134001000-134002400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr6:134001400-134001600	Enhancers	H1 Cell Line	embryonic stem cell
49	chr6:134001400-134002400	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr6:134001600-134001800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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