Variant report

Variant	nsv1022069
Chromosome Location	chr6:102470600-102598244
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:323)
CpG islands
(count:123)
Chromatin interactive
region (count:19)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:323 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:102521688-102521925	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr6:102474600-102474636	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr6:102486905-102487106	GM12878	blood:	n/a	chr6:102487063-102487072
4	CEBPB	chr6:102567664-102568032	HepG2	liver:	n/a	chr6:102567840-102567851 chr6:102567838-102567851 chr6:102567838-102567851 chr6:102567840-102567849 chr6:102567838-102567849
5	CEBPB	chr6:102567747-102567990	K562	blood:	n/a	chr6:102567840-102567851 chr6:102567838-102567851 chr6:102567838-102567851 chr6:102567840-102567849 chr6:102567838-102567849
6	CEBPB	chr6:102562336-102562652	MCF-7	breast:	n/a	n/a
7	CEBPB	chr6:102491082-102491340	HepG2	liver:	n/a	chr6:102491226-102491237
8	CEBPB	chr6:102534674-102535024	HepG2	liver:	n/a	chr6:102534766-102534779 chr6:102534850-102534861
9	CEBPB	chr6:102567721-102567930	H1-hESC	embryonic stem cell:	n/a	chr6:102567840-102567851 chr6:102567838-102567851 chr6:102567838-102567851 chr6:102567840-102567849 chr6:102567838-102567849
10	CEBPB	chr6:102534682-102535007	IMR90	lung:	n/a	chr6:102534766-102534779 chr6:102534850-102534861
11	CEBPB	chr6:102523521-102523806	MCF-7	breast:	n/a	n/a
12	CEBPB	chr6:102567662-102568016	IMR90	lung:	n/a	chr6:102567840-102567851 chr6:102567838-102567851 chr6:102567838-102567851 chr6:102567840-102567849 chr6:102567838-102567849
13	CEBPB	chr6:102567678-102568001	A549	lung:	n/a	chr6:102567840-102567851 chr6:102567838-102567851 chr6:102567838-102567851 chr6:102567840-102567849 chr6:102567838-102567849
14	CEBPB	chr6:102491061-102491357	IMR90	lung:	n/a	chr6:102491226-102491237
15	CEBPB	chr6:102580353-102580639	IMR90	lung:	n/a	n/a
16	CTCF	chr6:102562404-102562503	GM19240	blood:	n/a	n/a
17	CTCF	chr6:102562360-102562510	HepG2	liver:	n/a	n/a
18	CTCF	chr6:102533353-102533604	IMR90	lung:	n/a	chr6:102533472-102533481
19	CTCF	chr6:102562320-102562470	GM12801	blood:	n/a	n/a
20	CTCF	chr6:102562380-102562530	HRE	kidney:	n/a	n/a
21	CTCF	chr6:102533320-102533470	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr6:102562420-102562570	GM06990	blood:	n/a	n/a
23	CTCF	chr6:102562360-102562510	GM12866	blood:	n/a	n/a
24	CTCF	chr6:102562480-102562630	GM12871	blood:	n/a	n/a
25	CTCF	chr6:102562420-102562570	SAEC	small airway:	n/a	n/a
26	CTCF	chr6:102533420-102533570	BE2_C	brain:	n/a	chr6:102533472-102533481
27	CTCF	chr6:102562340-102562490	HFF	foreskin:	n/a	n/a
28	CTCF	chr6:102562860-102563010	HEK293	kidney:	n/a	n/a
29	CTCF	chr6:102562413-102562510	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr6:102562400-102562550	GM12874	blood:	n/a	n/a
31	CTCF	chr6:102562416-102562502	GM12892	blood:	n/a	n/a
32	CTCF	chr6:102533420-102533570	HBMEC	blood vessel:	n/a	chr6:102533472-102533481
33	CTCF	chr6:102562440-102562590	HCT-116	colon:	n/a	n/a
34	CTCF	chr6:102562360-102562510	GM12868	blood:	n/a	n/a
35	CTCF	chr6:102562400-102562550	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr6:102562380-102562530	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:102562375-102562536	Gliobla	brain:	n/a	n/a
38	CTCF	chr6:102562308-102562722	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:102562414-102562460	GM10266	blood:	n/a	n/a
40	CTCF	chr6:102562334-102562569	GM13977	blood:	n/a	n/a
41	CTCF	chr6:102562420-102562570	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr6:102562340-102562490	GM12868	blood:	n/a	n/a
43	CTCF	chr6:102562400-102562550	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr6:102562360-102562510	GM12870	blood:	n/a	n/a
45	CTCF	chr6:102562660-102562810	HEK293	kidney:	n/a	n/a
46	CTCF	chr6:102533380-102533530	NHEK	skin:	n/a	chr6:102533472-102533481
47	CTCF	chr6:102562417-102562508	NHEK	skin:	n/a	n/a
48	CTCF	chr6:102562340-102562490	GM12873	blood:	n/a	n/a
49	CTCF	chr6:102562369-102562542	GM19238	blood:	n/a	n/a
50	CTCF	chr6:102562420-102562570	HEEpiC	esophagus:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:102536421-102536471	AG10803	skin:	n/a
2	chr6:102536421-102536471	AG10803	skin:	n/a
3	chr6:102536421-102536471	AG09319	gingival:	n/a
4	chr6:102516590-102516640	MCF10A-Er-Src	breast:	n/a
5	chr6:102536421-102536471	ProgFib	skin:	n/a
6	chr6:102516590-102516640	A549	lung:	n/a
7	chr6:102516590-102516640	Hela-S3	cervix:	n/a
8	chr6:102536421-102536471	A549	lung:	n/a
9	chr6:102516590-102516640	H1-hESC	embryonic stem cell:	embryo
10	chr6:102536421-102536471	HRPEpiC	eye:	n/a
11	chr6:102536421-102536471	NHBE	bronchial:	n/a
12	chr6:102536421-102536471	SK-N-SH_RA	brain:	n/a
13	chr6:102516590-102516640	AG04450	lung:	fetal
14	chr6:102516590-102516640	NB4	blood:	n/a
15	chr6:102536421-102536471	GM12878	blood:	n/a
16	chr6:102536421-102536471	SKMC	muscle:	n/a
17	chr6:102516590-102516640	HCM	heart:	n/a
18	chr6:102536421-102536471	AG04449	skin:	fetal
19	chr6:102516590-102516640	HCF	heart:	n/a
20	chr6:102536421-102536471	AG09309	skin:	n/a
21	chr6:102516590-102516640	HUVEC	blood vessel:	n/a
22	chr6:102516590-102516640	AG10803	skin:	n/a
23	chr6:102516590-102516640	GM06990	blood:	n/a
24	chr6:102516590-102516640	ProgFib	skin:	n/a
25	chr6:102516590-102516640	T-47D	breast:	n/a
26	chr6:102536421-102536471	SK-N-SH	brain:	n/a
27	chr6:102516590-102516640	HNPCEpiC	eye:	n/a
28	chr6:102516590-102516640	Caco-2	colon:	n/a
29	chr6:102516590-102516640	NHBE	bronchial:	n/a
30	chr6:102536421-102536471	K562	blood:	n/a
31	chr6:102516590-102516640	AoSMC	blood vessel:	n/a
32	chr6:102536421-102536471	RPTEC	kidney:	n/a
33	chr6:102516590-102516640	HEEpiC	esophagus:	n/a
34	chr6:102516590-102516640	CMK	blood:	n/a
35	chr6:102516590-102516640	HRCEpiC	kidney:	n/a
36	chr6:102516590-102516640	PFSK-1	brain:	n/a
37	chr6:102536421-102536471	GM06990	blood:	n/a
38	chr6:102516590-102516640	ovcar-3	ovarian:	n/a
39	chr6:102516590-102516640	AG09319	gingival:	n/a
40	chr6:102516590-102516640	NH-A	brain:	n/a
41	chr6:102536421-102536471	Hepatocyte	liver:	n/a
42	chr6:102536421-102536471	GM19239	blood:	n/a
43	chr6:102516590-102516640	HEK293	kidney:	embryo
44	chr6:102516590-102516640	PANC-1	pancreas:	n/a
45	chr6:102536421-102536471	NHDF-neo	bronchial:	n/a
46	chr6:102536421-102536471	CMK	blood:	n/a
47	chr6:102536421-102536471	HCF	heart:	n/a
48	chr6:102536421-102536471	HRE	kidney:	n/a
49	chr6:102516590-102516640	PrEC	prostate:	n/a
50	chr6:102536421-102536471	PANC-1	pancreas:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:102476206..102478938-chr6:102479367..102481927,2	MCF-7	breast:
2	chr6:102594665..102597425-chr6:102597707..102599339,2	MCF-7	breast:
3	chr6:102569145..102571853-chr6:102574170..102575887,3	K562	blood:
4	chr6:102476206..102478938-chr6:102479367..102481927,2	MCF-7	breast:
5	chr6:102582072..102584846-chr6:102585321..102586983,2	MCF-7	breast:
6	chr6:102561781..102562640-chr6:103570762..103571536,2	MCF-7	breast:
7	chr6:102467652..102469278-chr6:102473178..102474761,2	MCF-7	breast:
8	chr6:102572254..102574562-chr6:102580095..102582205,2	MCF-7	breast:
9	chr6:102594665..102597425-chr6:102597707..102599339,2	MCF-7	breast:
10	chr6:102571736..102574356-chr6:102583811..102586926,3	K562	blood:
11	chr6:102582072..102584846-chr6:102585321..102586983,2	MCF-7	breast:
12	chr6:102569145..102571791-chr6:102574229..102575887,2	K562	blood:
13	chr6:102469224..102471750-chr6:102472091..102474956,2	K562	blood:
14	chr6:102572254..102574562-chr6:102580095..102582205,2	MCF-7	breast:
15	chr6:102569145..102571853-chr6:102574170..102575887,3	K562	blood:
16	chr6:102469224..102471750-chr6:102472091..102474956,2	K562	blood:
17	chr6:102569145..102571791-chr6:102574229..102575887,2	K562	blood:
18	chr6:102571736..102574356-chr6:102583811..102586926,3	K562	blood:
19	chr6:102368803..102370851-chr6:102488591..102491392,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASCC3-1	chr6:102575603-102575865	XLOC_005791
2	lnc-ASCC3-1	chr6:102580356-102580400	XLOC_005791
3	lnc-GRIK2-3	chr6:102526747-102527430	NONHSAT114174

No data

Variant related genes	Relation type
ENSG00000218536	TF binding region
ENSG00000218536	CpG island

Extended variants
information (count: 1000 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:1000 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188297216	chr6:102470609-102470610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs564384061	chr6:102470616-102470617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs1335023	chr6:102470673-102470674	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs549973252	chr6:102470764-102470765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs13191478	chr6:102470777-102470778	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs530248571	chr6:102470789-102470790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548156831	chr6:102470811-102470812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372039383	chr6:102470869-102470870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs9485585	chr6:102470881-102470882	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs527970715	chr6:102470917-102470918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs9485586	chr6:102470985-102470986	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs374382020	chr6:102471001-102471002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs13203019	chr6:102471005-102471006	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs538020166	chr6:102471026-102471027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375792952	chr6:102471051-102471052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114812436	chr6:102471107-102471108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs13203156	chr6:102471125-102471126	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs535589574	chr6:102471132-102471133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200325431	chr6:102471202-102471203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573848555	chr6:102471218-102471219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572028500	chr6:102471238-102471239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545819548	chr6:102471239-102471240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558057969	chr6:102471301-102471302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572214021	chr6:102471305-102471306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576304209	chr6:102471313-102471314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543237448	chr6:102471325-102471326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575539459	chr6:102471329-102471330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184549147	chr6:102471419-102471420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545986085	chr6:102471512-102471513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs145711740	chr6:102471598-102471599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560214874	chr6:102471605-102471606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573492939	chr6:102471672-102471673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs188677326	chr6:102471681-102471682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs564382532	chr6:102471719-102471720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552169489	chr6:102471729-102471730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs34827756	chr6:102471746-102471747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571039610	chr6:102471762-102471763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532057595	chr6:102471784-102471785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550101935	chr6:102471822-102471823	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs148497687	chr6:102471835-102471836	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs555465934	chr6:102471841-102471842	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs145470923	chr6:102471842-102471843	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs565803735	chr6:102471857-102471858	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs539407616	chr6:102471863-102471864	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs147700546	chr6:102471868-102471869	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs576236240	chr6:102471869-102471870	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs538777247	chr6:102471893-102471894	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs1335024	chr6:102471903-102471904	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs555264301	chr6:102471921-102471922	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs573741826	chr6:102471937-102471938	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

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
Endometrioid adenocarcinoma	16974079	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
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	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
Leukemia	18688285	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
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	17640729	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
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17170743	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21785460	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Obesity	21045960	CNVD
Liver carcinoma	19366792	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Urothelial carcinoma	21177765	CNVD
Autism	22543975	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:102463000-102471400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr6:102470400-102471000	Enhancers	Hela-S3	cervix
3	chr6:102471400-102471800	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr6:102471800-102472600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr6:102472600-102474000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr6:102474000-102475200	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr6:102486200-102487200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr6:102486600-102487600	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr6:102486800-102487400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:102486800-102487400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr6:102487000-102487400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr6:102487000-102487600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr6:102487000-102487600	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr6:102487200-102487600	Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr6:102487400-102487800	Active TSS	Stomach Smooth Muscle	stomach
16	chr6:102487600-102487800	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr6:102487600-102491200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr6:102514000-102514600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr6:102514600-102516400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr6:102515800-102516200	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr6:102516200-102516600	Enhancers	Rectal Smooth Muscle	rectum
22	chr6:102516200-102516800	Enhancers	Colon Smooth Muscle	Colon
23	chr6:102516200-102517000	Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr6:102516400-102517200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr6:102550800-102552000	Active TSS	H9 Cell Line	embryonic stem cell
26	chr6:102551000-102551200	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr6:102551200-102556200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr6:102556000-102556600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr6:102556200-102556400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr6:102556200-102557000	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr6:102556400-102557000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr6:102557000-102557200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr6:102563200-102563600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr6:102566200-102566800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr6:102573800-102574200	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr6:102573800-102575000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr6:102574000-102574400	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr6:102574000-102575400	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr6:102574000-102575600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:102574000-102575600	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr6:102574400-102574800	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr6:102574400-102575000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr6:102583600-102584000	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr6:102596200-102596600	Enhancers	Brain Germinal Matrix	brain
45	chr6:102596600-102597800	Weak transcription	Brain Germinal Matrix	brain
46	chr6:102597800-102598000	Enhancers	Brain Germinal Matrix	brain

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