Variant report

Variant	nsv1020900
Chromosome Location	chr6:163302262-163517812
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:642)
CpG islands
(count:671)
Chromatin interactive
region (count:20)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:642 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:163304083-163304357	HepG2	liver:	n/a	n/a
2	ATF2	chr6:163422341-163422769	GM12878	blood:	n/a	n/a
3	ATF3	chr6:163303817-163304198	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr6:163303885-163304152	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr6:163422365-163422747	GM12878	blood:	n/a	chr6:163422593-163422603
6	BATF	chr6:163422337-163422713	GM12878	blood:	n/a	chr6:163422593-163422603
7	BCL11A	chr6:163422413-163422668	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:163422425-163422741	GM12878	blood:	n/a	n/a
9	BCL3	chr6:163476237-163476563	GM12878	blood:	n/a	n/a
10	BCL3	chr6:163479255-163479599	GM12878	blood:	n/a	n/a
11	BCL3	chr6:163476202-163476485	GM12878	blood:	n/a	n/a
12	BCL3	chr6:163479336-163479590	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:163304111-163304430	HepG2	liver:	n/a	n/a
14	CBX3	chr6:163453013-163453248	K562	blood:	n/a	n/a
15	CBX3	chr6:163385583-163386388	HCT-116	colon:	n/a	n/a
16	CBX3	chr6:163385655-163386353	HCT-116	colon:	n/a	n/a
17	CCNT2	chr6:163334181-163334374	K562	blood:	n/a	n/a
18	CCNT2	chr6:163315115-163315237	K562	blood:	n/a	n/a
19	CCNT2	chr6:163484404-163484537	K562	blood:	n/a	n/a
20	CEBPB	chr6:163385672-163386327	HCT-116	colon:	n/a	n/a
21	CEBPB	chr6:163303993-163304101	HepG2	liver:	n/a	chr6:163304059-163304070
22	CEBPB	chr6:163325122-163325456	HepG2	liver:	n/a	chr6:163325287-163325298
23	CEBPB	chr6:163303878-163304389	HepG2	liver:	n/a	chr6:163304059-163304070
24	CEBPB	chr6:163513731-163513951	HepG2	liver:	n/a	chr6:163513809-163513820
25	CEBPB	chr6:163325142-163325406	H1-hESC	embryonic stem cell:	n/a	chr6:163325287-163325298
26	CEBPB	chr6:163478329-163478613	A549	lung:	n/a	chr6:163478503-163478514
27	CEBPB	chr6:163478280-163478773	A549	lung:	n/a	chr6:163478503-163478514
28	CEBPB	chr6:163325147-163325444	A549	lung:	n/a	chr6:163325287-163325298
29	CEBPB	chr6:163478324-163478696	IMR90	lung:	n/a	chr6:163478503-163478514
30	CEBPB	chr6:163478331-163478677	MCF-7	breast:	n/a	chr6:163478503-163478514
31	CEBPB	chr6:163478317-163478694	K562	blood:	n/a	chr6:163478503-163478514
32	CEBPB	chr6:163443243-163443443	HepG2	liver:	n/a	chr6:163443336-163443347
33	CEBPB	chr6:163303910-163304178	H1-hESC	embryonic stem cell:	n/a	chr6:163304059-163304070
34	CEBPB	chr6:163462678-163462805	HepG2	liver:	n/a	chr6:163462716-163462727 chr6:163462715-163462728 chr6:163462715-163462726 chr6:163462717-163462726 chr6:163462717-163462726 chr6:163462717-163462726 chr6:163462717-163462726
35	CEBPB	chr6:163385817-163386320	IMR90	lung:	n/a	n/a
36	CEBPB	chr6:163325129-163325412	IMR90	lung:	n/a	chr6:163325287-163325298
37	CEBPB	chr6:163325154-163325392	K562	blood:	n/a	chr6:163325287-163325298
38	CEBPB	chr6:163303869-163304224	HepG2	liver:	n/a	chr6:163304059-163304070
39	CEBPB	chr6:163478376-163478685	ECC-1	luminal epithelium:	n/a	chr6:163478503-163478514
40	CEBPB	chr6:163303926-163304412	A549	lung:	n/a	chr6:163304059-163304070
41	CEBPB	chr6:163478428-163478563	HepG2	liver:	n/a	chr6:163478503-163478514
42	CEBPB	chr6:163478412-163478549	K562	blood:	n/a	chr6:163478503-163478514
43	CEBPB	chr6:163315544-163315822	HepG2	liver:	n/a	chr6:163315679-163315690 chr6:163315678-163315691 chr6:163315678-163315689
44	CEBPB	chr6:163442088-163442410	HepG2	liver:	n/a	chr6:163442250-163442261
45	CEBPB	chr6:163303909-163304113	IMR90	lung:	n/a	chr6:163304059-163304070
46	CEBPB	chr6:163478305-163478612	K562	blood:	n/a	chr6:163478503-163478514
47	CEBPB	chr6:163442138-163442402	A549	lung:	n/a	chr6:163442250-163442261
48	CEBPB	chr6:163478322-163478694	A549	lung:	n/a	chr6:163478503-163478514
49	CEBPB	chr6:163478322-163478698	H1-hESC	embryonic stem cell:	n/a	chr6:163478503-163478514
50	CEBPB	chr6:163384837-163385142	IMR90	lung:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163475718-163475768	HMEC	breast:	n/a
2	chr6:163362155-163362205	BE2_C	brain:	n/a
3	chr6:163517573-163517623	ProgFib	skin:	n/a
4	chr6:163321305-163321355	HIPEpiC	eye:	n/a
5	chr6:163514605-163514655	GM06990	blood:	n/a
6	chr6:163321435-163321485	HEEpiC	esophagus:	n/a
7	chr6:163514605-163514655	SK-N-SH	brain:	n/a
8	chr6:163475324-163475374	GM12891	blood:	n/a
9	chr6:163321305-163321355	HCT-116	colon:	n/a
10	chr6:163475718-163475768	Hela-S3	cervix:	n/a
11	chr6:163475324-163475374	MCF-7	breast:	n/a
12	chr6:163321435-163321485	U87	brain:	n/a
13	chr6:163321157-163321207	K562	blood:	n/a
14	chr6:163321435-163321485	CMK	blood:	n/a
15	chr6:163475324-163475374	NHBE	bronchial:	n/a
16	chr6:163321435-163321485	LNCaP	prostate:	n/a
17	chr6:163517573-163517623	H1-hESC	embryonic stem cell:	embryo
18	chr6:163475324-163475374	GM19239	blood:	n/a
19	chr6:163517573-163517623	MCF-7	breast:	n/a
20	chr6:163321305-163321355	HRCEpiC	kidney:	n/a
21	chr6:163514605-163514655	AG09319	gingival:	n/a
22	chr6:163475252-163475302	GM12878	blood:	n/a
23	chr6:163321157-163321207	Hepatocyte	liver:	n/a
24	chr6:163514605-163514655	HRCEpiC	kidney:	n/a
25	chr6:163506790-163506840	BJ	skin:	n/a
26	chr6:163362155-163362205	HRCEpiC	kidney:	n/a
27	chr6:163517573-163517623	HL-60	blood:	n/a
28	chr6:163321305-163321355	NHDF-neo	bronchial:	n/a
29	chr6:163475718-163475768	SKMC	muscle:	n/a
30	chr6:163362155-163362205	NT2-D1	testis:	n/a
31	chr6:163517573-163517623	SK-N-SH_RA	brain:	n/a
32	chr6:163475252-163475302	HRPEpiC	eye:	n/a
33	chr6:163362155-163362205	SKMC	muscle:	n/a
34	chr6:163321305-163321355	GM19239	blood:	n/a
35	chr6:163475324-163475374	AG04450	lung:	fetal
36	chr6:163321435-163321485	ECC-1	luminal epithelium:	n/a
37	chr6:163321435-163321485	AG04449	skin:	fetal
38	chr6:163362155-163362205	K562	blood:	n/a
39	chr6:163321157-163321207	HAEpiC	amniotic membrane:	n/a
40	chr6:163517573-163517623	AG09309	skin:	n/a
41	chr6:163514605-163514655	HRE	kidney:	n/a
42	chr6:163321157-163321207	MCF10A-Er-Src	breast:	n/a
43	chr6:163321435-163321485	HIPEpiC	eye:	n/a
44	chr6:163321305-163321355	SKMC	muscle:	n/a
45	chr6:163321435-163321485	AG10803	skin:	n/a
46	chr6:163321305-163321355	MCF10A-Er-Src	breast:	n/a
47	chr6:163475252-163475302	MCF10A-Er-Src	breast:	n/a
48	chr6:163475324-163475374	A549	lung:	n/a
49	chr6:163506790-163506840	GM12891	blood:	n/a
50	chr6:163475333-163475383	HCF	heart:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:163320477..163321997-chr6:163470936..163472773,2	K562	blood:
2	chr6:163383289..163384996-chr6:163389712..163391752,2	MCF-7	breast:
3	chr6:163467143..163469243-chr6:163471356..163474324,2	K562	blood:
4	chr6:163332495..163335026-chr6:163337698..163339412,2	K562	blood:
5	chr12:104252627..104253426-chr6:163440642..163441162,2	MCF-7	breast:
6	chr6:163458107..163459739-chr6:163463183..163466142,2	K562	blood:
7	chr6:163312379..163314050-chr6:163315693..163317902,2	K562	blood:
8	chr6:163316641..163319996-chr6:163320032..163324686,4	K562	blood:
9	chr6:163383289..163384996-chr6:163389712..163391752,2	MCF-7	breast:
10	chr6:163426091..163427659-chr6:163429418..163431049,2	K562	blood:
11	chr6:163509761..163512247-chr6:163514199..163516689,2	K562	blood:
12	chr6:163429068..163430008-chrX:51497389..51498171,2	MCF-7	breast:
13	chr6:163467143..163469243-chr6:163471356..163474324,2	K562	blood:
14	chr6:163458107..163459739-chr6:163463183..163466142,2	K562	blood:
15	chr6:163332495..163335026-chr6:163337698..163339412,2	K562	blood:
16	chr6:163321321..163323965-chr6:163834423..163836018,2	MCF-7	breast:
17	chr6:163312379..163314050-chr6:163315693..163317902,2	K562	blood:
18	chr6:163426091..163427659-chr6:163429418..163431049,2	K562	blood:
19	chr6:163316641..163319996-chr6:163320032..163324686,4	K562	blood:
20	chr6:163509761..163512247-chr6:163514199..163516689,2	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL078585.1-1	chr6:163467616-163467715	ENSG00000225437.1
2	lnc-AL078585.1-1	chr6:163467616-163467717	ENSG00000225437.1
3	lnc-AL078585.1-1	chr6:163465681-163465778	ENSG00000225437.1
4	lnc-AL078585.1-1	chr6:163463589-163463729	ENSG00000225437.1
5	lnc-AL078585.1-13	chr6:163384002-163384191	ucscGeneNc_uc003qud_1
6	lnc-AL078585.1-1	chr6:163465681-163465778	ENSG00000225437.1
7	lnc-AL078585.1-1	chr6:163471578-163473064	NONHSAT115951
8	lnc-AL078585.1-13	chr6:163392282-163393054	ucscGeneNc_uc003qud_1
9	lnc-AL078585.1-1	chr6:163474957-163475173	NONHSAT115951
10	lnc-QKI-10	chr6:163307016-163311030	NONHSAT115946
11	lnc-AL078585.1-1	chr6:163464011-163464201	ENSG00000225437.1
12	lnc-AL078585.1-1	chr6:163464086-163464201	ENSG00000225437.1
13	lnc-AL078585.1-14	chr6:163378290-163378580	NONHSAT115947
14	lnc-AL078585.1-1	chr6:163474957-163475193	ENSG00000225437.1
15	lnc-AL078585.1-1	chr6:163472292-163473064	ENSG00000225437.1
16	lnc-AL078585.1-1	chr6:163467647-163467715	NONHSAT115951
17	lnc-AL078585.1-1	chr6:163472292-163472446	ENSG00000225437.1
18	lnc-AL078585.1-1	chr6:163464012-163464201	ENSG00000225437.1
19	lnc-AL078585.1-1	chr6:163467616-163467715	ENSG00000225437.1
20	lnc-AL078585.1-13	chr6:163387606-163387705	ucscGeneNc_uc003qud_1
21	lnc-AL078585.1-13	chr6:163394947-163395183	ucscGeneNc_uc003qud_1

No data

Variant related genes	Relation type
ENSG00000225437	TF binding region
PACRG	TF binding region
ENSG00000217557	TF binding region
ENSG00000225437	CpG island
PACRG	CpG island
ENSG00000217557	CpG island
ENSG00000270419	chromatin interactions
ENSG00000225437	chromatin interactions
ENSG00000112531	chromatin interactions

Extended variants
information (count: 5147 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:5147 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573833870	chr6:163302262-163302263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552296316	chr6:163302317-163302318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548498941	chr6:163302318-163302319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375851879	chr6:163302386-163302387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs68064523	chr6:163302402-163302403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534126285	chr6:163302424-163302425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569010705	chr6:163302426-163302427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182176560	chr6:163302439-163302440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558891798	chr6:163302481-163302482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577267339	chr6:163302563-163302564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554679709	chr6:163302616-163302617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369943968	chr6:163302645-163302646	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs77836784	chr6:163302650-163302651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150533239	chr6:163302655-163302656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs9458663	chr6:163302673-163302674	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs139915868	chr6:163302693-163302694	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546429452	chr6:163302721-163302722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6455853	chr6:163302725-163302726	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs375477322	chr6:163302791-163302792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576079672	chr6:163302898-163302899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541775937	chr6:163302907-163302908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561564462	chr6:163302949-163302950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187185434	chr6:163302954-163302955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540975441	chr6:163302962-163302963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369753081	chr6:163302993-163302994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550090540	chr6:163302995-163302996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs9765879	chr6:163302997-163302998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532925210	chr6:163302999-163303000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373586955	chr6:163303002-163303003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs57716241	chr6:163303047-163303048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs56913961	chr6:163303077-163303078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149818552	chr6:163303089-163303090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs184593265	chr6:163303092-163303093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542050826	chr6:163303095-163303096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531744738	chr6:163303115-163303116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569901995	chr6:163303123-163303124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548540834	chr6:163303129-163303130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560785867	chr6:163303132-163303133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568408733	chr6:163303160-163303161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188727893	chr6:163303164-163303165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554465194	chr6:163303171-163303172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34612817	chr6:163303192-163303193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571164289	chr6:163303217-163303218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs142358248	chr6:163303222-163303223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572310596	chr6:163303230-163303231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556812285	chr6:163303240-163303241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34686598	chr6:163303243-163303244	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs541591248	chr6:163303292-163303293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34739752	chr6:163303317-163303318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140210432	chr6:163303352-163303353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
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
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
Gastric cancer	17908304	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
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	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
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
abnormal development	18461090	CNVD
Cancer	20164919	CNVD

Chromatin state (count:585 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163295000-163303800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr6:163301000-163303600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:163302000-163309000	Weak transcription	Pancreas	Pancrea
4	chr6:163302400-163302800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:163302800-163303200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:163303200-163303600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:163303600-163303800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr6:163303600-163304000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:163303600-163304000	Enhancers	Liver	Liver
10	chr6:163303600-163304800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:163303800-163304000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:163303800-163304200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:163304000-163304600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr6:163304000-163305200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:163304000-163309000	Weak transcription	Liver	Liver
16	chr6:163304600-163304800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:163304800-163305800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:163306000-163306200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:163308800-163309600	Enhancers	Fetal Muscle Trunk	muscle
20	chr6:163308800-163309800	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr6:163309000-163309400	Enhancers	Right Atrium	heart
22	chr6:163309000-163309800	Enhancers	Duodenum Mucosa	Duodenum
23	chr6:163309000-163309800	Enhancers	Left Ventricle	heart
24	chr6:163309000-163309800	Enhancers	Pancreas	Pancrea
25	chr6:163309000-163311400	Enhancers	Liver	Liver
26	chr6:163309400-163309800	Enhancers	Psoas Muscle	Psoas
27	chr6:163309400-163309800	Enhancers	Spleen	Spleen
28	chr6:163309400-163310000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr6:163309600-163309800	Enhancers	Brain Angular Gyrus	brain
30	chr6:163309600-163311000	Enhancers	Brain Substantia Nigra	brain
31	chr6:163309800-163310200	Enhancers	Colonic Mucosa	Colon
32	chr6:163309800-163310200	Enhancers	Colon Smooth Muscle	Colon
33	chr6:163309800-163310200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
34	chr6:163309800-163310600	Weak transcription	Brain Angular Gyrus	brain
35	chr6:163309800-163313000	Weak transcription	Pancreas	Pancrea
36	chr6:163310000-163311000	Enhancers	Brain Anterior Caudate	brain
37	chr6:163310200-163311000	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr6:163310600-163310800	Enhancers	Brain Angular Gyrus	brain
39	chr6:163310800-163315200	Weak transcription	Brain Angular Gyrus	brain
40	chr6:163313000-163313200	ZNF genes & repeats	Pancreas	Pancrea
41	chr6:163313200-163318800	Weak transcription	Pancreas	Pancrea
42	chr6:163313600-163322800	Weak transcription	Gastric	stomach
43	chr6:163314800-163316000	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr6:163315000-163315200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr6:163315200-163315400	Enhancers	Brain Cingulate Gyrus	brain
46	chr6:163315200-163315600	Enhancers	Brain Angular Gyrus	brain
47	chr6:163315400-163316000	Enhancers	Brain Hippocampus Middle	brain
48	chr6:163316000-163322800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr6:163318800-163319000	ZNF genes & repeats	Pancreas	Pancrea
50	chr6:163318800-163329800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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