Variant report

Variant	nsv538525
Chromosome Location	chr6:163449712-163488528
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:53)
CpG islands
(count:244)
Chromatin interactive
region (count:4)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:53 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr6:163476202-163476485	GM12878	blood:	n/a	n/a
2	BCL3	chr6:163476237-163476563	GM12878	blood:	n/a	n/a
3	BCL3	chr6:163479255-163479599	GM12878	blood:	n/a	n/a
4	BCL3	chr6:163479336-163479590	GM12878	blood:	n/a	n/a
5	CBX3	chr6:163453013-163453248	K562	blood:	n/a	n/a
6	CCNT2	chr6:163484404-163484537	K562	blood:	n/a	n/a
7	CEBPB	chr6:163478280-163478773	A549	lung:	n/a	chr6:163478503-163478514
8	CEBPB	chr6:163478305-163478612	K562	blood:	n/a	chr6:163478503-163478514
9	CEBPB	chr6:163478412-163478549	K562	blood:	n/a	chr6:163478503-163478514
10	CEBPB	chr6:163478322-163478694	A549	lung:	n/a	chr6:163478503-163478514
11	CEBPB	chr6:163478322-163478698	H1-hESC	embryonic stem cell:	n/a	chr6:163478503-163478514
12	CEBPB	chr6:163478329-163478613	A549	lung:	n/a	chr6:163478503-163478514
13	CEBPB	chr6:163478317-163478694	K562	blood:	n/a	chr6:163478503-163478514
14	CEBPB	chr6:163478324-163478696	IMR90	lung:	n/a	chr6:163478503-163478514
15	CEBPB	chr6:163478331-163478677	MCF-7	breast:	n/a	chr6:163478503-163478514
16	CEBPB	chr6:163478376-163478685	ECC-1	luminal epithelium:	n/a	chr6:163478503-163478514
17	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
18	CEBPB	chr6:163478318-163478693	HepG2	liver:	n/a	chr6:163478503-163478514
19	CEBPB	chr6:163478428-163478563	HepG2	liver:	n/a	chr6:163478503-163478514
20	CTCF	chr6:163484300-163484450	GM12878	blood:	n/a	n/a
21	CTCF	chr6:163485536-163485560	Fibrobl	skin:	n/a	n/a
22	CTCF	chr6:163458799-163458848	Fibrobl	skin:	n/a	n/a
23	CTCF	chr6:163462440-163462590	HEK293	kidney:	n/a	n/a
24	CTCF	chr6:163475280-163475430	GM12867	blood:	n/a	n/a
25	GATA3	chr6:163469310-163469732	MCF-7	breast:	n/a	n/a
26	JUN	chr6:163487952-163488061	HepG2	liver:	n/a	chr6:163488004-163488013 chr6:163488003-163488016
27	JUND	chr6:163487883-163488170	HepG2	liver:	n/a	chr6:163488004-163488013
28	KAP1	chr6:163452759-163453297	K562	blood:	n/a	n/a
29	MAFF	chr6:163452210-163452232	K562	blood:	n/a	n/a
30	MAFF	chr6:163452069-163452377	HepG2	liver:	n/a	chr6:163452194-163452212
31	MAFK	chr6:163471855-163471946	HepG2	liver:	n/a	n/a
32	MAFK	chr6:163452039-163452378	HepG2	liver:	n/a	n/a
33	MAFK	chr6:163457470-163457670	HepG2	liver:	n/a	n/a
34	MAFK	chr6:163457550-163457650	HepG2	liver:	n/a	n/a
35	MAFK	chr6:163452054-163452341	HepG2	liver:	n/a	n/a
36	MAFK	chr6:163474909-163475107	HepG2	liver:	n/a	n/a
37	MAFK	chr6:163452089-163452321	IMR90	lung:	n/a	n/a
38	MAZ	chr6:163459755-163459774	HepG2	liver:	n/a	n/a
39	NFATC1	chr6:163476203-163476587	GM12878	blood:	n/a	n/a
40	PBX3	chr6:163476347-163476477	GM12878	blood:	n/a	n/a
41	POLR2A	chr6:163475688-163475785	K562	blood:	n/a	n/a
42	POLR2A	chr6:163455920-163455995	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr6:163470069-163470174	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr6:163471844-163471877	MCF10A-Er-Src	breast:	n/a	n/a
45	SETDB1	chr6:163471667-163471949	U2OS	brain:	n/a	n/a
46	SETDB1	chr6:163452786-163453572	U2OS	brain:	n/a	n/a
47	SETDB1	chr6:163480500-163480770	U2OS	brain:	n/a	n/a
48	SPI1	chr6:163450748-163451103	HL-60	blood:	n/a	n/a
49	STAT3	chr6:163458374-163458515	MCF10A-Er-Src	breast:	n/a	n/a
50	STAT3	chr6:163487349-163487433	MCF10A-Er-Src	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163475718-163475768	AG09309	skin:	n/a
2	chr6:163475333-163475383	MCF-7	breast:	n/a
3	chr6:163475252-163475302	BJ	skin:	n/a
4	chr6:163475252-163475302	NHDF-neo	bronchial:	n/a
5	chr6:163475333-163475383	HRCEpiC	kidney:	n/a
6	chr6:163475252-163475302	A549	lung:	n/a
7	chr6:163475333-163475383	BJ	skin:	n/a
8	chr6:163475252-163475302	HCT-116	colon:	n/a
9	chr6:163475324-163475374	GM12892	blood:	n/a
10	chr6:163475718-163475768	HCF	heart:	n/a
11	chr6:163475252-163475302	HRE	kidney:	n/a
12	chr6:163475333-163475383	HMEC	breast:	n/a
13	chr6:163475333-163475383	HNPCEpiC	eye:	n/a
14	chr6:163475333-163475383	K562	blood:	n/a
15	chr6:163475718-163475768	HAEpiC	amniotic membrane:	n/a
16	chr6:163475718-163475768	SK-N-SH	brain:	n/a
17	chr6:163475324-163475374	PANC-1	pancreas:	n/a
18	chr6:163475324-163475374	MCF10A-Er-Src	breast:	n/a
19	chr6:163475252-163475302	SK-N-MC	brain:	n/a
20	chr6:163475333-163475383	BE2_C	brain:	n/a
21	chr6:163475333-163475383	AG09319	gingival:	n/a
22	chr6:163475252-163475302	PFSK-1	brain:	n/a
23	chr6:163475252-163475302	HEEpiC	esophagus:	n/a
24	chr6:163475718-163475768	PFSK-1	brain:	n/a
25	chr6:163475718-163475768	ECC-1	luminal epithelium:	n/a
26	chr6:163475324-163475374	A549	lung:	n/a
27	chr6:163475718-163475768	HepG2	liver:	n/a
28	chr6:163475718-163475768	AG09319	gingival:	n/a
29	chr6:163475324-163475374	Jurkat	blood:	n/a
30	chr6:163475252-163475302	HL-60	blood:	n/a
31	chr6:163475324-163475374	Hepatocyte	liver:	n/a
32	chr6:163475324-163475374	HIPEpiC	eye:	n/a
33	chr6:163475718-163475768	Hepatocyte	liver:	n/a
34	chr6:163475718-163475768	HCPEpiC	choroid plexus:	n/a
35	chr6:163475718-163475768	GM12892	blood:	n/a
36	chr6:163475252-163475302	NH-A	brain:	n/a
37	chr6:163475324-163475374	SKMC	muscle:	n/a
38	chr6:163475252-163475302	Caco-2	colon:	n/a
39	chr6:163475718-163475768	AG04449	skin:	fetal
40	chr6:163475718-163475768	HUVEC	blood vessel:	n/a
41	chr6:163475333-163475383	T-47D	breast:	n/a
42	chr6:163475324-163475374	SK-N-MC	brain:	n/a
43	chr6:163475333-163475383	NH-A	brain:	n/a
44	chr6:163475333-163475383	SKMC	muscle:	n/a
45	chr6:163475252-163475302	HUVEC	blood vessel:	n/a
46	chr6:163475252-163475302	CMK	blood:	n/a
47	chr6:163475718-163475768	T-47D	breast:	n/a
48	chr6:163475324-163475374	MCF-7	breast:	n/a
49	chr6:163475333-163475383	HPAEpiC	pulmonary alveolar:	n/a
50	chr6:163475324-163475374	Hela-S3	cervix:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:163458107..163459739-chr6:163463183..163466142,2	K562	blood:
2	chr6:163458107..163459739-chr6:163463183..163466142,2	K562	blood:
3	chr6:163467143..163469243-chr6:163471356..163474324,2	K562	blood:
4	chr6:163467143..163469243-chr6:163471356..163474324,2	K562	blood:

(count:15 , 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	chr6:163463589-163463729	ENSG00000225437.1
3	lnc-AL078585.1-1	chr6:163472292-163472446	ENSG00000225437.1
4	lnc-AL078585.1-1	chr6:163474957-163475193	ENSG00000225437.1
5	lnc-AL078585.1-1	chr6:163467616-163467717	ENSG00000225437.1
6	lnc-AL078585.1-1	chr6:163472292-163473064	ENSG00000225437.1
7	lnc-AL078585.1-1	chr6:163467616-163467715	ENSG00000225437.1
8	lnc-AL078585.1-1	chr6:163465681-163465778	ENSG00000225437.1
9	lnc-AL078585.1-1	chr6:163474957-163475173	NONHSAT115951
10	lnc-AL078585.1-1	chr6:163465681-163465778	ENSG00000225437.1
11	lnc-AL078585.1-1	chr6:163464012-163464201	ENSG00000225437.1
12	lnc-AL078585.1-1	chr6:163471578-163473064	NONHSAT115951
13	lnc-AL078585.1-1	chr6:163464086-163464201	ENSG00000225437.1
14	lnc-AL078585.1-1	chr6:163464011-163464201	ENSG00000225437.1
15	lnc-AL078585.1-1	chr6:163467647-163467715	NONHSAT115951

No data

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

Extended variants
information (count: 845 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:845 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574354350	chr6:163456832-163456833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs187972473	chr6:163456857-163456858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2498498	chr6:163456858-163456859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs57629875	chr6:163456866-163456867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs533442923	chr6:163456868-163456869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544021871	chr6:163456899-163456900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563714527	chr6:163456990-163456991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148430616	chr6:163457021-163457022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75251176	chr6:163457115-163457116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs141682404	chr6:163457196-163457197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574023564	chr6:163457205-163457206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528051126	chr6:163457230-163457231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs73783991	chr6:163457296-163457297	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs146136368	chr6:163457300-163457301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs115075288	chr6:163457387-163457388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200818920	chr6:163457413-163457414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557156132	chr6:163457416-163457417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369489263	chr6:163457430-163457431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567319305	chr6:163457434-163457435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs62427571	chr6:163457475-163457476	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs6936045	chr6:163457499-163457500	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs572197806	chr6:163457560-163457561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140116840	chr6:163457580-163457581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs143768383	chr6:163457584-163457585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545573605	chr6:163457592-163457593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563887052	chr6:163457600-163457601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs369751636	chr6:163457670-163457671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192830516	chr6:163457677-163457678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374357196	chr6:163457711-163457712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543725731	chr6:163457717-163457718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184386468	chr6:163457729-163457730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs367981123	chr6:163457756-163457757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs59738972	chr6:163458685-163458686	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs546422911	chr6:163458695-163458696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146517299	chr6:163458696-163458697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs118077614	chr6:163458706-163458707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551416106	chr6:163458732-163458733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs57432193	chr6:163458755-163458756	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs60737521	chr6:163458762-163458763	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs140450249	chr6:163458774-163458775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534992821	chr6:163458845-163458846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372359747	chr6:163458890-163458891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2031436	chr6:163458898-163458899	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs574283180	chr6:163458918-163458919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568218249	chr6:163458932-163458933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528908522	chr6:163458938-163458939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370100243	chr6:163459011-163459012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147622547	chr6:163459012-163459013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs142192406	chr6:163459023-163459024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs568997755	chr6:163459051-163459052	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
abnormal development	18461090	CNVD
Cancer	20164919	CNVD

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163456800-163457400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:163457400-163457800	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr6:163458600-163459800	Enhancers	Fetal Heart	heart
4	chr6:163459800-163460000	Flanking Active TSS	Fetal Heart	heart
5	chr6:163460000-163460200	Active TSS	Fetal Heart	heart
6	chr6:163466000-163466200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:163466200-163470400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:163467000-163467400	Active TSS	Spleen	Spleen
9	chr6:163469400-163470400	Enhancers	Liver	Liver
10	chr6:163472200-163475800	Weak transcription	Pancreas	Pancrea
11	chr6:163473600-163474400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:163474000-163474600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr6:163474400-163474600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:163474600-163475000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:163474600-163475800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr6:163474800-163475600	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr6:163475000-163475200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:163475200-163475400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:163475400-163475600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:163475600-163476000	Enhancers	Spleen	Spleen
21	chr6:163475600-163476200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:163475800-163476000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:163475800-163476000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr6:163475800-163476000	ZNF genes & repeats	Pancreas	Pancrea
25	chr6:163476000-163477800	Weak transcription	Pancreas	Pancrea
26	chr6:163478000-163479000	Weak transcription	Pancreas	Pancrea
27	chr6:163479200-163479400	ZNF genes & repeats	Gastric	stomach
28	chr6:163479400-163481400	Weak transcription	Pancreas	Pancrea
29	chr6:163479400-163488200	Weak transcription	Gastric	stomach
30	chr6:163482200-163483200	ZNF genes & repeats	Pancreas	Pancrea
31	chr6:163482400-163488600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr6:163483200-163484000	Weak transcription	Pancreas	Pancrea
33	chr6:163484000-163484200	Strong transcription	Pancreas	Pancrea
34	chr6:163484200-163484400	ZNF genes & repeats	Pancreas	Pancrea
35	chr6:163484400-163486200	Weak transcription	Pancreas	Pancrea
36	chr6:163484800-163485000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr6:163485000-163486200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:163486000-163486400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:163486000-163487600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:163486200-163486600	Enhancers	Brain Anterior Caudate	brain
41	chr6:163486200-163486800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:163486800-163489200	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr6:163488200-163488400	ZNF genes & repeats	Gastric	stomach

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