Variant report

Variant	nsv605176
Chromosome Location	chr6:162980903-163079918
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	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
2	ATF2	chr6:163042363-163042635	GM12878	blood:	n/a	n/a
3	ATF3	chr6:163042298-163042684	HCT-116	colon:	n/a	n/a
4	BATF	chr6:163042398-163042636	GM12878	blood:	n/a	chr6:163042519-163042530
5	BATF	chr6:163042347-163042655	GM12878	blood:	n/a	chr6:163042519-163042530
6	BHLHE40	chr6:163042376-163042676	GM12878	blood:	n/a	n/a
7	CCNT2	chr6:163001825-163002025	K562	blood:	n/a	n/a
8	CEBPB	chr6:163036070-163036411	IMR90	lung:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
9	CEBPB	chr6:163063888-163064088	H1-hESC	embryonic stem cell:	n/a	chr6:163063991-163064002
10	CEBPB	chr6:163036055-163036678	HepG2	liver:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036565-163036582 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
11	CEBPB	chr6:163036133-163036384	Hela-S3	cervix:	n/a	chr6:163036237-163036246 chr6:163036237-163036246 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036236-163036247
12	CEBPB	chr6:163063853-163064152	HepG2	liver:	n/a	chr6:163063991-163064002
13	CEBPB	chr6:163036076-163036363	H1-hESC	embryonic stem cell:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
14	CEBPB	chr6:163042252-163042579	MCF-7	breast:	n/a	n/a
15	CEBPB	chr6:163063873-163064127	IMR90	lung:	n/a	chr6:163063991-163064002
16	CEBPB	chr6:163036084-163036403	A549	lung:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
17	CEBPB	chr6:163042256-163042790	HCT-116	colon:	n/a	n/a
18	CEBPB	chr6:163067647-163067800	HepG2	liver:	n/a	chr6:163067696-163067707
19	CEBPB	chr6:163042384-163042569	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr6:163024952-163025129	GM12878	blood:	n/a	n/a
21	CTCF	chr6:163033777-163033927	MCF-7	breast:	n/a	n/a
22	CTCF	chr6:163033760-163033910	MCF-7	breast:	n/a	n/a
23	CTCF	chr6:162986380-162986530	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr6:162984275-162984315	K562	blood:	n/a	n/a
25	CTCF	chr6:163033791-163033941	MCF-7	breast:	n/a	n/a
26	CTCF	chr6:163033844-163033900	HepG2	liver:	n/a	n/a
27	CTCF	chr6:163001780-163001930	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr6:163033680-163033970	MCF-7	breast:	n/a	n/a
29	CTCF	chr6:163033831-163033920	LNCaP	prostate:	n/a	n/a
30	CTCF	chr6:163001788-163001915	HepG2	liver:	n/a	n/a
31	CTCF	chr6:163033654-163034114	MCF-7	breast:	n/a	n/a
32	CTCF	chr6:162990462-162990514	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:163033681-163033971	MCF-7	breast:	n/a	n/a
34	CTCF	chr6:163033780-163033930	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr6:163001800-163001950	MCF-7	breast:	n/a	n/a
36	CTCF	chr6:163033780-163033930	BE2_C	brain:	n/a	n/a
37	CTCF	chr6:163033760-163033910	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr6:163033780-163033930	HepG2	liver:	n/a	n/a
39	CTCF	chr6:163033740-163033890	HEK293	kidney:	n/a	n/a
40	CTCF	chr6:162990380-162990530	HEK293	kidney:	n/a	n/a
41	CTCF	chr6:163001760-163001910	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr6:163033823-163033909	A549	lung:	n/a	n/a
43	CTCF	chr6:163033765-163033956	MCF-7	breast:	n/a	n/a
44	CTCF	chr6:162989674-162989762	GM20000	blood:	n/a	n/a
45	CTCF	chr6:162990358-162990589	HepG2	liver:	n/a	n/a
46	CTCF	chr6:163033770-163033924	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:163001742-163001906	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr6:163033767-163033941	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:163041298-163041411	GM12878	blood:	n/a	chr6:163041356-163041369 chr6:163041349-163041370 chr6:163041354-163041372
50	CTCF	chr6:163001780-163001930	HBMEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163024624-163024674	Caco-2	colon:	n/a
2	chr6:163024624-163024674	H1-hESC	embryonic stem cell:	embryo
3	chr6:163024624-163024674	HRPEpiC	eye:	n/a
4	chr6:163024624-163024674	SK-N-SH	brain:	n/a
5	chr6:163024624-163024674	GM06990	blood:	n/a
6	chr6:163024624-163024674	HEK293	kidney:	embryo
7	chr6:163024624-163024674	AG09319	gingival:	n/a
8	chr6:163024624-163024674	ovcar-3	ovarian:	n/a
9	chr6:163024624-163024674	BJ	skin:	n/a
10	chr6:163024624-163024674	AG10803	skin:	n/a
11	chr6:163024624-163024674	AoSMC	blood vessel:	n/a
12	chr6:163024624-163024674	SK-N-MC	brain:	n/a
13	chr6:163024624-163024674	HCPEpiC	choroid plexus:	n/a
14	chr6:163024624-163024674	T-47D	breast:	n/a
15	chr6:163024624-163024674	NH-A	brain:	n/a
16	chr6:163024624-163024674	HepG2	liver:	n/a
17	chr6:163024624-163024674	HCM	heart:	n/a
18	chr6:163024624-163024674	GM12878	blood:	n/a
19	chr6:163024624-163024674	HMEC	breast:	n/a
20	chr6:163024624-163024674	IMR90	lung:	fetal
21	chr6:163024624-163024674	Jurkat	blood:	n/a
22	chr6:163024624-163024674	NHDF-neo	bronchial:	n/a
23	chr6:163024624-163024674	AG04450	lung:	fetal
24	chr6:163024624-163024674	SK-N-SH_RA	brain:	n/a
25	chr6:163024624-163024674	PrEC	prostate:	n/a
26	chr6:163024624-163024674	Hela-S3	cervix:	n/a
27	chr6:163024624-163024674	K562	blood:	n/a
28	chr6:163024624-163024674	NT2-D1	testis:	n/a
29	chr6:163024624-163024674	AG09309	skin:	n/a
30	chr6:163024624-163024674	CMK	blood:	n/a
31	chr6:163024624-163024674	HNPCEpiC	eye:	n/a
32	chr6:163024624-163024674	HRE	kidney:	n/a
33	chr6:163024624-163024674	PANC-1	pancreas:	n/a
34	chr6:163024624-163024674	HCF	heart:	n/a
35	chr6:163024624-163024674	SKMC	muscle:	n/a
36	chr6:163024624-163024674	HRCEpiC	kidney:	n/a
37	chr6:163024624-163024674	HUVEC	blood vessel:	n/a
38	chr6:163024624-163024674	ProgFib	skin:	n/a
39	chr6:163024624-163024674	PFSK-1	brain:	n/a
40	chr6:163024624-163024674	MCF10A-Er-Src	breast:	n/a
41	chr6:163024624-163024674	U87	brain:	n/a
42	chr6:163024624-163024674	NB4	blood:	n/a
43	chr6:163024624-163024674	GM12891	blood:	n/a
44	chr6:163024624-163024674	MCF-7	breast:	n/a
45	chr6:163024624-163024674	HPAEpiC	pulmonary alveolar:	n/a
46	chr6:163024624-163024674	HIPEpiC	eye:	n/a
47	chr6:163024624-163024674	NHBE	bronchial:	n/a
48	chr6:163024624-163024674	GM12892	blood:	n/a
49	chr6:163024624-163024674	AG04449	skin:	fetal
50	chr6:163024624-163024674	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
2	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
3	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:

Variant related genes	Relation type
KRT8P44	TF binding region
KRT8P44	CpG island

Extended variants
information (count: 3923 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:3923 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9295192	chr6:162980903-162980904	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs552786633	chr6:162980913-162980914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs9295193	chr6:162980932-162980933	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs557782593	chr6:162980935-162980936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538620651	chr6:162980954-162980955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs9295194	chr6:162980955-162980956	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs575583770	chr6:162980974-162980975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544534355	chr6:162981004-162981005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554709659	chr6:162981055-162981056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs79351298	chr6:162981109-162981110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540471169	chr6:162981128-162981129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182710268	chr6:162981153-162981154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559585844	chr6:162981171-162981172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561459878	chr6:162981173-162981174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528600101	chr6:162981184-162981185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186506850	chr6:162981243-162981244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540828013	chr6:162981249-162981250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2023016	chr6:162981266-162981267	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs371261089	chr6:162981268-162981269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs13216615	chr6:162981315-162981316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191025559	chr6:162981316-162981317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144859145	chr6:162981346-162981347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560411979	chr6:162981350-162981351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs13201023	chr6:162981381-162981382	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs567995555	chr6:162981421-162981422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530221718	chr6:162981459-162981460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10945841	chr6:162981582-162981583	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs566421532	chr6:162981605-162981606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538761581	chr6:162981629-162981630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558554255	chr6:162981656-162981657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568880341	chr6:162981677-162981678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369475100	chr6:162981696-162981697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs9458595	chr6:162981739-162981740	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs574719180	chr6:162981765-162981766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549470297	chr6:162981804-162981805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377039858	chr6:162981884-162981885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373998794	chr6:162981885-162981886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10636480	chr6:162981886-162981887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs60391138	chr6:162981899-162981900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371981183	chr6:162981954-162981955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377550753	chr6:162981956-162981957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553963125	chr6:162981979-162981980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540643585	chr6:162982028-162982029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116285920	chr6:162982051-162982052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375330877	chr6:162982072-162982073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368817447	chr6:162982085-162982086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371356365	chr6:162982088-162982089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530807553	chr6:162982114-162982115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2803067	chr6:162982118-162982119	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs561407371	chr6:162982121-162982122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20838587	CNVD
Early-onset parkinson disease	21993715	CNVD
Glioblastoma	18772890	CNVD
Pancreatic cancer	20981101	CNVD
Autism	21360662	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Parkinson disease	0	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162941200-162989400	Weak transcription	Aorta	Aorta
2	chr6:162962600-162983400	Weak transcription	Left Ventricle	heart
3	chr6:162965600-162988800	Weak transcription	Stomach Smooth Muscle	stomach
4	chr6:162967800-162989400	Weak transcription	Pancreas	Pancrea
5	chr6:162969200-162989400	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr6:162975800-162986200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:162978600-162989400	Weak transcription	Ovary	ovary
8	chr6:162983200-162983400	Enhancers	Right Ventricle	heart
9	chr6:162983400-162984000	Enhancers	Left Ventricle	heart
10	chr6:162983400-162989600	Weak transcription	Right Ventricle	heart
11	chr6:162983400-162991600	Weak transcription	Brain Substantia Nigra	brain
12	chr6:162984000-162986400	Weak transcription	Left Ventricle	heart
13	chr6:162986400-162986800	ZNF genes & repeats	Left Ventricle	heart
14	chr6:162986800-162989200	Weak transcription	Left Ventricle	heart
15	chr6:162988200-162989400	Weak transcription	Gastric	stomach
16	chr6:162988800-162989400	ZNF genes & repeats	Stomach Smooth Muscle	stomach
17	chr6:162988800-162990200	ZNF genes & repeats	Adipose Nuclei	Adipose
18	chr6:162989000-162989200	Weak transcription	Fetal Kidney	kidney
19	chr6:162989000-162989600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr6:162989000-162990000	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr6:162989200-162989800	Weak transcription	Brain Hippocampus Middle	brain
22	chr6:162989200-162990400	Strong transcription	Left Ventricle	heart
23	chr6:162989200-162990400	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
24	chr6:162989200-162992600	Weak transcription	Colon Smooth Muscle	Colon
25	chr6:162989400-162989800	Strong transcription	Gastric	stomach
26	chr6:162989400-162989800	ZNF genes & repeats	Pancreas	Pancrea
27	chr6:162989400-162990400	ZNF genes & repeats	Aorta	Aorta
28	chr6:162989400-162990400	ZNF genes & repeats	Lung	lung
29	chr6:162989400-162990400	Strong transcription	Ovary	ovary
30	chr6:162989400-162990400	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
31	chr6:162989400-162990400	Strong transcription	Stomach Smooth Muscle	stomach
32	chr6:162989600-162990000	ZNF genes & repeats	Brain Cingulate Gyrus	brain
33	chr6:162989600-162990400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr6:162989600-162990400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr6:162989600-162990400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr6:162989600-162990600	ZNF genes & repeats	Esophagus	oesophagus
37	chr6:162989600-162990600	Genic enhancers	Right Ventricle	heart
38	chr6:162989600-162993600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr6:162989800-162990200	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
40	chr6:162989800-162990400	Strong transcription	Brain Hippocampus Middle	brain
41	chr6:162989800-162990600	ZNF genes & repeats	Gastric	stomach
42	chr6:162989800-163000200	Weak transcription	Pancreas	Pancrea
43	chr6:162990000-162990200	Strong transcription	Brain Cingulate Gyrus	brain
44	chr6:162990000-162990400	Strong transcription	Duodenum Smooth Muscle	Duodenum
45	chr6:162990200-162990800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
46	chr6:162990200-162994400	Weak transcription	Brain Cingulate Gyrus	brain
47	chr6:162990400-162992000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr6:162990400-162992000	Weak transcription	Stomach Smooth Muscle	stomach
49	chr6:162990400-162992200	Weak transcription	Brain Hippocampus Middle	brain
50	chr6:162990400-162993200	Weak transcription	Duodenum Smooth Muscle	Duodenum

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