Variant report

Variant	nsv604485
Chromosome Location	chr6:109959269-110054486
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1341)
CpG islands
(count:1588)
Chromatin interactive
region (count:34)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1341 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:110016756-110017015	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:110012148-110012516	K562	blood:	n/a	n/a
3	ARID3A	chr6:110016814-110017014	K562	blood:	n/a	n/a
4	ARID3A	chr6:110011916-110012560	HepG2	liver:	n/a	n/a
5	ATF1	chr6:110008403-110008832	K562	blood:	n/a	n/a
6	ATF2	chr6:110011764-110012271	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr6:110008348-110008671	K562	blood:	n/a	n/a
8	BCLAF1	chr6:110026282-110026872	GM12878	blood:	n/a	n/a
9	BCLAF1	chr6:110026327-110026828	GM12878	blood:	n/a	n/a
10	BCLAF1	chr6:110012118-110012892	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:110018469-110018860	K562	blood:	n/a	n/a
12	BHLHE40	chr6:110008452-110008919	K562	blood:	n/a	n/a
13	BHLHE40	chr6:110012001-110012958	K562	blood:	n/a	n/a
14	BHLHE40	chr6:110026449-110026718	HepG2	liver:	n/a	n/a
15	BHLHE40	chr6:110026358-110026784	GM12878	blood:	n/a	n/a
16	BHLHE40	chr6:110011547-110012800	GM12878	blood:	n/a	n/a
17	BRCA1	chr6:110012014-110012749	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr6:110026248-110026927	HCT-116	colon:	n/a	n/a
19	CCNT2	chr6:110011549-110011857	K562	blood:	n/a	n/a
20	CCNT2	chr6:110012207-110012744	K562	blood:	n/a	chr6:110012451-110012460
21	CEBPB	chr6:110008257-110008925	HCT-116	colon:	n/a	chr6:110008552-110008563
22	CEBPB	chr6:110018594-110018882	K562	blood:	n/a	n/a
23	CEBPB	chr6:110008251-110009063	HCT-116	colon:	n/a	chr6:110008552-110008563
24	CEBPB	chr6:110008365-110008934	IMR90	lung:	n/a	chr6:110008552-110008563
25	CEBPB	chr6:110018560-110018886	IMR90	lung:	n/a	n/a
26	CEBPB	chr6:110008480-110008680	HepG2	liver:	n/a	chr6:110008552-110008563
27	CEBPB	chr6:110008348-110008719	K562	blood:	n/a	chr6:110008552-110008563
28	CEBPB	chr6:110008384-110008743	Hela-S3	cervix:	n/a	chr6:110008552-110008563
29	CEBPB	chr6:110008450-110008602	K562	blood:	n/a	chr6:110008552-110008563
30	CEBPB	chr6:110008413-110008730	K562	blood:	n/a	chr6:110008552-110008563
31	CEBPB	chr6:110011810-110012545	GM12878	blood:	n/a	chr6:110012343-110012355
32	CHD1	chr6:110026322-110026941	IMR90	lung:	n/a	n/a
33	CHD1	chr6:110011967-110012344	GM12878	blood:	n/a	n/a
34	CHD2	chr6:110011712-110012932	Hela-S3	cervix:	n/a	chr6:110012873-110012880
35	CHD2	chr6:110012353-110012600	HepG2	liver:	n/a	n/a
36	CHD2	chr6:110012187-110012526	K562	blood:	n/a	n/a
37	CHD2	chr6:110011510-110012632	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr6:110000434-110000678	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr6:110011732-110012976	GM12878	blood:	n/a	chr6:110012873-110012880
40	CREB1	chr6:110012151-110012951	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr6:110016650-110016949	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr6:110012032-110012949	HepG2	liver:	n/a	n/a
43	CREB1	chr6:110012273-110012709	A549	lung:	n/a	n/a
44	CREB1	chr6:110012090-110012740	GM12878	blood:	n/a	n/a
45	CTBP2	chr6:110011570-110012908	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr6:110012620-110012770	NHEK	skin:	n/a	n/a
47	CTCF	chr6:110026197-110027014	K562	blood:	n/a	chr6:110026537-110026550 chr6:110026534-110026552 chr6:110026539-110026549 chr6:110026537-110026546 chr6:110026536-110026557 chr6:110026622-110026643
48	CTCF	chr6:110026500-110026650	Hela-S3	cervix:	n/a	chr6:110026537-110026550 chr6:110026534-110026552 chr6:110026539-110026549 chr6:110026537-110026546 chr6:110026536-110026557 chr6:110026622-110026643
49	CTCF	chr6:110016736-110017014	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:110026560-110026710	A549	lung:	n/a	chr6:110026622-110026643

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:110012366-110012416	HUVEC	blood vessel:	n/a
2	chr6:110012874-110012924	SK-N-SH_RA	brain:	n/a
3	chr6:110012366-110012416	HUVEC	blood vessel:	n/a
4	chr6:110012874-110012924	SK-N-SH_RA	brain:	n/a
5	chr6:110012478-110012528	GM12892	blood:	n/a
6	chr6:110012386-110012436	HCPEpiC	choroid plexus:	n/a
7	chr6:110012635-110012685	AG04450	lung:	fetal
8	chr6:110011999-110012049	NT2-D1	testis:	n/a
9	chr6:110012366-110012416	HMEC	breast:	n/a
10	chr6:110011968-110012018	SAEC	small airway:	n/a
11	chr6:110012632-110012682	AG10803	skin:	n/a
12	chr6:110012591-110012641	CMK	blood:	n/a
13	chr6:110011686-110011736	HEEpiC	esophagus:	n/a
14	chr6:110012180-110012230	BJ	skin:	n/a
15	chr6:110012577-110012627	PANC-1	pancreas:	n/a
16	chr6:110011686-110011736	HCPEpiC	choroid plexus:	n/a
17	chr6:110012263-110012313	NHBE	bronchial:	n/a
18	chr6:110012591-110012641	IMR90	lung:	fetal
19	chr6:110012478-110012528	MCF10A-Er-Src	breast:	n/a
20	chr6:110012488-110012538	LNCaP	prostate:	n/a
21	chr6:110012366-110012416	HEEpiC	esophagus:	n/a
22	chr6:110011968-110012018	HEK293	kidney:	embryo
23	chr6:110012723-110012773	IMR90	lung:	fetal
24	chr6:110011599-110011649	Caco-2	colon:	n/a
25	chr6:110011599-110011649	K562	blood:	n/a
26	chr6:110015052-110015102	AG09319	gingival:	n/a
27	chr6:110012574-110012624	Jurkat	blood:	n/a
28	chr6:110012378-110012428	AG04450	lung:	fetal
29	chr6:110012635-110012685	SK-N-SH_RA	brain:	n/a
30	chr6:110011686-110011736	GM12892	blood:	n/a
31	chr6:110012874-110012924	HCT-116	colon:	n/a
32	chr6:110012378-110012428	SK-N-MC	brain:	n/a
33	chr6:110011156-110011206	GM12891	blood:	n/a
34	chr6:110012180-110012230	HNPCEpiC	eye:	n/a
35	chr6:110015052-110015102	NH-A	brain:	n/a
36	chr6:109960018-109960068	HUVEC	blood vessel:	n/a
37	chr6:109960018-109960068	BJ	skin:	n/a
38	chr6:110012577-110012627	SK-N-SH	brain:	n/a
39	chr6:110012409-110012459	AG09309	skin:	n/a
40	chr6:110012874-110012924	NHDF-neo	bronchial:	n/a
41	chr6:110012409-110012459	HAEpiC	amniotic membrane:	n/a
42	chr6:110012366-110012416	AG09309	skin:	n/a
43	chr6:110015052-110015102	AG04450	lung:	fetal
44	chr6:110012874-110012924	HCM	heart:	n/a
45	chr6:110011999-110012049	HRPEpiC	eye:	n/a
46	chr6:109960018-109960068	PANC-1	pancreas:	n/a
47	chr6:110009743-110009793	NT2-D1	testis:	n/a
48	chr6:109960018-109960068	AG04449	skin:	fetal
49	chr6:110012591-110012641	HRE	kidney:	n/a
50	chr6:110012386-110012436	GM12878	blood:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:110026144..110026871-chr6:110500143..110501053,2	MCF-7	breast:
2	chr6:110009150..110010856-chr6:110010893..110012924,2	MCF-7	breast:
3	chr6:110006952..110010658-chr6:110010983..110015603,5	K562	blood:
4	chr6:109916966..109917798-chr6:110016397..110017380,5	MCF-7	breast:
5	chr6:109963602..109966014-chr6:110009596..110012309,2	MCF-7	breast:
6	chr6:110026127..110027055-chr6:110711820..110712448,2	MCF-7	breast:
7	chr6:110012433..110012940-chr8:145634538..145635256,2	Hela-S3	cervix:
8	chr6:110001528..110003303-chr6:110005576..110008412,2	MCF-7	breast:
9	chr6:109978242..109980545-chr6:109984478..109986308,2	K562	blood:
10	chr6:109996616..109999325-chr6:110011516..110013836,2	K562	blood:
11	chr6:110047914..110050234-chr6:110051143..110053248,2	MCF-7	breast:
12	chr6:110026116..110027123-chr6:110104149..110105170,4	MCF-7	breast:
13	chr6:110026132..110026688-chr6:110711506..110712260,2	MCF-7	breast:
14	chr6:110026617..110027143-chr6:110372925..110373520,2	MCF-7	breast:
15	chr6:110026208..110027002-chr6:110360378..110361549,3	K562	blood:
16	chr6:110026295..110027102-chr6:110374620..110375475,7	K562	blood:
17	chr6:110025993..110027032-chr6:110374302..110375553,10	MCF-7	breast:
18	chr6:110017902..110019926-chr6:110022450..110025001,2	K562	blood:
19	chr6:109982568..109985653-chr6:110007788..110010480,3	K562	blood:
20	chr6:110042492..110045032-chr6:110370097..110372632,2	MCF-7	breast:
21	chr6:110026131..110026685-chr6:110213854..110214493,2	MCF-7	breast:
22	chr6:110026058..110027053-chr6:110360200..110361829,12	MCF-7	breast:
23	chr6:110025954..110027208-chr6:110359665..110362381,41	MCF-7	breast:
24	chr6:109848106..109848779-chr6:110026265..110026944,2	MCF-7	breast:
25	chr6:110001528..110003303-chr6:110005576..110008412,2	MCF-7	breast:
26	chr6:109916901..109917812-chr6:110016606..110017379,4	MCF-7	breast:
27	chr6:109847917..109848863-chr6:110026120..110026805,4	MCF-7	breast:
28	chr6:109917095..109917599-chr6:110026112..110027051,2	MCF-7	breast:
29	chr6:109509121..109509682-chr6:110026304..110027085,2	K562	blood:
30	chr6:109983707..109985653-chr6:110007788..110010480,2	K562	blood:
31	chr6:110025916..110027085-chr6:110711360..110712730,11	K562	blood:
32	chr6:110024804..110028000-chr6:110359372..110362087,3	MCF-7	breast:
33	chr6:110026083..110027087-chr6:110374560..110375697,12	MCF-7	breast:
34	chr6:110047914..110050234-chr6:110051143..110053248,2	MCF-7	breast:

No data

Variant related genes	Relation type
AK9	TF binding region
FIG4	TF binding region
AK9	CpG island
FIG4	CpG island
ENSG00000155085	chromatin interactions
ENSG00000272115	chromatin interactions
ENSG00000112290	chromatin interactions
ENSG00000071894	chromatin interactions
ENSG00000112367	chromatin interactions

Extended variants
information (count: 3550 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:3550 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9386829	chr6:109959269-109959270	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs56070965	chr6:109959346-109959347	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs111560106	chr6:109959348-109959349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575567903	chr6:109959359-109959360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572669855	chr6:109959365-109959366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143299218	chr6:109959470-109959471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75372232	chr6:109959494-109959495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146724780	chr6:109959519-109959520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563481016	chr6:109959545-109959546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529045021	chr6:109959546-109959547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548908693	chr6:109959612-109959613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565937052	chr6:109959671-109959672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534627800	chr6:109959676-109959677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375381578	chr6:109959681-109959682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188003510	chr6:109959737-109959738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571243846	chr6:109959792-109959793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537092261	chr6:109959820-109959821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554320131	chr6:109959829-109959830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs116385471	chr6:109959856-109959857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs116068788	chr6:109959863-109959864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35578424	chr6:109959866-109959867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555696390	chr6:109959928-109959929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554447918	chr6:109959942-109959943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183523541	chr6:109959947-109959948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541340283	chr6:109959963-109959964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558076787	chr6:109960016-109960017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574389714	chr6:109960018-109960019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188561440	chr6:109960070-109960071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540078926	chr6:109960084-109960085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572240329	chr6:109960101-109960102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191520925	chr6:109960109-109960110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529391784	chr6:109960118-109960119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542773073	chr6:109960163-109960164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559267111	chr6:109960197-109960198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528318871	chr6:109960225-109960226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551699746	chr6:109960229-109960230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571610922	chr6:109960258-109960259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530468573	chr6:109960316-109960317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114958319	chr6:109960318-109960319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140307356	chr6:109960362-109960363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535948032	chr6:109960363-109960364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553059527	chr6:109960383-109960384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566139327	chr6:109960428-109960429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150363977	chr6:109960431-109960432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138100005	chr6:109960448-109960449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544341345	chr6:109960460-109960461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs57395711	chr6:109960472-109960473	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs543385141	chr6:109960473-109960474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371911124	chr6:109960510-109960511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373356886	chr6:109960513-109960514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
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
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Autism	17483303	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
abnormal development	18461090	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:109928000-109966400	Weak transcription	Pancreas	Pancrea
2	chr6:109933000-109962800	Weak transcription	Left Ventricle	heart
3	chr6:109933000-109966400	Weak transcription	Brain Germinal Matrix	brain
4	chr6:109933000-109985200	Weak transcription	Psoas Muscle	Psoas
5	chr6:109945400-109966400	Weak transcription	Duodenum Mucosa	Duodenum
6	chr6:109947200-109966800	Weak transcription	Gastric	stomach
7	chr6:109947400-109961200	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr6:109948000-109995000	Weak transcription	Brain Anterior Caudate	brain
9	chr6:109949600-109961200	Weak transcription	Lung	lung
10	chr6:109949600-109961200	Weak transcription	Spleen	Spleen
11	chr6:109949800-109961200	Weak transcription	Fetal Brain Female	brain
12	chr6:109952200-109961200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr6:109953200-109963000	Weak transcription	Stomach Smooth Muscle	stomach
14	chr6:109953200-109966200	Weak transcription	Fetal Intestine Small	intestine
15	chr6:109953600-109961200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr6:109953800-109961200	Weak transcription	Liver	Liver
17	chr6:109953800-109961200	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr6:109953800-109963000	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr6:109953800-109966400	Weak transcription	Primary hematopoietic stem cells	blood
20	chr6:109953800-109980800	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr6:109954000-109961200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr6:109954000-109963000	Weak transcription	Primary B cells from cord blood	blood
23	chr6:109954000-109965200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr6:109954400-109994800	Weak transcription	Brain Hippocampus Middle	brain
25	chr6:109957600-109961200	Weak transcription	Aorta	Aorta
26	chr6:109957600-109961200	Weak transcription	Thymus	Thymus
27	chr6:109958200-109959400	Enhancers	Primary T cells from cord blood	blood
28	chr6:109959400-109975200	Weak transcription	Primary T cells from cord blood	blood
29	chr6:109960000-109984000	Weak transcription	Brain Cingulate Gyrus	brain
30	chr6:109960800-109961200	Weak transcription	Right Ventricle	heart
31	chr6:109960800-109961200	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr6:109961200-109961400	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
33	chr6:109961200-109961600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
34	chr6:109961200-109961600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr6:109961200-109961600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr6:109961200-109961600	ZNF genes & repeats	Adipose Nuclei	Adipose
37	chr6:109961200-109961600	ZNF genes & repeats	Aorta	Aorta
38	chr6:109961200-109961600	ZNF genes & repeats	Liver	Liver
39	chr6:109961200-109961600	ZNF genes & repeats	Brain Angular Gyrus	brain
40	chr6:109961200-109961600	ZNF genes & repeats	Brain Substantia Nigra	brain
41	chr6:109961200-109961600	ZNF genes & repeats	Fetal Brain Female	brain
42	chr6:109961200-109961600	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
43	chr6:109961200-109961600	ZNF genes & repeats	Thymus	Thymus
44	chr6:109961200-109961600	ZNF genes & repeats	Spleen	Spleen
45	chr6:109961200-109961800	ZNF genes & repeats	Lung	lung
46	chr6:109961200-109961800	ZNF genes & repeats	Right Ventricle	heart
47	chr6:109961200-109962000	Strong transcription	Brain Inferior Temporal Lobe	brain
48	chr6:109961400-110000800	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr6:109961600-109963000	Weak transcription	Aorta	Aorta
50	chr6:109961600-109963200	Weak transcription	Liver	Liver

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