Variant report

Variant	nsv604484
Chromosome Location	chr6:109851937-109997529
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:430)
CpG islands
(count:368)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:109947743-109947775	HepG2	liver:	n/a	n/a
2	BATF	chr6:109953633-109953962	GM12878	blood:	n/a	n/a
3	BATF	chr6:109900545-109900857	GM12878	blood:	n/a	chr6:109900728-109900739
4	BATF	chr6:109900613-109900853	GM12878	blood:	n/a	chr6:109900728-109900739
5	BCL11A	chr6:109900625-109900952	GM12878	blood:	n/a	n/a
6	BCL11A	chr6:109900625-109900865	GM12878	blood:	n/a	n/a
7	BHLHE40	chr6:109901915-109901921	K562	blood:	n/a	n/a
8	CEBPB	chr6:109947555-109947885	HepG2	liver:	n/a	n/a
9	CEBPB	chr6:109952623-109952968	HepG2	liver:	n/a	chr6:109952785-109952796
10	CEBPB	chr6:109952629-109952933	A549	lung:	n/a	chr6:109952785-109952796
11	CEBPB	chr6:109861487-109861561	HepG2	liver:	n/a	chr6:109861533-109861544
12	CEBPB	chr6:109957648-109957810	K562	blood:	n/a	n/a
13	CEBPB	chr6:109952640-109952967	IMR90	lung:	n/a	chr6:109952785-109952796
14	CEBPB	chr6:109952735-109952897	K562	blood:	n/a	chr6:109952785-109952796
15	CEBPB	chr6:109957671-109957789	A549	lung:	n/a	n/a
16	CHD2	chr6:109853047-109853048	HepG2	liver:	n/a	n/a
17	CTCF	chr6:109917229-109917367	GM13976	blood:	n/a	n/a
18	CTCF	chr6:109917220-109917370	GM12866	blood:	n/a	n/a
19	CTCF	chr6:109917180-109917330	HAc	cerebellar:	n/a	n/a
20	CTCF	chr6:109917280-109917430	GM12873	blood:	n/a	n/a
21	CTCF	chr6:109851767-109852093	GM12878	blood:	n/a	n/a
22	CTCF	chr6:109917240-109917390	HepG2	liver:	n/a	n/a
23	CTCF	chr6:109917189-109917375	K562	blood:	n/a	n/a
24	CTCF	chr6:109917260-109917410	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr6:109917220-109917370	AG10803	skin:	n/a	n/a
26	CTCF	chr6:109917209-109917450	MCF-7	breast:	n/a	n/a
27	CTCF	chr6:109917260-109917410	HFF	foreskin:	n/a	n/a
28	CTCF	chr6:109917240-109917390	AG04449	skin:	n/a	n/a
29	CTCF	chr6:109917212-109917408	LNCaP	prostate:	n/a	n/a
30	CTCF	chr6:109917240-109917390	BE2_C	brain:	n/a	n/a
31	CTCF	chr6:109917240-109917390	GM12866	blood:	n/a	n/a
32	CTCF	chr6:109917300-109917450	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr6:109917260-109917410	HEK293	kidney:	n/a	n/a
34	CTCF	chr6:109917260-109917410	GM12872	blood:	n/a	n/a
35	CTCF	chr6:109917240-109917390	GM12875	blood:	n/a	n/a
36	CTCF	chr6:109917233-109917350	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr6:109917420-109917570	HAc	cerebellar:	n/a	n/a
38	CTCF	chr6:109917280-109917430	GM12874	blood:	n/a	n/a
39	CTCF	chr6:109949380-109949530	GM12868	blood:	n/a	n/a
40	CTCF	chr6:109917200-109917350	NB4	blood:	n/a	n/a
41	CTCF	chr6:109917240-109917390	GM12873	blood:	n/a	n/a
42	CTCF	chr6:109917215-109917423	NHEK	skin:	n/a	n/a
43	CTCF	chr6:109917280-109917430	HepG2	liver:	n/a	n/a
44	CTCF	chr6:109917360-109917510	WI-38	lung:	n/a	n/a
45	CTCF	chr6:109917224-109917398	GM10266	blood:	n/a	n/a
46	CTCF	chr6:109917260-109917410	SAEC	small airway:	n/a	n/a
47	CTCF	chr6:109978084-109978136	GM10248	blood:	n/a	n/a
48	CTCF	chr6:109917480-109917630	NHEK	skin:	n/a	n/a
49	CTCF	chr6:109917259-109917362	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr6:109917220-109917370	WI-38	lung:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:109868066-109868116	SAEC	small airway:	n/a
2	chr6:109868066-109868116	T-47D	breast:	n/a
3	chr6:109868066-109868116	SAEC	small airway:	n/a
4	chr6:109868066-109868116	T-47D	breast:	n/a
5	chr6:109868066-109868116	A549	lung:	n/a
6	chr6:109868066-109868116	BJ	skin:	n/a
7	chr6:109953157-109953207	A549	lung:	n/a
8	chr6:109960018-109960068	SK-N-MC	brain:	n/a
9	chr6:109953157-109953207	AG04450	lung:	fetal
10	chr6:109940408-109940458	HepG2	liver:	n/a
11	chr6:109868066-109868116	NB4	blood:	n/a
12	chr6:109868066-109868116	PrEC	prostate:	n/a
13	chr6:109941310-109941360	BE2_C	brain:	n/a
14	chr6:109953157-109953207	SKMC	muscle:	n/a
15	chr6:109868066-109868116	Hela-S3	cervix:	n/a
16	chr6:109953157-109953207	NHDF-neo	bronchial:	n/a
17	chr6:109868066-109868116	SK-N-SH	brain:	n/a
18	chr6:109953157-109953207	HNPCEpiC	eye:	n/a
19	chr6:109960018-109960068	HEEpiC	esophagus:	n/a
20	chr6:109941310-109941360	GM06990	blood:	n/a
21	chr6:109871787-109871837	HCF	heart:	n/a
22	chr6:109871787-109871837	PANC-1	pancreas:	n/a
23	chr6:109871787-109871837	NT2-D1	testis:	n/a
24	chr6:109960018-109960068	HEK293	kidney:	embryo
25	chr6:109953157-109953207	HEEpiC	esophagus:	n/a
26	chr6:109953157-109953207	SK-N-MC	brain:	n/a
27	chr6:109871787-109871837	HCPEpiC	choroid plexus:	n/a
28	chr6:109953157-109953207	RPTEC	kidney:	n/a
29	chr6:109960018-109960068	T-47D	breast:	n/a
30	chr6:109953157-109953207	AG10803	skin:	n/a
31	chr6:109868066-109868116	ProgFib	skin:	n/a
32	chr6:109871787-109871837	MCF10A-Er-Src	breast:	n/a
33	chr6:109953157-109953207	Caco-2	colon:	n/a
34	chr6:109941310-109941360	HCPEpiC	choroid plexus:	n/a
35	chr6:109941310-109941360	NT2-D1	testis:	n/a
36	chr6:109960018-109960068	AoSMC	blood vessel:	n/a
37	chr6:109941310-109941360	RPTEC	kidney:	n/a
38	chr6:109960018-109960068	Hepatocyte	liver:	n/a
39	chr6:109941310-109941360	SK-N-SH_RA	brain:	n/a
40	chr6:109960018-109960068	HCM	heart:	n/a
41	chr6:109941310-109941360	GM12878	blood:	n/a
42	chr6:109871787-109871837	AG04449	skin:	fetal
43	chr6:109940408-109940458	SK-N-SH	brain:	n/a
44	chr6:109871787-109871837	AoSMC	blood vessel:	n/a
45	chr6:109941310-109941360	PFSK-1	brain:	n/a
46	chr6:109960018-109960068	SAEC	small airway:	n/a
47	chr6:109940408-109940458	PFSK-1	brain:	n/a
48	chr6:109941310-109941360	AG04450	lung:	fetal
49	chr6:109868066-109868116	CMK	blood:	n/a
50	chr6:109940408-109940458	BE2_C	brain:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:109916901..109917812-chr6:110016606..110017379,4	MCF-7	breast:
2	chr6:109963602..109966014-chr6:110009596..110012309,2	MCF-7	breast:
3	chr6:109996616..109999325-chr6:110011516..110013836,2	K562	blood:
4	chr6:109978242..109980545-chr6:109984478..109986308,2	K562	blood:
5	chr6:109927783..109929912-chr6:109931522..109933858,2	K562	blood:
6	chr6:109932824..109934658-chr6:109936171..109939061,2	K562	blood:
7	chr6:109916966..109917798-chr6:110016397..110017380,5	MCF-7	breast:
8	chr6:109926146..109927722-chr6:109932421..109934095,2	MCF-7	breast:
9	chr6:109926146..109927722-chr6:109932421..109934095,2	MCF-7	breast:
10	chr6:109932824..109934658-chr6:109936171..109939061,2	K562	blood:
11	chr6:109927783..109929912-chr6:109931522..109933858,2	K562	blood:
12	chr6:109917095..109917599-chr6:110026112..110027051,2	MCF-7	breast:

No data

Variant related genes	Relation type
AK9	TF binding region
AK9	CpG island
ENSG00000112367	chromatin interactions
ENSG00000155085	chromatin interactions

Extended variants
information (count: 5554 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:5554 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11969939	chr6:109851937-109851938	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185375455	chr6:109851939-109851940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529571410	chr6:109852024-109852025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149845927	chr6:109852074-109852075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190626240	chr6:109852075-109852076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528547395	chr6:109852143-109852144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548881778	chr6:109852162-109852163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs111252195	chr6:109852179-109852180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182930342	chr6:109852189-109852190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs114785270	chr6:109852223-109852224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs143176119	chr6:109852224-109852225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185744645	chr6:109852236-109852237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536563553	chr6:109852239-109852240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552964561	chr6:109852240-109852241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528231327	chr6:109852244-109852245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs67553535	chr6:109852245-109852246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs4946983	chr6:109852249-109852250	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs146681000	chr6:109852275-109852276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs75435553	chr6:109852291-109852292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs575333266	chr6:109852298-109852299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543589356	chr6:109852348-109852349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75510907	chr6:109852386-109852387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs116328153	chr6:109852390-109852391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs190892756	chr6:109852421-109852422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77051723	chr6:109852472-109852473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536076569	chr6:109852499-109852500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555527006	chr6:109852533-109852534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs528475572	chr6:109852548-109852549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183683703	chr6:109852552-109852553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372062365	chr6:109852573-109852574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73523129	chr6:109852613-109852614	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs73523131	chr6:109852650-109852651	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs149387237	chr6:109852700-109852701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567478221	chr6:109852724-109852725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536503084	chr6:109852759-109852760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs188038275	chr6:109852788-109852789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192314937	chr6:109852793-109852794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538241481	chr6:109852844-109852845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183386035	chr6:109852856-109852857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575221922	chr6:109852858-109852859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs537564668	chr6:109852883-109852884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557095162	chr6:109852894-109852895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs573902445	chr6:109852911-109852912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs749517	chr6:109852916-109852917	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs187109948	chr6:109852922-109852923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573507385	chr6:109852933-109852934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs374694278	chr6:109852983-109852984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577932192	chr6:109853007-109853008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73523133	chr6:109853045-109853046	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs115147410	chr6:109853049-109853050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:653 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:109838600-109861400	Weak transcription	Thymus	Thymus
2	chr6:109848400-109865600	Weak transcription	Aorta	Aorta
3	chr6:109848400-109870400	Weak transcription	Primary B cells from peripheral blood	blood
4	chr6:109850800-109870000	Weak transcription	Left Ventricle	heart
5	chr6:109851000-109853000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr6:109851400-109854400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr6:109852200-109878400	Weak transcription	Pancreas	Pancrea
8	chr6:109852400-109853000	Enhancers	Stomach Smooth Muscle	stomach
9	chr6:109852400-109853200	Enhancers	HSMMtube	muscle
10	chr6:109853000-109853200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr6:109853000-109853600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr6:109853600-109853800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr6:109859200-109868000	Weak transcription	Spleen	Spleen
14	chr6:109859200-109873000	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr6:109860200-109870000	Weak transcription	Adipose Nuclei	Adipose
16	chr6:109860400-109861000	Weak transcription	Fetal Thymus	thymus
17	chr6:109860600-109870000	Weak transcription	Brain Hippocampus Middle	brain
18	chr6:109860800-109866400	Weak transcription	Primary T cells from cord blood	blood
19	chr6:109861000-109861600	ZNF genes & repeats	Fetal Thymus	thymus
20	chr6:109861000-109862600	Weak transcription	Stomach Smooth Muscle	stomach
21	chr6:109861200-109861800	ZNF genes & repeats	Lung	lung
22	chr6:109861200-109870200	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr6:109861400-109862200	ZNF genes & repeats	Thymus	Thymus
24	chr6:109861600-109862000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
25	chr6:109861600-109862200	ZNF genes & repeats	Primary B cells from cord blood	blood
26	chr6:109861600-109862200	Strong transcription	Fetal Thymus	thymus
27	chr6:109861600-109866400	Weak transcription	Ovary	ovary
28	chr6:109861800-109862200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
29	chr6:109861800-109862200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr6:109861800-109866400	Weak transcription	Lung	lung
31	chr6:109862000-109862200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr6:109862200-109866400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr6:109862200-109867200	Weak transcription	Fetal Thymus	thymus
34	chr6:109862200-109869600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr6:109862200-109869600	Weak transcription	Primary hematopoietic stem cells	blood
36	chr6:109862200-109870000	Weak transcription	Primary B cells from cord blood	blood
37	chr6:109862200-109878200	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr6:109862200-109878400	Weak transcription	Thymus	Thymus
39	chr6:109863000-109870000	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr6:109863200-109866000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr6:109863600-109867800	Weak transcription	Rectal Smooth Muscle	rectum
42	chr6:109864200-109870200	Weak transcription	Brain Anterior Caudate	brain
43	chr6:109864200-109870200	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr6:109865000-109867600	Weak transcription	Fetal Brain Female	brain
45	chr6:109865400-109870000	Weak transcription	Liver	Liver
46	chr6:109865600-109865800	ZNF genes & repeats	Aorta	Aorta
47	chr6:109865800-109866600	Weak transcription	Aorta	Aorta
48	chr6:109865800-109869000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:109866400-109866600	ZNF genes & repeats	Lung	lung
50	chr6:109866400-109867000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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