Variant report

Variant	nsv538416
Chromosome Location	chr6:109868058-109987502
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:377)
CpG islands
(count:367)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr6:109900613-109900853	GM12878	blood:	n/a	chr6:109900728-109900739
3	BATF	chr6:109900545-109900857	GM12878	blood:	n/a	chr6:109900728-109900739
4	BATF	chr6:109953633-109953962	GM12878	blood:	n/a	n/a
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	chr6:109957648-109957810	K562	blood:	n/a	n/a
9	CEBPB	chr6:109957671-109957789	A549	lung:	n/a	n/a
10	CEBPB	chr6:109952735-109952897	K562	blood:	n/a	chr6:109952785-109952796
11	CEBPB	chr6:109952629-109952933	A549	lung:	n/a	chr6:109952785-109952796
12	CEBPB	chr6:109952623-109952968	HepG2	liver:	n/a	chr6:109952785-109952796
13	CEBPB	chr6:109947555-109947885	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:109952640-109952967	IMR90	lung:	n/a	chr6:109952785-109952796
15	CTCF	chr6:109917240-109917390	AG09319	gingival:	n/a	n/a
16	CTCF	chr6:109917220-109917370	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr6:109917200-109917418	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr6:109917303-109917397	GM12891	blood:	n/a	n/a
19	CTCF	chr6:109898007-109898101	GM10248	blood:	n/a	n/a
20	CTCF	chr6:109917200-109917350	HVMF	connective:	n/a	n/a
21	CTCF	chr6:109898025-109898080	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr6:109917211-109917449	Gliobla	brain:	n/a	n/a
23	CTCF	chr6:109917260-109917410	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr6:109917256-109917405	MCF-7	breast:	n/a	n/a
25	CTCF	chr6:109917260-109917410	AG09309	skin:	n/a	n/a
26	CTCF	chr6:109917209-109917450	MCF-7	breast:	n/a	n/a
27	CTCF	chr6:109917280-109917430	HPF	lung:	n/a	n/a
28	CTCF	chr6:109917220-109917370	GM12873	blood:	n/a	n/a
29	CTCF	chr6:109917520-109917670	GM12875	blood:	n/a	n/a
30	CTCF	chr6:109917180-109917330	HFF-Myc	foreskin:	n/a	n/a
31	CTCF	chr6:109917200-109917350	GM12867	blood:	n/a	n/a
32	CTCF	chr6:109917240-109917390	HMF	breast:	n/a	n/a
33	CTCF	chr6:109917240-109917390	HMEC	breast:	n/a	n/a
34	CTCF	chr6:109917240-109917390	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr6:109917240-109917390	K562	blood:	n/a	n/a
36	CTCF	chr6:109917115-109917493	GM12878	blood:	n/a	n/a
37	CTCF	chr6:109917240-109917390	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr6:109917200-109917350	Caco-2	colon:	n/a	n/a
39	CTCF	chr6:109917222-109917396	GM13977	blood:	n/a	n/a
40	CTCF	chr6:109917220-109917370	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr6:109917220-109917370	AG10803	skin:	n/a	n/a
42	CTCF	chr6:109917201-109917417	LNCaP	prostate:	n/a	n/a
43	CTCF	chr6:109917115-109917474	IMR90	lung:	n/a	n/a
44	CTCF	chr6:109917200-109917350	HPF	lung:	n/a	n/a
45	CTCF	chr6:109917240-109917390	GM12866	blood:	n/a	n/a
46	CTCF	chr6:109917220-109917370	HMEC	breast:	n/a	n/a
47	CTCF	chr6:109916983-109917494	HCT-116	colon:	n/a	n/a
48	CTCF	chr6:109917225-109917414	K562	blood:	n/a	n/a
49	CTCF	chr6:109917220-109917370	GM06990	blood:	n/a	n/a
50	CTCF	chr6:109917240-109917390	WERI-Rb-1	eye:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:109960018-109960068	GM06990	blood:	n/a
2	chr6:109960018-109960068	GM06990	blood:	n/a
3	chr6:109940408-109940458	GM06990	blood:	n/a
4	chr6:109868066-109868116	HepG2	liver:	n/a
5	chr6:109868066-109868116	K562	blood:	n/a
6	chr6:109960018-109960068	NB4	blood:	n/a
7	chr6:109960018-109960068	HRPEpiC	eye:	n/a
8	chr6:109953157-109953207	SK-N-MC	brain:	n/a
9	chr6:109868066-109868116	HMEC	breast:	n/a
10	chr6:109871787-109871837	NB4	blood:	n/a
11	chr6:109941310-109941360	HIPEpiC	eye:	n/a
12	chr6:109940408-109940458	ProgFib	skin:	n/a
13	chr6:109960018-109960068	AG04450	lung:	fetal
14	chr6:109940408-109940458	Caco-2	colon:	n/a
15	chr6:109941310-109941360	K562	blood:	n/a
16	chr6:109868066-109868116	PFSK-1	brain:	n/a
17	chr6:109871787-109871837	HCM	heart:	n/a
18	chr6:109868066-109868116	PANC-1	pancreas:	n/a
19	chr6:109868066-109868116	AG09319	gingival:	n/a
20	chr6:109871787-109871837	BE2_C	brain:	n/a
21	chr6:109868066-109868116	H1-hESC	embryonic stem cell:	embryo
22	chr6:109871787-109871837	MCF-7	breast:	n/a
23	chr6:109940408-109940458	A549	lung:	n/a
24	chr6:109941310-109941360	HRCEpiC	kidney:	n/a
25	chr6:109941310-109941360	Caco-2	colon:	n/a
26	chr6:109941310-109941360	HPAEpiC	pulmonary alveolar:	n/a
27	chr6:109868066-109868116	AG04449	skin:	fetal
28	chr6:109940408-109940458	PANC-1	pancreas:	n/a
29	chr6:109871787-109871837	LNCaP	prostate:	n/a
30	chr6:109941310-109941360	GM12891	blood:	n/a
31	chr6:109953157-109953207	SK-N-SH_RA	brain:	n/a
32	chr6:109940408-109940458	NHDF-neo	bronchial:	n/a
33	chr6:109940408-109940458	SAEC	small airway:	n/a
34	chr6:109960018-109960068	GM12878	blood:	n/a
35	chr6:109960018-109960068	CMK	blood:	n/a
36	chr6:109940408-109940458	AG09319	gingival:	n/a
37	chr6:109940408-109940458	HepG2	liver:	n/a
38	chr6:109871787-109871837	HEEpiC	esophagus:	n/a
39	chr6:109940408-109940458	HCF	heart:	n/a
40	chr6:109868066-109868116	HCF	heart:	n/a
41	chr6:109953157-109953207	MCF10A-Er-Src	breast:	n/a
42	chr6:109868066-109868116	U87	brain:	n/a
43	chr6:109940408-109940458	HRCEpiC	kidney:	n/a
44	chr6:109871787-109871837	NHBE	bronchial:	n/a
45	chr6:109953157-109953207	MCF-7	breast:	n/a
46	chr6:109960018-109960068	Jurkat	blood:	n/a
47	chr6:109871787-109871837	PFSK-1	brain:	n/a
48	chr6:109871787-109871837	AG04449	skin:	fetal
49	chr6:109953157-109953207	HRE	kidney:	n/a
50	chr6:109871787-109871837	HNPCEpiC	eye:	n/a

(count:11 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 4474 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:4474 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187743726	chr6:109868067-109868068	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs192643956	chr6:109868071-109868072	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs183138645	chr6:109868099-109868100	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs546271316	chr6:109868128-109868129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566238718	chr6:109868261-109868262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542496615	chr6:109868262-109868263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562088263	chr6:109868277-109868278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562778096	chr6:109868297-109868298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368256049	chr6:109868298-109868299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527666532	chr6:109868312-109868313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547405720	chr6:109868327-109868328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564216789	chr6:109868330-109868331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs17070705	chr6:109868340-109868341	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs9487144	chr6:109868364-109868365	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs374081360	chr6:109868368-109868369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187228232	chr6:109868377-109868378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549278747	chr6:109868411-109868412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191680136	chr6:109868474-109868475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138550135	chr6:109868480-109868481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs9480973	chr6:109868519-109868520	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs142672101	chr6:109868528-109868529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146936399	chr6:109868554-109868555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184538306	chr6:109868613-109868614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188903770	chr6:109868623-109868624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs114273467	chr6:109868624-109868625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs193138267	chr6:109868636-109868637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs137974866	chr6:109868639-109868640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527541085	chr6:109868669-109868670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112741832	chr6:109868680-109868681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540983249	chr6:109868731-109868732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs9480974	chr6:109868764-109868765	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs533212912	chr6:109868806-109868807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73523152	chr6:109868807-109868808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535020435	chr6:109868821-109868822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376530730	chr6:109868835-109868836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529068098	chr6:109868874-109868875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185663455	chr6:109868895-109868896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189294319	chr6:109869017-109869018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116181618	chr6:109869018-109869019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551353079	chr6:109869023-109869024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200969609	chr6:109869050-109869051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74940921	chr6:109869051-109869052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs55899214	chr6:109869064-109869065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556687120	chr6:109869065-109869066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs398002587	chr6:109869068-109869069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs62436123	chr6:109869071-109869072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571209660	chr6:109869094-109869095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536693028	chr6:109869106-109869107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565277377	chr6:109869248-109869249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs146510845	chr6:109869254-109869255	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:555 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:109848400-109870400	Weak transcription	Primary B cells from peripheral blood	blood
2	chr6:109850800-109870000	Weak transcription	Left Ventricle	heart
3	chr6:109852200-109878400	Weak transcription	Pancreas	Pancrea
4	chr6:109859200-109873000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr6:109860200-109870000	Weak transcription	Adipose Nuclei	Adipose
6	chr6:109860600-109870000	Weak transcription	Brain Hippocampus Middle	brain
7	chr6:109861200-109870200	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr6:109862200-109869600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr6:109862200-109869600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr6:109862200-109870000	Weak transcription	Primary B cells from cord blood	blood
11	chr6:109862200-109878200	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr6:109862200-109878400	Weak transcription	Thymus	Thymus
13	chr6:109863000-109870000	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr6:109864200-109870200	Weak transcription	Brain Anterior Caudate	brain
15	chr6:109864200-109870200	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr6:109865400-109870000	Weak transcription	Liver	Liver
17	chr6:109865800-109869000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr6:109866400-109870200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr6:109867000-109869600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr6:109867000-109885800	Weak transcription	Ovary	ovary
21	chr6:109867400-109869600	Weak transcription	Primary T cells from cord blood	blood
22	chr6:109869600-109870600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
23	chr6:109869600-109870600	Strong transcription	Primary T cells from cord blood	blood
24	chr6:109869600-109870800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
25	chr6:109869600-109870800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr6:109869800-109870600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr6:109870000-109870600	ZNF genes & repeats	Adipose Nuclei	Adipose
28	chr6:109870000-109870600	ZNF genes & repeats	Brain Hippocampus Middle	brain
29	chr6:109870000-109870600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
30	chr6:109870000-109870600	ZNF genes & repeats	Left Ventricle	heart
31	chr6:109870000-109870800	Strong transcription	Primary B cells from cord blood	blood
32	chr6:109870000-109870800	ZNF genes & repeats	Liver	Liver
33	chr6:109870200-109870600	ZNF genes & repeats	Brain Anterior Caudate	brain
34	chr6:109870200-109870800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr6:109870200-109870800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
36	chr6:109870200-109871400	Strong transcription	Skeletal Muscle Male	skeletal muscle
37	chr6:109870400-109870800	Strong transcription	Primary B cells from peripheral blood	blood
38	chr6:109870400-109870800	ZNF genes & repeats	Psoas Muscle	Psoas
39	chr6:109870600-109872000	Weak transcription	Brain Anterior Caudate	brain
40	chr6:109870600-109878400	Weak transcription	Left Ventricle	heart
41	chr6:109870600-109878800	Weak transcription	Primary T cells from cord blood	blood
42	chr6:109870800-109873000	Weak transcription	Primary B cells from peripheral blood	blood
43	chr6:109870800-109873200	Weak transcription	Primary B cells from cord blood	blood
44	chr6:109871400-109884000	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr6:109873400-109873800	Enhancers	Dnd41	blood
46	chr6:109878200-109878400	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
47	chr6:109878400-109878800	ZNF genes & repeats	Pancreas	Pancrea
48	chr6:109878400-109879000	ZNF genes & repeats	Left Ventricle	heart
49	chr6:109878400-109879000	ZNF genes & repeats	Thymus	Thymus
50	chr6:109878400-109879600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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