Variant report

Variant	nsv886160
Chromosome Location	chr6:74305276-74341589
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	ARID3A	chr6:74320193-74320518	K562	blood:	n/a	n/a
2	ARID3A	chr6:74318607-74318812	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:74320184-74320573	HepG2	liver:	n/a	n/a
4	BACH1	chr6:74307995-74308040	K562	blood:	n/a	n/a
5	BCLAF1	chr6:74320128-74320611	GM12878	blood:	n/a	n/a
6	CEBPB	chr6:74305419-74305551	A549	lung:	n/a	n/a
7	CEBPB	chr6:74305413-74305544	K562	blood:	n/a	n/a
8	CEBPB	chr6:74327490-74327557	K562	blood:	n/a	n/a
9	CEBPB	chr6:74334641-74334960	K562	blood:	n/a	chr6:74334817-74334828
10	CEBPB	chr6:74332408-74332484	K562	blood:	n/a	chr6:74332449-74332460 chr6:74332411-74332424 chr6:74332449-74332460
11	CEBPB	chr6:74305386-74305580	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr6:74320256-74320489	Medullo	brain:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
13	CTCF	chr6:74320107-74320630	HCT-116	colon:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
14	CTCF	chr6:74320147-74320586	GM12878	blood:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
15	CTCF	chr6:74320280-74320430	GM12872	blood:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
16	CTCF	chr6:74320241-74320485	Hela-S3	cervix:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
17	CTCF	chr6:74320260-74320410	GM12870	blood:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
18	CTCF	chr6:74320540-74320690	GM12874	blood:	n/a	n/a
19	CTCF	chr6:74324741-74324853	K562	blood:	n/a	n/a
20	CTCF	chr6:74320280-74320430	HUVEC	blood vessel:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
21	CTCF	chr6:74320280-74320430	HFF	foreskin:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
22	CTCF	chr6:74320320-74320470	HCM	heart:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
23	CTCF	chr6:74320300-74320450	HCPEpiC	choroid plexus:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
24	CTCF	chr6:74324720-74324870	Caco-2	colon:	n/a	n/a
25	CTCF	chr6:74316226-74316426	K562	blood:	n/a	n/a
26	CTCF	chr6:74316304-74316413	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr6:74320300-74320450	Hela-S3	cervix:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
28	CTCF	chr6:74320320-74320470	AG09319	gingival:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
29	CTCF	chr6:74320280-74320430	A549	lung:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
30	CTCF	chr6:74316298-74316428	GM12878	blood:	n/a	n/a
31	CTCF	chr6:74316306-74316406	MCF-7	breast:	n/a	n/a
32	CTCF	chr6:74320280-74320430	GM12873	blood:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
33	CTCF	chr6:74316317-74316386	MCF-7	breast:	n/a	n/a
34	CTCF	chr6:74320240-74320390	NB4	blood:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
35	CTCF	chr6:74320096-74320580	K562	blood:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
36	CTCF	chr6:74320360-74320510	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr6:74320280-74320430	AG09309	skin:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
38	CTCF	chr6:74320240-74320390	Hela-S3	cervix:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
39	CTCF	chr6:74316322-74316391	GM12891	blood:	n/a	n/a
40	CTCF	chr6:74320300-74320450	BE2_C	brain:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
41	CTCF	chr6:74320240-74320390	HRPEpiC	eye:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
42	CTCF	chr6:74320290-74320478	GM10248	blood:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
43	CTCF	chr6:74320257-74320491	Pancreas_OC	pancreas:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
44	CTCF	chr6:74320280-74320430	GM12867	blood:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
45	CTCF	chr6:74320032-74320711	A549	lung:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
46	CTCF	chr6:74320280-74320430	HPAF	blood vessel:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
47	CTCF	chr6:74320276-74320475	LNCaP	prostate:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
48	CTCF	chr6:74320240-74320390	HEK293	kidney:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
49	CTCF	chr6:74320229-74320523	Spleen_OC	spleen:	n/a	chr6:74320353-74320374 chr6:74320358-74320376
50	CTCF	chr6:74324636-74324905	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:74294601..74296941-chr6:74314591..74316170,2	K562	blood:
2	chr6:74223088..74226507-chr6:74303403..74307438,4	K562	blood:
3	chr6:74304294..74306000-chr6:74307805..74310134,2	MCF-7	breast:
4	chr6:74219940..74235097-chr6:74314890..74324923,44	MCF-7	breast:
5	chr6:74287356..74290171-chr6:74314710..74316586,2	MCF-7	breast:
6	chr6:74304109..74305737-chr6:74318220..74319814,2	K562	blood:
7	chr6:74231875..74233471-chr6:74332835..74334648,2	K562	blood:
8	chr6:74303250..74306152-chr6:74307378..74309370,2	K562	blood:
9	chr6:74312525..74315005-chr6:74316974..74319869,2	K562	blood:
10	chr6:74315170..74318004-chr6:74318140..74320478,4	K562	blood:
11	chr6:74304109..74305737-chr6:74318220..74319814,2	K562	blood:
12	chr6:74304294..74306000-chr6:74307805..74310134,2	MCF-7	breast:
13	chr6:74224257..74227085-chr6:74333037..74337394,5	K562	blood:
14	chr6:74310744..74313637-chr6:74316920..74318819,2	MCF-7	breast:
15	chr6:74313794..74316156-chr6:74316863..74318391,2	MCF-7	breast:
16	chr6:74311981..74314645-chr6:74316596..74320386,3	MCF-7	breast:
17	chr6:74293673..74296243-chr6:74316721..74319519,2	MCF-7	breast:
18	chr6:74227785..74235725-chr6:74313522..74322840,21	MCF-7	breast:
19	chr6:74236818..74238643-chr6:74323624..74325300,2	K562	blood:
20	chr6:74321133..74323534-chr6:74341281..74343940,2	K562	blood:
21	chr6:74230217..74232050-chr6:74335341..74337314,2	MCF-7	breast:
22	chr6:74236552..74238220-chr6:74320205..74322243,2	MCF-7	breast:
23	chr6:74310744..74313637-chr6:74316920..74318819,2	MCF-7	breast:
24	chr6:74218426..74219208-chr6:74319917..74320421,2	K562	blood:
25	chr6:74313794..74316156-chr6:74316863..74318391,2	MCF-7	breast:
26	chr6:74221668..74234853-chr6:74311080..74327130,62	K562	blood:
27	chr6:74231646..74233694-chr6:74302777..74306194,3	MCF-7	breast:
28	chr6:74305928..74307842-chr6:74313274..74316085,2	K562	blood:
29	chr6:74317037..74319356-chr6:74320974..74322634,2	MCF-7	breast:
30	chr6:74229410..74231742-chr6:74312645..74314509,2	MCF-7	breast:
31	chr6:74217534..74219125-chr6:74306574..74309139,2	MCF-7	breast:
32	chr6:74225454..74225974-chr6:74319966..74320496,2	K562	blood:
33	chr6:74341293..74343216-chr6:74345270..74346833,2	MCF-7	breast:
34	chr6:74317037..74319356-chr6:74320974..74322634,2	MCF-7	breast:
35	chr6:74225322..74227120-chr6:74304460..74305982,2	K562	blood:
36	chr6:74158484..74160884-chr6:74318973..74320604,2	MCF-7	breast:
37	chr6:74229155..74231796-chr6:74303421..74306313,3	MCF-7	breast:
38	chr6:74311981..74314645-chr6:74316596..74320386,3	MCF-7	breast:
39	chr6:74295297..74298408-chr6:74308010..74309896,3	MCF-7	breast:
40	chr6:74228508..74231368-chr6:74339913..74342882,2	K562	blood:
41	chr6:74305928..74307842-chr6:74313274..74316085,2	K562	blood:
42	chr6:74318714..74320214-chr6:74328892..74331642,2	MCF-7	breast:
43	chr6:74303250..74306152-chr6:74307378..74309370,2	K562	blood:
44	chr6:74321133..74323534-chr6:74341281..74343940,2	K562	blood:
45	chr6:74321340..74324338-chr6:74361477..74364146,2	MCF-7	breast:
46	chr6:74320124..74323054-chr6:74351713..74353933,2	MCF-7	breast:
47	chr6:74318714..74320214-chr6:74328892..74331642,2	MCF-7	breast:
48	chr6:74313554..74316552-chr6:74335667..74338657,2	K562	blood:
49	chr6:74228636..74231731-chr6:74306040..74309055,4	K562	blood:
50	chr6:74221323..74236726-chr6:74306065..74338770,101	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD109-4	chr6:74328069-74328320	NONHSAT113576

Variant related genes	Relation type
RPS27P15	TF binding region
ENSG00000229862	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000223967	chromatin interactions
ENSG00000119899	chromatin interactions

Extended variants
information (count: 1612 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1612 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12528608	chr6:74305276-74305277	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553216331	chr6:74305355-74305356	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs72947457	chr6:74305393-74305394	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs530277782	chr6:74305399-74305400	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs112632355	chr6:74305463-74305464	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs453979	chr6:74305477-74305478	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs445098	chr6:74305479-74305480	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs540213663	chr6:74305493-74305494	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs190612494	chr6:74305496-74305497	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs552151546	chr6:74305504-74305505	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs375131280	chr6:74305505-74305506	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs368506243	chr6:74305524-74305525	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs560477642	chr6:74305531-74305532	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs145295573	chr6:74305542-74305543	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs532292859	chr6:74305593-74305594	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs550817698	chr6:74305627-74305628	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs569514807	chr6:74305628-74305629	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs536406299	chr6:74305639-74305640	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs548415801	chr6:74305640-74305641	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs566562810	chr6:74305652-74305653	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs62438427	chr6:74305656-74305657	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs9442926	chr6:74305661-74305662	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs201350274	chr6:74305671-74305672	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs192979886	chr6:74305686-74305687	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs137925056	chr6:74305705-74305706	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs140942085	chr6:74305709-74305710	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs537456758	chr6:74305772-74305773	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs374505330	chr6:74305790-74305791	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs556785226	chr6:74305820-74305821	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs13207999	chr6:74305851-74305852	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs9352012	chr6:74305875-74305876	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs545004578	chr6:74305881-74305882	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs541977730	chr6:74305931-74305932	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs564896449	chr6:74305963-74305964	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs144578132	chr6:74305973-74305974	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs546313939	chr6:74306072-74306073	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs564439219	chr6:74306074-74306075	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs184274806	chr6:74306104-74306105	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs549913484	chr6:74306108-74306109	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs562763383	chr6:74306118-74306119	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs138538841	chr6:74306160-74306161	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs548399606	chr6:74306182-74306183	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs566699339	chr6:74306241-74306242	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs76816192	chr6:74306270-74306271	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs367599983	chr6:74306271-74306272	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs12191213	chr6:74306282-74306283	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs570475602	chr6:74306297-74306298	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs537800877	chr6:74306318-74306319	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs188652477	chr6:74306350-74306351	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs574791003	chr6:74306351-74306352	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	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
Prostate cancer	16573809	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:930 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74289600-74309600	Weak transcription	Lung	lung
2	chr6:74289600-74323800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:74290600-74305800	Weak transcription	Fetal Muscle Trunk	muscle
4	chr6:74290600-74318400	Weak transcription	Small Intestine	intestine
5	chr6:74290600-74338800	Weak transcription	Ovary	ovary
6	chr6:74291000-74307200	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr6:74291000-74315800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr6:74291000-74323600	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr6:74295200-74321800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr6:74296000-74317200	Weak transcription	Fetal Brain Female	brain
11	chr6:74296200-74317800	Weak transcription	Colonic Mucosa	Colon
12	chr6:74296200-74317800	Weak transcription	Gastric	stomach
13	chr6:74296200-74322200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:74296200-74322400	Weak transcription	Brain Germinal Matrix	brain
15	chr6:74296200-74332000	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr6:74296400-74307200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr6:74296400-74307200	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr6:74296400-74307400	Weak transcription	Brain Cingulate Gyrus	brain
19	chr6:74296400-74309000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr6:74296400-74309000	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr6:74296400-74316000	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr6:74296400-74316400	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr6:74296400-74318400	Weak transcription	Aorta	Aorta
24	chr6:74296400-74318400	Weak transcription	Rectal Smooth Muscle	rectum
25	chr6:74296400-74325800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr6:74296400-74354800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr6:74296400-74354800	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr6:74296400-74355000	Weak transcription	Fetal Brain Male	brain
29	chr6:74296600-74307400	Weak transcription	Brain Angular Gyrus	brain
30	chr6:74296600-74307400	Weak transcription	Brain Anterior Caudate	brain
31	chr6:74296600-74308000	Weak transcription	NHEK	skin
32	chr6:74296600-74309000	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr6:74296600-74317600	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr6:74296600-74317800	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr6:74296600-74319200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr6:74296600-74324000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr6:74296600-74324200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr6:74296600-74324400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr6:74296600-74344000	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr6:74296800-74307400	Weak transcription	Brain Hippocampus Middle	brain
41	chr6:74296800-74309200	Weak transcription	NH-A	brain
42	chr6:74296800-74316200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr6:74296800-74334000	Weak transcription	Fetal Lung	lung
44	chr6:74297000-74307200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr6:74297000-74307200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr6:74297000-74307400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr6:74297000-74307400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr6:74297000-74313200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr6:74297000-74313400	Weak transcription	Primary hematopoietic stem cells	blood
50	chr6:74297000-74313800	Weak transcription	Fetal Thymus	thymus

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