Variant report

Variant	nsv884000
Chromosome Location	chr6:29924728-29937924
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:983)
CpG islands
(count:611)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:983 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:29935249-29935871	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:29931139-29931164	K562	blood:	n/a	n/a
3	ARID3A	chr6:29933775-29934240	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:29933748-29934309	K562	blood:	n/a	n/a
5	ARID3A	chr6:29934522-29934914	K562	blood:	n/a	n/a
6	ARID3A	chr6:29935252-29935904	K562	blood:	n/a	n/a
7	ARID3A	chr6:29932477-29933236	K562	blood:	n/a	n/a
8	ARID3A	chr6:29937042-29937091	K562	blood:	n/a	n/a
9	ARID3A	chr6:29932290-29932954	HepG2	liver:	n/a	n/a
10	ATF1	chr6:29935286-29935585	K562	blood:	n/a	n/a
11	ATF1	chr6:29932584-29933076	K562	blood:	n/a	n/a
12	ATF2	chr6:29932488-29932978	GM12878	blood:	n/a	n/a
13	ATF2	chr6:29932433-29933091	GM12878	blood:	n/a	n/a
14	ATF3	chr6:29932615-29932943	K562	blood:	n/a	n/a
15	ATF3	chr6:29932539-29933023	K562	blood:	n/a	n/a
16	BACH1	chr6:29932608-29933062	K562	blood:	n/a	n/a
17	BACH1	chr6:29932453-29933278	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr6:29932612-29932987	GM12878	blood:	n/a	chr6:29932797-29932808 chr6:29932798-29932808
19	BATF	chr6:29932589-29933017	GM12878	blood:	n/a	chr6:29932797-29932808 chr6:29932798-29932808
20	BCL11A	chr6:29932639-29932881	GM12878	blood:	n/a	chr6:29932797-29932806
21	BCL11A	chr6:29932602-29932969	GM12878	blood:	n/a	chr6:29932797-29932806
22	BCL3	chr6:29932533-29932943	GM12878	blood:	n/a	chr6:29932797-29932806
23	BCLAF1	chr6:29932428-29933119	GM12878	blood:	n/a	chr6:29932797-29932806
24	BCLAF1	chr6:29932494-29933203	GM12878	blood:	n/a	chr6:29932797-29932806
25	BHLHE40	chr6:29932569-29933159	K562	blood:	n/a	n/a
26	BHLHE40	chr6:29934607-29934610	GM12878	blood:	n/a	n/a
27	BHLHE40	chr6:29932548-29933279	GM12878	blood:	n/a	n/a
28	BHLHE40	chr6:29935166-29935758	K562	blood:	n/a	n/a
29	BHLHE40	chr6:29933714-29934091	HepG2	liver:	n/a	n/a
30	BHLHE40	chr6:29933866-29934118	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:29933686-29934301	K562	blood:	n/a	n/a
32	CBX3	chr6:29932403-29933273	HCT-116	colon:	n/a	n/a
33	CBX3	chr6:29935109-29935665	K562	blood:	n/a	n/a
34	CBX3	chr6:29935860-29936460	HCT-116	colon:	n/a	n/a
35	CBX3	chr6:29932608-29932997	K562	blood:	n/a	n/a
36	CBX3	chr6:29933685-29934511	HCT-116	colon:	n/a	n/a
37	CBX3	chr6:29935905-29936437	HCT-116	colon:	n/a	n/a
38	CBX3	chr6:29932504-29933475	K562	blood:	n/a	n/a
39	CCNT2	chr6:29935317-29935569	K562	blood:	n/a	n/a
40	CCNT2	chr6:29932623-29932970	K562	blood:	n/a	n/a
41	CEBPB	chr6:29935138-29935549	K562	blood:	n/a	chr6:29935249-29935260 chr6:29935210-29935221
42	CEBPB	chr6:29932426-29933189	K562	blood:	n/a	n/a
43	CEBPB	chr6:29932409-29933285	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr6:29933654-29933956	HepG2	liver:	n/a	n/a
45	CEBPB	chr6:29929562-29929884	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:29934230-29934543	IMR90	lung:	n/a	n/a
47	CEBPB	chr6:29936002-29936359	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr6:29935064-29935418	HepG2	liver:	n/a	chr6:29935249-29935260 chr6:29935210-29935221
49	CEBPB	chr6:29935073-29935816	K562	blood:	n/a	chr6:29935249-29935260 chr6:29935210-29935221
50	CEBPB	chr6:29932577-29933269	K562	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29933411-29933461	HCF	heart:	n/a
2	chr6:29933411-29933461	HCF	heart:	n/a
3	chr6:29933971-29934021	HRCEpiC	kidney:	n/a
4	chr6:29933915-29933965	HEEpiC	esophagus:	n/a
5	chr6:29928362-29928412	U87	brain:	n/a
6	chr6:29933971-29934021	HMEC	breast:	n/a
7	chr6:29928362-29928412	CMK	blood:	n/a
8	chr6:29928362-29928412	MCF10A-Er-Src	breast:	n/a
9	chr6:29933971-29934021	AG04449	skin:	fetal
10	chr6:29933411-29933461	HCM	heart:	n/a
11	chr6:29933915-29933965	HEK293	kidney:	embryo
12	chr6:29933925-29933975	ovcar-3	ovarian:	n/a
13	chr6:29932743-29932793	HAEpiC	amniotic membrane:	n/a
14	chr6:29933511-29933561	HepG2	liver:	n/a
15	chr6:29933697-29933747	HMEC	breast:	n/a
16	chr6:29932864-29932914	HCF	heart:	n/a
17	chr6:29932864-29932914	HCT-116	colon:	n/a
18	chr6:29928362-29928412	PrEC	prostate:	n/a
19	chr6:29933411-29933461	HCT-116	colon:	n/a
20	chr6:29932743-29932793	NB4	blood:	n/a
21	chr6:29933925-29933975	HUVEC	blood vessel:	n/a
22	chr6:29933971-29934021	HIPEpiC	eye:	n/a
23	chr6:29933411-29933461	NB4	blood:	n/a
24	chr6:29932864-29932914	AG04450	lung:	fetal
25	chr6:29933925-29933975	CMK	blood:	n/a
26	chr6:29933511-29933561	CMK	blood:	n/a
27	chr6:29933925-29933975	GM06990	blood:	n/a
28	chr6:29933971-29934021	PrEC	prostate:	n/a
29	chr6:29928362-29928412	HIPEpiC	eye:	n/a
30	chr6:29933697-29933747	ovcar-3	ovarian:	n/a
31	chr6:29933511-29933561	Hepatocyte	liver:	n/a
32	chr6:29933697-29933747	NHDF-neo	bronchial:	n/a
33	chr6:29933915-29933965	GM06990	blood:	n/a
34	chr6:29933511-29933561	IMR90	lung:	fetal
35	chr6:29933697-29933747	AoSMC	blood vessel:	n/a
36	chr6:29933925-29933975	AG09309	skin:	n/a
37	chr6:29932621-29932671	HCM	heart:	n/a
38	chr6:29933697-29933747	MCF10A-Er-Src	breast:	n/a
39	chr6:29933915-29933965	H1-hESC	embryonic stem cell:	embryo
40	chr6:29932621-29932671	CMK	blood:	n/a
41	chr6:29933925-29933975	AG04450	lung:	fetal
42	chr6:29928362-29928412	HEEpiC	esophagus:	n/a
43	chr6:29933511-29933561	PANC-1	pancreas:	n/a
44	chr6:29933511-29933561	HCT-116	colon:	n/a
45	chr6:29933697-29933747	HRE	kidney:	n/a
46	chr6:29933915-29933965	HCM	heart:	n/a
47	chr6:29933915-29933965	NHDF-neo	bronchial:	n/a
48	chr6:29933971-29934021	SAEC	small airway:	n/a
49	chr6:29932864-29932914	NH-A	brain:	n/a
50	chr6:29933511-29933561	H1-hESC	embryonic stem cell:	embryo

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:29937399..29939324-chr6:29949163..29951713,2	K562	blood:
2	chr6:29917413..29919975-chr6:29932108..29934788,2	K562	blood:
3	chr6:29937339..29939716-chr6:29942275..29944965,3	MCF-7	breast:
4	chr6:29927397..29931336-chr6:29932208..29936273,8	K562	blood:
5	chr6:29937696..29939359-chr6:30032545..30034517,2	K562	blood:
6	chr6:29931492..29933251-chr6:30034694..30036479,2	K562	blood:
7	chr6:29929604..29934270-chr6:29942846..29948120,6	K562	blood:
8	chr6:29820786..29821478-chr6:29935191..29935715,2	MCF-7	breast:
9	chr6:29932263..29935141-chr6:29936079..29939709,3	K562	blood:
10	chr6:29931653..29934276-chr6:29943760..29946372,5	K562	blood:
11	chr6:29927397..29931336-chr6:29932208..29936273,8	K562	blood:
12	chr6:29931972..29934794-chr6:30027595..30029471,2	K562	blood:
13	chr6:29926306..29930004-chr6:29943804..29947247,3	K562	blood:
14	chr6:29932263..29935141-chr6:29936079..29939709,3	K562	blood:
15	chr6:29933916..29936718-chr6:29943405..29945040,3	MCF-7	breast:
16	chr6:29820931..29821695-chr6:29935492..29936150,2	MCF-7	breast:
17	chr6:29815528..29816550-chr6:29935117..29936165,4	MCF-7	breast:
18	chr6:29921960..29924230-chr6:29934596..29936833,2	K562	blood:
19	chr6:29920527..29922060-chr6:29926055..29928693,2	K562	blood:
20	chr6:29920547..29922811-chr6:29925895..29928597,2	MCF-7	breast:
21	chr6:29892582..29894711-chr6:29932418..29935205,2	K562	blood:
22	chr14:77247003..77248532-chr6:29931290..29933642,2	K562	blood:

No data

Variant related genes	Relation type
HCG9	TF binding region
HCG9	CpG island
ENSG00000066379	chromatin interactions
ENSG00000204619	chromatin interactions
ENSG00000230795	chromatin interactions
ENSG00000204623	chromatin interactions
ENSG00000204625	chromatin interactions
ENSG00000259081	chromatin interactions

Extended variants
information (count: 747 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:747 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs892666	chr6:29924728-29924729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs533928663	chr6:29924731-29924732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147575963	chr6:29924732-29924733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12665039	chr6:29924779-29924780	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs539090104	chr6:29924803-29924804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs428905	chr6:29924822-29924823	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs386698626	chr6:29924831-29924832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs9260671	chr6:29924833-29924834	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs554994627	chr6:29924834-29924835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530053395	chr6:29924844-29924845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs2517702	chr6:29924889-29924890	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs529969172	chr6:29924918-29924919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370607467	chr6:29924935-29924936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369578198	chr6:29924936-29924937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs75409837	chr6:29924942-29924943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371397008	chr6:29924970-29924971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150137844	chr6:29924984-29924985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs9260672	chr6:29924996-29924997	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs17179921	chr6:29924997-29924998	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs181580476	chr6:29925004-29925005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs17179929	chr6:29925073-29925074	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs527515840	chr6:29925078-29925079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2523942	chr6:29925086-29925087	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs114193679	chr6:29925103-29925104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138614182	chr6:29925104-29925105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs2844809	chr6:29925127-29925128	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs535099297	chr6:29925131-29925132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149317413	chr6:29925133-29925134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10947038	chr6:29925134-29925135	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs534153597	chr6:29925159-29925160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553970041	chr6:29925186-29925187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575188818	chr6:29925206-29925207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369300344	chr6:29925224-29925225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374265577	chr6:29925250-29925251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114313991	chr6:29925256-29925257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201394357	chr6:29925274-29925275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs117485380	chr6:29925281-29925282	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
38	rs17179936	chr6:29925298-29925299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2571395	chr6:29925331-29925332	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs562191258	chr6:29925370-29925371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185690597	chr6:29925397-29925398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142736905	chr6:29925398-29925399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564312100	chr6:29925420-29925421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs11757135	chr6:29925438-29925439	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs550094807	chr6:29925447-29925448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs138846438	chr6:29925456-29925457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs117274630	chr6:29925457-29925458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565311264	chr6:29925480-29925481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs75288083	chr6:29925491-29925492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs111300603	chr6:29925492-29925493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD

Chromatin state (count:691 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29913400-29932200	Weak transcription	Brain Anterior Caudate	brain
2	chr6:29913400-29932600	Weak transcription	Brain Substantia Nigra	brain
3	chr6:29913600-29925400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr6:29913800-29932200	Weak transcription	Small Intestine	intestine
5	chr6:29914000-29932200	Weak transcription	Colon Smooth Muscle	Colon
6	chr6:29914600-29932200	Weak transcription	Colonic Mucosa	Colon
7	chr6:29914800-29932200	Weak transcription	Right Ventricle	heart
8	chr6:29915400-29931800	Weak transcription	Fetal Thymus	thymus
9	chr6:29915600-29932000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr6:29916400-29926400	Weak transcription	GM12878-XiMat	blood
11	chr6:29916800-29928200	Weak transcription	HepG2	liver
12	chr6:29916800-29930000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr6:29916800-29932200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr6:29916800-29932200	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr6:29916800-29932200	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr6:29916800-29933000	Weak transcription	Esophagus	oesophagus
17	chr6:29916800-29933000	Weak transcription	Pancreas	Pancrea
18	chr6:29916800-29933200	Weak transcription	Lung	lung
19	chr6:29916800-29940200	Weak transcription	Gastric	stomach
20	chr6:29917000-29926800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr6:29917000-29931800	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr6:29917200-29926000	Weak transcription	Adipose Nuclei	Adipose
23	chr6:29917200-29926000	Weak transcription	Spleen	Spleen
24	chr6:29917200-29932000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr6:29917200-29932200	Weak transcription	Liver	Liver
26	chr6:29917200-29932200	Weak transcription	Brain Hippocampus Middle	brain
27	chr6:29917400-29927400	Weak transcription	Fetal Muscle Leg	muscle
28	chr6:29917800-29926400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr6:29917800-29932200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr6:29918000-29926000	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr6:29918000-29926600	Weak transcription	Primary B cells from peripheral blood	blood
32	chr6:29918000-29926600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr6:29918000-29932000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr6:29918000-29932200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr6:29918000-29932200	Weak transcription	Fetal Intestine Small	intestine
36	chr6:29918200-29925600	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr6:29918200-29926600	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr6:29918200-29931800	Weak transcription	Primary T cells from cord blood	blood
39	chr6:29918400-29925600	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr6:29918400-29927400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr6:29919000-29926800	Weak transcription	Primary B cells from cord blood	blood
42	chr6:29920400-29932200	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr6:29921800-29926000	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr6:29921800-29929400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr6:29921800-29929600	Weak transcription	Psoas Muscle	Psoas
46	chr6:29921800-29932200	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr6:29922000-29929600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr6:29922400-29927600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr6:29922800-29926000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr6:29924200-29924800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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