Variant report

Variant	nsv883992
Chromosome Location	chr6:29924130-29937833
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:985)
CpG islands
(count:1223)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:985 , 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	chr6:29932290-29932954	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:29931139-29931164	K562	blood:	n/a	n/a
4	ARID3A	chr6:29933775-29934240	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:29934522-29934914	K562	blood:	n/a	n/a
6	ARID3A	chr6:29933748-29934309	K562	blood:	n/a	n/a
7	ARID3A	chr6:29937042-29937091	K562	blood:	n/a	n/a
8	ARID3A	chr6:29932477-29933236	K562	blood:	n/a	n/a
9	ARID3A	chr6:29935252-29935904	K562	blood:	n/a	n/a
10	ATF1	chr6:29932584-29933076	K562	blood:	n/a	n/a
11	ATF1	chr6:29935286-29935585	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	chr6:29932539-29933023	K562	blood:	n/a	n/a
15	ATF3	chr6:29932615-29932943	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	chr6:29932494-29933203	GM12878	blood:	n/a	chr6:29932797-29932806
24	BCLAF1	chr6:29932428-29933119	GM12878	blood:	n/a	chr6:29932797-29932806
25	BHLHE40	chr6:29932548-29933279	GM12878	blood:	n/a	n/a
26	BHLHE40	chr6:29933686-29934301	K562	blood:	n/a	n/a
27	BHLHE40	chr6:29935166-29935758	K562	blood:	n/a	n/a
28	BHLHE40	chr6:29932569-29933159	K562	blood:	n/a	n/a
29	BHLHE40	chr6:29933714-29934091	HepG2	liver:	n/a	n/a
30	BHLHE40	chr6:29934607-29934610	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:29933866-29934118	GM12878	blood:	n/a	n/a
32	CBX3	chr6:29932403-29933273	HCT-116	colon:	n/a	n/a
33	CBX3	chr6:29935905-29936437	HCT-116	colon:	n/a	n/a
34	CBX3	chr6:29933685-29934511	HCT-116	colon:	n/a	n/a
35	CBX3	chr6:29935860-29936460	HCT-116	colon:	n/a	n/a
36	CBX3	chr6:29932608-29932997	K562	blood:	n/a	n/a
37	CBX3	chr6:29932504-29933475	K562	blood:	n/a	n/a
38	CBX3	chr6:29935109-29935665	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	chr6:29932577-29933269	K562	blood:	n/a	n/a
43	CEBPB	chr6:29929562-29929884	HepG2	liver:	n/a	n/a
44	CEBPB	chr6:29935064-29935418	HepG2	liver:	n/a	chr6:29935249-29935260 chr6:29935210-29935221
45	CEBPB	chr6:29936002-29936359	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr6:29935073-29935816	K562	blood:	n/a	chr6:29935249-29935260 chr6:29935210-29935221
47	CEBPB	chr6:29934230-29934543	IMR90	lung:	n/a	n/a
48	CEBPB	chr6:29932451-29933116	GM12878	blood:	n/a	n/a
49	CEBPB	chr6:29929504-29929848	K562	blood:	n/a	n/a
50	CEBPB	chr6:29932409-29933285	Hela-S3	cervix:	n/a	n/a

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29924471-29924521	SAEC	small airway:	n/a
2	chr6:29924256-29924306	CMK	blood:	n/a
3	chr6:29924202-29924252	PANC-1	pancreas:	n/a
4	chr6:29924471-29924521	SAEC	small airway:	n/a
5	chr6:29924256-29924306	CMK	blood:	n/a
6	chr6:29924202-29924252	PANC-1	pancreas:	n/a
7	chr6:29933915-29933965	SK-N-SH	brain:	n/a
8	chr6:29924207-29924257	HRCEpiC	kidney:	n/a
9	chr6:29924247-29924297	HCPEpiC	choroid plexus:	n/a
10	chr6:29924310-29924360	NHBE	bronchial:	n/a
11	chr6:29924310-29924360	HCM	heart:	n/a
12	chr6:29924407-29924457	RPTEC	kidney:	n/a
13	chr6:29924299-29924349	HCPEpiC	choroid plexus:	n/a
14	chr6:29924207-29924257	HRE	kidney:	n/a
15	chr6:29924256-29924306	K562	blood:	n/a
16	chr6:29924471-29924521	ProgFib	skin:	n/a
17	chr6:29933511-29933561	SAEC	small airway:	n/a
18	chr6:29924256-29924306	HPAEpiC	pulmonary alveolar:	n/a
19	chr6:29933411-29933461	NHBE	bronchial:	n/a
20	chr6:29928362-29928412	H1-hESC	embryonic stem cell:	embryo
21	chr6:29924207-29924257	HEK293	kidney:	embryo
22	chr6:29924256-29924306	U87	brain:	n/a
23	chr6:29924471-29924521	K562	blood:	n/a
24	chr6:29924407-29924457	PANC-1	pancreas:	n/a
25	chr6:29924310-29924360	HCT-116	colon:	n/a
26	chr6:29932743-29932793	HCF	heart:	n/a
27	chr6:29933697-29933747	HCM	heart:	n/a
28	chr6:29924475-29924525	ProgFib	skin:	n/a
29	chr6:29933925-29933975	CMK	blood:	n/a
30	chr6:29924404-29924454	GM12878	blood:	n/a
31	chr6:29933697-29933747	RPTEC	kidney:	n/a
32	chr6:29932621-29932671	AoSMC	blood vessel:	n/a
33	chr6:29932743-29932793	HPAEpiC	pulmonary alveolar:	n/a
34	chr6:29924299-29924349	AG09309	skin:	n/a
35	chr6:29924471-29924521	LNCaP	prostate:	n/a
36	chr6:29933925-29933975	HRCEpiC	kidney:	n/a
37	chr6:29933925-29933975	H1-hESC	embryonic stem cell:	embryo
38	chr6:29924471-29924521	HMEC	breast:	n/a
39	chr6:29924207-29924257	NT2-D1	testis:	n/a
40	chr6:29924202-29924252	BJ	skin:	n/a
41	chr6:29933915-29933965	HUVEC	blood vessel:	n/a
42	chr6:29932864-29932914	BE2_C	brain:	n/a
43	chr6:29928362-29928412	HCF	heart:	n/a
44	chr6:29924310-29924360	IMR90	lung:	fetal
45	chr6:29933697-29933747	HMEC	breast:	n/a
46	chr6:29924475-29924525	NT2-D1	testis:	n/a
47	chr6:29933925-29933975	GM19239	blood:	n/a
48	chr6:29933511-29933561	ProgFib	skin:	n/a
49	chr6:29924256-29924306	HepG2	liver:	n/a
50	chr6:29924404-29924454	HCF	heart:	n/a

(count:23 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 797 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:797 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9260657	chr6:29924130-29924131	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549864249	chr6:29924137-29924138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs9260658	chr6:29924141-29924142	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs9260659	chr6:29924158-29924159	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs41265804	chr6:29924159-29924160	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs73725597	chr6:29924166-29924167	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs386698623	chr6:29924170-29924171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs9260661	chr6:29924172-29924173	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs575354200	chr6:29924208-29924209	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs2571392	chr6:29924220-29924221	Enhancers Weak transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs9260662	chr6:29924231-29924232	Enhancers Weak transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs9260663	chr6:29924247-29924248	Enhancers Weak transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs567544918	chr6:29924287-29924288	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs386698624	chr6:29924288-29924289	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs73725598	chr6:29924294-29924295	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs149627224	chr6:29924297-29924298	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs576874987	chr6:29924299-29924300	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs139785736	chr6:29924315-29924316	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs149758668	chr6:29924317-29924318	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs537839399	chr6:29924318-29924319	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs375960190	chr6:29924321-29924322	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs386698625	chr6:29924357-29924358	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs2735089	chr6:29924359-29924360	Enhancers Weak transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs551138466	chr6:29924378-29924379	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2571393	chr6:29924386-29924387	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs2571394	chr6:29924389-29924390	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs9260665	chr6:29924408-29924409	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs3893538	chr6:29924425-29924426	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
29	rs17179851	chr6:29924440-29924441	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs9260667	chr6:29924454-29924455	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs147766075	chr6:29924458-29924459	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs6907082	chr6:29924482-29924483	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs6907230	chr6:29924490-29924491	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs75124665	chr6:29924491-29924492	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2019775	chr6:29924495-29924496	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs17186258	chr6:29924496-29924497	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs570225325	chr6:29924501-29924502	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs141162588	chr6:29924506-29924507	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs114591208	chr6:29924516-29924517	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189295372	chr6:29924523-29924524	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556019133	chr6:29924532-29924533	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs1808199	chr6:29924542-29924543	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs1808198	chr6:29924555-29924556	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs17179879	chr6:29924619-29924620	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs3129013	chr6:29924626-29924627	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs59264191	chr6:29924641-29924642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574351730	chr6:29924647-29924648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560412666	chr6:29924651-29924652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs59781164	chr6:29924652-29924653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs202244611	chr6:29924655-29924656	Enhancers Weak transcription	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:705 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29912800-29924200	Weak transcription	Right Atrium	heart
2	chr6:29913000-29924200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:29913400-29932200	Weak transcription	Brain Anterior Caudate	brain
4	chr6:29913400-29932600	Weak transcription	Brain Substantia Nigra	brain
5	chr6:29913600-29924400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr6:29913600-29925400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr6:29913800-29932200	Weak transcription	Small Intestine	intestine
8	chr6:29914000-29924200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr6:29914000-29932200	Weak transcription	Colon Smooth Muscle	Colon
10	chr6:29914600-29932200	Weak transcription	Colonic Mucosa	Colon
11	chr6:29914800-29932200	Weak transcription	Right Ventricle	heart
12	chr6:29915400-29931800	Weak transcription	Fetal Thymus	thymus
13	chr6:29915600-29932000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr6:29916400-29926400	Weak transcription	GM12878-XiMat	blood
15	chr6:29916800-29924400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr6:29916800-29928200	Weak transcription	HepG2	liver
17	chr6:29916800-29930000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr6:29916800-29932200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr6:29916800-29932200	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr6:29916800-29932200	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr6:29916800-29933000	Weak transcription	Esophagus	oesophagus
22	chr6:29916800-29933000	Weak transcription	Pancreas	Pancrea
23	chr6:29916800-29933200	Weak transcription	Lung	lung
24	chr6:29916800-29940200	Weak transcription	Gastric	stomach
25	chr6:29917000-29926800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr6:29917000-29931800	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr6:29917200-29926000	Weak transcription	Adipose Nuclei	Adipose
28	chr6:29917200-29926000	Weak transcription	Spleen	Spleen
29	chr6:29917200-29932000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr6:29917200-29932200	Weak transcription	Liver	Liver
31	chr6:29917200-29932200	Weak transcription	Brain Hippocampus Middle	brain
32	chr6:29917400-29927400	Weak transcription	Fetal Muscle Leg	muscle
33	chr6:29917800-29926400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr6:29917800-29932200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr6:29918000-29926000	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr6:29918000-29926600	Weak transcription	Primary B cells from peripheral blood	blood
37	chr6:29918000-29926600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr6:29918000-29932000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr6:29918000-29932200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr6:29918000-29932200	Weak transcription	Fetal Intestine Small	intestine
41	chr6:29918200-29925600	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr6:29918200-29926600	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr6:29918200-29931800	Weak transcription	Primary T cells from cord blood	blood
44	chr6:29918400-29925600	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr6:29918400-29927400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr6:29919000-29926800	Weak transcription	Primary B cells from cord blood	blood
47	chr6:29919800-29924200	Weak transcription	Left Ventricle	heart
48	chr6:29920400-29932200	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr6:29921800-29926000	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr6:29921800-29929400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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