Variant report

Variant	nsv1024516
Chromosome Location	chr6:128184182-128298278
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:498)
CpG islands
(count:488)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:128200736-128201193	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr6:128200833-128201174	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr6:128267687-128267775	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:128258975-128259009	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:128259903-128260275	K562	blood:	n/a	chr6:128260016-128260030
6	BACH1	chr6:128259660-128261287	H1-hESC	embryonic stem cell:	n/a	chr6:128260016-128260030
7	BACH1	chr6:128260872-128261034	K562	blood:	n/a	n/a
8	BACH1	chr6:128201742-128201923	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr6:128198445-128198715	GM12878	blood:	n/a	n/a
10	BATF	chr6:128229097-128229441	GM12878	blood:	n/a	n/a
11	BATF	chr6:128198483-128198700	GM12878	blood:	n/a	n/a
12	BATF	chr6:128229136-128229403	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:128201515-128201808	GM12878	blood:	n/a	n/a
14	CEBPB	chr6:128285225-128285505	HepG2	liver:	n/a	n/a
15	CEBPB	chr6:128258895-128259274	IMR90	lung:	n/a	chr6:128259099-128259112 chr6:128259099-128259112 chr6:128259099-128259110 chr6:128259100-128259111
16	CEBPB	chr6:128258922-128259247	HepG2	liver:	n/a	chr6:128259099-128259112 chr6:128259099-128259112 chr6:128259099-128259110 chr6:128259100-128259111
17	CEBPB	chr6:128235492-128235686	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr6:128293042-128293770	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr6:128280512-128280675	A549	lung:	n/a	chr6:128280625-128280633
20	CEBPB	chr6:128193671-128193672	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr6:128212473-128212767	HepG2	liver:	n/a	chr6:128212631-128212642
22	CEBPB	chr6:128293106-128293483	MCF-7	breast:	n/a	n/a
23	CEBPB	chr6:128212553-128212676	HepG2	liver:	n/a	chr6:128212631-128212642
24	CEBPB	chr6:128246557-128246843	HepG2	liver:	n/a	n/a
25	CEBPB	chr6:128212541-128212741	H1-hESC	embryonic stem cell:	n/a	chr6:128212631-128212642
26	CEBPB	chr6:128246631-128246768	A549	lung:	n/a	n/a
27	CHD1	chr6:128293057-128293169	GM12878	blood:	n/a	n/a
28	CREB1	chr6:128214641-128215104	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr6:128200733-128201245	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr6:128200853-128201182	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTBP2	chr6:128200447-128201220	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr6:128277452-128277767	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:128277500-128277650	HFF-Myc	foreskin:	n/a	n/a
34	CTCF	chr6:128289720-128289870	HUVEC	blood vessel:	n/a	chr6:128289730-128289751 chr6:128289735-128289753 chr6:128289736-128289752
35	CTCF	chr6:128277500-128277650	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr6:128207320-128207470	AG09319	gingival:	n/a	n/a
37	CTCF	chr6:128277500-128277650	AG04450	lung:	n/a	n/a
38	CTCF	chr6:128285591-128285626	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:128277480-128277630	HEK293	kidney:	n/a	n/a
40	CTCF	chr6:128207800-128207950	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr6:128277540-128277690	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr6:128289940-128290090	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr6:128289680-128289830	HMEC	breast:	n/a	chr6:128289730-128289751 chr6:128289735-128289753 chr6:128289736-128289752
44	CTCF	chr6:128289620-128289770	HRE	kidney:	n/a	chr6:128289730-128289751 chr6:128289735-128289753 chr6:128289736-128289752
45	CTCF	chr6:128277540-128277690	WI-38	lung:	n/a	n/a
46	CTCF	chr6:128277500-128277650	HEK293	kidney:	n/a	n/a
47	CTCF	chr6:128277500-128277650	HMF	breast:	n/a	n/a
48	CTCF	chr6:128277511-128277587	Fibrobl	skin:	n/a	n/a
49	CTCF	chr6:128289600-128289750	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr6:128277534-128277665	Gliobla	brain:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:128222378-128222428	AG04450	lung:	fetal
2	chr6:128239611-128239661	GM12878	blood:	n/a
3	chr6:128240363-128240413	PrEC	prostate:	n/a
4	chr6:128239611-128239661	GM06990	blood:	n/a
5	chr6:128222053-128222103	HRE	kidney:	n/a
6	chr6:128239611-128239661	NT2-D1	testis:	n/a
7	chr6:128259318-128259368	MCF10A-Er-Src	breast:	n/a
8	chr6:128199727-128199777	SK-N-MC	brain:	n/a
9	chr6:128222390-128222440	U87	brain:	n/a
10	chr6:128222053-128222103	CMK	blood:	n/a
11	chr6:128199727-128199777	HRPEpiC	eye:	n/a
12	chr6:128259318-128259368	HUVEC	blood vessel:	n/a
13	chr6:128240363-128240413	NT2-D1	testis:	n/a
14	chr6:128259318-128259368	AG04449	skin:	fetal
15	chr6:128259318-128259368	GM19239	blood:	n/a
16	chr6:128199727-128199777	HEK293	kidney:	embryo
17	chr6:128239611-128239661	HIPEpiC	eye:	n/a
18	chr6:128222390-128222440	AG09309	skin:	n/a
19	chr6:128290073-128290123	AG04450	lung:	fetal
20	chr6:128222053-128222103	GM06990	blood:	n/a
21	chr6:128222053-128222103	BJ	skin:	n/a
22	chr6:128259318-128259368	HCT-116	colon:	n/a
23	chr6:128222378-128222428	HepG2	liver:	n/a
24	chr6:128199727-128199777	ProgFib	skin:	n/a
25	chr6:128222390-128222440	PFSK-1	brain:	n/a
26	chr6:128290073-128290123	GM12878	blood:	n/a
27	chr6:128240363-128240413	SKMC	muscle:	n/a
28	chr6:128290073-128290123	SAEC	small airway:	n/a
29	chr6:128222053-128222103	GM12878	blood:	n/a
30	chr6:128290073-128290123	NT2-D1	testis:	n/a
31	chr6:128259318-128259368	GM06990	blood:	n/a
32	chr6:128222390-128222440	RPTEC	kidney:	n/a
33	chr6:128239611-128239661	Jurkat	blood:	n/a
34	chr6:128240363-128240413	HPAEpiC	pulmonary alveolar:	n/a
35	chr6:128222378-128222428	HPAEpiC	pulmonary alveolar:	n/a
36	chr6:128222378-128222428	AG04449	skin:	fetal
37	chr6:128290073-128290123	SK-N-SH_RA	brain:	n/a
38	chr6:128199727-128199777	HCPEpiC	choroid plexus:	n/a
39	chr6:128222390-128222440	NB4	blood:	n/a
40	chr6:128290073-128290123	BJ	skin:	n/a
41	chr6:128239611-128239661	AG04450	lung:	fetal
42	chr6:128222390-128222440	HRPEpiC	eye:	n/a
43	chr6:128199727-128199777	NB4	blood:	n/a
44	chr6:128222053-128222103	AG10803	skin:	n/a
45	chr6:128199727-128199777	NHDF-neo	bronchial:	n/a
46	chr6:128199727-128199777	HPAEpiC	pulmonary alveolar:	n/a
47	chr6:128222053-128222103	HRPEpiC	eye:	n/a
48	chr6:128290073-128290123	H1-hESC	embryonic stem cell:	embryo
49	chr6:128222390-128222440	MCF10A-Er-Src	breast:	n/a
50	chr6:128240363-128240413	HRCEpiC	kidney:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:128290855..128292622-chr6:128292665..128294749,2	MCF-7	breast:
2	chr6:128183469..128185798-chr6:128259779..128262240,2	K562	blood:
3	chr6:128283049..128285690-chr6:128287675..128290328,2	MCF-7	breast:
4	chr6:128289419..128291149-chr6:128295395..128297962,2	MCF-7	breast:
5	chr6:128057816..128058584-chr6:128289323..128290031,2	MCF-7	breast:
6	chr6:128183469..128185798-chr6:128259779..128262240,2	K562	blood:
7	chr6:128259450..128262289-chr6:128263884..128266852,3	MCF-7	breast:
8	chr6:128259450..128262289-chr6:128263884..128266852,3	MCF-7	breast:
9	chr6:128057292..128059744-chr6:128288447..128291098,2	MCF-7	breast:
10	chr6:128290855..128292622-chr6:128292665..128294749,2	MCF-7	breast:
11	chr2:165475774..165478358-chr6:128205269..128207397,2	MCF-7	breast:
12	chr6:128215641..128218449-chr6:128221466..128223378,2	MCF-7	breast:
13	chr6:128289419..128291149-chr6:128295395..128297962,2	MCF-7	breast:
14	chr6:128283049..128285690-chr6:128287675..128290328,2	MCF-7	breast:
15	chr6:128216642..128219486-chr6:128221737..128224434,2	MCF-7	breast:

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PTPRK	hsa-miR-30a-5p	chr6:128290204-128290197
2	PTPRK	hsa-miR-9-5p	chr6:128290802-128290796
3	PTPRK	hsa-miR-9-5p	chr6:128290797-128290820
4	PTPRK	hsa-miR-30a-5p	chr6:128290198-128290219
5	PTPRK	hsa-miR-133b	chr6:128290489-128290482
6	PTPRK	hsa-miR-133b	chr6:128290483-128290505
7	PTPRK	hsa-miR-149-5p	chr6:128291314-128291336

Variant related genes	Relation type
THEMIS	TF binding region
THEMIS	CpG island
ENSG00000172673	chromatin interactions
ENSG00000115290	chromatin interactions

Extended variants
information (count: 4375 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:4375 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145575344	chr6:128184373-128184374	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs545522256	chr6:128184381-128184382	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532859477	chr6:128184432-128184433	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs72973339	chr6:128184450-128184451	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs550973419	chr6:128184451-128184452	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs76983671	chr6:128184456-128184457	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376813652	chr6:128184515-128184516	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs567897092	chr6:128184561-128184562	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536641262	chr6:128184676-128184677	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs270041	chr6:128184738-128184739	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs559309233	chr6:128184751-128184752	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566975086	chr6:128184770-128184771	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184453033	chr6:128184793-128184794	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553149153	chr6:128184794-128184795	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs75417849	chr6:128184814-128184815	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs148442637	chr6:128184818-128184819	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556827523	chr6:128184833-128184834	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187673957	chr6:128184857-128184858	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192375739	chr6:128184874-128184875	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560505175	chr6:128184879-128184880	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572907275	chr6:128184966-128184967	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539919441	chr6:128184973-128184974	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565504982	chr6:128184979-128184980	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142567416	chr6:128185000-128185001	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551338757	chr6:128185007-128185008	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs270042	chr6:128185084-128185085	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs184753699	chr6:128185108-128185109	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375129499	chr6:128185111-128185112	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566838487	chr6:128185204-128185205	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534322513	chr6:128185227-128185228	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs189004437	chr6:128185319-128185320	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs180900760	chr6:128185330-128185331	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538450606	chr6:128185334-128185335	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556690378	chr6:128185355-128185356	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575182889	chr6:128185357-128185358	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs373674877	chr6:128185364-128185365	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534390810	chr6:128185401-128185402	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78079949	chr6:128185515-128185516	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs150968790	chr6:128185561-128185562	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201484860	chr6:128185596-128185597	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540360866	chr6:128185641-128185642	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530292009	chr6:128185658-128185659	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs558363290	chr6:128185683-128185684	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs561131145	chr6:128185698-128185699	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577416182	chr6:128185751-128185752	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs544824279	chr6:128185765-128185766	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563031573	chr6:128185773-128185774	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs142062860	chr6:128185784-128185785	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542513680	chr6:128185792-128185793	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551321356	chr6:128185797-128185798	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
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
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
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Neurocytoma	17123091	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Ependymoma	18628472	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21958427	CNVD
Mental retardation	17847001	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1570 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128178800-128190800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr6:128179200-128190400	Weak transcription	Brain Cingulate Gyrus	brain
3	chr6:128180400-128184600	Weak transcription	Thymus	Thymus
4	chr6:128180400-128189600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr6:128180400-128190600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr6:128180600-128184600	Weak transcription	Brain Hippocampus Middle	brain
7	chr6:128180600-128189600	Weak transcription	Brain Substantia Nigra	brain
8	chr6:128181200-128184200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr6:128181600-128184200	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr6:128181600-128184600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr6:128181600-128185400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr6:128181600-128185800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr6:128181800-128185400	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr6:128183200-128185600	Strong transcription	Fetal Thymus	thymus
15	chr6:128183400-128185200	Genic enhancers	Primary T helper cells fromperipheralblood	blood
16	chr6:128183600-128184600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr6:128183600-128184800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr6:128183800-128184400	Strong transcription	Primary T cells from cord blood	blood
19	chr6:128183800-128187000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr6:128184200-128186000	Strong transcription	Primary T cells fromperipheralblood	blood
21	chr6:128184200-128186200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr6:128184400-128186400	Genic enhancers	Primary T cells from cord blood	blood
23	chr6:128184600-128185000	Enhancers	Brain Hippocampus Middle	brain
24	chr6:128184600-128185000	Enhancers	Thymus	Thymus
25	chr6:128184600-128186200	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr6:128184600-128186800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
27	chr6:128184800-128185000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr6:128185000-128185600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr6:128185000-128185600	Weak transcription	Thymus	Thymus
30	chr6:128185200-128186000	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr6:128185400-128185600	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr6:128185400-128187400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr6:128185600-128186200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr6:128185600-128186200	Genic enhancers	Fetal Thymus	thymus
35	chr6:128185600-128186400	Genic enhancers	Thymus	Thymus
36	chr6:128185600-128186600	Enhancers	Fetal Intestine Large	intestine
37	chr6:128185600-128187200	Genic enhancers	Primary T helper cells PMA-I stimulated	--
38	chr6:128185800-128186600	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr6:128185800-128186600	Enhancers	HepG2	liver
40	chr6:128186000-128186200	Genic enhancers	Primary T helper cells fromperipheralblood	blood
41	chr6:128186000-128186400	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr6:128186000-128186400	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr6:128186000-128186600	Genic enhancers	Primary T cells fromperipheralblood	blood
44	chr6:128186200-128186400	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr6:128186200-128186600	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr6:128186200-128186600	Enhancers	Fetal Intestine Small	intestine
47	chr6:128186200-128187200	Enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr6:128186200-128187200	Strong transcription	Fetal Thymus	thymus
49	chr6:128186200-128188400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr6:128186400-128188200	Weak transcription	Primary T helper cells fromperipheralblood	blood

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