Variant report

Variant	nsv600990
Chromosome Location	chr6:11710554-11733777
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:618)
CpG islands
(count:185)
Chromatin interactive
region (count:27)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:618 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:11730661-11731349	GM12878	blood:	n/a	n/a
2	ATF2	chr6:11714151-11715184	GM12878	blood:	n/a	n/a
3	ATF2	chr6:11731922-11733068	GM12878	blood:	n/a	n/a
4	ATF2	chr6:11714214-11715173	GM12878	blood:	n/a	n/a
5	ATF2	chr6:11723045-11723597	GM12878	blood:	n/a	n/a
6	ATF2	chr6:11711528-11713514	GM12878	blood:	n/a	n/a
7	ATF2	chr6:11731801-11733023	GM12878	blood:	n/a	n/a
8	ATF2	chr6:11711447-11713475	GM12878	blood:	n/a	n/a
9	ATF2	chr6:11730505-11731420	GM12878	blood:	n/a	n/a
10	BATF	chr6:11711882-11712232	GM12878	blood:	n/a	n/a
11	BATF	chr6:11711547-11712383	GM12878	blood:	n/a	chr6:11711685-11711694
12	BATF	chr6:11732109-11732917	GM12878	blood:	n/a	n/a
13	BATF	chr6:11712540-11713419	GM12878	blood:	n/a	n/a
14	BATF	chr6:11714642-11715052	GM12878	blood:	n/a	n/a
15	BATF	chr6:11730786-11731338	GM12878	blood:	n/a	n/a
16	BATF	chr6:11732110-11732812	GM12878	blood:	n/a	n/a
17	BCL11A	chr6:11732094-11732861	GM12878	blood:	n/a	chr6:11732311-11732320
18	BCL11A	chr6:11730847-11731256	GM12878	blood:	n/a	n/a
19	BCL11A	chr6:11711922-11712242	GM12878	blood:	n/a	n/a
20	BCL11A	chr6:11732306-11732763	GM12878	blood:	n/a	chr6:11732311-11732320
21	BCL11A	chr6:11711536-11712395	GM12878	blood:	n/a	n/a
22	BCL3	chr6:11730744-11731237	GM12878	blood:	n/a	n/a
23	BCL3	chr6:11712499-11713504	GM12878	blood:	n/a	n/a
24	BCL3	chr6:11711595-11712338	GM12878	blood:	n/a	n/a
25	BCL3	chr6:11732274-11732811	GM12878	blood:	n/a	chr6:11732311-11732320
26	BCL3	chr6:11732080-11732799	GM12878	blood:	n/a	chr6:11732311-11732320
27	BCL3	chr6:11714513-11715130	GM12878	blood:	n/a	n/a
28	BCL3	chr6:11711932-11712192	GM12878	blood:	n/a	n/a
29	BCLAF1	chr6:11731982-11732930	GM12878	blood:	n/a	chr6:11732311-11732320
30	BCLAF1	chr6:11732086-11732876	GM12878	blood:	n/a	chr6:11732311-11732320
31	BCLAF1	chr6:11714163-11715205	GM12878	blood:	n/a	n/a
32	BCLAF1	chr6:11711690-11713903	GM12878	blood:	n/a	n/a
33	BCLAF1	chr6:11714232-11715211	GM12878	blood:	n/a	n/a
34	BCLAF1	chr6:11730806-11731469	GM12878	blood:	n/a	n/a
35	BCLAF1	chr6:11730695-11731446	GM12878	blood:	n/a	n/a
36	BCLAF1	chr6:11711524-11713689	GM12878	blood:	n/a	n/a
37	BCLAF1	chr6:11722434-11723694	GM12878	blood:	n/a	n/a
38	BHLHE40	chr6:11732155-11733052	GM12878	blood:	n/a	n/a
39	BHLHE40	chr6:11714410-11715020	GM12878	blood:	n/a	n/a
40	BHLHE40	chr6:11722467-11722764	GM12878	blood:	n/a	n/a
41	BHLHE40	chr6:11711736-11713655	GM12878	blood:	n/a	n/a
42	BHLHE40	chr6:11731691-11731988	HepG2	liver:	n/a	n/a
43	BHLHE40	chr6:11730813-11731297	GM12878	blood:	n/a	n/a
44	BRCA1	chr6:11732522-11732831	GM12878	blood:	n/a	n/a
45	BRCA1	chr6:11711708-11711891	GM12878	blood:	n/a	n/a
46	CCNT2	chr6:11729222-11729419	K562	blood:	n/a	chr6:11729362-11729382
47	CCNT2	chr6:11712579-11712815	K562	blood:	n/a	n/a
48	CEBPB	chr6:11728313-11728513	IMR90	lung:	n/a	chr6:11728366-11728377 chr6:11728366-11728379 chr6:11728368-11728379
49	CEBPB	chr6:11712923-11713275	A549	lung:	n/a	chr6:11713111-11713120 chr6:11713111-11713120 chr6:11713111-11713120 chr6:11713111-11713120 chr6:11713109-11713120 chr6:11713109-11713122 chr6:11713109-11713122
50	CEBPB	chr6:11728412-11728415	K562	blood:	n/a	n/a

(count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:11714562-11714612	Caco-2	colon:	n/a
2	chr6:11714562-11714612	MCF10A-Er-Src	breast:	n/a
3	chr6:11714562-11714612	Caco-2	colon:	n/a
4	chr6:11714562-11714612	MCF10A-Er-Src	breast:	n/a
5	chr6:11711971-11712021	SK-N-SH_RA	brain:	n/a
6	chr6:11714562-11714612	U87	brain:	n/a
7	chr6:11711971-11712021	AG04449	skin:	fetal
8	chr6:11714562-11714612	HRE	kidney:	n/a
9	chr6:11710597-11710647	IMR90	lung:	fetal
10	chr6:11710597-11710647	HMEC	breast:	n/a
11	chr6:11714562-11714612	AoSMC	blood vessel:	n/a
12	chr6:11714562-11714612	GM19239	blood:	n/a
13	chr6:11710597-11710647	SK-N-SH_RA	brain:	n/a
14	chr6:11714562-11714612	NB4	blood:	n/a
15	chr6:11714562-11714612	HCM	heart:	n/a
16	chr6:11714562-11714612	HEK293	kidney:	embryo
17	chr6:11714562-11714612	HMEC	breast:	n/a
18	chr6:11714562-11714612	PFSK-1	brain:	n/a
19	chr6:11711971-11712021	LNCaP	prostate:	n/a
20	chr6:11710597-11710647	NT2-D1	testis:	n/a
21	chr6:11710597-11710647	PrEC	prostate:	n/a
22	chr6:11711971-11712021	H1-hESC	embryonic stem cell:	embryo
23	chr6:11711971-11712021	BE2_C	brain:	n/a
24	chr6:11711971-11712021	GM12891	blood:	n/a
25	chr6:11711971-11712021	NB4	blood:	n/a
26	chr6:11714562-11714612	SK-N-MC	brain:	n/a
27	chr6:11711971-11712021	HAEpiC	amniotic membrane:	n/a
28	chr6:11711971-11712021	HUVEC	blood vessel:	n/a
29	chr6:11710597-11710647	HEK293	kidney:	embryo
30	chr6:11714562-11714612	AG04450	lung:	fetal
31	chr6:11714562-11714612	RPTEC	kidney:	n/a
32	chr6:11714562-11714612	AG09309	skin:	n/a
33	chr6:11711971-11712021	MCF10A-Er-Src	breast:	n/a
34	chr6:11710597-11710647	HepG2	liver:	n/a
35	chr6:11710597-11710647	SK-N-MC	brain:	n/a
36	chr6:11714562-11714612	HAEpiC	amniotic membrane:	n/a
37	chr6:11711971-11712021	AG04450	lung:	fetal
38	chr6:11710597-11710647	SAEC	small airway:	n/a
39	chr6:11710597-11710647	HCM	heart:	n/a
40	chr6:11710597-11710647	ovcar-3	ovarian:	n/a
41	chr6:11711971-11712021	HPAEpiC	pulmonary alveolar:	n/a
42	chr6:11711971-11712021	MCF-7	breast:	n/a
43	chr6:11714562-11714612	LNCaP	prostate:	n/a
44	chr6:11710597-11710647	HPAEpiC	pulmonary alveolar:	n/a
45	chr6:11714562-11714612	Hela-S3	cervix:	n/a
46	chr6:11710597-11710647	HCF	heart:	n/a
47	chr6:11710597-11710647	SKMC	muscle:	n/a
48	chr6:11714562-11714612	HPAEpiC	pulmonary alveolar:	n/a
49	chr6:11711971-11712021	ECC-1	luminal epithelium:	n/a
50	chr6:11711971-11712021	HL-60	blood:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:11722035..11725191-chr6:11730801..11735491,4	K562	blood:
2	chr6:11707605..11709932-chr6:11714222..11716200,2	K562	blood:
3	chr6:11728883..11730943-chr6:11731032..11732727,2	K562	blood:
4	chr6:11710777..11713015-chr6:11730009..11731518,2	K562	blood:
5	chr6:11723063..11725185-chr6:11732645..11735491,2	K562	blood:
6	chr6:11717459..11719677-chr6:11722650..11725386,2	MCF-7	breast:
7	chr6:11718348..11720271-chr6:11754971..11757663,2	K562	blood:
8	chr6:11733150..11736062-chr6:12007778..12010289,2	K562	blood:
9	chr6:11717348..11719875-chr6:11747463..11750048,2	MCF-7	breast:
10	chr6:11723063..11725185-chr6:11732645..11735491,2	K562	blood:
11	chr6:11677849..11680603-chr6:11722462..11724414,2	K562	blood:
12	chr6:11720548..11722758-chr6:11726915..11729775,2	MCF-7	breast:
13	chr6:11723926..11725711-chr6:11733477..11735503,2	MCF-7	breast:
14	chr6:11722035..11725191-chr6:11730801..11735491,4	K562	blood:
15	chr6:11717459..11719677-chr6:11722650..11725386,2	MCF-7	breast:
16	chr6:11731733..11734169-chr6:11735074..11737583,2	K562	blood:
17	chr6:11732175..11734663-chr6:11982258..11984188,2	MCF-7	breast:
18	chr6:11728883..11730943-chr6:11731032..11732727,2	K562	blood:
19	chr6:11729664..11733352-chr6:11734064..11737412,4	K562	blood:
20	chr6:11723926..11725711-chr6:11733477..11735503,2	MCF-7	breast:
21	chr6:11715212..11717961-chr6:11734201..11736485,2	K562	blood:
22	chr6:11710372..11713269-chr6:11723329..11725416,2	K562	blood:
23	chr6:11716333..11720276-chr6:11720959..11723559,3	K562	blood:
24	chr6:11726535..11729461-chr6:11731362..11733356,2	MCF-7	breast:
25	chr6:11710777..11713015-chr6:11730009..11731518,2	K562	blood:
26	chr6:11716333..11720276-chr6:11720959..11723559,3	K562	blood:
27	chr6:11710372..11713269-chr6:11723329..11725416,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NEDD9-2	chr6:11723582-11723733	NONHSAT107762
2	lnc-NEDD9-2	chr6:11728560-11728790	NONHSAT107763
3	lnc-NEDD9-2	chr6:11717542-11717647	NONHSAT107762
4	lnc-NEDD9-2	chr6:11714187-11714745	NONHSAT107763
5	lnc-NEDD9-2	chr6:11713908-11714745	NONHSAT107762
6	lnc-NEDD9-2	chr6:11723582-11723733	NONHSAT107763

No data

Variant related genes	Relation type
ADTRP	TF binding region
ADTRP	CpG island
ENSG00000229896	chromatin interactions
ENSG00000095951	chromatin interactions
ENSG00000111863	chromatin interactions

Extended variants
information (count: 895 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:895 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs210920	chr6:11710554-11710555	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs210919	chr6:11710560-11710561	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs567178542	chr6:11710597-11710598	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs140890635	chr6:11710598-11710599	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs558694144	chr6:11710626-11710627	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs572283220	chr6:11710659-11710660	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs536226737	chr6:11710704-11710705	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs374464325	chr6:11710749-11710750	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs144796087	chr6:11710769-11710770	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs555191698	chr6:11710775-11710776	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs145552207	chr6:11710819-11710820	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs112933947	chr6:11710858-11710859	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs563813861	chr6:11710920-11710921	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs532650781	chr6:11710928-11710929	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs566595201	chr6:11710937-11710938	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs568586523	chr6:11710938-11710939	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs528800552	chr6:11710948-11710949	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs114141554	chr6:11710951-11710952	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs566929501	chr6:11710992-11710993	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs535881193	chr6:11710993-11710994	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs143582534	chr6:11710994-11710995	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs565812574	chr6:11711027-11711028	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs190146077	chr6:11711045-11711046	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs538691561	chr6:11711051-11711052	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs148058055	chr6:11711100-11711101	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs538710273	chr6:11711104-11711105	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs143050234	chr6:11711112-11711113	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs367739201	chr6:11711117-11711118	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs62395240	chr6:11711178-11711179	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs534615768	chr6:11711190-11711191	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs545296432	chr6:11711226-11711227	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs115297493	chr6:11711235-11711236	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs78456828	chr6:11711275-11711276	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs114146929	chr6:11711276-11711277	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs563652052	chr6:11711302-11711303	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs577450311	chr6:11711312-11711313	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs368731789	chr6:11711342-11711343	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs546246615	chr6:11711348-11711349	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs559721612	chr6:11711353-11711354	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs528641676	chr6:11711402-11711403	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs548614484	chr6:11711473-11711474	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs551079819	chr6:11711476-11711477	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs147032058	chr6:11711478-11711479	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs549090355	chr6:11711510-11711511	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs578211344	chr6:11711519-11711520	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs537392768	chr6:11711521-11711522	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs557613571	chr6:11711522-11711523	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs7747449	chr6:11711539-11711540	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs549397734	chr6:11711600-11711601	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs569274309	chr6:11711668-11711669	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	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
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
small cell lung cancer	20016488	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
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Cancer	21183584	CNVD
Acute myeloid leukemia	18000384	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Metastatic melanoma	18483359	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:681 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11688800-11711000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr6:11701800-11713000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:11703200-11711200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:11703200-11711400	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr6:11703200-11711400	Weak transcription	HSMM	muscle
6	chr6:11703600-11712600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:11703800-11711200	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr6:11704200-11714800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:11705800-11712000	Weak transcription	Adipose Nuclei	Adipose
10	chr6:11706600-11712000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr6:11707200-11711600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr6:11708000-11710800	Enhancers	Fetal Muscle Leg	muscle
13	chr6:11708200-11714800	Enhancers	Primary T cells fromperipheralblood	blood
14	chr6:11708400-11710600	Weak transcription	Fetal Muscle Trunk	muscle
15	chr6:11708400-11716800	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr6:11709000-11710600	Enhancers	Primary T cells from cord blood	blood
17	chr6:11709000-11710600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
18	chr6:11709000-11711200	Weak transcription	Psoas Muscle	Psoas
19	chr6:11709000-11714800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr6:11709000-11715800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr6:11709000-11716400	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr6:11709200-11710800	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr6:11709400-11710600	Weak transcription	Duodenum Mucosa	Duodenum
24	chr6:11709800-11711200	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr6:11709800-11716400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr6:11710000-11711200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr6:11710000-11711200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr6:11710000-11711600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
29	chr6:11710000-11712200	Enhancers	Fetal Stomach	stomach
30	chr6:11710000-11715200	Enhancers	Fetal Thymus	thymus
31	chr6:11710200-11711800	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr6:11710400-11710600	Enhancers	Primary B cells from peripheral blood	blood
33	chr6:11710400-11710800	Enhancers	Stomach Smooth Muscle	stomach
34	chr6:11710400-11710800	Flanking Active TSS	GM12878-XiMat	blood
35	chr6:11710400-11711000	Enhancers	Fetal Brain Female	brain
36	chr6:11710400-11711000	Enhancers	HSMMtube	muscle
37	chr6:11710400-11711200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr6:11710400-11711200	Enhancers	Brain Cingulate Gyrus	brain
39	chr6:11710400-11711400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr6:11710400-11711400	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr6:11710400-11711400	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr6:11710400-11711600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr6:11710400-11711800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
44	chr6:11710400-11711800	Enhancers	Fetal Heart	heart
45	chr6:11710400-11711800	Enhancers	Fetal Kidney	kidney
46	chr6:11710400-11712200	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr6:11710400-11712800	Enhancers	NHEK	skin
48	chr6:11710400-11713200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr6:11710400-11713400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr6:11710400-11713400	Enhancers	Spleen	Spleen

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