Variant report

Variant	nsv602948
Chromosome Location	chr6:36646788-36651889
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:57)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:36518339..36520561-chr6:36646946..36648999,2	K562	blood:
2	chr6:36648865..36650746-chr6:36679299..36682231,2	K562	blood:
3	chr6:36646643..36648189-chr6:36817431..36818959,2	MCF-7	breast:
4	chr6:36648503..36650842-chr6:36690770..36692686,2	MCF-7	breast:
5	chr6:36649332..36651548-chr6:36829968..36831540,2	MCF-7	breast:
6	chr6:36606453..36608701-chr6:36645452..36648033,2	MCF-7	breast:
7	chr22:29137882..29138609-chr6:36646475..36646984,2	Hela-S3	cervix:
8	chr1:40042208..40042835-chr6:36646343..36646854,2	HCT-116	colon:
9	chr6:36560711..36564837-chr6:36645733..36649715,9	K562	blood:
10	chr17:56708601..56709445-chr6:36647024..36647582,2	Hela-S3	cervix:
11	chr12:81050417..81052003-chr6:36650116..36652674,2	MCF-7	breast:
12	chr6:36581748..36603537-chr6:36641861..36652365,77	MCF-7	breast:
13	chr10:11865096..11865789-chr6:36646486..36647024,2	Hela-S3	cervix:
14	chr17:56707748..56709290-chr6:36645821..36647810,2	MCF-7	breast:
15	chr6:36590906..36591946-chr6:36647029..36648637,8	MCF-7	breast:
16	chr6:36590986..36591856-chr6:36647878..36648875,10	K562	blood:
17	chr6:36584731..36585313-chr6:36649604..36650477,2	MCF-7	breast:
18	chr6:36649100..36652081-chr6:36702052..36705068,3	MCF-7	breast:
19	chr6:36581224..36597272-chr6:36642199..36659412,120	MCF-7	breast:
20	chr6:36589971..36596625-chr6:36645571..36650576,10	K562	blood:
21	chr6:36644040..36648031-chr6:36680924..36685784,5	MCF-7	breast:
22	chr6:36577436..36580901-chr6:36648470..36651354,3	K562	blood:
23	chr6:36631889..36633994-chr6:36649894..36652299,3	K562	blood:
24	chr6:36650316..36652178-chr6:36659155..36660681,2	MCF-7	breast:
25	chr6:36560538..36562550-chr6:36650769..36653257,2	MCF-7	breast:
26	chr17:41437979..41438687-chr6:36647348..36648127,2	Hela-S3	cervix:
27	chr6:36589213..36595227-chr6:36645571..36651666,9	K562	blood:
28	chr6:36570219..36573404-chr6:36646918..36650255,3	K562	blood:
29	chr6:36646719..36650011-chr6:36657952..36660291,4	MCF-7	breast:
30	chr6:36561682..36564550-chr6:36650223..36652038,2	K562	blood:
31	chr6:36584612..36585297-chr6:36648004..36648751,2	MCF-7	breast:
32	chr17:57914670..57916833-chr6:36645394..36647964,3	MCF-7	breast:
33	chr6:27100904..27101438-chr6:36648004..36648546,2	Hela-S3	cervix:
34	chr6:36647044..36648855-chr6:36663270..36664993,2	MCF-7	breast:
35	chr6:36646406..36647008-chr9:130213190..130213761,2	Hela-S3	cervix:
36	chr6:36649873..36651499-chr6:36688995..36691220,2	MCF-7	breast:
37	chr6:36564965..36566976-chr6:36648126..36649999,2	K562	blood:
38	chr6:36650715..36656032-chr6:36664945..36667924,5	MCF-7	breast:
39	chr6:36650647..36652675-chr6:36655883..36658117,2	MCF-7	breast:
40	chr6:36592351..36593048-chr6:36648313..36648819,2	K562	blood:
41	chr6:36645391..36647920-chr6:36680659..36684331,3	MCF-7	breast:
42	chr6:36578466..36580870-chr6:36647924..36649824,2	MCF-7	breast:
43	chr6:36644838..36653438-chr6:36718524..36730954,23	MCF-7	breast:
44	chr6:36646585..36648136-chr6:36723645..36726426,2	K562	blood:
45	chr6:36571904..36574235-chr6:36647480..36649037,2	K562	blood:
46	chr6:36650057..36652668-chr6:36663338..36666266,2	K562	blood:
47	chr6:36645102..36656546-chr6:36717974..36730993,29	MCF-7	breast:
48	chr6:36561535..36562422-chr6:36647947..36648663,2	K562	blood:
49	chr6:36634794..36635467-chr6:36647053..36647864,2	MCF-7	breast:
50	chr6:36560285..36563984-chr6:36645642..36649715,8	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAB44-3	chr6:36648251-36648457	NONHSAT112229

No data

Variant related genes	Relation type
ENSG00000139641	chromatin interactions
ENSG00000220349	chromatin interactions
ENSG00000197958	chromatin interactions
ENSG00000124772	chromatin interactions
ENSG00000112081	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000263894	chromatin interactions
ENSG00000183765	chromatin interactions
ENSG00000255587	chromatin interactions
ENSG00000090621	chromatin interactions
ENSG00000100209	chromatin interactions
ENSG00000213500	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000148426	chromatin interactions
ENSG00000238554	chromatin interactions

Extended variants
information (count: 227 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:227 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3176320	chr6:36646788-36646789	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs3176321	chr6:36646807-36646808	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs200966207	chr6:36646811-36646812	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
4	rs3176323	chr6:36646849-36646850	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs141318160	chr6:36646922-36646923	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
6	rs545871553	chr6:36646930-36646931	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
7	rs3176324	chr6:36646950-36646951	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs377177083	chr6:36646959-36646960	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
9	rs541349344	chr6:36646966-36646967	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
10	rs3176325	chr6:36646970-36646971	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
11	rs141423474	chr6:36646982-36646983	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
12	rs4647892	chr6:36647030-36647031	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs368810826	chr6:36647032-36647033	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs191982478	chr6:36647033-36647034	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs4647893	chr6:36647161-36647162	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs563904290	chr6:36647186-36647187	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs557501324	chr6:36647196-36647197	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs577481656	chr6:36647245-36647246	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs371003992	chr6:36647275-36647276	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs3176326	chr6:36647289-36647290	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs3176327	chr6:36647328-36647329	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs4647894	chr6:36647398-36647399	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs528459025	chr6:36647412-36647413	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs376613761	chr6:36647419-36647420	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs3176328	chr6:36647457-36647458	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs3176329	chr6:36647463-36647464	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs3176330	chr6:36647490-36647491	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs370270986	chr6:36647493-36647494	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs568995125	chr6:36647505-36647506	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs3176331	chr6:36647525-36647526	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs543276323	chr6:36647538-36647539	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs550258064	chr6:36647625-36647626	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs4135240	chr6:36647680-36647681	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs539878419	chr6:36647760-36647761	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs566731902	chr6:36647765-36647766	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs554921943	chr6:36647768-36647769	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs575077828	chr6:36647809-36647810	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs191070763	chr6:36647866-36647867	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs563733227	chr6:36647957-36647958	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs201410543	chr6:36648054-36648055	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs147436240	chr6:36648065-36648066	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs531105241	chr6:36648080-36648081	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs113663599	chr6:36648117-36648118	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs59807512	chr6:36648118-36648119	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs59454180	chr6:36648122-36648123	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs141793353	chr6:36648123-36648124	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs546333743	chr6:36648170-36648171	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs374550548	chr6:36648209-36648210	Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs199912677	chr6:36648211-36648212	Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs73412231	chr6:36648217-36648218	Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
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
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	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
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	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
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Ovarian cancer	21720365	CNVD

Chromatin state (count:784 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36644200-36647600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr6:36645600-36647000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
3	chr6:36645600-36648600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
4	chr6:36645800-36646800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr6:36645800-36647400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
6	chr6:36646000-36646800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr6:36646000-36646800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr6:36646000-36646800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr6:36646000-36647000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr6:36646000-36647200	Flanking Active TSS	Primary B cells from peripheral blood	blood
11	chr6:36646000-36647400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
12	chr6:36646000-36647400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
13	chr6:36646000-36647400	Flanking Active TSS	Colonic Mucosa	Colon
14	chr6:36646000-36647400	Flanking Active TSS	Placenta Amnion	Placenta Amnion
15	chr6:36646000-36647600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
16	chr6:36646000-36647800	Bivalent Enhancer	Fetal Brain Male	brain
17	chr6:36646000-36648000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
18	chr6:36646000-36648000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
19	chr6:36646000-36648000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
20	chr6:36646000-36648400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr6:36646000-36648400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:36646000-36648600	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
23	chr6:36646000-36648600	Active TSS	Duodenum Smooth Muscle	Duodenum
24	chr6:36646000-36648800	Active TSS	Aorta	Aorta
25	chr6:36646000-36648800	Active TSS	Psoas Muscle	Psoas
26	chr6:36646000-36649000	Flanking Active TSS	Primary B cells from cord blood	blood
27	chr6:36646000-36650200	Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr6:36646200-36646800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
29	chr6:36646200-36647000	Active TSS	Brain Cingulate Gyrus	brain
30	chr6:36646200-36647000	Active TSS	Brain Inferior Temporal Lobe	brain
31	chr6:36646200-36647000	Active TSS	Rectal Smooth Muscle	rectum
32	chr6:36646200-36647000	Active TSS	Monocytes-CD14+_RO01746	blood
33	chr6:36646200-36647200	Active TSS	Primary T killer memory cells from peripheral blood	blood
34	chr6:36646200-36647400	Flanking Active TSS	K562	blood
35	chr6:36646200-36647600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
36	chr6:36646200-36647600	Flanking Bivalent TSS/Enh	Thymus	Thymus
37	chr6:36646200-36648000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
38	chr6:36646200-36648200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr6:36646200-36648400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr6:36646200-36648400	Active TSS	Muscle Satellite Cultured Cells	--
41	chr6:36646200-36648400	Active TSS	Liver	Liver
42	chr6:36646200-36648400	Active TSS	Brain Angular Gyrus	brain
43	chr6:36646200-36648400	Active TSS	Hela-S3	cervix
44	chr6:36646200-36648400	Active TSS	NHDF-Ad	bronchial
45	chr6:36646200-36648400	Active TSS	Osteobl	bone
46	chr6:36646200-36648600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr6:36646200-36648600	Active TSS	Brain Anterior Caudate	brain
48	chr6:36646200-36648600	Active TSS	Colon Smooth Muscle	Colon
49	chr6:36646200-36648600	Active TSS	Duodenum Mucosa	Duodenum
50	chr6:36646200-36648600	Active TSS	Fetal Kidney	kidney

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