Variant report

Variant	nsv1023808
Chromosome Location	chr6:27656049-27674354
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:59)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:27526508..27528799-chr6:27655486..27657530,2	K562	blood:
2	chr6:27650810..27652452-chr6:27664583..27667295,2	MCF-7	breast:
3	chr6:27661665..27662337-chr6:27720402..27720938,2	MCF-7	breast:
4	chr14:24682276..24682781-chr6:27661990..27662656,2	Hela-S3	cervix:
5	chr6:27660759..27663376-chr6:27861041..27863812,2	K562	blood:
6	chr6:27655786..27657671-chr6:27777694..27780064,2	K562	blood:
7	chr6:27653789..27659338-chr6:27659392..27663401,13	K562	blood:
8	chr6:27652252..27653760-chr6:27657291..27659495,2	MCF-7	breast:
9	chr6:27657772..27659329-chr6:27759649..27761328,2	K562	blood:
10	chr6:27656124..27658141-chr6:27861315..27864462,3	K562	blood:
11	chr6:27651170..27656145-chr6:27660253..27663653,4	MCF-7	breast:
12	chr6:27114783..27117247-chr6:27654285..27656648,2	K562	blood:
13	chr6:27661813..27662703-chr6:27719579..27720188,2	MCF-7	breast:
14	chr6:27568300..27570576-chr6:27654240..27656534,2	K562	blood:
15	chr6:27100391..27103275-chr6:27661781..27664479,3	K562	blood:
16	chr6:27663855..27666018-chr6:27668315..27670242,2	MCF-7	breast:
17	chr6:27653789..27659338-chr6:27659392..27663401,13	K562	blood:
18	chr6:27517580..27520296-chr6:27658437..27660745,2	K562	blood:
19	chr6:27660759..27663752-chr6:27861076..27863812,2	K562	blood:
20	chr6:27202749..27204748-chr6:27656090..27658081,2	K562	blood:
21	chr6:27659790..27663314-chr6:27665578..27668905,6	K562	blood:
22	chr6:27659151..27662876-chr6:27687364..27691190,4	K562	blood:
23	chr6:27559025..27560718-chr6:27653331..27656285,2	K562	blood:
24	chr6:27179126..27181346-chr6:27660529..27662958,2	K562	blood:
25	chr6:27658926..27663446-chr6:27685398..27690588,6	K562	blood:
26	chr6:27663855..27666018-chr6:27668315..27670242,2	MCF-7	breast:
27	chr6:27661399..27663799-chr6:27664607..27667603,2	MCF-7	breast:
28	chr6:27638340..27640249-chr6:27659440..27661461,2	K562	blood:
29	chr6:27651230..27653525-chr6:27660393..27663354,2	MCF-7	breast:
30	chr6:27651170..27656145-chr6:27660253..27663653,4	MCF-7	breast:
31	chr6:27655564..27658376-chr6:27856463..27858379,2	K562	blood:
32	chr6:27661331..27663089-chr6:27665763..27668347,2	K562	blood:
33	chr6:27661478..27663340-chr6:27680780..27682655,2	K562	blood:
34	chr6:27114898..27117828-chr6:27655156..27657411,2	MCF-7	breast:
35	chr6:27662005..27662637-chr6:31619681..31620477,2	Hela-S3	cervix:
36	chr6:27661232..27663489-chr6:27678201..27680638,2	K562	blood:
37	chr6:27260766..27263711-chr6:27659606..27661608,2	K562	blood:
38	chr6:27670250..27673191-chr6:27723819..27726632,2	K562	blood:
39	chr6:27655233..27656837-chr6:27693147..27694855,2	K562	blood:
40	chr6:27661606..27663243-chr6:27719625..27721150,2	K562	blood:
41	chr6:27656133..27659088-chr6:27710854..27712483,2	K562	blood:
42	chr6:27669358..27671049-chr6:27700076..27702911,2	K562	blood:
43	chr6:27104177..27107088-chr6:27654712..27657071,2	K562	blood:
44	chr6:27655370..27657742-chr6:27715050..27717959,2	K562	blood:
45	chr6:27655233..27657099-chr6:27693355..27695720,2	K562	blood:
46	chr6:27665264..27666796-chr6:27688059..27690362,2	K562	blood:
47	chr6:26595641..26598321-chr6:27660238..27661908,2	K562	blood:
48	chr6:27518096..27521091-chr6:27655240..27657826,2	K562	blood:
49	chr6:27654225..27656931-chr6:27719778..27721751,2	K562	blood:
50	chr6:27654652..27657286-chr6:27777694..27780046,3	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HIST1H2BL-2	chr6:27672956-27673553	NONHSAT108399
2	lnc-HIST1H2AI-3	chr6:27661814-27662285	XLOC_005219
3	lnc-HIST1H2AI-3	chr6:27661858-27662005	NONHSAT108398
4	lnc-HIST1H2AI-3	chr6:27661865-27662005	XLOC_005219
5	lnc-HIST1H2AI-3	chr6:27670093-27670196	XLOC_005219
6	lnc-HIST1H2AI-3	chr6:27667376-27667442	NONHSAT108397
7	lnc-HIST1H2AI-3	chr6:27661814-27662285	XLOC_005219
8	lnc-HIST1H2AI-3	chr6:27661814-27662005	XLOC_005219
9	lnc-HIST1H2AI-3	chr6:27670093-27670196	NONHSAT108398
10	lnc-HIST1H2AI-3	chr6:27670093-27670196	XLOC_005219
11	lnc-HIST1H2BL-2	chr6:27672903-27672947	NONHSAT108399
12	lnc-HIST1H2AI-3	chr6:27661814-27662285	NONHSAT108394
13	lnc-HIST1H2AI-3	chr6:27670093-27670196	XLOC_005219
14	lnc-HIST1H2AI-3	chr6:27661814-27662285	NONHSAT108395
15	lnc-HIST1H2AI-3	chr6:27670093-27670196	NONHSAT108394
16	lnc-HIST1H2AI-3	chr6:27670093-27670196	XLOC_005219
17	lnc-HIST1H2AI-3	chr6:27670093-27670196	NONHSAT108395
18	lnc-HIST1H2AI-3	chr6:27670093-27670198	NONHSAT108397
19	lnc-HIST1H2AI-3	chr6:27661858-27662005	ENSG00000246046
20	lnc-HIST1H2AI-3	chr6:27661843-27662285	NONHSAT108397
21	lnc-HIST1H2AI-3	chr6:27670093-27670196	ENSG00000246046

No data

Variant related genes	Relation type
ENSG00000146109	chromatin interactions
ENSG00000203813	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000124635	chromatin interactions
ENSG00000254505	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000265565	chromatin interactions
ENSG00000187837	chromatin interactions
ENSG00000254692	chromatin interactions
ENSG00000196331	chromatin interactions
ENSG00000198339	chromatin interactions
ENSG00000184825	chromatin interactions
BRD8	miRNA target sites
VAPA	miRNA target sites
TOP1	miRNA target sites
POLR2D	miRNA target sites

Extended variants
information (count: 729 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:729 , 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	rs191937477	chr6:27656050-27656051	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs115680175	chr6:27656053-27656054	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs148693769	chr6:27656055-27656056	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs549424608	chr6:27656056-27656057	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs566173250	chr6:27656058-27656059	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs116171085	chr6:27656061-27656062	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs141300966	chr6:27656069-27656070	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs112227551	chr6:27656073-27656074	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs16867901	chr6:27656076-27656077	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs369258543	chr6:27656080-27656081	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs574023897	chr6:27656088-27656089	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs9348772	chr6:27656090-27656091	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs552591476	chr6:27656098-27656099	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs572809071	chr6:27656104-27656105	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs139129217	chr6:27656105-27656106	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs374471256	chr6:27656108-27656109	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs564902350	chr6:27656111-27656112	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs145168562	chr6:27656120-27656121	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs9393845	chr6:27656122-27656123	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs565965173	chr6:27656132-27656133	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs561142447	chr6:27656136-27656137	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs200877522	chr6:27656137-27656138	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs530062281	chr6:27656138-27656139	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs543004818	chr6:27656139-27656140	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs559788321	chr6:27656145-27656146	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs528550422	chr6:27656157-27656158	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs146165301	chr6:27656161-27656162	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs369802842	chr6:27656163-27656164	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs551869194	chr6:27656168-27656169	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs571686941	chr6:27656198-27656199	Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs374046589	chr6:27656203-27656204	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs376977408	chr6:27656231-27656232	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs111392566	chr6:27656242-27656243	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs550810653	chr6:27656243-27656244	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs10946943	chr6:27656255-27656256	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs536556534	chr6:27656271-27656272	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs147583250	chr6:27656291-27656292	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs566483103	chr6:27656328-27656329	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs185314299	chr6:27656339-27656340	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs34834027	chr6:27656374-27656375	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs11412338	chr6:27656375-27656376	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs538318856	chr6:27656380-27656381	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs398001069	chr6:27656391-27656392	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs12055685	chr6:27656400-27656401	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs530991781	chr6:27656423-27656424	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs575271890	chr6:27656431-27656432	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs187788311	chr6:27656470-27656471	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs9380006	chr6:27656499-27656500	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs551251110	chr6:27656517-27656518	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs548338360	chr6:27656538-27656539	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
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
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	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
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
Breast cancer	22032731	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
T-cell lymphomas	19863542	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
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:631 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:27653600-27656600	Active TSS	HUES6 Cell Line	embryonic stem cell
2	chr6:27654200-27656600	Active TSS	H1 Cell Line	embryonic stem cell
3	chr6:27654600-27656400	Active TSS	HUES48 Cell Line	embryonic stem cell
4	chr6:27654600-27656600	Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr6:27654800-27656200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:27654800-27656400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr6:27654800-27656400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr6:27654800-27656400	Active TSS	HMEC	breast
9	chr6:27654800-27656600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:27654800-27656600	Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr6:27654800-27656600	Active TSS	iPS-18 Cell Line	embryonic stem cell
12	chr6:27654800-27656600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:27654800-27656600	Active TSS	A549	lung
14	chr6:27654800-27656600	Flanking Active TSS	Dnd41	blood
15	chr6:27654800-27657200	Active TSS	K562	blood
16	chr6:27655000-27656200	Active TSS	Brain Anterior Caudate	brain
17	chr6:27655000-27656200	Active TSS	Brain Substantia Nigra	brain
18	chr6:27655000-27656200	Active TSS	Colon Smooth Muscle	Colon
19	chr6:27655000-27656200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
20	chr6:27655000-27656200	Active TSS	Right Ventricle	heart
21	chr6:27655000-27656200	Active TSS	HSMM	muscle
22	chr6:27655000-27656200	Active TSS	HSMMtube	muscle
23	chr6:27655000-27656200	Flanking Active TSS	HUVEC	blood vessel
24	chr6:27655000-27656200	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
25	chr6:27655000-27656400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:27655000-27656400	Active TSS	H9 Cell Line	embryonic stem cell
27	chr6:27655000-27656400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr6:27655000-27656400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr6:27655000-27656400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr6:27655000-27656400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr6:27655000-27656400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
32	chr6:27655000-27656400	Flanking Active TSS	Primary B cells from peripheral blood	blood
33	chr6:27655000-27656400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
34	chr6:27655000-27656400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr6:27655000-27656400	Active TSS	Brain Cingulate Gyrus	brain
36	chr6:27655000-27656400	Active TSS	Brain Inferior Temporal Lobe	brain
37	chr6:27655000-27656400	Active TSS	Fetal Brain Male	brain
38	chr6:27655000-27656400	Bivalent/Poised TSS	Fetal Kidney	kidney
39	chr6:27655000-27656400	Active TSS	Fetal Lung	lung
40	chr6:27655000-27656400	Active TSS	Ovary	ovary
41	chr6:27655000-27656400	Active TSS	Rectal Smooth Muscle	rectum
42	chr6:27655000-27656400	Active TSS	Hela-S3	cervix
43	chr6:27655000-27656400	Active TSS	NHDF-Ad	bronchial
44	chr6:27655000-27656600	Active TSS	ES-I3 Cell Line	embryonic stem cell
45	chr6:27655000-27656600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
46	chr6:27655000-27656600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr6:27655000-27656600	Active TSS	iPS-15b Cell Line	embryonic stem cell
48	chr6:27655200-27656200	Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr6:27655200-27656200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
50	chr6:27655200-27656200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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