Variant report

Variant	nsv601204
Chromosome Location	chr6:27655564-27689502
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:88)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:27659151..27662876-chr6:27687364..27691190,4	K562	blood:
2	chr6:27655370..27657742-chr6:27715050..27717959,2	K562	blood:
3	chr6:27665264..27666796-chr6:27688059..27690362,2	K562	blood:
4	chr6:27662005..27662637-chr6:31619681..31620477,2	Hela-S3	cervix:
5	chr6:27114783..27117247-chr6:27654285..27656648,2	K562	blood:
6	chr6:27638340..27640249-chr6:27659440..27661461,2	K562	blood:
7	chr6:27658926..27663446-chr6:27685398..27690588,6	K562	blood:
8	chr6:27653789..27659338-chr6:27659392..27663401,13	K562	blood:
9	chr6:27114795..27117088-chr6:27688794..27690487,2	K562	blood:
10	chr6:27671590..27673866-chr6:27681015..27683164,2	K562	blood:
11	chr6:27114898..27117828-chr6:27655156..27657411,2	MCF-7	breast:
12	chr6:27671590..27673866-chr6:27681015..27683164,2	K562	blood:
13	chr6:27517580..27520296-chr6:27658437..27660745,2	K562	blood:
14	chr6:27655564..27658376-chr6:27856463..27858379,2	K562	blood:
15	chr6:27585302..27586142-chr6:27655326..27655973,2	K562	blood:
16	chr6:27644939..27650269-chr6:27651814..27657274,7	K562	blood:
17	chr6:27688928..27690631-chr6:27710497..27712546,2	MCF-7	breast:
18	chr6:27676712..27678626-chr6:27679096..27681049,2	K562	blood:
19	chr6:27677806..27681371-chr6:27682071..27685052,3	K562	blood:
20	chr6:27661232..27663489-chr6:27678201..27680638,2	K562	blood:
21	chr6:27683083..27685640-chr6:27686917..27688772,2	MCF-7	breast:
22	chr6:27636299..27636853-chr6:27655225..27655832,2	K562	blood:
23	chr6:27653789..27659338-chr6:27659392..27663401,13	K562	blood:
24	chr6:27651170..27656145-chr6:27660253..27663653,4	MCF-7	breast:
25	chr6:27659790..27663314-chr6:27665578..27668905,6	K562	blood:
26	chr6:27656133..27659088-chr6:27710854..27712483,2	K562	blood:
27	chr6:27596183..27599052-chr6:27654192..27655700,2	K562	blood:
28	chr6:27100391..27103275-chr6:27661781..27664479,3	K562	blood:
29	chr6:27683083..27685640-chr6:27686917..27688772,2	MCF-7	breast:
30	chr6:27660759..27663376-chr6:27861041..27863812,2	K562	blood:
31	chr6:27676712..27678626-chr6:27679096..27681049,2	K562	blood:
32	chr6:26595641..26598321-chr6:27660238..27661908,2	K562	blood:
33	chr6:27598632..27599274-chr6:27655396..27655916,2	K562	blood:
34	chr6:27661665..27662337-chr6:27720402..27720938,2	MCF-7	breast:
35	chr6:27660759..27663752-chr6:27861076..27863812,2	K562	blood:
36	chr6:27654225..27656931-chr6:27719778..27721751,2	K562	blood:
37	chr6:27526508..27528799-chr6:27655486..27657530,2	K562	blood:
38	chr6:27518096..27521091-chr6:27655240..27657826,2	K562	blood:
39	chr6:27676729..27679149-chr6:27683111..27685492,2	K562	blood:
40	chr6:27670250..27673191-chr6:27723819..27726632,2	K562	blood:
41	chr6:27202749..27204748-chr6:27656090..27658081,2	K562	blood:
42	chr6:27687897..27691780-chr6:27691811..27694513,3	MCF-7	breast:
43	chr6:27179126..27181346-chr6:27660529..27662958,2	K562	blood:
44	chr6:27641336..27643543-chr6:27677360..27680125,2	K562	blood:
45	chr6:27655233..27657099-chr6:27693355..27695720,2	K562	blood:
46	chr6:27659790..27663314-chr6:27665578..27668905,6	K562	blood:
47	chr6:27104177..27107088-chr6:27654712..27657071,2	K562	blood:
48	chr6:27676729..27679149-chr6:27683111..27685492,2	K562	blood:
49	chr6:27655786..27657671-chr6:27777694..27780064,2	K562	blood:
50	chr6:27660493..27662208-chr6:27687324..27689056,2	MCF-7	breast:

(count:36 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HIST1H2AI-3	chr6:27670093-27670196	NONHSAT108395
2	lnc-HIST1H2AI-3	chr6:27678460-27678670	NONHSAT108397
3	lnc-HIST1H2AI-2	chr6:27677989-27678004	XLOC_005220
4	lnc-HIST1H2BL-2	chr6:27672956-27673553	NONHSAT108399
5	lnc-HIST1H2AI-3	chr6:27661814-27662285	XLOC_005219
6	lnc-HIST1H2AI-3	chr6:27661814-27662285	NONHSAT108394
7	lnc-HIST1H2AI-3	chr6:27674418-27676936	NONHSAT108398
8	lnc-HIST1H2BL-2	chr6:27672903-27672947	NONHSAT108399
9	lnc-HIST1H2AI-3	chr6:27674418-27676935	ENSG00000246046
10	lnc-HIST1H2AI-3	chr6:27661814-27662005	XLOC_005219
11	lnc-HIST1H2AI-3	chr6:27661858-27662005	ENSG00000246046
12	lnc-HIST1H2BL-2	chr6:27674985-27675450	NONHSAT108399
13	lnc-HIST1H2AI-3	chr6:27670093-27670196	XLOC_005219
14	lnc-HIST1H2AI-2	chr6:27680783-27680876	XLOC_005220
15	lnc-HIST1H2AI-3	chr6:27674418-27674530	XLOC_005219
16	lnc-HIST1H2AI-3	chr6:27680783-27681184	NONHSAT108397
17	lnc-HIST1H2BL-2	chr6:27680492-27681059	NONHSAT108399
18	lnc-HIST1H2AI-3	chr6:27670093-27670196	ENSG00000246046
19	lnc-HIST1H2AI-3	chr6:27670093-27670196	NONHSAT108398
20	lnc-HIST1H2AI-3	chr6:27661858-27662005	NONHSAT108398
21	lnc-HIST1H2AI-3	chr6:27670093-27670196	NONHSAT108394
22	lnc-HIST1H2AI-3	chr6:27670093-27670196	XLOC_005219
23	lnc-HIST1H2AI-3	chr6:27667376-27667442	NONHSAT108397
24	lnc-HIST1H2AI-3	chr6:27677903-27678001	NONHSAT108394
25	lnc-HIST1H2AI-3	chr6:27661865-27662005	XLOC_005219
26	lnc-HIST1H2AI-3	chr6:27661814-27662285	XLOC_005219
27	lnc-HIST1H2AI-3	chr6:27670093-27670196	XLOC_005219
28	lnc-HIST1H2AI-3	chr6:27670093-27670196	XLOC_005219
29	lnc-HIST1H2AI-3	chr6:27674418-27676935	XLOC_005219
30	lnc-HIST1H2AI-2	chr6:27678460-27678668	XLOC_005220
31	lnc-HIST1H2AI-3	chr6:27675118-27675276	NONHSAT108397
32	lnc-HIST1H2AI-3	chr6:27670093-27670198	NONHSAT108397
33	lnc-HIST1H2AI-3	chr6:27661843-27662285	NONHSAT108397
34	lnc-HIST1H2AI-3	chr6:27677903-27678001	NONHSAT108395
35	lnc-HIST1H2AI-3	chr6:27675118-27675195	NONHSAT108395
36	lnc-HIST1H2AI-3	chr6:27661814-27662285	NONHSAT108395

No data

Variant related genes	Relation type
ENSG00000124635	chromatin interactions
ENSG00000146109	chromatin interactions
ENSG00000187837	chromatin interactions
ENSG00000203813	chromatin interactions
ENSG00000184825	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000238648	chromatin interactions
ENSG00000265565	chromatin interactions
ENSG00000254692	chromatin interactions
ENSG00000196331	chromatin interactions
ENSG00000254505	chromatin interactions
ENSG00000198339	chromatin interactions
ENSG00000204463	chromatin interactions
POLR2D	miRNA target sites
TOP1	miRNA target sites
BRD8	miRNA target sites
VAPA	miRNA target sites

Extended variants
information (count: 1321 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1321 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1010261	chr6:27655564-27655565	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563306671	chr6:27655589-27655590	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs568072039	chr6:27655601-27655602	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs62401400	chr6:27655630-27655631	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs535159125	chr6:27655700-27655701	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs528911586	chr6:27655704-27655705	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs181675067	chr6:27655744-27655745	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs559088454	chr6:27655790-27655791	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs371740218	chr6:27655795-27655796	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs528255555	chr6:27655797-27655798	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs372929817	chr6:27655821-27655822	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs565031655	chr6:27655825-27655826	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs186220259	chr6:27655935-27655936	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs549866406	chr6:27655943-27655944	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs570068026	chr6:27655946-27655947	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs191461676	chr6:27655954-27655955	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs182359831	chr6:27655957-27655958	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs188052367	chr6:27655958-27655959	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs190829516	chr6:27655959-27655960	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs183382877	chr6:27655967-27655968	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs578159053	chr6:27655971-27655972	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs375522708	chr6:27655977-27655978	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs9393844	chr6:27655981-27655982	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs556513724	chr6:27655982-27655983	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs573317457	chr6:27655987-27655988	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs1555021	chr6:27655994-27655995	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs376636798	chr6:27655997-27655998	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs531478843	chr6:27656000-27656001	Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs559002434	chr6:27656003-27656004	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	rs200081838	chr6:27656007-27656008	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	rs572650443	chr6:27656009-27656010	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
32	rs368899656	chr6:27656016-27656017	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
33	rs372010290	chr6:27656018-27656019	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
34	rs146043275	chr6:27656020-27656021	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
35	rs530669452	chr6:27656034-27656035	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
36	rs187838445	chr6:27656039-27656040	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
37	rs376773718	chr6:27656047-27656048	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
38	rs373376749	chr6:27656048-27656049	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
39	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
40	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
41	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
42	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
43	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
44	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
45	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
46	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
47	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
48	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
49	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
50	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

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:900 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

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	chr6:27654800-27656000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr6:27654800-27656200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:27654800-27656400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr6:27654800-27656400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr6:27654800-27656400	Active TSS	HMEC	breast
10	chr6:27654800-27656600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:27654800-27656600	Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr6:27654800-27656600	Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chr6:27654800-27656600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr6:27654800-27656600	Active TSS	A549	lung
15	chr6:27654800-27656600	Flanking Active TSS	Dnd41	blood
16	chr6:27654800-27657200	Active TSS	K562	blood
17	chr6:27655000-27655600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
18	chr6:27655000-27655600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
19	chr6:27655000-27655600	Flanking Bivalent TSS/Enh	Placenta	Placenta
20	chr6:27655000-27655800	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
21	chr6:27655000-27655800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
22	chr6:27655000-27655800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
23	chr6:27655000-27656000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr6:27655000-27656000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr6:27655000-27656000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr6:27655000-27656000	Flanking Active TSS	Primary B cells from cord blood	blood
27	chr6:27655000-27656000	Flanking Active TSS	Primary hematopoietic stem cells	blood
28	chr6:27655000-27656000	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
29	chr6:27655000-27656000	Flanking Active TSS	Adipose Nuclei	Adipose
30	chr6:27655000-27656000	Flanking Active TSS	Duodenum Mucosa	Duodenum
31	chr6:27655000-27656000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
32	chr6:27655000-27656000	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
33	chr6:27655000-27656000	Bivalent/Poised TSS	HepG2	liver
34	chr6:27655000-27656000	Active TSS	NHLF	lung
35	chr6:27655000-27656200	Active TSS	Brain Anterior Caudate	brain
36	chr6:27655000-27656200	Active TSS	Brain Substantia Nigra	brain
37	chr6:27655000-27656200	Active TSS	Colon Smooth Muscle	Colon
38	chr6:27655000-27656200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
39	chr6:27655000-27656200	Active TSS	Right Ventricle	heart
40	chr6:27655000-27656200	Active TSS	HSMM	muscle
41	chr6:27655000-27656200	Active TSS	HSMMtube	muscle
42	chr6:27655000-27656200	Flanking Active TSS	HUVEC	blood vessel
43	chr6:27655000-27656200	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
44	chr6:27655000-27656400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr6:27655000-27656400	Active TSS	H9 Cell Line	embryonic stem cell
46	chr6:27655000-27656400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:27655000-27656400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr6:27655000-27656400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr6:27655000-27656400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr6:27655000-27656400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell

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