Variant report

Variant	nsv970084
Chromosome Location	chr6:26183939-26184583
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:191)
CpG islands
(count:245)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:191 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:26183349-26185499	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr6:26183368-26185155	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr6:26183994-26184443	GM12878	blood:	n/a	n/a
4	BCL11A	chr6:26183924-26184436	GM12878	blood:	n/a	chr6:26183985-26183994
5	BCL11A	chr6:26184012-26184420	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:26183650-26184078	GM12878	blood:	n/a	n/a
7	CEBPB	chr6:26183490-26184613	GM12878	blood:	n/a	n/a
8	CEBPB	chr6:26184352-26184354	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD1	chr6:26184325-26184513	GM12878	blood:	n/a	n/a
10	CHD1	chr6:26183988-26185281	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr6:26183487-26184118	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr6:26184430-26184617	H1-hESC	embryonic stem cell:	n/a	n/a
13	EBF1	chr6:26184035-26184441	GM12878	blood:	n/a	n/a
14	EP300	chr6:26183598-26184171	SK-N-SH	brain:	n/a	chr6:26183985-26183999
15	EP300	chr6:26183925-26184505	GM12878	blood:	n/a	chr6:26183985-26183999
16	EP300	chr6:26183986-26184363	GM12878	blood:	n/a	n/a
17	EP300	chr6:26183835-26184211	A549	lung:	n/a	chr6:26183985-26183999
18	FOSL2	chr6:26183955-26184367	HepG2	liver:	n/a	chr6:26183987-26183996
19	FOXA1	chr6:26184098-26184396	HepG2	liver:	n/a	n/a
20	FOXA2	chr6:26184176-26184475	A549	lung:	n/a	n/a
21	FOXM1	chr6:26183759-26184435	GM12878	blood:	n/a	n/a
22	GABPA	chr6:26184203-26184333	Hela-S3	cervix:	n/a	n/a
23	GABPA	chr6:26184162-26184375	Hela-S3	cervix:	n/a	n/a
24	GATA1	chr6:26183608-26184668	PBDE	blood:	n/a	n/a
25	GTF2F1	chr6:26183409-26184349	H1-hESC	embryonic stem cell:	n/a	n/a
26	HEY1	chr6:26183880-26184391	HepG2	liver:	n/a	n/a
27	HEY1	chr6:26183919-26184477	K562	blood:	n/a	n/a
28	HEY1	chr6:26183991-26184355	HepG2	liver:	n/a	n/a
29	HEY1	chr6:26183891-26184443	K562	blood:	n/a	n/a
30	IRF4	chr6:26183943-26184485	GM12878	blood:	n/a	n/a
31	IRF4	chr6:26183894-26184456	GM12878	blood:	n/a	n/a
32	JUND	chr6:26184265-26184453	H1-hESC	embryonic stem cell:	n/a	n/a
33	JUND	chr6:26183950-26184175	H1-hESC	embryonic stem cell:	n/a	chr6:26183987-26183996
34	JUND	chr6:26184191-26184358	HepG2	liver:	n/a	n/a
35	JUND	chr6:26183409-26184565	H1-hESC	embryonic stem cell:	n/a	chr6:26183851-26183860 chr6:26183987-26183996
36	JUND	chr6:26183978-26184311	A549	lung:	n/a	chr6:26183987-26183996
37	MAFK	chr6:26183943-26184208	H1-hESC	embryonic stem cell:	n/a	n/a
38	MAFK	chr6:26183717-26184192	IMR90	lung:	n/a	n/a
39	MAX	chr6:26184312-26184399	GM12878	blood:	n/a	n/a
40	MAX	chr6:26183511-26184246	SK-N-SH	brain:	n/a	n/a
41	MAX	chr6:26183692-26184130	NB4	blood:	n/a	n/a
42	MTA3	chr6:26183764-26184787	GM12878	blood:	n/a	n/a
43	MXI1	chr6:26183987-26184395	GM12878	blood:	n/a	n/a
44	MXI1	chr6:26184567-26184595	H1-hESC	embryonic stem cell:	n/a	n/a
45	MYC	chr6:26184050-26184270	MCF-7	breast:	n/a	n/a
46	MYC	chr6:26184159-26184394	MCF-7	breast:	n/a	n/a
47	NFATC1	chr6:26183760-26184514	GM12878	blood:	n/a	n/a
48	NFIC	chr6:26183594-26184827	GM12878	blood:	n/a	n/a
49	NFIC	chr6:26183711-26184357	GM12878	blood:	n/a	n/a
50	NFYA	chr6:26183750-26183993	GM12878	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26184227-26184277	HEK293	kidney:	embryo
2	chr6:26184227-26184277	HEK293	kidney:	embryo
3	chr6:26184227-26184277	IMR90	lung:	fetal
4	chr6:26184037-26184087	HPAEpiC	pulmonary alveolar:	n/a
5	chr6:26184227-26184277	NHBE	bronchial:	n/a
6	chr6:26184245-26184295	NHDF-neo	bronchial:	n/a
7	chr6:26184037-26184087	HUVEC	blood vessel:	n/a
8	chr6:26183899-26183949	NT2-D1	testis:	n/a
9	chr6:26184227-26184277	ProgFib	skin:	n/a
10	chr6:26184037-26184087	SK-N-SH	brain:	n/a
11	chr6:26184037-26184087	BE2_C	brain:	n/a
12	chr6:26184227-26184277	SKMC	muscle:	n/a
13	chr6:26184227-26184277	AG09309	skin:	n/a
14	chr6:26184227-26184277	HUVEC	blood vessel:	n/a
15	chr6:26184037-26184087	AoSMC	blood vessel:	n/a
16	chr6:26184037-26184087	HRPEpiC	eye:	n/a
17	chr6:26184245-26184295	HUVEC	blood vessel:	n/a
18	chr6:26183899-26183949	HAEpiC	amniotic membrane:	n/a
19	chr6:26184037-26184087	NHBE	bronchial:	n/a
20	chr6:26183899-26183949	AG10803	skin:	n/a
21	chr6:26184037-26184087	HEEpiC	esophagus:	n/a
22	chr6:26184227-26184277	BE2_C	brain:	n/a
23	chr6:26184227-26184277	RPTEC	kidney:	n/a
24	chr6:26183899-26183949	MCF-7	breast:	n/a
25	chr6:26184037-26184087	AG10803	skin:	n/a
26	chr6:26184227-26184277	LNCaP	prostate:	n/a
27	chr6:26184037-26184087	HCT-116	colon:	n/a
28	chr6:26183899-26183949	PrEC	prostate:	n/a
29	chr6:26184227-26184277	T-47D	breast:	n/a
30	chr6:26183899-26183949	AG04449	skin:	fetal
31	chr6:26184245-26184295	AG09319	gingival:	n/a
32	chr6:26184245-26184295	GM12892	blood:	n/a
33	chr6:26184037-26184087	Caco-2	colon:	n/a
34	chr6:26184245-26184295	NHBE	bronchial:	n/a
35	chr6:26184245-26184295	IMR90	lung:	fetal
36	chr6:26183899-26183949	HNPCEpiC	eye:	n/a
37	chr6:26183899-26183949	HepG2	liver:	n/a
38	chr6:26184227-26184277	GM06990	blood:	n/a
39	chr6:26183899-26183949	Hepatocyte	liver:	n/a
40	chr6:26184037-26184087	HRCEpiC	kidney:	n/a
41	chr6:26184037-26184087	PANC-1	pancreas:	n/a
42	chr6:26184245-26184295	HCPEpiC	choroid plexus:	n/a
43	chr6:26184245-26184295	Hepatocyte	liver:	n/a
44	chr6:26184227-26184277	HRPEpiC	eye:	n/a
45	chr6:26184245-26184295	H1-hESC	embryonic stem cell:	embryo
46	chr6:26183899-26183949	HMEC	breast:	n/a
47	chr6:26184227-26184277	SK-N-SH_RA	brain:	n/a
48	chr6:26184245-26184295	HAEpiC	amniotic membrane:	n/a
49	chr6:26184037-26184087	NB4	blood:	n/a
50	chr6:26184227-26184277	SK-N-MC	brain:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26032288..26035408-chr6:26183846..26189517,7	MCF-7	breast:
2	chr2:97534211..97537154-chr6:26181504..26183977,2	MCF-7	breast:
3	chr6:26044671..26047980-chr6:26183838..26186075,3	MCF-7	breast:
4	chr6:26183122..26184759-chr9:135545223..135546937,2	MCF-7	breast:
5	chr6:26181774..26184572-chr6:27859696..27862295,2	MCF-7	breast:
6	chr6:26183858..26185495-chr7:104652929..104654673,2	MCF-7	breast:
7	chr6:26182173..26185335-chr6:27780962..27783737,3	MCF-7	breast:
8	chr6:26054953..26059351-chr6:26183267..26187731,5	MCF-7	breast:
9	chr6:26158163..26159015-chr6:26183506..26184251,2	MCF-7	breast:
10	chr6:26183066..26187877-chr6:27774821..27779151,5	MCF-7	breast:

No data

Variant related genes	Relation type
HIST1H2BE	TF binding region
HIST1H2BE	CpG island
ENSG00000137259	chromatin interactions
ENSG00000203813	chromatin interactions
ENSG00000125484	chromatin interactions
ENSG00000217862	chromatin interactions
ENSG00000196747	chromatin interactions
ENSG00000005483	chromatin interactions
ENSG00000185130	chromatin interactions
ENSG00000124693	chromatin interactions
ENSG00000196532	chromatin interactions
ENSG00000239569	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000125485	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000187837	chromatin interactions
ENSG00000233224	chromatin interactions
ENSG00000168758	chromatin interactions
ENSG00000196374	chromatin interactions
ENSG00000182611	chromatin interactions
ENSG00000196331	chromatin interactions

Extended variants
information (count: 62 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:62 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181407485	chr6:26183950-26183951	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
2	rs574468451	chr6:26183954-26183955	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
3	rs577228714	chr6:26183955-26183956	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
4	rs528799710	chr6:26183956-26183957	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
5	rs377528815	chr6:26183980-26183981	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
6	rs529730207	chr6:26183982-26183983	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
7	rs370696344	chr6:26183989-26183990	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
8	rs138620090	chr6:26183991-26183992	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
9	rs576902929	chr6:26183998-26183999	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
10	rs574400757	chr6:26184008-26184009	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
11	rs116848504	chr6:26184011-26184012	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
12	rs114173719	chr6:26184013-26184014	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
13	rs201385344	chr6:26184033-26184034	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
14	rs148688357	chr6:26184034-26184035	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
15	rs16891375	chr6:26184041-26184042	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs146757427	chr6:26184043-26184044	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
17	rs145468173	chr6:26184055-26184056	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
18	rs368968049	chr6:26184064-26184065	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
19	rs371930376	chr6:26184065-26184066	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
20	rs570095612	chr6:26184074-26184075	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
21	rs374387585	chr6:26184075-26184076	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
22	rs529756458	chr6:26184080-26184081	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
23	rs61978632	chr6:26184082-26184083	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs141005448	chr6:26184083-26184084	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
25	rs371699016	chr6:26184089-26184090	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
26	rs549755584	chr6:26184091-26184092	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
27	rs374653390	chr6:26184098-26184099	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
28	rs7766641	chr6:26184102-26184103	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs552518996	chr6:26184112-26184113	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
30	rs369028901	chr6:26184143-26184144	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
31	rs112927641	chr6:26184149-26184150	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
32	rs569385193	chr6:26184203-26184204	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
33	rs538164578	chr6:26184206-26184207	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
34	rs185241633	chr6:26184207-26184208	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
35	rs568409555	chr6:26184218-26184219	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
36	rs371923151	chr6:26184224-26184225	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
37	rs138743711	chr6:26184231-26184232	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
38	rs199592828	chr6:26184267-26184268	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
39	rs572484796	chr6:26184272-26184273	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
40	rs553736996	chr6:26184278-26184279	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
41	rs201769089	chr6:26184284-26184285	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
42	rs191131837	chr6:26184286-26184287	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
43	rs149352594	chr6:26184291-26184292	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
44	rs558477628	chr6:26184295-26184296	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
45	rs143792250	chr6:26184308-26184309	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
46	rs146191676	chr6:26184317-26184318	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
47	rs143978911	chr6:26184338-26184339	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
48	rs370186182	chr6:26184354-26184355	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
49	rs374025158	chr6:26184368-26184369	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
50	rs147307438	chr6:26184371-26184372	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Multiple myeloma	17550852	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
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	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
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Williams-beuren syndrome	16971481	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Autism	22495309	CNVD
Lung cancer	21569311	CNVD
Breast cancer	21509527	CNVD
Autism	20808228	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26179200-26184000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:26182000-26193000	Weak transcription	Dnd41	blood
3	chr6:26183000-26184400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:26183000-26184400	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr6:26183000-26184400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr6:26183000-26185000	Active TSS	iPS-15b Cell Line	embryonic stem cell
7	chr6:26183200-26184000	Active TSS	Rectal Mucosa Donor 31	rectum
8	chr6:26183200-26184200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr6:26183200-26184400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr6:26183200-26184400	Active TSS	Breast Myoepithelial Primary Cells	Breast
11	chr6:26183200-26184400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:26183200-26184400	Active TSS	Brain Hippocampus Middle	brain
13	chr6:26183200-26184400	Active TSS	Duodenum Mucosa	Duodenum
14	chr6:26183200-26184400	Active TSS	Fetal Brain Male	brain
15	chr6:26183200-26184400	Active TSS	Fetal Thymus	thymus
16	chr6:26183200-26184400	Active TSS	Rectal Mucosa Donor 29	rectum
17	chr6:26183200-26184600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
18	chr6:26183200-26184600	Active TSS	Fetal Kidney	kidney
19	chr6:26183200-26184800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
20	chr6:26183200-26184800	Active TSS	H1 Cell Line	embryonic stem cell
21	chr6:26183200-26184800	Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr6:26183200-26184800	Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr6:26183200-26184800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
24	chr6:26183200-26184800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr6:26183200-26184800	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr6:26183200-26184800	Active TSS	Right Ventricle	heart
27	chr6:26183200-26185000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr6:26183200-26185000	Active TSS	Fetal Brain Female	brain
29	chr6:26183200-26185200	Active TSS	ES-I3 Cell Line	embryonic stem cell
30	chr6:26183200-26185400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr6:26183400-26184000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr6:26183400-26184000	Active TSS	Fetal Muscle Trunk	muscle
33	chr6:26183400-26184000	Active TSS	Lung	lung
34	chr6:26183400-26184000	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
35	chr6:26183400-26184200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
36	chr6:26183400-26184200	Active TSS	Placenta	Placenta
37	chr6:26183400-26184400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr6:26183400-26184400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:26183400-26184400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:26183400-26184400	Active TSS	Primary T cells from cord blood	blood
41	chr6:26183400-26184400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr6:26183400-26184400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr6:26183400-26184400	Active TSS	Brain Germinal Matrix	brain
44	chr6:26183400-26184400	Active TSS	Brain Inferior Temporal Lobe	brain
45	chr6:26183400-26184400	Active TSS	Colon Smooth Muscle	Colon
46	chr6:26183400-26184400	Active TSS	Duodenum Smooth Muscle	Duodenum
47	chr6:26183400-26184400	Active TSS	Fetal Heart	heart
48	chr6:26183400-26184400	Active TSS	Fetal Intestine Large	intestine
49	chr6:26183400-26184400	Active TSS	Fetal Intestine Small	intestine
50	chr6:26183400-26184400	Active TSS	Fetal Muscle Leg	muscle

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