Variant report

Variant	nsv1034359
Chromosome Location	chr6:167359643-167384714
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1512)
CpG islands
(count:856)
Chromatin interactive
region (count:30)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1512 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167371809-167372105	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167370020-167370428	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167364761-167365174	K562	blood:	n/a	n/a
4	ARID3A	chr6:167371261-167371329	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167372448-167372816	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167372891-167373023	K562	blood:	n/a	n/a
7	ATF1	chr6:167372668-167373071	K562	blood:	n/a	n/a
8	ATF1	chr6:167364441-167365172	K562	blood:	n/a	n/a
9	ATF2	chr6:167368553-167369203	GM12878	blood:	n/a	n/a
10	ATF2	chr6:167363635-167364298	GM12878	blood:	n/a	n/a
11	ATF2	chr6:167372716-167373205	GM12878	blood:	n/a	n/a
12	ATF2	chr6:167364472-167365159	GM12878	blood:	n/a	n/a
13	ATF2	chr6:167370572-167371300	GM12878	blood:	n/a	n/a
14	ATF2	chr6:167364414-167365219	GM12878	blood:	n/a	n/a
15	ATF3	chr6:167364420-167364692	GM12878	blood:	n/a	n/a
16	ATF3	chr6:167364469-167364752	K562	blood:	n/a	n/a
17	ATF3	chr6:167364440-167364776	K562	blood:	n/a	n/a
18	BACH1	chr6:167364962-167364983	K562	blood:	n/a	n/a
19	BACH1	chr6:167370745-167371043	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr6:167369850-167370482	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr6:167380221-167380224	K562	blood:	n/a	n/a
22	BACH1	chr6:167364844-167365106	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr6:167369879-167369882	K562	blood:	n/a	n/a
24	BATF	chr6:167368788-167369068	GM12878	blood:	n/a	n/a
25	BATF	chr6:167364411-167365081	GM12878	blood:	n/a	n/a
26	BATF	chr6:167363731-167364205	GM12878	blood:	n/a	n/a
27	BATF	chr6:167368743-167369035	GM12878	blood:	n/a	n/a
28	BATF	chr6:167363773-167364130	GM12878	blood:	n/a	n/a
29	BATF	chr6:167364402-167365169	GM12878	blood:	n/a	n/a
30	BCL11A	chr6:167364668-167365155	GM12878	blood:	n/a	n/a
31	BCL11A	chr6:167368671-167369160	GM12878	blood:	n/a	n/a
32	BCL11A	chr6:167364500-167365184	GM12878	blood:	n/a	n/a
33	BCL3	chr6:167368500-167369041	GM12878	blood:	n/a	n/a
34	BCL3	chr6:167363740-167364297	GM12878	blood:	n/a	chr6:167363938-167363947
35	BCL3	chr6:167364471-167365127	GM12878	blood:	n/a	n/a
36	BCL3	chr6:167368548-167369042	GM12878	blood:	n/a	n/a
37	BCLAF1	chr6:167368538-167369203	GM12878	blood:	n/a	n/a
38	BCLAF1	chr6:167370078-167370833	GM12878	blood:	n/a	n/a
39	BCLAF1	chr6:167368650-167369198	GM12878	blood:	n/a	n/a
40	BCLAF1	chr6:167364453-167365197	GM12878	blood:	n/a	n/a
41	BCLAF1	chr6:167363456-167364277	GM12878	blood:	n/a	chr6:167363938-167363947
42	BCLAF1	chr6:167363682-167364306	GM12878	blood:	n/a	chr6:167363938-167363947
43	BCLAF1	chr6:167364413-167365232	GM12878	blood:	n/a	n/a
44	BHLHE40	chr6:167371321-167371930	HepG2	liver:	n/a	n/a
45	BHLHE40	chr6:167369637-167371205	K562	blood:	n/a	chr6:167369798-167369814 chr6:167369784-167369800 chr6:167370180-167370196
46	BHLHE40	chr6:167365579-167366412	GM12878	blood:	n/a	chr6:167365904-167365913
47	BHLHE40	chr6:167363679-167365192	K562	blood:	n/a	n/a
48	BHLHE40	chr6:167369913-167371100	HepG2	liver:	n/a	chr6:167370180-167370196
49	BHLHE40	chr6:167368762-167369399	K562	blood:	n/a	n/a
50	BHLHE40	chr6:167363687-167365191	GM12878	blood:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167370224-167370274	HL-60	blood:	n/a
2	chr6:167369491-167369541	Hepatocyte	liver:	n/a
3	chr6:167370224-167370274	HL-60	blood:	n/a
4	chr6:167369491-167369541	Hepatocyte	liver:	n/a
5	chr6:167370648-167370698	H1-hESC	embryonic stem cell:	embryo
6	chr6:167370648-167370698	HCPEpiC	choroid plexus:	n/a
7	chr6:167370266-167370316	AG09309	skin:	n/a
8	chr6:167370276-167370326	HepG2	liver:	n/a
9	chr6:167369491-167369541	PrEC	prostate:	n/a
10	chr6:167370266-167370316	K562	blood:	n/a
11	chr6:167363345-167363395	HCF	heart:	n/a
12	chr6:167370529-167370579	SKMC	muscle:	n/a
13	chr6:167369504-167369554	PFSK-1	brain:	n/a
14	chr6:167368657-167368707	NT2-D1	testis:	n/a
15	chr6:167370587-167370637	NT2-D1	testis:	n/a
16	chr6:167370587-167370637	HCF	heart:	n/a
17	chr6:167369941-167369991	NT2-D1	testis:	n/a
18	chr6:167370648-167370698	PANC-1	pancreas:	n/a
19	chr6:167370224-167370274	PFSK-1	brain:	n/a
20	chr6:167370587-167370637	AG10803	skin:	n/a
21	chr6:167370266-167370316	MCF10A-Er-Src	breast:	n/a
22	chr6:167369504-167369554	HUVEC	blood vessel:	n/a
23	chr6:167370529-167370579	MCF10A-Er-Src	breast:	n/a
24	chr6:167370587-167370637	SAEC	small airway:	n/a
25	chr6:167370224-167370274	ovcar-3	ovarian:	n/a
26	chr6:167369941-167369991	HAEpiC	amniotic membrane:	n/a
27	chr6:167366683-167366733	A549	lung:	n/a
28	chr6:167370224-167370274	A549	lung:	n/a
29	chr6:167373233-167373283	Hepatocyte	liver:	n/a
30	chr6:167370276-167370326	Hela-S3	cervix:	n/a
31	chr6:167363345-167363395	NHBE	bronchial:	n/a
32	chr6:167363345-167363395	Caco-2	colon:	n/a
33	chr6:167370215-167370265	HNPCEpiC	eye:	n/a
34	chr6:167369941-167369991	T-47D	breast:	n/a
35	chr6:167373233-167373283	K562	blood:	n/a
36	chr6:167370587-167370637	ECC-1	luminal epithelium:	n/a
37	chr6:167370276-167370326	GM12878	blood:	n/a
38	chr6:167366683-167366733	HCPEpiC	choroid plexus:	n/a
39	chr6:167363345-167363395	SK-N-SH_RA	brain:	n/a
40	chr6:167363345-167363395	NT2-D1	testis:	n/a
41	chr6:167370224-167370274	HCPEpiC	choroid plexus:	n/a
42	chr6:167370276-167370326	Caco-2	colon:	n/a
43	chr6:167370587-167370637	PrEC	prostate:	n/a
44	chr6:167363345-167363395	H1-hESC	embryonic stem cell:	embryo
45	chr6:167366683-167366733	IMR90	lung:	fetal
46	chr6:167370648-167370698	A549	lung:	n/a
47	chr6:167370224-167370274	HCM	heart:	n/a
48	chr6:167370276-167370326	AG09309	skin:	n/a
49	chr6:167370587-167370637	IMR90	lung:	fetal
50	chr6:167363345-167363395	PFSK-1	brain:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167358096..167360750-chr6:167361902..167364646,4	K562	blood:
2	chr6:167362668..167365438-chr6:167411450..167414365,2	MCF-7	breast:
3	chr6:167367121..167370566-chr6:167371148..167375087,4	K562	blood:
4	chr6:167355022..167357881-chr6:167358676..167361500,2	K562	blood:
5	chr6:167370784..167372453-chr6:167373625..167375404,2	K562	blood:
6	chr6:167327598..167330047-chr6:167367070..167369538,2	K562	blood:
7	chr6:167383062..167385710-chr6:167390180..167391984,2	MCF-7	breast:
8	chr6:167372022..167374249-chr6:167383520..167385172,2	K562	blood:
9	chr6:167361983..167365004-chr6:167367480..167371949,7	MCF-7	breast:
10	chr6:167364990..167367805-chr6:167369090..167372947,3	K562	blood:
11	chr6:167382648..167385296-chr6:167441304..167444220,2	K562	blood:
12	chr6:167376063..167378279-chr6:167383576..167385467,2	K562	blood:
13	chr6:167368947..167370452-chr6:167382818..167385059,2	K562	blood:
14	chr6:167368947..167371010-chr6:167382080..167384318,2	K562	blood:
15	chr6:167370784..167372453-chr6:167373625..167375404,2	K562	blood:
16	chr6:167372022..167374249-chr6:167383520..167385172,2	K562	blood:
17	chr6:167380676..167382734-chr6:167385661..167387748,2	K562	blood:
18	chr6:167376063..167378279-chr6:167383576..167385467,2	K562	blood:
19	chr6:167372682..167375031-chr6:167410586..167412884,3	K562	blood:
20	chr6:167368436..167372370-chr6:167409956..167415121,7	MCF-7	breast:
21	chr6:167369620..167371640-chr6:167412068..167415220,3	K562	blood:
22	chr6:167353412..167356832-chr6:167362421..167365420,3	MCF-7	breast:
23	chr6:167370155..167372073-chr6:167409744..167411701,2	K562	blood:
24	chr6:167274608..167276505-chr6:167368344..167370567,2	MCF-7	breast:
25	chr6:167364990..167367805-chr6:167369090..167372947,3	K562	blood:
26	chr6:167383885..167385840-chr6:167392702..167394703,2	K562	blood:
27	chr6:167356381..167359345-chr6:167359373..167361500,2	K562	blood:
28	chr6:167368335..167372073-chr6:167409735..167414257,6	K562	blood:
29	chr6:167368539..167373039-chr6:167409933..167412837,4	MCF-7	breast:
30	chr6:167374431..167376778-chr6:167389828..167392620,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGFR1OP-9	chr6:167374299-167374866	expReg_chr6_12870_+
2	lnc-RNASET2-2	chr6:167370437-167370679	NONHSAT116063
3	lnc-RNASET2-2	chr6:167369585-167369679	NONHSAT116063
4	lnc-RPS6KA2-2	chr6:167357853-167360151	NONHSAT116065

No data

Variant related genes	Relation type
ENSG00000249141	TF binding region
ENSG00000197146	TF binding region
RNASET2	TF binding region
ENSG00000249141	CpG island
ENSG00000197146	CpG island
RNASET2	CpG island
ENSG00000197146	chromatin interactions
ENSG00000249141	chromatin interactions
ENSG00000227598	chromatin interactions
ENSG00000213066	chromatin interactions
ENSG00000071242	chromatin interactions
ENSG00000026297	chromatin interactions
ENSG00000265828	chromatin interactions
ENSG00000272980	chromatin interactions

Extended variants
information (count: 1150 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1150 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9459809	chr6:167359643-167359644	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs558240193	chr6:167359663-167359664	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs530486387	chr6:167359709-167359710	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs187884694	chr6:167359740-167359741	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs545510212	chr6:167359773-167359774	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs192782643	chr6:167359817-167359818	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs373265580	chr6:167359842-167359843	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs182260819	chr6:167359847-167359848	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs3215702	chr6:167359848-167359849	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs563800796	chr6:167359851-167359852	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs530946361	chr6:167359860-167359861	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs552567230	chr6:167359865-167359866	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs188071260	chr6:167359881-167359882	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs9459810	chr6:167359882-167359883	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs111311477	chr6:167359894-167359895	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	mRNA abundance
16	rs2236310	chr6:167359905-167359906	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs536030027	chr6:167359913-167359914	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs529078146	chr6:167359917-167359918	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs548477345	chr6:167359918-167359919	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs569573744	chr6:167359926-167359927	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs536652213	chr6:167359927-167359928	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs558125847	chr6:167359979-167359980	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs576569534	chr6:167359986-167359987	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs192353881	chr6:167359997-167359998	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs553320115	chr6:167360004-167360005	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs375534540	chr6:167360012-167360013	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs2236311	chr6:167360020-167360021	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs1077453	chr6:167360024-167360025	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs575964972	chr6:167360075-167360076	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs533460130	chr6:167360094-167360095	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs2236312	chr6:167360104-167360105	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs370580293	chr6:167360126-167360127	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs373038850	chr6:167360135-167360136	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs564455321	chr6:167360136-167360137	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs112364937	chr6:167360153-167360154	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs537395639	chr6:167360164-167360165	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs376713057	chr6:167360182-167360183	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs540739308	chr6:167360215-167360216	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs115956642	chr6:167360217-167360218	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs184572250	chr6:167360224-167360225	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs190110862	chr6:167360334-167360335	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs569660637	chr6:167360386-167360387	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs2236313	chr6:167360389-167360390	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
44	rs567926184	chr6:167360450-167360451	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs535266934	chr6:167360452-167360453	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs551790668	chr6:167360515-167360516	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs192748659	chr6:167360543-167360544	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs534294918	chr6:167360601-167360602	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs77025052	chr6:167360605-167360606	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs149205912	chr6:167360627-167360628	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	17440070	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1337 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167337600-167363400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr6:167340000-167363000	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr6:167340000-167363000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr6:167340200-167362800	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr6:167340400-167363000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr6:167340600-167363000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr6:167341000-167368800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr6:167341200-167368800	Weak transcription	Colon Smooth Muscle	Colon
9	chr6:167341400-167361400	Strong transcription	Rectal Mucosa Donor 31	rectum
10	chr6:167342400-167368600	Weak transcription	Fetal Heart	heart
11	chr6:167344200-167364000	Weak transcription	Brain Angular Gyrus	brain
12	chr6:167344200-167368600	Weak transcription	Right Atrium	heart
13	chr6:167344400-167362000	Strong transcription	GM12878-XiMat	blood
14	chr6:167344400-167363600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr6:167344400-167364000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:167344800-167359800	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr6:167345600-167361400	Strong transcription	Duodenum Mucosa	Duodenum
18	chr6:167346400-167362200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr6:167348400-167364800	Weak transcription	Brain Substantia Nigra	brain
20	chr6:167350000-167363600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr6:167350600-167359800	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr6:167350600-167361000	Strong transcription	Primary B cells from peripheral blood	blood
23	chr6:167350600-167363200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr6:167350600-167366400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr6:167350600-167367600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr6:167351000-167362000	Strong transcription	Primary B cells from cord blood	blood
27	chr6:167351600-167360600	Weak transcription	Stomach Mucosa	stomach
28	chr6:167352200-167360400	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr6:167352200-167363200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr6:167352200-167368800	Weak transcription	Fetal Kidney	kidney
31	chr6:167352400-167360400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr6:167352400-167360600	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr6:167352400-167363200	Weak transcription	Small Intestine	intestine
34	chr6:167352400-167364800	Weak transcription	Right Ventricle	heart
35	chr6:167353600-167360400	Weak transcription	Fetal Brain Female	brain
36	chr6:167353600-167364000	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr6:167353800-167366600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr6:167354200-167363200	Weak transcription	Brain Germinal Matrix	brain
39	chr6:167354400-167362200	Strong transcription	HepG2	liver
40	chr6:167354400-167364800	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr6:167354600-167362200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr6:167354600-167363200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr6:167354600-167364800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr6:167354600-167368800	Weak transcription	HSMM	muscle
45	chr6:167354600-167369000	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr6:167354600-167369000	Weak transcription	A549	lung
47	chr6:167354800-167363400	Weak transcription	Brain Anterior Caudate	brain
48	chr6:167356000-167362000	Strong transcription	Fetal Stomach	stomach
49	chr6:167356400-167361200	Strong transcription	Lung	lung
50	chr6:167356400-167366800	Strong transcription	Fetal Intestine Small	intestine

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