Variant report

Variant	nsv518835
Chromosome Location	chr6:139770067-139800892
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:249)
CpG islands
(count:61)
Chromatin interactive
region (count:47)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:249 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:139789389-139789547	K562	blood:	n/a	n/a
2	ARID3A	chr6:139795562-139796544	K562	blood:	n/a	n/a
3	ARID3A	chr6:139768143-139771468	K562	blood:	n/a	chr6:139770457-139770473
4	ARID3A	chr6:139796869-139797310	K562	blood:	n/a	n/a
5	ATF3	chr6:139779919-139780153	K562	blood:	n/a	n/a
6	BACH1	chr6:139770285-139770345	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:139770079-139771598	K562	blood:	n/a	n/a
8	BACH1	chr6:139770635-139771184	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr6:139787322-139787458	K562	blood:	n/a	n/a
10	BATF	chr6:139795415-139795733	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:139795949-139796275	K562	blood:	n/a	chr6:139796167-139796188
12	BHLHE40	chr6:139769999-139770718	K562	blood:	n/a	n/a
13	CCNT2	chr6:139770812-139771155	K562	blood:	n/a	n/a
14	CCNT2	chr6:139768955-139770403	K562	blood:	n/a	n/a
15	CEBPB	chr6:139773657-139773921	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr6:139773630-139773992	K562	blood:	n/a	n/a
17	CEBPB	chr6:139792367-139792663	K562	blood:	n/a	chr6:139792514-139792527 chr6:139792516-139792527 chr6:139792514-139792525
18	CEBPB	chr6:139792367-139792627	IMR90	lung:	n/a	chr6:139792514-139792527 chr6:139792516-139792527 chr6:139792514-139792525
19	CEBPB	chr6:139795425-139796097	K562	blood:	n/a	n/a
20	CEBPB	chr6:139779919-139780234	K562	blood:	n/a	chr6:139780077-139780088
21	CEBPB	chr6:139773669-139773960	IMR90	lung:	n/a	n/a
22	CEBPB	chr6:139780861-139781056	HepG2	liver:	n/a	chr6:139780889-139780900
23	CEBPB	chr6:139792354-139792629	HepG2	liver:	n/a	chr6:139792514-139792527 chr6:139792516-139792527 chr6:139792514-139792525
24	CEBPB	chr6:139780059-139780121	HepG2	liver:	n/a	chr6:139780077-139780088
25	CEBPB	chr6:139773566-139773925	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr6:139779923-139780244	IMR90	lung:	n/a	chr6:139780077-139780088
27	CEBPB	chr6:139773607-139773898	K562	blood:	n/a	n/a
28	CEBPB	chr6:139773698-139773962	HepG2	liver:	n/a	n/a
29	CEBPB	chr6:139800311-139800418	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:139795405-139795739	K562	blood:	n/a	n/a
31	CEBPB	chr6:139773114-139774011	Hela-S3	cervix:	n/a	chr6:139773440-139773453
32	CEBPB	chr6:139790974-139791187	K562	blood:	n/a	chr6:139791053-139791064
33	CHD2	chr6:139795439-139796241	K562	blood:	n/a	chr6:139795785-139795795
34	CHD2	chr6:139795444-139796218	GM12878	blood:	n/a	chr6:139795785-139795795
35	CHD2	chr6:139794440-139794604	K562	blood:	n/a	n/a
36	CHD2	chr6:139800504-139800758	K562	blood:	n/a	n/a
37	CTCF	chr6:139795538-139795787	K562	blood:	n/a	n/a
38	CTCF	chr6:139774360-139774510	GM12869	blood:	n/a	n/a
39	CTCF	chr6:139794400-139794550	NHEK	skin:	n/a	n/a
40	CTCF	chr6:139794460-139794610	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr6:139794560-139794710	AG09309	skin:	n/a	n/a
42	CTCF	chr6:139772102-139772159	GM10248	blood:	n/a	n/a
43	CTCF	chr6:139796900-139797143	K562	blood:	n/a	n/a
44	CTCF	chr6:139794480-139794630	AG09309	skin:	n/a	n/a
45	CTCF	chr6:139796960-139797110	HCM	heart:	n/a	n/a
46	CUX1	chr6:139768279-139770641	K562	blood:	n/a	n/a
47	CUX1	chr6:139794351-139794404	K562	blood:	n/a	n/a
48	CUX1	chr6:139796419-139796846	K562	blood:	n/a	n/a
49	CUX1	chr6:139795910-139796185	K562	blood:	n/a	n/a
50	E2F4	chr6:139774724-139774864	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:139795527-139795577	BJ	skin:	n/a
2	chr6:139795527-139795577	SK-N-MC	brain:	n/a
3	chr6:139795527-139795577	HIPEpiC	eye:	n/a
4	chr6:139795527-139795577	GM12892	blood:	n/a
5	chr6:139795527-139795577	NB4	blood:	n/a
6	chr6:139795527-139795577	HCF	heart:	n/a
7	chr6:139795527-139795577	Hela-S3	cervix:	n/a
8	chr6:139795527-139795577	HCPEpiC	choroid plexus:	n/a
9	chr6:139795527-139795577	HUVEC	blood vessel:	n/a
10	chr6:139795527-139795577	HL-60	blood:	n/a
11	chr6:139795527-139795577	HRPEpiC	eye:	n/a
12	chr6:139795527-139795577	GM06990	blood:	n/a
13	chr6:139795527-139795577	HRE	kidney:	n/a
14	chr6:139795527-139795577	HCM	heart:	n/a
15	chr6:139795527-139795577	H1-hESC	embryonic stem cell:	embryo
16	chr6:139795527-139795577	SKMC	muscle:	n/a
17	chr6:139795527-139795577	AoSMC	blood vessel:	n/a
18	chr6:139795527-139795577	A549	lung:	n/a
19	chr6:139795527-139795577	Hepatocyte	liver:	n/a
20	chr6:139795527-139795577	HEEpiC	esophagus:	n/a
21	chr6:139795527-139795577	AG10803	skin:	n/a
22	chr6:139795527-139795577	ProgFib	skin:	n/a
23	chr6:139795527-139795577	AG09319	gingival:	n/a
24	chr6:139795527-139795577	GM12891	blood:	n/a
25	chr6:139795527-139795577	HRCEpiC	kidney:	n/a
26	chr6:139795527-139795577	ECC-1	luminal epithelium:	n/a
27	chr6:139795527-139795577	RPTEC	kidney:	n/a
28	chr6:139795527-139795577	SK-N-SH_RA	brain:	n/a
29	chr6:139795527-139795577	NHBE	bronchial:	n/a
30	chr6:139795527-139795577	HMEC	breast:	n/a
31	chr6:139795527-139795577	ovcar-3	ovarian:	n/a
32	chr6:139795527-139795577	NH-A	brain:	n/a
33	chr6:139795527-139795577	GM12878	blood:	n/a
34	chr6:139795527-139795577	HAEpiC	amniotic membrane:	n/a
35	chr6:139795527-139795577	LNCaP	prostate:	n/a
36	chr6:139795527-139795577	PANC-1	pancreas:	n/a
37	chr6:139795527-139795577	PFSK-1	brain:	n/a
38	chr6:139795527-139795577	HepG2	liver:	n/a
39	chr6:139795527-139795577	IMR90	lung:	fetal
40	chr6:139795527-139795577	MCF10A-Er-Src	breast:	n/a
41	chr6:139795527-139795577	MCF-7	breast:	n/a
42	chr6:139795527-139795577	HEK293	kidney:	embryo
43	chr6:139795527-139795577	PrEC	prostate:	n/a
44	chr6:139795527-139795577	SAEC	small airway:	n/a
45	chr6:139795527-139795577	HCT-116	colon:	n/a
46	chr6:139795527-139795577	U87	brain:	n/a
47	chr6:139795527-139795577	AG04450	lung:	fetal
48	chr6:139795527-139795577	SK-N-SH	brain:	n/a
49	chr6:139795527-139795577	NHDF-neo	bronchial:	n/a
50	chr6:139795527-139795577	BE2_C	brain:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:139786016..139787706-chr6:139797791..139799773,2	MCF-7	breast:
2	chr6:139792312..139793885-chr6:139793947..139796899,2	K562	blood:
3	chr6:139797675..139799727-chr6:139800146..139801985,2	K562	blood:
4	chr6:139693217..139702760-chr6:139758637..139773636,35	K562	blood:
5	chr6:139797780..139800668-chr6:139802147..139805671,5	K562	blood:
6	chr6:139797780..139799711-chr6:139803256..139805008,2	K562	blood:
7	chr6:139794045..139795703-chr6:139798060..139801025,2	MCF-7	breast:
8	chr6:139766736..139768408-chr6:139772895..139775718,3	K562	blood:
9	chr6:139762168..139766688-chr6:139768523..139772512,5	K562	blood:
10	chr6:139769856..139771450-chr6:139849684..139852218,2	K562	blood:
11	chr6:139693530..139699538-chr6:139762864..139774913,28	K562	blood:
12	chr6:139693137..139696900-chr6:139799148..139803009,4	K562	blood:
13	chr6:139775888..139779489-chr6:139779881..139783220,3	K562	blood:
14	chr6:139768879..139771871-chr6:139917556..139920182,2	K562	blood:
15	chr6:139777830..139780367-chr6:139781270..139784794,3	MCF-7	breast:
16	chr6:139775888..139779489-chr6:139779881..139783220,3	K562	blood:
17	chr6:139769744..139772558-chr6:139778063..139781285,3	K562	blood:
18	chr6:139769744..139772558-chr6:139778063..139781285,3	K562	blood:
19	chr6:139694833..139697691-chr6:139800681..139802869,2	K562	blood:
20	chr6:139786016..139787706-chr6:139797791..139799773,2	MCF-7	breast:
21	chr6:139788753..139790765-chr6:139796325..139798435,2	K562	blood:
22	chr6:139795343..139797706-chr6:139807680..139810551,2	K562	blood:
23	chr6:139774426..139776095-chr6:139793362..139796039,2	K562	blood:
24	chr6:139793418..139795524-chr6:139796922..139799226,2	K562	blood:
25	chr6:139799627..139801775-chr6:140085865..140087472,2	K562	blood:
26	chr6:139746639..139749113-chr6:139772562..139774559,2	K562	blood:
27	chr6:139694047..139695995-chr6:139771490..139773794,2	MCF-7	breast:
28	chr6:139797675..139799727-chr6:139800146..139801985,2	K562	blood:
29	chr6:139773415..139775962-chr6:140133812..140135963,2	K562	blood:
30	chr6:139770584..139773183-chr6:139828829..139830952,2	K562	blood:
31	chr6:139771786..139774405-chr6:139971662..139973387,2	MCF-7	breast:
32	chr6:139795946..139798274-chr6:139802764..139804469,2	MCF-7	breast:
33	chr6:139786911..139790685-chr6:139791747..139796190,4	K562	blood:
34	chr6:139763145..139764911-chr6:139778606..139780976,2	K562	blood:
35	chr6:139799364..139800954-chr6:139840362..139842649,2	K562	blood:
36	chr6:139794471..139796039-chr6:139865082..139867209,2	K562	blood:
37	chr6:139696316..139699290-chr6:139794575..139797588,3	MCF-7	breast:
38	chr6:139773028..139775843-chr6:139903683..139906144,2	K562	blood:
39	chr6:139799661..139802615-chr6:139804179..139806515,2	MCF-7	breast:
40	chr6:139694106..139695782-chr6:139792309..139794051,2	K562	blood:
41	chr6:139777830..139780367-chr6:139781270..139784794,3	MCF-7	breast:
42	chr6:139793599..139796116-chr6:139799932..139801605,2	K562	blood:
43	chr6:139693348..139695724-chr6:139794532..139798166,3	K562	blood:
44	chr6:139693565..139697388-chr6:139794842..139800531,8	K562	blood:
45	chr6:139765322..139769157-chr6:139769413..139772627,5	K562	blood:
46	chr6:139693038..139695067-chr6:139768698..139770405,2	MCF-7	breast:
47	chr6:139788753..139790765-chr6:139796325..139798435,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CITED2-1	chr6:139794069-139794192	XLOC_005856
2	lnc-CITED2-1	chr6:139793664-139793732	XLOC_005856
3	lnc-CITED2-1	chr6:139778813-139778994	XLOC_005856
4	lnc-CITED2-1	chr6:139794069-139794109	XLOC_005856
5	lnc-CITED2-1	chr6:139795703-139795733	XLOC_005856
6	lnc-CITED2-1	chr6:139795703-139795737	XLOC_005856
7	lnc-CITED2-1	chr6:139794069-139794192	XLOC_005856
8	lnc-CITED2-1	chr6:139794069-139794192	XLOC_005856
9	lnc-CITED2-1	chr6:139778813-139778994	XLOC_005856
10	lnc-CITED2-1	chr6:139790132-139791597	XLOC_005856
11	lnc-CITED2-1	chr6:139791301-139791597	XLOC_005856
12	lnc-CITED2-1	chr6:139793664-139793732	XLOC_005856
13	lnc-CITED2-1	chr6:139793664-139793732	XLOC_005856
14	lnc-CITED2-1	chr6:139793664-139793732	XLOC_005856
15	lnc-CITED2-1	chr6:139781234-139781278	XLOC_005856
16	lnc-CITED2-1	chr6:139777987-139778994	XLOC_005856

No data

Variant related genes	Relation type
ENSG00000238099	TF binding region
ENSG00000238099	CpG island
ENSG00000164442	chromatin interactions
ENSG00000238099	chromatin interactions
SLC17A5	miRNA target sites
ELF4	miRNA target sites
FBXO17	miRNA target sites
HBP1	miRNA target sites
HBEGF	miRNA target sites

Extended variants
information (count: 921 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:921 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17406820	chr6:139770067-139770068	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs17068684	chr6:139770085-139770086	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs17068686	chr6:139770108-139770109	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs542270187	chr6:139770114-139770115	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs200551165	chr6:139770150-139770151	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs560894154	chr6:139770163-139770164	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs531353150	chr6:139770193-139770194	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs58805273	chr6:139770200-139770201	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs180839077	chr6:139770279-139770280	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs185295214	chr6:139770311-139770312	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs532195407	chr6:139770322-139770323	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs189637382	chr6:139770354-139770355	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs565845117	chr6:139770358-139770359	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs551954090	chr6:139770364-139770365	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs536499891	chr6:139770367-139770368	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs181673952	chr6:139770409-139770410	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs186896613	chr6:139770420-139770421	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs537574656	chr6:139770456-139770457	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs6932165	chr6:139770461-139770462	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs577386450	chr6:139770478-139770479	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs571751142	chr6:139770492-139770493	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs140507457	chr6:139770525-139770526	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs553567171	chr6:139770567-139770568	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs117660161	chr6:139770590-139770591	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs192232175	chr6:139770628-139770629	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs9495482	chr6:139770642-139770643	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs183549132	chr6:139770650-139770651	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs375687453	chr6:139770706-139770707	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs542984973	chr6:139770731-139770732	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs554358177	chr6:139770758-139770759	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs9495483	chr6:139770889-139770890	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs532036995	chr6:139770967-139770968	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs185311128	chr6:139771011-139771012	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs189666127	chr6:139771072-139771073	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs182332936	chr6:139771074-139771075	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs535805300	chr6:139771079-139771080	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs569827343	chr6:139771083-139771084	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs375363591	chr6:139771096-139771097	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs548447029	chr6:139771146-139771147	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs569977797	chr6:139771173-139771174	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs537466135	chr6:139771176-139771177	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs112142274	chr6:139771180-139771181	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs187048173	chr6:139771189-139771190	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs150425473	chr6:139771233-139771234	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs192750647	chr6:139771252-139771253	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs553338261	chr6:139771253-139771254	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs138167266	chr6:139771307-139771308	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs183596867	chr6:139771336-139771337	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs557613174	chr6:139771338-139771339	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs556396258	chr6:139771387-139771388	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Autism	21448237	CNVD
Autism	22495311	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
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	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
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
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	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
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Basal cell lymphoma	21115979	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD

Chromatin state (count:565 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:139765200-139770600	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr6:139765200-139772800	Weak transcription	HSMMtube	muscle
3	chr6:139767600-139771600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:139768200-139770800	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr6:139768200-139771400	Flanking Active TSS	K562	blood
6	chr6:139768200-139771800	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr6:139768200-139774000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr6:139768400-139770400	Enhancers	GM12878-XiMat	blood
9	chr6:139768400-139771200	Weak transcription	Ovary	ovary
10	chr6:139768400-139771400	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr6:139768800-139770600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr6:139768800-139771600	Weak transcription	Fetal Kidney	kidney
13	chr6:139769000-139770200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:139769000-139770400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr6:139769000-139772000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr6:139769200-139770200	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr6:139769200-139770600	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr6:139769200-139773400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr6:139769400-139770400	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr6:139769400-139773200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr6:139769600-139770600	Weak transcription	NHDF-Ad	bronchial
22	chr6:139769600-139770800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr6:139769600-139773400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr6:139769800-139770200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr6:139769800-139770200	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr6:139769800-139770600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr6:139769800-139770800	Weak transcription	Adipose Nuclei	Adipose
28	chr6:139770000-139770400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr6:139770000-139770400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr6:139770000-139770400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr6:139770000-139771400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr6:139770200-139770600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
33	chr6:139770200-139771400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr6:139770200-139771800	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr6:139770200-139771800	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr6:139770400-139770600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr6:139770400-139771400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:139770400-139771400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr6:139770400-139771400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr6:139770400-139771400	Enhancers	Osteobl	bone
41	chr6:139770400-139771800	Enhancers	Muscle Satellite Cultured Cells	--
42	chr6:139770600-139770800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr6:139770600-139771200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr6:139770600-139771200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr6:139770600-139771400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr6:139770600-139771400	Enhancers	NHDF-Ad	bronchial
47	chr6:139770600-139773400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr6:139770600-139773600	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr6:139770800-139771000	Enhancers	Adipose Nuclei	Adipose
50	chr6:139770800-139771200	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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