Variant report

Variant	nsv886763
Chromosome Location	chr6:150091219-150174507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1404)
CpG islands
(count:427)
Chromatin interactive
region (count:119)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:150168716-150169082	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:150152146-150152752	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:150168290-150168454	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:150161741-150161972	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:150168782-150169147	K562	blood:	n/a	n/a
6	ATF1	chr6:150168706-150169270	K562	blood:	n/a	n/a
7	ATF1	chr6:150173313-150173520	K562	blood:	n/a	n/a
8	ATF2	chr6:150137007-150137303	GM12878	blood:	n/a	n/a
9	ATF3	chr6:150168612-150169050	K562	blood:	n/a	n/a
10	ATF3	chr6:150168738-150168916	K562	blood:	n/a	n/a
11	BACH1	chr6:150167601-150167781	H1-hESC	embryonic stem cell:	n/a	chr6:150167713-150167727
12	BACH1	chr6:150092456-150092554	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr6:150168873-150168948	K562	blood:	n/a	n/a
14	BACH1	chr6:150092348-150092664	K562	blood:	n/a	n/a
15	BATF	chr6:150168706-150168953	GM12878	blood:	n/a	chr6:150168857-150168868
16	BCL3	chr6:150100819-150100990	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:150161823-150162025	K562	blood:	n/a	n/a
18	BHLHE40	chr6:150167552-150167782	K562	blood:	n/a	n/a
19	BHLHE40	chr6:150168496-150168544	K562	blood:	n/a	n/a
20	BHLHE40	chr6:150116979-150117158	K562	blood:	n/a	chr6:150117065-150117086 chr6:150117070-150117079
21	BHLHE40	chr6:150173366-150173514	K562	blood:	n/a	n/a
22	BHLHE40	chr6:150168195-150169061	HepG2	liver:	n/a	n/a
23	BHLHE40	chr6:150168827-150169113	K562	blood:	n/a	n/a
24	BRCA1	chr6:150161750-150161934	HepG2	liver:	n/a	n/a
25	BRCA1	chr6:150168141-150168320	HepG2	liver:	n/a	n/a
26	CBX3	chr6:150155610-150156720	HCT-116	colon:	n/a	n/a
27	CCNT2	chr6:150167478-150167598	K562	blood:	n/a	n/a
28	CCNT2	chr6:150095023-150095118	K562	blood:	n/a	n/a
29	CCNT2	chr6:150168743-150168947	K562	blood:	n/a	n/a
30	CCNT2	chr6:150173335-150173611	K562	blood:	n/a	chr6:150173456-150173476
31	CCNT2	chr6:150142723-150142923	K562	blood:	n/a	n/a
32	CEBPB	chr6:150168148-150168444	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr6:150166283-150166564	HepG2	liver:	n/a	chr6:150166430-150166439
34	CEBPB	chr6:150168674-150169066	K562	blood:	n/a	n/a
35	CEBPB	chr6:150172626-150172905	A549	lung:	n/a	n/a
36	CEBPB	chr6:150102801-150103114	HepG2	liver:	n/a	chr6:150102954-150102965
37	CEBPB	chr6:150172569-150172960	IMR90	lung:	n/a	n/a
38	CEBPB	chr6:150161857-150162254	IMR90	lung:	n/a	n/a
39	CEBPB	chr6:150168711-150169234	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr6:150172555-150172976	A549	lung:	n/a	n/a
41	CEBPB	chr6:150166292-150166530	IMR90	lung:	n/a	chr6:150166430-150166439
42	CEBPB	chr6:150151929-150152302	IMR90	lung:	n/a	n/a
43	CEBPB	chr6:150098433-150098649	IMR90	lung:	n/a	n/a
44	CEBPB	chr6:150102851-150103103	IMR90	lung:	n/a	chr6:150102954-150102965
45	CEBPB	chr6:150128928-150129144	HepG2	liver:	n/a	n/a
46	CEBPB	chr6:150167414-150167744	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr6:150102851-150103107	K562	blood:	n/a	chr6:150102954-150102965
48	CEBPB	chr6:150168779-150169032	A549	lung:	n/a	n/a
49	CEBPB	chr6:150106213-150106402	K562	blood:	n/a	n/a
50	CEBPB	chr6:150168731-150169014	K562	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150128134-150128184	HMEC	breast:	n/a
2	chr6:150152522-150152572	NHBE	bronchial:	n/a
3	chr6:150152522-150152572	HEEpiC	esophagus:	n/a
4	chr6:150160468-150160518	ProgFib	skin:	n/a
5	chr6:150128134-150128184	SK-N-SH	brain:	n/a
6	chr6:150159984-150160034	HCM	heart:	n/a
7	chr6:150160468-150160518	PANC-1	pancreas:	n/a
8	chr6:150128134-150128184	HCT-116	colon:	n/a
9	chr6:150174215-150174265	HCM	heart:	n/a
10	chr6:150159984-150160034	GM12878	blood:	n/a
11	chr6:150128134-150128184	Hela-S3	cervix:	n/a
12	chr6:150167359-150167409	A549	lung:	n/a
13	chr6:150159984-150160034	PANC-1	pancreas:	n/a
14	chr6:150128134-150128184	NB4	blood:	n/a
15	chr6:150174215-150174265	H1-hESC	embryonic stem cell:	embryo
16	chr6:150160468-150160518	AG04450	lung:	fetal
17	chr6:150161689-150161739	GM12878	blood:	n/a
18	chr6:150161689-150161739	AoSMC	blood vessel:	n/a
19	chr6:150161689-150161739	NT2-D1	testis:	n/a
20	chr6:150174215-150174265	SAEC	small airway:	n/a
21	chr6:150152522-150152572	SK-N-SH_RA	brain:	n/a
22	chr6:150152522-150152572	MCF-7	breast:	n/a
23	chr6:150128134-150128184	HL-60	blood:	n/a
24	chr6:150159984-150160034	HIPEpiC	eye:	n/a
25	chr6:150174215-150174265	U87	brain:	n/a
26	chr6:150161689-150161739	HUVEC	blood vessel:	n/a
27	chr6:150159984-150160034	T-47D	breast:	n/a
28	chr6:150160468-150160518	NB4	blood:	n/a
29	chr6:150174215-150174265	RPTEC	kidney:	n/a
30	chr6:150167359-150167409	HEEpiC	esophagus:	n/a
31	chr6:150159984-150160034	ProgFib	skin:	n/a
32	chr6:150174215-150174265	Hela-S3	cervix:	n/a
33	chr6:150160468-150160518	HRCEpiC	kidney:	n/a
34	chr6:150174215-150174265	HCPEpiC	choroid plexus:	n/a
35	chr6:150160468-150160518	SAEC	small airway:	n/a
36	chr6:150161689-150161739	ECC-1	luminal epithelium:	n/a
37	chr6:150159984-150160034	NT2-D1	testis:	n/a
38	chr6:150161689-150161739	Hela-S3	cervix:	n/a
39	chr6:150174215-150174265	HUVEC	blood vessel:	n/a
40	chr6:150128134-150128184	HRCEpiC	kidney:	n/a
41	chr6:150128134-150128184	PANC-1	pancreas:	n/a
42	chr6:150152522-150152572	MCF10A-Er-Src	breast:	n/a
43	chr6:150161689-150161739	HCPEpiC	choroid plexus:	n/a
44	chr6:150159984-150160034	NH-A	brain:	n/a
45	chr6:150167359-150167409	BJ	skin:	n/a
46	chr6:150161689-150161739	HMEC	breast:	n/a
47	chr6:150161689-150161739	MCF-7	breast:	n/a
48	chr6:150152522-150152572	HEK293	kidney:	embryo
49	chr6:150167359-150167409	MCF-7	breast:	n/a
50	chr6:150128134-150128184	HIPEpiC	eye:	n/a

(count:119 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:150069990..150071882-chr6:150109798..150112486,2	MCF-7	breast:
2	chr6:150169785..150171423-chr6:150184398..150186335,2	K562	blood:
3	chr6:150103039..150105538-chr6:150109602..150113560,4	K562	blood:
4	chr6:150044766..150045296-chr6:150144284..150144787,2	MCF-7	breast:
5	chr6:150166050..150170337-chr6:150173456..150176763,5	MCF-7	breast:
6	chr6:150146365..150148189-chr6:150149570..150152826,3	K562	blood:
7	chr6:150166079..150172408-chr6:150181587..150186360,13	MCF-7	breast:
8	chr6:150154401..150157118-chr6:150163961..150165886,2	MCF-7	breast:
9	chr6:150133046..150135763-chr6:150140364..150142175,2	K562	blood:
10	chr6:150154949..150156625-chr6:150185486..150186813,8	MCF-7	breast:
11	chr6:150138887..150141566-chr6:150185525..150187707,2	K562	blood:
12	chr6:150120002..150121687-chr6:150123365..150125710,2	K562	blood:
13	chr6:150037962..150039498-chr6:150131610..150134476,2	K562	blood:
14	chr6:150055968..150058286-chr6:150092691..150095282,2	K562	blood:
15	chr6:150155341..150156327-chr6:150247051..150248024,4	K562	blood:
16	chr6:150160122..150165164-chr6:150183114..150187569,12	MCF-7	breast:
17	chr6:150140253..150142421-chr6:150147806..150149368,2	K562	blood:
18	chr6:150157110..150158839-chr6:150161991..150164233,2	K562	blood:
19	chr6:150154902..150156132-chr6:150246873..150248035,8	MCF-7	breast:
20	chr6:150115210..150117160-chr6:150126668..150131060,3	MCF-7	breast:
21	chr6:150103642..150105538-chr6:150109602..150112158,2	K562	blood:
22	chr6:150116018..150118922-chr6:150120645..150124683,3	K562	blood:
23	chr6:150103684..150106554-chr6:150183972..150185592,2	MCF-7	breast:
24	chr6:150103186..150105713-chr6:150110065..150112313,2	MCF-7	breast:
25	chr6:150164239..150168667-chr6:150168889..150173398,4	K562	blood:
26	chr6:150068088..150071586-chr6:150150186..150152200,3	K562	blood:
27	chr6:149884418..149886657-chr6:150140173..150142192,2	K562	blood:
28	chr6:150147289..150147851-chr6:150168101..150168897,2	K562	blood:
29	chr6:150127289..150128879-chr6:150131415..150134275,2	K562	blood:
30	chr6:150103642..150105538-chr6:150109602..150112158,2	K562	blood:
31	chr6:150161516..150164235-chr6:150221796..150224745,2	K562	blood:
32	chr6:150138857..150141317-chr6:150147239..150149220,2	K562	blood:
33	chr6:150155755..150156389-chr6:150185932..150186700,2	MCF-7	breast:
34	chr6:150127349..150128879-chr6:150131415..150134215,2	K562	blood:
35	chr6:150151705..150153570-chr6:150183035..150185955,2	MCF-7	breast:
36	chr6:150123377..150125799-chr6:150184381..150186208,2	MCF-7	breast:
37	chr6:150160714..150164051-chr6:150166023..150170073,4	MCF-7	breast:
38	chr6:150133046..150135763-chr6:150140364..150142175,2	K562	blood:
39	chr6:150160714..150164051-chr6:150166023..150170073,4	MCF-7	breast:
40	chr6:150145482..150148001-chr6:150150634..150152826,2	K562	blood:
41	chr6:150154861..150155845-chr6:150337730..150338274,2	K562	blood:
42	chr6:150134530..150136218-chr6:150140152..150141893,2	MCF-7	breast:
43	chr6:150085048..150087027-chr6:150091947..150093777,2	MCF-7	breast:
44	chr6:150157068..150159142-chr6:150224629..150226824,2	MCF-7	breast:
45	chr6:150166110..150169897-chr6:150177295..150181208,4	MCF-7	breast:
46	chr6:150127349..150128879-chr6:150131415..150134215,2	K562	blood:
47	chr6:150069279..150071165-chr6:150089916..150092656,2	MCF-7	breast:
48	chr6:150141029..150142944-chr6:150146310..150148674,2	MCF-7	breast:
49	chr6:150134530..150136218-chr6:150140152..150141893,2	MCF-7	breast:
50	chr6:150155391..150156182-chr6:150239663..150240372,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAET1E-4	chr6:150147247-150147495	NONHSAT115512
2	lnc-LRP11-1	chr6:150118392-150118575	ENSG00000231760.1
3	lnc-LRP11-1	chr6:150117711-150118575	ENSG00000231760.2
4	lnc-LRP11-1	chr6:150119057-150119308	ENSG00000231760.2
5	lnc-LRP11-1	chr6:150119057-150119308	ENSG00000231760.1
6	lnc-ULBP2-6	chr6:150131176-150131259	NONHSAT115511
7	lnc-ULBP2-6	chr6:150131752-150132044	NONHSAT115511
8	lnc-RAET1E-4	chr6:150157221-150157335	NONHSAT115512

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	PCMT1	hsa-miR-16-5p	chr6:150132505-150132527
2	LRP11	hsa-miR-122-5p	chr6:150140403-150140426
3	PCMT1	hsa-miR-16-5p	chr6:150132435-150132456
4	PCMT1	hsa-miR-16-5p	chr6:150124321-150124327

Variant related genes	Relation type
PCMT1	TF binding region
ENSG00000219433	TF binding region
LRP11	TF binding region
ENSG00000231760	TF binding region
ENSG00000273132	TF binding region
PCMT1	CpG island
ENSG00000219433	CpG island
LRP11	CpG island
ENSG00000231760	CpG island
ENSG00000273132	CpG island
ENSG00000203722	chromatin interactions
ENSG00000120265	chromatin interactions
ENSG00000120253	chromatin interactions
ENSG00000131023	chromatin interactions
ENSG00000216906	chromatin interactions
ENSG00000120256	chromatin interactions
ENSG00000179743	chromatin interactions
ENSG00000273132	chromatin interactions
ENSG00000219433	chromatin interactions
ENSG00000155918	chromatin interactions
ENSG00000268592	chromatin interactions

Extended variants
information (count: 3122 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3122 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34172531	chr6:150091219-150091220	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs192942050	chr6:150091327-150091328	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs146315850	chr6:150091384-150091385	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs373458856	chr6:150091448-150091449	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs545841896	chr6:150091573-150091574	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs559411750	chr6:150091592-150091593	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs568607172	chr6:150091618-150091619	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs185545649	chr6:150091724-150091725	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs561582342	chr6:150091732-150091733	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs530781408	chr6:150091749-150091750	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs9689694	chr6:150091773-150091774	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs142717584	chr6:150091790-150091791	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs551076438	chr6:150091861-150091862	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs190518934	chr6:150091862-150091863	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs373681896	chr6:150091887-150091888	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs9688867	chr6:150091912-150091913	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs139955237	chr6:150091964-150091965	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs140505162	chr6:150091988-150091989	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs201250582	chr6:150091989-150091990	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs141352764	chr6:150091990-150091991	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs10677539	chr6:150091991-150091992	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs200329531	chr6:150091992-150091993	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs555090933	chr6:150091996-150091997	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs574826785	chr6:150092027-150092028	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs537684076	chr6:150092084-150092085	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs557249752	chr6:150092087-150092088	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs553360734	chr6:150092115-150092116	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs201532086	chr6:150092137-150092138	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs577485069	chr6:150092223-150092224	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs546535672	chr6:150092225-150092226	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs370470455	chr6:150092248-150092249	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs371406788	chr6:150092263-150092264	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs34017825	chr6:150092264-150092265	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs560046916	chr6:150092284-150092285	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs11540602	chr6:150092342-150092343	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs374534669	chr6:150092351-150092352	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs11540596	chr6:150092357-150092358	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs572879221	chr6:150092419-150092420	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs368948790	chr6:150092440-150092441	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs371986421	chr6:150092441-150092442	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs541458563	chr6:150092449-150092450	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs561863787	chr6:150092470-150092471	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs572252478	chr6:150092574-150092575	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs111907716	chr6:150092579-150092580	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs561980906	chr6:150092599-150092600	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs180783698	chr6:150092715-150092716	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs534889166	chr6:150092722-150092723	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs532931432	chr6:150092727-150092728	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs554482078	chr6:150092773-150092774	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs562974813	chr6:150092796-150092797	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
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
Follicular lymphoma	20505157	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
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:2378 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150071800-150092600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:150071800-150092800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr6:150071800-150100200	Weak transcription	Gastric	stomach
4	chr6:150072000-150094200	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr6:150072000-150111000	Weak transcription	Fetal Kidney	kidney
6	chr6:150072000-150152000	Weak transcription	Aorta	Aorta
7	chr6:150072400-150104600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr6:150072400-150111400	Weak transcription	Colonic Mucosa	Colon
9	chr6:150073000-150094400	Weak transcription	Lung	lung
10	chr6:150073800-150182400	Weak transcription	Fetal Brain Male	brain
11	chr6:150074200-150101000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr6:150075800-150094800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr6:150077000-150115400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr6:150077200-150118400	Weak transcription	Pancreas	Pancrea
15	chr6:150077400-150142400	Weak transcription	Fetal Heart	heart
16	chr6:150077800-150118400	Weak transcription	Psoas Muscle	Psoas
17	chr6:150078200-150092600	Weak transcription	Left Ventricle	heart
18	chr6:150081600-150101200	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr6:150081800-150092800	Weak transcription	Spleen	Spleen
20	chr6:150081800-150092800	Weak transcription	HSMMtube	muscle
21	chr6:150082400-150092800	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr6:150083600-150092800	Weak transcription	Ovary	ovary
23	chr6:150084800-150092200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr6:150086200-150092800	Weak transcription	Rectal Smooth Muscle	rectum
25	chr6:150087000-150093800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr6:150087000-150096600	Weak transcription	Esophagus	oesophagus
27	chr6:150087200-150095400	Strong transcription	Primary T cells from cord blood	blood
28	chr6:150087200-150154000	Weak transcription	Small Intestine	intestine
29	chr6:150087400-150091400	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr6:150087400-150134000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr6:150087600-150092200	Weak transcription	Stomach Smooth Muscle	stomach
32	chr6:150087600-150092400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr6:150087600-150092600	Weak transcription	HUVEC	blood vessel
34	chr6:150087600-150117400	Weak transcription	Brain Substantia Nigra	brain
35	chr6:150087800-150092200	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr6:150087800-150092600	Weak transcription	NHLF	lung
37	chr6:150087800-150092800	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr6:150087800-150092800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr6:150087800-150092800	Weak transcription	Brain Anterior Caudate	brain
40	chr6:150087800-150092800	Weak transcription	Duodenum Mucosa	Duodenum
41	chr6:150087800-150093000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr6:150087800-150093000	Weak transcription	Brain Cingulate Gyrus	brain
43	chr6:150087800-150093200	Weak transcription	HMEC	breast
44	chr6:150087800-150094000	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr6:150087800-150101600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr6:150087800-150112000	Weak transcription	Right Ventricle	heart
47	chr6:150087800-150112400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr6:150088000-150091400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr6:150088000-150092200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:150088000-150092200	Weak transcription	HUES64 Cell Line	embryonic stem cell

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