Variant report

Variant	nsv887629
Chromosome Location	chr7:12304555-12400837
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:825)
CpG islands
(count:183)
Chromatin interactive
region (count:61)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:825 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:12361928-12362236	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:12309141-12309418	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:12361970-12362233	K562	blood:	n/a	n/a
4	ATF1	chr7:12391517-12391830	K562	blood:	n/a	n/a
5	ATF1	chr7:12360907-12361152	K562	blood:	n/a	n/a
6	ATF2	chr7:12397170-12397485	GM12878	blood:	n/a	n/a
7	BATF	chr7:12362561-12362908	GM12878	blood:	n/a	chr7:12362724-12362735
8	BATF	chr7:12362529-12362819	GM12878	blood:	n/a	chr7:12362724-12362735
9	BCL11A	chr7:12362562-12362789	GM12878	blood:	n/a	n/a
10	BCL11A	chr7:12362543-12362825	GM12878	blood:	n/a	n/a
11	BCL3	chr7:12370808-12371350	K562	blood:	n/a	n/a
12	BCL3	chr7:12397240-12397520	GM12878	blood:	n/a	n/a
13	BHLHE40	chr7:12371392-12371475	A549	lung:	n/a	n/a
14	BHLHE40	chr7:12309159-12309475	HepG2	liver:	n/a	n/a
15	BHLHE40	chr7:12361210-12361233	K562	blood:	n/a	n/a
16	BHLHE40	chr7:12362651-12362754	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:12391626-12391783	K562	blood:	n/a	n/a
18	BRCA1	chr7:12309199-12309288	HepG2	liver:	n/a	n/a
19	BRCA1	chr7:12310930-12310977	GM12878	blood:	n/a	n/a
20	BRCA1	chr7:12363238-12363314	GM12878	blood:	n/a	n/a
21	CBX3	chr7:12338999-12339376	K562	blood:	n/a	n/a
22	CBX3	chr7:12330934-12331289	K562	blood:	n/a	n/a
23	CCNT2	chr7:12383002-12383143	K562	blood:	n/a	n/a
24	CCNT2	chr7:12391547-12391847	K562	blood:	n/a	n/a
25	CCNT2	chr7:12360909-12361396	K562	blood:	n/a	n/a
26	CEBPB	chr7:12360899-12361157	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr7:12341270-12341440	K562	blood:	n/a	n/a
28	CEBPB	chr7:12376796-12377033	K562	blood:	n/a	chr7:12376957-12376970 chr7:12376957-12376968 chr7:12376957-12376970
29	CEBPB	chr7:12365884-12365914	H1-hESC	embryonic stem cell:	n/a	chr7:12365903-12365914
30	CEBPB	chr7:12360962-12361174	K562	blood:	n/a	n/a
31	CEBPB	chr7:12357399-12357607	A549	lung:	n/a	chr7:12357510-12357521
32	CEBPB	chr7:12376799-12377121	HepG2	liver:	n/a	chr7:12376957-12376970 chr7:12376957-12376968 chr7:12376957-12376970
33	CEBPB	chr7:12309133-12309386	HepG2	liver:	n/a	chr7:12309255-12309266
34	CEBPB	chr7:12337404-12337716	MCF-7	breast:	n/a	n/a
35	CEBPB	chr7:12376804-12377018	IMR90	lung:	n/a	chr7:12376957-12376970 chr7:12376957-12376968 chr7:12376957-12376970
36	CEBPB	chr7:12357363-12357592	IMR90	lung:	n/a	chr7:12357510-12357521
37	CEBPB	chr7:12309067-12309463	HepG2	liver:	n/a	chr7:12309255-12309266
38	CEBPB	chr7:12397108-12397677	GM12878	blood:	n/a	n/a
39	CEBPB	chr7:12309194-12309370	A549	lung:	n/a	chr7:12309255-12309266
40	CEBPB	chr7:12357353-12357682	K562	blood:	n/a	chr7:12357510-12357521
41	CEBPB	chr7:12345750-12345982	A549	lung:	n/a	n/a
42	CEBPB	chr7:12365869-12365957	K562	blood:	n/a	chr7:12365903-12365914 chr7:12365903-12365916 chr7:12365903-12365916 chr7:12365903-12365916
43	CEBPB	chr7:12368645-12369574	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr7:12376790-12377114	A549	lung:	n/a	chr7:12376957-12376970 chr7:12376957-12376968 chr7:12376957-12376970
45	CEBPB	chr7:12309070-12309489	HepG2	liver:	n/a	chr7:12309255-12309266
46	CEBPB	chr7:12357429-12357629	HepG2	liver:	n/a	chr7:12357510-12357521
47	CEBPB	chr7:12309079-12309453	HepG2	liver:	n/a	chr7:12309255-12309266
48	CEBPB	chr7:12309229-12309233	K562	blood:	n/a	n/a
49	CEBPD	chr7:12309210-12309392	HepG2	liver:	n/a	n/a
50	CEBPD	chr7:12309155-12309378	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12363490-12363540	GM12891	blood:	n/a
2	chr7:12370351-12370401	U87	brain:	n/a
3	chr7:12376625-12376675	HCF	heart:	n/a
4	chr7:12363490-12363540	NH-A	brain:	n/a
5	chr7:12370351-12370401	NB4	blood:	n/a
6	chr7:12376625-12376675	SK-N-MC	brain:	n/a
7	chr7:12363490-12363540	ovcar-3	ovarian:	n/a
8	chr7:12376625-12376675	BJ	skin:	n/a
9	chr7:12363490-12363540	SK-N-SH	brain:	n/a
10	chr7:12363490-12363540	AG09319	gingival:	n/a
11	chr7:12370351-12370401	Caco-2	colon:	n/a
12	chr7:12363490-12363540	PrEC	prostate:	n/a
13	chr7:12363490-12363540	BE2_C	brain:	n/a
14	chr7:12376625-12376675	NHDF-neo	bronchial:	n/a
15	chr7:12376625-12376675	HCT-116	colon:	n/a
16	chr7:12376625-12376675	HRE	kidney:	n/a
17	chr7:12363490-12363540	ECC-1	luminal epithelium:	n/a
18	chr7:12370351-12370401	HNPCEpiC	eye:	n/a
19	chr7:12370351-12370401	H1-hESC	embryonic stem cell:	embryo
20	chr7:12363490-12363540	MCF10A-Er-Src	breast:	n/a
21	chr7:12370351-12370401	MCF-7	breast:	n/a
22	chr7:12363490-12363540	HRCEpiC	kidney:	n/a
23	chr7:12370351-12370401	PrEC	prostate:	n/a
24	chr7:12376625-12376675	NT2-D1	testis:	n/a
25	chr7:12363490-12363540	Hela-S3	cervix:	n/a
26	chr7:12363490-12363540	SK-N-MC	brain:	n/a
27	chr7:12376625-12376675	ECC-1	luminal epithelium:	n/a
28	chr7:12376625-12376675	Hela-S3	cervix:	n/a
29	chr7:12370351-12370401	HRE	kidney:	n/a
30	chr7:12376625-12376675	HRCEpiC	kidney:	n/a
31	chr7:12376625-12376675	H1-hESC	embryonic stem cell:	embryo
32	chr7:12376625-12376675	MCF-7	breast:	n/a
33	chr7:12376625-12376675	CMK	blood:	n/a
34	chr7:12363490-12363540	HCM	heart:	n/a
35	chr7:12363490-12363540	HNPCEpiC	eye:	n/a
36	chr7:12376625-12376675	HRPEpiC	eye:	n/a
37	chr7:12363490-12363540	SK-N-SH_RA	brain:	n/a
38	chr7:12363490-12363540	HUVEC	blood vessel:	n/a
39	chr7:12363490-12363540	AoSMC	blood vessel:	n/a
40	chr7:12376625-12376675	HCM	heart:	n/a
41	chr7:12363490-12363540	GM12878	blood:	n/a
42	chr7:12363490-12363540	HCPEpiC	choroid plexus:	n/a
43	chr7:12370351-12370401	SKMC	muscle:	n/a
44	chr7:12370351-12370401	GM06990	blood:	n/a
45	chr7:12370351-12370401	NT2-D1	testis:	n/a
46	chr7:12363490-12363540	NT2-D1	testis:	n/a
47	chr7:12370351-12370401	HL-60	blood:	n/a
48	chr7:12370351-12370401	ProgFib	skin:	n/a
49	chr7:12363490-12363540	K562	blood:	n/a
50	chr7:12370351-12370401	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr7:12380686..12382239-chr7:12385639..12388082,2	K562	blood:
2	chr7:12398772..12400728-chr7:12416119..12417972,2	K562	blood:
3	chr7:12311161..12313996-chr7:12317609..12319933,2	K562	blood:
4	chr7:12382799..12385098-chr7:12438700..12441052,2	K562	blood:
5	chr7:12249029..12251264-chr7:12355308..12358122,2	MCF-7	breast:
6	chr7:12392619..12394669-chr7:12398215..12400869,2	K562	blood:
7	chr7:12319256..12322046-chr7:12323185..12326325,3	K562	blood:
8	chr7:12378441..12379998-chr7:12382677..12384554,2	K562	blood:
9	chr7:12399201..12400947-chr7:12402626..12404166,2	K562	blood:
10	chr7:12382924..12384916-chr7:12389053..12391966,2	K562	blood:
11	chr7:12237104..12239270-chr7:12329420..12331412,2	K562	blood:
12	chr7:12391914..12394742-chr7:12414391..12416688,2	K562	blood:
13	chr7:12389607..12392285-chr7:12392419..12394302,2	K562	blood:
14	chr7:12362049..12364322-chr7:12365857..12368217,3	K562	blood:
15	chr7:12382924..12384916-chr7:12389053..12391966,2	K562	blood:
16	chr7:12380686..12382239-chr7:12385639..12388082,2	K562	blood:
17	chr7:12248340..12250610-chr7:12341759..12344659,2	K562	blood:
18	chr7:12362078..12365720-chr7:12370304..12373327,3	K562	blood:
19	chr7:12365317..12367228-chr7:12375967..12378342,2	K562	blood:
20	chr7:12391712..12393347-chr7:12394959..12396471,2	K562	blood:
21	chr7:12385242..12386819-chr7:12390082..12392750,2	K562	blood:
22	chr7:12359785..12361369-chr7:12363361..12365480,2	K562	blood:
23	chr7:12326033..12327864-chr7:12530775..12532531,2	K562	blood:
24	chr7:12385242..12386819-chr7:12390082..12392750,2	K562	blood:
25	chr7:12359785..12361369-chr7:12363361..12365480,2	K562	blood:
26	chr7:12392619..12394669-chr7:12398215..12400869,2	K562	blood:
27	chr7:12304154..12306342-chr7:12308310..12310160,2	K562	blood:
28	chr7:12311161..12313996-chr7:12317609..12319933,2	K562	blood:
29	chr7:12249110..12251929-chr7:12341759..12344024,2	K562	blood:
30	chr7:12390586..12393212-chr7:12394959..12396886,2	K562	blood:
31	chr7:12353391..12355072-chr7:12357011..12359494,3	K562	blood:
32	chr7:12363684..12366465-chr7:12393124..12396040,2	K562	blood:
33	chr7:12378441..12379998-chr7:12382677..12384554,2	K562	blood:
34	chr7:12391134..12392692-chr7:12402911..12404517,2	K562	blood:
35	chr7:12362049..12364322-chr7:12365857..12368217,3	K562	blood:
36	chr7:12391712..12393347-chr7:12394959..12396471,2	K562	blood:
37	chr7:12380686..12382573-chr7:12386582..12389339,2	K562	blood:
38	chr7:12376678..12378667-chr7:12443118..12444758,2	K562	blood:
39	chr7:12359587..12361942-chr7:12364993..12366787,2	K562	blood:
40	chr7:12356830..12359604-chr7:12404989..12406571,2	K562	blood:
41	chr7:12249722..12251364-chr7:12307905..12310601,2	MCF-7	breast:
42	chr7:12251087..12251775-chr7:12361635..12362202,4	MCF-7	breast:
43	chr7:12365317..12367228-chr7:12375967..12378342,2	K562	blood:
44	chr7:12333884..12336168-chr7:12337724..12340459,4	K562	blood:
45	chr7:12353391..12355072-chr7:12357011..12359494,3	K562	blood:
46	chr7:12351255..12355072-chr7:12355211..12359779,5	K562	blood:
47	chr7:12390586..12393212-chr7:12394959..12396886,2	K562	blood:
48	chr7:12304154..12306342-chr7:12308310..12310160,2	K562	blood:
49	chr7:12363684..12366465-chr7:12393124..12396040,2	K562	blood:
50	chr7:12106923..12107696-chr7:12361667..12362587,3	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-THSD7A-7	chr7:12380807-12381047	expReg_chr7_1129_-
2	lnc-THSD7A-4	chr7:12370513-12370823	NONHSAT119227
3	lnc-THSD7A-4	chr7:12373091-12373352	NONHSAT119227
4	lnc-VWDE-5	chr7:12360180-12360643	expReg_chr7_1116_-
5	lnc-THSD7A-8	chr7:12381149-12381601	expReg_chr7_1130_-
6	lnc-THSD7A-6	chr7:12378965-12379591	expReg_chr7_1128_-
7	lnc-THSD7A-5	chr7:12376785-12377015	expReg_chr7_1125_-

No data

Variant related genes	Relation type
VWDE	TF binding region
VWDE	CpG island
ENSG00000106460	chromatin interactions
ENSG00000146530	chromatin interactions

Extended variants
information (count: 4238 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:4238 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550540403	chr7:12307946-12307947	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs569650285	chr7:12307978-12307979	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs75994414	chr7:12307992-12307993	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs548926891	chr7:12307997-12307998	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs565820811	chr7:12308012-12308013	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs115318903	chr7:12308028-12308029	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs551540476	chr7:12308098-12308099	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs6976341	chr7:12308110-12308111	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs4721068	chr7:12308136-12308137	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs7808979	chr7:12308175-12308176	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs556965397	chr7:12308180-12308181	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs184556467	chr7:12308197-12308198	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs530949133	chr7:12308210-12308211	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs536906487	chr7:12308211-12308212	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs189697318	chr7:12308226-12308227	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs115564342	chr7:12308258-12308259	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs545195363	chr7:12308315-12308316	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs56259269	chr7:12308332-12308333	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs367834471	chr7:12308345-12308346	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs544214922	chr7:12308357-12308358	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs560917214	chr7:12308390-12308391	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs578256913	chr7:12308399-12308400	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs73290038	chr7:12308402-12308403	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs77504689	chr7:12308416-12308417	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs386710398	chr7:12308430-12308431	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs181332557	chr7:12308432-12308433	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs115549788	chr7:12308435-12308436	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs7776877	chr7:12308455-12308456	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs537118235	chr7:12308476-12308477	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs7795892	chr7:12308487-12308488	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs567215077	chr7:12308523-12308524	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs12699347	chr7:12308570-12308571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs56047724	chr7:12308612-12308613	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs573437205	chr7:12308616-12308617	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs536594839	chr7:12308627-12308628	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs544190819	chr7:12308661-12308662	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs367952315	chr7:12308697-12308698	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs111424789	chr7:12308723-12308724	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs544251805	chr7:12308724-12308725	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs185973230	chr7:12308754-12308755	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs574815699	chr7:12308790-12308791	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs540263392	chr7:12308816-12308817	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs557038989	chr7:12308821-12308822	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs528376684	chr7:12308849-12308850	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs73290041	chr7:12308884-12308885	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs562549971	chr7:12308900-12308901	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs530633323	chr7:12308918-12308919	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs573618257	chr7:12308934-12308935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs533410333	chr7:12308937-12308938	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs78505888	chr7:12309010-12309011	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Autism	22495309	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Multiple myeloma	17550852	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:270 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12308400-12308600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:12308400-12310600	Enhancers	Fetal Intestine Large	intestine
3	chr7:12308600-12308800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:12308600-12310000	Enhancers	Fetal Intestine Small	intestine
5	chr7:12308800-12309200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:12308800-12309600	Enhancers	Liver	Liver
7	chr7:12308800-12310000	Enhancers	HepG2	liver
8	chr7:12309200-12309400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr7:12309400-12310000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:12317800-12318000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr7:12317800-12318200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr7:12317800-12318400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr7:12317800-12329400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:12323600-12324000	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr7:12326800-12327800	Enhancers	Brain Germinal Matrix	brain
16	chr7:12327800-12328600	Weak transcription	Brain Germinal Matrix	brain
17	chr7:12328600-12328800	Enhancers	Brain Germinal Matrix	brain
18	chr7:12329000-12329200	Enhancers	H9 Cell Line	embryonic stem cell
19	chr7:12329200-12330400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:12329400-12330000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr7:12330200-12330600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr7:12330400-12331000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr7:12331000-12331200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
24	chr7:12331200-12331400	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr7:12331400-12332400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr7:12334000-12335000	Enhancers	Primary B cells from peripheral blood	blood
27	chr7:12334400-12335000	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr7:12335200-12336200	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr7:12335200-12336200	Enhancers	Esophagus	oesophagus
30	chr7:12335200-12338400	Enhancers	Placenta	Placenta
31	chr7:12335600-12336200	Enhancers	NHEK	skin
32	chr7:12335800-12336200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr7:12335800-12336200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr7:12335800-12336200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr7:12335800-12336200	Enhancers	HMEC	breast
36	chr7:12335800-12336400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr7:12336200-12336400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr7:12336200-12337200	Weak transcription	NHEK	skin
39	chr7:12336200-12338000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr7:12336200-12342400	Weak transcription	HMEC	breast
41	chr7:12336400-12337000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr7:12336400-12337600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr7:12337000-12337600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr7:12337000-12337600	Enhancers	Fetal Kidney	kidney
45	chr7:12337000-12338400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr7:12337200-12337600	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr7:12337200-12338000	Enhancers	NHEK	skin
48	chr7:12337400-12337800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr7:12337400-12338600	Enhancers	H1 Cell Line	embryonic stem cell
50	chr7:12337600-12342400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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