Variant report

Variant	nsv887630
Chromosome Location	chr7:12323757-12400837
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:763)
CpG islands
(count:183)
Chromatin interactive
region (count:54)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:763 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:12361970-12362233	K562	blood:	n/a	n/a
2	ARID3A	chr7:12361928-12362236	HepG2	liver:	n/a	n/a
3	ATF1	chr7:12360907-12361152	K562	blood:	n/a	n/a
4	ATF1	chr7:12391517-12391830	K562	blood:	n/a	n/a
5	ATF2	chr7:12397170-12397485	GM12878	blood:	n/a	n/a
6	BATF	chr7:12362561-12362908	GM12878	blood:	n/a	chr7:12362724-12362735
7	BATF	chr7:12362529-12362819	GM12878	blood:	n/a	chr7:12362724-12362735
8	BCL11A	chr7:12362543-12362825	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:12362562-12362789	GM12878	blood:	n/a	n/a
10	BCL3	chr7:12397240-12397520	GM12878	blood:	n/a	n/a
11	BCL3	chr7:12370808-12371350	K562	blood:	n/a	n/a
12	BHLHE40	chr7:12371392-12371475	A549	lung:	n/a	n/a
13	BHLHE40	chr7:12362651-12362754	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:12361210-12361233	K562	blood:	n/a	n/a
15	BHLHE40	chr7:12391626-12391783	K562	blood:	n/a	n/a
16	BRCA1	chr7:12363238-12363314	GM12878	blood:	n/a	n/a
17	CBX3	chr7:12330934-12331289	K562	blood:	n/a	n/a
18	CBX3	chr7:12338999-12339376	K562	blood:	n/a	n/a
19	CCNT2	chr7:12391547-12391847	K562	blood:	n/a	n/a
20	CCNT2	chr7:12360909-12361396	K562	blood:	n/a	n/a
21	CCNT2	chr7:12383002-12383143	K562	blood:	n/a	n/a
22	CEBPB	chr7:12365869-12365957	K562	blood:	n/a	chr7:12365903-12365914 chr7:12365903-12365916 chr7:12365903-12365916 chr7:12365903-12365916
23	CEBPB	chr7:12337404-12337716	MCF-7	breast:	n/a	n/a
24	CEBPB	chr7:12376799-12377121	HepG2	liver:	n/a	chr7:12376957-12376970 chr7:12376957-12376968 chr7:12376957-12376970
25	CEBPB	chr7:12376790-12377114	A549	lung:	n/a	chr7:12376957-12376970 chr7:12376957-12376968 chr7:12376957-12376970
26	CEBPB	chr7:12357363-12357592	IMR90	lung:	n/a	chr7:12357510-12357521
27	CEBPB	chr7:12360962-12361174	K562	blood:	n/a	n/a
28	CEBPB	chr7:12365884-12365914	H1-hESC	embryonic stem cell:	n/a	chr7:12365903-12365914
29	CEBPB	chr7:12341270-12341440	K562	blood:	n/a	n/a
30	CEBPB	chr7:12357399-12357607	A549	lung:	n/a	chr7:12357510-12357521
31	CEBPB	chr7:12397108-12397677	GM12878	blood:	n/a	n/a
32	CEBPB	chr7:12345750-12345982	A549	lung:	n/a	n/a
33	CEBPB	chr7:12376804-12377018	IMR90	lung:	n/a	chr7:12376957-12376970 chr7:12376957-12376968 chr7:12376957-12376970
34	CEBPB	chr7:12376796-12377033	K562	blood:	n/a	chr7:12376957-12376970 chr7:12376957-12376968 chr7:12376957-12376970
35	CEBPB	chr7:12357353-12357682	K562	blood:	n/a	chr7:12357510-12357521
36	CEBPB	chr7:12368645-12369574	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr7:12357429-12357629	HepG2	liver:	n/a	chr7:12357510-12357521
38	CEBPB	chr7:12360899-12361157	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr7:12363089-12363397	HepG2	liver:	n/a	n/a
40	CHD2	chr7:12363091-12363608	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr7:12363065-12363428	GM12878	blood:	n/a	n/a
42	CHD2	chr7:12391646-12391710	K562	blood:	n/a	n/a
43	CTCF	chr7:12362040-12362190	HFF-Myc	foreskin:	n/a	chr7:12362097-12362118 chr7:12362102-12362120
44	CTCF	chr7:12331620-12331770	NHEK	skin:	n/a	n/a
45	CTCF	chr7:12361914-12362255	SK-N-SH_RA	brain:	n/a	chr7:12362097-12362118 chr7:12362102-12362120
46	CTCF	chr7:12362060-12362210	HCT-116	colon:	n/a	chr7:12362097-12362118 chr7:12362102-12362120
47	CTCF	chr7:12362040-12362190	HUVEC	blood vessel:	n/a	chr7:12362097-12362118 chr7:12362102-12362120
48	CTCF	chr7:12331600-12331750	GM12872	blood:	n/a	n/a
49	CTCF	chr7:12361875-12362312	T-47D	breast:	n/a	chr7:12362097-12362118 chr7:12362102-12362120
50	CTCF	chr7:12362000-12362150	HA-sp	spinal cord:	n/a	chr7:12362097-12362118 chr7:12362102-12362120

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12376625-12376675	HCF	heart:	n/a
2	chr7:12363490-12363540	HCF	heart:	n/a
3	chr7:12363490-12363540	ECC-1	luminal epithelium:	n/a
4	chr7:12370351-12370401	HL-60	blood:	n/a
5	chr7:12376625-12376675	SK-N-MC	brain:	n/a
6	chr7:12363490-12363540	HRE	kidney:	n/a
7	chr7:12376625-12376675	RPTEC	kidney:	n/a
8	chr7:12363490-12363540	HUVEC	blood vessel:	n/a
9	chr7:12363490-12363540	SK-N-MC	brain:	n/a
10	chr7:12363490-12363540	HEK293	kidney:	embryo
11	chr7:12363490-12363540	GM12891	blood:	n/a
12	chr7:12363490-12363540	HCM	heart:	n/a
13	chr7:12370351-12370401	ProgFib	skin:	n/a
14	chr7:12363490-12363540	NH-A	brain:	n/a
15	chr7:12363490-12363540	Hepatocyte	liver:	n/a
16	chr7:12370351-12370401	H1-hESC	embryonic stem cell:	embryo
17	chr7:12376625-12376675	HEEpiC	esophagus:	n/a
18	chr7:12376625-12376675	SAEC	small airway:	n/a
19	chr7:12363490-12363540	BE2_C	brain:	n/a
20	chr7:12370351-12370401	Jurkat	blood:	n/a
21	chr7:12376625-12376675	BJ	skin:	n/a
22	chr7:12363490-12363540	SKMC	muscle:	n/a
23	chr7:12370351-12370401	ovcar-3	ovarian:	n/a
24	chr7:12376625-12376675	A549	lung:	n/a
25	chr7:12363490-12363540	AG04450	lung:	fetal
26	chr7:12363490-12363540	GM06990	blood:	n/a
27	chr7:12370351-12370401	AG04449	skin:	fetal
28	chr7:12376625-12376675	HCM	heart:	n/a
29	chr7:12376625-12376675	HUVEC	blood vessel:	n/a
30	chr7:12376625-12376675	AG09319	gingival:	n/a
31	chr7:12376625-12376675	PANC-1	pancreas:	n/a
32	chr7:12370351-12370401	NHDF-neo	bronchial:	n/a
33	chr7:12376625-12376675	Hepatocyte	liver:	n/a
34	chr7:12363490-12363540	GM12892	blood:	n/a
35	chr7:12370351-12370401	LNCaP	prostate:	n/a
36	chr7:12363490-12363540	NHBE	bronchial:	n/a
37	chr7:12376625-12376675	HL-60	blood:	n/a
38	chr7:12376625-12376675	CMK	blood:	n/a
39	chr7:12376625-12376675	GM12891	blood:	n/a
40	chr7:12370351-12370401	SKMC	muscle:	n/a
41	chr7:12376625-12376675	MCF10A-Er-Src	breast:	n/a
42	chr7:12370351-12370401	Caco-2	colon:	n/a
43	chr7:12376625-12376675	SK-N-SH	brain:	n/a
44	chr7:12376625-12376675	PrEC	prostate:	n/a
45	chr7:12363490-12363540	HepG2	liver:	n/a
46	chr7:12363490-12363540	HEEpiC	esophagus:	n/a
47	chr7:12363490-12363540	HMEC	breast:	n/a
48	chr7:12363490-12363540	NT2-D1	testis:	n/a
49	chr7:12370351-12370401	CMK	blood:	n/a
50	chr7:12370351-12370401	T-47D	breast:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:12359785..12361369-chr7:12363361..12365480,2	K562	blood:
2	chr7:12237104..12239270-chr7:12329420..12331412,2	K562	blood:
3	chr7:12385242..12386819-chr7:12390082..12392750,2	K562	blood:
4	chr7:12390586..12393212-chr7:12394959..12396886,2	K562	blood:
5	chr7:12106833..12107747-chr7:12331137..12332178,5	MCF-7	breast:
6	chr7:12351255..12355072-chr7:12355211..12359779,5	K562	blood:
7	chr7:12391712..12393347-chr7:12394959..12396471,2	K562	blood:
8	chr7:12378441..12379998-chr7:12382677..12384554,2	K562	blood:
9	chr7:12362078..12365720-chr7:12370304..12373327,3	K562	blood:
10	chr7:12351255..12355072-chr7:12355211..12359779,5	K562	blood:
11	chr7:12359785..12361369-chr7:12363361..12365480,2	K562	blood:
12	chr7:12391712..12393347-chr7:12394959..12396471,2	K562	blood:
13	chr7:12389607..12392285-chr7:12392419..12394302,2	K562	blood:
14	chr7:12333884..12336168-chr7:12337724..12340459,4	K562	blood:
15	chr7:12391914..12394742-chr7:12414391..12416688,2	K562	blood:
16	chr7:12399201..12400947-chr7:12402626..12404166,2	K562	blood:
17	chr7:12249029..12251264-chr7:12355308..12358122,2	MCF-7	breast:
18	chr7:12380686..12382239-chr7:12385639..12388082,2	K562	blood:
19	chr7:12106923..12107696-chr7:12361667..12362587,3	MCF-7	breast:
20	chr7:12391134..12392692-chr7:12402911..12404517,2	K562	blood:
21	chr7:12378441..12379998-chr7:12382677..12384554,2	K562	blood:
22	chr7:12356830..12359604-chr7:12404989..12406571,2	K562	blood:
23	chr7:12398772..12400728-chr7:12416119..12417972,2	K562	blood:
24	chr7:12248340..12250610-chr7:12341759..12344659,2	K562	blood:
25	chr7:12392619..12394669-chr7:12398215..12400869,2	K562	blood:
26	chr7:12380686..12382573-chr7:12386582..12389339,2	K562	blood:
27	chr7:12353391..12355072-chr7:12357011..12359494,3	K562	blood:
28	chr7:12359587..12361942-chr7:12364993..12366787,2	K562	blood:
29	chr7:12362049..12364322-chr7:12365857..12368217,3	K562	blood:
30	chr7:12382799..12385098-chr7:12438700..12441052,2	K562	blood:
31	chr7:12392619..12394669-chr7:12398215..12400869,2	K562	blood:
32	chr7:12363684..12366465-chr7:12393124..12396040,2	K562	blood:
33	chr7:12382924..12384916-chr7:12389053..12391966,2	K562	blood:
34	chr7:12365317..12367228-chr7:12375967..12378342,2	K562	blood:
35	chr7:12390586..12393212-chr7:12394959..12396886,2	K562	blood:
36	chr7:12319256..12322046-chr7:12323185..12326325,3	K562	blood:
37	chr7:12326033..12327864-chr7:12530775..12532531,2	K562	blood:
38	chr7:12365317..12367228-chr7:12375967..12378342,2	K562	blood:
39	chr7:12333884..12336168-chr7:12337724..12340459,4	K562	blood:
40	chr7:12359587..12361942-chr7:12364993..12366787,2	K562	blood:
41	chr7:12363684..12366465-chr7:12393124..12396040,2	K562	blood:
42	chr7:12353391..12355072-chr7:12357011..12359494,3	K562	blood:
43	chr7:12249110..12251929-chr7:12341759..12344024,2	K562	blood:
44	chr7:12389607..12392285-chr7:12392419..12394302,2	K562	blood:
45	chr7:12362078..12365720-chr7:12370304..12373327,3	K562	blood:
46	chr7:12380686..12382239-chr7:12385639..12388082,2	K562	blood:
47	chr7:12252737..12254776-chr7:12374517..12377204,2	K562	blood:
48	chr7:12385242..12386819-chr7:12390082..12392750,2	K562	blood:
49	chr7:12376678..12378667-chr7:12443118..12444758,2	K562	blood:
50	chr7:12354059..12356452-chr7:12416852..12418898,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 3808 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:3808 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10247702	chr7:12323757-12323758	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531752129	chr7:12323801-12323802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112674889	chr7:12323814-12323815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548572990	chr7:12323819-12323820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567569649	chr7:12323841-12323842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536506121	chr7:12323844-12323845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546575226	chr7:12323877-12323878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112801596	chr7:12323913-12323914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143086097	chr7:12323933-12323934	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6977974	chr7:12323936-12323937	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs535925356	chr7:12323940-12323941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs72238989	chr7:12323992-12323993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189197974	chr7:12324017-12324018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10277566	chr7:12324026-12324027	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs10248101	chr7:12324035-12324036	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs545413214	chr7:12324048-12324049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148208556	chr7:12324069-12324070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540965847	chr7:12324073-12324074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560599062	chr7:12324113-12324114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577399633	chr7:12324181-12324182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146172736	chr7:12324182-12324183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs6978326	chr7:12324183-12324184	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs531791101	chr7:12324189-12324190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75096814	chr7:12324217-12324218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562153506	chr7:12324272-12324273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs527663374	chr7:12324296-12324297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546908064	chr7:12324320-12324321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10274502	chr7:12324330-12324331	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs181953631	chr7:12324343-12324344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10258758	chr7:12324351-12324352	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs10258988	chr7:12324355-12324356	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs537592555	chr7:12324372-12324373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554237359	chr7:12324388-12324389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574399280	chr7:12324390-12324391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185784185	chr7:12324404-12324405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554462348	chr7:12324431-12324432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs111337906	chr7:12324434-12324435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530253154	chr7:12324439-12324440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546421498	chr7:12324447-12324448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556754661	chr7:12324453-12324454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576700695	chr7:12324473-12324474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs9969145	chr7:12324485-12324486	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs562026378	chr7:12324521-12324522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546759619	chr7:12324651-12324652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113680594	chr7:12324692-12324693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192033722	chr7:12324748-12324749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532235266	chr7:12324776-12324777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78501733	chr7:12324822-12324823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12699359	chr7:12324844-12324845	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs60322048	chr7:12324853-12324854	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:91)

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
Multiple myeloma	17550852	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12317800-12329400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:12323600-12324000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr7:12326800-12327800	Enhancers	Brain Germinal Matrix	brain
4	chr7:12327800-12328600	Weak transcription	Brain Germinal Matrix	brain
5	chr7:12328600-12328800	Enhancers	Brain Germinal Matrix	brain
6	chr7:12329000-12329200	Enhancers	H9 Cell Line	embryonic stem cell
7	chr7:12329200-12330400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:12329400-12330000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr7:12330200-12330600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr7:12330400-12331000	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr7:12331000-12331200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
12	chr7:12331200-12331400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr7:12331400-12332400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr7:12334000-12335000	Enhancers	Primary B cells from peripheral blood	blood
15	chr7:12334400-12335000	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr7:12335200-12336200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr7:12335200-12336200	Enhancers	Esophagus	oesophagus
18	chr7:12335200-12338400	Enhancers	Placenta	Placenta
19	chr7:12335600-12336200	Enhancers	NHEK	skin
20	chr7:12335800-12336200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr7:12335800-12336200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:12335800-12336200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr7:12335800-12336200	Enhancers	HMEC	breast
24	chr7:12335800-12336400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr7:12336200-12336400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr7:12336200-12337200	Weak transcription	NHEK	skin
27	chr7:12336200-12338000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr7:12336200-12342400	Weak transcription	HMEC	breast
29	chr7:12336400-12337000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr7:12336400-12337600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr7:12337000-12337600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr7:12337000-12337600	Enhancers	Fetal Kidney	kidney
33	chr7:12337000-12338400	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr7:12337200-12337600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr7:12337200-12338000	Enhancers	NHEK	skin
36	chr7:12337400-12337800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:12337400-12338600	Enhancers	H1 Cell Line	embryonic stem cell
38	chr7:12337600-12342400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr7:12337800-12338200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr7:12338000-12338400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr7:12338000-12338600	Enhancers	Placenta Amnion	Placenta Amnion
42	chr7:12338000-12342200	Weak transcription	NHEK	skin
43	chr7:12338200-12338400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:12338200-12338800	Enhancers	Adipose Nuclei	Adipose
45	chr7:12338400-12359200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr7:12339600-12360000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr7:12340800-12342000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr7:12342000-12342800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr7:12342000-12342800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr7:12342200-12342600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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