Variant report

Variant	nsv882688
Chromosome Location	chr5:107595383-107715746
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:875)
CpG islands
(count:244)
Chromatin interactive
region (count:59)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:875 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:107620107-107620141	K562	blood:	n/a	n/a
2	ARID3A	chr5:107674937-107675137	K562	blood:	n/a	n/a
3	ARID3A	chr5:107600098-107600210	K562	blood:	n/a	n/a
4	ARID3A	chr5:107606643-107607282	K562	blood:	n/a	n/a
5	ARID3A	chr5:107715451-107716224	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:107681343-107681626	K562	blood:	n/a	n/a
7	ATF1	chr5:107596189-107596594	K562	blood:	n/a	n/a
8	ATF1	chr5:107624684-107624909	K562	blood:	n/a	n/a
9	ATF1	chr5:107696104-107696307	K562	blood:	n/a	n/a
10	ATF1	chr5:107606855-107607320	K562	blood:	n/a	n/a
11	ATF1	chr5:107602038-107602338	K562	blood:	n/a	n/a
12	BATF	chr5:107596353-107596643	GM12878	blood:	n/a	chr5:107596536-107596545
13	BATF	chr5:107596322-107596630	GM12878	blood:	n/a	chr5:107596536-107596545
14	BCL3	chr5:107666346-107666596	GM12878	blood:	n/a	n/a
15	BCLAF1	chr5:107596309-107596680	GM12878	blood:	n/a	n/a
16	BHLHE40	chr5:107606875-107607203	K562	blood:	n/a	n/a
17	BHLHE40	chr5:107666323-107666558	K562	blood:	n/a	n/a
18	BHLHE40	chr5:107596297-107596574	K562	blood:	n/a	n/a
19	CBX3	chr5:107711447-107711797	K562	blood:	n/a	n/a
20	CBX3	chr5:107708074-107708501	K562	blood:	n/a	n/a
21	CBX3	chr5:107711457-107711756	K562	blood:	n/a	n/a
22	CBX3	chr5:107709172-107709413	K562	blood:	n/a	n/a
23	CBX3	chr5:107709123-107709498	K562	blood:	n/a	n/a
24	CBX3	chr5:107709123-107709557	HCT-116	colon:	n/a	n/a
25	CBX3	chr5:107708110-107708382	K562	blood:	n/a	n/a
26	CCNT2	chr5:107606596-107607245	K562	blood:	n/a	chr5:107607043-107607063
27	CCNT2	chr5:107645829-107646060	K562	blood:	n/a	n/a
28	CEBPB	chr5:107631605-107632100	Hela-S3	cervix:	n/a	chr5:107631760-107631771 chr5:107631760-107631769
29	CEBPB	chr5:107645842-107646112	A549	lung:	n/a	chr5:107646013-107646024
30	CEBPB	chr5:107601995-107602342	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr5:107660681-107660854	HepG2	liver:	n/a	n/a
32	CEBPB	chr5:107715494-107715884	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr5:107713722-107714042	IMR90	lung:	n/a	chr5:107713885-107713896
34	CEBPB	chr5:107715466-107715915	HepG2	liver:	n/a	n/a
35	CEBPB	chr5:107713802-107714063	A549	lung:	n/a	chr5:107713885-107713896
36	CEBPB	chr5:107631604-107632130	IMR90	lung:	n/a	chr5:107631760-107631771 chr5:107631760-107631769
37	CEBPB	chr5:107596323-107596668	Hela-S3	cervix:	n/a	chr5:107596520-107596531
38	CEBPB	chr5:107660629-107660991	HepG2	liver:	n/a	n/a
39	CEBPB	chr5:107657017-107657483	ECC-1	luminal epithelium:	n/a	chr5:107657276-107657287 chr5:107657275-107657288
40	CEBPB	chr5:107617025-107617253	HepG2	liver:	n/a	n/a
41	CEBPB	chr5:107713835-107714023	H1-hESC	embryonic stem cell:	n/a	chr5:107713885-107713896
42	CEBPB	chr5:107713803-107714027	Hela-S3	cervix:	n/a	chr5:107713885-107713896
43	CEBPB	chr5:107606936-107607452	K562	blood:	n/a	n/a
44	CEBPB	chr5:107596354-107596582	H1-hESC	embryonic stem cell:	n/a	chr5:107596520-107596531
45	CEBPB	chr5:107713768-107714065	K562	blood:	n/a	chr5:107713885-107713896
46	CEBPB	chr5:107631617-107631834	H1-hESC	embryonic stem cell:	n/a	chr5:107631760-107631771 chr5:107631760-107631769
47	CEBPB	chr5:107657031-107657431	ECC-1	luminal epithelium:	n/a	chr5:107657276-107657287 chr5:107657275-107657288
48	CEBPB	chr5:107715571-107715791	IMR90	lung:	n/a	n/a
49	CEBPB	chr5:107713722-107714030	HepG2	liver:	n/a	chr5:107713885-107713896
50	CEBPB	chr5:107657261-107657436	HepG2	liver:	n/a	chr5:107657276-107657287 chr5:107657275-107657288

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:107713125-107713175	ovcar-3	ovarian:	n/a
2	chr5:107614099-107614149	Caco-2	colon:	n/a
3	chr5:107713125-107713175	RPTEC	kidney:	n/a
4	chr5:107614099-107614149	HepG2	liver:	n/a
5	chr5:107595754-107595804	ProgFib	skin:	n/a
6	chr5:107702185-107702235	RPTEC	kidney:	n/a
7	chr5:107702185-107702235	HEK293	kidney:	embryo
8	chr5:107614099-107614149	BE2_C	brain:	n/a
9	chr5:107595754-107595804	LNCaP	prostate:	n/a
10	chr5:107713125-107713175	HAEpiC	amniotic membrane:	n/a
11	chr5:107702185-107702235	AG04450	lung:	fetal
12	chr5:107702185-107702235	SK-N-SH_RA	brain:	n/a
13	chr5:107595754-107595804	PFSK-1	brain:	n/a
14	chr5:107595754-107595804	MCF-7	breast:	n/a
15	chr5:107713125-107713175	NH-A	brain:	n/a
16	chr5:107614099-107614149	HCT-116	colon:	n/a
17	chr5:107614099-107614149	Hepatocyte	liver:	n/a
18	chr5:107614099-107614149	HRPEpiC	eye:	n/a
19	chr5:107595754-107595804	ECC-1	luminal epithelium:	n/a
20	chr5:107595754-107595804	PrEC	prostate:	n/a
21	chr5:107614099-107614149	T-47D	breast:	n/a
22	chr5:107595754-107595804	T-47D	breast:	n/a
23	chr5:107614099-107614149	Hela-S3	cervix:	n/a
24	chr5:107713125-107713175	HNPCEpiC	eye:	n/a
25	chr5:107614099-107614149	NB4	blood:	n/a
26	chr5:107702185-107702235	HAEpiC	amniotic membrane:	n/a
27	chr5:107713125-107713175	HEEpiC	esophagus:	n/a
28	chr5:107713125-107713175	PFSK-1	brain:	n/a
29	chr5:107713125-107713175	CMK	blood:	n/a
30	chr5:107614099-107614149	RPTEC	kidney:	n/a
31	chr5:107702185-107702235	NHBE	bronchial:	n/a
32	chr5:107713125-107713175	SK-N-SH	brain:	n/a
33	chr5:107713125-107713175	HEK293	kidney:	embryo
34	chr5:107702185-107702235	HCM	heart:	n/a
35	chr5:107595754-107595804	AG04449	skin:	fetal
36	chr5:107595754-107595804	HL-60	blood:	n/a
37	chr5:107595754-107595804	NH-A	brain:	n/a
38	chr5:107702185-107702235	PANC-1	pancreas:	n/a
39	chr5:107614099-107614149	K562	blood:	n/a
40	chr5:107614099-107614149	MCF10A-Er-Src	breast:	n/a
41	chr5:107595754-107595804	AG10803	skin:	n/a
42	chr5:107595754-107595804	Jurkat	blood:	n/a
43	chr5:107614099-107614149	HCM	heart:	n/a
44	chr5:107614099-107614149	CMK	blood:	n/a
45	chr5:107614099-107614149	NH-A	brain:	n/a
46	chr5:107614099-107614149	GM12878	blood:	n/a
47	chr5:107713125-107713175	PANC-1	pancreas:	n/a
48	chr5:107595754-107595804	HMEC	breast:	n/a
49	chr5:107614099-107614149	AG09309	skin:	n/a
50	chr5:107595754-107595804	BE2_C	brain:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:107595024..107598091-chr5:107715832..107718425,3	K562	blood:
2	chr5:107705977..107708184-chr5:107711910..107713807,2	MCF-7	breast:
3	chr5:107652768..107655007-chr5:107665345..107667956,2	K562	blood:
4	chr5:107695811..107698012-chr5:107701922..107703734,2	K562	blood:
5	chr5:107591521..107593328-chr5:107594496..107596431,3	MCF-7	breast:
6	chr5:107602916..107603688-chr6:91564315..91565066,2	MCF-7	breast:
7	chr5:102896315..102898883-chr5:107715677..107718329,2	K562	blood:
8	chr5:107700578..107705838-chr5:107715421..107718628,5	K562	blood:
9	chr5:107687278..107689541-chr5:107694592..107696182,2	K562	blood:
10	chr5:107696924..107698880-chr5:107700620..107702301,2	MCF-7	breast:
11	chr5:107629129..107630886-chr5:107639365..107641581,2	K562	blood:
12	chr5:107687278..107689541-chr5:107694592..107696182,2	K562	blood:
13	chr5:107705544..107707049-chr5:107712715..107714654,2	K562	blood:
14	chr5:107703017..107709518-chr5:107714821..107720551,7	MCF-7	breast:
15	chr5:107705544..107707049-chr5:107712715..107714654,2	K562	blood:
16	chr5:107641389..107643591-chr5:107717199..107720025,2	MCF-7	breast:
17	chr5:107596357..107597019-chr5:107678266..107678805,2	MCF-7	breast:
18	chr11:393917..395827-chr5:107707504..107710114,2	MCF-7	breast:
19	chr5:107596085..107596926-chr5:107614295..107614996,3	MCF-7	breast:
20	chr5:107705977..107708184-chr5:107711910..107713807,2	MCF-7	breast:
21	chr5:107715063..107717038-chr5:110074735..110077588,2	K562	blood:
22	chr5:107703017..107709518-chr5:107714821..107720551,7	MCF-7	breast:
23	chr5:107595947..107596960-chr5:107681100..107682005,3	MCF-7	breast:
24	chr5:107637065..107639701-chr5:107665572..107668280,2	K562	blood:
25	chr5:107696924..107698880-chr5:107700620..107702301,2	MCF-7	breast:
26	chr5:107662350..107665061-chr5:107666147..107667939,2	MCF-7	breast:
27	chr5:107693754..107695689-chr5:107714400..107716161,2	K562	blood:
28	chr20:15213744..15214594-chr5:107680986..107681674,2	MCF-7	breast:
29	chr5:107697658..107700570-chr5:107705243..107707964,2	K562	blood:
30	chr5:107702113..107704886-chr5:107707019..107708765,2	K562	blood:
31	chr5:107703047..107709148-chr5:107715421..107721287,10	K562	blood:
32	chr5:107593297..107597338-chr5:107716343..107718522,3	MCF-7	breast:
33	chr5:107674221..107676262-chr5:107681301..107685297,3	K562	blood:
34	chr5:107700359..107701872-chr5:107716648..107719223,2	MCF-7	breast:
35	chr5:107637065..107639701-chr5:107665572..107668280,2	K562	blood:
36	chr5:107678990..107681640-chr5:107716469..107719656,3	MCF-7	breast:
37	chr5:107699675..107702509-chr5:107715943..107717724,2	K562	blood:
38	chr5:107630732..107633907-chr5:107716808..107719263,3	MCF-7	breast:
39	chr5:107652768..107655007-chr5:107665345..107667956,2	K562	blood:
40	chr5:107697169..107698902-chr5:107715827..107718166,2	K562	blood:
41	chr5:107696918..107699388-chr5:107716914..107718993,2	K562	blood:
42	chr5:107596085..107596926-chr5:107614295..107614996,3	MCF-7	breast:
43	chr5:107596383..107598517-chr5:107717279..107719570,2	MCF-7	breast:
44	chr5:107693754..107695689-chr5:107714400..107716161,2	K562	blood:
45	chr5:107703047..107709148-chr5:107715421..107721287,10	K562	blood:
46	chr5:107690532..107692643-chr5:107717200..107720124,2	K562	blood:
47	chr5:107700578..107705838-chr5:107715421..107718628,5	K562	blood:
48	chr5:107705561..107708007-chr5:107713920..107718411,4	MCF-7	breast:
49	chr5:107692103..107694932-chr5:107716321..107718109,2	MCF-7	breast:
50	chr5:107703071..107704967-chr5:107714002..107715919,2	MCF-7	breast:

No data

Variant related genes	Relation type
FBXL17	TF binding region
FBXL17	CpG island
ENSG00000164209	chromatin interactions
ENSG00000184363	chromatin interactions
ENSG00000145743	chromatin interactions
ENSG00000112874	chromatin interactions

Extended variants
information (count: 4511 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4511 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10051605	chr5:107595383-107595384	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532472072	chr5:107595509-107595510	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs565332427	chr5:107595518-107595519	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs575532789	chr5:107595525-107595526	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs143990607	chr5:107595529-107595530	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs188602704	chr5:107595546-107595547	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs529974787	chr5:107595561-107595562	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs7726195	chr5:107595562-107595563	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs12519091	chr5:107595650-107595651	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs111840389	chr5:107595687-107595688	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs531932342	chr5:107595713-107595714	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs111960335	chr5:107595722-107595723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs398065088	chr5:107595733-107595734	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs76686204	chr5:107595735-107595736	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs72240923	chr5:107595736-107595737	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs202174228	chr5:107595745-107595746	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs182078529	chr5:107595795-107595796	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs568575859	chr5:107595830-107595831	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs186853304	chr5:107595837-107595838	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs550920309	chr5:107595927-107595928	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs567844622	chr5:107595953-107595954	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs146410600	chr5:107595968-107595969	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs149222674	chr5:107595970-107595971	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs559425748	chr5:107596029-107596030	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs368577977	chr5:107596040-107596041	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs540618924	chr5:107596065-107596066	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs112621910	chr5:107596086-107596087	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs191693777	chr5:107596181-107596182	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs183921119	chr5:107596204-107596205	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs143379978	chr5:107596229-107596230	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs544672907	chr5:107596247-107596248	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs7730637	chr5:107596249-107596250	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs35417290	chr5:107596250-107596251	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs574569147	chr5:107596280-107596281	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs148371360	chr5:107596293-107596294	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs116396471	chr5:107596312-107596313	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs186079052	chr5:107596329-107596330	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs551788331	chr5:107596368-107596369	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs189904779	chr5:107596406-107596407	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs531351661	chr5:107596451-107596452	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs562853053	chr5:107596460-107596461	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs368291437	chr5:107596470-107596471	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs111404361	chr5:107596478-107596479	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs544124050	chr5:107596496-107596497	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs530267626	chr5:107596524-107596525	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs564016808	chr5:107596537-107596538	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs147086309	chr5:107596555-107596556	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs4957551	chr5:107596575-107596576	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs539325162	chr5:107596600-107596601	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs569657166	chr5:107596604-107596605	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1035 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:107575200-107596200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:107575400-107617600	Weak transcription	Primary B cells from cord blood	blood
3	chr5:107577000-107616000	Weak transcription	Primary T cells from cord blood	blood
4	chr5:107585000-107617800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:107589200-107595800	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr5:107591800-107596200	Weak transcription	Ovary	ovary
7	chr5:107592000-107595800	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr5:107592000-107596000	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr5:107593200-107596400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr5:107593600-107595400	Enhancers	HSMM	muscle
11	chr5:107593600-107596400	Enhancers	HSMMtube	muscle
12	chr5:107593600-107596600	Enhancers	Fetal Heart	heart
13	chr5:107593600-107614000	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr5:107593800-107596000	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr5:107593800-107596200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr5:107594000-107596000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr5:107594000-107596200	Enhancers	Muscle Satellite Cultured Cells	--
18	chr5:107594000-107596400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr5:107594200-107596800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr5:107594400-107596000	Enhancers	HUVEC	blood vessel
21	chr5:107594400-107596400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr5:107594600-107595400	Enhancers	Colon Smooth Muscle	Colon
23	chr5:107594600-107596200	Enhancers	Osteobl	bone
24	chr5:107594800-107596000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr5:107594800-107596200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr5:107594800-107596400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr5:107595000-107595400	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr5:107595000-107595400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr5:107595000-107595400	Enhancers	Fetal Lung	lung
30	chr5:107595000-107595600	Enhancers	Liver	Liver
31	chr5:107595000-107595600	Enhancers	Fetal Kidney	kidney
32	chr5:107595000-107595600	Enhancers	Rectal Smooth Muscle	rectum
33	chr5:107595000-107595800	Enhancers	Fetal Intestine Large	intestine
34	chr5:107595000-107596000	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr5:107595000-107596400	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr5:107595000-107596400	Enhancers	Right Ventricle	heart
37	chr5:107595000-107596400	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr5:107595000-107596400	Enhancers	NHDF-Ad	bronchial
39	chr5:107595000-107596800	Enhancers	NH-A	brain
40	chr5:107595200-107595400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr5:107595200-107595600	Weak transcription	Psoas Muscle	Psoas
42	chr5:107595200-107596000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr5:107595200-107596000	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr5:107595200-107596000	Weak transcription	Stomach Smooth Muscle	stomach
45	chr5:107595200-107596200	Weak transcription	GM12878-XiMat	blood
46	chr5:107595200-107596200	Enhancers	K562	blood
47	chr5:107595200-107596400	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr5:107595200-107596400	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr5:107595200-107596400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr5:107595200-107596400	Enhancers	Fetal Intestine Small	intestine

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