Variant report

Variant	nsv1020948
Chromosome Location	chr8:8087144-8145999
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2154)
CpG islands
(count:305)
Chromatin interactive
region (count:55)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2154 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8092931-8093297	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:8105314-8105669	K562	blood:	n/a	n/a
3	ARID3A	chr8:8136392-8136433	K562	blood:	n/a	n/a
4	ARID3A	chr8:8127158-8127358	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:8091892-8091896	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:8101412-8102391	K562	blood:	n/a	n/a
7	ARID3A	chr8:8126032-8126609	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:8114109-8114421	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:8145751-8146493	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:8127880-8128214	HepG2	liver:	n/a	n/a
11	ARID3A	chr8:8111412-8112067	HepG2	liver:	n/a	n/a
12	ARID3A	chr8:8101041-8101072	HepG2	liver:	n/a	n/a
13	ARID3A	chr8:8102923-8103018	K562	blood:	n/a	n/a
14	ARID3A	chr8:8130676-8131061	HepG2	liver:	n/a	n/a
15	ARID3A	chr8:8105348-8105599	HepG2	liver:	n/a	n/a
16	ATF1	chr8:8101961-8102473	K562	blood:	n/a	n/a
17	ATF1	chr8:8118490-8118523	K562	blood:	n/a	n/a
18	ATF1	chr8:8144090-8144415	K562	blood:	n/a	n/a
19	ATF2	chr8:8141903-8142578	GM12878	blood:	n/a	n/a
20	ATF2	chr8:8126192-8126618	GM12878	blood:	n/a	n/a
21	ATF2	chr8:8136646-8137350	GM12878	blood:	n/a	n/a
22	ATF2	chr8:8143907-8144515	GM12878	blood:	n/a	n/a
23	ATF2	chr8:8141766-8142478	GM12878	blood:	n/a	n/a
24	ATF2	chr8:8126203-8126652	GM12878	blood:	n/a	n/a
25	ATF2	chr8:8143978-8144540	GM12878	blood:	n/a	n/a
26	ATF2	chr8:8096080-8096557	GM12878	blood:	n/a	n/a
27	ATF3	chr8:8145708-8146540	HCT-116	colon:	n/a	n/a
28	ATF3	chr8:8096172-8096477	K562	blood:	n/a	n/a
29	ATF3	chr8:8127796-8128282	A549	lung:	n/a	n/a
30	ATF3	chr8:8101821-8102415	K562	blood:	n/a	n/a
31	ATF3	chr8:8145728-8146513	A549	lung:	n/a	n/a
32	ATF3	chr8:8145720-8146548	HCT-116	colon:	n/a	n/a
33	ATF3	chr8:8101985-8102287	K562	blood:	n/a	n/a
34	ATF3	chr8:8145665-8146549	A549	lung:	n/a	n/a
35	BACH1	chr8:8130683-8130937	K562	blood:	n/a	n/a
36	BATF	chr8:8126297-8126540	GM12878	blood:	n/a	chr8:8126405-8126416 chr8:8126421-8126431 chr8:8126417-8126427 chr8:8126420-8126431
37	BATF	chr8:8144052-8144469	GM12878	blood:	n/a	n/a
38	BATF	chr8:8096176-8096555	GM12878	blood:	n/a	n/a
39	BATF	chr8:8143371-8143632	GM12878	blood:	n/a	n/a
40	BATF	chr8:8136381-8136667	GM12878	blood:	n/a	n/a
41	BATF	chr8:8143398-8143620	GM12878	blood:	n/a	n/a
42	BATF	chr8:8137532-8137784	GM12878	blood:	n/a	chr8:8137667-8137678 chr8:8137668-8137678
43	BATF	chr8:8141982-8142461	GM12878	blood:	n/a	n/a
44	BATF	chr8:8126185-8126638	GM12878	blood:	n/a	chr8:8126405-8126416 chr8:8126421-8126431 chr8:8126417-8126427 chr8:8126420-8126431
45	BATF	chr8:8144007-8144450	GM12878	blood:	n/a	n/a
46	BATF	chr8:8130779-8131070	GM12878	blood:	n/a	n/a
47	BATF	chr8:8091245-8091594	GM12878	blood:	n/a	n/a
48	BATF	chr8:8095764-8096661	GM12878	blood:	n/a	n/a
49	BATF	chr8:8086780-8087231	GM12878	blood:	n/a	chr8:8086859-8086869
50	BATF	chr8:8086957-8087326	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8090460-8090510	GM06990	blood:	n/a
2	chr8:8102121-8102171	HAEpiC	amniotic membrane:	n/a
3	chr8:8090460-8090510	AG10803	skin:	n/a
4	chr8:8102392-8102442	LNCaP	prostate:	n/a
5	chr8:8102121-8102171	NH-A	brain:	n/a
6	chr8:8102392-8102442	ECC-1	luminal epithelium:	n/a
7	chr8:8102121-8102171	BE2_C	brain:	n/a
8	chr8:8102121-8102171	GM06990	blood:	n/a
9	chr8:8120624-8120674	BJ	skin:	n/a
10	chr8:8102392-8102442	GM12878	blood:	n/a
11	chr8:8131077-8131127	HRCEpiC	kidney:	n/a
12	chr8:8131077-8131127	Hepatocyte	liver:	n/a
13	chr8:8120624-8120674	Hepatocyte	liver:	n/a
14	chr8:8131077-8131127	CMK	blood:	n/a
15	chr8:8120624-8120674	HUVEC	blood vessel:	n/a
16	chr8:8131077-8131127	Hela-S3	cervix:	n/a
17	chr8:8131077-8131127	K562	blood:	n/a
18	chr8:8102392-8102442	HAEpiC	amniotic membrane:	n/a
19	chr8:8131077-8131127	LNCaP	prostate:	n/a
20	chr8:8102392-8102442	HRCEpiC	kidney:	n/a
21	chr8:8102392-8102442	BE2_C	brain:	n/a
22	chr8:8102121-8102171	HRPEpiC	eye:	n/a
23	chr8:8131077-8131127	HUVEC	blood vessel:	n/a
24	chr8:8090460-8090510	SK-N-SH	brain:	n/a
25	chr8:8120624-8120674	PANC-1	pancreas:	n/a
26	chr8:8090460-8090510	BJ	skin:	n/a
27	chr8:8102392-8102442	PFSK-1	brain:	n/a
28	chr8:8131077-8131127	MCF-7	breast:	n/a
29	chr8:8102121-8102171	GM12891	blood:	n/a
30	chr8:8102121-8102171	Caco-2	colon:	n/a
31	chr8:8102392-8102442	GM19239	blood:	n/a
32	chr8:8102392-8102442	T-47D	breast:	n/a
33	chr8:8102121-8102171	PANC-1	pancreas:	n/a
34	chr8:8131077-8131127	SKMC	muscle:	n/a
35	chr8:8131077-8131127	ovcar-3	ovarian:	n/a
36	chr8:8120624-8120674	NHBE	bronchial:	n/a
37	chr8:8131077-8131127	A549	lung:	n/a
38	chr8:8090460-8090510	HL-60	blood:	n/a
39	chr8:8102392-8102442	AG04449	skin:	fetal
40	chr8:8102121-8102171	HNPCEpiC	eye:	n/a
41	chr8:8131077-8131127	AG04450	lung:	fetal
42	chr8:8102121-8102171	AG09309	skin:	n/a
43	chr8:8090460-8090510	HEEpiC	esophagus:	n/a
44	chr8:8102392-8102442	HEK293	kidney:	embryo
45	chr8:8090460-8090510	PFSK-1	brain:	n/a
46	chr8:8102392-8102442	GM12892	blood:	n/a
47	chr8:8102392-8102442	H1-hESC	embryonic stem cell:	embryo
48	chr8:8120624-8120674	Hela-S3	cervix:	n/a
49	chr8:8102121-8102171	Hepatocyte	liver:	n/a
50	chr8:8090460-8090510	H1-hESC	embryonic stem cell:	embryo

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:8084641..8087551-chr8:8098301..8100358,2	K562	blood:
2	chr8:8093979..8097330-chr8:8100546..8105094,4	K562	blood:
3	chr8:8098254..8100230-chr8:8106571..8108592,2	K562	blood:
4	chr8:8130511..8132438-chr8:8135661..8137544,2	K562	blood:
5	chr8:8108549..8111183-chr8:8240516..8242778,2	MCF-7	breast:
6	chr8:8128833..8131355-chr8:8136442..8139093,2	MCF-7	breast:
7	chr8:8118434..8122893-chr8:8123384..8125953,5	MCF-7	breast:
8	chr8:8130421..8131300-chr8:8175825..8176932,3	K562	blood:
9	chr8:8125550..8129443-chr8:8243752..8245349,3	MCF-7	breast:
10	chr8:8142878..8144520-chr8:8146399..8149197,2	MCF-7	breast:
11	chr8:8084641..8087551-chr8:8098301..8100358,2	K562	blood:
12	chr8:8105578..8107200-chr8:8525517..8527239,2	MCF-7	breast:
13	chr8:8086683..8088508-chr8:8193858..8196209,2	MCF-7	breast:
14	chr8:8126556..8131624-chr8:8143035..8148399,10	MCF-7	breast:
15	chr8:8130511..8132438-chr8:8135661..8137544,2	K562	blood:
16	chr8:8104258..8105835-chr8:8243426..8245376,2	MCF-7	breast:
17	chr8:8093979..8096897-chr8:8099466..8105094,8	K562	blood:
18	chr8:8131655..8133179-chr8:8135431..8137292,2	MCF-7	breast:
19	chr8:8145815..8148362-chr8:8152420..8155525,4	MCF-7	breast:
20	chr8:8105059..8106011-chr8:8526943..8527953,6	MCF-7	breast:
21	chr8:8141970..8144276-chr8:8242374..8245136,3	MCF-7	breast:
22	chr8:8093979..8097330-chr8:8100546..8105094,4	K562	blood:
23	chr8:8144375..8149679-chr8:8240479..8246459,10	MCF-7	breast:
24	chr8:8145045..8147805-chr8:8168275..8170393,2	MCF-7	breast:
25	chr8:8101157..8102709-chr8:8124508..8126459,2	MCF-7	breast:
26	chr8:8128833..8131355-chr8:8136442..8139093,2	MCF-7	breast:
27	chr8:8092255..8094353-chr8:8097556..8100076,2	K562	blood:
28	chr8:8138288..8140321-chr8:8142532..8144155,2	MCF-7	breast:
29	chr8:8138288..8140321-chr8:8142532..8144155,2	MCF-7	breast:
30	chr8:8134812..8136654-chr8:8146118..8147961,3	K562	blood:
31	chr8:8142616..8145069-chr8:8226333..8228141,2	MCF-7	breast:
32	chr8:8126556..8131624-chr8:8143035..8148399,10	MCF-7	breast:
33	chr8:8118434..8122893-chr8:8123384..8125953,5	MCF-7	breast:
34	chr8:8126193..8127836-chr8:8129384..8131743,2	MCF-7	breast:
35	chr8:8129344..8132133-chr8:8525629..8527896,2	MCF-7	breast:
36	chr8:8140760..8143388-chr8:8146728..8148425,2	K562	blood:
37	chr8:8094651..8097727-chr8:8099626..8103713,3	MCF-7	breast:
38	chr8:8131655..8133179-chr8:8135431..8137292,2	MCF-7	breast:
39	chr8:8145200..8147453-chr8:8312155..8314860,2	MCF-7	breast:
40	chr8:8092255..8094353-chr8:8097556..8100076,2	K562	blood:
41	chr8:8130384..8131365-chr8:8526780..8528280,9	K562	blood:
42	chr8:8144670..8146200-chr8:8236707..8239376,2	MCF-7	breast:
43	chr8:8101610..8104492-chr8:8112542..8114092,2	K562	blood:
44	chr8:8093979..8096897-chr8:8099466..8105094,8	K562	blood:
45	chr8:8094096..8094629-chr8:8147947..8148540,2	MCF-7	breast:
46	chr8:8130411..8130935-chr8:8374466..8375028,2	K562	blood:
47	chr8:8094104..8094693-chr8:8146401..8147333,2	MCF-7	breast:
48	chr8:8101610..8104279-chr8:8111391..8114092,2	K562	blood:
49	chr8:8094651..8097727-chr8:8099626..8103713,3	MCF-7	breast:
50	chr8:8105365..8106008-chr8:8526894..8527465,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC068020.1-1	chr8:8099150-8099484	NONHSAT124868
2	lnc-PRAGMIN.1-7	chr8:8095696-8095860	NONHSAT124863
3	lnc-AC068020.1-1	chr8:8095815-8096448	NONHSAT124861
4	lnc-PRAGMIN.1-7	chr8:8097728-8097835	NONHSAT124863
5	lnc-PRAGMIN.1-7	chr8:8097960-8098070	NONHSAT124863
6	lnc-PRAGMIN.1-7	chr8:8093525-8093885	NONHSAT124858
7	lnc-AC068020.1-1	chr8:8094730-8094797	NONHSAT124861
8	lnc-PRAGMIN.1-7	chr8:8097015-8097098	NONHSAT124863
9	lnc-AC068020.1-1	chr8:8101621-8101684	NONHSAT124868
10	lnc-PRAGMIN.1-7	chr8:8094648-8095823	NONHSAT124860
11	lnc-AC068020.1-1	chr8:8101621-8101707	NONHSAT124867
12	lnc-PRAGMIN.1-7	chr8:8097017-8097128	NONHSAT124860
13	lnc-AC068020.1-1	chr8:8097891-8099954	NONHSAT124866
14	lnc-AC068020.1-1	chr8:8101621-8102385	NONHSAT124866
15	lnc-AC068020.1-1	chr8:8098797-8099202	NONHSAT124867
16	lnc-PRAGMIN.1-7	chr8:8098818-8098933	NONHSAT124863
17	lnc-PRAGMIN.1-7	chr8:8095713-8095872	NONHSAT124858

No data

Variant related genes	Relation type
FAM86B3P	TF binding region
FAM85B	TF binding region
ALG1L13P	TF binding region
FAM86B3P	CpG island
FAM85B	CpG island
ALG1L13P	CpG island
ENSG00000253958	chromatin interactions
ENSG00000253981	chromatin interactions
ENSG00000254153	chromatin interactions
ENSG00000182319	chromatin interactions
ENSG00000176305	chromatin interactions
ENSG00000173295	chromatin interactions

Extended variants
information (count: 3417 )
Associated
traits (count: 144 )

Variant overlapped rSNPs/rCNVs (count:3417 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3989610	chr8:8087144-8087145	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs3989611	chr8:8087171-8087172	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs555734050	chr8:8087175-8087176	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs3989612	chr8:8087214-8087215	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs556143984	chr8:8087246-8087247	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs199851301	chr8:8087262-8087263	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs535487671	chr8:8087264-8087265	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs569958084	chr8:8087271-8087272	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs3989613	chr8:8087276-8087277	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs3989581	chr8:8087290-8087291	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs3958844	chr8:8087301-8087302	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs201170693	chr8:8087333-8087334	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs35342497	chr8:8087349-8087350	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs202110871	chr8:8087357-8087358	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs555579668	chr8:8087376-8087377	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs3989582	chr8:8087379-8087380	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs3989583	chr8:8087385-8087386	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs3989584	chr8:8087411-8087412	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs187846464	chr8:8087429-8087430	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs3989585	chr8:8087442-8087443	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs540737700	chr8:8087445-8087446	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs3958845	chr8:8087451-8087452	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs201559696	chr8:8087464-8087465	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs557858225	chr8:8087465-8087466	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs142608332	chr8:8087495-8087496	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs3989586	chr8:8087506-8087507	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs3989587	chr8:8087507-8087508	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs189726193	chr8:8087518-8087519	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs71513182	chr8:8087533-8087534	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs3958846	chr8:8087580-8087581	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs3989588	chr8:8087594-8087595	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs3989589	chr8:8087603-8087604	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs3989590	chr8:8087615-8087616	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs563174199	chr8:8087622-8087623	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs534496768	chr8:8087646-8087647	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs200542827	chr8:8087649-8087650	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs3989591	chr8:8087650-8087651	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs201158543	chr8:8087666-8087667	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs192941457	chr8:8087713-8087714	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs376903860	chr8:8087762-8087763	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs371632286	chr8:8087767-8087768	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs529538785	chr8:8087773-8087774	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs112960395	chr8:8087784-8087785	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs9771806	chr8:8087826-8087827	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs200476458	chr8:8087838-8087839	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs201052274	chr8:8087854-8087855	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs559504675	chr8:8087873-8087874	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs370164517	chr8:8087910-8087911	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs528674627	chr8:8087947-8087948	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs551555470	chr8:8087949-8087950	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:144)

Disease	PMID	Source
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Incontinentia Pigmenti	22033527	CNVD
Williams Syndrome	20824207	CNVD
Urothelial carcinoma	21177765	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	21346763	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Glioblastoma multiforme	21138945	CNVD

Chromatin state (count:820 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8084200-8087200	Active TSS	iPS-20b Cell Line	embryonic stem cell
2	chr8:8085000-8087200	Active TSS	NHLF	lung
3	chr8:8086400-8087200	Enhancers	Primary T cells fromperipheralblood	blood
4	chr8:8086400-8087600	Flanking Active TSS	Hela-S3	cervix
5	chr8:8086600-8091600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:8086600-8094600	Weak transcription	Ovary	ovary
7	chr8:8086600-8096000	Weak transcription	Fetal Thymus	thymus
8	chr8:8086600-8100600	Weak transcription	Aorta	Aorta
9	chr8:8086800-8087200	Weak transcription	Osteobl	bone
10	chr8:8086800-8087400	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr8:8086800-8087400	Enhancers	Muscle Satellite Cultured Cells	--
12	chr8:8086800-8087600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr8:8086800-8091600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr8:8086800-8091600	Weak transcription	Placenta	Placenta
15	chr8:8086800-8091600	Weak transcription	Stomach Mucosa	stomach
16	chr8:8086800-8092000	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr8:8086800-8093000	Weak transcription	K562	blood
18	chr8:8086800-8093200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr8:8086800-8093200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr8:8086800-8093200	Weak transcription	Gastric	stomach
21	chr8:8086800-8093200	Weak transcription	Spleen	Spleen
22	chr8:8086800-8093400	Weak transcription	Fetal Intestine Large	intestine
23	chr8:8086800-8094600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:8086800-8096200	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr8:8086800-8096200	Weak transcription	Thymus	Thymus
26	chr8:8086800-8096600	Weak transcription	Fetal Stomach	stomach
27	chr8:8086800-8097600	Weak transcription	Brain Anterior Caudate	brain
28	chr8:8086800-8099400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr8:8086800-8100000	Weak transcription	Fetal Muscle Leg	muscle
30	chr8:8086800-8101400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr8:8086800-8101600	Weak transcription	Pancreas	Pancrea
32	chr8:8086800-8108400	Weak transcription	NHEK	skin
33	chr8:8087000-8087200	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr8:8087000-8087400	Enhancers	A549	lung
35	chr8:8087000-8087400	Enhancers	Dnd41	blood
36	chr8:8087000-8087800	Enhancers	GM12878-XiMat	blood
37	chr8:8087000-8091600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr8:8087000-8091600	Weak transcription	Duodenum Mucosa	Duodenum
39	chr8:8087000-8091800	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr8:8087000-8092800	Weak transcription	Fetal Intestine Small	intestine
41	chr8:8087000-8093000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr8:8087000-8093200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr8:8087000-8093800	Weak transcription	Liver	Liver
44	chr8:8087000-8094400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr8:8087000-8094600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr8:8087000-8095600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr8:8087000-8096000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:8087000-8096800	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr8:8087000-8097600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr8:8087000-8100000	Weak transcription	Skeletal Muscle Male	skeletal muscle

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