Variant report

Variant	nsv917158
Chromosome Location	chr8:126101990-126255266
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3593)
CpG islands
(count:1284)
Chromatin interactive
region (count:274)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3593 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:126241351-126241412	K562	blood:	n/a	n/a
2	ARID3A	chr8:126137840-126138449	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:126236934-126238105	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:126231220-126232539	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:126231583-126232204	K562	blood:	n/a	n/a
6	ARID3A	chr8:126181075-126181466	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:126192989-126193546	K562	blood:	n/a	n/a
8	ARID3A	chr8:126123079-126123444	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:126187724-126188020	K562	blood:	n/a	n/a
10	ARID3A	chr8:126203662-126204538	K562	blood:	n/a	n/a
11	ARID3A	chr8:126242926-126243239	HepG2	liver:	n/a	n/a
12	ARID3A	chr8:126175560-126175995	K562	blood:	n/a	n/a
13	ARID3A	chr8:126103958-126104181	K562	blood:	n/a	n/a
14	ARID3A	chr8:126179999-126180572	HepG2	liver:	n/a	n/a
15	ARID3A	chr8:126130748-126130992	HepG2	liver:	n/a	n/a
16	ARID3A	chr8:126245063-126245443	HepG2	liver:	n/a	n/a
17	ATF1	chr8:126112310-126112668	K562	blood:	n/a	n/a
18	ATF1	chr8:126175607-126176029	K562	blood:	n/a	n/a
19	ATF1	chr8:126231603-126231818	K562	blood:	n/a	n/a
20	ATF1	chr8:126187630-126187894	K562	blood:	n/a	n/a
21	ATF1	chr8:126103865-126104330	K562	blood:	n/a	n/a
22	ATF1	chr8:126204921-126205249	K562	blood:	n/a	n/a
23	ATF1	chr8:126193133-126193508	K562	blood:	n/a	n/a
24	ATF1	chr8:126203917-126204525	K562	blood:	n/a	n/a
25	ATF2	chr8:126103850-126104314	GM12878	blood:	n/a	n/a
26	ATF2	chr8:126232120-126233204	GM12878	blood:	n/a	n/a
27	ATF2	chr8:126175599-126176032	GM12878	blood:	n/a	n/a
28	ATF2	chr8:126187394-126188097	GM12878	blood:	n/a	n/a
29	ATF2	chr8:126122831-126123528	GM12878	blood:	n/a	n/a
30	ATF2	chr8:126103769-126104224	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr8:126237362-126238019	GM12878	blood:	n/a	n/a
32	ATF2	chr8:126103692-126104350	GM12878	blood:	n/a	n/a
33	ATF2	chr8:126203832-126204543	GM12878	blood:	n/a	n/a
34	ATF2	chr8:126187455-126188118	GM12878	blood:	n/a	n/a
35	ATF2	chr8:126122876-126123398	GM12878	blood:	n/a	n/a
36	ATF2	chr8:126232601-126233086	GM12878	blood:	n/a	n/a
37	ATF2	chr8:126163713-126164853	GM12878	blood:	n/a	n/a
38	ATF2	chr8:126203868-126204603	GM12878	blood:	n/a	n/a
39	ATF2	chr8:126221258-126221864	GM12878	blood:	n/a	n/a
40	ATF2	chr8:126163697-126164982	GM12878	blood:	n/a	n/a
41	ATF2	chr8:126175509-126176085	GM12878	blood:	n/a	n/a
42	ATF2	chr8:126221321-126221861	GM12878	blood:	n/a	n/a
43	ATF3	chr8:126244936-126245430	A549	lung:	n/a	n/a
44	ATF3	chr8:126122989-126123429	A549	lung:	n/a	n/a
45	ATF3	chr8:126103857-126104348	K562	blood:	n/a	chr8:126104019-126104028 chr8:126104073-126104093 chr8:126104055-126104064
46	ATF3	chr8:126103795-126104229	K562	blood:	n/a	chr8:126104019-126104028 chr8:126104073-126104093 chr8:126104055-126104064
47	ATF3	chr8:126103829-126104250	HepG2	liver:	n/a	chr8:126104019-126104028 chr8:126104073-126104093 chr8:126104055-126104064
48	ATF3	chr8:126103727-126104223	H1-hESC	embryonic stem cell:	n/a	chr8:126104019-126104028 chr8:126104073-126104093 chr8:126104055-126104064
49	ATF3	chr8:126103848-126104199	K562	blood:	n/a	chr8:126104019-126104028 chr8:126104073-126104093 chr8:126104055-126104064
50	ATF3	chr8:126231328-126232041	A549	lung:	n/a	n/a

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:126186709-126186759	AG04450	lung:	fetal
2	chr8:126202653-126202703	U87	brain:	n/a
3	chr8:126154086-126154136	HIPEpiC	eye:	n/a
4	chr8:126186709-126186759	AG04450	lung:	fetal
5	chr8:126202653-126202703	U87	brain:	n/a
6	chr8:126154086-126154136	HIPEpiC	eye:	n/a
7	chr8:126154086-126154136	LNCaP	prostate:	n/a
8	chr8:126202653-126202703	AoSMC	blood vessel:	n/a
9	chr8:126216633-126216683	HNPCEpiC	eye:	n/a
10	chr8:126250639-126250689	SK-N-MC	brain:	n/a
11	chr8:126103992-126104042	HPAEpiC	pulmonary alveolar:	n/a
12	chr8:126181478-126181528	AG09319	gingival:	n/a
13	chr8:126103343-126103393	HEEpiC	esophagus:	n/a
14	chr8:126103980-126104030	MCF-7	breast:	n/a
15	chr8:126216633-126216683	SAEC	small airway:	n/a
16	chr8:126217943-126217993	NH-A	brain:	n/a
17	chr8:126195405-126195455	HEEpiC	esophagus:	n/a
18	chr8:126181478-126181528	AG09309	skin:	n/a
19	chr8:126142264-126142314	HEK293	kidney:	embryo
20	chr8:126217943-126217993	HCT-116	colon:	n/a
21	chr8:126104329-126104379	ovcar-3	ovarian:	n/a
22	chr8:126142264-126142314	NT2-D1	testis:	n/a
23	chr8:126162903-126162953	AG10803	skin:	n/a
24	chr8:126103681-126103731	HPAEpiC	pulmonary alveolar:	n/a
25	chr8:126216633-126216683	PANC-1	pancreas:	n/a
26	chr8:126103343-126103393	Jurkat	blood:	n/a
27	chr8:126103980-126104030	AG09319	gingival:	n/a
28	chr8:126103992-126104042	U87	brain:	n/a
29	chr8:126104387-126104437	NHBE	bronchial:	n/a
30	chr8:126103980-126104030	SAEC	small airway:	n/a
31	chr8:126103343-126103393	HIPEpiC	eye:	n/a
32	chr8:126195405-126195455	ovcar-3	ovarian:	n/a
33	chr8:126103343-126103393	K562	blood:	n/a
34	chr8:126250639-126250689	RPTEC	kidney:	n/a
35	chr8:126154086-126154136	Hela-S3	cervix:	n/a
36	chr8:126104540-126104590	PFSK-1	brain:	n/a
37	chr8:126162903-126162953	T-47D	breast:	n/a
38	chr8:126103980-126104030	HCM	heart:	n/a
39	chr8:126104387-126104437	HPAEpiC	pulmonary alveolar:	n/a
40	chr8:126103343-126103393	SK-N-MC	brain:	n/a
41	chr8:126216633-126216683	GM06990	blood:	n/a
42	chr8:126103980-126104030	H1-hESC	embryonic stem cell:	embryo
43	chr8:126142264-126142314	AoSMC	blood vessel:	n/a
44	chr8:126154086-126154136	AG10803	skin:	n/a
45	chr8:126104368-126104418	Hepatocyte	liver:	n/a
46	chr8:126204966-126205016	HIPEpiC	eye:	n/a
47	chr8:126104329-126104379	MCF10A-Er-Src	breast:	n/a
48	chr8:126250639-126250689	HCPEpiC	choroid plexus:	n/a
49	chr8:126204966-126205016	CMK	blood:	n/a
50	chr8:126103343-126103393	HUVEC	blood vessel:	n/a

(count:274 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr8:126123285..126125941-chr8:126128325..126132031,4	MCF-7	breast:
2	chr8:126192451..126194569-chr8:126196843..126198953,2	MCF-7	breast:
3	chr8:126238065..126239621-chr8:126240641..126243197,2	MCF-7	breast:
4	chr8:126198688..126200568-chr8:126203635..126206517,2	K562	blood:
5	chr8:126233946..126236339-chr8:126236823..126239784,3	K562	blood:
6	chr8:126102769..126104821-chr8:126238208..126240450,2	MCF-7	breast:
7	chr8:126235461..126238167-chr8:126248077..126250279,2	K562	blood:
8	chr8:126242492..126244562-chr8:126657053..126658910,2	MCF-7	breast:
9	chr8:126147030..126148722-chr8:126158702..126160766,2	K562	blood:
10	chr8:126130235..126131316-chr8:126242799..126243406,4	MCF-7	breast:
11	chr8:126123285..126125941-chr8:126128325..126132031,4	MCF-7	breast:
12	chr8:126010080..126012320-chr8:126100351..126105467,4	MCF-7	breast:
13	chr8:126130347..126130874-chr8:126656532..126657354,2	K562	blood:
14	chr8:126130677..126131235-chr8:126444045..126444954,3	K562	blood:
15	chr8:126100915..126106135-chr8:126441974..126444669,8	MCF-7	breast:
16	chr8:126102962..126105480-chr8:126105597..126108613,3	MCF-7	breast:
17	chr8:126191373..126194129-chr8:126441234..126444333,3	MCF-7	breast:
18	chr8:126112265..126115118-chr8:126118237..126122453,5	MCF-7	breast:
19	chr8:126182429..126184249-chr8:126522972..126525365,2	K562	blood:
20	chr8:126130646..126131207-chr8:126707551..126708054,2	MCF-7	breast:
21	chr8:126239983..126246163-chr8:126440449..126448219,20	MCF-7	breast:
22	chr8:126176328..126178254-chr8:126189530..126191092,2	MCF-7	breast:
23	chr8:126182582..126184381-chr8:126186885..126189550,2	K562	blood:
24	chr8:126178763..126181013-chr8:126182364..126184931,3	MCF-7	breast:
25	chr8:126163871..126166452-chr8:126194576..126197466,2	K562	blood:
26	chr8:126104927..126107896-chr8:126108427..126111358,2	K562	blood:
27	chr8:126101740..126106410-chr8:126441508..126444796,5	MCF-7	breast:
28	chr8:126175201..126177309-chr8:126182431..126184742,3	K562	blood:
29	chr8:126222075..126223796-chr8:126224521..126227219,2	K562	blood:
30	chr8:126217433..126218974-chr8:126675802..126677421,2	MCF-7	breast:
31	chr8:126237669..126239441-chr8:126440944..126443387,2	K562	blood:
32	chr8:126202633..126205386-chr8:126440752..126443830,3	MCF-7	breast:
33	chr8:126094932..126099483-chr8:126100368..126105771,7	K562	blood:
34	chr8:126184387..126187013-chr8:126442001..126443979,2	MCF-7	breast:
35	chr8:126079813..126082557-chr8:126108973..126111318,2	MCF-7	breast:
36	chr8:126214703..126218445-chr8:126219117..126223784,5	MCF-7	breast:
37	chr2:241499998..241500585-chr8:126103535..126104092,2	Hela-S3	cervix:
38	chr8:126155085..126158836-chr8:126194107..126197268,3	MCF-7	breast:
39	chr8:126213738..126215975-chr8:126217898..126220188,2	K562	blood:
40	chr8:126188966..126191727-chr8:126193252..126196746,4	MCF-7	breast:
41	chr8:126104927..126107896-chr8:126108427..126111358,2	K562	blood:
42	chr8:126101602..126103969-chr8:126231664..126234229,2	K562	blood:
43	chr8:126130824..126131576-chr8:126241852..126242626,2	MCF-7	breast:
44	chr8:126167671..126170997-chr8:126171128..126173953,3	MCF-7	breast:
45	chr8:126242654..126243238-chr8:126601971..126602543,2	MCF-7	breast:
46	chr8:126214703..126218445-chr8:126219117..126223784,5	MCF-7	breast:
47	chr8:126132005..126134785-chr8:126149699..126151451,2	K562	blood:
48	chr8:126147732..126149263-chr8:126155870..126158265,2	K562	blood:
49	chr8:126169503..126171101-chr8:126173955..126176588,2	K562	blood:
50	chr8:126138185..126141108-chr8:126441359..126446173,6	MCF-7	breast:

No data

Variant related genes	Relation type
KIAA0196	TF binding region
NSMCE2	TF binding region
KIAA0196	CpG island
NSMCE2	CpG island
ENSG00000168216	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000173334	chromatin interactions
ENSG00000139718	chromatin interactions
ENSG00000147684	chromatin interactions
ENSG00000156831	chromatin interactions
ENSG00000187634	chromatin interactions
ENSG00000144504	chromatin interactions
ENSG00000242170	chromatin interactions
ENSG00000212694	chromatin interactions
ENSG00000255491	chromatin interactions
ENSG00000139725	chromatin interactions
ENSG00000164961	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000143333	chromatin interactions
ENSG00000253513	chromatin interactions
ENSG00000147687	chromatin interactions
ENSG00000104549	chromatin interactions
ENSG00000188542	chromatin interactions

Extended variants
information (count: 5503 )
Associated
traits (count: 154 )

Variant overlapped rSNPs/rCNVs (count:5503 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539327230	chr8:126102005-126102006	Weak transcription Enhancers Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs558630231	chr8:126102034-126102035	Weak transcription Enhancers Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs12550607	chr8:126102072-126102073	Weak transcription Enhancers Active TSS	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs543394581	chr8:126102077-126102078	Weak transcription Enhancers Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs144365373	chr8:126102108-126102109	Weak transcription Enhancers Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs12545690	chr8:126102114-126102115	Weak transcription Enhancers Active TSS	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs574448287	chr8:126102134-126102135	Weak transcription Enhancers Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs75553573	chr8:126102142-126102143	Weak transcription Enhancers Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs529894827	chr8:126102147-126102148	Weak transcription Enhancers Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs532313801	chr8:126102165-126102166	Weak transcription Enhancers Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs150147787	chr8:126102172-126102173	Weak transcription Enhancers Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs562815368	chr8:126102175-126102176	Weak transcription Enhancers Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs12545710	chr8:126102198-126102199	Weak transcription Enhancers Active TSS	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs527699356	chr8:126102200-126102201	Weak transcription Enhancers Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs547740858	chr8:126102230-126102231	Weak transcription Enhancers Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs533493473	chr8:126102260-126102261	Weak transcription Enhancers Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs372027287	chr8:126102273-126102274	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs192675012	chr8:126102281-126102282	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs74681210	chr8:126102318-126102319	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs563572006	chr8:126102343-126102344	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs75622842	chr8:126102359-126102360	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs570257892	chr8:126102369-126102370	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs60388854	chr8:126102398-126102399	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs559276259	chr8:126102400-126102401	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs566330538	chr8:126102430-126102431	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs551720970	chr8:126102471-126102472	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs534345947	chr8:126102484-126102485	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs567954682	chr8:126102607-126102608	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs148799393	chr8:126102745-126102746	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs7357374	chr8:126102788-126102789	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs7357375	chr8:126102820-126102821	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs185070267	chr8:126102836-126102837	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs548025137	chr8:126102896-126102897	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs72720529	chr8:126102937-126102938	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs545727637	chr8:126102945-126102946	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs12544110	chr8:126103087-126103088	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs537279593	chr8:126103112-126103113	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs559408958	chr8:126103133-126103134	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs528341088	chr8:126103141-126103142	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs539183542	chr8:126103146-126103147	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs551448142	chr8:126103161-126103162	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs541075089	chr8:126103187-126103188	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs561326560	chr8:126103243-126103244	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs113976845	chr8:126103262-126103263	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs530261972	chr8:126103268-126103269	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs557662884	chr8:126103271-126103272	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs142254336	chr8:126103273-126103274	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs571129643	chr8:126103287-126103288	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs201143172	chr8:126103371-126103372	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs570294018	chr8:126103382-126103383	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:154)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Gastric cancer	18160780	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Ovarian cancer	21240255	CNVD
Lung adenocarcinoma	21935476	CNVD
Glioma	20126413	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:4786 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:126029800-126103000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:126052800-126103200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr8:126064200-126102800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr8:126071800-126103000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr8:126084000-126102400	Weak transcription	Fetal Heart	heart
6	chr8:126085400-126102400	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr8:126085400-126102600	Weak transcription	Stomach Mucosa	stomach
8	chr8:126090800-126102800	Weak transcription	Aorta	Aorta
9	chr8:126091000-126103000	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr8:126091200-126102600	Weak transcription	Fetal Brain Male	brain
11	chr8:126091200-126102600	Weak transcription	NHLF	lung
12	chr8:126091200-126103000	Weak transcription	Esophagus	oesophagus
13	chr8:126091200-126103000	Weak transcription	Pancreas	Pancrea
14	chr8:126091200-126103200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:126091800-126103200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr8:126093000-126102800	Weak transcription	Small Intestine	intestine
17	chr8:126093000-126103000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr8:126094000-126102200	Weak transcription	Fetal Brain Female	brain
19	chr8:126094000-126103000	Weak transcription	Lung	lung
20	chr8:126094000-126103000	Weak transcription	Right Ventricle	heart
21	chr8:126094200-126102400	Weak transcription	Rectal Smooth Muscle	rectum
22	chr8:126094400-126102600	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr8:126094400-126102800	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr8:126094400-126102800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr8:126094400-126102800	Weak transcription	HSMMtube	muscle
26	chr8:126094400-126103000	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr8:126094400-126103000	Weak transcription	Left Ventricle	heart
28	chr8:126094400-126103000	Weak transcription	Ovary	ovary
29	chr8:126094600-126102400	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr8:126094600-126102600	Weak transcription	A549	lung
31	chr8:126094600-126103000	Weak transcription	Colonic Mucosa	Colon
32	chr8:126094800-126102800	Weak transcription	NH-A	brain
33	chr8:126095000-126102600	Weak transcription	Fetal Kidney	kidney
34	chr8:126095000-126102600	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr8:126095000-126102800	Weak transcription	Stomach Smooth Muscle	stomach
36	chr8:126095000-126103000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr8:126095400-126102400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr8:126095400-126102400	Weak transcription	NHEK	skin
39	chr8:126095400-126102600	Weak transcription	HSMM	muscle
40	chr8:126095400-126102800	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr8:126095600-126102400	Weak transcription	Osteobl	bone
42	chr8:126095600-126102600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr8:126095800-126102400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr8:126095800-126102400	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr8:126095800-126102600	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr8:126096000-126102600	Weak transcription	HMEC	breast
47	chr8:126096200-126102400	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr8:126096200-126102600	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr8:126096600-126102400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr8:126096600-126102600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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