Variant report

Variant	nsv612148
Chromosome Location	chr8:126068197-126132816
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1504)
CpG islands
(count:857)
Chromatin interactive
region (count:153)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1504 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:126103958-126104181	K562	blood:	n/a	n/a
2	ARID3A	chr8:126123079-126123444	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:126130748-126130992	HepG2	liver:	n/a	n/a
4	ATF1	chr8:126112310-126112668	K562	blood:	n/a	n/a
5	ATF1	chr8:126103865-126104330	K562	blood:	n/a	n/a
6	ATF1	chr8:126098132-126098234	K562	blood:	n/a	n/a
7	ATF2	chr8:126103769-126104224	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr8:126122876-126123398	GM12878	blood:	n/a	n/a
9	ATF2	chr8:126103850-126104314	GM12878	blood:	n/a	n/a
10	ATF2	chr8:126103692-126104350	GM12878	blood:	n/a	n/a
11	ATF2	chr8:126122831-126123528	GM12878	blood:	n/a	n/a
12	ATF3	chr8:126103727-126104223	H1-hESC	embryonic stem cell:	n/a	chr8:126104019-126104028 chr8:126104073-126104093 chr8:126104055-126104064
13	ATF3	chr8:126103631-126104460	A549	lung:	n/a	chr8:126104019-126104028 chr8:126104073-126104093 chr8:126104055-126104064
14	ATF3	chr8:126122989-126123429	A549	lung:	n/a	n/a
15	ATF3	chr8:126103696-126104400	A549	lung:	n/a	chr8:126104019-126104028 chr8:126104073-126104093 chr8:126104055-126104064
16	ATF3	chr8:126103745-126104401	HepG2	liver:	n/a	chr8:126104019-126104028 chr8:126104073-126104093 chr8:126104055-126104064
17	ATF3	chr8:126103754-126104224	H1-hESC	embryonic stem cell:	n/a	chr8:126104019-126104028 chr8:126104073-126104093 chr8:126104055-126104064
18	ATF3	chr8:126103848-126104199	K562	blood:	n/a	chr8:126104019-126104028 chr8:126104073-126104093 chr8:126104055-126104064
19	ATF3	chr8:126103793-126104436	GM12878	blood:	n/a	chr8:126104019-126104028 chr8:126104073-126104093 chr8:126104055-126104064
20	ATF3	chr8:126103829-126104250	HepG2	liver:	n/a	chr8:126104019-126104028 chr8:126104073-126104093 chr8:126104055-126104064
21	ATF3	chr8:126103795-126104229	K562	blood:	n/a	chr8:126104019-126104028 chr8:126104073-126104093 chr8:126104055-126104064
22	ATF3	chr8:126103857-126104348	K562	blood:	n/a	chr8:126104019-126104028 chr8:126104073-126104093 chr8:126104055-126104064
23	ATF3	chr8:126103861-126104152	GM12878	blood:	n/a	chr8:126104019-126104028 chr8:126104073-126104093 chr8:126104055-126104064
24	BACH1	chr8:126103744-126104173	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr8:126103060-126103208	K562	blood:	n/a	n/a
26	BACH1	chr8:126104048-126104235	K562	blood:	n/a	n/a
27	BATF	chr8:126122995-126123460	GM12878	blood:	n/a	n/a
28	BATF	chr8:126131396-126131670	GM12878	blood:	n/a	chr8:126131602-126131612
29	BATF	chr8:126103848-126104235	GM12878	blood:	n/a	n/a
30	BATF	chr8:126122944-126123463	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:126123023-126123393	GM12878	blood:	n/a	chr8:126123178-126123187
32	BCL11A	chr8:126123051-126123376	GM12878	blood:	n/a	chr8:126123178-126123187
33	BCL3	chr8:126103733-126104371	A549	lung:	n/a	chr8:126103791-126103804
34	BCL3	chr8:126103710-126104405	A549	lung:	n/a	chr8:126103791-126103804
35	BCLAF1	chr8:126103798-126104311	GM12878	blood:	n/a	n/a
36	BCLAF1	chr8:126122855-126123393	GM12878	blood:	n/a	chr8:126123178-126123187
37	BCLAF1	chr8:126131367-126131705	GM12878	blood:	n/a	chr8:126131604-126131613
38	BHLHE40	chr8:126103595-126104339	K562	blood:	n/a	n/a
39	BHLHE40	chr8:126122959-126123354	GM12878	blood:	n/a	n/a
40	BHLHE40	chr8:126131300-126131583	GM12878	blood:	n/a	n/a
41	BHLHE40	chr8:126111763-126111963	K562	blood:	n/a	n/a
42	BHLHE40	chr8:126103729-126104221	HepG2	liver:	n/a	n/a
43	BHLHE40	chr8:126103596-126104245	GM12878	blood:	n/a	n/a
44	BHLHE40	chr8:126131578-126131647	K562	blood:	n/a	n/a
45	BRCA1	chr8:126103863-126104239	H1-hESC	embryonic stem cell:	n/a	n/a
46	BRCA1	chr8:126103925-126104249	HepG2	liver:	n/a	n/a
47	BRCA1	chr8:126103881-126104279	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr8:126103938-126104179	GM12878	blood:	n/a	n/a
49	BRCA1	chr8:126131336-126131728	Hela-S3	cervix:	n/a	n/a
50	CBX3	chr8:126131147-126131836	HCT-116	colon:	n/a	n/a

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:126103980-126104030	MCF10A-Er-Src	breast:	n/a
2	chr8:126082720-126082770	GM19239	blood:	n/a
3	chr8:126097158-126097208	Jurkat	blood:	n/a
4	chr8:126103980-126104030	MCF10A-Er-Src	breast:	n/a
5	chr8:126082720-126082770	GM19239	blood:	n/a
6	chr8:126097158-126097208	Jurkat	blood:	n/a
7	chr8:126082720-126082770	T-47D	breast:	n/a
8	chr8:126096148-126096198	PFSK-1	brain:	n/a
9	chr8:126097158-126097208	H1-hESC	embryonic stem cell:	embryo
10	chr8:126100743-126100793	NH-A	brain:	n/a
11	chr8:126103969-126104019	ovcar-3	ovarian:	n/a
12	chr8:126096148-126096198	HCM	heart:	n/a
13	chr8:126104329-126104379	NB4	blood:	n/a
14	chr8:126107457-126107507	HCPEpiC	choroid plexus:	n/a
15	chr8:126096148-126096198	HMEC	breast:	n/a
16	chr8:126103681-126103731	PFSK-1	brain:	n/a
17	chr8:126103969-126104019	SAEC	small airway:	n/a
18	chr8:126103343-126103393	CMK	blood:	n/a
19	chr8:126104368-126104418	HepG2	liver:	n/a
20	chr8:126082720-126082770	HCT-116	colon:	n/a
21	chr8:126104368-126104418	HCPEpiC	choroid plexus:	n/a
22	chr8:126103681-126103731	Jurkat	blood:	n/a
23	chr8:126103992-126104042	LNCaP	prostate:	n/a
24	chr8:126104329-126104379	HCT-116	colon:	n/a
25	chr8:126107457-126107507	NHBE	bronchial:	n/a
26	chr8:126107457-126107507	HPAEpiC	pulmonary alveolar:	n/a
27	chr8:126104540-126104590	NHBE	bronchial:	n/a
28	chr8:126107457-126107507	PANC-1	pancreas:	n/a
29	chr8:126104329-126104379	A549	lung:	n/a
30	chr8:126103992-126104042	A549	lung:	n/a
31	chr8:126097158-126097208	AoSMC	blood vessel:	n/a
32	chr8:126103992-126104042	K562	blood:	n/a
33	chr8:126104540-126104590	HCF	heart:	n/a
34	chr8:126103969-126104019	GM12878	blood:	n/a
35	chr8:126103681-126103731	HepG2	liver:	n/a
36	chr8:126100743-126100793	GM19239	blood:	n/a
37	chr8:126082720-126082770	HL-60	blood:	n/a
38	chr8:126096148-126096198	HPAEpiC	pulmonary alveolar:	n/a
39	chr8:126097158-126097208	SK-N-SH_RA	brain:	n/a
40	chr8:126103969-126104019	HNPCEpiC	eye:	n/a
41	chr8:126097158-126097208	GM12878	blood:	n/a
42	chr8:126103681-126103731	ECC-1	luminal epithelium:	n/a
43	chr8:126107457-126107507	AG04449	skin:	fetal
44	chr8:126097158-126097208	RPTEC	kidney:	n/a
45	chr8:126107457-126107507	IMR90	lung:	fetal
46	chr8:126103980-126104030	AG04449	skin:	fetal
47	chr8:126104329-126104379	ProgFib	skin:	n/a
48	chr8:126103969-126104019	NHBE	bronchial:	n/a
49	chr8:126100743-126100793	Caco-2	colon:	n/a
50	chr8:126104387-126104437	HRPEpiC	eye:	n/a

(count:153 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr8:126122099..126124809-chr8:126126071..126128199,2	MCF-7	breast:
2	chr8:126130720..126131864-chr8:126438477..126439411,5	MCF-7	breast:
3	chr8:126065661..126068015-chr8:126076648..126079016,2	MCF-7	breast:
4	chr8:126065375..126068867-chr8:126072932..126075617,3	MCF-7	breast:
5	chr8:126132393..126134587-chr8:126146402..126148822,2	K562	blood:
6	chr8:126054260..126055838-chr8:126069090..126070904,2	K562	blood:
7	chr8:126100915..126106135-chr8:126441974..126444669,8	MCF-7	breast:
8	chr8:126109384..126111604-chr8:126122578..126124828,2	MCF-7	breast:
9	chr8:126102962..126105480-chr8:126105597..126108613,3	MCF-7	breast:
10	chr8:125485708..125487232-chr8:126075795..126078177,2	MCF-7	breast:
11	chr8:126125572..126128289-chr8:126130309..126132372,2	MCF-7	breast:
12	chr8:126072198..126074417-chr8:126098170..126100467,2	MCF-7	breast:
13	chr8:126070042..126072649-chr8:126091335..126093606,2	MCF-7	breast:
14	chr8:126130990..126132733-chr8:126709106..126710611,2	MCF-7	breast:
15	chr8:126092989..126095480-chr8:126096326..126098536,2	K562	blood:
16	chr8:126086426..126089939-chr8:126095460..126099490,6	MCF-7	breast:
17	chr8:126103818..126106100-chr8:126441528..126444004,2	K562	blood:
18	chr8:125665322..125667736-chr8:126082032..126083680,2	MCF-7	breast:
19	chr8:126122076..126124828-chr8:126440286..126443846,3	MCF-7	breast:
20	chr8:126094932..126099483-chr8:126100368..126105771,7	K562	blood:
21	chr8:126123096..126125735-chr8:126439490..126442539,3	MCF-7	breast:
22	chr8:126117610..126119168-chr8:126119754..126122274,2	MCF-7	breast:
23	chr8:126080962..126083848-chr8:126442611..126444645,2	MCF-7	breast:
24	chr8:125826373..125828748-chr8:126103559..126105908,3	K562	blood:
25	chr12:120729365..120731964-chr8:126101720..126104275,2	MCF-7	breast:
26	chr8:126130496..126132117-chr8:126655992..126657468,16	MCF-7	breast:
27	chr8:125550215..125552814-chr8:126108940..126110942,2	MCF-7	breast:
28	chr8:126104927..126107896-chr8:126108427..126111358,2	K562	blood:
29	chr8:125485690..125488438-chr8:126066764..126069152,2	MCF-7	breast:
30	chr8:126080675..126083902-chr8:126087679..126091293,3	MCF-7	breast:
31	chr8:126122099..126124809-chr8:126126071..126128199,2	MCF-7	breast:
32	chr8:126062714..126065233-chr8:126075717..126077360,2	MCF-7	breast:
33	chr8:126107482..126112486-chr8:126114879..126119066,5	MCF-7	breast:
34	chr8:126107482..126112486-chr8:126114879..126119066,5	MCF-7	breast:
35	chr8:126081874..126084254-chr8:126086357..126088747,2	MCF-7	breast:
36	chr8:126130563..126131277-chr8:126709482..126710133,2	MCF-7	breast:
37	chr8:126094988..126096800-chr8:126109412..126111250,2	MCF-7	breast:
38	chr8:126102864..126104610-chr8:126121575..126124532,2	K562	blood:
39	chr8:126089121..126090954-chr8:126122040..126124119,2	K562	blood:
40	chr8:125548946..125551897-chr8:126103590..126105323,2	MCF-7	breast:
41	chr8:125590158..125592640-chr8:126086582..126088559,2	K562	blood:
42	chr19:921473..922000-chr8:126084096..126084596,3	K562	blood:
43	chr8:126102968..126106954-chr8:126119806..126124843,7	MCF-7	breast:
44	chr8:126116223..126117724-chr8:126119342..126121125,2	K562	blood:
45	chr8:126081493..126082982-chrX:149209259..149210130,5	MCF-7	breast:
46	chr8:126004345..126006985-chr8:126108210..126109732,2	MCF-7	breast:
47	chr8:126081874..126084254-chr8:126086357..126088747,2	MCF-7	breast:
48	chr8:126130319..126132027-chr8:126443795..126444880,8	MCF-7	breast:
49	chr8:126092867..126094913-chr8:126103512..126105513,2	K562	blood:
50	chr8:126121150..126124061-chr8:126446457..126448780,3	K562	blood:

No data

Variant related genes	Relation type
KIAA0196	TF binding region
NSMCE2	TF binding region
KIAA0196	CpG island
NSMCE2	CpG island
ENSG00000147684	chromatin interactions
ENSG00000272486	chromatin interactions
ENSG00000173334	chromatin interactions
ENSG00000170881	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000168216	chromatin interactions
ENSG00000245149	chromatin interactions
ENSG00000188542	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000255491	chromatin interactions
ENSG00000147687	chromatin interactions
ENSG00000253513	chromatin interactions
ENSG00000164961	chromatin interactions
ENSG00000144504	chromatin interactions
ENSG00000156831	chromatin interactions
ENSG00000104549	chromatin interactions

Extended variants
information (count: 2657 )
Associated
traits (count: 151 )

Variant overlapped rSNPs/rCNVs (count:2657 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2303525	chr8:126068197-126068198	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs2303524	chr8:126068215-126068216	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs74895604	chr8:126068236-126068237	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs376815976	chr8:126068244-126068245	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs4421364	chr8:126068246-126068247	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs139226089	chr8:126068261-126068262	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs190256515	chr8:126068265-126068266	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs554832415	chr8:126068274-126068275	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs376753803	chr8:126068283-126068284	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs534162460	chr8:126068286-126068287	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs72720515	chr8:126068289-126068290	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs4421365	chr8:126068308-126068309	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs35037331	chr8:126068355-126068356	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs149414397	chr8:126068428-126068429	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs556398467	chr8:126068443-126068444	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs575952268	chr8:126068475-126068476	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs373696962	chr8:126068480-126068481	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs544987469	chr8:126068484-126068485	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs559506068	chr8:126068485-126068486	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs4570178	chr8:126068490-126068491	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs116929049	chr8:126068526-126068527	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs528226026	chr8:126068540-126068541	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs369491901	chr8:126068566-126068567	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs561090689	chr8:126068595-126068596	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs562572805	chr8:126068597-126068598	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs4425776	chr8:126068616-126068617	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs144836658	chr8:126068656-126068657	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs4339662	chr8:126068662-126068663	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs563569289	chr8:126068700-126068701	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs531646644	chr8:126068709-126068710	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs182489220	chr8:126068804-126068805	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs571676611	chr8:126068823-126068824	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs527806849	chr8:126068846-126068847	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs112492995	chr8:126068848-126068849	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs2303523	chr8:126068873-126068874	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs118088197	chr8:126068879-126068880	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs2303522	chr8:126068886-126068887	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs201263481	chr8:126068898-126068899	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs556487107	chr8:126068970-126068971	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs148951367	chr8:126068972-126068973	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs371128991	chr8:126068994-126068995	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs143678667	chr8:126068998-126068999	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs377530564	chr8:126069015-126069016	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs376352332	chr8:126069038-126069039	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs80338867	chr8:126069059-126069060	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs367667154	chr8:126069088-126069089	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs570321404	chr8:126069089-126069090	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs2303521	chr8:126069142-126069143	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs34744854	chr8:126069149-126069150	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs571921658	chr8:126069165-126069166	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:151)

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

Chromatin state (count:2487 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:126015400-126098000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr8:126019600-126071800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr8:126023600-126099000	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr8:126028200-126072000	Strong transcription	Primary T helper cells PMA-I stimulated	--
5	chr8:126028600-126097400	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr8:126028800-126072200	Strong transcription	Adipose Nuclei	Adipose
7	chr8:126029800-126097400	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr8:126029800-126103000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr8:126038800-126097200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr8:126039400-126072000	Strong transcription	Duodenum Mucosa	Duodenum
11	chr8:126039400-126091400	Strong transcription	Duodenum Smooth Muscle	Duodenum
12	chr8:126039600-126071800	Strong transcription	Stomach Smooth Muscle	stomach
13	chr8:126042200-126084000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr8:126042400-126096800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr8:126042600-126098600	Strong transcription	Primary T helper cells fromperipheralblood	blood
16	chr8:126042600-126098800	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr8:126042800-126071800	Strong transcription	Sigmoid Colon	Sigmoid Colon
18	chr8:126042800-126072600	Strong transcription	Rectal Mucosa Donor 31	rectum
19	chr8:126042800-126084200	Strong transcription	Fetal Intestine Large	intestine
20	chr8:126043000-126075800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
21	chr8:126043000-126084000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr8:126043000-126096000	Strong transcription	Liver	Liver
23	chr8:126043000-126098000	Strong transcription	Fetal Thymus	thymus
24	chr8:126043800-126075800	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr8:126043800-126076400	Strong transcription	HUES48 Cell Line	embryonic stem cell
26	chr8:126043800-126082400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr8:126044000-126072200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr8:126044600-126071600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr8:126044800-126071800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
30	chr8:126045600-126095000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr8:126046200-126070400	Strong transcription	Placenta	Placenta
32	chr8:126046200-126081800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr8:126046600-126072200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr8:126046600-126099600	Strong transcription	Primary B cells from peripheral blood	blood
35	chr8:126046800-126096200	Strong transcription	Rectal Mucosa Donor 29	rectum
36	chr8:126047000-126071600	Strong transcription	Primary hematopoietic stem cells	blood
37	chr8:126048000-126072600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr8:126048600-126071800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr8:126049800-126071800	Strong transcription	Fetal Brain Female	brain
40	chr8:126050200-126089000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr8:126052400-126080600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr8:126052800-126103200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr8:126053000-126071800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr8:126053200-126071400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr8:126054600-126071200	Strong transcription	Thymus	Thymus
46	chr8:126054600-126071800	Strong transcription	Left Ventricle	heart
47	chr8:126055200-126071800	Strong transcription	Brain Inferior Temporal Lobe	brain
48	chr8:126055600-126071800	Strong transcription	Brain Anterior Caudate	brain
49	chr8:126055600-126072200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
50	chr8:126055800-126088600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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