Variant report

Variant	nsv6236
Chromosome Location	chr8:67359312-67403981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:899)
CpG islands
(count:366)
Chromatin interactive
region (count:46)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:899 , 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	chr8:67376527-67376760	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:67374833-67375041	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:67385678-67385869	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:67375399-67376000	HepG2	liver:	n/a	chr8:67375704-67375720 chr8:67375703-67375719
5	ATF2	chr8:67400544-67401075	GM12878	blood:	n/a	n/a
6	ATF2	chr8:67397821-67398395	GM12878	blood:	n/a	n/a
7	ATF2	chr8:67397862-67398274	GM12878	blood:	n/a	n/a
8	ATF2	chr8:67400567-67400993	GM12878	blood:	n/a	n/a
9	BCL3	chr8:67368420-67368775	GM12878	blood:	n/a	n/a
10	BHLHE40	chr8:67397932-67398528	GM12878	blood:	n/a	n/a
11	BHLHE40	chr8:67373688-67373999	HepG2	liver:	n/a	n/a
12	BHLHE40	chr8:67400587-67401234	GM12878	blood:	n/a	n/a
13	BRCA1	chr8:67371394-67371470	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr8:67383595-67383967	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr8:67371310-67371559	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr8:67389916-67390143	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr8:67383537-67383999	HCT-116	colon:	n/a	n/a
18	CBX3	chr8:67385302-67385959	HCT-116	colon:	n/a	n/a
19	CEBPB	chr8:67383582-67383903	A549	lung:	n/a	n/a
20	CEBPB	chr8:67395823-67396125	IMR90	lung:	n/a	n/a
21	CEBPB	chr8:67403961-67404105	A549	lung:	n/a	chr8:67404012-67404023
22	CEBPB	chr8:67389943-67390258	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr8:67372076-67372290	A549	lung:	n/a	n/a
24	CEBPB	chr8:67370894-67371714	Hela-S3	cervix:	n/a	chr8:67371520-67371533
25	CEBPB	chr8:67384997-67385194	A549	lung:	n/a	chr8:67385137-67385148
26	CEBPB	chr8:67385016-67385148	H1-hESC	embryonic stem cell:	n/a	chr8:67385137-67385148
27	CEBPB	chr8:67383574-67383955	IMR90	lung:	n/a	n/a
28	CEBPB	chr8:67403938-67404180	HepG2	liver:	n/a	chr8:67404012-67404023
29	CEBPB	chr8:67393590-67393751	Hela-S3	cervix:	n/a	chr8:67393690-67393701 chr8:67393690-67393703
30	CEBPB	chr8:67384973-67385233	K562	blood:	n/a	chr8:67385137-67385148
31	CEBPB	chr8:67365427-67365776	IMR90	lung:	n/a	chr8:67365733-67365745 chr8:67365574-67365585
32	CEBPB	chr8:67368099-67368832	IMR90	lung:	n/a	n/a
33	CEBPB	chr8:67383127-67383379	A549	lung:	n/a	n/a
34	CEBPB	chr8:67386137-67386462	HepG2	liver:	n/a	n/a
35	CEBPB	chr8:67365444-67365737	HepG2	liver:	n/a	chr8:67365574-67365585
36	CEBPB	chr8:67375578-67376146	A549	lung:	n/a	n/a
37	CEBPB	chr8:67383447-67384093	A549	lung:	n/a	n/a
38	CEBPB	chr8:67371342-67371702	IMR90	lung:	n/a	chr8:67371520-67371533
39	CEBPB	chr8:67375039-67375044	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr8:67376696-67377167	IMR90	lung:	n/a	n/a
41	CEBPB	chr8:67375426-67376095	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr8:67365493-67365724	H1-hESC	embryonic stem cell:	n/a	chr8:67365574-67365585
43	CEBPB	chr8:67389979-67390289	IMR90	lung:	n/a	n/a
44	CEBPB	chr8:67365465-67365718	A549	lung:	n/a	chr8:67365574-67365585
45	CEBPB	chr8:67385511-67385788	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr8:67365451-67365715	K562	blood:	n/a	chr8:67365574-67365585
47	CEBPB	chr8:67393601-67393691	A549	lung:	n/a	n/a
48	CEBPB	chr8:67398113-67398309	HepG2	liver:	n/a	chr8:67398151-67398162
49	CEBPB	chr8:67385092-67385175	HepG2	liver:	n/a	chr8:67385137-67385148
50	CEBPB	chr8:67383544-67383955	Hela-S3	cervix:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:67380613-67380663	HNPCEpiC	eye:	n/a
2	chr8:67371088-67371138	HCM	heart:	n/a
3	chr8:67365340-67365390	HNPCEpiC	eye:	n/a
4	chr8:67401313-67401363	GM19239	blood:	n/a
5	chr8:67380613-67380663	HPAEpiC	pulmonary alveolar:	n/a
6	chr8:67401313-67401363	Hela-S3	cervix:	n/a
7	chr8:67384873-67384923	Hela-S3	cervix:	n/a
8	chr8:67401313-67401363	HIPEpiC	eye:	n/a
9	chr8:67371088-67371138	NHDF-neo	bronchial:	n/a
10	chr8:67365340-67365390	PANC-1	pancreas:	n/a
11	chr8:67380613-67380663	Jurkat	blood:	n/a
12	chr8:67401313-67401363	H1-hESC	embryonic stem cell:	embryo
13	chr8:67371088-67371138	U87	brain:	n/a
14	chr8:67365340-67365390	NT2-D1	testis:	n/a
15	chr8:67384873-67384923	HRE	kidney:	n/a
16	chr8:67401313-67401363	AG04450	lung:	fetal
17	chr8:67380613-67380663	HCF	heart:	n/a
18	chr8:67373171-67373221	NH-A	brain:	n/a
19	chr8:67373171-67373221	HRPEpiC	eye:	n/a
20	chr8:67371088-67371138	HIPEpiC	eye:	n/a
21	chr8:67365340-67365390	SK-N-SH_RA	brain:	n/a
22	chr8:67365340-67365390	LNCaP	prostate:	n/a
23	chr8:67365340-67365390	GM06990	blood:	n/a
24	chr8:67371088-67371138	HCF	heart:	n/a
25	chr8:67401313-67401363	PFSK-1	brain:	n/a
26	chr8:67384873-67384923	BE2_C	brain:	n/a
27	chr8:67401313-67401363	T-47D	breast:	n/a
28	chr8:67365340-67365390	AG04449	skin:	fetal
29	chr8:67401313-67401363	AG09319	gingival:	n/a
30	chr8:67384873-67384923	HRPEpiC	eye:	n/a
31	chr8:67365340-67365390	Jurkat	blood:	n/a
32	chr8:67365340-67365390	Caco-2	colon:	n/a
33	chr8:67380613-67380663	HRCEpiC	kidney:	n/a
34	chr8:67384873-67384923	HPAEpiC	pulmonary alveolar:	n/a
35	chr8:67384873-67384923	AG04450	lung:	fetal
36	chr8:67371088-67371138	K562	blood:	n/a
37	chr8:67365340-67365390	BE2_C	brain:	n/a
38	chr8:67401313-67401363	SK-N-SH_RA	brain:	n/a
39	chr8:67401313-67401363	A549	lung:	n/a
40	chr8:67401313-67401363	MCF10A-Er-Src	breast:	n/a
41	chr8:67373171-67373221	HAEpiC	amniotic membrane:	n/a
42	chr8:67384873-67384923	HepG2	liver:	n/a
43	chr8:67373171-67373221	HEK293	kidney:	embryo
44	chr8:67380613-67380663	Hela-S3	cervix:	n/a
45	chr8:67401313-67401363	HRE	kidney:	n/a
46	chr8:67371088-67371138	SKMC	muscle:	n/a
47	chr8:67373171-67373221	MCF10A-Er-Src	breast:	n/a
48	chr8:67384873-67384923	GM06990	blood:	n/a
49	chr8:67384873-67384923	ProgFib	skin:	n/a
50	chr8:67380613-67380663	HAEpiC	amniotic membrane:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:67358722..67361670-chr8:67363913..67366041,2	MCF-7	breast:
2	chr8:67360323..67362172-chr8:67364568..67366628,2	K562	blood:
3	chr8:67385468..67387907-chr8:67392199..67395140,2	K562	blood:
4	chr8:67343368..67345307-chr8:67372235..67374136,2	K562	blood:
5	chr8:67352250..67355147-chr8:67358287..67360742,2	K562	blood:
6	chr8:67373381..67375489-chr8:67836418..67838496,2	MCF-7	breast:
7	chr8:67374805..67375440-chr8:67626072..67626739,2	MCF-7	breast:
8	chr8:67372183..67373683-chr8:67623863..67626623,2	MCF-7	breast:
9	chr8:67347726..67350540-chr8:67362226..67363853,2	K562	blood:
10	chr8:67371423..67376205-chr8:67520601..67527002,8	MCF-7	breast:
11	chr8:67370489..67372991-chr8:67834453..67837306,2	MCF-7	breast:
12	chr8:67373363..67378961-chr8:67380708..67384244,6	MCF-7	breast:
13	chr8:67378228..67380679-chr8:67388244..67390416,2	MCF-7	breast:
14	chr8:67385468..67387907-chr8:67392199..67395140,2	K562	blood:
15	chr8:67366507..67368766-chr8:67466802..67469221,2	K562	blood:
16	chr8:67358368..67361034-chr8:67361272..67364476,3	K562	blood:
17	chr8:67358368..67361034-chr8:67361272..67364476,3	K562	blood:
18	chr8:67378110..67380525-chr8:67519992..67522222,2	MCF-7	breast:
19	chr8:67358722..67361670-chr8:67363913..67366041,2	MCF-7	breast:
20	chr8:67344388..67346218-chr8:67359592..67361320,2	K562	blood:
21	chr8:67400231..67403065-chr8:67433723..67435649,2	MCF-7	breast:
22	chr8:67343549..67345743-chr8:67361458..67364132,2	K562	blood:
23	chr8:67401130..67402872-chr8:67415894..67418363,2	K562	blood:
24	chr8:67379259..67381817-chr8:67625879..67628203,2	MCF-7	breast:
25	chr8:67370426..67372835-chr8:67375511..67377950,2	K562	blood:
26	chr8:67385031..67386596-chr8:67579677..67581320,2	K562	blood:
27	chr8:67401678..67404150-chr8:67442018..67444245,2	K562	blood:
28	chr16:731520..732080-chr8:67384069..67384716,2	HCT-116	colon:
29	chr8:67383309..67385950-chr8:67398891..67400480,2	MCF-7	breast:
30	chr16:729976..731206-chr8:67384019..67385398,14	HCT-116	colon:
31	chr8:67385020..67386788-chr8:67389859..67392152,2	MCF-7	breast:
32	chr8:67365709..67368396-chr8:67368954..67371561,2	MCF-7	breast:
33	chr8:67399013..67400552-chr8:67401503..67403129,2	MCF-7	breast:
34	chr8:67360913..67363800-chr8:67364065..67366392,2	MCF-7	breast:
35	chr17:57920618..57922939-chr8:67379137..67382122,2	MCF-7	breast:
36	chr8:67378228..67380679-chr8:67388244..67390416,2	MCF-7	breast:
37	chr8:67341492..67343356-chr8:67372946..67374948,2	MCF-7	breast:
38	chr8:67387606..67389202-chr8:67836916..67838423,2	MCF-7	breast:
39	chr8:67347340..67349444-chr8:67372672..67374895,2	K562	blood:
40	chr8:67367251..67370240-chr8:67562662..67564942,2	K562	blood:
41	chr8:67373454..67375848-chr8:67443609..67445864,2	MCF-7	breast:
42	chr8:67363456..67365486-chr8:67368972..67371866,2	K562	blood:
43	chr8:67374151..67375671-chr8:67623910..67626033,2	MCF-7	breast:
44	chr8:67398115..67399973-chr8:67424030..67426495,2	MCF-7	breast:
45	chr8:67399013..67400552-chr8:67401503..67403129,2	MCF-7	breast:
46	chr8:67368485..67371409-chr8:67521786..67525460,5	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADHFE1-2	chr8:67392883-67393721	NONHSAT127031
2	lnc-ADHFE1-1	chr8:67385661-67386173	XLOC_006828
3	lnc-ADHFE1-1	chr8:67387028-67387496	XLOC_006828
4	lnc-ADHFE1-1	chr8:67386021-67386173	XLOC_006828
5	lnc-ADHFE1-1	chr8:67387028-67387240	XLOC_006828
6	lnc-ADHFE1-1	chr8:67383684-67383853	XLOC_006828

No data

Variant related genes	Relation type
ENSG00000253623	TF binding region
C8orf46	TF binding region
ADHFE1	TF binding region
ENSG00000253623	CpG island
C8orf46	CpG island
ADHFE1	CpG island
ENSG00000185697	chromatin interactions
ENSG00000103266	chromatin interactions
ENSG00000245910	chromatin interactions
ENSG00000169085	chromatin interactions
ENSG00000253623	chromatin interactions
ENSG00000104205	chromatin interactions
ENSG00000213865	chromatin interactions
ENSG00000254341	chromatin interactions
ENSG00000270024	chromatin interactions
ENSG00000147576	chromatin interactions
LCOR	miRNA target sites

Extended variants
information (count: 1699 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1699 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567109243	chr8:67359327-67359328	Weak transcription Bivalent Enhancer Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs556205992	chr8:67359344-67359345	Weak transcription Bivalent Enhancer Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs115759076	chr8:67359356-67359357	Weak transcription Bivalent Enhancer Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs539241937	chr8:67359426-67359427	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538443206	chr8:67359465-67359466	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs376838868	chr8:67359468-67359469	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139680830	chr8:67359553-67359554	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142885020	chr8:67359574-67359575	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73253646	chr8:67359602-67359603	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs183698232	chr8:67359642-67359643	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs375726482	chr8:67359669-67359670	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs554596558	chr8:67359682-67359683	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs188985882	chr8:67359710-67359711	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs543492645	chr8:67359711-67359712	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs563803918	chr8:67359721-67359722	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs115103361	chr8:67359825-67359826	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs57142328	chr8:67359830-67359831	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs367921797	chr8:67359906-67359907	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs546331383	chr8:67359929-67359930	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs544346995	chr8:67359940-67359941	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs374258530	chr8:67359944-67359945	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs559954689	chr8:67359988-67359989	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs538021703	chr8:67360024-67360025	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs528716269	chr8:67360135-67360136	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs149059314	chr8:67360155-67360156	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs562276228	chr8:67360165-67360166	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs529680269	chr8:67360176-67360177	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs551249357	chr8:67360223-67360224	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs377235746	chr8:67360257-67360258	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs554488222	chr8:67360285-67360286	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs569313632	chr8:67360297-67360298	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs75310501	chr8:67360321-67360322	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs551869795	chr8:67360350-67360351	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs565518309	chr8:67360360-67360361	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs78921147	chr8:67360392-67360393	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574692134	chr8:67360405-67360406	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs192958229	chr8:67360496-67360497	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs144669843	chr8:67360510-67360511	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs371716638	chr8:67360600-67360601	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs577326985	chr8:67360613-67360614	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs546288748	chr8:67360675-67360676	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs138546767	chr8:67360697-67360698	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs1030420	chr8:67360725-67360726	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
44	rs542096010	chr8:67360737-67360738	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs1030421	chr8:67360762-67360763	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs140228003	chr8:67360793-67360794	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs551266113	chr8:67360817-67360818	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs562909080	chr8:67360869-67360870	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs182867767	chr8:67360878-67360879	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs551841376	chr8:67360908-67360909	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	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
Salivary gland tumor	18059337	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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1096 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67352000-67363600	Weak transcription	Esophagus	oesophagus
2	chr8:67352200-67360200	Weak transcription	Lung	lung
3	chr8:67352200-67360200	Weak transcription	Ovary	ovary
4	chr8:67352200-67360600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:67352200-67361000	Weak transcription	Spleen	Spleen
6	chr8:67352200-67361200	Weak transcription	Gastric	stomach
7	chr8:67352200-67361200	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr8:67352200-67364600	Weak transcription	Psoas Muscle	Psoas
9	chr8:67352400-67360200	Weak transcription	Right Ventricle	heart
10	chr8:67352400-67360800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr8:67352400-67361600	Weak transcription	Duodenum Mucosa	Duodenum
12	chr8:67352400-67363600	Weak transcription	Rectal Smooth Muscle	rectum
13	chr8:67352400-67366600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr8:67352600-67363600	Weak transcription	Colon Smooth Muscle	Colon
15	chr8:67353200-67361000	Weak transcription	Primary hematopoietic stem cells	blood
16	chr8:67353200-67361200	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr8:67353400-67365400	Weak transcription	Fetal Brain Male	brain
18	chr8:67353400-67368000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr8:67353600-67360600	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr8:67353600-67365200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr8:67353600-67372400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr8:67354000-67360000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr8:67354000-67367800	Weak transcription	Stomach Mucosa	stomach
24	chr8:67354200-67360400	Weak transcription	Placenta	Placenta
25	chr8:67354800-67359400	Weak transcription	Fetal Intestine Large	intestine
26	chr8:67355000-67361200	Weak transcription	Fetal Intestine Small	intestine
27	chr8:67355000-67365200	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr8:67355400-67361000	Weak transcription	Fetal Stomach	stomach
29	chr8:67356200-67359400	Strong transcription	Adipose Nuclei	Adipose
30	chr8:67356200-67360600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr8:67356200-67360800	Weak transcription	Fetal Muscle Trunk	muscle
32	chr8:67356200-67362200	Strong transcription	Skeletal Muscle Male	skeletal muscle
33	chr8:67356200-67374400	Strong transcription	Liver	Liver
34	chr8:67356400-67361800	Strong transcription	Skeletal Muscle Female	skeletal muscle
35	chr8:67356400-67366000	Weak transcription	Fetal Brain Female	brain
36	chr8:67356800-67365600	Strong transcription	Stomach Smooth Muscle	stomach
37	chr8:67357200-67360800	Weak transcription	Fetal Muscle Leg	muscle
38	chr8:67357400-67365000	Weak transcription	Primary T cells from cord blood	blood
39	chr8:67357800-67359400	Enhancers	Brain Anterior Caudate	brain
40	chr8:67357800-67363400	Strong transcription	Left Ventricle	heart
41	chr8:67358200-67359400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr8:67358200-67359400	Flanking Active TSS	GM12878-XiMat	blood
43	chr8:67358400-67359400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
44	chr8:67358400-67360800	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr8:67358400-67364200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr8:67358600-67364600	Weak transcription	Right Atrium	heart
47	chr8:67358600-67365800	Strong transcription	Fetal Lung	lung
48	chr8:67358800-67359800	Strong transcription	Fetal Heart	heart
49	chr8:67358800-67360200	Weak transcription	Aorta	Aorta
50	chr8:67358800-67360800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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