Variant report

Variant	esv3369267
Chromosome Location	chr9:103188781-103190679
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:559)
CpG islands
(count:244)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:559 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:103190045-103190238	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:103188063-103189399	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:103188363-103189299	K562	blood:	n/a	n/a
4	BACH1	chr9:103188440-103190245	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr9:103188917-103189625	GM12878	blood:	n/a	chr9:103189368-103189384
6	BHLHE40	chr9:103188563-103189560	K562	blood:	n/a	chr9:103189368-103189384
7	BHLHE40	chr9:103188737-103189546	HepG2	liver:	n/a	chr9:103189368-103189384
8	BRCA1	chr9:103188584-103188964	HepG2	liver:	n/a	n/a
9	BRCA1	chr9:103188660-103189306	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr9:103189222-103189407	HepG2	liver:	n/a	n/a
11	CBX3	chr9:103188665-103189324	K562	blood:	n/a	n/a
12	CCNT2	chr9:103188565-103190134	K562	blood:	n/a	n/a
13	CEBPB	chr9:103190053-103190347	HepG2	liver:	n/a	n/a
14	CEBPB	chr9:103189952-103190522	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr9:103188513-103189127	K562	blood:	n/a	chr9:103188703-103188714
16	CEBPB	chr9:103188521-103189192	A549	lung:	n/a	chr9:103188703-103188714
17	CEBPB	chr9:103188581-103189030	HepG2	liver:	n/a	chr9:103188703-103188714
18	CEBPB	chr9:103188542-103189010	K562	blood:	n/a	chr9:103188703-103188714
19	CEBPB	chr9:103188599-103188919	A549	lung:	n/a	chr9:103188703-103188714
20	CEBPB	chr9:103190186-103190269	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr9:103188510-103189120	IMR90	lung:	n/a	chr9:103188703-103188714
22	CEBPB	chr9:103188275-103189337	Hela-S3	cervix:	n/a	chr9:103188703-103188714
23	CEBPD	chr9:103189102-103189484	HepG2	liver:	n/a	n/a
24	CHD1	chr9:103189163-103189529	GM12878	blood:	n/a	n/a
25	CHD1	chr9:103187954-103192506	IMR90	lung:	n/a	n/a
26	CHD2	chr9:103189985-103190183	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr9:103188938-103189429	GM12878	blood:	n/a	n/a
28	CHD2	chr9:103188819-103189269	HepG2	liver:	n/a	n/a
29	CHD2	chr9:103188811-103189354	K562	blood:	n/a	n/a
30	CHD2	chr9:103188584-103190336	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr9:103189607-103190047	K562	blood:	n/a	n/a
32	CREB1	chr9:103189127-103189737	A549	lung:	n/a	n/a
33	CTBP2	chr9:103189918-103190298	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr9:103189000-103189150	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr9:103189320-103189470	HepG2	liver:	n/a	chr9:103189359-103189368
36	CTCF	chr9:103189529-103189530	GM13977	blood:	n/a	n/a
37	CTCF	chr9:103189421-103189489	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr9:103189880-103190030	GM12865	blood:	n/a	chr9:103189989-103189997
39	CTCF	chr9:103189360-103189510	GM12874	blood:	n/a	n/a
40	CTCF	chr9:103189336-103189527	MCF-7	breast:	n/a	chr9:103189359-103189368
41	CTCF	chr9:103189357-103189510	MCF-7	breast:	n/a	chr9:103189359-103189368
42	CTCF	chr9:103189900-103190050	GM12866	blood:	n/a	chr9:103189989-103189997
43	CTCF	chr9:103189120-103189270	BJ	skin:	n/a	n/a
44	CTCF	chr9:103189326-103189512	GM12892	blood:	n/a	chr9:103189359-103189368
45	CTCF	chr9:103189800-103189950	AG04449	skin:	n/a	n/a
46	CTCF	chr9:103189180-103189330	GM12873	blood:	n/a	n/a
47	CTCF	chr9:103189340-103189490	HCPEpiC	choroid plexus:	n/a	chr9:103189359-103189368
48	CTCF	chr9:103189340-103189490	AG04449	skin:	n/a	chr9:103189359-103189368
49	CTCF	chr9:103189155-103189721	IMR90	lung:	n/a	chr9:103189359-103189368
50	CTCF	chr9:103189386-103189488	Fibrobl	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:103190019-103190069	SK-N-MC	brain:	n/a
2	chr9:103189168-103189218	PrEC	prostate:	n/a
3	chr9:103188942-103188992	GM12892	blood:	n/a
4	chr9:103190019-103190069	MCF10A-Er-Src	breast:	n/a
5	chr9:103189158-103189208	MCF10A-Er-Src	breast:	n/a
6	chr9:103190019-103190069	Hela-S3	cervix:	n/a
7	chr9:103188942-103188992	MCF-7	breast:	n/a
8	chr9:103188942-103188992	AG09309	skin:	n/a
9	chr9:103189168-103189218	HL-60	blood:	n/a
10	chr9:103190019-103190069	NB4	blood:	n/a
11	chr9:103189158-103189208	HCPEpiC	choroid plexus:	n/a
12	chr9:103189168-103189218	HRE	kidney:	n/a
13	chr9:103190019-103190069	H1-hESC	embryonic stem cell:	embryo
14	chr9:103188942-103188992	HRCEpiC	kidney:	n/a
15	chr9:103189168-103189218	AoSMC	blood vessel:	n/a
16	chr9:103189158-103189208	PrEC	prostate:	n/a
17	chr9:103190019-103190069	U87	brain:	n/a
18	chr9:103190019-103190069	HMEC	breast:	n/a
19	chr9:103190019-103190069	A549	lung:	n/a
20	chr9:103190019-103190069	HCT-116	colon:	n/a
21	chr9:103188942-103188992	HRE	kidney:	n/a
22	chr9:103189168-103189218	HRCEpiC	kidney:	n/a
23	chr9:103189158-103189208	NT2-D1	testis:	n/a
24	chr9:103189158-103189208	SK-N-SH	brain:	n/a
25	chr9:103189158-103189208	Jurkat	blood:	n/a
26	chr9:103189158-103189208	ovcar-3	ovarian:	n/a
27	chr9:103190019-103190069	NHDF-neo	bronchial:	n/a
28	chr9:103189168-103189218	HEEpiC	esophagus:	n/a
29	chr9:103188942-103188992	U87	brain:	n/a
30	chr9:103189168-103189218	IMR90	lung:	fetal
31	chr9:103189158-103189208	HPAEpiC	pulmonary alveolar:	n/a
32	chr9:103189168-103189218	RPTEC	kidney:	n/a
33	chr9:103189168-103189218	HepG2	liver:	n/a
34	chr9:103188942-103188992	HEEpiC	esophagus:	n/a
35	chr9:103188942-103188992	HAEpiC	amniotic membrane:	n/a
36	chr9:103189168-103189218	GM12878	blood:	n/a
37	chr9:103189168-103189218	SK-N-SH	brain:	n/a
38	chr9:103189158-103189208	NHDF-neo	bronchial:	n/a
39	chr9:103189168-103189218	AG04450	lung:	fetal
40	chr9:103189168-103189218	NH-A	brain:	n/a
41	chr9:103189168-103189218	HCM	heart:	n/a
42	chr9:103189168-103189218	U87	brain:	n/a
43	chr9:103188942-103188992	NHBE	bronchial:	n/a
44	chr9:103189158-103189208	NHBE	bronchial:	n/a
45	chr9:103188942-103188992	HRPEpiC	eye:	n/a
46	chr9:103190019-103190069	PrEC	prostate:	n/a
47	chr9:103188942-103188992	HepG2	liver:	n/a
48	chr9:103190019-103190069	RPTEC	kidney:	n/a
49	chr9:103188942-103188992	AG10803	skin:	n/a
50	chr9:103189168-103189218	Hepatocyte	liver:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:103112743..103119519-chr9:103186928..103191502,9	MCF-7	breast:
2	chr9:103187168..103189222-chr9:103356564..103358499,2	K562	blood:
3	chr9:102581117..102583683-chr9:103188604..103191068,4	K562	blood:
4	chr9:103185149..103186826-chr9:103187204..103188970,2	K562	blood:
5	chr9:103187999..103190908-chr9:103233595..103236918,6	MCF-7	breast:
6	chr9:103105076..103107773-chr9:103190189..103193187,3	MCF-7	breast:
7	chr9:103188255..103190992-chr9:103234182..103236159,2	MCF-7	breast:
8	chr9:103108891..103111879-chr9:103188016..103191736,3	K562	blood:
9	chr12:56510216..56511089-chr9:103188467..103189444,2	Hela-S3	cervix:
10	chr9:101982434..101984283-chr9:103190237..103193103,2	MCF-7	breast:
11	chr9:102587074..102589303-chr9:103188855..103190578,2	MCF-7	breast:
12	chr9:103112020..103116853-chr9:103187928..103193300,12	MCF-7	breast:
13	chr3:57678348..57678964-chr9:103188755..103189418,2	Hela-S3	cervix:
14	chr9:102580552..102583439-chr9:103187663..103189259,2	MCF-7	breast:
15	chr16:88519591..88520195-chr9:103189245..103190084,2	HCT-116	colon:
16	chr9:103113279..103116752-chr9:103187119..103190910,6	K562	blood:
17	chr9:103108916..103110922-chr9:103189088..103192439,3	MCF-7	breast:
18	chr9:103113751..103117482-chr9:103187755..103190910,6	K562	blood:
19	chr2:15731552..15732171-chr9:103189458..103190114,2	Hela-S3	cervix:
20	chr9:103182521..103185122-chr9:103187370..103189359,3	K562	blood:
21	chr6:3000150..3000654-chr9:103188910..103189655,2	Hela-S3	cervix:
22	chr11:62608651..62609649-chr9:103188677..103189695,4	Hela-S3	cervix:

No data

Variant related genes	Relation type
MSANTD3	TF binding region
MSANTD3	CpG island
ENSG00000174839	chromatin interactions
ENSG00000241933	chromatin interactions
ENSG00000241697	chromatin interactions
ENSG00000079785	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000119523	chromatin interactions
ENSG00000136891	chromatin interactions
ENSG00000179588	chromatin interactions
ENSG00000124588	chromatin interactions
ENSG00000237461	chromatin interactions
ENSG00000229117	chromatin interactions
ENSG00000119508	chromatin interactions

Extended variants
information (count: 52 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:52 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143346015	chr9:103188783-103188784	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs73655536	chr9:103188826-103188827	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs554813453	chr9:103189004-103189005	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs73655537	chr9:103189010-103189011	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs72735110	chr9:103189031-103189032	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs140315131	chr9:103189053-103189054	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs537015421	chr9:103189196-103189197	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs375771913	chr9:103189205-103189206	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs577294538	chr9:103189216-103189217	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs545873358	chr9:103189292-103189293	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
11	rs62579389	chr9:103189320-103189321	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
12	rs558368917	chr9:103189326-103189327	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
13	rs571904434	chr9:103189330-103189331	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
14	rs540928180	chr9:103189336-103189337	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
15	rs112932999	chr9:103189338-103189339	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs560986385	chr9:103189339-103189340	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs544373839	chr9:103189341-103189342	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
18	rs574391207	chr9:103189392-103189393	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
19	rs191173698	chr9:103189530-103189531	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs183786527	chr9:103189560-103189561	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs563275299	chr9:103189607-103189608	Active TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs559519841	chr9:103189708-103189709	Active TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs532143384	chr9:103189721-103189722	Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs188954095	chr9:103189743-103189744	Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs112914133	chr9:103189746-103189747	Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs560036473	chr9:103189757-103189758	Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs10989089	chr9:103189912-103189913	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs528650604	chr9:103189921-103189922	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs376349544	chr9:103189934-103189935	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs568631445	chr9:103189967-103189968	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs182652981	chr9:103189973-103189974	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs77626545	chr9:103190051-103190052	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs370416860	chr9:103190069-103190070	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs374120879	chr9:103190107-103190108	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs13286882	chr9:103190174-103190175	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs570812240	chr9:103190178-103190179	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs539589366	chr9:103190180-103190181	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs529906096	chr9:103190190-103190191	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs553000685	chr9:103190191-103190192	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs538695943	chr9:103190203-103190204	Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs187034722	chr9:103190205-103190206	Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs138044560	chr9:103190225-103190226	Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs142050400	chr9:103190333-103190334	Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs574673817	chr9:103190349-103190350	Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs145811485	chr9:103190394-103190395	Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs75837288	chr9:103190435-103190436	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs56050588	chr9:103190456-103190457	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs545919459	chr9:103190623-103190624	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs559454653	chr9:103190645-103190646	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs528716524	chr9:103190668-103190669	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Mantle cell lymphoma	19029149	CNVD
Intracranial aneurysm	16715129	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:423 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:103174600-103188800	Weak transcription	Esophagus	oesophagus
2	chr9:103188000-103188800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:103188000-103188800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr9:103188200-103188800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr9:103188200-103188800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
6	chr9:103188200-103188800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr9:103188200-103188800	Enhancers	Stomach Mucosa	stomach
8	chr9:103188200-103189000	Enhancers	Fetal Heart	heart
9	chr9:103188200-103189000	Flanking Active TSS	Hela-S3	cervix
10	chr9:103188200-103189000	Flanking Active TSS	HMEC	breast
11	chr9:103188200-103189000	Flanking Active TSS	NHEK	skin
12	chr9:103188400-103188800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr9:103188400-103188800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr9:103188400-103188800	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr9:103188400-103188800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr9:103188400-103188800	Flanking Active TSS	Brain Angular Gyrus	brain
17	chr9:103188400-103188800	Enhancers	Brain Cingulate Gyrus	brain
18	chr9:103188400-103188800	Enhancers	Duodenum Mucosa	Duodenum
19	chr9:103188400-103188800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
20	chr9:103188400-103188800	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr9:103188400-103188800	Flanking Active TSS	HSMMtube	muscle
22	chr9:103188400-103189000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr9:103188400-103189000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr9:103188400-103189200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr9:103188400-103189200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
26	chr9:103188400-103189200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr9:103188400-103189200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr9:103188400-103189200	Flanking Active TSS	HUVEC	blood vessel
29	chr9:103188400-103189800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr9:103188400-103190200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr9:103188400-103190200	Active TSS	HepG2	liver
32	chr9:103188400-103190600	Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr9:103188400-103191000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr9:103188600-103188800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr9:103188600-103188800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr9:103188600-103188800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr9:103188600-103188800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
38	chr9:103188600-103188800	Enhancers	Primary B cells from peripheral blood	blood
39	chr9:103188600-103188800	Flanking Active TSS	Primary T cells from cord blood	blood
40	chr9:103188600-103188800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr9:103188600-103188800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
42	chr9:103188600-103188800	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr9:103188600-103188800	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
44	chr9:103188600-103188800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr9:103188600-103188800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr9:103188600-103188800	Active TSS	Primary T killer memory cells from peripheral blood	blood
47	chr9:103188600-103188800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
48	chr9:103188600-103188800	Flanking Active TSS	Aorta	Aorta
49	chr9:103188600-103188800	Enhancers	Brain Hippocampus Middle	brain
50	chr9:103188600-103188800	Flanking Active TSS	Fetal Intestine Large	intestine

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