Variant report

Variant	esv3372349
Chromosome Location	chr10:96161987-96164835
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:686)
CpG islands
(count:732)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:686 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:96163791-96164005	HepG2	liver:	n/a	chr10:96163926-96163942
2	ARID3A	chr10:96161938-96162456	HepG2	liver:	n/a	n/a
3	ATF1	chr10:96161937-96162267	K562	blood:	n/a	n/a
4	ATF2	chr10:96161841-96162276	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr10:96161816-96162293	A549	lung:	n/a	n/a
6	BACH1	chr10:96161959-96163255	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr10:96161717-96162346	A549	lung:	n/a	chr10:96162279-96162292 chr10:96162275-96162288
8	BCL3	chr10:96161704-96162598	A549	lung:	n/a	chr10:96162279-96162292 chr10:96162275-96162288 chr10:96162345-96162358
9	BCLAF1	chr10:96161767-96162712	GM12878	blood:	n/a	chr10:96162279-96162292 chr10:96162275-96162288 chr10:96162345-96162358
10	BCLAF1	chr10:96161801-96162945	GM12878	blood:	n/a	chr10:96162279-96162292 chr10:96162275-96162288 chr10:96162345-96162358
11	BCLAF1	chr10:96163071-96163931	GM12878	blood:	n/a	n/a
12	BHLHE40	chr10:96161860-96162771	K562	blood:	n/a	chr10:96162269-96162285
13	BHLHE40	chr10:96161931-96162433	HepG2	liver:	n/a	chr10:96162269-96162285
14	BHLHE40	chr10:96161878-96163759	GM12878	blood:	n/a	chr10:96162269-96162285
15	BHLHE40	chr10:96163367-96163651	K562	blood:	n/a	n/a
16	BRCA1	chr10:96163594-96164067	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr10:96161930-96162118	GM12878	blood:	n/a	n/a
18	CBX3	chr10:96161771-96162241	K562	blood:	n/a	n/a
19	CBX3	chr10:96161648-96162699	HCT-116	colon:	n/a	n/a
20	CBX3	chr10:96161727-96162379	K562	blood:	n/a	n/a
21	CCNT2	chr10:96162008-96163594	K562	blood:	n/a	n/a
22	CEBPB	chr10:96163540-96163989	A549	lung:	n/a	n/a
23	CEBPB	chr10:96161693-96162588	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr10:96163593-96163951	A549	lung:	n/a	n/a
25	CEBPB	chr10:96161853-96162658	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr10:96163655-96163933	K562	blood:	n/a	n/a
27	CEBPB	chr10:96163115-96164024	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr10:96163592-96163973	IMR90	lung:	n/a	n/a
29	CEBPB	chr10:96163599-96163949	HepG2	liver:	n/a	n/a
30	CEBPB	chr10:96161752-96162087	HepG2	liver:	n/a	n/a
31	CEBPB	chr10:96163600-96163967	K562	blood:	n/a	n/a
32	CEBPB	chr10:96163597-96163926	MCF-7	breast:	n/a	n/a
33	CEBPB	chr10:96163200-96163986	Hela-S3	cervix:	n/a	n/a
34	CEBPD	chr10:96162024-96162440	HepG2	liver:	n/a	n/a
35	CHD1	chr10:96163205-96163467	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD1	chr10:96162753-96162837	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr10:96162127-96163963	GM12878	blood:	n/a	n/a
38	CHD2	chr10:96161910-96162820	GM12878	blood:	n/a	n/a
39	CHD2	chr10:96161949-96162261	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr10:96162018-96162281	HepG2	liver:	n/a	n/a
41	CHD2	chr10:96161884-96163836	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr10:96163039-96163700	GM12878	blood:	n/a	n/a
43	CHD2	chr10:96162751-96162799	K562	blood:	n/a	n/a
44	CHD2	chr10:96162586-96162957	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr10:96162486-96162758	HepG2	liver:	n/a	n/a
46	CREB1	chr10:96161983-96162256	A549	lung:	n/a	n/a
47	CREB1	chr10:96161777-96163798	HepG2	liver:	n/a	n/a
48	CREB1	chr10:96163115-96163632	A549	lung:	n/a	n/a
49	CREB1	chr10:96161849-96162867	A549	lung:	n/a	n/a
50	CREB1	chr10:96161934-96162453	ECC-1	luminal epithelium:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:96162173-96162223	HMEC	breast:	n/a
2	chr10:96162146-96162196	HMEC	breast:	n/a
3	chr10:96162988-96163038	CMK	blood:	n/a
4	chr10:96162133-96162183	RPTEC	kidney:	n/a
5	chr10:96162173-96162223	HNPCEpiC	eye:	n/a
6	chr10:96162178-96162228	U87	brain:	n/a
7	chr10:96162189-96162239	PrEC	prostate:	n/a
8	chr10:96163157-96163207	HCF	heart:	n/a
9	chr10:96162173-96162223	NT2-D1	testis:	n/a
10	chr10:96162173-96162223	K562	blood:	n/a
11	chr10:96162809-96162859	NT2-D1	testis:	n/a
12	chr10:96162284-96162334	HEEpiC	esophagus:	n/a
13	chr10:96163371-96163421	HEK293	kidney:	embryo
14	chr10:96162133-96162183	HCF	heart:	n/a
15	chr10:96162809-96162859	Hela-S3	cervix:	n/a
16	chr10:96163371-96163421	GM19239	blood:	n/a
17	chr10:96162066-96162116	Caco-2	colon:	n/a
18	chr10:96162809-96162859	SAEC	small airway:	n/a
19	chr10:96163371-96163421	ProgFib	skin:	n/a
20	chr10:96162988-96163038	HCT-116	colon:	n/a
21	chr10:96162988-96163038	LNCaP	prostate:	n/a
22	chr10:96162988-96163038	MCF-7	breast:	n/a
23	chr10:96162809-96162859	PANC-1	pancreas:	n/a
24	chr10:96163371-96163421	AoSMC	blood vessel:	n/a
25	chr10:96162809-96162859	LNCaP	prostate:	n/a
26	chr10:96163371-96163421	AG10803	skin:	n/a
27	chr10:96162988-96163038	HEEpiC	esophagus:	n/a
28	chr10:96162189-96162239	SK-N-SH	brain:	n/a
29	chr10:96162162-96162212	GM19239	blood:	n/a
30	chr10:96162146-96162196	HCPEpiC	choroid plexus:	n/a
31	chr10:96162178-96162228	HNPCEpiC	eye:	n/a
32	chr10:96162189-96162239	IMR90	lung:	fetal
33	chr10:96162146-96162196	MCF-7	breast:	n/a
34	chr10:96162146-96162196	HRE	kidney:	n/a
35	chr10:96162189-96162239	GM12892	blood:	n/a
36	chr10:96163371-96163421	HRCEpiC	kidney:	n/a
37	chr10:96162162-96162212	Jurkat	blood:	n/a
38	chr10:96162133-96162183	AG09319	gingival:	n/a
39	chr10:96162178-96162228	K562	blood:	n/a
40	chr10:96162066-96162116	PFSK-1	brain:	n/a
41	chr10:96162066-96162116	K562	blood:	n/a
42	chr10:96163371-96163421	HPAEpiC	pulmonary alveolar:	n/a
43	chr10:96162178-96162228	SK-N-SH_RA	brain:	n/a
44	chr10:96162189-96162239	AoSMC	blood vessel:	n/a
45	chr10:96162173-96162223	SKMC	muscle:	n/a
46	chr10:96162189-96162239	HPAEpiC	pulmonary alveolar:	n/a
47	chr10:96162284-96162334	SK-N-SH	brain:	n/a
48	chr10:96163371-96163421	Caco-2	colon:	n/a
49	chr10:96162809-96162859	NB4	blood:	n/a
50	chr10:96162066-96162116	HRCEpiC	kidney:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:96121306..96124383-chr10:96159927..96163798,5	MCF-7	breast:
2	chr10:96162320..96165263-chr10:96165537..96170524,5	K562	blood:
3	chr10:96089068..96091434-chr10:96163469..96165336,2	K562	blood:
4	chr10:96159758..96162488-chr10:96305268..96307065,2	K562	blood:
5	chr10:96120934..96124258-chr10:96160439..96165957,6	MCF-7	breast:
6	chr10:96162368..96164918-chr10:96174079..96176855,3	K562	blood:
7	chr10:96162673..96164608-chr10:96201520..96204137,3	MCF-7	breast:
8	chr10:96121730..96122942-chr10:96161863..96162614,3	Hela-S3	cervix:
9	chr10:96161889..96162635-chr9:88897007..88897760,2	Hela-S3	cervix:
10	chr10:96121005..96123981-chr10:96160609..96162843,2	K562	blood:
11	chr10:96122660..96124273-chr10:96159058..96162494,4	K562	blood:
12	chr10:96162267..96164235-chr10:96185502..96188240,3	MCF-7	breast:
13	chr10:96162017..96163519-chr15:65596803..65598979,2	MCF-7	breast:
14	chr10:96160448..96164371-chr10:96304138..96307716,8	MCF-7	breast:
15	chr10:96162891..96164490-chr10:96175616..96177129,2	MCF-7	breast:
16	chr10:96119763..96122726-chr10:96163965..96166273,2	MCF-7	breast:
17	chr10:96162121..96162677-chr5:154317419..154318125,2	HCT-116	colon:
18	chr10:96162530..96165019-chr10:96199067..96201077,2	MCF-7	breast:

No data

Variant related genes	Relation type
TBC1D12	TF binding region
TBC1D12	CpG island
ENSG00000119969	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000173145	chromatin interactions
ENSG00000082516	chromatin interactions
ENSG00000135070	chromatin interactions

Extended variants
information (count: 119 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:119 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562203540	chr10:96161989-96161990	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs552772114	chr10:96162000-96162001	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs187727356	chr10:96162004-96162005	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs564475459	chr10:96162062-96162063	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs533469281	chr10:96162065-96162066	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs191398638	chr10:96162069-96162070	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs560412728	chr10:96162075-96162076	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs529487905	chr10:96162151-96162152	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs549126346	chr10:96162191-96162192	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs536775916	chr10:96162213-96162214	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs556534030	chr10:96162219-96162220	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs537919248	chr10:96162231-96162232	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs182777817	chr10:96162241-96162242	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs187198222	chr10:96162254-96162255	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs112161698	chr10:96162260-96162261	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs376037737	chr10:96162265-96162266	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs554154479	chr10:96162291-96162292	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs192014520	chr10:96162320-96162321	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs199804945	chr10:96162342-96162343	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs201614754	chr10:96162402-96162403	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs375547585	chr10:96162417-96162418	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs575668165	chr10:96162426-96162427	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs371794719	chr10:96162430-96162431	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs200798014	chr10:96162443-96162444	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs573344096	chr10:96162453-96162454	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs373772939	chr10:96162461-96162462	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs371213453	chr10:96162463-96162464	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs578007960	chr10:96162496-96162497	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs540259659	chr10:96162506-96162507	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs560424908	chr10:96162548-96162549	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs529499164	chr10:96162592-96162593	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs146846523	chr10:96162619-96162620	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs562709067	chr10:96162682-96162683	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs531797574	chr10:96162685-96162686	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs551482751	chr10:96162693-96162694	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs367696898	chr10:96162730-96162731	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs200792738	chr10:96162766-96162767	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs527322317	chr10:96162792-96162793	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs547374715	chr10:96162795-96162796	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs567567845	chr10:96162801-96162802	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs536521261	chr10:96162827-96162828	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs556406071	chr10:96162888-96162889	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs1111067	chr10:96162920-96162921	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs569863734	chr10:96162933-96162934	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs538454677	chr10:96162979-96162980	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs558274229	chr10:96163008-96163009	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs2477534	chr10:96163039-96163040	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs540236850	chr10:96163049-96163050	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs553722737	chr10:96163052-96163053	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs538323881	chr10:96163120-96163121	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Intracranial aneurysm	16715129	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic cancer	17952125	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:389 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96155800-96162000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:96161200-96162400	Active TSS	Fetal Brain Male	brain
3	chr10:96161200-96164000	Active TSS	Placenta	Placenta
4	chr10:96161400-96162000	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
5	chr10:96161600-96163800	Active TSS	Rectal Mucosa Donor 29	rectum
6	chr10:96161600-96164200	Active TSS	Brain Inferior Temporal Lobe	brain
7	chr10:96161600-96164600	Active TSS	Rectal Smooth Muscle	rectum
8	chr10:96161600-96164800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr10:96161600-96164800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
10	chr10:96161600-96164800	Active TSS	Stomach Smooth Muscle	stomach
11	chr10:96161600-96164800	Active TSS	Hela-S3	cervix
12	chr10:96161600-96165000	Active TSS	Brain Anterior Caudate	brain
13	chr10:96161600-96165000	Active TSS	Fetal Intestine Large	intestine
14	chr10:96161600-96165400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr10:96161800-96162000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr10:96161800-96162000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
17	chr10:96161800-96162000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr10:96161800-96162000	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
19	chr10:96161800-96162000	Flanking Active TSS	Primary hematopoietic stem cells	blood
20	chr10:96161800-96162000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
21	chr10:96161800-96162000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
22	chr10:96161800-96162000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
23	chr10:96161800-96162000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr10:96161800-96162000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
25	chr10:96161800-96162000	Flanking Active TSS	Fetal Brain Female	brain
26	chr10:96161800-96162000	Enhancers	Fetal Heart	heart
27	chr10:96161800-96162000	Flanking Active TSS	Fetal Intestine Small	intestine
28	chr10:96161800-96162000	Flanking Active TSS	Fetal Muscle Leg	muscle
29	chr10:96161800-96162000	Flanking Active TSS	Lung	lung
30	chr10:96161800-96162000	Enhancers	Placenta Amnion	Placenta Amnion
31	chr10:96161800-96162000	Flanking Active TSS	Right Ventricle	heart
32	chr10:96161800-96162000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
33	chr10:96161800-96162000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
34	chr10:96161800-96162000	Flanking Active TSS	Stomach Mucosa	stomach
35	chr10:96161800-96162000	Flanking Active TSS	A549	lung
36	chr10:96161800-96162000	Flanking Active TSS	HepG2	liver
37	chr10:96161800-96162000	Flanking Active TSS	HSMM	muscle
38	chr10:96161800-96162000	Flanking Active TSS	HSMMtube	muscle
39	chr10:96161800-96162000	Flanking Active TSS	NH-A	brain
40	chr10:96161800-96162000	Flanking Active TSS	NHDF-Ad	bronchial
41	chr10:96161800-96162000	Flanking Active TSS	NHEK	skin
42	chr10:96161800-96162200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr10:96161800-96162200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr10:96161800-96162200	Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr10:96161800-96162200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr10:96161800-96162200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr10:96161800-96162200	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
48	chr10:96161800-96162200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
49	chr10:96161800-96162200	Bivalent/Poised TSS	Primary B cells from cord blood	blood
50	chr10:96161800-96162200	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--

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