Variant report

Variant	esv1006379
Chromosome Location	chr19:35798572-35810821
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:492)
CpG islands
(count:367)
Chromatin interactive
region (count:50)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:492 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:35800871-35801058	K562	blood:	n/a	n/a
2	ARID3A	chr19:35798744-35798763	K562	blood:	n/a	n/a
3	ARID3A	chr19:35807639-35807843	HepG2	liver:	n/a	n/a
4	ATF3	chr19:35808447-35808621	K562	blood:	n/a	n/a
5	ATF3	chr19:35809873-35810229	K562	blood:	n/a	n/a
6	BHLHE40	chr19:35800541-35801165	K562	blood:	n/a	n/a
7	BHLHE40	chr19:35808385-35808689	K562	blood:	n/a	n/a
8	BHLHE40	chr19:35809614-35810369	K562	blood:	n/a	chr19:35810081-35810090 chr19:35810078-35810091 chr19:35810080-35810089 chr19:35810080-35810089
9	BHLHE40	chr19:35809901-35810260	A549	lung:	n/a	chr19:35810081-35810090 chr19:35810078-35810091 chr19:35810080-35810089 chr19:35810080-35810089
10	BHLHE40	chr19:35806795-35807157	K562	blood:	n/a	n/a
11	BHLHE40	chr19:35798958-35799074	K562	blood:	n/a	n/a
12	BHLHE40	chr19:35809843-35810360	HepG2	liver:	n/a	chr19:35810081-35810090 chr19:35810078-35810091 chr19:35810080-35810089 chr19:35810080-35810089
13	BHLHE40	chr19:35809868-35810291	GM12878	blood:	n/a	chr19:35810081-35810090 chr19:35810078-35810091 chr19:35810080-35810089 chr19:35810080-35810089
14	BHLHE40	chr19:35805792-35806150	K562	blood:	n/a	n/a
15	BRCA1	chr19:35807607-35807721	HepG2	liver:	n/a	n/a
16	BRCA1	chr19:35809644-35810243	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr19:35800317-35801218	K562	blood:	n/a	n/a
18	CBX3	chr19:35800783-35801102	K562	blood:	n/a	n/a
19	CBX3	chr19:35809344-35810321	K562	blood:	n/a	n/a
20	CCNT2	chr19:35800600-35801108	K562	blood:	n/a	n/a
21	CCNT2	chr19:35806853-35807065	K562	blood:	n/a	n/a
22	CEBPB	chr19:35800410-35800834	K562	blood:	n/a	n/a
23	CEBPB	chr19:35800307-35800639	HepG2	liver:	n/a	n/a
24	CEBPB	chr19:35800318-35800664	K562	blood:	n/a	n/a
25	CEBPB	chr19:35809845-35810403	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr19:35800464-35800492	IMR90	lung:	n/a	n/a
27	CEBPD	chr19:35806814-35807265	K562	blood:	n/a	n/a
28	CHD2	chr19:35800447-35801162	K562	blood:	n/a	n/a
29	CHD2	chr19:35809658-35810465	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr19:35809776-35809889	K562	blood:	n/a	n/a
31	CHD2	chr19:35804517-35804797	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr19:35807551-35807744	HepG2	liver:	n/a	n/a
33	CTCF	chr19:35801720-35801870	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr19:35801620-35801770	HEK293	kidney:	n/a	chr19:35801713-35801731 chr19:35801719-35801728
35	CTCF	chr19:35806820-35806970	GM12872	blood:	n/a	n/a
36	CTCF	chr19:35806690-35807037	K562	blood:	n/a	n/a
37	CTCF	chr19:35800470-35800618	K562	blood:	n/a	n/a
38	CTCF	chr19:35806700-35806850	GM12873	blood:	n/a	n/a
39	CTCF	chr19:35806820-35806970	A549	lung:	n/a	n/a
40	CTCF	chr19:35806785-35807072	HepG2	liver:	n/a	n/a
41	CTCF	chr19:35806820-35806970	K562	blood:	n/a	n/a
42	CTCF	chr19:35806861-35806990	GM19239	blood:	n/a	n/a
43	CTCF	chr19:35806920-35807070	K562	blood:	n/a	n/a
44	CTCF	chr19:35806800-35806950	HepG2	liver:	n/a	n/a
45	CTCF	chr19:35800640-35800790	HepG2	liver:	n/a	n/a
46	CTCF	chr19:35806808-35806968	GM12878	blood:	n/a	n/a
47	CTCF	chr19:35806780-35806930	Caco-2	colon:	n/a	n/a
48	CTCF	chr19:35806780-35806930	GM06990	blood:	n/a	n/a
49	CTCF	chr19:35806717-35807076	K562	blood:	n/a	n/a
50	CTCF	chr19:35806813-35806955	GM10248	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:35800925-35800975	GM19239	blood:	n/a
2	chr19:35800925-35800975	GM19239	blood:	n/a
3	chr19:35800743-35800793	ovcar-3	ovarian:	n/a
4	chr19:35800925-35800975	AG10803	skin:	n/a
5	chr19:35800743-35800793	SKMC	muscle:	n/a
6	chr19:35800743-35800793	SAEC	small airway:	n/a
7	chr19:35801215-35801265	AG04449	skin:	fetal
8	chr19:35800743-35800793	BJ	skin:	n/a
9	chr19:35801215-35801265	U87	brain:	n/a
10	chr19:35801014-35801064	ovcar-3	ovarian:	n/a
11	chr19:35800743-35800793	A549	lung:	n/a
12	chr19:35800589-35800639	HIPEpiC	eye:	n/a
13	chr19:35801014-35801064	Hepatocyte	liver:	n/a
14	chr19:35800743-35800793	HEK293	kidney:	embryo
15	chr19:35801014-35801064	ECC-1	luminal epithelium:	n/a
16	chr19:35800589-35800639	SAEC	small airway:	n/a
17	chr19:35803340-35803390	AG09309	skin:	n/a
18	chr19:35801014-35801064	HCT-116	colon:	n/a
19	chr19:35800589-35800639	BJ	skin:	n/a
20	chr19:35801215-35801265	HAEpiC	amniotic membrane:	n/a
21	chr19:35800589-35800639	GM12892	blood:	n/a
22	chr19:35801215-35801265	HRPEpiC	eye:	n/a
23	chr19:35803340-35803390	SK-N-SH	brain:	n/a
24	chr19:35800589-35800639	HPAEpiC	pulmonary alveolar:	n/a
25	chr19:35800589-35800639	AG09309	skin:	n/a
26	chr19:35801215-35801265	HepG2	liver:	n/a
27	chr19:35803340-35803390	HIPEpiC	eye:	n/a
28	chr19:35803340-35803390	LNCaP	prostate:	n/a
29	chr19:35800925-35800975	K562	blood:	n/a
30	chr19:35800589-35800639	NB4	blood:	n/a
31	chr19:35800925-35800975	MCF10A-Er-Src	breast:	n/a
32	chr19:35801014-35801064	BJ	skin:	n/a
33	chr19:35801014-35801064	SK-N-SH	brain:	n/a
34	chr19:35800925-35800975	HPAEpiC	pulmonary alveolar:	n/a
35	chr19:35801215-35801265	BJ	skin:	n/a
36	chr19:35800925-35800975	GM12891	blood:	n/a
37	chr19:35800925-35800975	HMEC	breast:	n/a
38	chr19:35800589-35800639	ProgFib	skin:	n/a
39	chr19:35800743-35800793	AG09309	skin:	n/a
40	chr19:35800589-35800639	HCPEpiC	choroid plexus:	n/a
41	chr19:35800589-35800639	PANC-1	pancreas:	n/a
42	chr19:35800743-35800793	ProgFib	skin:	n/a
43	chr19:35803340-35803390	T-47D	breast:	n/a
44	chr19:35801014-35801064	HCF	heart:	n/a
45	chr19:35801014-35801064	GM19239	blood:	n/a
46	chr19:35801215-35801265	Hepatocyte	liver:	n/a
47	chr19:35800925-35800975	HEEpiC	esophagus:	n/a
48	chr19:35800743-35800793	GM12891	blood:	n/a
49	chr19:35801014-35801064	SKMC	muscle:	n/a
50	chr19:35800743-35800793	ECC-1	luminal epithelium:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:35807993..35809012-chr19:36044708..36045631,5	MCF-7	breast:
2	chr19:35491237..35491794-chr19:35808497..35809009,2	MCF-7	breast:
3	chr19:35646046..35647977-chr19:35796625..35798576,2	K562	blood:
4	chr19:35758596..35761330-chr19:35808386..35811398,6	MCF-7	breast:
5	chr19:35807878..35810423-chr19:36035383..36039227,3	MCF-7	breast:
6	chr19:35778338..35780262-chr19:35804621..35807184,2	MCF-7	breast:
7	chr19:35757352..35763490-chr19:35798817..35804347,10	MCF-7	breast:
8	chr19:35808879..35811383-chr19:35819038..35823207,3	K562	blood:
9	chr19:35794837..35799903-chr19:35800719..35807404,10	MCF-7	breast:
10	chr19:35782103..35783478-chr19:35808039..35808940,5	MCF-7	breast:
11	chr19:35604701..35607129-chr19:35809231..35811359,2	MCF-7	breast:
12	chr19:35757193..35760230-chr19:35795583..35800096,4	K562	blood:
13	chr19:35781735..35783754-chr19:35799663..35801226,2	MCF-7	breast:
14	chr19:35762096..35762857-chr19:35804524..35805135,2	MCF-7	breast:
15	chr19:35607895..35610299-chr19:35808518..35810247,2	MCF-7	breast:
16	chr19:35798397..35800415-chr19:35842184..35843828,2	MCF-7	breast:
17	chr19:35762082..35763038-chr19:35808435..35809008,4	MCF-7	breast:
18	chr19:35780282..35782569-chr19:35797611..35799728,2	MCF-7	breast:
19	chr19:35753841..35756119-chr19:35797821..35799359,2	MCF-7	breast:
20	chr19:35794875..35797641-chr19:35798078..35800124,2	MCF-7	breast:
21	chr19:35788326..35791177-chr19:35803354..35807024,3	MCF-7	breast:
22	chr19:35807993..35809012-chr19:36044708..36045631,4	MCF-7	breast:
23	chr19:35759321..35763199-chr19:35795656..35798701,4	MCF-7	breast:
24	chr19:35761264..35763399-chr19:35801388..35804082,2	K562	blood:
25	chr19:35771719..35773722-chr19:35808312..35810561,2	K562	blood:
26	chr19:35800092..35801659-chr19:35829023..35831587,2	K562	blood:
27	chr19:35808228..35808955-chr19:36059823..36060624,3	MCF-7	breast:
28	chr19:35797829..35800128-chr19:35823862..35825668,2	MCF-7	breast:
29	chr19:35738973..35741505-chr19:35806828..35808599,2	MCF-7	breast:
30	chr19:35757351..35762248-chr19:35804679..35808319,5	MCF-7	breast:
31	chr19:35807787..35809317-chr19:35810235..35812842,2	K562	blood:
32	chr19:35606400..35608352-chr19:35800705..35803047,2	MCF-7	breast:
33	chr19:35614004..35615566-chr19:35808376..35809985,2	MCF-7	breast:
34	chr19:35738675..35740393-chr19:35799543..35801412,2	MCF-7	breast:
35	chr19:35796764..35800582-chr19:36132788..36136056,3	K562	blood:
36	chr19:35760570..35761203-chr19:35808161..35808860,2	MCF-7	breast:
37	chr19:35801054..35803091-chr19:35805182..35806855,2	MCF-7	breast:
38	chr19:35490912..35491745-chr19:35808049..35808930,2	MCF-7	breast:
39	chr19:35762082..35763038-chr19:35808102..35809008,5	MCF-7	breast:
40	chr19:35807998..35809046-chr19:40971871..40972634,3	MCF-7	breast:
41	chr19:35738491..35740445-chr19:35800431..35803185,3	MCF-7	breast:
42	chr19:35782451..35783179-chr19:35808099..35808940,2	MCF-7	breast:
43	chr19:35755149..35764508-chr19:35799437..35813142,44	MCF-7	breast:
44	chr19:35808141..35808673-chr19:35999936..36000808,2	MCF-7	breast:
45	chr19:35760524..35761090-chr19:35804405..35805080,2	MCF-7	breast:
46	chr19:35779735..35782128-chr19:35802752..35804567,2	MCF-7	breast:
47	chr19:35760384..35761203-chr19:35808161..35809024,2	MCF-7	breast:
48	chr19:35740175..35741891-chr19:35807694..35809845,2	MCF-7	breast:
49	chr19:35801834..35808584-chr19:35810190..35813576,7	MCF-7	breast:
50	chr19:35759827..35760405-chr19:35809677..35810195,2	MCF-7	breast:

No data

Variant related genes	Relation type
MAG	TF binding region
CD22	TF binding region
MAG	CpG island
CD22	CpG island
ENSG00000012124	chromatin interactions
ENSG00000105698	chromatin interactions
ENSG00000089351	chromatin interactions
ENSG00000160460	chromatin interactions
ENSG00000089356	chromatin interactions
ENSG00000269553	chromatin interactions
ENSG00000126266	chromatin interactions
ENSG00000105697	chromatin interactions
ENSG00000105677	chromatin interactions
ENSG00000105672	chromatin interactions
ENSG00000236144	chromatin interactions
ENSG00000105699	chromatin interactions
ENSG00000269303	chromatin interactions
ENSG00000105695	chromatin interactions

Extended variants
information (count: 569 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138684764	chr19:35798583-35798584	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs141316819	chr19:35798584-35798585	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs530704525	chr19:35798642-35798643	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs201749290	chr19:35798645-35798646	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs534021794	chr19:35798646-35798647	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs182878845	chr19:35798664-35798665	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs2285449	chr19:35798668-35798669	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs369275721	chr19:35798680-35798681	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs529869340	chr19:35798701-35798702	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs546404638	chr19:35798702-35798703	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs187486614	chr19:35798792-35798793	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs3214112	chr19:35798802-35798803	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs397839904	chr19:35798807-35798808	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs532103671	chr19:35798817-35798818	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs370664156	chr19:35798861-35798862	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs568877257	chr19:35798904-35798905	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs193298561	chr19:35798932-35798933	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs557586697	chr19:35798966-35798967	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs116478508	chr19:35798973-35798974	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs536811076	chr19:35798975-35798976	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs10402632	chr19:35798976-35798977	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs573369815	chr19:35799009-35799010	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs545558131	chr19:35799073-35799074	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs80128691	chr19:35799119-35799120	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs185467294	chr19:35799122-35799123	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs552587530	chr19:35799154-35799155	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs76597311	chr19:35799197-35799198	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs561580350	chr19:35799198-35799199	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs1034597	chr19:35799200-35799201	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs575203975	chr19:35799202-35799203	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs73031728	chr19:35799230-35799231	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs187999856	chr19:35799242-35799243	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs556522777	chr19:35799256-35799257	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs377353040	chr19:35799296-35799297	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs551816913	chr19:35799298-35799299	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs192215390	chr19:35799299-35799300	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs574988828	chr19:35799320-35799321	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs531311061	chr19:35799328-35799329	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs2269756	chr19:35799371-35799372	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs567936009	chr19:35799372-35799373	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs536976974	chr19:35799391-35799392	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs2872113	chr19:35799452-35799453	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs138104172	chr19:35799472-35799473	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs12185485	chr19:35799506-35799507	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs149455147	chr19:35799523-35799524	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs184897965	chr19:35799591-35799592	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs538221050	chr19:35799685-35799686	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs114401203	chr19:35799742-35799743	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs140350949	chr19:35799743-35799744	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs188393501	chr19:35799744-35799745	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Gastric cancer	21811585	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD

Chromatin state (count:337 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35774800-35809600	Weak transcription	Right Atrium	heart
2	chr19:35791400-35798800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr19:35792800-35801400	Genic enhancers	Brain Hippocampus Middle	brain
4	chr19:35794400-35810000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr19:35794600-35799400	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr19:35795000-35800400	Enhancers	HepG2	liver
7	chr19:35795200-35798800	Weak transcription	Spleen	Spleen
8	chr19:35796200-35799200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr19:35796200-35799600	Enhancers	Primary B cells from peripheral blood	blood
10	chr19:35796800-35800600	Enhancers	Ovary	ovary
11	chr19:35796800-35801000	Weak transcription	Fetal Thymus	thymus
12	chr19:35797000-35799000	Enhancers	GM12878-XiMat	blood
13	chr19:35797000-35800800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr19:35797200-35799400	Enhancers	Primary hematopoietic stem cells	blood
15	chr19:35797200-35800000	Enhancers	Primary B cells from cord blood	blood
16	chr19:35797200-35802200	Weak transcription	Brain Anterior Caudate	brain
17	chr19:35797600-35804000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr19:35797800-35798800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr19:35797800-35799000	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr19:35797800-35800000	Enhancers	Fetal Lung	lung
21	chr19:35797800-35800200	Enhancers	Fetal Kidney	kidney
22	chr19:35797800-35800800	Genic enhancers	Brain Substantia Nigra	brain
23	chr19:35797800-35809600	Weak transcription	Brain Angular Gyrus	brain
24	chr19:35798000-35801400	Enhancers	Fetal Muscle Trunk	muscle
25	chr19:35798000-35801800	Enhancers	Fetal Stomach	stomach
26	chr19:35798000-35802600	Enhancers	Placenta	Placenta
27	chr19:35798200-35799000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr19:35798200-35799200	Weak transcription	Brain Cingulate Gyrus	brain
29	chr19:35798200-35801400	Enhancers	Fetal Muscle Leg	muscle
30	chr19:35798200-35802800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr19:35798200-35811400	Weak transcription	Liver	Liver
32	chr19:35798400-35800000	Enhancers	K562	blood
33	chr19:35798800-35799000	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr19:35798800-35799200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr19:35798800-35799400	Enhancers	Spleen	Spleen
36	chr19:35799000-35799200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr19:35799000-35799800	Strong transcription	Brain Inferior Temporal Lobe	brain
38	chr19:35799000-35800400	Weak transcription	GM12878-XiMat	blood
39	chr19:35799200-35799600	Strong transcription	Brain Cingulate Gyrus	brain
40	chr19:35799200-35801200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr19:35799200-35804000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr19:35799400-35800600	Weak transcription	Spleen	Spleen
43	chr19:35799400-35800800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr19:35799400-35804200	Weak transcription	Primary hematopoietic stem cells	blood
45	chr19:35799600-35800000	Weak transcription	Primary B cells from peripheral blood	blood
46	chr19:35799600-35801400	Genic enhancers	Brain Cingulate Gyrus	brain
47	chr19:35799600-35803400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr19:35799800-35800000	Genic enhancers	Brain Inferior Temporal Lobe	brain
49	chr19:35799800-35801200	Enhancers	Duodenum Mucosa	Duodenum
50	chr19:35800000-35800200	Enhancers	Primary B cells from peripheral blood	blood

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