Variant report

Variant	nsv900878
Chromosome Location	chr13:91619133-91717352
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:914)
CpG islands
(count:122)
Chromatin interactive
region (count:54)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:914 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:91643944-91643967	K562	blood:	n/a	n/a
2	ARID3A	chr13:91697893-91697942	K562	blood:	n/a	n/a
3	ARID3A	chr13:91669638-91669971	K562	blood:	n/a	n/a
4	ATF1	chr13:91697590-91697810	K562	blood:	n/a	n/a
5	ATF1	chr13:91677141-91677313	K562	blood:	n/a	n/a
6	ATF1	chr13:91668475-91668544	K562	blood:	n/a	n/a
7	BACH1	chr13:91639971-91640005	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr13:91627168-91627255	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr13:91709086-91709378	GM12878	blood:	n/a	n/a
10	BCL11A	chr13:91709063-91709372	GM12878	blood:	n/a	n/a
11	BHLHE40	chr13:91653765-91653931	K562	blood:	n/a	n/a
12	BHLHE40	chr13:91669629-91669890	K562	blood:	n/a	n/a
13	BHLHE40	chr13:91709142-91709344	GM12878	blood:	n/a	n/a
14	BRCA1	chr13:91620939-91620966	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr13:91669569-91669951	K562	blood:	n/a	n/a
16	CEBPB	chr13:91684273-91684471	HepG2	liver:	n/a	n/a
17	CEBPB	chr13:91676825-91677073	HepG2	liver:	n/a	chr13:91676935-91676946
18	CEBPB	chr13:91697258-91697284	HepG2	liver:	n/a	n/a
19	CEBPB	chr13:91677758-91678048	HepG2	liver:	n/a	chr13:91677906-91677915 chr13:91677904-91677917 chr13:91677906-91677917 chr13:91677904-91677915 chr13:91677906-91677915 chr13:91677904-91677917 chr13:91677906-91677915 chr13:91677904-91677917 chr13:91677906-91677915
20	CEBPB	chr13:91699807-91699836	HepG2	liver:	n/a	n/a
21	CEBPB	chr13:91677751-91678023	A549	lung:	n/a	chr13:91677906-91677915 chr13:91677904-91677917 chr13:91677906-91677917 chr13:91677904-91677915 chr13:91677906-91677915 chr13:91677904-91677917 chr13:91677906-91677915 chr13:91677904-91677917 chr13:91677906-91677915
22	CEBPB	chr13:91669345-91670004	Hela-S3	cervix:	n/a	chr13:91669480-91669491 chr13:91669479-91669492
23	CEBPB	chr13:91712749-91713020	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr13:91705109-91705112	K562	blood:	n/a	n/a
25	CEBPB	chr13:91641587-91641816	A549	lung:	n/a	n/a
26	CEBPB	chr13:91677726-91678084	K562	blood:	n/a	chr13:91677906-91677915 chr13:91677904-91677917 chr13:91677906-91677917 chr13:91677904-91677915 chr13:91677906-91677915 chr13:91677904-91677917 chr13:91677906-91677915 chr13:91677904-91677917 chr13:91677906-91677915
27	CEBPB	chr13:91669298-91669934	K562	blood:	n/a	chr13:91669480-91669491 chr13:91669479-91669492
28	CEBPB	chr13:91626532-91627109	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr13:91701651-91701778	K562	blood:	n/a	n/a
30	CEBPB	chr13:91701581-91701854	HepG2	liver:	n/a	n/a
31	CEBPB	chr13:91699744-91699923	A549	lung:	n/a	chr13:91699877-91699888 chr13:91699877-91699890 chr13:91699877-91699890 chr13:91699877-91699888
32	CEBPB	chr13:91701526-91701880	A549	lung:	n/a	n/a
33	CEBPB	chr13:91669327-91669620	HepG2	liver:	n/a	chr13:91669480-91669491 chr13:91669479-91669492
34	CEBPB	chr13:91684264-91684439	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD1	chr13:91709072-91709181	GM12878	blood:	n/a	n/a
36	CHD2	chr13:91683888-91684034	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr13:91708898-91709392	GM12878	blood:	n/a	n/a
38	CREB1	chr13:91708950-91709506	GM12878	blood:	n/a	n/a
39	CTCF	chr13:91669740-91669890	GM12878	blood:	n/a	chr13:91669777-91669795 chr13:91669772-91669793 chr13:91669779-91669792 chr13:91669779-91669792 chr13:91669783-91669792
40	CTCF	chr13:91669669-91669853	HepG2	liver:	n/a	chr13:91669777-91669795 chr13:91669772-91669793 chr13:91669779-91669792 chr13:91669779-91669792 chr13:91669783-91669792
41	CTCF	chr13:91620880-91621030	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr13:91683900-91684050	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr13:91669684-91669875	GM12891	blood:	n/a	chr13:91669777-91669795 chr13:91669772-91669793 chr13:91669779-91669792 chr13:91669779-91669792 chr13:91669783-91669792
44	CTCF	chr13:91620860-91621010	GM12872	blood:	n/a	n/a
45	CTCF	chr13:91620900-91621050	GM12866	blood:	n/a	n/a
46	CTCF	chr13:91697820-91697970	NB4	blood:	n/a	chr13:91697868-91697889 chr13:91697874-91697890 chr13:91697873-91697891
47	CTCF	chr13:91683920-91684070	BE2_C	brain:	n/a	n/a
48	CTCF	chr13:91697780-91697930	HMF	breast:	n/a	chr13:91697868-91697889 chr13:91697874-91697890 chr13:91697873-91697891
49	CTCF	chr13:91697800-91697950	GM06990	blood:	n/a	chr13:91697868-91697889 chr13:91697874-91697890 chr13:91697873-91697891
50	CTCF	chr13:91699280-91699430	RPTEC	kidney:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:91624536-91624586	NHBE	bronchial:	n/a
2	chr13:91627026-91627076	BJ	skin:	n/a
3	chr13:91624536-91624586	CMK	blood:	n/a
4	chr13:91624536-91624586	GM12892	blood:	n/a
5	chr13:91627026-91627076	HIPEpiC	eye:	n/a
6	chr13:91627026-91627076	K562	blood:	n/a
7	chr13:91624536-91624586	SK-N-MC	brain:	n/a
8	chr13:91627026-91627076	MCF10A-Er-Src	breast:	n/a
9	chr13:91624536-91624586	RPTEC	kidney:	n/a
10	chr13:91627026-91627076	HCF	heart:	n/a
11	chr13:91627026-91627076	HL-60	blood:	n/a
12	chr13:91627026-91627076	NHDF-neo	bronchial:	n/a
13	chr13:91624536-91624586	Caco-2	colon:	n/a
14	chr13:91627026-91627076	NHBE	bronchial:	n/a
15	chr13:91624536-91624586	HEK293	kidney:	embryo
16	chr13:91624536-91624586	U87	brain:	n/a
17	chr13:91627026-91627076	AG10803	skin:	n/a
18	chr13:91624536-91624586	BJ	skin:	n/a
19	chr13:91624536-91624586	Hepatocyte	liver:	n/a
20	chr13:91624536-91624586	IMR90	lung:	fetal
21	chr13:91624536-91624586	NT2-D1	testis:	n/a
22	chr13:91627026-91627076	SK-N-SH	brain:	n/a
23	chr13:91624536-91624586	NB4	blood:	n/a
24	chr13:91624536-91624586	HepG2	liver:	n/a
25	chr13:91627026-91627076	HPAEpiC	pulmonary alveolar:	n/a
26	chr13:91627026-91627076	NH-A	brain:	n/a
27	chr13:91627026-91627076	GM06990	blood:	n/a
28	chr13:91624536-91624586	AG09309	skin:	n/a
29	chr13:91627026-91627076	PANC-1	pancreas:	n/a
30	chr13:91624536-91624586	SK-N-SH	brain:	n/a
31	chr13:91624536-91624586	GM19239	blood:	n/a
32	chr13:91624536-91624586	AoSMC	blood vessel:	n/a
33	chr13:91627026-91627076	HNPCEpiC	eye:	n/a
34	chr13:91627026-91627076	HCPEpiC	choroid plexus:	n/a
35	chr13:91627026-91627076	SK-N-MC	brain:	n/a
36	chr13:91624536-91624586	ovcar-3	ovarian:	n/a
37	chr13:91624536-91624586	BE2_C	brain:	n/a
38	chr13:91624536-91624586	HRCEpiC	kidney:	n/a
39	chr13:91624536-91624586	HRE	kidney:	n/a
40	chr13:91627026-91627076	SAEC	small airway:	n/a
41	chr13:91624536-91624586	PFSK-1	brain:	n/a
42	chr13:91624536-91624586	GM06990	blood:	n/a
43	chr13:91627026-91627076	GM19239	blood:	n/a
44	chr13:91624536-91624586	MCF10A-Er-Src	breast:	n/a
45	chr13:91624536-91624586	HMEC	breast:	n/a
46	chr13:91624536-91624586	Hela-S3	cervix:	n/a
47	chr13:91627026-91627076	GM12892	blood:	n/a
48	chr13:91627026-91627076	Caco-2	colon:	n/a
49	chr13:91627026-91627076	ECC-1	luminal epithelium:	n/a
50	chr13:91627026-91627076	HRPEpiC	eye:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:91712535..91717054-chr13:91999404..92002931,4	K562	blood:
2	chr13:91711254..91714185-chr13:91714775..91716673,3	K562	blood:
3	chr13:91684109..91685768-chr13:91709350..91711880,2	K562	blood:
4	chr13:91631852..91633535-chr13:91636429..91638322,2	K562	blood:
5	chr13:91527534..91530490-chr13:91638435..91640751,2	K562	blood:
6	chr13:91535395..91538269-chr13:91626547..91628248,2	K562	blood:
7	chr13:91520684..91521356-chr13:91620487..91621149,2	MCF-7	breast:
8	chr13:91666492..91668285-chr13:92006589..92008125,2	K562	blood:
9	chr13:91682803..91684784-chr13:91688040..91691032,2	K562	blood:
10	chr13:91624778..91626545-chr13:91641725..91644502,2	K562	blood:
11	chr13:91711634..91714185-chr13:91714775..91716444,2	K562	blood:
12	chr13:91660431..91663097-chr13:91765114..91768066,3	K562	blood:
13	chr13:91624778..91626545-chr13:91641725..91644502,2	K562	blood:
14	chr13:91631852..91633535-chr13:91636429..91638322,2	K562	blood:
15	chr13:91627930..91630698-chr13:92093262..92096251,2	K562	blood:
16	chr13:91535763..91536557-chr13:91620508..91621127,3	MCF-7	breast:
17	chr13:91645861..91648178-chr13:91998721..92001281,2	K562	blood:
18	chr13:91711680..91715085-chr13:91718150..91721561,4	K562	blood:
19	chr13:91711634..91714185-chr13:91714775..91716444,2	K562	blood:
20	chr13:91590964..91593450-chr13:91647110..91649272,2	K562	blood:
21	chr13:91666607..91668886-chr13:91670518..91672068,2	K562	blood:
22	chr13:91683791..91685341-chr13:92005987..92008919,2	K562	blood:
23	chr13:91678702..91681179-chr13:91682905..91684742,2	K562	blood:
24	chr13:91705962..91707850-chr13:91709398..91711486,2	K562	blood:
25	chr13:91639571..91641593-chr13:91646155..91648079,2	K562	blood:
26	chr13:91714010..91717064-chr13:91759391..91762967,3	K562	blood:
27	chr13:91692018..91694558-chr13:92011037..92013238,2	K562	blood:
28	chr13:91665398..91666903-chr13:91667898..91670513,2	K562	blood:
29	chr13:91639571..91641593-chr13:91646155..91648079,2	K562	blood:
30	chr13:91670732..91673372-chr13:91673630..91676630,3	K562	blood:
31	chr13:91614487..91617150-chr13:91618821..91620598,2	K562	blood:
32	chr13:91653705..91655534-chr13:91733936..91735797,2	K562	blood:
33	chr13:91665398..91666903-chr13:91667898..91670513,2	K562	blood:
34	chr13:91067650..91070177-chr13:91643740..91645578,2	K562	blood:
35	chr13:91645606..91647803-chr13:91665875..91668500,2	K562	blood:
36	chr13:91627499..91629287-chr13:91636601..91638840,2	K562	blood:
37	chr13:91711254..91714185-chr13:91714775..91716673,3	K562	blood:
38	chr13:91696836..91698844-chr13:91999135..92000969,2	K562	blood:
39	chr13:91669308..91669910-chr5:74664857..74665857,2	K562	blood:
40	chr13:91618328..91620916-chr13:91623249..91624814,2	K562	blood:
41	chr13:91666607..91668886-chr13:91670518..91672068,2	K562	blood:
42	chr13:91654397..91657081-chr13:91966360..91968645,2	K562	blood:
43	chr13:91682803..91684784-chr13:91688040..91691032,2	K562	blood:
44	chr13:91656873..91659047-chr13:92007660..92010033,2	K562	blood:
45	chr13:91710530..91712184-chr13:91999258..92001269,2	K562	blood:
46	chr13:91693894..91695601-chr13:91720462..91722439,2	K562	blood:
47	chr13:91618328..91620916-chr13:91623249..91624814,2	K562	blood:
48	chr13:91678702..91681179-chr13:91682905..91684742,2	K562	blood:
49	chr13:91684109..91685768-chr13:91709350..91711880,2	K562	blood:
50	chr13:91645606..91647803-chr13:91665875..91668500,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DCT-18	chr13:91675986-91676208	NONHSAT034657

No data

Variant related genes	Relation type
BRK1P2	TF binding region
BRK1P2	CpG island
ENSG00000215417	chromatin interactions
ENSG00000227983	chromatin interactions

Extended variants
information (count: 2232 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2232 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4347494	chr13:91619201-91619202	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs17667497	chr13:91619229-91619230	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs553656205	chr13:91619230-91619231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs140316008	chr13:91619246-91619247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144174409	chr13:91619260-91619261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557452612	chr13:91619263-91619264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188447870	chr13:91619277-91619278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs75689370	chr13:91619316-91619317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192881917	chr13:91619321-91619322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545655934	chr13:91619328-91619329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528462049	chr13:91619329-91619330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185302194	chr13:91619352-91619353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564794496	chr13:91619462-91619463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs16944982	chr13:91619508-91619509	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs188668125	chr13:91619573-91619574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192567820	chr13:91619592-91619593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs184821754	chr13:91619606-91619607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566478656	chr13:91619671-91619672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533730294	chr13:91619711-91619712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547333631	chr13:91619723-91619724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571944708	chr13:91619724-91619725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs72633899	chr13:91619747-91619748	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs557309348	chr13:91619748-91619749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575787514	chr13:91619762-91619763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs148839841	chr13:91619802-91619803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554593081	chr13:91619812-91619813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188079350	chr13:91619828-91619829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540198034	chr13:91619855-91619856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564856018	chr13:91619907-91619908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142638318	chr13:91619912-91619913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs58006253	chr13:91619927-91619928	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs562193665	chr13:91619999-91620000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs140897964	chr13:91620026-91620027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529851525	chr13:91620035-91620036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548316408	chr13:91620060-91620061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs560255925	chr13:91620109-91620110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs9515864	chr13:91620124-91620125	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs552232046	chr13:91620157-91620158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570415730	chr13:91620199-91620200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541688754	chr13:91620288-91620289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs75973260	chr13:91620299-91620300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs181024892	chr13:91620361-91620362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7325495	chr13:91620397-91620398	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs116609177	chr13:91620399-91620400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572973401	chr13:91620405-91620406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529086319	chr13:91620468-91620469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs7324977	chr13:91620492-91620493	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs184725972	chr13:91620513-91620514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577158809	chr13:91620606-91620607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs80133029	chr13:91620627-91620628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:91619200-91620600	Enhancers	Rectal Smooth Muscle	rectum
2	chr13:91619400-91619600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr13:91619600-91622400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr13:91620600-91621000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr13:91620800-91621800	Enhancers	Fetal Lung	lung
6	chr13:91621000-91621200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr13:91621000-91621400	Enhancers	Rectal Smooth Muscle	rectum
8	chr13:91621000-91621600	Enhancers	Brain Substantia Nigra	brain
9	chr13:91621000-91621800	Enhancers	Brain Cingulate Gyrus	brain
10	chr13:91621000-91621800	Enhancers	Colon Smooth Muscle	Colon
11	chr13:91621200-91625600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr13:91621400-91622000	Enhancers	Duodenum Smooth Muscle	Duodenum
13	chr13:91622400-91623000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr13:91622600-91623200	Enhancers	Primary hematopoietic stem cells	blood
15	chr13:91622600-91623200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr13:91624200-91624400	Enhancers	H1 Cell Line	embryonic stem cell
17	chr13:91624400-91625400	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr13:91625200-91626200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr13:91625200-91626800	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr13:91625400-91625800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr13:91625400-91626400	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr13:91625400-91628600	Enhancers	H1 Cell Line	embryonic stem cell
23	chr13:91625600-91626200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr13:91625600-91626400	Enhancers	H9 Cell Line	embryonic stem cell
25	chr13:91625600-91626400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr13:91625800-91627000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr13:91626200-91626400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
28	chr13:91626200-91626800	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr13:91626200-91627200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr13:91626200-91627800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr13:91626400-91626600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr13:91626400-91626800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr13:91626400-91627600	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr13:91626400-91627600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr13:91626600-91626800	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr13:91626800-91627000	Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr13:91626800-91627200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr13:91626800-91627200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr13:91626800-91627200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
40	chr13:91626800-91628600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr13:91627000-91627400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr13:91627000-91627400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr13:91627200-91627400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr13:91627200-91627400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr13:91627200-91628000	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr13:91627200-91628000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr13:91627200-91628600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr13:91627400-91627800	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr13:91627400-91630800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr13:91627600-91627800	Enhancers	H9 Cell Line	embryonic stem cell

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