Variant report

Variant	esv3433889
Chromosome Location	chr13:50365601-50367799
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:851)
CpG islands
(count:916)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:851 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:50366846-50367514	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:50365984-50366120	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:50365302-50365701	HepG2	liver:	n/a	n/a
4	ATF2	chr13:50366842-50367554	GM12878	blood:	n/a	n/a
5	ATF2	chr13:50366922-50367551	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr13:50366738-50367057	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr13:50366730-50367199	HepG2	liver:	n/a	chr13:50366853-50366862 chr13:50366877-50366897
8	ATF3	chr13:50366713-50367215	GM12878	blood:	n/a	chr13:50366853-50366862 chr13:50366877-50366897
9	ATF3	chr13:50366740-50366957	GM12878	blood:	n/a	chr13:50366853-50366862 chr13:50366877-50366897
10	ATF3	chr13:50366758-50367176	HepG2	liver:	n/a	chr13:50366853-50366862 chr13:50366877-50366897
11	ATF3	chr13:50366712-50367018	K562	blood:	n/a	chr13:50366853-50366862 chr13:50366877-50366897
12	ATF3	chr13:50366747-50367052	H1-hESC	embryonic stem cell:	n/a	chr13:50366853-50366862 chr13:50366877-50366897
13	BACH1	chr13:50366820-50367599	H1-hESC	embryonic stem cell:	n/a	n/a
14	BHLHE40	chr13:50365417-50366252	GM12878	blood:	n/a	n/a
15	BHLHE40	chr13:50366705-50367096	A549	lung:	n/a	n/a
16	BHLHE40	chr13:50365474-50367685	HepG2	liver:	n/a	chr13:50366364-50366380 chr13:50366375-50366391 chr13:50366423-50366439 chr13:50366367-50366383
17	BHLHE40	chr13:50365829-50366233	K562	blood:	n/a	n/a
18	BHLHE40	chr13:50366566-50367565	K562	blood:	n/a	n/a
19	BHLHE40	chr13:50366529-50367473	GM12878	blood:	n/a	n/a
20	BRCA1	chr13:50366766-50367665	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr13:50366994-50367517	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr13:50367029-50367219	HepG2	liver:	n/a	n/a
23	BRCA1	chr13:50366184-50366318	H1-hESC	embryonic stem cell:	n/a	n/a
24	CBX3	chr13:50366737-50367385	K562	blood:	n/a	n/a
25	CCNT2	chr13:50366034-50367396	K562	blood:	n/a	chr13:50366046-50366055
26	CEBPB	chr13:50367482-50367734	IMR90	lung:	n/a	n/a
27	CEBPB	chr13:50365429-50366116	Hela-S3	cervix:	n/a	chr13:50365665-50365678 chr13:50365665-50365676
28	CEBPB	chr13:50367451-50367671	K562	blood:	n/a	n/a
29	CEBPB	chr13:50366935-50367179	HepG2	liver:	n/a	n/a
30	CEBPB	chr13:50366807-50367734	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr13:50365542-50365772	H1-hESC	embryonic stem cell:	n/a	chr13:50365665-50365678 chr13:50365665-50365676
32	CEBPB	chr13:50367488-50367701	HepG2	liver:	n/a	n/a
33	CEBPD	chr13:50366425-50366737	HepG2	liver:	n/a	n/a
34	CEBPD	chr13:50366876-50367347	HepG2	liver:	n/a	n/a
35	CHD1	chr13:50365648-50366511	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD1	chr13:50365433-50366337	GM12878	blood:	n/a	n/a
37	CHD1	chr13:50366903-50367142	H1-hESC	embryonic stem cell:	n/a	chr13:50367048-50367058
38	CHD1	chr13:50366902-50367627	GM12878	blood:	n/a	chr13:50367048-50367058
39	CHD2	chr13:50366604-50367762	H1-hESC	embryonic stem cell:	n/a	chr13:50367048-50367058 chr13:50366798-50366808
40	CHD2	chr13:50366642-50367694	HepG2	liver:	n/a	chr13:50367048-50367058 chr13:50366798-50366808
41	CHD2	chr13:50365471-50367514	GM12878	blood:	n/a	chr13:50367048-50367058 chr13:50366798-50366808
42	CHD2	chr13:50366562-50367411	K562	blood:	n/a	chr13:50367048-50367058 chr13:50366798-50366808
43	CHD2	chr13:50365961-50366216	HepG2	liver:	n/a	n/a
44	CHD2	chr13:50365461-50367498	Hela-S3	cervix:	n/a	chr13:50367048-50367058 chr13:50366798-50366808
45	CHD2	chr13:50365746-50366153	K562	blood:	n/a	n/a
46	CREB1	chr13:50366541-50367836	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr13:50365934-50367817	HepG2	liver:	n/a	n/a
48	CREB1	chr13:50366559-50367841	K562	blood:	n/a	n/a
49	CREB1	chr13:50366582-50367861	HepG2	liver:	n/a	n/a
50	CREB1	chr13:50366032-50367805	GM12878	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:50367279-50367329	Hela-S3	cervix:	n/a
2	chr13:50367279-50367329	Hela-S3	cervix:	n/a
3	chr13:50367395-50367445	NH-A	brain:	n/a
4	chr13:50366559-50366609	GM12892	blood:	n/a
5	chr13:50367173-50367223	RPTEC	kidney:	n/a
6	chr13:50366190-50366240	A549	lung:	n/a
7	chr13:50367060-50367110	HPAEpiC	pulmonary alveolar:	n/a
8	chr13:50367114-50367164	SK-N-MC	brain:	n/a
9	chr13:50367395-50367445	AG09319	gingival:	n/a
10	chr13:50367064-50367114	ovcar-3	ovarian:	n/a
11	chr13:50367340-50367390	Jurkat	blood:	n/a
12	chr13:50366546-50366596	GM12878	blood:	n/a
13	chr13:50367340-50367390	SAEC	small airway:	n/a
14	chr13:50367060-50367110	HUVEC	blood vessel:	n/a
15	chr13:50367114-50367164	NHBE	bronchial:	n/a
16	chr13:50367095-50367145	GM12892	blood:	n/a
17	chr13:50366559-50366609	HRCEpiC	kidney:	n/a
18	chr13:50365574-50365624	Jurkat	blood:	n/a
19	chr13:50366648-50366698	NHBE	bronchial:	n/a
20	chr13:50367395-50367445	HL-60	blood:	n/a
21	chr13:50366559-50366609	ovcar-3	ovarian:	n/a
22	chr13:50367060-50367110	SKMC	muscle:	n/a
23	chr13:50367095-50367145	HRCEpiC	kidney:	n/a
24	chr13:50367095-50367145	AG10803	skin:	n/a
25	chr13:50367064-50367114	HEK293	kidney:	embryo
26	chr13:50367173-50367223	T-47D	breast:	n/a
27	chr13:50367279-50367329	HCPEpiC	choroid plexus:	n/a
28	chr13:50367095-50367145	ovcar-3	ovarian:	n/a
29	chr13:50367173-50367223	AG09319	gingival:	n/a
30	chr13:50367295-50367345	AoSMC	blood vessel:	n/a
31	chr13:50367173-50367223	PrEC	prostate:	n/a
32	chr13:50367114-50367164	LNCaP	prostate:	n/a
33	chr13:50367295-50367345	HAEpiC	amniotic membrane:	n/a
34	chr13:50366546-50366596	PANC-1	pancreas:	n/a
35	chr13:50367279-50367329	AoSMC	blood vessel:	n/a
36	chr13:50367064-50367114	HRCEpiC	kidney:	n/a
37	chr13:50367095-50367145	SK-N-SH	brain:	n/a
38	chr13:50367340-50367390	AG09309	skin:	n/a
39	chr13:50367057-50367107	PFSK-1	brain:	n/a
40	chr13:50367395-50367445	HEK293	kidney:	embryo
41	chr13:50367295-50367345	HIPEpiC	eye:	n/a
42	chr13:50367095-50367145	MCF-7	breast:	n/a
43	chr13:50366190-50366240	GM19239	blood:	n/a
44	chr13:50366559-50366609	AG09319	gingival:	n/a
45	chr13:50367173-50367223	H1-hESC	embryonic stem cell:	embryo
46	chr13:50367064-50367114	PFSK-1	brain:	n/a
47	chr13:50367057-50367107	NT2-D1	testis:	n/a
48	chr13:50366546-50366596	NHDF-neo	bronchial:	n/a
49	chr13:50367395-50367445	ProgFib	skin:	n/a
50	chr13:50367114-50367164	GM12892	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:50242498..50244504-chr13:50366051..50367551,2	MCF-7	breast:
2	chr13:50366438..50367362-chr9:91925263..91926169,2	NB4	blood:
3	chr13:50365136..50367359-chr13:50509492..50511604,3	MCF-7	breast:
4	chr13:50365087..50367801-chr13:50569333..50572997,5	MCF-7	breast:
5	chr13:50262508..50268089-chr13:50363531..50368771,13	MCF-7	breast:
6	chr13:50263387..50265868-chr13:50365424..50368677,3	K562	blood:
7	chr13:50263387..50266299-chr13:50365424..50368132,3	K562	blood:
8	chr12:57472055..57474451-chr13:50366783..50368850,2	K562	blood:
9	chr13:50365172..50367900-chr13:50655465..50657230,2	K562	blood:
10	chr13:50363476..50366040-chr13:51498906..51500626,2	K562	blood:
11	chr13:50253326..50254069-chr13:50365169..50365855,3	MCF-7	breast:
12	chr13:50366691..50367418-chr3:40350564..40351423,2	NB4	blood:
13	chr13:50278979..50281390-chr13:50365910..50368755,2	MCF-7	breast:
14	chr10:104210318..104210821-chr13:50367293..50367793,2	NB4	blood:
15	chr13:50261767..50269137-chr13:50365068..50368535,12	MCF-7	breast:
16	chr13:50367116..50367723-chr7:128170990..128171600,2	NB4	blood:
17	chr13:50366935..50367602-chr14:73524591..73525438,2	NB4	blood:
18	chr13:50363329..50366279-chr13:50509762..50511637,2	MCF-7	breast:
19	chr13:50366632..50367555-chr15:65588352..65589049,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
KPNA3	TF binding region
KPNA3	CpG island
ENSG00000176124	chromatin interactions
ENSG00000114784	chromatin interactions
ENSG00000119707	chromatin interactions
ENSG00000269609	chromatin interactions
ENSG00000166881	chromatin interactions
ENSG00000123975	chromatin interactions
ENSG00000204977	chromatin interactions
ENSG00000231607	chromatin interactions
ENSG00000123179	chromatin interactions
ENSG00000123178	chromatin interactions
ENSG00000203547	chromatin interactions
ENSG00000102753	chromatin interactions
ENSG00000264864	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000273270	chromatin interactions

Extended variants
information (count: 92 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:92 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556520501	chr13:50365616-50365617	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs577964531	chr13:50365625-50365626	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs545062144	chr13:50365631-50365632	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs202144253	chr13:50365662-50365663	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs11391029	chr13:50365665-50365666	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs3215725	chr13:50365666-50365667	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs145623267	chr13:50365680-50365681	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs527422613	chr13:50365681-50365682	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs80089392	chr13:50365706-50365707	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs560784358	chr13:50365725-50365726	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs79213152	chr13:50365751-50365752	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs138230691	chr13:50365767-50365768	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs36098008	chr13:50365786-50365787	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs562854153	chr13:50365802-50365803	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs9568332	chr13:50365819-50365820	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs551411782	chr13:50365830-50365831	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs201425990	chr13:50365851-50365852	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs566509283	chr13:50365946-50365947	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs2236354	chr13:50365966-50365967	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs549472472	chr13:50365972-50365973	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs567627872	chr13:50365992-50365993	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs143018043	chr13:50366051-50366052	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs556383339	chr13:50366055-50366056	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs578031584	chr13:50366056-50366057	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs564352836	chr13:50366063-50366064	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs553837859	chr13:50366074-50366075	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs572019678	chr13:50366099-50366100	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs542227325	chr13:50366205-50366206	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs561039270	chr13:50366212-50366213	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs117219709	chr13:50366224-50366225	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	mRNA abundance
31	rs544446767	chr13:50366370-50366371	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs562741723	chr13:50366510-50366511	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs533475975	chr13:50366541-50366542	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs369465748	chr13:50366549-50366550	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs200563678	chr13:50366555-50366556	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs560589166	chr13:50366561-50366562	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs374104014	chr13:50366653-50366654	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs200365157	chr13:50366665-50366666	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs199509096	chr13:50366672-50366673	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs374334924	chr13:50366674-50366675	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs377544239	chr13:50366680-50366681	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs375322361	chr13:50366681-50366682	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs567760110	chr13:50366686-50366687	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs376163982	chr13:50366687-50366688	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs538338299	chr13:50366696-50366697	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs550028434	chr13:50366709-50366710	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs571451190	chr13:50366714-50366715	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs532345061	chr13:50366718-50366719	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs538803285	chr13:50366721-50366722	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs554127749	chr13:50366737-50366738	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	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
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21990379	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute promyelocytic leukemia	19109227	CNVD

Chromatin state (count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50363400-50365800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr13:50363800-50365800	Enhancers	Small Intestine	intestine
3	chr13:50364000-50367600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr13:50364200-50367800	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr13:50364600-50365800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr13:50364600-50365800	Flanking Active TSS	Fetal Brain Female	brain
7	chr13:50364600-50365800	Enhancers	Placenta Amnion	Placenta Amnion
8	chr13:50364600-50366000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr13:50364600-50366000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr13:50364600-50367600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr13:50364600-50367800	Active TSS	Aorta	Aorta
12	chr13:50364600-50368000	Active TSS	H1 Cell Line	embryonic stem cell
13	chr13:50364600-50368000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr13:50364600-50368000	Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr13:50364800-50365800	Flanking Active TSS	HUVEC	blood vessel
16	chr13:50364800-50365800	Flanking Active TSS	NH-A	brain
17	chr13:50364800-50366000	Flanking Active TSS	Adipose Nuclei	Adipose
18	chr13:50364800-50366000	Flanking Active TSS	Liver	Liver
19	chr13:50364800-50366600	Active TSS	Right Atrium	heart
20	chr13:50364800-50367600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr13:50364800-50367600	Active TSS	Colonic Mucosa	Colon
22	chr13:50364800-50367800	Active TSS	A549	lung
23	chr13:50364800-50368000	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr13:50365000-50365800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr13:50365000-50365800	Flanking Active TSS	Dnd41	blood
26	chr13:50365000-50366000	Flanking Active TSS	Primary hematopoietic stem cells	blood
27	chr13:50365000-50366000	Active TSS	Fetal Brain Male	brain
28	chr13:50365000-50367400	Active TSS	Cortex derived primary cultured neurospheres	brain
29	chr13:50365000-50367400	Active TSS	Fetal Intestine Large	intestine
30	chr13:50365000-50367400	Active TSS	Skeletal Muscle Male	skeletal muscle
31	chr13:50365000-50367400	Active TSS	Skeletal Muscle Female	skeletal muscle
32	chr13:50365000-50367400	Active TSS	HMEC	breast
33	chr13:50365000-50367400	Active TSS	NHLF	lung
34	chr13:50365000-50367600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr13:50365000-50367600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr13:50365000-50367600	Active TSS	Fetal Intestine Small	intestine
37	chr13:50365000-50367600	Active TSS	Fetal Kidney	kidney
38	chr13:50365000-50367600	Active TSS	GM12878-XiMat	blood
39	chr13:50365000-50367600	Active TSS	K562	blood
40	chr13:50365000-50367600	Active TSS	NHDF-Ad	bronchial
41	chr13:50365000-50367800	Active TSS	HSMMtube	muscle
42	chr13:50365000-50368000	Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr13:50365000-50368000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr13:50365200-50365800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
45	chr13:50365200-50365800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
46	chr13:50365200-50365800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
47	chr13:50365200-50365800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
48	chr13:50365200-50365800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
49	chr13:50365200-50365800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr13:50365200-50365800	Flanking Active TSS	Brain Angular Gyrus	brain

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