Variant report

Variant	esv3421253
Chromosome Location	chr13:50364151-50368649
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:884)
CpG islands
(count:916)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:884 , 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	chr13:50365302-50365701	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:50365984-50366120	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:50366846-50367514	HepG2	liver:	n/a	n/a
4	ATF2	chr13:50366922-50367551	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr13:50366842-50367554	GM12878	blood:	n/a	n/a
6	ATF2	chr13:50366738-50367057	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr13:50366740-50366957	GM12878	blood:	n/a	chr13:50366853-50366862 chr13:50366877-50366897
8	ATF3	chr13:50366758-50367176	HepG2	liver:	n/a	chr13:50366853-50366862 chr13:50366877-50366897
9	ATF3	chr13:50366747-50367052	H1-hESC	embryonic stem cell:	n/a	chr13:50366853-50366862 chr13:50366877-50366897
10	ATF3	chr13:50366730-50367199	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	chr13:50366713-50367215	GM12878	blood:	n/a	chr13:50366853-50366862 chr13:50366877-50366897
13	BACH1	chr13:50366820-50367599	H1-hESC	embryonic stem cell:	n/a	n/a
14	BHLHE40	chr13:50366705-50367096	A549	lung:	n/a	n/a
15	BHLHE40	chr13:50365417-50366252	GM12878	blood:	n/a	n/a
16	BHLHE40	chr13:50366566-50367565	K562	blood:	n/a	n/a
17	BHLHE40	chr13:50365829-50366233	K562	blood:	n/a	n/a
18	BHLHE40	chr13:50365474-50367685	HepG2	liver:	n/a	chr13:50366364-50366380 chr13:50366375-50366391 chr13:50366423-50366439 chr13:50366367-50366383
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	chr13:50366184-50366318	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr13:50367029-50367219	HepG2	liver:	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	chr13:50366935-50367179	HepG2	liver:	n/a	n/a
27	CEBPB	chr13:50366807-50367734	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr13:50367451-50367671	K562	blood:	n/a	n/a
29	CEBPB	chr13:50367488-50367701	HepG2	liver:	n/a	n/a
30	CEBPB	chr13:50365429-50366116	Hela-S3	cervix:	n/a	chr13:50365665-50365678 chr13:50365665-50365676
31	CEBPB	chr13:50365542-50365772	H1-hESC	embryonic stem cell:	n/a	chr13:50365665-50365678 chr13:50365665-50365676
32	CEBPB	chr13:50367482-50367734	IMR90	lung:	n/a	n/a
33	CEBPD	chr13:50366876-50367347	HepG2	liver:	n/a	n/a
34	CEBPD	chr13:50366425-50366737	HepG2	liver:	n/a	n/a
35	CHD1	chr13:50366903-50367142	H1-hESC	embryonic stem cell:	n/a	chr13:50367048-50367058
36	CHD1	chr13:50365648-50366511	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr13:50366902-50367627	GM12878	blood:	n/a	chr13:50367048-50367058
38	CHD1	chr13:50365433-50366337	GM12878	blood:	n/a	n/a
39	CHD2	chr13:50366642-50367694	HepG2	liver:	n/a	chr13:50367048-50367058 chr13:50366798-50366808
40	CHD2	chr13:50365471-50367514	GM12878	blood:	n/a	chr13:50367048-50367058 chr13:50366798-50366808
41	CHD2	chr13:50366604-50367762	H1-hESC	embryonic stem cell:	n/a	chr13:50367048-50367058 chr13:50366798-50366808
42	CHD2	chr13:50365961-50366216	HepG2	liver:	n/a	n/a
43	CHD2	chr13:50366562-50367411	K562	blood:	n/a	chr13:50367048-50367058 chr13:50366798-50366808
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	chr13:50366582-50367861	HepG2	liver:	n/a	n/a
47	CREB1	chr13:50366032-50367805	GM12878	blood:	n/a	n/a
48	CREB1	chr13:50365934-50367817	HepG2	liver:	n/a	n/a
49	CREB1	chr13:50366559-50367841	K562	blood:	n/a	n/a
50	CREB1	chr13:50366592-50367928	H1-hESC	embryonic stem cell:	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	chr13:50365574-50365624	SK-N-MC	brain:	n/a
2	chr13:50365574-50365624	SK-N-MC	brain:	n/a
3	chr13:50367395-50367445	HNPCEpiC	eye:	n/a
4	chr13:50366546-50366596	NHBE	bronchial:	n/a
5	chr13:50367173-50367223	MCF-7	breast:	n/a
6	chr13:50367095-50367145	PFSK-1	brain:	n/a
7	chr13:50367295-50367345	GM12878	blood:	n/a
8	chr13:50366546-50366596	Jurkat	blood:	n/a
9	chr13:50366559-50366609	SK-N-MC	brain:	n/a
10	chr13:50367064-50367114	MCF-7	breast:	n/a
11	chr13:50367173-50367223	A549	lung:	n/a
12	chr13:50367279-50367329	HepG2	liver:	n/a
13	chr13:50367057-50367107	HRE	kidney:	n/a
14	chr13:50366546-50366596	GM12891	blood:	n/a
15	chr13:50367057-50367107	H1-hESC	embryonic stem cell:	embryo
16	chr13:50366190-50366240	HUVEC	blood vessel:	n/a
17	chr13:50367340-50367390	AG04450	lung:	fetal
18	chr13:50367114-50367164	U87	brain:	n/a
19	chr13:50367064-50367114	GM19239	blood:	n/a
20	chr13:50367395-50367445	HCPEpiC	choroid plexus:	n/a
21	chr13:50367114-50367164	AG09309	skin:	n/a
22	chr13:50367114-50367164	AG04449	skin:	fetal
23	chr13:50367340-50367390	HEK293	kidney:	embryo
24	chr13:50367340-50367390	HRE	kidney:	n/a
25	chr13:50366559-50366609	GM12878	blood:	n/a
26	chr13:50366546-50366596	NH-A	brain:	n/a
27	chr13:50367173-50367223	GM19239	blood:	n/a
28	chr13:50365574-50365624	Caco-2	colon:	n/a
29	chr13:50367279-50367329	GM06990	blood:	n/a
30	chr13:50367095-50367145	SAEC	small airway:	n/a
31	chr13:50367060-50367110	ProgFib	skin:	n/a
32	chr13:50367114-50367164	HCT-116	colon:	n/a
33	chr13:50367340-50367390	LNCaP	prostate:	n/a
34	chr13:50367395-50367445	HUVEC	blood vessel:	n/a
35	chr13:50367095-50367145	BE2_C	brain:	n/a
36	chr13:50367279-50367329	SK-N-MC	brain:	n/a
37	chr13:50367060-50367110	HPAEpiC	pulmonary alveolar:	n/a
38	chr13:50366190-50366240	IMR90	lung:	fetal
39	chr13:50367295-50367345	HNPCEpiC	eye:	n/a
40	chr13:50367340-50367390	HNPCEpiC	eye:	n/a
41	chr13:50367340-50367390	Jurkat	blood:	n/a
42	chr13:50366190-50366240	H1-hESC	embryonic stem cell:	embryo
43	chr13:50367340-50367390	RPTEC	kidney:	n/a
44	chr13:50367279-50367329	K562	blood:	n/a
45	chr13:50367060-50367110	MCF10A-Er-Src	breast:	n/a
46	chr13:50366546-50366596	PrEC	prostate:	n/a
47	chr13:50365574-50365624	NHDF-neo	bronchial:	n/a
48	chr13:50367064-50367114	AG10803	skin:	n/a
49	chr13:50367095-50367145	Jurkat	blood:	n/a
50	chr13:50366648-50366698	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:50365136..50367359-chr13:50509492..50511604,3	MCF-7	breast:
2	chr13:50363308..50365589-chr13:50370131..50372850,2	K562	blood:
3	chr12:57472055..57474451-chr13:50366783..50368850,2	K562	blood:
4	chr13:50263387..50266299-chr13:50365424..50368132,3	K562	blood:
5	chr13:50366438..50367362-chr9:91925263..91926169,2	NB4	blood:
6	chr13:50363476..50366040-chr13:51498906..51500626,2	K562	blood:
7	chr13:50266035..50267824-chr13:50362193..50365135,2	K562	blood:
8	chr10:104210318..104210821-chr13:50367293..50367793,2	NB4	blood:
9	chr13:50263387..50265868-chr13:50365424..50368677,3	K562	blood:
10	chr13:50365172..50367900-chr13:50655465..50657230,2	K562	blood:
11	chr13:50262508..50268089-chr13:50363531..50368771,13	MCF-7	breast:
12	chr13:50253326..50254069-chr13:50365169..50365855,3	MCF-7	breast:
13	chr13:50366935..50367602-chr14:73524591..73525438,2	NB4	blood:
14	chr13:50363119..50364738-chr13:50365543..50368287,2	MCF-7	breast:
15	chr13:50366632..50367555-chr15:65588352..65589049,2	Hela-S3	cervix:
16	chr13:50363329..50366279-chr13:50509762..50511637,2	MCF-7	breast:
17	chr13:50242498..50244504-chr13:50366051..50367551,2	MCF-7	breast:
18	chr13:50365087..50367801-chr13:50569333..50572997,5	MCF-7	breast:
19	chr13:50278979..50281390-chr13:50365910..50368755,2	MCF-7	breast:
20	chr13:50366691..50367418-chr3:40350564..40351423,2	NB4	blood:
21	chr13:50261767..50269137-chr13:50365068..50368535,12	MCF-7	breast:
22	chr13:50367116..50367723-chr7:128170990..128171600,2	NB4	blood:

No data

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

Extended variants
information (count: 166 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:166 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550348842	chr13:50364151-50364152	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs186141635	chr13:50364174-50364175	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs533088154	chr13:50364253-50364254	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs191073180	chr13:50364256-50364257	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs533086315	chr13:50364294-50364295	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs181386264	chr13:50364317-50364318	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs528718593	chr13:50364355-50364356	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs547129814	chr13:50364366-50364367	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs117766481	chr13:50364368-50364369	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs75105811	chr13:50364369-50364370	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs557104396	chr13:50364423-50364424	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs3782931	chr13:50364464-50364465	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs78301088	chr13:50364558-50364559	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs113600973	chr13:50364580-50364581	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs572957123	chr13:50364608-50364609	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs185937118	chr13:50364621-50364622	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs552012218	chr13:50364629-50364630	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs190600363	chr13:50364672-50364673	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs150152977	chr13:50364691-50364692	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs573901861	chr13:50364724-50364725	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs183206400	chr13:50364733-50364734	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs115133181	chr13:50364758-50364759	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs532974490	chr13:50364766-50364767	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs73485742	chr13:50364790-50364791	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs187817699	chr13:50364878-50364879	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs527369025	chr13:50365016-50365017	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs113039018	chr13:50365058-50365059	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs182449883	chr13:50365105-50365106	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs145756985	chr13:50365121-50365122	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs187871248	chr13:50365186-50365187	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs569177925	chr13:50365188-50365189	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs539448515	chr13:50365213-50365214	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs61961487	chr13:50365248-50365249	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs11617584	chr13:50365319-50365320	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs534299619	chr13:50365341-50365342	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs527636182	chr13:50365355-50365356	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs571600228	chr13:50365454-50365455	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs571641734	chr13:50365460-50365461	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs12584870	chr13:50365586-50365587	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs77369521	chr13:50365599-50365600	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs556520501	chr13:50365616-50365617	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs577964531	chr13:50365625-50365626	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs545062144	chr13:50365631-50365632	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs202144253	chr13:50365662-50365663	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs11391029	chr13:50365665-50365666	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs3215725	chr13:50365666-50365667	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs145623267	chr13:50365680-50365681	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs527422613	chr13:50365681-50365682	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs80089392	chr13:50365706-50365707	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs560784358	chr13:50365725-50365726	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	6 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:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50336200-50364800	Weak transcription	Fetal Intestine Small	intestine
2	chr13:50336800-50364600	Weak transcription	NHLF	lung
3	chr13:50349600-50365400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr13:50349600-50365400	Weak transcription	Lung	lung
5	chr13:50351200-50364200	Weak transcription	HSMM	muscle
6	chr13:50351200-50364600	Weak transcription	HSMMtube	muscle
7	chr13:50352000-50365200	Weak transcription	Fetal Thymus	thymus
8	chr13:50352400-50364400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr13:50352600-50364800	Weak transcription	A549	lung
10	chr13:50354200-50364400	Weak transcription	Right Atrium	heart
11	chr13:50354200-50365400	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr13:50354400-50365400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr13:50356200-50364800	Weak transcription	NHEK	skin
14	chr13:50356400-50365200	Weak transcription	Right Ventricle	heart
15	chr13:50356600-50365000	Weak transcription	Fetal Kidney	kidney
16	chr13:50356800-50364600	Weak transcription	Primary B cells from cord blood	blood
17	chr13:50357000-50364400	Weak transcription	Ovary	ovary
18	chr13:50357800-50364200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr13:50357800-50364600	Weak transcription	Fetal Stomach	stomach
20	chr13:50357800-50365200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr13:50358400-50364400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr13:50358400-50364600	Weak transcription	Aorta	Aorta
23	chr13:50358400-50365200	Weak transcription	Stomach Mucosa	stomach
24	chr13:50358400-50365600	Weak transcription	Gastric	stomach
25	chr13:50359600-50365200	Weak transcription	Fetal Muscle Leg	muscle
26	chr13:50360600-50364600	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr13:50361000-50364400	Weak transcription	Fetal Intestine Large	intestine
28	chr13:50361400-50364400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr13:50361400-50364600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr13:50362400-50364200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr13:50362600-50364400	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr13:50362600-50364600	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr13:50362600-50365000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr13:50362600-50365200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr13:50362800-50364400	Weak transcription	NHDF-Ad	bronchial
36	chr13:50362800-50364800	Enhancers	HepG2	liver
37	chr13:50362800-50365600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr13:50363000-50364200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr13:50363000-50364600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr13:50363000-50364600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr13:50363000-50364800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr13:50363000-50364800	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr13:50363000-50365200	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr13:50363000-50365200	Enhancers	Brain Hippocampus Middle	brain
45	chr13:50363000-50365200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
46	chr13:50363000-50365200	Enhancers	Fetal Heart	heart
47	chr13:50363000-50365400	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr13:50363200-50364200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr13:50363200-50364200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr13:50363200-50364200	Enhancers	Brain Germinal Matrix	brain

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