Variant report

Variant	nsv948334
Chromosome Location	chr5:61891622-62197219
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1761)
CpG islands
(count:613)
Chromatin interactive
region (count:57)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1761 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:61948019-61948444	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:62037767-62038406	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:61896465-61897039	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:61953771-61953952	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:61976936-61977433	HepG2	liver:	n/a	n/a
6	ATF1	chr5:62004400-62004644	K562	blood:	n/a	n/a
7	ATF3	chr5:62015871-62016064	K562	blood:	n/a	n/a
8	BACH1	chr5:61986215-61986345	K562	blood:	n/a	n/a
9	BACH1	chr5:61917202-61917344	K562	blood:	n/a	n/a
10	BCL3	chr5:62073699-62074050	GM12878	blood:	n/a	n/a
11	BCL3	chr5:62056284-62056836	GM12878	blood:	n/a	n/a
12	BHLHE40	chr5:61927952-61927976	K562	blood:	n/a	n/a
13	BHLHE40	chr5:62072439-62072720	K562	blood:	n/a	n/a
14	BHLHE40	chr5:61945436-61945510	K562	blood:	n/a	n/a
15	BHLHE40	chr5:61917176-61917369	K562	blood:	n/a	n/a
16	BHLHE40	chr5:62058497-62058551	GM12878	blood:	n/a	n/a
17	BHLHE40	chr5:62015797-62016298	GM12878	blood:	n/a	n/a
18	BHLHE40	chr5:62015830-62016143	K562	blood:	n/a	n/a
19	BHLHE40	chr5:62015848-62016138	HepG2	liver:	n/a	n/a
20	BRCA1	chr5:61968131-61968149	GM12878	blood:	n/a	n/a
21	CBX3	chr5:61917097-61917474	K562	blood:	n/a	n/a
22	CBX3	chr5:62004057-62004283	K562	blood:	n/a	n/a
23	CEBPB	chr5:61946289-61946587	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr5:62009272-62009475	K562	blood:	n/a	n/a
25	CEBPB	chr5:61979912-61980050	HepG2	liver:	n/a	chr5:61979937-61979950 chr5:61979938-61979949
26	CEBPB	chr5:62086170-62086530	IMR90	lung:	n/a	chr5:62086349-62086360
27	CEBPB	chr5:62004388-62004553	K562	blood:	n/a	n/a
28	CEBPB	chr5:61891893-61892222	IMR90	lung:	n/a	n/a
29	CEBPB	chr5:62074801-62075107	Hela-S3	cervix:	n/a	chr5:62074994-62075011
30	CEBPB	chr5:61915587-61915728	K562	blood:	n/a	n/a
31	CEBPB	chr5:62086239-62086436	HepG2	liver:	n/a	chr5:62086349-62086360
32	CEBPB	chr5:62069399-62069579	K562	blood:	n/a	chr5:62069514-62069525
33	CEBPB	chr5:62183927-62184242	IMR90	lung:	n/a	chr5:62184085-62184096
34	CEBPB	chr5:62183940-62184226	A549	lung:	n/a	chr5:62184085-62184096
35	CEBPB	chr5:62069352-62069685	HepG2	liver:	n/a	chr5:62069514-62069525
36	CEBPB	chr5:62074833-62075055	A549	lung:	n/a	chr5:62074994-62075011
37	CEBPB	chr5:62150450-62150720	HepG2	liver:	n/a	n/a
38	CEBPB	chr5:61986071-61986164	K562	blood:	n/a	n/a
39	CEBPB	chr5:62037711-62038383	HepG2	liver:	n/a	chr5:62037824-62037837
40	CEBPB	chr5:62081409-62081741	HepG2	liver:	n/a	chr5:62081560-62081571
41	CEBPB	chr5:61917154-61917355	K562	blood:	n/a	n/a
42	CEBPB	chr5:61949390-61949600	IMR90	lung:	n/a	chr5:61949494-61949505 chr5:61949493-61949504
43	CEBPB	chr5:62086159-62086542	Hela-S3	cervix:	n/a	chr5:62086349-62086360
44	CEBPB	chr5:61986088-61986273	HepG2	liver:	n/a	n/a
45	CEBPB	chr5:61953709-61953841	HepG2	liver:	n/a	chr5:61953773-61953784
46	CEBPB	chr5:62184008-62184220	H1-hESC	embryonic stem cell:	n/a	chr5:62184085-62184096
47	CEBPB	chr5:61921186-61921290	K562	blood:	n/a	chr5:61921213-61921226 chr5:61921213-61921224
48	CEBPB	chr5:61932390-61932490	HepG2	liver:	n/a	n/a
49	CEBPB	chr5:62086167-62086547	HepG2	liver:	n/a	chr5:62086349-62086360
50	CEBPB	chr5:62122961-62123018	HepG2	liver:	n/a	chr5:62122995-62123006

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:62073161-62073211	HIPEpiC	eye:	n/a
2	chr5:62071572-62071622	HCM	heart:	n/a
3	chr5:61923204-61923254	SK-N-SH	brain:	n/a
4	chr5:62073161-62073211	HIPEpiC	eye:	n/a
5	chr5:62071572-62071622	HCM	heart:	n/a
6	chr5:61923204-61923254	SK-N-SH	brain:	n/a
7	chr5:62100540-62100590	HPAEpiC	pulmonary alveolar:	n/a
8	chr5:62072660-62072710	AG09309	skin:	n/a
9	chr5:62073161-62073211	HAEpiC	amniotic membrane:	n/a
10	chr5:62073161-62073211	SK-N-SH	brain:	n/a
11	chr5:61917363-61917413	HCF	heart:	n/a
12	chr5:61923204-61923254	HPAEpiC	pulmonary alveolar:	n/a
13	chr5:61917363-61917413	RPTEC	kidney:	n/a
14	chr5:62073161-62073211	AG09309	skin:	n/a
15	chr5:61923204-61923254	HUVEC	blood vessel:	n/a
16	chr5:62074261-62074311	HAEpiC	amniotic membrane:	n/a
17	chr5:62073161-62073211	ovcar-3	ovarian:	n/a
18	chr5:62100540-62100590	SK-N-SH	brain:	n/a
19	chr5:62014804-62014854	Hepatocyte	liver:	n/a
20	chr5:62071572-62071622	ECC-1	luminal epithelium:	n/a
21	chr5:61917363-61917413	HIPEpiC	eye:	n/a
22	chr5:62071572-62071622	GM12878	blood:	n/a
23	chr5:62074572-62074622	Caco-2	colon:	n/a
24	chr5:62073161-62073211	GM06990	blood:	n/a
25	chr5:62071572-62071622	U87	brain:	n/a
26	chr5:62014804-62014854	SK-N-MC	brain:	n/a
27	chr5:62073623-62073673	PANC-1	pancreas:	n/a
28	chr5:62074572-62074622	NB4	blood:	n/a
29	chr5:62072660-62072710	Hela-S3	cervix:	n/a
30	chr5:62074261-62074311	PFSK-1	brain:	n/a
31	chr5:62074261-62074311	MCF-7	breast:	n/a
32	chr5:61917363-61917413	ECC-1	luminal epithelium:	n/a
33	chr5:61917363-61917413	SKMC	muscle:	n/a
34	chr5:61917363-61917413	T-47D	breast:	n/a
35	chr5:61923204-61923254	AG04449	skin:	fetal
36	chr5:62074572-62074622	BE2_C	brain:	n/a
37	chr5:61917363-61917413	GM12892	blood:	n/a
38	chr5:62074261-62074311	HEK293	kidney:	embryo
39	chr5:62074572-62074622	PrEC	prostate:	n/a
40	chr5:62071572-62071622	AG04449	skin:	fetal
41	chr5:62100540-62100590	PrEC	prostate:	n/a
42	chr5:62074261-62074311	Hela-S3	cervix:	n/a
43	chr5:62014804-62014854	Jurkat	blood:	n/a
44	chr5:62071572-62071622	IMR90	lung:	fetal
45	chr5:62014804-62014854	HRPEpiC	eye:	n/a
46	chr5:61923204-61923254	HCM	heart:	n/a
47	chr5:62100540-62100590	NHDF-neo	bronchial:	n/a
48	chr5:62074261-62074311	HPAEpiC	pulmonary alveolar:	n/a
49	chr5:62100540-62100590	GM19239	blood:	n/a
50	chr5:62073161-62073211	GM12891	blood:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:61756022..61757748-chr5:62074424..62075807,9	MCF-7	breast:
2	chr5:61897835..61900758-chr5:61901696..61904448,2	K562	blood:
3	chr5:62071591..62073108-chr5:62074194..62077077,2	K562	blood:
4	chr5:61912906..61915006-chr5:61917150..61920034,2	K562	blood:
5	chr5:61912906..61915006-chr5:61917150..61920034,2	K562	blood:
6	chr5:61929416..61931059-chr5:61937366..61939285,2	K562	blood:
7	chr5:62036443..62039207-chr5:62041195..62044511,3	K562	blood:
8	chr5:62000604..62002658-chr5:62007528..62009304,2	K562	blood:
9	chr5:61929416..61931059-chr5:61937366..61939285,2	K562	blood:
10	chr5:62002817..62004465-chr5:62011306..62013415,2	K562	blood:
11	chr5:62061013..62063521-chr5:62063661..62066191,2	K562	blood:
12	chr5:61893060..61895061-chr5:61895378..61897801,2	K562	blood:
13	chr5:61898028..61900560-chr5:61910431..61912053,2	MCF-7	breast:
14	chr5:62030684..62032945-chr5:62039649..62042488,2	MCF-7	breast:
15	chr5:62000604..62002658-chr5:62007528..62009304,2	K562	blood:
16	chr5:62078011..62080327-chr5:62081236..62083654,2	K562	blood:
17	chr5:61925893..61927703-chr5:61935030..61937549,2	K562	blood:
18	chr5:61936086..61938123-chr5:61944668..61946794,2	K562	blood:
19	chr5:61756416..61757318-chr5:62074341..62075268,4	K562	blood:
20	chr5:62017098..62019061-chr5:62042354..62044460,2	K562	blood:
21	chr5:61892474..61895061-chr5:61895378..61897729,2	K562	blood:
22	chr5:61944121..61945939-chr5:61947041..61949118,2	K562	blood:
23	chr5:62030684..62032945-chr5:62039649..62042488,2	MCF-7	breast:
24	chr5:62017098..62019061-chr5:62042354..62044460,2	K562	blood:
25	chr5:61909872..61912743-chr5:61916842..61918403,2	MCF-7	breast:
26	chr5:62193925..62195577-chr5:62201485..62203661,2	MCF-7	breast:
27	chr5:61915873..61918235-chr5:61922517..61925303,2	K562	blood:
28	chr5:62002817..62004465-chr5:62011306..62013415,2	K562	blood:
29	chr5:61898028..61900560-chr5:61910431..61912053,2	MCF-7	breast:
30	chr5:61936086..61938123-chr5:61944668..61946794,2	K562	blood:
31	chr5:61944121..61945939-chr5:61947041..61949118,2	K562	blood:
32	chr5:61905876..61908467-chr5:61910449..61913197,3	K562	blood:
33	chr5:61940617..61943358-chr5:61943464..61946144,3	K562	blood:
34	chr5:62068406..62072262-chr5:62073628..62078748,5	K562	blood:
35	chr5:62078011..62080327-chr5:62081236..62083654,2	K562	blood:
36	chr5:61978360..61980328-chr5:61986158..61988132,2	K562	blood:
37	chr5:62177885..62179876-chr5:62180704..62182544,2	K562	blood:
38	chr5:61756074..61756595-chr5:61927958..61928492,2	MCF-7	breast:
39	chr5:61897835..61900758-chr5:61901696..61904448,2	K562	blood:
40	chr5:62069461..62071077-chr5:62076501..62078748,2	K562	blood:
41	chr5:62177885..62179876-chr5:62180704..62182544,2	K562	blood:
42	chr5:61905876..61908467-chr5:61910449..61913197,3	K562	blood:
43	chr5:62069461..62071077-chr5:62076501..62078748,2	K562	blood:
44	chr5:61940617..61943358-chr5:61943464..61946144,3	K562	blood:
45	chr5:62068406..62072262-chr5:62073628..62078748,5	K562	blood:
46	chr5:61886779..61891355-chr5:61892416..61896612,4	K562	blood:
47	chr5:62036443..62039207-chr5:62041195..62044511,3	K562	blood:
48	chr5:61925893..61927703-chr5:61935030..61937549,2	K562	blood:
49	chr5:62061013..62063521-chr5:62063661..62066191,2	K562	blood:
50	chr5:62018815..62021360-chr5:62022661..62025357,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IPO11-2	chr5:61957255-61957780	NONHSAT101718
2	lnc-DIMT1-3	chr5:61938348-61938891	NONHSAT101717
3	lnc-DIMT1-3	chr5:61937940-61938054	NONHSAT101717
4	lnc-IPO11-2	chr5:61963594-61963682	NONHSAT101718

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	IPO11	hsa-miR-16-5p	chr5:61923396-61923417

Variant related genes	Relation type
IPO11	TF binding region
ISCA1P1	TF binding region
IPO11	CpG island
ISCA1P1	CpG island
ENSG00000217416	chromatin interactions
ENSG00000086200	chromatin interactions

Extended variants
information (count: 6377 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:6377 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1477358	chr5:61891622-61891623	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs368738868	chr5:61891666-61891667	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551429292	chr5:61891718-61891719	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs16890854	chr5:61891755-61891756	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs527524747	chr5:61891808-61891809	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541549624	chr5:61891828-61891829	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs62375052	chr5:61891922-61891923	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs79160696	chr5:61891924-61891925	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs76615058	chr5:61891925-61891926	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547175887	chr5:61891950-61891951	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559571636	chr5:61891986-61891987	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567087155	chr5:61892056-61892057	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs375703978	chr5:61892095-61892096	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs3077487	chr5:61892110-61892111	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs180906833	chr5:61892132-61892133	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs139618639	chr5:61892154-61892155	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs184192148	chr5:61892157-61892158	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs545388244	chr5:61892203-61892204	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs115103706	chr5:61892327-61892328	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs73108093	chr5:61892342-61892343	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs568050205	chr5:61892471-61892472	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs149729016	chr5:61892592-61892593	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs534940573	chr5:61892643-61892644	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs555224358	chr5:61892657-61892658	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs190704168	chr5:61892671-61892672	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs115850033	chr5:61892675-61892676	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs557481743	chr5:61892686-61892687	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs577216526	chr5:61892698-61892699	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs201076691	chr5:61892745-61892746	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs546159484	chr5:61892747-61892748	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs115080659	chr5:61892762-61892763	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs181882767	chr5:61892792-61892793	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs186204094	chr5:61892810-61892811	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs563984326	chr5:61892839-61892840	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs190625030	chr5:61892854-61892855	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs529796148	chr5:61892868-61892869	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs61308671	chr5:61892926-61892927	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs569728571	chr5:61892961-61892962	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs532038522	chr5:61892983-61892984	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs144051295	chr5:61893022-61893023	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs181416462	chr5:61893035-61893036	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs535340788	chr5:61893074-61893075	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs116210039	chr5:61893078-61893079	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs75650113	chr5:61893083-61893084	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs78834418	chr5:61893084-61893085	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs146442578	chr5:61893105-61893106	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs111353742	chr5:61893239-61893240	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs537641408	chr5:61893258-61893259	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs557520352	chr5:61893275-61893276	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs543331079	chr5:61893378-61893379	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1238 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61764200-61895800	Weak transcription	Pancreas	Pancrea
2	chr5:61793600-61905000	Weak transcription	NHEK	skin
3	chr5:61796800-61899000	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr5:61803000-61904400	Weak transcription	Fetal Kidney	kidney
5	chr5:61827400-61899200	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr5:61834800-61899200	Weak transcription	Esophagus	oesophagus
7	chr5:61848200-61939600	Weak transcription	Brain Anterior Caudate	brain
8	chr5:61856400-61906400	Weak transcription	Colon Smooth Muscle	Colon
9	chr5:61861400-61902600	Weak transcription	Brain Cingulate Gyrus	brain
10	chr5:61862200-61902600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr5:61863200-61910200	Weak transcription	Right Ventricle	heart
12	chr5:61864200-61899200	Weak transcription	Thymus	Thymus
13	chr5:61864800-61945800	Weak transcription	HSMMtube	muscle
14	chr5:61875000-61906600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr5:61875000-61922200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr5:61875400-61893200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr5:61876200-61904400	Weak transcription	Fetal Muscle Leg	muscle
18	chr5:61879600-61908800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr5:61881400-61939400	Weak transcription	Spleen	Spleen
20	chr5:61881800-61892600	Weak transcription	NHLF	lung
21	chr5:61881800-61901200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr5:61881800-61905200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr5:61882000-61916400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr5:61882200-61902600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr5:61882200-61925400	Weak transcription	Rectal Smooth Muscle	rectum
26	chr5:61883400-61925800	Weak transcription	Psoas Muscle	Psoas
27	chr5:61884000-61910200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr5:61885400-61896200	Weak transcription	HepG2	liver
29	chr5:61885800-61904400	Weak transcription	Brain Hippocampus Middle	brain
30	chr5:61886000-61891800	Weak transcription	Fetal Brain Female	brain
31	chr5:61886800-61941200	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr5:61887000-61912000	Weak transcription	Brain Angular Gyrus	brain
33	chr5:61887000-61922800	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr5:61887400-61903800	Weak transcription	Placenta	Placenta
35	chr5:61888000-61899400	Weak transcription	Fetal Lung	lung
36	chr5:61888200-61898400	Weak transcription	Liver	Liver
37	chr5:61888600-61901000	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr5:61888800-61898800	Weak transcription	Hela-S3	cervix
39	chr5:61888800-61899000	Weak transcription	Ovary	ovary
40	chr5:61888800-61899200	Weak transcription	Duodenum Mucosa	Duodenum
41	chr5:61888800-61899200	Weak transcription	Fetal Stomach	stomach
42	chr5:61888800-61899400	Weak transcription	Aorta	Aorta
43	chr5:61888800-61901600	Weak transcription	Primary T cells fromperipheralblood	blood
44	chr5:61888800-61904800	Weak transcription	Fetal Intestine Small	intestine
45	chr5:61888800-61905000	Weak transcription	GM12878-XiMat	blood
46	chr5:61888800-61905600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr5:61888800-61910400	Weak transcription	Lung	lung
48	chr5:61888800-61928000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr5:61888800-61937000	Weak transcription	Gastric	stomach
50	chr5:61889000-61898400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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