Variant report

Variant	nsv600452
Chromosome Location	chr5:178180299-178241495
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178205915-178206235	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:178214229-178214360	HepG2	liver:	n/a	n/a
3	BACH1	chr5:178214042-178214427	K562	blood:	n/a	n/a
4	BCL3	chr5:178220955-178221285	GM12878	blood:	n/a	n/a
5	BHLHE40	chr5:178213106-178213236	K562	blood:	n/a	n/a
6	BHLHE40	chr5:178223819-178224462	GM12878	blood:	n/a	chr5:178223892-178223901 chr5:178223891-178223900 chr5:178223893-178223902 chr5:178223892-178223901
7	BHLHE40	chr5:178214113-178214496	K562	blood:	n/a	n/a
8	BHLHE40	chr5:178214114-178214477	HepG2	liver:	n/a	n/a
9	BHLHE40	chr5:178205865-178206066	HepG2	liver:	n/a	n/a
10	BHLHE40	chr5:178223850-178223909	K562	blood:	n/a	chr5:178223892-178223901 chr5:178223891-178223900 chr5:178223893-178223902 chr5:178223892-178223901
11	BHLHE40	chr5:178205860-178206179	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:178217335-178217632	Hela-S3	cervix:	n/a	chr5:178217452-178217463 chr5:178217454-178217463
13	CEBPB	chr5:178217367-178217564	HepG2	liver:	n/a	chr5:178217452-178217463 chr5:178217454-178217463
14	CEBPB	chr5:178217275-178217650	HepG2	liver:	n/a	chr5:178217452-178217463 chr5:178217454-178217463
15	CEBPB	chr5:178231504-178231802	MCF-7	breast:	n/a	chr5:178231622-178231633
16	CEBPB	chr5:178213997-178214855	A549	lung:	n/a	chr5:178214591-178214602
17	CEBPB	chr5:178208112-178208488	HepG2	liver:	n/a	chr5:178208294-178208307 chr5:178208295-178208306 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208294-178208307
18	CEBPB	chr5:178208102-178208484	Hela-S3	cervix:	n/a	chr5:178208294-178208307 chr5:178208295-178208306 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208294-178208307
19	CEBPB	chr5:178217180-178217731	MCF-7	breast:	n/a	chr5:178217452-178217463 chr5:178217454-178217463
20	CEBPB	chr5:178212801-178213317	A549	lung:	n/a	chr5:178213039-178213050
21	CEBPB	chr5:178212900-178213209	HepG2	liver:	n/a	chr5:178213039-178213050
22	CEBPB	chr5:178217322-178217546	HepG2	liver:	n/a	chr5:178217452-178217463 chr5:178217454-178217463
23	CEBPB	chr5:178213967-178214852	MCF-7	breast:	n/a	chr5:178214591-178214602
24	CEBPB	chr5:178208159-178208469	K562	blood:	n/a	chr5:178208294-178208307 chr5:178208295-178208306 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208294-178208307
25	CEBPB	chr5:178208108-178208499	A549	lung:	n/a	chr5:178208294-178208307 chr5:178208295-178208306 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208294-178208307
26	CEBPB	chr5:178234405-178234452	HepG2	liver:	n/a	n/a
27	CEBPB	chr5:178208145-178208506	A549	lung:	n/a	chr5:178208294-178208307 chr5:178208295-178208306 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208294-178208307
28	CEBPB	chr5:178231520-178231709	HepG2	liver:	n/a	chr5:178231622-178231633
29	CEBPB	chr5:178208109-178208562	K562	blood:	n/a	chr5:178208294-178208307 chr5:178208295-178208306 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208294-178208307
30	CEBPB	chr5:178217294-178217603	IMR90	lung:	n/a	chr5:178217452-178217463 chr5:178217454-178217463
31	CEBPB	chr5:178196790-178196860	K562	blood:	n/a	n/a
32	CEBPB	chr5:178212822-178213356	A549	lung:	n/a	chr5:178213039-178213050
33	CEBPB	chr5:178208178-178208473	H1-hESC	embryonic stem cell:	n/a	chr5:178208294-178208307 chr5:178208295-178208306 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208294-178208307
34	CEBPB	chr5:178214110-178214713	A549	lung:	n/a	chr5:178214591-178214602
35	CEBPB	chr5:178217276-178217625	K562	blood:	n/a	chr5:178217452-178217463 chr5:178217454-178217463
36	CEBPB	chr5:178217265-178217644	HepG2	liver:	n/a	chr5:178217452-178217463 chr5:178217454-178217463
37	CEBPB	chr5:178208056-178208589	MCF-7	breast:	n/a	chr5:178208294-178208307 chr5:178208295-178208306 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208294-178208307
38	CEBPB	chr5:178217238-178217831	MCF-7	breast:	n/a	chr5:178217452-178217463 chr5:178217454-178217463
39	CEBPB	chr5:178217311-178217619	A549	lung:	n/a	chr5:178217452-178217463 chr5:178217454-178217463
40	CEBPB	chr5:178208119-178208486	IMR90	lung:	n/a	chr5:178208294-178208307 chr5:178208295-178208306 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208294-178208307
41	CEBPB	chr5:178214500-178214659	HepG2	liver:	n/a	chr5:178214591-178214602
42	CEBPB	chr5:178208119-178208539	MCF-7	breast:	n/a	chr5:178208294-178208307 chr5:178208295-178208306 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208296-178208305 chr5:178208294-178208307
43	CEBPD	chr5:178217357-178217583	HepG2	liver:	n/a	chr5:178217453-178217464
44	CHD2	chr5:178224169-178224347	GM12878	blood:	n/a	n/a
45	CTCF	chr5:178220240-178220390	HFF-Myc	foreskin:	n/a	chr5:178220357-178220367 chr5:178220355-178220368 chr5:178220352-178220370 chr5:178220354-178220375 chr5:178220355-178220364
46	CTCF	chr5:178220211-178220515	MCF-7	breast:	n/a	chr5:178220357-178220367 chr5:178220355-178220368 chr5:178220352-178220370 chr5:178220354-178220375 chr5:178220355-178220364
47	CTCF	chr5:178214240-178214390	SAEC	small airway:	n/a	n/a
48	CTCF	chr5:178186730-178186766	Lung_OC	lung:	n/a	n/a
49	CTCF	chr5:178194591-178194881	K562	blood:	n/a	chr5:178194716-178194729 chr5:178194713-178194731
50	CTCF	chr5:178220229-178220484	K562	blood:	n/a	chr5:178220357-178220367 chr5:178220355-178220368 chr5:178220352-178220370 chr5:178220354-178220375 chr5:178220355-178220364

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178195589-178195639	SK-N-SH	brain:	n/a
2	chr5:178195589-178195639	SK-N-SH	brain:	n/a
3	chr5:178195556-178195606	HRCEpiC	kidney:	n/a
4	chr5:178204356-178204406	PANC-1	pancreas:	n/a
5	chr5:178220967-178221017	HCM	heart:	n/a
6	chr5:178213543-178213593	HAEpiC	amniotic membrane:	n/a
7	chr5:178215887-178215937	GM12891	blood:	n/a
8	chr5:178204766-178204816	GM06990	blood:	n/a
9	chr5:178208957-178209007	Jurkat	blood:	n/a
10	chr5:178209272-178209322	SAEC	small airway:	n/a
11	chr5:178203469-178203519	SKMC	muscle:	n/a
12	chr5:178208550-178208600	NT2-D1	testis:	n/a
13	chr5:178204356-178204406	ovcar-3	ovarian:	n/a
14	chr5:178215887-178215937	HRE	kidney:	n/a
15	chr5:178204356-178204406	GM19239	blood:	n/a
16	chr5:178208550-178208600	ECC-1	luminal epithelium:	n/a
17	chr5:178208957-178209007	HIPEpiC	eye:	n/a
18	chr5:178220967-178221017	HEEpiC	esophagus:	n/a
19	chr5:178209272-178209322	HCT-116	colon:	n/a
20	chr5:178199408-178199458	HIPEpiC	eye:	n/a
21	chr5:178203469-178203519	HPAEpiC	pulmonary alveolar:	n/a
22	chr5:178195589-178195639	SK-N-SH_RA	brain:	n/a
23	chr5:178204356-178204406	IMR90	lung:	fetal
24	chr5:178213543-178213593	PANC-1	pancreas:	n/a
25	chr5:178208610-178208660	GM12892	blood:	n/a
26	chr5:178208957-178209007	NHDF-neo	bronchial:	n/a
27	chr5:178195556-178195606	GM12891	blood:	n/a
28	chr5:178204763-178204813	HCT-116	colon:	n/a
29	chr5:178220238-178220288	GM06990	blood:	n/a
30	chr5:178203469-178203519	A549	lung:	n/a
31	chr5:178220967-178221017	K562	blood:	n/a
32	chr5:178220238-178220288	AG04449	skin:	fetal
33	chr5:178204763-178204813	T-47D	breast:	n/a
34	chr5:178209272-178209322	HCM	heart:	n/a
35	chr5:178209199-178209249	GM06990	blood:	n/a
36	chr5:178203432-178203482	K562	blood:	n/a
37	chr5:178195556-178195606	SK-N-MC	brain:	n/a
38	chr5:178220967-178221017	Hepatocyte	liver:	n/a
39	chr5:178209759-178209809	ProgFib	skin:	n/a
40	chr5:178208957-178209007	ovcar-3	ovarian:	n/a
41	chr5:178208957-178209007	AG04449	skin:	fetal
42	chr5:178208610-178208660	NT2-D1	testis:	n/a
43	chr5:178204763-178204813	HRPEpiC	eye:	n/a
44	chr5:178199408-178199458	NB4	blood:	n/a
45	chr5:178204356-178204406	SK-N-MC	brain:	n/a
46	chr5:178195589-178195639	Hela-S3	cervix:	n/a
47	chr5:178220238-178220288	NT2-D1	testis:	n/a
48	chr5:178195589-178195639	HMEC	breast:	n/a
49	chr5:178204766-178204816	AG09319	gingival:	n/a
50	chr5:178204766-178204816	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:177630127..177632197-chr5:178212770..178214294,2	MCF-7	breast:
2	chr5:178217515..178219756-chr5:178222476..178225165,2	MCF-7	breast:
3	chr5:178157501..178158373-chr5:178219857..178220443,3	MCF-7	breast:
4	chr5:178219922..178220838-chr5:178920668..178921270,2	MCF-7	breast:
5	chr5:178219826..178220832-chr5:178266011..178266987,10	MCF-7	breast:
6	chr5:178211735..178215494-chr5:178218190..178221753,4	MCF-7	breast:
7	chr5:178211735..178215494-chr5:178218190..178221753,4	MCF-7	breast:
8	chr5:178189340..178191048-chr5:178195069..178197316,2	MCF-7	breast:
9	chr5:178223973..178226497-chr5:178266303..178268866,2	MCF-7	breast:
10	chr5:178195480..178197937-chr5:178198452..178200736,2	MCF-7	breast:
11	chr5:178219935..178220578-chr5:178266097..178266710,3	MCF-7	breast:
12	chr5:178238402..178240858-chr5:178245759..178247482,2	K562	blood:
13	chr5:178189340..178191048-chr5:178195069..178197316,2	MCF-7	breast:
14	chr5:178219952..178220766-chr5:178688074..178688887,3	MCF-7	breast:
15	chr5:178209012..178209534-chr7:62475815..62476717,2	MCF-7	breast:
16	chr5:177659037..177660828-chr5:178212887..178215227,2	MCF-7	breast:
17	chr5:178214124..178214763-chr5:178265905..178266637,2	MCF-7	breast:
18	chr5:178219841..178220793-chr5:178920740..178921735,2	MCF-7	breast:
19	chr5:177657932..177660784-chr5:178214332..178216670,2	MCF-7	breast:
20	chr5:178195480..178197937-chr5:178198452..178200736,2	MCF-7	breast:
21	chr1:149207614..149210594-chr5:178225995..178227496,2	MCF-7	breast:
22	chr5:170259431..170263893-chr5:178180791..178183224,3	MCF-7	breast:
23	chr5:178155431..178159106-chr5:178210602..178214832,4	MCF-7	breast:
24	chr5:178219910..178220433-chr5:178257274..178257901,2	MCF-7	breast:
25	chr5:178228775..178231759-chr5:178257850..178260513,2	MCF-7	breast:
26	chr5:178157437..178158143-chr5:178214195..178215016,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF354A-3	chr5:178181044-178181218	NONHSAT105547

Variant related genes	Relation type
AACSP1	TF binding region
AACSP1	CpG island
ENSG00000169131	chromatin interactions
ENSG00000253725	chromatin interactions
ENSG00000250420	chromatin interactions
ENSG00000175309	chromatin interactions
ENSG00000197451	chromatin interactions

Extended variants
information (count: 3351 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:3351 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4280887	chr5:178180299-178180300	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188962513	chr5:178180302-178180303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138463394	chr5:178180306-178180307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs527274273	chr5:178180393-178180394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370114248	chr5:178180400-178180401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs552102940	chr5:178180429-178180430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570662882	chr5:178180430-178180431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532013787	chr5:178180446-178180447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368062373	chr5:178180478-178180479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs34739968	chr5:178180483-178180484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10074058	chr5:178180484-178180485	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs556104872	chr5:178180517-178180518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568221662	chr5:178180527-178180528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs536391256	chr5:178180529-178180530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554643747	chr5:178180554-178180555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186487469	chr5:178180586-178180587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190976453	chr5:178180588-178180589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181042888	chr5:178180671-178180672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577489323	chr5:178180677-178180678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561791236	chr5:178180728-178180729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544868419	chr5:178180763-178180764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562974698	chr5:178180781-178180782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554795265	chr5:178180831-178180832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530307454	chr5:178180833-178180834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372447648	chr5:178180855-178180856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73804481	chr5:178180865-178180866	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs13175048	chr5:178180868-178180869	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs72812657	chr5:178180874-178180875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141490733	chr5:178180901-178180902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs13154686	chr5:178180916-178180917	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs201313230	chr5:178180976-178180977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550042135	chr5:178180987-178180988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs62393873	chr5:178180991-178180992	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs535274761	chr5:178181004-178181005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs370370425	chr5:178181009-178181010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553511696	chr5:178181015-178181016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs146187468	chr5:178181022-178181023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534271979	chr5:178181028-178181029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558710762	chr5:178181065-178181066	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs538679082	chr5:178181090-178181091	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs577154332	chr5:178181102-178181103	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs12513687	chr5:178181111-178181112	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs535095350	chr5:178181134-178181135	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs386695501	chr5:178181145-178181146	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs73804482	chr5:178181147-178181148	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs538162926	chr5:178181162-178181163	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs187378264	chr5:178181173-178181174	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs560632102	chr5:178181189-178181190	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs572190398	chr5:178181236-178181237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs190853345	chr5:178181256-178181257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
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
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:174 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178166600-178224000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr5:178179800-178181000	Weak transcription	Fetal Kidney	kidney
3	chr5:178180200-178180800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:178180600-178181200	Enhancers	Fetal Intestine Large	intestine
5	chr5:178181000-178182000	Enhancers	Fetal Kidney	kidney
6	chr5:178181400-178186200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr5:178182000-178182400	Weak transcription	Fetal Kidney	kidney
8	chr5:178182400-178183000	Enhancers	Fetal Kidney	kidney
9	chr5:178183400-178213200	Weak transcription	K562	blood
10	chr5:178185200-178188000	Enhancers	Placenta	Placenta
11	chr5:178188000-178189400	Weak transcription	Placenta	Placenta
12	chr5:178189400-178190600	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr5:178189400-178190600	Enhancers	Placenta	Placenta
14	chr5:178189600-178190000	Enhancers	Esophagus	oesophagus
15	chr5:178189800-178190000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr5:178190000-178190400	Weak transcription	Esophagus	oesophagus
17	chr5:178190000-178192800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr5:178190400-178190600	Enhancers	Esophagus	oesophagus
19	chr5:178190600-178192600	Weak transcription	Esophagus	oesophagus
20	chr5:178192600-178195000	Enhancers	Esophagus	oesophagus
21	chr5:178192800-178193000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr5:178194000-178194200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr5:178194200-178195800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr5:178195000-178195200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr5:178195600-178196400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr5:178195800-178196000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr5:178196000-178199400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr5:178196400-178197000	Enhancers	Pancreas	Pancrea
29	chr5:178196600-178197000	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr5:178196600-178197200	Enhancers	Adipose Nuclei	Adipose
31	chr5:178196600-178197200	Enhancers	Fetal Lung	lung
32	chr5:178196600-178197400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr5:178196800-178197200	Enhancers	Esophagus	oesophagus
34	chr5:178196800-178197200	Enhancers	Fetal Muscle Leg	muscle
35	chr5:178197600-178198400	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr5:178198400-178202800	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr5:178199400-178199600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr5:178199400-178199600	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
39	chr5:178199600-178199800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr5:178199800-178200800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr5:178200600-178201000	Bivalent Enhancer	HepG2	liver
42	chr5:178200800-178201000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr5:178201000-178201800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr5:178201800-178203000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr5:178202000-178202600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr5:178202800-178204400	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr5:178202800-178208400	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr5:178203000-178203200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr5:178203000-178203400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr5:178203000-178206600	Enhancers	Primary neutrophils fromperipheralblood	blood

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