Variant report

Variant	nsv427720
Chromosome Location	chr5:58913581-59086987
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2467)
CpG islands
(count:672)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:2467 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:59055857-59056165	HepG2	liver:	n/a	chr5:59056128-59056144
2	ARID3A	chr5:59052164-59052634	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:58969309-58969587	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:58957641-58958039	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:58960994-58961180	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:59047127-59047447	HepG2	liver:	n/a	n/a
7	ATF2	chr5:59005081-59005496	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr5:59005135-59005567	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr5:59055287-59055893	A549	lung:	n/a	n/a
10	BACH1	chr5:59069118-59069478	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:58918847-58919049	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:59009027-59009230	K562	blood:	n/a	n/a
13	BATF	chr5:58981051-58981275	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:59005221-59005381	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr5:59005117-59005450	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL11A	chr5:58948417-58948651	GM12878	blood:	n/a	n/a
17	BCL3	chr5:59052219-59052547	GM12878	blood:	n/a	n/a
18	BCL3	chr5:59052168-59052553	GM12878	blood:	n/a	n/a
19	BCL3	chr5:59041912-59042688	A549	lung:	n/a	n/a
20	BCL3	chr5:59052159-59052701	A549	lung:	n/a	n/a
21	BCL3	chr5:59051983-59052744	A549	lung:	n/a	chr5:59051989-59051998
22	BCL3	chr5:59041024-59041803	A549	lung:	n/a	n/a
23	BCL3	chr5:59047253-59047586	GM12878	blood:	n/a	chr5:59047326-59047335
24	BCL3	chr5:59086057-59086868	A549	lung:	n/a	n/a
25	BCL3	chr5:59055323-59055863	A549	lung:	n/a	n/a
26	BCL3	chr5:59063625-59065317	A549	lung:	n/a	chr5:59064669-59064682
27	BCL3	chr5:59063930-59064948	A549	lung:	n/a	chr5:59064669-59064682
28	BCL3	chr5:59042027-59042748	A549	lung:	n/a	n/a
29	BCL3	chr5:59054989-59056388	A549	lung:	n/a	chr5:59055995-59056004
30	BHLHE40	chr5:59064450-59064828	HepG2	liver:	n/a	n/a
31	BHLHE40	chr5:59041278-59041705	A549	lung:	n/a	n/a
32	BHLHE40	chr5:58945013-58945327	K562	blood:	n/a	n/a
33	BHLHE40	chr5:58956285-58956315	GM12878	blood:	n/a	n/a
34	BHLHE40	chr5:59052269-59052540	HepG2	liver:	n/a	n/a
35	BRCA1	chr5:59067948-59069744	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr5:59082267-59082761	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr5:59063436-59065003	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr5:59040298-59042224	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr5:59017406-59017428	GM12878	blood:	n/a	n/a
40	BRCA1	chr5:59086174-59086936	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr5:59052295-59052858	HepG2	liver:	n/a	chr5:59052679-59052690
42	CEBPB	chr5:58999729-58999865	A549	lung:	n/a	n/a
43	CEBPB	chr5:59082134-59082821	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr5:58974871-58975073	A549	lung:	n/a	chr5:58974960-58974971 chr5:58974962-58974971 chr5:58975045-58975058
45	CEBPB	chr5:58944191-58944463	Hela-S3	cervix:	n/a	chr5:58944238-58944247 chr5:58944238-58944249
46	CEBPB	chr5:58918730-58919007	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr5:58974841-58975128	Hela-S3	cervix:	n/a	chr5:58974960-58974971 chr5:58974962-58974971 chr5:58975045-58975058
48	CEBPB	chr5:59047750-59048047	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr5:59052496-59052768	Hela-S3	cervix:	n/a	chr5:59052679-59052690
50	CEBPB	chr5:59041225-59041521	IMR90	lung:	n/a	chr5:59041353-59041366

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:59064378-59064428	IMR90	lung:	fetal
2	chr5:59064378-59064428	IMR90	lung:	fetal
3	chr5:59064389-59064439	SK-N-SH_RA	brain:	n/a
4	chr5:59064235-59064285	NT2-D1	testis:	n/a
5	chr5:59064523-59064573	GM06990	blood:	n/a
6	chr5:59064378-59064428	HNPCEpiC	eye:	n/a
7	chr5:59064579-59064629	SK-N-MC	brain:	n/a
8	chr5:59064630-59064680	GM06990	blood:	n/a
9	chr5:59064517-59064567	SKMC	muscle:	n/a
10	chr5:59064389-59064439	GM12891	blood:	n/a
11	chr5:59064235-59064285	GM19239	blood:	n/a
12	chr5:59064378-59064428	HCF	heart:	n/a
13	chr5:59064579-59064629	ProgFib	skin:	n/a
14	chr5:59086432-59086482	AG04450	lung:	fetal
15	chr5:59064378-59064428	NB4	blood:	n/a
16	chr5:59064517-59064567	AG10803	skin:	n/a
17	chr5:59064630-59064680	PFSK-1	brain:	n/a
18	chr5:59064682-59064732	ProgFib	skin:	n/a
19	chr5:59086432-59086482	ProgFib	skin:	n/a
20	chr5:59064378-59064428	T-47D	breast:	n/a
21	chr5:59064523-59064573	HL-60	blood:	n/a
22	chr5:59086432-59086482	HPAEpiC	pulmonary alveolar:	n/a
23	chr5:59086432-59086482	NB4	blood:	n/a
24	chr5:59064579-59064629	HCM	heart:	n/a
25	chr5:59064682-59064732	HCT-116	colon:	n/a
26	chr5:59064235-59064285	AG09309	skin:	n/a
27	chr5:59064517-59064567	GM12878	blood:	n/a
28	chr5:59064579-59064629	LNCaP	prostate:	n/a
29	chr5:59064235-59064285	PrEC	prostate:	n/a
30	chr5:59086432-59086482	SK-N-SH	brain:	n/a
31	chr5:59072686-59072736	AG09309	skin:	n/a
32	chr5:59064389-59064439	H1-hESC	embryonic stem cell:	embryo
33	chr5:59064389-59064439	HepG2	liver:	n/a
34	chr5:59086432-59086482	HNPCEpiC	eye:	n/a
35	chr5:59086432-59086482	Hepatocyte	liver:	n/a
36	chr5:58957910-58957960	AG10803	skin:	n/a
37	chr5:59064517-59064567	PANC-1	pancreas:	n/a
38	chr5:59064630-59064680	SK-N-MC	brain:	n/a
39	chr5:59064389-59064439	K562	blood:	n/a
40	chr5:59064389-59064439	SAEC	small airway:	n/a
41	chr5:58957910-58957960	HCT-116	colon:	n/a
42	chr5:59072686-59072736	HIPEpiC	eye:	n/a
43	chr5:59072686-59072736	LNCaP	prostate:	n/a
44	chr5:59086432-59086482	Jurkat	blood:	n/a
45	chr5:59064517-59064567	ProgFib	skin:	n/a
46	chr5:59064517-59064567	HRE	kidney:	n/a
47	chr5:59072686-59072736	HCM	heart:	n/a
48	chr5:59064682-59064732	HEEpiC	esophagus:	n/a
49	chr5:59064235-59064285	U87	brain:	n/a
50	chr5:59064235-59064285	IMR90	lung:	fetal

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:58802090..58802764-chr5:58956093..58957045,3	MCF-7	breast:
2	chr5:59042416..59043177-chr6:10415490..10415996,2	Hela-S3	cervix:
3	chr5:58919593..58921213-chr5:58924380..58926616,2	MCF-7	breast:
4	chr5:58915352..58918200-chr5:58918396..58920310,2	MCF-7	breast:
5	chr5:58803075..58803840-chr5:58956390..58957074,2	MCF-7	breast:
6	chr11:65268788..65269336-chr5:59059488..59060259,2	Hela-S3	cervix:
7	chr12:53139319..53140001-chr5:58956637..58957236,2	MCF-7	breast:
8	chr5:58938220..58940371-chr5:58941651..58943411,2	MCF-7	breast:
9	chr5:58821597..58822483-chr5:58956197..58956887,3	MCF-7	breast:
10	chr5:58685998..58686505-chr5:58956311..58957192,2	MCF-7	breast:
11	chr5:58921699..58924088-chr5:58961415..58963109,2	MCF-7	breast:
12	chr5:58909037..58911630-chr5:58912245..58914996,2	K562	blood:
13	chr10:99093900..99094504-chr5:59063199..59063729,2	Hela-S3	cervix:
14	chr5:58801867..58802786-chr5:58968976..58969858,3	MCF-7	breast:
15	chr5:58803367..58805536-chr5:58956722..58959458,2	MCF-7	breast:
16	chr5:58921699..58924088-chr5:58961415..58963109,2	MCF-7	breast:
17	chr5:58915352..58918200-chr5:58918396..58920310,2	MCF-7	breast:
18	chr5:58956441..58957361-chr5:58968943..58969531,2	MCF-7	breast:
19	chr5:59022602..59025084-chr5:59040662..59042603,2	MCF-7	breast:
20	chr5:59002219..59005898-chr5:59006477..59009673,3	K562	blood:
21	chr5:58938220..58940371-chr5:58941651..58943411,2	MCF-7	breast:
22	chr5:58801995..58802802-chr5:58968998..58969985,2	MCF-7	breast:
23	chr5:58956441..58957361-chr5:58968943..58969531,2	MCF-7	breast:
24	chr5:59022602..59025084-chr5:59040662..59042603,2	MCF-7	breast:
25	chr5:59085744..59087906-chr5:59088999..59091482,2	K562	blood:
26	chr1:28969284..28970055-chr5:59064238..59065007,2	Hela-S3	cervix:
27	chr5:58968638..58970043-chr5:59019689..59021106,4	MCF-7	breast:
28	chr12:17875088..17875599-chr5:58957118..58957618,2	Hela-S3	cervix:
29	chr5:58919593..58921213-chr5:58924380..58926616,2	MCF-7	breast:
30	chr5:58801963..58802644-chr5:58962690..58963296,2	MCF-7	breast:
31	chr11:62608526..62609390-chr5:59060896..59061540,2	Hela-S3	cervix:
32	chr5:59085766..59086766-chr9:132250884..132251680,2	Hela-S3	cervix:
33	chr5:58969044..58969563-chr5:59095719..59096533,2	MCF-7	breast:
34	chr3:12882807..12883499-chr5:59064404..59064928,2	Hela-S3	cervix:
35	chr14:81687360..81688109-chr5:59063848..59064610,2	Hela-S3	cervix:
36	chr5:58801872..58802902-chr5:58956210..58957251,7	MCF-7	breast:
37	chr5:58801703..58803307-chr5:58968055..58970489,2	MCF-7	breast:
38	chr5:59085744..59088656-chr5:59089982..59093707,3	K562	blood:
39	chr5:58968638..58970043-chr5:59019689..59021106,4	MCF-7	breast:
40	chr5:59002219..59005898-chr5:59006477..59009673,3	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-582-3p	chr5:58999456-58999477	MIMAT0004797
hsa-miR-582-5p	chr5:58999492-58999514	MIMAT0003247

No data

Variant related genes	Relation type
MIR582	TF binding region
PDE4D	TF binding region
MIR582	CpG island
PDE4D	CpG island
ENSG00000120656	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000144713	chromatin interactions
ENSG00000225850	chromatin interactions
ENSG00000165417	chromatin interactions
ENSG00000204054	chromatin interactions
ENSG00000181274	chromatin interactions
ENSG00000229388	chromatin interactions
MCL1	Mature miRNA region

Extended variants
information (count: 6055 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:6055 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552921038	chr5:58913594-58913595	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs144372768	chr5:58913629-58913630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573003292	chr5:58913701-58913702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs79153638	chr5:58913716-58913717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561835800	chr5:58913720-58913721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531057304	chr5:58913743-58913744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs149234107	chr5:58913746-58913747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs12653257	chr5:58913770-58913771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs62355584	chr5:58913794-58913795	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs298017	chr5:58913833-58913834	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs552221735	chr5:58913834-58913835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564519628	chr5:58913836-58913837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565640907	chr5:58913861-58913862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144442777	chr5:58913875-58913876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs148584585	chr5:58913878-58913879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568127403	chr5:58913895-58913896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536883763	chr5:58913928-58913929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144135608	chr5:58913973-58913974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs62355585	chr5:58913988-58913989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs570677129	chr5:58914086-58914087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182018793	chr5:58914127-58914128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs7710565	chr5:58914128-58914129	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs572940854	chr5:58914181-58914182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186902903	chr5:58914226-58914227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555689293	chr5:58914254-58914255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535453741	chr5:58914293-58914294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555467243	chr5:58914307-58914308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575676565	chr5:58914317-58914318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs544492316	chr5:58914387-58914388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs564671372	chr5:58914398-58914399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557276858	chr5:58914411-58914412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs578195875	chr5:58914466-58914467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540971505	chr5:58914517-58914518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10056137	chr5:58914562-58914563	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs528123975	chr5:58914575-58914576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536441106	chr5:58914646-58914647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575742979	chr5:58914651-58914652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372533357	chr5:58914703-58914704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191445924	chr5:58914714-58914715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183761866	chr5:58914724-58914725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530600444	chr5:58914725-58914726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186170781	chr5:58914728-58914729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190260356	chr5:58914788-58914789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10037874	chr5:58914803-58914804	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs182190923	chr5:58914835-58914836	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs186750262	chr5:58914856-58914857	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs140893639	chr5:58914891-58914892	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs192432028	chr5:58914915-58914916	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs10805516	chr5:58914930-58914931	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs575668071	chr5:58915023-58915024	Weak transcription Genic enhancers	n/a	n/a	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
Autism	22495311	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
Acute myeloid leukemia	20729466	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	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
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD

Chromatin state (count:2189 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:58897600-58915800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:58905600-58915800	Weak transcription	HSMMtube	muscle
3	chr5:58908400-58915600	Weak transcription	Primary B cells from cord blood	blood
4	chr5:58910400-58913600	Enhancers	A549	lung
5	chr5:58911400-58929600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr5:58911600-58915200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:58911800-58915200	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr5:58911800-58915200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr5:58911800-58915200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr5:58911800-58915400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr5:58911800-58915800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr5:58911800-58916600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr5:58911800-58918400	Weak transcription	Hela-S3	cervix
14	chr5:58912200-58915400	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr5:58912400-58915200	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr5:58912400-58915800	Weak transcription	HSMM	muscle
17	chr5:58912600-58916000	Weak transcription	Osteobl	bone
18	chr5:58913000-58913600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
19	chr5:58913000-58913800	Enhancers	Fetal Intestine Small	intestine
20	chr5:58913000-58914400	Enhancers	Psoas Muscle	Psoas
21	chr5:58913200-58913600	Active TSS	Duodenum Mucosa	Duodenum
22	chr5:58913200-58913600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
23	chr5:58913200-58913600	Flanking Active TSS	Stomach Mucosa	stomach
24	chr5:58913200-58913800	Enhancers	Placenta Amnion	Placenta Amnion
25	chr5:58913400-58913600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr5:58913400-58913800	Enhancers	Aorta	Aorta
27	chr5:58913400-58914400	Enhancers	Colon Smooth Muscle	Colon
28	chr5:58913600-58913800	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr5:58913600-58914200	Enhancers	Stomach Mucosa	stomach
30	chr5:58913600-58914400	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr5:58913600-58914400	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr5:58913600-58914800	Weak transcription	A549	lung
33	chr5:58913800-58914200	Weak transcription	Aorta	Aorta
34	chr5:58913800-58918800	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr5:58914200-58914400	Enhancers	Aorta	Aorta
36	chr5:58914200-58919200	Weak transcription	Stomach Mucosa	stomach
37	chr5:58914400-58915400	Weak transcription	Aorta	Aorta
38	chr5:58914400-58922600	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr5:58914400-58923400	Weak transcription	Colon Smooth Muscle	Colon
40	chr5:58914400-58923400	Weak transcription	Psoas Muscle	Psoas
41	chr5:58914800-58915400	Genic enhancers	A549	lung
42	chr5:58915200-58915600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr5:58915200-58915600	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr5:58915200-58915800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr5:58915200-58915800	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr5:58915200-58916000	Enhancers	H9 Cell Line	embryonic stem cell
47	chr5:58915200-58917600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr5:58915400-58915600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr5:58915400-58916200	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr5:58915400-58916200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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