Variant report

Variant	nsv830316
Chromosome Location	chr5:59480269-59689829
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1591)
CpG islands
(count:244)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1591 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:59573336-59573776	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:59553354-59554437	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:59502114-59502626	HepG2	liver:	n/a	n/a
4	ATF1	chr5:59666959-59667190	K562	blood:	n/a	n/a
5	ATF1	chr5:59560365-59560521	K562	blood:	n/a	n/a
6	ATF1	chr5:59514975-59515053	K562	blood:	n/a	n/a
7	ATF1	chr5:59591131-59591303	K562	blood:	n/a	n/a
8	ATF2	chr5:59628380-59628787	GM12878	blood:	n/a	n/a
9	ATF2	chr5:59638900-59639325	GM12878	blood:	n/a	n/a
10	ATF2	chr5:59636629-59637086	GM12878	blood:	n/a	n/a
11	ATF2	chr5:59628371-59628819	GM12878	blood:	n/a	n/a
12	BACH1	chr5:59589412-59589738	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr5:59628471-59628765	GM12878	blood:	n/a	chr5:59628607-59628617
14	BATF	chr5:59544689-59545104	GM12878	blood:	n/a	n/a
15	BATF	chr5:59636767-59637051	GM12878	blood:	n/a	n/a
16	BATF	chr5:59638975-59639243	GM12878	blood:	n/a	chr5:59639144-59639153
17	BATF	chr5:59636663-59637052	GM12878	blood:	n/a	n/a
18	BATF	chr5:59628408-59629278	GM12878	blood:	n/a	chr5:59628607-59628617
19	BATF	chr5:59638945-59639333	GM12878	blood:	n/a	chr5:59639144-59639153
20	BCL11A	chr5:59544756-59545152	GM12878	blood:	n/a	n/a
21	BCL11A	chr5:59675732-59676009	GM12878	blood:	n/a	n/a
22	BCL11A	chr5:59558736-59559148	GM12878	blood:	n/a	n/a
23	BCL11A	chr5:59636664-59637040	GM12878	blood:	n/a	n/a
24	BCL11A	chr5:59544746-59545162	GM12878	blood:	n/a	n/a
25	BCLAF1	chr5:59635114-59635571	GM12878	blood:	n/a	chr5:59635449-59635458
26	BCLAF1	chr5:59544682-59545205	GM12878	blood:	n/a	n/a
27	BCLAF1	chr5:59636663-59637114	GM12878	blood:	n/a	n/a
28	BHLHE40	chr5:59503027-59503254	GM12878	blood:	n/a	n/a
29	BHLHE40	chr5:59558766-59559019	GM12878	blood:	n/a	n/a
30	BHLHE40	chr5:59481108-59481445	GM12878	blood:	n/a	n/a
31	BHLHE40	chr5:59635331-59635475	GM12878	blood:	n/a	n/a
32	BHLHE40	chr5:59675753-59676051	GM12878	blood:	n/a	n/a
33	BRCA1	chr5:59492191-59492593	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr5:59591368-59591596	HepG2	liver:	n/a	n/a
35	CBX3	chr5:59582918-59583409	HCT-116	colon:	n/a	n/a
36	CCNT2	chr5:59520133-59520333	K562	blood:	n/a	n/a
37	CEBPB	chr5:59599732-59600028	IMR90	lung:	n/a	n/a
38	CEBPB	chr5:59565465-59565782	A549	lung:	n/a	chr5:59565595-59565606
39	CEBPB	chr5:59591285-59591644	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:59642259-59642588	Hela-S3	cervix:	n/a	chr5:59642344-59642355 chr5:59642344-59642355 chr5:59642340-59642351
41	CEBPB	chr5:59591309-59591702	A549	lung:	n/a	n/a
42	CEBPB	chr5:59642215-59642550	A549	lung:	n/a	chr5:59642344-59642355 chr5:59642344-59642355 chr5:59642340-59642351
43	CEBPB	chr5:59591290-59591652	A549	lung:	n/a	n/a
44	CEBPB	chr5:59680462-59680758	A549	lung:	n/a	n/a
45	CEBPB	chr5:59591291-59591686	MCF-7	breast:	n/a	n/a
46	CEBPB	chr5:59591279-59591650	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr5:59502022-59502560	HepG2	liver:	n/a	chr5:59502187-59502200 chr5:59502377-59502390
48	CEBPB	chr5:59495113-59495419	IMR90	lung:	n/a	chr5:59495276-59495289 chr5:59495278-59495287 chr5:59495134-59495146 chr5:59495276-59495287
49	CEBPB	chr5:59664424-59664526	Hela-S3	cervix:	n/a	chr5:59664510-59664521
50	CEBPB	chr5:59680471-59680692	Hela-S3	cervix:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:59619821-59619871	HepG2	liver:	n/a
2	chr5:59559180-59559230	HCF	heart:	n/a
3	chr5:59619821-59619871	Hepatocyte	liver:	n/a
4	chr5:59559218-59559268	AG04450	lung:	fetal
5	chr5:59619821-59619871	PANC-1	pancreas:	n/a
6	chr5:59559180-59559230	HNPCEpiC	eye:	n/a
7	chr5:59559062-59559112	U87	brain:	n/a
8	chr5:59559062-59559112	LNCaP	prostate:	n/a
9	chr5:59559218-59559268	MCF10A-Er-Src	breast:	n/a
10	chr5:59619821-59619871	AG09319	gingival:	n/a
11	chr5:59619821-59619871	HEK293	kidney:	embryo
12	chr5:59559180-59559230	SKMC	muscle:	n/a
13	chr5:59559062-59559112	HIPEpiC	eye:	n/a
14	chr5:59559062-59559112	PrEC	prostate:	n/a
15	chr5:59559062-59559112	GM06990	blood:	n/a
16	chr5:59619821-59619871	K562	blood:	n/a
17	chr5:59559180-59559230	HL-60	blood:	n/a
18	chr5:59559180-59559230	CMK	blood:	n/a
19	chr5:59559218-59559268	GM12878	blood:	n/a
20	chr5:59559062-59559112	NB4	blood:	n/a
21	chr5:59559062-59559112	NHDF-neo	bronchial:	n/a
22	chr5:59559218-59559268	HAEpiC	amniotic membrane:	n/a
23	chr5:59559062-59559112	HCF	heart:	n/a
24	chr5:59559180-59559230	Hepatocyte	liver:	n/a
25	chr5:59619821-59619871	HIPEpiC	eye:	n/a
26	chr5:59559218-59559268	HIPEpiC	eye:	n/a
27	chr5:59559062-59559112	CMK	blood:	n/a
28	chr5:59559180-59559230	ovcar-3	ovarian:	n/a
29	chr5:59559180-59559230	SK-N-MC	brain:	n/a
30	chr5:59559180-59559230	NHBE	bronchial:	n/a
31	chr5:59619821-59619871	ECC-1	luminal epithelium:	n/a
32	chr5:59619821-59619871	HRE	kidney:	n/a
33	chr5:59619821-59619871	GM12891	blood:	n/a
34	chr5:59559180-59559230	BJ	skin:	n/a
35	chr5:59559180-59559230	HCPEpiC	choroid plexus:	n/a
36	chr5:59559218-59559268	ovcar-3	ovarian:	n/a
37	chr5:59619821-59619871	PFSK-1	brain:	n/a
38	chr5:59559062-59559112	K562	blood:	n/a
39	chr5:59559218-59559268	SKMC	muscle:	n/a
40	chr5:59559218-59559268	NHDF-neo	bronchial:	n/a
41	chr5:59559218-59559268	HUVEC	blood vessel:	n/a
42	chr5:59559062-59559112	ProgFib	skin:	n/a
43	chr5:59559218-59559268	PFSK-1	brain:	n/a
44	chr5:59559062-59559112	SK-N-SH_RA	brain:	n/a
45	chr5:59619821-59619871	ProgFib	skin:	n/a
46	chr5:59559180-59559230	SK-N-SH_RA	brain:	n/a
47	chr5:59559180-59559230	MCF-7	breast:	n/a
48	chr5:59559062-59559112	HCM	heart:	n/a
49	chr5:59559062-59559112	H1-hESC	embryonic stem cell:	embryo
50	chr5:59559062-59559112	HMEC	breast:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:59109870..59110665-chr5:59582813..59583691,3	MCF-7	breast:
2	chr5:59105509..59106419-chr5:59678283..59679226,3	MCF-7	breast:
3	chr5:59590922..59592157-chr5:59678281..59679194,10	MCF-7	breast:
4	chr5:59105855..59106437-chr5:59582746..59583636,2	MCF-7	breast:
5	chr5:59636747..59637753-chr5:59650701..59651624,3	MCF-7	breast:
6	chr5:59105757..59106471-chr5:59582762..59583638,3	MCF-7	breast:
7	chr5:59590961..59591565-chr5:59678761..59679630,2	MCF-7	breast:
8	chr5:59525141..59527803-chr5:59530452..59533157,2	MCF-7	breast:
9	chr5:59590922..59592157-chr5:59678281..59679194,10	MCF-7	breast:
10	chr5:59630941..59633052-chr5:59638055..59640413,2	K562	blood:
11	chr5:59624456..59627842-chr5:59630040..59632479,3	K562	blood:
12	chr5:59589888..59590741-chr5:59944874..59945467,2	MCF-7	breast:
13	chr5:59590976..59591892-chr5:59964196..59965108,2	MCF-7	breast:
14	chr5:59591035..59591843-chr5:59881984..59882629,2	MCF-7	breast:
15	chr5:59591127..59591873-chr5:59964222..59965152,2	MCF-7	breast:
16	chr5:59109357..59110129-chr5:59582693..59583574,6	MCF-7	breast:
17	chr5:59678290..59679528-chr5:59881870..59883189,3	MCF-7	breast:
18	chr5:59636747..59637753-chr5:59650701..59651624,3	MCF-7	breast:
19	chr5:59630941..59633052-chr5:59638055..59640413,2	K562	blood:
20	chr5:59549482..59552233-chr5:59553881..59555409,2	K562	blood:
21	chr5:59525141..59527803-chr5:59530452..59533157,2	MCF-7	breast:
22	chr5:59109590..59110214-chr5:59678255..59679111,2	MCF-7	breast:
23	chr5:59590961..59591565-chr5:59678761..59679630,2	MCF-7	breast:
24	chr5:59549482..59552233-chr5:59553881..59555409,2	K562	blood:
25	chr11:288802..289567-chr5:59528126..59528944,2	NB4	blood:
26	chr5:59624456..59627842-chr5:59630040..59632479,3	K562	blood:

No data

Variant related genes	Relation type
RNU6-806P	TF binding region
PDE4D	TF binding region
RNU6-806P	CpG island
PDE4D	CpG island
ENSG00000142102	chromatin interactions

Extended variants
information (count: 6282 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:6282 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148744193	chr5:59480293-59480294	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs368623029	chr5:59480324-59480325	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs57996583	chr5:59480425-59480426	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535013053	chr5:59480431-59480432	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564862259	chr5:59480444-59480445	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532107939	chr5:59480447-59480448	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142250491	chr5:59480483-59480484	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575145930	chr5:59480512-59480513	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181550964	chr5:59480548-59480549	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557562760	chr5:59480557-59480558	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549897373	chr5:59480582-59480583	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536580556	chr5:59480642-59480643	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577385033	chr5:59480644-59480645	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562386735	chr5:59480651-59480652	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529850903	chr5:59480653-59480654	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146798681	chr5:59480665-59480666	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548320892	chr5:59480681-59480682	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564973217	chr5:59480697-59480698	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566677433	chr5:59480709-59480710	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs527444947	chr5:59480763-59480764	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540617829	chr5:59480787-59480788	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186261318	chr5:59480800-59480801	Strong transcription Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs12515241	chr5:59480816-59480817	Strong transcription Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191421108	chr5:59480843-59480844	Strong transcription Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569696769	chr5:59480894-59480895	Strong transcription Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs549677721	chr5:59481010-59481011	Strong transcription Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs16877736	chr5:59481106-59481107	Strong transcription Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs139969276	chr5:59481128-59481129	Strong transcription Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532312112	chr5:59481145-59481146	Strong transcription Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552132490	chr5:59481248-59481249	Active TSS Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs182773624	chr5:59481299-59481300	Active TSS Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs370728234	chr5:59481457-59481458	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs186583057	chr5:59481458-59481459	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs377739811	chr5:59481477-59481478	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs568489055	chr5:59481478-59481479	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs546714148	chr5:59481488-59481489	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs143510155	chr5:59481503-59481504	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs557619619	chr5:59481509-59481510	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs539182831	chr5:59481531-59481532	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs577497319	chr5:59481611-59481612	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs540023693	chr5:59481616-59481617	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs190639187	chr5:59481628-59481629	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs146721975	chr5:59481630-59481631	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs140264265	chr5:59481631-59481632	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs560511416	chr5:59481657-59481658	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs574077577	chr5:59481714-59481715	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs543041961	chr5:59481749-59481750	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs565095739	chr5:59481763-59481764	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs11451682	chr5:59481764-59481765	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs563594311	chr5:59481777-59481778	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:808 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59471600-59500800	Weak transcription	Primary B cells from cord blood	blood
2	chr5:59476400-59484000	Weak transcription	Aorta	Aorta
3	chr5:59478400-59481200	Weak transcription	HepG2	liver
4	chr5:59479000-59482000	Strong transcription	Primary neutrophils fromperipheralblood	blood
5	chr5:59479200-59481200	Enhancers	Fetal Kidney	kidney
6	chr5:59479600-59480600	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr5:59479600-59480600	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr5:59480200-59480800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr5:59480600-59481200	Enhancers	Brain Substantia Nigra	brain
10	chr5:59480600-59482800	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr5:59480800-59481600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr5:59481000-59481600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr5:59481200-59481400	Bivalent Enhancer	HUVEC	blood vessel
14	chr5:59481200-59481600	Active TSS	Duodenum Mucosa	Duodenum
15	chr5:59481200-59481600	Flanking Active TSS	Fetal Kidney	kidney
16	chr5:59481200-59481800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr5:59481400-59481800	Enhancers	Duodenum Smooth Muscle	Duodenum
18	chr5:59481400-59481800	Enhancers	Fetal Brain Male	brain
19	chr5:59481600-59481800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr5:59481600-59483000	Enhancers	Fetal Kidney	kidney
21	chr5:59481800-59482200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr5:59481800-59483800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr5:59482000-59492000	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr5:59482800-59483000	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr5:59482800-59483200	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr5:59483200-59492000	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr5:59483800-59486400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr5:59484000-59484400	ZNF genes & repeats	Aorta	Aorta
29	chr5:59484400-59492200	Weak transcription	Aorta	Aorta
30	chr5:59486400-59487000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr5:59487000-59491400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr5:59491400-59493800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr5:59491600-59492000	Enhancers	A549	lung
34	chr5:59491600-59494000	Enhancers	Hela-S3	cervix
35	chr5:59491800-59492200	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr5:59491800-59492400	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr5:59491800-59492400	Enhancers	Placenta Amnion	Placenta Amnion
38	chr5:59491800-59492600	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr5:59491800-59492800	Enhancers	HMEC	breast
40	chr5:59491800-59493000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr5:59491800-59493200	Enhancers	Muscle Satellite Cultured Cells	--
42	chr5:59492000-59492200	Active TSS	Osteobl	bone
43	chr5:59492000-59492400	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr5:59492000-59492400	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr5:59492000-59492800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr5:59492000-59492800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr5:59492000-59492800	Flanking Active TSS	A549	lung
48	chr5:59492000-59492800	Enhancers	HSMMtube	muscle
49	chr5:59492000-59492800	Enhancers	HUVEC	blood vessel
50	chr5:59492000-59492800	Enhancers	NH-A	brain

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