Variant report

Variant	nsv830434
Chromosome Location	chr5:104059364-104242396
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:473)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:473 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:104223199-104223207	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr5:104087774-104088008	GM12878	blood:	n/a	chr5:104087867-104087878
3	BATF	chr5:104087746-104087944	GM12878	blood:	n/a	chr5:104087867-104087878
4	CEBPB	chr5:104090393-104090670	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr5:104136224-104136540	IMR90	lung:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
6	CEBPB	chr5:104068408-104068610	HepG2	liver:	n/a	chr5:104068507-104068518
7	CEBPB	chr5:104136117-104136616	MCF-7	breast:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
8	CEBPB	chr5:104195064-104195524	A549	lung:	n/a	chr5:104195252-104195263
9	CEBPB	chr5:104177422-104177540	K562	blood:	n/a	n/a
10	CEBPB	chr5:104136123-104136646	HCT-116	colon:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
11	CEBPB	chr5:104195089-104195447	ECC-1	luminal epithelium:	n/a	chr5:104195252-104195263
12	CEBPB	chr5:104136032-104136689	MCF-7	breast:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
13	CEBPB	chr5:104195099-104195433	H1-hESC	embryonic stem cell:	n/a	chr5:104195252-104195263
14	CEBPB	chr5:104136228-104136514	Hela-S3	cervix:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
15	CEBPB	chr5:104136186-104136537	K562	blood:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
16	CEBPB	chr5:104195080-104195455	K562	blood:	n/a	chr5:104195252-104195263
17	CEBPB	chr5:104195098-104195441	HepG2	liver:	n/a	chr5:104195252-104195263
18	CEBPB	chr5:104136061-104136624	A549	lung:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
19	CEBPB	chr5:104136136-104136548	A549	lung:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
20	CEBPB	chr5:104195135-104195333	K562	blood:	n/a	chr5:104195252-104195263
21	CEBPB	chr5:104102501-104102787	A549	lung:	n/a	chr5:104102656-104102667
22	CEBPB	chr5:104136190-104136565	H1-hESC	embryonic stem cell:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
23	CEBPB	chr5:104195172-104195487	MCF-7	breast:	n/a	chr5:104195252-104195263
24	CEBPB	chr5:104136209-104136550	A549	lung:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
25	CEBPB	chr5:104136255-104136426	K562	blood:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
26	CEBPB	chr5:104195078-104195490	Hela-S3	cervix:	n/a	chr5:104195252-104195263
27	CEBPB	chr5:104195073-104195449	IMR90	lung:	n/a	chr5:104195252-104195263
28	CEBPB	chr5:104136258-104136502	HepG2	liver:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
29	CEBPB	chr5:104136181-104136567	HepG2	liver:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
30	CEBPB	chr5:104195095-104195389	MCF-7	breast:	n/a	chr5:104195252-104195263
31	CEBPB	chr5:104136188-104136569	K562	blood:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
32	CEBPB	chr5:104136178-104136571	HepG2	liver:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
33	CEBPB	chr5:104136225-104136497	HepG2	liver:	n/a	chr5:104136365-104136376 chr5:104136380-104136391
34	CEBPB	chr5:104171648-104171720	HepG2	liver:	n/a	n/a
35	CEBPB	chr5:104195083-104195431	A549	lung:	n/a	chr5:104195252-104195263
36	CEBPB	chr5:104102566-104102783	HepG2	liver:	n/a	chr5:104102656-104102667
37	CEBPD	chr5:104179642-104179910	K562	blood:	n/a	n/a
38	CEBPD	chr5:104136280-104136473	HepG2	liver:	n/a	n/a
39	CTCF	chr5:104136240-104136390	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr5:104136240-104136390	HCFaa	heart:	n/a	n/a
41	CTCF	chr5:104136260-104136410	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr5:104136260-104136410	AG09319	gingival:	n/a	n/a
43	CTCF	chr5:104136253-104136461	LNCaP	prostate:	n/a	n/a
44	CTCF	chr5:104136191-104136536	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr5:104136200-104136350	A549	lung:	n/a	n/a
46	CTCF	chr5:104136260-104136410	HMEC	breast:	n/a	n/a
47	CTCF	chr5:104136246-104136408	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr5:104136260-104136410	GM12870	blood:	n/a	n/a
49	CTCF	chr5:104070060-104070210	GM12866	blood:	n/a	n/a
50	CTCF	chr5:104136260-104136410	HUVEC	blood vessel:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104090236-104090286	SAEC	small airway:	n/a
2	chr5:104090236-104090286	HL-60	blood:	n/a
3	chr5:104090236-104090286	GM12892	blood:	n/a
4	chr5:104090236-104090286	AG04449	skin:	fetal
5	chr5:104090236-104090286	CMK	blood:	n/a
6	chr5:104090236-104090286	SK-N-MC	brain:	n/a
7	chr5:104090236-104090286	IMR90	lung:	fetal
8	chr5:104090236-104090286	SKMC	muscle:	n/a
9	chr5:104090236-104090286	RPTEC	kidney:	n/a
10	chr5:104090236-104090286	HepG2	liver:	n/a
11	chr5:104090236-104090286	HCM	heart:	n/a
12	chr5:104090236-104090286	HCT-116	colon:	n/a
13	chr5:104090236-104090286	Hepatocyte	liver:	n/a
14	chr5:104090236-104090286	K562	blood:	n/a
15	chr5:104090236-104090286	GM12891	blood:	n/a
16	chr5:104090236-104090286	HCF	heart:	n/a
17	chr5:104090236-104090286	AG09319	gingival:	n/a
18	chr5:104090236-104090286	SK-N-SH_RA	brain:	n/a
19	chr5:104090236-104090286	NH-A	brain:	n/a
20	chr5:104090236-104090286	HMEC	breast:	n/a
21	chr5:104090236-104090286	BJ	skin:	n/a
22	chr5:104090236-104090286	AG10803	skin:	n/a
23	chr5:104090236-104090286	GM19239	blood:	n/a
24	chr5:104090236-104090286	HAEpiC	amniotic membrane:	n/a
25	chr5:104090236-104090286	HUVEC	blood vessel:	n/a
26	chr5:104090236-104090286	PANC-1	pancreas:	n/a
27	chr5:104090236-104090286	MCF-7	breast:	n/a
28	chr5:104090236-104090286	HIPEpiC	eye:	n/a
29	chr5:104090236-104090286	A549	lung:	n/a
30	chr5:104090236-104090286	PFSK-1	brain:	n/a
31	chr5:104090236-104090286	HRCEpiC	kidney:	n/a
32	chr5:104090236-104090286	HRE	kidney:	n/a
33	chr5:104090236-104090286	HEEpiC	esophagus:	n/a
34	chr5:104090236-104090286	T-47D	breast:	n/a
35	chr5:104090236-104090286	BE2_C	brain:	n/a
36	chr5:104090236-104090286	GM12878	blood:	n/a
37	chr5:104090236-104090286	HCPEpiC	choroid plexus:	n/a
38	chr5:104090236-104090286	ECC-1	luminal epithelium:	n/a
39	chr5:104090236-104090286	NHDF-neo	bronchial:	n/a
40	chr5:104090236-104090286	SK-N-SH	brain:	n/a
41	chr5:104090236-104090286	PrEC	prostate:	n/a
42	chr5:104090236-104090286	U87	brain:	n/a
43	chr5:104090236-104090286	HPAEpiC	pulmonary alveolar:	n/a
44	chr5:104090236-104090286	Hela-S3	cervix:	n/a
45	chr5:104090236-104090286	Caco-2	colon:	n/a
46	chr5:104090236-104090286	ProgFib	skin:	n/a
47	chr5:104090236-104090286	MCF10A-Er-Src	breast:	n/a
48	chr5:104090236-104090286	AoSMC	blood vessel:	n/a
49	chr5:104090236-104090286	HNPCEpiC	eye:	n/a
50	chr5:104090236-104090286	Jurkat	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:104091669..104093962-chr5:104097846..104099466,2	MCF-7	breast:
2	chr5:104091669..104093962-chr5:104097846..104099466,2	MCF-7	breast:
3	chr5:104080992..104082950-chr5:104084605..104086219,2	K562	blood:
4	chr5:104226367..104227906-chr5:104228376..104230821,2	MCF-7	breast:
5	chr5:104239889..104241844-chr5:104241951..104244541,2	MCF-7	breast:
6	chr5:104223049..104225474-chr5:104235768..104238593,2	MCF-7	breast:
7	chr5:104223049..104225474-chr5:104235768..104238593,2	MCF-7	breast:
8	chr5:104086946..104088891-chr5:104090048..104092847,2	MCF-7	breast:
9	chr5:104227529..104229773-chr5:104240979..104242491,2	MCF-7	breast:
10	chr5:104234931..104236476-chr5:104238248..104241105,2	MCF-7	breast:
11	chr5:104239889..104241844-chr5:104241951..104244541,2	MCF-7	breast:
12	chr5:104227529..104229773-chr5:104240979..104242491,2	MCF-7	breast:
13	chr5:104226367..104227906-chr5:104228376..104230821,2	MCF-7	breast:
14	chr5:104086946..104088891-chr5:104090048..104092847,2	MCF-7	breast:
15	chr5:104234931..104236476-chr5:104238248..104241105,2	MCF-7	breast:

(count:36 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-13	chr5:104137254-104137422	l_2988_chr5:104103131-104137422_testes
2	lnc-NUDT12-5	chr5:104109314-104109361	ENSG00000251574
3	lnc-NUDT12-5	chr5:104080291-104080310	NONHSAT103088
4	lnc-NUDT12-13	chr5:104118423-104118445	l_2988_chr5:104103131-104137422_testes
5	lnc-NUDT12-5	chr5:104074998-104075113	ENSG00000251574
6	lnc-NUDT12-5	chr5:104072462-104072616	ENSG00000251574
7	lnc-C5orf30-2	chr5:104098977-104099084	XLOC_004497
8	lnc-NUDT12-5	chr5:104079736-104079892	ENSG00000251574
9	lnc-NUDT12-5	chr5:104098981-104099084	NONHSAT103081
10	lnc-NUDT12-5	chr5:104098981-104099084	NONHSAT103082
11	lnc-NUDT12-5	chr5:104079393-104079555	ENSG00000251574
12	lnc-NUDT12-5	chr5:104109434-104109524	NONHSAT103081
13	lnc-NUDT12-6	chr5:104222559-104222676	ENSG00000251574
14	lnc-C5orf30-3	chr5:104135007-104135473	ENSG00000253776
15	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
16	lnc-NUDT12-5	chr5:104109434-104109523	ENSG00000251574
17	lnc-NUDT12-13	chr5:104103132-104103235	l_2988_chr5:104103131-104137422_testes
18	lnc-NUDT12-5	chr5:104075198-104075336	ENSG00000251574
19	lnc-C5orf30-2	chr5:104079736-104079888	XLOC_004497
20	lnc-NUDT12-5	chr5:104074962-104075113	ENSG00000251574
21	lnc-NUDT12-5	chr5:104075198-104075336	ENSG00000251574
22	lnc-NUDT12-5	chr5:104109314-104109524	NONHSAT103082
23	lnc-NUDT12-5	chr5:104074955-104075113	ENSG00000251574
24	lnc-NUDT12-5	chr5:104075198-104075242	ENSG00000251574
25	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
26	lnc-NUDT12-6	chr5:104222559-104222676	ENSG00000251574
27	lnc-NUDT12-5	chr5:104098932-104099084	ENSG00000251574
28	lnc-NUDT12-5	chr5:104081064-104081147	NONHSAT103088
29	lnc-C5orf30-3	chr5:104109342-104109441	ENSG00000253776
30	lnc-NUDT12-5	chr5:104109314-104109485	ENSG00000251574
31	lnc-NUDT12-5	chr5:104109314-104109524	NONHSAT103088
32	lnc-NUDT12-5	chr5:104082242-104082310	ENSG00000251574
33	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
34	lnc-NUDT12-5	chr5:104098981-104099084	ENSG00000251574
35	lnc-NUDT12-5	chr5:104109314-104109492	ENSG00000251574
36	lnc-NUDT12-5	chr5:104109314-104109397	ENSG00000251574

No data

Variant related genes	Relation type
ENSG00000253776	TF binding region
RNU6-334P	TF binding region
ENSG00000251574	TF binding region
ENSG00000253776	CpG island
RNU6-334P	CpG island
ENSG00000251574	CpG island
ENSG00000251574	chromatin interactions
CREB3L2	miRNA target sites

Extended variants
information (count: 2332 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2332 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554415685	chr5:104065401-104065402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs161787	chr5:104065427-104065428	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs545750049	chr5:104065465-104065466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116908721	chr5:104065467-104065468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs79061578	chr5:104065481-104065482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs372917871	chr5:104065485-104065486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368746669	chr5:104065525-104065526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541955242	chr5:104065527-104065528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560898856	chr5:104065540-104065541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529871390	chr5:104065568-104065569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192355560	chr5:104065586-104065587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs145002691	chr5:104065632-104065633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143056273	chr5:104065664-104065665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532455101	chr5:104065705-104065706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552679045	chr5:104065748-104065749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs55797241	chr5:104065755-104065756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531415165	chr5:104065794-104065795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149048599	chr5:104065827-104065828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143074196	chr5:104065829-104065830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534367872	chr5:104065838-104065839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534978388	chr5:104065839-104065840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555020011	chr5:104065939-104065940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183355921	chr5:104065949-104065950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188049466	chr5:104065985-104065986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539789348	chr5:104066015-104066016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575158006	chr5:104066048-104066049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192660095	chr5:104066049-104066050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78849424	chr5:104066059-104066060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541844879	chr5:104066066-104066067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377722990	chr5:104066072-104066073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537770529	chr5:104066079-104066080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs172876	chr5:104066174-104066175	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs141102821	chr5:104066176-104066177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs74440847	chr5:104066230-104066231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs116885425	chr5:104066234-104066235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs386690729	chr5:104066258-104066259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184450589	chr5:104066268-104066269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs62361861	chr5:104066283-104066284	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs62361862	chr5:104066369-104066370	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs562443305	chr5:104066390-104066391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs35287481	chr5:104066439-104066440	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs547890267	chr5:104066479-104066480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568106663	chr5:104066494-104066495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527397714	chr5:104066727-104066728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547966636	chr5:104066756-104066757	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373218210	chr5:104066758-104066759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77824854	chr5:104066774-104066775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370315486	chr5:104066780-104066781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570030623	chr5:104066887-104066888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535418748	chr5:104066900-104066901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
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
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	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
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
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Obesity	20622171	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104065400-104065800	Enhancers	Rectal Smooth Muscle	rectum
2	chr5:104065800-104066200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr5:104065800-104067800	Enhancers	Fetal Lung	lung
4	chr5:104066200-104066400	Enhancers	Rectal Smooth Muscle	rectum
5	chr5:104066400-104067600	Weak transcription	Rectal Smooth Muscle	rectum
6	chr5:104067200-104067600	Enhancers	Colon Smooth Muscle	Colon
7	chr5:104067600-104068200	Enhancers	Rectal Smooth Muscle	rectum
8	chr5:104067600-104069200	Weak transcription	Colon Smooth Muscle	Colon
9	chr5:104068200-104068600	Weak transcription	Rectal Smooth Muscle	rectum
10	chr5:104068600-104070200	Enhancers	Rectal Smooth Muscle	rectum
11	chr5:104069200-104070200	Enhancers	Colon Smooth Muscle	Colon
12	chr5:104089600-104090800	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr5:104089800-104090000	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr5:104089800-104090200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr5:104089800-104091200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr5:104089800-104091200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr5:104089800-104091200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr5:104089800-104091200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr5:104089800-104091400	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr5:104090000-104090600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr5:104090000-104090600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr5:104090200-104090400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr5:104090200-104090600	Enhancers	Brain Germinal Matrix	brain
24	chr5:104090200-104091000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr5:104090400-104090800	Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr5:104090600-104090800	Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr5:104090800-104091000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr5:104091200-104092600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr5:104091400-104095000	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr5:104095000-104095800	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr5:104112400-104113000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr5:104112600-104113000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr5:104124800-104125400	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr5:104124800-104125400	Enhancers	Rectal Smooth Muscle	rectum
35	chr5:104124800-104125600	Enhancers	Fetal Lung	lung
36	chr5:104124800-104126400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr5:104126400-104130000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr5:104127800-104129000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:104128400-104129800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr5:104128600-104129000	Enhancers	Fetal Intestine Small	intestine
41	chr5:104128600-104129000	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr5:104128600-104129200	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr5:104128600-104129400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr5:104128600-104129400	Enhancers	Rectal Mucosa Donor 29	rectum
45	chr5:104128600-104130000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
46	chr5:104128600-104130200	Enhancers	Fetal Intestine Large	intestine
47	chr5:104128800-104129200	Enhancers	NH-A	brain
48	chr5:104129000-104129400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
49	chr5:104129000-104129400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr5:104129200-104129400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell

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