Variant report

Variant	nsv597844
Chromosome Location	chr5:37287836-37567851
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2955)
CpG islands
(count:1712)
Chromatin interactive
region (count:134)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2955 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:37435399-37435833	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:37371072-37371329	HepG2	liver:	n/a	chr5:37371175-37371187
3	ARID3A	chr5:37552742-37553918	K562	blood:	n/a	n/a
4	ARID3A	chr5:37412949-37413405	K562	blood:	n/a	n/a
5	ARID3A	chr5:37555087-37555396	K562	blood:	n/a	n/a
6	ARID3A	chr5:37424736-37424788	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:37554224-37554305	K562	blood:	n/a	n/a
8	ARID3A	chr5:37349046-37349675	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:37435813-37436000	K562	blood:	n/a	chr5:37435891-37435907
10	ARID3A	chr5:37379206-37379473	K562	blood:	n/a	n/a
11	ARID3A	chr5:37561556-37561928	K562	blood:	n/a	n/a
12	ARID3A	chr5:37371166-37371527	K562	blood:	n/a	chr5:37371175-37371187
13	ARID3A	chr5:37413045-37413386	HepG2	liver:	n/a	n/a
14	ARID3A	chr5:37566412-37566482	K562	blood:	n/a	n/a
15	ATF1	chr5:37370938-37371803	K562	blood:	n/a	n/a
16	ATF1	chr5:37552974-37553744	K562	blood:	n/a	n/a
17	ATF1	chr5:37413139-37413402	K562	blood:	n/a	n/a
18	ATF1	chr5:37379197-37379483	K562	blood:	n/a	n/a
19	ATF2	chr5:37370963-37371677	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr5:37370974-37371643	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr5:37370933-37371743	GM12878	blood:	n/a	n/a
22	ATF2	chr5:37379198-37379480	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr5:37379058-37379502	GM12878	blood:	n/a	n/a
24	ATF2	chr5:37370951-37371687	GM12878	blood:	n/a	n/a
25	ATF3	chr5:37379172-37379508	A549	lung:	n/a	n/a
26	ATF3	chr5:37370910-37371420	GM12878	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
27	ATF3	chr5:37370993-37371683	A549	lung:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
28	ATF3	chr5:37370943-37371319	H1-hESC	embryonic stem cell:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
29	ATF3	chr5:37413096-37413476	K562	blood:	n/a	n/a
30	ATF3	chr5:37371001-37371307	HepG2	liver:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
31	ATF3	chr5:37371024-37371385	H1-hESC	embryonic stem cell:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
32	ATF3	chr5:37370782-37371385	K562	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
33	ATF3	chr5:37379108-37379491	K562	blood:	n/a	n/a
34	ATF3	chr5:37371073-37371320	GM12878	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
35	ATF3	chr5:37370920-37371369	K562	blood:	n/a	chr5:37371209-37371223 chr5:37371172-37371181
36	ATF3	chr5:37379100-37379507	A549	lung:	n/a	n/a
37	BACH1	chr5:37305059-37305259	K562	blood:	n/a	n/a
38	BACH1	chr5:37371532-37371839	K562	blood:	n/a	n/a
39	BACH1	chr5:37553100-37553687	K562	blood:	n/a	n/a
40	BACH1	chr5:37512136-37512171	K562	blood:	n/a	n/a
41	BATF	chr5:37379223-37379461	GM12878	blood:	n/a	n/a
42	BATF	chr5:37413135-37413360	GM12878	blood:	n/a	n/a
43	BCL11A	chr5:37436356-37436593	GM12878	blood:	n/a	n/a
44	BCL3	chr5:37379009-37379598	A549	lung:	n/a	n/a
45	BCL3	chr5:37379056-37379575	A549	lung:	n/a	n/a
46	BCL3	chr5:37370886-37371778	A549	lung:	n/a	chr5:37371215-37371224
47	BCL3	chr5:37370732-37371729	A549	lung:	n/a	chr5:37371215-37371224
48	BCLAF1	chr5:37379111-37379567	GM12878	blood:	n/a	n/a
49	BCLAF1	chr5:37370930-37371950	GM12878	blood:	n/a	chr5:37371215-37371224
50	BCLAF1	chr5:37379066-37379572	K562	blood:	n/a	n/a

(count:1712 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37371074-37371124	LNCaP	prostate:	n/a
2	chr5:37379461-37379511	HPAEpiC	pulmonary alveolar:	n/a
3	chr5:37378229-37378279	NHBE	bronchial:	n/a
4	chr5:37371213-37371263	AoSMC	blood vessel:	n/a
5	chr5:37371074-37371124	LNCaP	prostate:	n/a
6	chr5:37379461-37379511	HPAEpiC	pulmonary alveolar:	n/a
7	chr5:37378229-37378279	NHBE	bronchial:	n/a
8	chr5:37371213-37371263	AoSMC	blood vessel:	n/a
9	chr5:37379822-37379872	GM06990	blood:	n/a
10	chr5:37371082-37371132	SK-N-MC	brain:	n/a
11	chr5:37379461-37379511	Caco-2	colon:	n/a
12	chr5:37371047-37371097	PANC-1	pancreas:	n/a
13	chr5:37370947-37370997	SKMC	muscle:	n/a
14	chr5:37379396-37379446	Caco-2	colon:	n/a
15	chr5:37484025-37484075	MCF10A-Er-Src	breast:	n/a
16	chr5:37371179-37371229	GM12878	blood:	n/a
17	chr5:37371053-37371103	HCM	heart:	n/a
18	chr5:37371056-37371106	HMEC	breast:	n/a
19	chr5:37371047-37371097	HRCEpiC	kidney:	n/a
20	chr5:37371074-37371124	H1-hESC	embryonic stem cell:	embryo
21	chr5:37371056-37371106	Hela-S3	cervix:	n/a
22	chr5:37370947-37370997	GM12892	blood:	n/a
23	chr5:37379374-37379424	Hela-S3	cervix:	n/a
24	chr5:37371213-37371263	H1-hESC	embryonic stem cell:	embryo
25	chr5:37371213-37371263	SAEC	small airway:	n/a
26	chr5:37379374-37379424	ECC-1	luminal epithelium:	n/a
27	chr5:37371056-37371106	A549	lung:	n/a
28	chr5:37370967-37371017	SAEC	small airway:	n/a
29	chr5:37371053-37371103	ProgFib	skin:	n/a
30	chr5:37371628-37371678	HAEpiC	amniotic membrane:	n/a
31	chr5:37371213-37371263	HEK293	kidney:	embryo
32	chr5:37371192-37371242	NHBE	bronchial:	n/a
33	chr5:37379822-37379872	MCF-7	breast:	n/a
34	chr5:37371047-37371097	LNCaP	prostate:	n/a
35	chr5:37379358-37379408	AG09319	gingival:	n/a
36	chr5:37379822-37379872	GM12878	blood:	n/a
37	chr5:37371213-37371263	HCPEpiC	choroid plexus:	n/a
38	chr5:37379269-37379319	SK-N-MC	brain:	n/a
39	chr5:37370947-37370997	HUVEC	blood vessel:	n/a
40	chr5:37379272-37379322	AG09319	gingival:	n/a
41	chr5:37371213-37371263	HCF	heart:	n/a
42	chr5:37379822-37379872	BJ	skin:	n/a
43	chr5:37371082-37371132	GM12891	blood:	n/a
44	chr5:37370967-37371017	HMEC	breast:	n/a
45	chr5:37379396-37379446	IMR90	lung:	fetal
46	chr5:37379374-37379424	HCF	heart:	n/a
47	chr5:37371213-37371263	Jurkat	blood:	n/a
48	chr5:37371074-37371124	ECC-1	luminal epithelium:	n/a
49	chr5:37371179-37371229	GM06990	blood:	n/a
50	chr5:37322183-37322233	ProgFib	skin:	n/a

(count:134 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:37539872..37542556-chr5:37548847..37552617,3	K562	blood:
2	chr5:37412800..37413850-chr5:37837177..37838175,5	MCF-7	breast:
3	chr5:37308340..37310527-chr5:37313095..37315302,2	K562	blood:
4	chr5:37313041..37316016-chr5:37316235..37320190,3	K562	blood:
5	chr12:7052910..7053902-chr5:37371084..37371594,2	Hela-S3	cervix:
6	chr5:21459174..21459727-chr5:37379374..37379881,2	Hela-S3	cervix:
7	chr5:37543508..37545182-chr5:37552537..37554107,2	K562	blood:
8	chr5:37550616..37553710-chr5:37559318..37562633,4	K562	blood:
9	chr5:37329127..37329843-chr5:37340391..37341109,2	Hela-S3	cervix:
10	chr2:61404229..61405117-chr5:37371163..37371819,2	Hela-S3	cervix:
11	chr5:37541266..37543534-chr5:37545440..37547559,2	K562	blood:
12	chr5:37412788..37413557-chr5:38023669..38024455,2	MCF-7	breast:
13	chr5:37536707..37538331-chr5:37538401..37541156,2	K562	blood:
14	chr5:37539872..37542556-chr5:37548847..37552617,3	K562	blood:
15	chr5:37550784..37553523-chr5:37560304..37561961,2	MCF-7	breast:
16	chr5:37423699..37426165-chr5:37428640..37431370,2	MCF-7	breast:
17	chr5:37553408..37554969-chr5:37565315..37567049,2	K562	blood:
18	chr5:37358150..37361413-chr5:37362395..37366227,3	K562	blood:
19	chr5:37412806..37413850-chr5:37900474..37901433,3	MCF-7	breast:
20	chr5:37370138..37373249-chr5:37374935..37377740,7	K562	blood:
21	chr5:37392088..37394720-chr5:37398631..37400477,2	K562	blood:
22	chr5:37488881..37490858-chr5:37567347..37569058,2	K562	blood:
23	chr5:37358150..37361413-chr5:37362395..37366227,3	K562	blood:
24	chr5:37348597..37351209-chr5:37351351..37353763,2	K562	blood:
25	chr5:37551824..37554603-chr5:37555317..37558093,4	K562	blood:
26	chr5:37402668..37405027-chr5:37408741..37410429,2	K562	blood:
27	chr5:37318176..37320415-chr5:37333622..37336534,2	K562	blood:
28	chr5:37369760..37372730-chr5:37375256..37380889,7	MCF-7	breast:
29	chr5:37288508..37291349-chr5:37291892..37294572,2	K562	blood:
30	chr5:37496762..37498368-chr5:37500019..37501730,2	MCF-7	breast:
31	chr5:37398413..37401041-chr5:37401249..37404698,3	K562	blood:
32	chr5:37349723..37351295-chr5:37369578..37371440,2	K562	blood:
33	chr5:37326722..37329430-chr5:37348015..37351389,3	K562	blood:
34	chr5:37412852..37413708-chr5:37554717..37555628,3	MCF-7	breast:
35	chr5:37477675..37480288-chr5:37486843..37489829,2	K562	blood:
36	chr5:37389025..37391631-chr5:37392336..37394905,2	K562	blood:
37	chr5:37550272..37552016-chr5:37552928..37554782,2	MCF-7	breast:
38	chr5:37550784..37553523-chr5:37560304..37561961,2	MCF-7	breast:
39	chr5:37395673..37397370-chr5:37410862..37413241,2	MCF-7	breast:
40	chr5:37536707..37538331-chr5:37538401..37541156,2	K562	blood:
41	chr5:37389025..37391631-chr5:37392336..37394905,2	K562	blood:
42	chr5:37353747..37356748-chr5:37369994..37371965,3	K562	blood:
43	chr19:10443916..10444436-chr5:37370772..37371335,2	NB4	blood:
44	chr5:37370138..37373249-chr5:37374935..37377740,7	K562	blood:
45	chr17:61358570..61359089-chr5:37412803..37413392,2	MCF-7	breast:
46	chr5:37299270..37301087-chr5:37332798..37335148,2	K562	blood:
47	chr5:37343556..37345615-chr5:37366480..37369895,3	K562	blood:
48	chr5:37369538..37373129-chr5:37377393..37380859,4	MCF-7	breast:
49	chr15:94515130..94515844-chr5:37350902..37351467,2	MCF-7	breast:
50	chr1:11967776..11968487-chr5:37370635..37371332,2	Hela-S3	cervix:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NIPBL-7	chr5:37379404-37379494	NONHSAT101065
2	lnc-NIPBL-7	chr5:37379591-37379656	NONHSAT101065
3	lnc-C5orf42-5	chr5:37324306-37324596	expReg_chr5_1217_-
4	lnc-WDR70-4	chr5:37377986-37378073	NONHSAT101062
5	lnc-WDR70-4	chr5:37377151-37377385	NONHSAT101062
6	lnc-NUP155-5	chr5:37505790-37506959	NONHSAT101066
7	lnc-NIPBL-7	chr5:37381704-37381911	NONHSAT101065

No data

Variant related genes	Relation type
ENSG00000250455	TF binding region
ENSG00000270558	TF binding region
WDR70	TF binding region
ENSG00000248216	TF binding region
RNU7-75P	TF binding region
NUP155	TF binding region
ENSG00000250455	CpG island
ENSG00000270558	CpG island
WDR70	CpG island
ENSG00000248216	CpG island
RNU7-75P	CpG island
NUP155	CpG island
ENSG00000250455	chromatin interactions
ENSG00000145741	chromatin interactions
ENSG00000104549	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000197603	chromatin interactions
ENSG00000272173	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000154222	chromatin interactions
ENSG00000161847	chromatin interactions
ENSG00000082068	chromatin interactions
ENSG00000248587	chromatin interactions
ENSG00000183666	chromatin interactions
ENSG00000215190	chromatin interactions
ENSG00000236137	chromatin interactions
ENSG00000113569	chromatin interactions
ENSG00000173209	chromatin interactions
ENSG00000164190	chromatin interactions
ENSG00000253513	chromatin interactions
ENSG00000251880	chromatin interactions

Extended variants
information (count: 10718 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:10718 , 50 per page) page: 1 2 3 4 5 6 7 ... 215

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11953538	chr5:37287836-37287837	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560054654	chr5:37287837-37287838	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs556040750	chr5:37287841-37287842	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs528854134	chr5:37287873-37287874	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs574350532	chr5:37287969-37287970	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs188992625	chr5:37287995-37287996	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs76299857	chr5:37288019-37288020	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs553722851	chr5:37288078-37288079	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs545285434	chr5:37288096-37288097	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs116172229	chr5:37288117-37288118	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
11	rs181635745	chr5:37288155-37288156	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs564417278	chr5:37288166-37288167	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs55960428	chr5:37288306-37288307	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs568520484	chr5:37288377-37288378	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs576627002	chr5:37288382-37288383	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs140084812	chr5:37288390-37288391	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs143565183	chr5:37288442-37288443	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs530963480	chr5:37288447-37288448	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs151260734	chr5:37288517-37288518	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs10473043	chr5:37288535-37288536	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs141531535	chr5:37288537-37288538	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs142232930	chr5:37288544-37288545	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs188717549	chr5:37288553-37288554	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs140388294	chr5:37288589-37288590	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs180897690	chr5:37288649-37288650	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs185968587	chr5:37288696-37288697	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs56044954	chr5:37288702-37288703	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs192125665	chr5:37288733-37288734	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs537658325	chr5:37288812-37288813	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs113364318	chr5:37288843-37288844	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs371786888	chr5:37288873-37288874	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs549532264	chr5:37288876-37288877	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs372473048	chr5:37288881-37288882	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs182187513	chr5:37288892-37288893	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs186860783	chr5:37288924-37288925	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs140491224	chr5:37288935-37288936	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs530234333	chr5:37288940-37288941	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs572446963	chr5:37288947-37288948	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs539449899	chr5:37288983-37288984	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs1143189	chr5:37288996-37288997	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs113574938	chr5:37289011-37289012	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs78406874	chr5:37289023-37289024	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs183151400	chr5:37289032-37289033	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs10070875	chr5:37289041-37289042	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs11750291	chr5:37289049-37289050	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs544050317	chr5:37289066-37289067	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs573627772	chr5:37289103-37289104	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs574266392	chr5:37289128-37289129	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs541784549	chr5:37289151-37289152	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs559791856	chr5:37289157-37289158	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	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
Bladder cancer	21909424	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
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Autism	22549408	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:5550 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37282400-37290400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr5:37283600-37288600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr5:37284200-37289000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:37284400-37289400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:37284600-37290200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr5:37285200-37288400	Weak transcription	Dnd41	blood
7	chr5:37285400-37297000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr5:37285600-37289200	Weak transcription	Fetal Thymus	thymus
9	chr5:37285600-37289400	Weak transcription	Hela-S3	cervix
10	chr5:37285600-37289600	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr5:37285600-37298000	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr5:37285800-37289200	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr5:37285800-37289200	Weak transcription	Thymus	Thymus
14	chr5:37286000-37289200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr5:37286000-37289200	Weak transcription	Pancreas	Pancrea
16	chr5:37286000-37289200	Weak transcription	A549	lung
17	chr5:37286000-37289600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr5:37286000-37290200	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr5:37286000-37290200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr5:37286000-37290600	Weak transcription	Primary T cells from cord blood	blood
21	chr5:37286200-37289400	Weak transcription	Liver	Liver
22	chr5:37286200-37289600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr5:37286200-37290000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr5:37286200-37290200	Weak transcription	Adipose Nuclei	Adipose
25	chr5:37286400-37288200	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr5:37286400-37288400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr5:37286400-37289400	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr5:37286800-37289200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr5:37287000-37289200	Weak transcription	Fetal Muscle Trunk	muscle
30	chr5:37287000-37289400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr5:37287000-37289400	Weak transcription	Fetal Muscle Leg	muscle
32	chr5:37287000-37289400	Weak transcription	Placenta	Placenta
33	chr5:37287000-37289400	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr5:37287000-37289600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr5:37287000-37290200	Weak transcription	Fetal Kidney	kidney
36	chr5:37287000-37290200	Weak transcription	Fetal Stomach	stomach
37	chr5:37287000-37290400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr5:37287000-37296800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr5:37287000-37298800	Weak transcription	Fetal Brain Male	brain
40	chr5:37287200-37288000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
41	chr5:37287200-37289200	Weak transcription	HSMM	muscle
42	chr5:37287200-37289400	Weak transcription	HMEC	breast
43	chr5:37287200-37289600	Weak transcription	Primary B cells from cord blood	blood
44	chr5:37287200-37296800	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr5:37287200-37297400	Weak transcription	Brain Cingulate Gyrus	brain
46	chr5:37287400-37288400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr5:37287400-37289000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr5:37287400-37289200	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr5:37287400-37289400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr5:37287400-37289800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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