Variant report

Variant	nsv830353
Chromosome Location	chr5:74961520-75152609
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1907)
CpG islands
(count:1344)
Chromatin interactive
region (count:94)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1907 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:75016714-75017107	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:74964985-74965304	K562	blood:	n/a	n/a
3	ARID3A	chr5:75012873-75013653	K562	blood:	n/a	n/a
4	ARID3A	chr5:75003873-75004464	K562	blood:	n/a	n/a
5	ARID3A	chr5:75002735-75003318	K562	blood:	n/a	n/a
6	ARID3A	chr5:75012722-75013708	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:74977101-74977345	K562	blood:	n/a	n/a
8	ARID3A	chr5:74974294-74974363	K562	blood:	n/a	n/a
9	ARID3A	chr5:75017531-75017690	K562	blood:	n/a	n/a
10	ARID3A	chr5:74976935-74977330	HepG2	liver:	n/a	n/a
11	ATF1	chr5:75017575-75017756	K562	blood:	n/a	n/a
12	ATF1	chr5:75114533-75114536	K562	blood:	n/a	n/a
13	ATF1	chr5:75012865-75013638	K562	blood:	n/a	n/a
14	ATF1	chr5:75002668-75002999	K562	blood:	n/a	n/a
15	ATF1	chr5:74964828-74965541	K562	blood:	n/a	n/a
16	ATF2	chr5:75012610-75013409	GM12878	blood:	n/a	n/a
17	ATF2	chr5:75143015-75143908	GM12878	blood:	n/a	n/a
18	ATF2	chr5:75133129-75133647	GM12878	blood:	n/a	n/a
19	ATF2	chr5:74964701-74965511	GM12878	blood:	n/a	n/a
20	ATF2	chr5:75012659-75013437	GM12878	blood:	n/a	n/a
21	ATF2	chr5:74964607-74965672	GM12878	blood:	n/a	n/a
22	ATF2	chr5:75143016-75143983	GM12878	blood:	n/a	n/a
23	ATF3	chr5:75012887-75013324	K562	blood:	n/a	n/a
24	ATF3	chr5:75017407-75017825	K562	blood:	n/a	n/a
25	ATF3	chr5:74964960-74965310	K562	blood:	n/a	n/a
26	ATF3	chr5:75012817-75013399	A549	lung:	n/a	chr5:75013389-75013398 chr5:75013337-75013346
27	BACH1	chr5:74965141-74965322	K562	blood:	n/a	n/a
28	BACH1	chr5:75032146-75032464	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr5:75031171-75031207	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr5:75012859-75013622	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr5:75012979-75013333	K562	blood:	n/a	n/a
32	BATF	chr5:74964664-74965323	GM12878	blood:	n/a	n/a
33	BATF	chr5:75012773-75013177	GM12878	blood:	n/a	n/a
34	BATF	chr5:75143255-75143843	GM12878	blood:	n/a	n/a
35	BATF	chr5:75062439-75062727	GM12878	blood:	n/a	n/a
36	BATF	chr5:74964753-74965201	GM12878	blood:	n/a	n/a
37	BATF	chr5:75143260-75143829	GM12878	blood:	n/a	n/a
38	BATF	chr5:75062447-75062640	GM12878	blood:	n/a	n/a
39	BCL11A	chr5:75143255-75143876	GM12878	blood:	n/a	chr5:75143541-75143550 chr5:75143634-75143643
40	BCL11A	chr5:75143279-75143764	GM12878	blood:	n/a	chr5:75143541-75143550 chr5:75143634-75143643
41	BCL11A	chr5:75012822-75013335	GM12878	blood:	n/a	n/a
42	BCL3	chr5:75012667-75013410	A549	lung:	n/a	chr5:75013351-75013364 chr5:75013389-75013402
43	BCL3	chr5:75143295-75143812	GM12878	blood:	n/a	chr5:75143541-75143550 chr5:75143634-75143643
44	BCL3	chr5:75012710-75013385	A549	lung:	n/a	chr5:75013351-75013364
45	BCLAF1	chr5:75143147-75143817	GM12878	blood:	n/a	chr5:75143541-75143550 chr5:75143634-75143643
46	BCLAF1	chr5:75143072-75143934	GM12878	blood:	n/a	chr5:75143541-75143550 chr5:75143634-75143643
47	BCLAF1	chr5:74964622-74965257	GM12878	blood:	n/a	chr5:74965005-74965014
48	BCLAF1	chr5:75012548-75013687	GM12878	blood:	n/a	chr5:75013351-75013364 chr5:75013389-75013402
49	BCLAF1	chr5:74964648-74965421	GM12878	blood:	n/a	chr5:74965005-74965014
50	BCLAF1	chr5:75012549-75013317	GM12878	blood:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:75013471-75013521	HPAEpiC	pulmonary alveolar:	n/a
2	chr5:75013490-75013540	SK-N-SH_RA	brain:	n/a
3	chr5:75013471-75013521	HPAEpiC	pulmonary alveolar:	n/a
4	chr5:75013490-75013540	SK-N-SH_RA	brain:	n/a
5	chr5:75013682-75013732	RPTEC	kidney:	n/a
6	chr5:75013342-75013392	HIPEpiC	eye:	n/a
7	chr5:75013329-75013379	HEEpiC	esophagus:	n/a
8	chr5:75013227-75013277	U87	brain:	n/a
9	chr5:75013227-75013277	HL-60	blood:	n/a
10	chr5:75013185-75013235	HNPCEpiC	eye:	n/a
11	chr5:75127862-75127912	ProgFib	skin:	n/a
12	chr5:75016955-75017005	HRPEpiC	eye:	n/a
13	chr5:75013329-75013379	HL-60	blood:	n/a
14	chr5:75012816-75012866	Hela-S3	cervix:	n/a
15	chr5:75009014-75009064	Hela-S3	cervix:	n/a
16	chr5:74978020-74978070	HUVEC	blood vessel:	n/a
17	chr5:75013227-75013277	GM12891	blood:	n/a
18	chr5:75127862-75127912	Hepatocyte	liver:	n/a
19	chr5:75013682-75013732	Hela-S3	cervix:	n/a
20	chr5:75013329-75013379	RPTEC	kidney:	n/a
21	chr5:75013592-75013642	HepG2	liver:	n/a
22	chr5:75012816-75012866	HCPEpiC	choroid plexus:	n/a
23	chr5:74965039-74965089	BE2_C	brain:	n/a
24	chr5:75013592-75013642	HUVEC	blood vessel:	n/a
25	chr5:75013227-75013277	MCF-7	breast:	n/a
26	chr5:75012313-75012363	MCF10A-Er-Src	breast:	n/a
27	chr5:75009428-75009478	AG09319	gingival:	n/a
28	chr5:75016955-75017005	AG04449	skin:	fetal
29	chr5:74991826-74991876	Jurkat	blood:	n/a
30	chr5:75013392-75013442	H1-hESC	embryonic stem cell:	embryo
31	chr5:75013392-75013442	NH-A	brain:	n/a
32	chr5:75013329-75013379	HEK293	kidney:	embryo
33	chr5:75127862-75127912	BJ	skin:	n/a
34	chr5:74991826-74991876	PrEC	prostate:	n/a
35	chr5:75013490-75013540	ECC-1	luminal epithelium:	n/a
36	chr5:75013471-75013521	AG09309	skin:	n/a
37	chr5:75009428-75009478	SK-N-SH_RA	brain:	n/a
38	chr5:75013131-75013181	NB4	blood:	n/a
39	chr5:75127862-75127912	MCF-7	breast:	n/a
40	chr5:75009014-75009064	GM12891	blood:	n/a
41	chr5:75013329-75013379	H1-hESC	embryonic stem cell:	embryo
42	chr5:75013342-75013392	ovcar-3	ovarian:	n/a
43	chr5:75013227-75013277	HCT-116	colon:	n/a
44	chr5:74991826-74991876	K562	blood:	n/a
45	chr5:75013471-75013521	HRCEpiC	kidney:	n/a
46	chr5:75016955-75017005	HCM	heart:	n/a
47	chr5:75013227-75013277	CMK	blood:	n/a
48	chr5:75009428-75009478	GM12891	blood:	n/a
49	chr5:75127929-75127979	GM12892	blood:	n/a
50	chr5:75013592-75013642	AoSMC	blood vessel:	n/a

(count:94 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:74959970..74961673-chr5:74963157..74964976,2	K562	blood:
2	chr5:75012010..75014731-chr5:75028709..75032386,3	MCF-7	breast:
3	chr5:74972829..74974939-chr5:74988828..74991642,2	K562	blood:
4	chr5:75001323..75004306-chr5:75007634..75010552,4	K562	blood:
5	chr5:74980503..74982901-chr5:74987691..74991437,3	K562	blood:
6	chr5:74983383..74985816-chr5:74986584..74989106,2	MCF-7	breast:
7	chr5:75034732..75038167-chr5:75039040..75042363,3	K562	blood:
8	chr5:75011834..75014480-chr5:75016534..75018144,2	MCF-7	breast:
9	chr5:75008837..75011583-chr5:75016834..75018987,2	K562	blood:
10	chr5:74961965..74963917-chr5:74970216..74971914,2	K562	blood:
11	chr5:75001250..75005615-chr5:75010572..75014500,9	K562	blood:
12	chr5:74880212..74881196-chr5:74962425..74963375,4	MCF-7	breast:
13	chr5:75030757..75031393-chr5:75551873..75552728,2	K562	blood:
14	chr5:75004216..75010579-chr5:75011703..75014378,6	MCF-7	breast:
15	chr5:74991379..74992986-chr5:75011800..75013427,2	K562	blood:
16	chr5:74959970..74961673-chr5:74963157..74964976,2	K562	blood:
17	chr20:49340007..49342985-chr5:75118339..75121338,3	MCF-7	breast:
18	chr5:74965127..74967340-chr5:75010605..75013451,3	K562	blood:
19	chr20:49341351..49342130-chr5:75119338..75119859,2	MCF-7	breast:
20	chr5:74980613..74983267-chr5:74984574..74986964,2	K562	blood:
21	chr5:74997231..74999217-chr5:75000460..75002166,2	K562	blood:
22	chr5:75032759..75033454-chr5:151772671..151773601,2	HCT-116	colon:
23	chr5:75030809..75031718-chr5:75181454..75182073,2	MCF-7	breast:
24	chr5:75012994..75014594-chr5:75126997..75129169,2	K562	blood:
25	chr5:74983383..74985816-chr5:74986584..74989106,2	MCF-7	breast:
26	chr5:74880501..74881472-chr5:74976763..74977639,2	MCF-7	breast:
27	chr5:74986971..74989471-chr5:74989787..74992402,2	MCF-7	breast:
28	chr5:75012994..75014594-chr5:75126997..75129169,2	K562	blood:
29	chr5:74880080..74881244-chr5:74962362..74964218,14	MCF-7	breast:
30	chr5:75001250..75005615-chr5:75010572..75014500,9	K562	blood:
31	chr5:74735308..74738290-chr5:74961776..74964047,2	K562	blood:
32	chr17:3571470..3572129-chr5:75012688..75013610,2	Hela-S3	cervix:
33	chr5:74996831..74999207-chr5:75004311..75007242,2	K562	blood:
34	chr5:75050757..75053657-chr5:75055621..75057191,2	K562	blood:
35	chr5:74756440..74758113-chr5:75010084..75012046,2	K562	blood:
36	chr5:74532317..74532921-chr5:74976842..74977712,2	K562	blood:
37	chr5:74997231..74999217-chr5:75000460..75002166,2	K562	blood:
38	chr5:74951852..74953716-chr5:74968580..74970630,2	K562	blood:
39	chr5:75018075..75020883-chr5:75022591..75024693,2	K562	blood:
40	chr5:74955921..74958847-chr5:74961478..74964262,3	K562	blood:
41	chr5:74998769..75000533-chr5:75008112..75009856,2	MCF-7	breast:
42	chr5:74956949..74958847-chr5:74961293..74964249,2	K562	blood:
43	chr5:75018075..75020883-chr5:75022591..75024693,2	K562	blood:
44	chr5:75036533..75039419-chr5:75045719..75047617,2	K562	blood:
45	chr5:74633002..74635499-chr5:74966644..74968332,2	K562	blood:
46	chr5:75030589..75031686-chr5:75551613..75552708,6	MCF-7	breast:
47	chr3:112738070..112738697-chr5:75013074..75013717,2	HCT-116	colon:
48	chr5:74952495..74955459-chr5:74961686..74963716,2	K562	blood:
49	chr5:74986233..74988640-chr5:74991256..74992996,3	K562	blood:
50	chr5:74959210..74961845-chr5:74965195..74967227,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKDD1B-4	chr5:74998373-74998574	ucscGeneNc_uc010izt_1
2	lnc-POLK-2	chr5:74966804-74967175	NONHSAT102216
3	lnc-ANKDD1B-4	chr5:75002560-75002734	ucscGeneNc_uc010izt_1
4	lnc-ANKDD1B-5	chr5:75018947-75019386	NONHSAT102223
5	lnc-POLK-2	chr5:74965019-74965208	NONHSAT102216
6	lnc-ANKDD1B-4	chr5:74994975-74995070	ucscGeneNc_uc010izt_1
7	lnc-POC5-3	chr5:75048395-75049304	NONHSAT102224
8	lnc-ANKDD1B-4	chr5:74990864-74990962	ucscGeneNc_uc010izt_1
9	lnc-ANKDD1B-4	chr5:74984723-74984821	ucscGeneNc_uc010izt_1
10	lnc-ANKDD1B-4	chr5:74987610-74987708	ucscGeneNc_uc010izt_1

No data

Variant related genes	Relation type
POC5	TF binding region
ENSG00000251419	TF binding region
SLC25A5P9	TF binding region
RNU6-680P	TF binding region
POC5	CpG island
ENSG00000251419	CpG island
SLC25A5P9	CpG island
RNU6-680P	CpG island
ENSG00000113161	chromatin interactions
ENSG00000240057	chromatin interactions
ENSG00000163608	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000207333	chromatin interactions
ENSG00000247372	chromatin interactions
ENSG00000213977	chromatin interactions
ENSG00000152359	chromatin interactions
ENSG00000127774	chromatin interactions
ENSG00000251078	chromatin interactions
ENSG00000251419	chromatin interactions
ENSG00000145700	chromatin interactions

Extended variants
information (count: 4014 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4014 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576443384	chr5:74961530-74961531	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566689239	chr5:74961582-74961583	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545363722	chr5:74961596-74961597	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190303202	chr5:74961610-74961611	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199500032	chr5:74961614-74961615	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375020490	chr5:74961618-74961619	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576038788	chr5:74961641-74961642	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371381725	chr5:74961756-74961757	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542047751	chr5:74961794-74961795	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561730016	chr5:74961795-74961796	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34356	chr5:74961796-74961797	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs148525918	chr5:74961852-74961853	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186169308	chr5:74961903-74961904	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115752025	chr5:74961921-74961922	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs151023459	chr5:74961922-74961923	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142644518	chr5:74961943-74961944	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529361435	chr5:74961951-74961952	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs367582234	chr5:74961993-74961994	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549603417	chr5:74962059-74962060	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557385494	chr5:74962097-74962098	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144916501	chr5:74962105-74962106	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534850550	chr5:74962108-74962109	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558050148	chr5:74962118-74962119	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571585258	chr5:74962127-74962128	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577316099	chr5:74962203-74962204	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs17563395	chr5:74962242-74962243	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs555874065	chr5:74962278-74962279	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540522440	chr5:74962337-74962338	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191020119	chr5:74962394-74962395	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs111425767	chr5:74962410-74962411	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs555459745	chr5:74962411-74962412	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs572284717	chr5:74962416-74962417	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs73124765	chr5:74962440-74962441	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs386689138	chr5:74962456-74962457	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs377299292	chr5:74962458-74962459	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs533249604	chr5:74962468-74962469	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs10561485	chr5:74962469-74962470	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs79141566	chr5:74962470-74962471	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs374666519	chr5:74962472-74962473	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs542881413	chr5:74962482-74962483	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs559405152	chr5:74962489-74962490	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs10035878	chr5:74962514-74962515	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs549222518	chr5:74962515-74962516	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs80063566	chr5:74962546-74962547	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs141726698	chr5:74962562-74962563	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs182169897	chr5:74962643-74962644	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs370286315	chr5:74962687-74962688	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs571646791	chr5:74962694-74962695	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs79580703	chr5:74962723-74962724	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs6453139	chr5:74962768-74962769	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:91)

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
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
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	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
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
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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	22355333	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2086 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74921800-74964400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:74945000-74962800	Weak transcription	Fetal Intestine Large	intestine
3	chr5:74952600-74964200	Weak transcription	Stomach Mucosa	stomach
4	chr5:74952800-74964000	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr5:74952800-74964200	Weak transcription	Right Ventricle	heart
6	chr5:74952800-74964400	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr5:74952800-74981400	Weak transcription	Psoas Muscle	Psoas
8	chr5:74953000-74964200	Weak transcription	Fetal Muscle Leg	muscle
9	chr5:74953000-74964400	Weak transcription	Adipose Nuclei	Adipose
10	chr5:74953000-74964400	Weak transcription	Fetal Kidney	kidney
11	chr5:74953000-74964400	Weak transcription	Fetal Stomach	stomach
12	chr5:74953000-74964600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr5:74956000-74965000	Weak transcription	NHEK	skin
14	chr5:74956600-74964400	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr5:74956800-74962800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr5:74956800-74964600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr5:74957400-74966000	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr5:74957400-74966000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr5:74958000-74964600	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr5:74958400-74964400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr5:74959200-74965200	Enhancers	Brain Substantia Nigra	brain
22	chr5:74959400-74963000	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr5:74960000-74962000	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr5:74960000-74962600	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr5:74960200-74963000	Weak transcription	Brain Anterior Caudate	brain
26	chr5:74960200-74968600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr5:74960600-74962000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr5:74960800-74963200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr5:74960800-74965400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr5:74961000-74963200	Weak transcription	Brain Cingulate Gyrus	brain
31	chr5:74961000-74964200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr5:74961000-74976800	Weak transcription	Colon Smooth Muscle	Colon
33	chr5:74961000-74987800	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr5:74961200-74962000	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr5:74961200-74962200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr5:74961200-74964000	Strong transcription	Fetal Intestine Small	intestine
37	chr5:74961200-74964600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr5:74961200-74965000	Enhancers	Brain Hippocampus Middle	brain
39	chr5:74961200-74968000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr5:74961400-74961600	Enhancers	Fetal Brain Male	brain
41	chr5:74961400-74962000	Enhancers	Primary hematopoietic stem cells	blood
42	chr5:74961400-74962000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr5:74961400-74963200	Weak transcription	Brain Angular Gyrus	brain
44	chr5:74961600-74963400	Weak transcription	Fetal Brain Male	brain
45	chr5:74961800-74962000	Enhancers	H1 Cell Line	embryonic stem cell
46	chr5:74961800-74963000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr5:74962000-74962400	Enhancers	Brain Germinal Matrix	brain
48	chr5:74962000-74962800	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr5:74962000-74963000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr5:74962000-74964000	Weak transcription	Primary hematopoietic stem cells	blood

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