Variant report

Variant	nsv537089
Chromosome Location	chr4:48580484-49032909
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6064)
CpG islands
(count:4275)
Chromatin interactive
region (count:313)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:6064 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:48781987-48783049	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:48669405-48669518	K562	blood:	n/a	n/a
3	ARID3A	chr4:48720801-48721430	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:48701999-48702183	K562	blood:	n/a	n/a
5	ARID3A	chr4:48900896-48901613	K562	blood:	n/a	n/a
6	ARID3A	chr4:48949857-48949997	K562	blood:	n/a	n/a
7	ARID3A	chr4:48806867-48807112	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:48628294-48628494	K562	blood:	n/a	n/a
9	ARID3A	chr4:48741003-48741162	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:48781053-48781304	K562	blood:	n/a	n/a
11	ARID3A	chr4:48782070-48782746	K562	blood:	n/a	n/a
12	ARID3A	chr4:48741537-48742064	K562	blood:	n/a	n/a
13	ARID3A	chr4:48780185-48780773	K562	blood:	n/a	chr4:48780342-48780358
14	ARID3A	chr4:48965071-48965451	K562	blood:	n/a	n/a
15	ARID3A	chr4:48779668-48779711	K562	blood:	n/a	n/a
16	ARID3A	chr4:48700373-48700768	K562	blood:	n/a	n/a
17	ARID3A	chr4:48685726-48686787	K562	blood:	n/a	n/a
18	ARID3A	chr4:48580424-48580701	HepG2	liver:	n/a	n/a
19	ARID3A	chr4:48605411-48605798	HepG2	liver:	n/a	n/a
20	ARID3A	chr4:48781608-48781746	HepG2	liver:	n/a	n/a
21	ARID3A	chr4:48742647-48743070	K562	blood:	n/a	n/a
22	ARID3A	chr4:48731313-48731501	K562	blood:	n/a	n/a
23	ARID3A	chr4:48625256-48625761	K562	blood:	n/a	n/a
24	ARID3A	chr4:48965068-48965466	HepG2	liver:	n/a	n/a
25	ARID3A	chr4:48682969-48684161	K562	blood:	n/a	chr4:48683524-48683540
26	ARID3A	chr4:48834700-48834957	K562	blood:	n/a	n/a
27	ARID3A	chr4:48728717-48728995	K562	blood:	n/a	n/a
28	ARID3A	chr4:48832949-48833248	HepG2	liver:	n/a	n/a
29	ARID3A	chr4:48902033-48902294	K562	blood:	n/a	n/a
30	ARID3A	chr4:48689608-48689783	K562	blood:	n/a	n/a
31	ARID3A	chr4:48593472-48593744	K562	blood:	n/a	n/a
32	ARID3A	chr4:48597297-48597435	K562	blood:	n/a	n/a
33	ARID3A	chr4:48855685-48856516	K562	blood:	n/a	n/a
34	ARID3A	chr4:48911807-48911825	K562	blood:	n/a	n/a
35	ARID3A	chr4:48907437-48907684	HepG2	liver:	n/a	n/a
36	ARID3A	chr4:48625367-48625761	HepG2	liver:	n/a	n/a
37	ATF1	chr4:48702001-48702239	K562	blood:	n/a	n/a
38	ATF1	chr4:48960603-48960934	K562	blood:	n/a	n/a
39	ATF1	chr4:48901179-48901510	K562	blood:	n/a	n/a
40	ATF1	chr4:48823576-48823694	K562	blood:	n/a	n/a
41	ATF1	chr4:48782242-48782757	K562	blood:	n/a	n/a
42	ATF1	chr4:48855906-48856194	K562	blood:	n/a	n/a
43	ATF1	chr4:48593488-48593917	K562	blood:	n/a	n/a
44	ATF1	chr4:48685798-48686486	K562	blood:	n/a	n/a
45	ATF1	chr4:48741571-48741881	K562	blood:	n/a	n/a
46	ATF1	chr4:48631400-48631866	K562	blood:	n/a	n/a
47	ATF1	chr4:48740483-48740490	K562	blood:	n/a	n/a
48	ATF1	chr4:48625474-48625805	K562	blood:	n/a	n/a
49	ATF1	chr4:48683063-48683464	K562	blood:	n/a	n/a
50	ATF1	chr4:48700313-48700663	K562	blood:	n/a	n/a

(count:4275 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:48925826-48925876	GM12892	blood:	n/a
2	chr4:48912027-48912077	AG09309	skin:	n/a
3	chr4:48779921-48779971	GM12892	blood:	n/a
4	chr4:48833041-48833091	HEEpiC	esophagus:	n/a
5	chr4:48833292-48833342	HCF	heart:	n/a
6	chr4:48925826-48925876	GM12892	blood:	n/a
7	chr4:48912027-48912077	AG09309	skin:	n/a
8	chr4:48779921-48779971	GM12892	blood:	n/a
9	chr4:48833041-48833091	HEEpiC	esophagus:	n/a
10	chr4:48833292-48833342	HCF	heart:	n/a
11	chr4:48832808-48832858	A549	lung:	n/a
12	chr4:48785918-48785968	GM19239	blood:	n/a
13	chr4:48833056-48833106	BE2_C	brain:	n/a
14	chr4:48987791-48987841	MCF10A-Er-Src	breast:	n/a
15	chr4:48906555-48906605	GM12892	blood:	n/a
16	chr4:48782551-48782601	NT2-D1	testis:	n/a
17	chr4:48779921-48779971	AG04450	lung:	fetal
18	chr4:48909057-48909107	NT2-D1	testis:	n/a
19	chr4:48833088-48833138	U87	brain:	n/a
20	chr4:48835877-48835927	HPAEpiC	pulmonary alveolar:	n/a
21	chr4:48656001-48656051	ECC-1	luminal epithelium:	n/a
22	chr4:48695242-48695292	IMR90	lung:	fetal
23	chr4:48991973-48992023	AoSMC	blood vessel:	n/a
24	chr4:48781332-48781382	K562	blood:	n/a
25	chr4:48779921-48779971	K562	blood:	n/a
26	chr4:48906555-48906605	HEEpiC	esophagus:	n/a
27	chr4:48754953-48755003	ovcar-3	ovarian:	n/a
28	chr4:48833193-48833243	HUVEC	blood vessel:	n/a
29	chr4:48754953-48755003	AG04449	skin:	fetal
30	chr4:48833568-48833618	CMK	blood:	n/a
31	chr4:48829788-48829838	ECC-1	luminal epithelium:	n/a
32	chr4:48833206-48833256	RPTEC	kidney:	n/a
33	chr4:48908902-48908952	HCF	heart:	n/a
34	chr4:48777471-48777521	BJ	skin:	n/a
35	chr4:48835877-48835927	NH-A	brain:	n/a
36	chr4:48777471-48777521	Caco-2	colon:	n/a
37	chr4:48832808-48832858	HRPEpiC	eye:	n/a
38	chr4:48833292-48833342	T-47D	breast:	n/a
39	chr4:48832808-48832858	HL-60	blood:	n/a
40	chr4:48833388-48833438	ECC-1	luminal epithelium:	n/a
41	chr4:48908902-48908952	H1-hESC	embryonic stem cell:	embryo
42	chr4:48991973-48992023	HCPEpiC	choroid plexus:	n/a
43	chr4:48908902-48908952	SKMC	muscle:	n/a
44	chr4:48833041-48833091	HepG2	liver:	n/a
45	chr4:48833206-48833256	HIPEpiC	eye:	n/a
46	chr4:48906555-48906605	SK-N-SH_RA	brain:	n/a
47	chr4:48833130-48833180	BJ	skin:	n/a
48	chr4:48832952-48833002	HUVEC	blood vessel:	n/a
49	chr4:48908696-48908746	HCT-116	colon:	n/a
50	chr4:48987791-48987841	HRE	kidney:	n/a

(count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr4:48572897..48575148-chr4:48625721..48628316,2	K562	blood:
2	chr4:48685624..48689755-chr4:48691004..48694286,4	K562	blood:
3	chr4:48737815..48740027-chr4:48780633..48782409,2	MCF-7	breast:
4	chr4:48580097..48581053-chr4:48964810..48965685,4	K562	blood:
5	chr4:48699623..48702132-chr4:48702246..48705129,3	K562	blood:
6	chr4:48814564..48816145-chr4:48829057..48831720,2	K562	blood:
7	chr4:48580146..48580771-chr4:48964761..48965396,2	MCF-7	breast:
8	chr4:48951539..48954783-chr4:48955167..48956810,3	MCF-7	breast:
9	chr4:48834344..48836920-chr4:48860620..48862528,2	K562	blood:
10	chr4:48689702..48692594-chr4:48697555..48699219,2	K562	blood:
11	chr4:48772195..48774601-chr4:48832586..48834543,2	K562	blood:
12	chr4:48683162..48685673-chr4:48779626..48783041,3	MCF-7	breast:
13	chr4:48831337..48833457-chr4:48856864..48859835,2	MCF-7	breast:
14	chr4:48622305..48625029-chr4:48654656..48657313,2	K562	blood:
15	chr4:48832331..48834187-chr4:48907329..48910001,2	MCF-7	breast:
16	chr4:48892295..48895717-chr4:48900323..48903334,3	MCF-7	breast:
17	chr1:149222104..149224886-chr4:48870472..48871972,2	MCF-7	breast:
18	chr4:48794659..48797818-chr4:48831784..48834674,3	MCF-7	breast:
19	chr4:48949861..48952069-chr4:48952330..48953887,2	MCF-7	breast:
20	chr4:48964805..48966894-chr4:48969035..48971406,2	K562	blood:
21	chr4:48862851..48865784-chr4:48884723..48887077,2	MCF-7	breast:
22	chr4:48896623..48898148-chr4:48938034..48940839,2	MCF-7	breast:
23	chr4:48626369..48628098-chr4:48781487..48784150,2	MCF-7	breast:
24	chr4:48832329..48839135-chr4:48842644..48848925,12	K562	blood:
25	chr4:48945137..48946034-chr4:48964617..48965701,8	MCF-7	breast:
26	chr4:48615973..48618309-chr4:48625425..48627835,2	K562	blood:
27	chr4:48702489..48705093-chr4:48707646..48709743,2	MCF-7	breast:
28	chr4:48781848..48784199-chr4:48833719..48835866,2	K562	blood:
29	chr4:48780694..48783941-chr4:48830567..48835952,11	MCF-7	breast:
30	chr4:48576864..48578418-chr4:48583302..48585934,2	K562	blood:
31	chr4:48782469..48785403-chr4:48787452..48790375,2	MCF-7	breast:
32	chr4:48946560..48948277-chr4:48957901..48960344,2	K562	blood:
33	chr4:48673422..48675692-chr4:48679955..48681969,2	MCF-7	breast:
34	chr4:48580146..48580771-chr4:48964761..48965396,2	MCF-7	breast:
35	chr4:48853235..48855592-chr4:48860236..48864497,3	MCF-7	breast:
36	chr4:48854871..48855704-chr4:48963569..48964287,2	MCF-7	breast:
37	chr4:48652921..48654969-chr4:48656237..48658200,2	K562	blood:
38	chr4:48628287..48631259-chr4:48635735..48637672,2	MCF-7	breast:
39	chr2:97303523..97304125-chr4:48781852..48782604,2	Hela-S3	cervix:
40	chr4:48780865..48783297-chr4:48796375..48799379,3	K562	blood:
41	chr4:48644058..48646870-chr4:48657277..48658947,3	K562	blood:
42	chr4:48832608..48834805-chr4:48835909..48838129,2	MCF-7	breast:
43	chr4:48900749..48905906-chr4:48906266..48908973,4	MCF-7	breast:
44	chr4:48749888..48752045-chr4:48754340..48756455,2	K562	blood:
45	chr4:48780685..48782941-chr4:48832386..48835907,3	MCF-7	breast:
46	chr4:48580476..48581095-chr4:48946367..48946964,2	K562	blood:
47	chr4:48848263..48850422-chr4:48852195..48854552,3	K562	blood:
48	chr4:48907349..48910637-chr4:48932106..48935377,4	MCF-7	breast:
49	chr4:48627219..48628721-chr4:48636980..48639563,2	K562	blood:
50	chr4:48949781..48950345-chr4:48964835..48965506,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CWH43-1	chr4:48938599-48938897	NONHSAT096305
2	lnc-OCIAD2-3	chr4:48686690-48686812	NONHSAT096292
3	lnc-OCIAD2-3	chr4:48712536-48712715	NONHSAT096293
4	lnc-CWH43-3	chr4:48862742-48862876	NONHSAT096297
5	lnc-CWH43-3	chr4:48854209-48854521	NONHSAT096297
6	lnc-OCIAD2-3	chr4:48636435-48636507	NONHSAT096290
7	lnc-OCIAD2-3	chr4:48686690-48686812	NONHSAT096291
8	lnc-OCIAD2-3	chr4:48782095-48782284	NONHSAT096290
9	lnc-OCIAD2-3	chr4:48712536-48712715	NONHSAT096290
10	lnc-OCIAD2-3	chr4:48636435-48636507	NONHSAT096291
11	lnc-OCIAD2-3	chr4:48782095-48782146	NONHSAT096293
12	lnc-OCIAD2-3	chr4:48782095-48782339	NONHSAT096291
13	lnc-OCIAD2-3	chr4:48686690-48686812	NONHSAT096293
14	lnc-OCIAD2-3	chr4:48638867-48640580	NONHSAT096292
15	lnc-OCIAD2-3	chr4:48647986-48648034	NONHSAT096293
16	lnc-OCIAD2-1	chr4:48854025-48854242	ENSG00000248256.1
17	lnc-OCIAD2-1	chr4:48862174-48862220	ENSG00000248256.1
18	lnc-OCIAD2-3	chr4:48782095-48782288	NONHSAT096292
19	lnc-OCIAD2-3	chr4:48729448-48729508	NONHSAT096293

No data

Variant related genes	Relation type
RNU6-158P	TF binding region
TPI1P4	TF binding region
OCIAD2	TF binding region
OCIAD1	TF binding region
FRYL	TF binding region
ENSG00000251334	TF binding region
OCIAD1-AS1	TF binding region
CWH43	TF binding region
RNU5E-3P	TF binding region
RNU6-158P	CpG island
TPI1P4	CpG island
OCIAD2	CpG island
OCIAD1	CpG island
FRYL	CpG island
ENSG00000251334	CpG island
OCIAD1-AS1	CpG island
CWH43	CpG island
RNU5E-3P	CpG island
ENSG00000248256	chromatin interactions
ENSG00000143970	chromatin interactions
ENSG00000114982	chromatin interactions
ENSG00000147162	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000150459	chromatin interactions
ENSG00000185238	chromatin interactions
ENSG00000109182	chromatin interactions
ENSG00000251722	chromatin interactions
ENSG00000075539	chromatin interactions
ENSG00000145247	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000252913	chromatin interactions
ENSG00000251334	chromatin interactions
ENSG00000109180	chromatin interactions

Extended variants
information (count: 15640 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:15640 , 50 per page) page: 1 2 3 4 5 6 7 ... 313

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111362813	chr4:48580503-48580504	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs146312277	chr4:48580535-48580536	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs552030823	chr4:48580540-48580541	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs528094098	chr4:48580610-48580611	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs569986452	chr4:48580656-48580657	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs17656189	chr4:48580683-48580684	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs555425288	chr4:48580699-48580700	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs573803877	chr4:48580745-48580746	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs375467977	chr4:48580747-48580748	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs201210077	chr4:48580751-48580752	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs185719492	chr4:48580802-48580803	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs552793838	chr4:48580831-48580832	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs76338164	chr4:48580853-48580854	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs200436808	chr4:48581017-48581018	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs373573217	chr4:48581039-48581040	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs544935208	chr4:48581047-48581048	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs377039573	chr4:48581068-48581069	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs75542681	chr4:48581089-48581090	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs575421561	chr4:48581099-48581100	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs569486031	chr4:48581150-48581151	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs560682735	chr4:48581158-48581159	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs372665399	chr4:48581177-48581178	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs375600105	chr4:48581220-48581221	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs188966880	chr4:48581258-48581259	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs78710838	chr4:48581285-48581286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs367939638	chr4:48581304-48581305	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533554222	chr4:48581317-48581318	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374362554	chr4:48581436-48581437	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs532886802	chr4:48581440-48581441	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs564875282	chr4:48581487-48581488	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs570329075	chr4:48581511-48581512	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs181647695	chr4:48581559-48581560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549396887	chr4:48581600-48581601	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186225335	chr4:48581628-48581629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191890576	chr4:48581776-48581777	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs534817868	chr4:48581796-48581797	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs553033262	chr4:48581843-48581844	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs144557409	chr4:48581896-48581897	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs182590774	chr4:48581935-48581936	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs556831251	chr4:48581978-48581979	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs146150481	chr4:48581994-48581995	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs185905206	chr4:48582008-48582009	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs542548788	chr4:48582032-48582033	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs191055627	chr4:48582034-48582035	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs572856438	chr4:48582035-48582036	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs113000095	chr4:48582085-48582086	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs386400020	chr4:48582086-48582087	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs11375529	chr4:48582092-48582093	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs370544577	chr4:48582093-48582094	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs540365765	chr4:48582189-48582190	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Basal cell lymphoma	21115979	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	20952505	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:9897 , 50 per page) page: 1 2 3 4 5 6 7 ... 198

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:48498600-48593000	Strong transcription	Rectal Mucosa Donor 31	rectum
2	chr4:48499000-48589400	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr4:48499600-48581400	Strong transcription	Dnd41	blood
4	chr4:48500200-48588800	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr4:48515800-48625000	Weak transcription	Hela-S3	cervix
6	chr4:48525000-48595600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr4:48528200-48596000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr4:48541000-48580600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr4:48541000-48587800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr4:48541200-48594000	Strong transcription	Rectal Mucosa Donor 29	rectum
11	chr4:48541400-48581200	Strong transcription	Primary T cells fromperipheralblood	blood
12	chr4:48541600-48581400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:48542800-48604400	Weak transcription	A549	lung
14	chr4:48545200-48618200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr4:48546400-48596400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr4:48547400-48593600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr4:48556000-48581400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr4:48557800-48622400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr4:48559800-48604400	Weak transcription	HepG2	liver
20	chr4:48561200-48581200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr4:48561400-48604400	Weak transcription	Stomach Mucosa	stomach
22	chr4:48562600-48596600	Weak transcription	Fetal Brain Male	brain
23	chr4:48562800-48590400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:48562800-48623200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr4:48563000-48637400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr4:48563200-48587000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr4:48563400-48593600	Weak transcription	Spleen	Spleen
28	chr4:48566600-48587600	Weak transcription	Colon Smooth Muscle	Colon
29	chr4:48572600-48582600	Weak transcription	Brain Germinal Matrix	brain
30	chr4:48573200-48586200	Weak transcription	Psoas Muscle	Psoas
31	chr4:48573200-48590000	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr4:48573200-48604600	Weak transcription	NHLF	lung
33	chr4:48573200-48605600	Weak transcription	Pancreas	Pancrea
34	chr4:48573200-48605600	Weak transcription	Small Intestine	intestine
35	chr4:48573800-48590000	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr4:48574000-48584400	Weak transcription	Fetal Heart	heart
37	chr4:48575000-48582800	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr4:48575000-48586400	Weak transcription	Left Ventricle	heart
39	chr4:48575000-48590000	Weak transcription	Right Ventricle	heart
40	chr4:48575000-48590400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr4:48575200-48582800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr4:48575200-48584400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr4:48575200-48586200	Weak transcription	NHDF-Ad	bronchial
44	chr4:48575200-48643000	Weak transcription	HSMMtube	muscle
45	chr4:48575400-48582400	Weak transcription	Brain Angular Gyrus	brain
46	chr4:48575400-48583400	Weak transcription	Fetal Brain Female	brain
47	chr4:48576400-48589000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr4:48577000-48580600	Strong transcription	Sigmoid Colon	Sigmoid Colon
49	chr4:48577000-48581200	Strong transcription	Primary T cells from cord blood	blood
50	chr4:48577400-48583400	Weak transcription	NH-A	brain

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