Variant report

Variant	nsv461357
Chromosome Location	chr4:48248258-48274152
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1013)
CpG islands
(count:1223)
Chromatin interactive
region (count:57)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1013 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:48271156-48271462	K562	blood:	n/a	n/a
2	ARID3A	chr4:48260893-48260896	K562	blood:	n/a	n/a
3	ARID3A	chr4:48271978-48272494	K562	blood:	n/a	n/a
4	ARID3A	chr4:48249420-48249934	K562	blood:	n/a	n/a
5	ATF1	chr4:48257322-48257741	K562	blood:	n/a	n/a
6	ATF1	chr4:48272999-48273508	K562	blood:	n/a	n/a
7	ATF1	chr4:48254522-48254801	K562	blood:	n/a	n/a
8	ATF1	chr4:48249224-48249377	K562	blood:	n/a	n/a
9	ATF2	chr4:48271888-48272435	GM12878	blood:	n/a	n/a
10	ATF2	chr4:48272043-48272668	GM12878	blood:	n/a	n/a
11	ATF2	chr4:48249067-48249653	GM12878	blood:	n/a	n/a
12	ATF2	chr4:48271260-48271747	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr4:48271289-48271867	GM12878	blood:	n/a	n/a
14	ATF3	chr4:48257249-48257555	K562	blood:	n/a	n/a
15	BACH1	chr4:48271474-48271674	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr4:48271610-48271743	K562	blood:	n/a	n/a
17	BACH1	chr4:48272139-48272826	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr4:48249168-48249564	K562	blood:	n/a	n/a
19	BACH1	chr4:48272285-48272805	K562	blood:	n/a	n/a
20	BACH1	chr4:48253636-48253639	K562	blood:	n/a	n/a
21	BATF	chr4:48249189-48249516	GM12878	blood:	n/a	chr4:48249376-48249387
22	BATF	chr4:48249174-48249528	GM12878	blood:	n/a	chr4:48249376-48249387
23	BATF	chr4:48273182-48273516	GM12878	blood:	n/a	n/a
24	BCL11A	chr4:48249198-48249489	GM12878	blood:	n/a	n/a
25	BCL3	chr4:48271926-48272500	GM12878	blood:	n/a	chr4:48272028-48272041
26	BCL3	chr4:48252364-48252729	GM12878	blood:	n/a	n/a
27	BCL3	chr4:48252361-48252701	GM12878	blood:	n/a	n/a
28	BCL3	chr4:48254027-48254418	GM12878	blood:	n/a	n/a
29	BCLAF1	chr4:48272931-48273514	GM12878	blood:	n/a	n/a
30	BCLAF1	chr4:48249095-48249588	GM12878	blood:	n/a	n/a
31	BCLAF1	chr4:48271899-48272596	GM12878	blood:	n/a	chr4:48272028-48272041
32	BCLAF1	chr4:48271929-48272686	GM12878	blood:	n/a	chr4:48272028-48272041
33	BHLHE40	chr4:48273012-48273470	GM12878	blood:	n/a	n/a
34	BHLHE40	chr4:48269776-48272702	K562	blood:	n/a	chr4:48272386-48272407 chr4:48272391-48272400 chr4:48271167-48271176 chr4:48271162-48271183
35	BHLHE40	chr4:48271031-48271331	A549	lung:	n/a	chr4:48271167-48271176 chr4:48271162-48271183
36	BHLHE40	chr4:48257006-48257710	K562	blood:	n/a	n/a
37	BHLHE40	chr4:48271106-48272528	HepG2	liver:	n/a	chr4:48272386-48272407 chr4:48272391-48272400 chr4:48271167-48271176 chr4:48271162-48271183
38	BHLHE40	chr4:48270826-48272646	GM12878	blood:	n/a	chr4:48272386-48272407 chr4:48272391-48272400 chr4:48271167-48271176 chr4:48271162-48271183
39	BRCA1	chr4:48271992-48272307	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr4:48272079-48272126	GM12878	blood:	n/a	n/a
41	BRCA1	chr4:48271475-48271779	Hela-S3	cervix:	n/a	n/a
42	CBX3	chr4:48271849-48272872	K562	blood:	n/a	n/a
43	CBX3	chr4:48257117-48257708	K562	blood:	n/a	n/a
44	CBX3	chr4:48273536-48274046	K562	blood:	n/a	n/a
45	CBX3	chr4:48257024-48257830	K562	blood:	n/a	n/a
46	CBX3	chr4:48248575-48249490	K562	blood:	n/a	n/a
47	CBX3	chr4:48271080-48271811	K562	blood:	n/a	n/a
48	CCNT2	chr4:48249671-48249885	K562	blood:	n/a	n/a
49	CCNT2	chr4:48271298-48272389	K562	blood:	n/a	n/a
50	CCNT2	chr4:48257456-48257726	K562	blood:	n/a	n/a

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:48271826-48271876	U87	brain:	n/a
2	chr4:48271149-48271199	HepG2	liver:	n/a
3	chr4:48273240-48273290	NH-A	brain:	n/a
4	chr4:48271826-48271876	U87	brain:	n/a
5	chr4:48271149-48271199	HepG2	liver:	n/a
6	chr4:48273240-48273290	NH-A	brain:	n/a
7	chr4:48272120-48272170	MCF-7	breast:	n/a
8	chr4:48271149-48271199	HRCEpiC	kidney:	n/a
9	chr4:48271918-48271968	AoSMC	blood vessel:	n/a
10	chr4:48272297-48272347	AoSMC	blood vessel:	n/a
11	chr4:48269743-48269793	HRPEpiC	eye:	n/a
12	chr4:48269743-48269793	SK-N-SH_RA	brain:	n/a
13	chr4:48271072-48271122	GM12892	blood:	n/a
14	chr4:48272297-48272347	U87	brain:	n/a
15	chr4:48272297-48272347	BE2_C	brain:	n/a
16	chr4:48272266-48272316	AoSMC	blood vessel:	n/a
17	chr4:48257144-48257194	Jurkat	blood:	n/a
18	chr4:48257144-48257194	HepG2	liver:	n/a
19	chr4:48272297-48272347	SAEC	small airway:	n/a
20	chr4:48272266-48272316	HRPEpiC	eye:	n/a
21	chr4:48271107-48271157	HepG2	liver:	n/a
22	chr4:48271923-48271973	GM12891	blood:	n/a
23	chr4:48271826-48271876	PANC-1	pancreas:	n/a
24	chr4:48272297-48272347	HCF	heart:	n/a
25	chr4:48271072-48271122	AoSMC	blood vessel:	n/a
26	chr4:48272120-48272170	Caco-2	colon:	n/a
27	chr4:48257144-48257194	HNPCEpiC	eye:	n/a
28	chr4:48273240-48273290	PFSK-1	brain:	n/a
29	chr4:48257144-48257194	HIPEpiC	eye:	n/a
30	chr4:48257144-48257194	GM06990	blood:	n/a
31	chr4:48272082-48272132	PANC-1	pancreas:	n/a
32	chr4:48272266-48272316	Jurkat	blood:	n/a
33	chr4:48271918-48271968	A549	lung:	n/a
34	chr4:48271107-48271157	SAEC	small airway:	n/a
35	chr4:48271942-48271992	HPAEpiC	pulmonary alveolar:	n/a
36	chr4:48271918-48271968	SK-N-SH	brain:	n/a
37	chr4:48271107-48271157	AoSMC	blood vessel:	n/a
38	chr4:48272059-48272109	HNPCEpiC	eye:	n/a
39	chr4:48271835-48271885	T-47D	breast:	n/a
40	chr4:48273240-48273290	SAEC	small airway:	n/a
41	chr4:48271923-48271973	SK-N-SH_RA	brain:	n/a
42	chr4:48269743-48269793	A549	lung:	n/a
43	chr4:48271893-48271943	K562	blood:	n/a
44	chr4:48272513-48272563	Caco-2	colon:	n/a
45	chr4:48272297-48272347	PFSK-1	brain:	n/a
46	chr4:48269743-48269793	SK-N-MC	brain:	n/a
47	chr4:48272120-48272170	AG10803	skin:	n/a
48	chr4:48272297-48272347	Caco-2	colon:	n/a
49	chr4:48257144-48257194	HRE	kidney:	n/a
50	chr4:48271149-48271199	HEK293	kidney:	embryo

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:56511687..56512571-chr4:48271561..48272061,2	Hela-S3	cervix:
2	chr4:48248192..48249902-chr4:48342443..48344604,2	K562	blood:
3	chr4:48238892..48241068-chr4:48247777..48249287,2	K562	blood:
4	chr19:40931605..40932510-chr4:48271137..48271845,2	Hela-S3	cervix:
5	chr4:48253065..48255231-chr4:48264308..48266240,2	K562	blood:
6	chr4:48269261..48273807-chr4:48342628..48344865,6	K562	blood:
7	chr4:48255521..48259627-chr4:48261501..48267509,10	K562	blood:
8	chr4:48258706..48261232-chr4:48269979..48272552,2	MCF-7	breast:
9	chr4:48167349..48169980-chr4:48272046..48273556,2	K562	blood:
10	chr4:48248411..48250691-chr4:48255149..48257827,3	K562	blood:
11	chr4:48270141..48273598-chr4:48341900..48344865,7	K562	blood:
12	chr4:48260906..48263782-chr4:48270701..48273043,3	K562	blood:
13	chr4:48257479..48259057-chr4:48261577..48263259,2	MCF-7	breast:
14	chr4:48253624..48256243-chr4:48267800..48270613,3	MCF-7	breast:
15	chr4:48200101..48201896-chr4:48269773..48271789,2	K562	blood:
16	chr4:48264189..48268843-chr4:48269527..48273164,9	K562	blood:
17	chr4:48251770..48253352-chr4:48260141..48262130,2	K562	blood:
18	chr4:48271855..48272497-chr7:75544014..75544536,2	NB4	blood:
19	chr3:156392017..156392697-chr4:48272003..48272899,2	NB4	blood:
20	chr12:120729424..120730098-chr4:48271378..48272195,2	Hela-S3	cervix:
21	chr4:48255487..48257034-chr4:48270351..48271892,2	K562	blood:
22	chr4:48251827..48254565-chr4:48270153..48272053,2	K562	blood:
23	chr4:48260906..48263782-chr4:48270701..48272361,2	K562	blood:
24	chr4:48272391..48273974-chr4:48279554..48281442,2	MCF-7	breast:
25	chr4:48250701..48254731-chr4:48255352..48259390,5	K562	blood:
26	chr4:48264879..48267835-chr4:48269527..48271829,4	K562	blood:
27	chr4:48264879..48267835-chr4:48269527..48271829,4	K562	blood:
28	chr4:48262092..48265166-chr4:48265573..48268015,3	K562	blood:
29	chr4:48247444..48251511-chr4:48269586..48272868,4	K562	blood:
30	chr4:48253065..48255231-chr4:48264308..48266240,2	K562	blood:
31	chr4:48255521..48259627-chr4:48261501..48267509,10	K562	blood:
32	chr1:36234965..36235557-chr4:48271368..48271893,2	Hela-S3	cervix:
33	chr4:48248891..48252665-chr4:48270333..48273467,3	MCF-7	breast:
34	chr4:48255711..48257883-chr4:48270489..48272038,2	MCF-7	breast:
35	chr4:48256167..48259627-chr4:48260322..48264297,6	K562	blood:
36	chr4:48262092..48265166-chr4:48265573..48268015,3	K562	blood:
37	chr4:48251770..48253352-chr4:48260141..48262130,2	K562	blood:
38	chr17:42297784..42298646-chr4:48271426..48272068,2	Hela-S3	cervix:
39	chr4:48191298..48193401-chr4:48269923..48271820,2	K562	blood:
40	chr1:110090966..110091798-chr4:48271404..48272367,2	Hela-S3	cervix:
41	chr4:48175041..48176757-chr4:48255815..48257585,2	K562	blood:
42	chr16:9185283..9185902-chr4:48271309..48272302,2	Hela-S3	cervix:
43	chr4:48231874..48234490-chr4:48252410..48255133,2	K562	blood:
44	chr4:48253624..48256243-chr4:48267800..48270613,3	MCF-7	breast:
45	chr4:48250701..48254731-chr4:48255352..48259390,5	K562	blood:
46	chr2:96873932..96874574-chr4:48271406..48272081,2	Hela-S3	cervix:
47	chr4:48255045..48260439-chr4:48268334..48274456,6	K562	blood:
48	chr4:48265765..48268538-chr4:48269206..48271993,2	MCF-7	breast:
49	chr4:48257479..48259057-chr4:48261577..48263259,2	MCF-7	breast:
50	chr4:48270358..48273390-chr4:48340605..48344777,4	MCF-7	breast:

No data

Variant related genes	Relation type
TEC	TF binding region
TEC	CpG island
ENSG00000204685	chromatin interactions
ENSG00000145248	chromatin interactions
ENSG00000127948	chromatin interactions
ENSG00000084090	chromatin interactions
ENSG00000135605	chromatin interactions
ENSG00000175931	chromatin interactions
ENSG00000197019	chromatin interactions
ENSG00000065135	chromatin interactions
ENSG00000182831	chromatin interactions
ENSG00000243926	chromatin interactions
ENSG00000108312	chromatin interactions
ENSG00000180035	chromatin interactions
ENSG00000109171	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000092853	chromatin interactions
ENSG00000139641	chromatin interactions
ENSG00000265020	chromatin interactions
ENSG00000129673	chromatin interactions
ENSG00000163659	chromatin interactions
ENSG00000202538	chromatin interactions

Extended variants
information (count: 873 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:873 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12643804	chr4:48248258-48248259	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs2457413	chr4:48248298-48248299	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs55994932	chr4:48248309-48248310	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs570116527	chr4:48248327-48248328	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs536873971	chr4:48248341-48248342	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs541990705	chr4:48248360-48248361	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs11945482	chr4:48248416-48248417	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs567577384	chr4:48248418-48248419	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs11945483	chr4:48248421-48248422	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs534866624	chr4:48248468-48248469	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs34988086	chr4:48248485-48248486	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs553298234	chr4:48248508-48248509	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs577750902	chr4:48248521-48248522	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs538610726	chr4:48248539-48248540	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs150310727	chr4:48248554-48248555	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs575270937	chr4:48248614-48248615	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs543669700	chr4:48248615-48248616	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs137914540	chr4:48248680-48248681	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs9996158	chr4:48248691-48248692	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs541365816	chr4:48248776-48248777	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs559602834	chr4:48248787-48248788	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs533186044	chr4:48248808-48248809	Weak transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs551134535	chr4:48248912-48248913	Weak transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs550561639	chr4:48248924-48248925	Weak transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs149468245	chr4:48248945-48248946	Weak transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs116114037	chr4:48248946-48248947	Weak transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs143016036	chr4:48248955-48248956	Weak transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs192133200	chr4:48248960-48248961	Weak transcription Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs567512815	chr4:48249039-48249040	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs534797472	chr4:48249056-48249057	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs377055397	chr4:48249057-48249058	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs142640354	chr4:48249147-48249148	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs374435559	chr4:48249150-48249151	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs571544548	chr4:48249158-48249159	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs566559144	chr4:48249191-48249192	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs538277997	chr4:48249198-48249199	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs556880945	chr4:48249200-48249201	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs371321194	chr4:48249208-48249209	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs185386283	chr4:48249338-48249339	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs55666922	chr4:48249339-48249340	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs141816785	chr4:48249395-48249396	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs573931049	chr4:48249500-48249501	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs190313997	chr4:48249523-48249524	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs139173089	chr4:48249539-48249540	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs573257731	chr4:48249540-48249541	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs193267075	chr4:48249579-48249580	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs548631610	chr4:48249727-48249728	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs578173597	chr4:48249796-48249797	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs545083389	chr4:48249804-48249805	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs146249977	chr4:48249819-48249820	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	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
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
Breast cancer	22522925	CNVD

Chromatin state (count:682 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:48242600-48252600	Weak transcription	Aorta	Aorta
2	chr4:48245600-48249000	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr4:48245600-48249200	ZNF genes & repeats	GM12878-XiMat	blood
4	chr4:48245800-48250200	Weak transcription	Primary B cells from peripheral blood	blood
5	chr4:48246200-48248800	Weak transcription	Primary hematopoietic stem cells	blood
6	chr4:48246400-48249600	Weak transcription	Fetal Intestine Large	intestine
7	chr4:48246600-48248400	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr4:48246600-48249200	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr4:48247000-48249200	Weak transcription	K562	blood
10	chr4:48247200-48249000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr4:48247400-48248800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr4:48248400-48249000	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr4:48248800-48249400	Active TSS	Primary hematopoietic stem cells	blood
14	chr4:48248800-48255200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr4:48248800-48270600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr4:48249000-48249400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr4:48249000-48249600	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr4:48249000-48249600	Enhancers	Primary B cells from cord blood	blood
19	chr4:48249000-48249800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:48249000-48250600	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr4:48249000-48250600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr4:48249200-48249400	Active TSS	GM12878-XiMat	blood
23	chr4:48249200-48249600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr4:48249200-48249600	Flanking Active TSS	K562	blood
25	chr4:48249200-48249600	Enhancers	NHLF	lung
26	chr4:48249200-48249800	Enhancers	Muscle Satellite Cultured Cells	--
27	chr4:48249200-48249800	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr4:48249200-48249800	Enhancers	NHDF-Ad	bronchial
29	chr4:48249200-48250400	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr4:48249200-48250400	Enhancers	Fetal Heart	heart
31	chr4:48249400-48250200	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr4:48249400-48250600	Enhancers	Primary hematopoietic stem cells	blood
33	chr4:48249400-48251000	Flanking Active TSS	GM12878-XiMat	blood
34	chr4:48249600-48249800	Enhancers	Fetal Intestine Large	intestine
35	chr4:48249600-48251000	Enhancers	Liver	Liver
36	chr4:48249600-48251000	Enhancers	K562	blood
37	chr4:48249600-48252600	Weak transcription	Primary B cells from cord blood	blood
38	chr4:48249600-48261600	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr4:48249800-48250400	Weak transcription	Fetal Intestine Large	intestine
40	chr4:48249800-48254200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr4:48249800-48255800	Weak transcription	NHDF-Ad	bronchial
42	chr4:48250000-48250600	Enhancers	Small Intestine	intestine
43	chr4:48250000-48252600	Enhancers	Fetal Lung	lung
44	chr4:48250200-48250400	Enhancers	Primary B cells from peripheral blood	blood
45	chr4:48250200-48250600	Enhancers	Left Ventricle	heart
46	chr4:48250200-48254600	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr4:48250400-48250800	Enhancers	Fetal Intestine Large	intestine
48	chr4:48250400-48251600	Weak transcription	Fetal Heart	heart
49	chr4:48250400-48254400	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr4:48250600-48250800	Enhancers	Rectal Mucosa Donor 31	rectum

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