Variant report

Variant	nsv872528
Chromosome Location	chr1:168341866-168384168
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:812)
CpG islands
(count:489)
Chromatin interactive
region (count:35)
LncRNA
region (count:7)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:812 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:168378059-168378372	K562	blood:	n/a	chr1:168378107-168378123
2	ARID3A	chr1:168343229-168343407	K562	blood:	n/a	n/a
3	ARID3A	chr1:168368284-168368533	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:168368098-168368571	K562	blood:	n/a	n/a
5	ARID3A	chr1:168378183-168378313	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:168371924-168371935	K562	blood:	n/a	n/a
7	ATF1	chr1:168342118-168342700	K562	blood:	n/a	n/a
8	ATF1	chr1:168377170-168377200	K562	blood:	n/a	n/a
9	ATF1	chr1:168378142-168378410	K562	blood:	n/a	n/a
10	ATF1	chr1:168343203-168343424	K562	blood:	n/a	n/a
11	ATF1	chr1:168341584-168341901	K562	blood:	n/a	n/a
12	ATF1	chr1:168373187-168373436	K562	blood:	n/a	n/a
13	ATF2	chr1:168356434-168356843	H1-hESC	embryonic stem cell:	n/a	chr1:168356575-168356589 chr1:168356577-168356588
14	ATF2	chr1:168356361-168357102	H1-hESC	embryonic stem cell:	n/a	chr1:168356575-168356589 chr1:168356577-168356588
15	ATF3	chr1:168368138-168368658	K562	blood:	n/a	n/a
16	ATF3	chr1:168355801-168356057	K562	blood:	n/a	n/a
17	ATF3	chr1:168368315-168368701	K562	blood:	n/a	n/a
18	ATF3	chr1:168378036-168378503	K562	blood:	n/a	chr1:168378273-168378287
19	ATF3	chr1:168377592-168378665	HCT-116	colon:	n/a	chr1:168378273-168378287
20	ATF3	chr1:168343126-168343426	K562	blood:	n/a	n/a
21	BACH1	chr1:168368283-168368645	H1-hESC	embryonic stem cell:	n/a	chr1:168368437-168368451
22	BACH1	chr1:168361870-168362573	K562	blood:	n/a	chr1:168362330-168362344
23	BACH1	chr1:168362166-168362509	H1-hESC	embryonic stem cell:	n/a	chr1:168362330-168362344
24	BACH1	chr1:168368271-168368612	K562	blood:	n/a	chr1:168368437-168368451
25	BACH1	chr1:168361902-168361929	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr1:168357056-168357360	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr1:168376500-168376541	K562	blood:	n/a	n/a
28	BACH1	chr1:168356174-168356821	H1-hESC	embryonic stem cell:	n/a	n/a
29	BATF	chr1:168378115-168378443	GM12878	blood:	n/a	chr1:168378273-168378284 chr1:168378253-168378263 chr1:168378274-168378284 chr1:168378252-168378263
30	BATF	chr1:168378152-168378447	GM12878	blood:	n/a	chr1:168378273-168378284 chr1:168378253-168378263 chr1:168378274-168378284 chr1:168378252-168378263
31	BCL11A	chr1:168379657-168379970	GM12878	blood:	n/a	n/a
32	BCL3	chr1:168348281-168348839	A549	lung:	n/a	chr1:168348563-168348572 chr1:168348562-168348571
33	BHLHE40	chr1:168347732-168348156	K562	blood:	n/a	n/a
34	BHLHE40	chr1:168362300-168362316	K562	blood:	n/a	n/a
35	BHLHE40	chr1:168379683-168380026	GM12878	blood:	n/a	n/a
36	BHLHE40	chr1:168343187-168343406	K562	blood:	n/a	n/a
37	BHLHE40	chr1:168368298-168368602	K562	blood:	n/a	n/a
38	BHLHE40	chr1:168367875-168367885	K562	blood:	n/a	n/a
39	BHLHE40	chr1:168371828-168371933	K562	blood:	n/a	n/a
40	BHLHE40	chr1:168341818-168342686	K562	blood:	n/a	n/a
41	BRCA1	chr1:168366205-168366816	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr1:168377700-168378424	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr1:168361083-168361740	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr1:168375019-168375412	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr1:168379159-168379169	GM12878	blood:	n/a	n/a
46	BRCA1	chr1:168356568-168356732	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr1:168359647-168359700	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr1:168374736-168375745	HCT-116	colon:	n/a	n/a
49	CBX3	chr1:168377435-168379361	HCT-116	colon:	n/a	n/a
50	CBX3	chr1:168368139-168368604	K562	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:168344264-168344314	SK-N-SH_RA	brain:	n/a
2	chr1:168344264-168344314	SK-N-SH_RA	brain:	n/a
3	chr1:168343945-168343995	HAEpiC	amniotic membrane:	n/a
4	chr1:168356673-168356723	NB4	blood:	n/a
5	chr1:168356673-168356723	BE2_C	brain:	n/a
6	chr1:168344264-168344314	BJ	skin:	n/a
7	chr1:168356591-168356641	HCF	heart:	n/a
8	chr1:168344264-168344314	U87	brain:	n/a
9	chr1:168343945-168343995	SK-N-SH_RA	brain:	n/a
10	chr1:168343945-168343995	CMK	blood:	n/a
11	chr1:168343339-168343389	LNCaP	prostate:	n/a
12	chr1:168356591-168356641	SKMC	muscle:	n/a
13	chr1:168356606-168356656	NH-A	brain:	n/a
14	chr1:168356591-168356641	Hepatocyte	liver:	n/a
15	chr1:168356606-168356656	HEK293	kidney:	embryo
16	chr1:168356591-168356641	MCF10A-Er-Src	breast:	n/a
17	chr1:168343339-168343389	IMR90	lung:	fetal
18	chr1:168356537-168356587	AoSMC	blood vessel:	n/a
19	chr1:168344184-168344234	PFSK-1	brain:	n/a
20	chr1:168343945-168343995	GM12892	blood:	n/a
21	chr1:168343339-168343389	HRCEpiC	kidney:	n/a
22	chr1:168344264-168344314	NB4	blood:	n/a
23	chr1:168343339-168343389	SK-N-SH	brain:	n/a
24	chr1:168343339-168343389	ProgFib	skin:	n/a
25	chr1:168344264-168344314	AG10803	skin:	n/a
26	chr1:168343339-168343389	HL-60	blood:	n/a
27	chr1:168356537-168356587	HIPEpiC	eye:	n/a
28	chr1:168356606-168356656	ProgFib	skin:	n/a
29	chr1:168344184-168344234	AG09309	skin:	n/a
30	chr1:168356673-168356723	A549	lung:	n/a
31	chr1:168343339-168343389	MCF10A-Er-Src	breast:	n/a
32	chr1:168344184-168344234	Hepatocyte	liver:	n/a
33	chr1:168356673-168356723	SKMC	muscle:	n/a
34	chr1:168356591-168356641	HCT-116	colon:	n/a
35	chr1:168356591-168356641	HRE	kidney:	n/a
36	chr1:168356537-168356587	SK-N-SH_RA	brain:	n/a
37	chr1:168343339-168343389	Jurkat	blood:	n/a
38	chr1:168356537-168356587	ProgFib	skin:	n/a
39	chr1:168356591-168356641	RPTEC	kidney:	n/a
40	chr1:168343339-168343389	BE2_C	brain:	n/a
41	chr1:168343339-168343389	HCF	heart:	n/a
42	chr1:168356591-168356641	MCF-7	breast:	n/a
43	chr1:168343945-168343995	HCT-116	colon:	n/a
44	chr1:168356537-168356587	BJ	skin:	n/a
45	chr1:168356673-168356723	PFSK-1	brain:	n/a
46	chr1:168356673-168356723	HUVEC	blood vessel:	n/a
47	chr1:168356606-168356656	GM12878	blood:	n/a
48	chr1:168356673-168356723	BJ	skin:	n/a
49	chr1:168356673-168356723	HepG2	liver:	n/a
50	chr1:168356606-168356656	AoSMC	blood vessel:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:168360896..168362544-chr1:168366659..168368237,2	K562	blood:
2	chr1:168368481..168370115-chr1:168372441..168374527,2	K562	blood:
3	chr1:168366951..168368657-chr1:168370802..168373547,2	K562	blood:
4	chr1:168335359..168337795-chr1:168345574..168348326,2	K562	blood:
5	chr1:168343623..168346188-chr1:168350297..168353036,3	K562	blood:
6	chr1:168372698..168375484-chr1:168376700..168379733,3	K562	blood:
7	chr1:168342866..168344756-chr1:168372914..168374516,2	K562	blood:
8	chr1:168356981..168360579-chr1:168363528..168366891,3	MCF-7	breast:
9	chr1:168346129..168348064-chr1:168353010..168355199,2	K562	blood:
10	chr1:168368481..168370115-chr1:168372441..168374527,2	K562	blood:
11	chr1:168380061..168382502-chr1:168391417..168394284,2	K562	blood:
12	chr1:168342866..168344756-chr1:168372914..168374516,2	K562	blood:
13	chr1:168366951..168368452-chr1:168372047..168373905,2	K562	blood:
14	chr1:168380376..168383489-chr1:168385353..168387780,3	K562	blood:
15	chr1:168338940..168340901-chr1:168341151..168343365,2	MCF-7	breast:
16	chr1:168346129..168348064-chr1:168353010..168355199,2	K562	blood:
17	chr1:168356981..168360579-chr1:168363528..168366891,3	MCF-7	breast:
18	chr1:168348118..168353414-chr1:168355151..168359007,7	MCF-7	breast:
19	chr1:168341145..168343864-chr1:168357058..168358969,2	K562	blood:
20	chr1:168187433..168189118-chr1:168341371..168344286,2	K562	blood:
21	chr1:168366951..168368452-chr1:168372047..168373905,2	K562	blood:
22	chr1:168349449..168351805-chr1:168370757..168373468,2	K562	blood:
23	chr1:168311615..168313900-chr1:168348090..168350975,2	MCF-7	breast:
24	chr1:168355026..168356826-chr1:168398882..168401309,2	K562	blood:
25	chr1:168348118..168353414-chr1:168355151..168359007,7	MCF-7	breast:
26	chr1:168376462..168378908-chr20:55839505..55841906,2	MCF-7	breast:
27	chr1:168372698..168375484-chr1:168376700..168379733,3	K562	blood:
28	chr1:168360896..168362544-chr1:168366659..168368237,2	K562	blood:
29	chr1:168357609..168359334-chr1:168366941..168369901,2	K562	blood:
30	chr1:168334562..168336538-chr1:168357801..168359534,2	K562	blood:
31	chr1:168341145..168343864-chr1:168357058..168358969,2	K562	blood:
32	chr1:168366951..168368657-chr1:168370802..168373547,2	K562	blood:
33	chr1:168344082..168345767-chr1:168346742..168349715,2	K562	blood:
34	chr1:168349449..168351805-chr1:168370757..168373468,2	K562	blood:
35	chr1:168357609..168359334-chr1:168366941..168369901,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-XCL2-2	chr1:168370721-168370768	XLOC_001083
2	lnc-XCL2-2	chr1:168376477-168376512	XLOC_001083
3	lnc-XCL2-2	chr1:168382031-168382174	NONHSAT007437
4	lnc-XCL2-2	chr1:168370067-168371581	XLOC_001083
5	lnc-XCL2-2	chr1:168369427-168371581	NONHSAT007437
6	lnc-XCL2-2	chr1:168371277-168371581	XLOC_001083
7	lnc-XCL2-2	chr1:168382031-168382174	XLOC_001083

miRNA name	Chromosome Location	mirBase accession
hsa-miR-557	chr1:168344822-168344844	MIMAT0003221

No data

Variant related genes	Relation type
MIR557	TF binding region
ENSG00000228697	TF binding region
MIR557	CpG island
ENSG00000228697	CpG island
ENSG00000228697	chromatin interactions
ENSG00000207974	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000226308	chromatin interactions

Extended variants
information (count: 1546 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1546 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2268554	chr1:168341866-168341867	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545453934	chr1:168341872-168341873	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs554112929	chr1:168341903-168341904	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs565270656	chr1:168341963-168341964	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs572695400	chr1:168342109-168342110	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs7534721	chr1:168342128-168342129	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs386636547	chr1:168342162-168342163	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs7534799	chr1:168342163-168342164	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs543998615	chr1:168342175-168342176	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs7534807	chr1:168342185-168342186	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs76978773	chr1:168342196-168342197	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs551138803	chr1:168342217-168342218	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs545659849	chr1:168342246-168342247	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs7534901	chr1:168342264-168342265	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs548866180	chr1:168342333-168342334	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs113855366	chr1:168342340-168342341	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs111486776	chr1:168342373-168342374	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs187813456	chr1:168342374-168342375	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs146269620	chr1:168342380-168342381	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs549548801	chr1:168342381-168342382	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs7535163	chr1:168342391-168342392	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs371843581	chr1:168342392-168342393	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs7512256	chr1:168342402-168342403	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs553935891	chr1:168342429-168342430	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs374220439	chr1:168342459-168342460	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs200905285	chr1:168342465-168342466	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs192625911	chr1:168342529-168342530	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs536621349	chr1:168342557-168342558	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs555318274	chr1:168342570-168342571	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs139141085	chr1:168342578-168342579	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs74123925	chr1:168342579-168342580	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs531082518	chr1:168342604-168342605	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs142329250	chr1:168342629-168342630	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs565474156	chr1:168342705-168342706	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs577706091	chr1:168342768-168342769	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs72701786	chr1:168342847-168342848	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs567859056	chr1:168342851-168342852	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs35100235	chr1:168342857-168342858	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs201877602	chr1:168342859-168342860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184319417	chr1:168342873-168342874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs149684631	chr1:168342894-168342895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs531384126	chr1:168342946-168342947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548532114	chr1:168342958-168342959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546913167	chr1:168342975-168342976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539265101	chr1:168343003-168343004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs560882352	chr1:168343004-168343005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531480366	chr1:168343036-168343037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189650525	chr1:168343101-168343102	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs145351418	chr1:168343102-168343103	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs571409353	chr1:168343148-168343149	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168338000-168343000	Weak transcription	Aorta	Aorta
2	chr1:168338000-168343200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:168338200-168343400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:168338400-168348200	Weak transcription	HepG2	liver
5	chr1:168340400-168342200	Enhancers	Colon Smooth Muscle	Colon
6	chr1:168340400-168342200	Enhancers	Fetal Muscle Leg	muscle
7	chr1:168340800-168342200	Enhancers	Rectal Smooth Muscle	rectum
8	chr1:168340800-168342600	Enhancers	Right Atrium	heart
9	chr1:168341000-168342000	Weak transcription	Fetal Lung	lung
10	chr1:168341200-168342800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr1:168341400-168342200	Enhancers	Right Ventricle	heart
12	chr1:168341400-168342600	Enhancers	Placenta	Placenta
13	chr1:168341400-168342800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr1:168341600-168342000	Enhancers	Stomach Smooth Muscle	stomach
15	chr1:168341600-168342800	Enhancers	Fetal Heart	heart
16	chr1:168341600-168342800	Flanking Active TSS	K562	blood
17	chr1:168341800-168342200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr1:168341800-168342800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr1:168341800-168343400	Enhancers	Placenta Amnion	Placenta Amnion
20	chr1:168342000-168342200	Enhancers	Spleen	Spleen
21	chr1:168342000-168342400	Enhancers	Fetal Lung	lung
22	chr1:168342000-168342600	Enhancers	Left Ventricle	heart
23	chr1:168342000-168343400	Enhancers	Primary hematopoietic stem cells	blood
24	chr1:168342200-168343800	Weak transcription	Right Ventricle	heart
25	chr1:168342600-168343600	Weak transcription	Placenta	Placenta
26	chr1:168342600-168347400	Weak transcription	Right Atrium	heart
27	chr1:168342800-168345600	Enhancers	K562	blood
28	chr1:168343200-168343800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:168343600-168344800	Enhancers	Placenta	Placenta
30	chr1:168344400-168345600	Enhancers	Fetal Intestine Large	intestine
31	chr1:168344400-168345600	Enhancers	Fetal Intestine Small	intestine
32	chr1:168345600-168348000	Weak transcription	K562	blood
33	chr1:168346800-168347800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr1:168347000-168347800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:168348000-168349000	Enhancers	K562	blood
36	chr1:168348200-168348600	Enhancers	HepG2	liver
37	chr1:168348200-168349000	Enhancers	A549	lung
38	chr1:168348400-168348600	Enhancers	H9 Cell Line	embryonic stem cell
39	chr1:168348600-168354200	Weak transcription	HepG2	liver
40	chr1:168348600-168356600	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr1:168349400-168350800	Weak transcription	Aorta	Aorta
42	chr1:168350000-168356200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr1:168354200-168354800	Strong transcription	HepG2	liver
44	chr1:168354800-168367600	Weak transcription	HepG2	liver
45	chr1:168355200-168358800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr1:168355800-168356200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
47	chr1:168355800-168356400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr1:168355800-168357800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr1:168356000-168356200	Enhancers	Gastric	stomach
50	chr1:168356000-168356400	Enhancers	Primary T helper cells PMA-I stimulated	--

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