Variant report

Variant	nsv1049774
Chromosome Location	chr15:55759573-56044600
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3118)
CpG islands
(count:3787)
Chromatin interactive
region (count:108)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:3118 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:56001018-56001195	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:55806152-55806285	K562	blood:	n/a	n/a
3	ARID3A	chr15:55772283-55772392	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:55790421-55790685	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:55933818-55934139	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:55818712-55819023	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:56035308-56035658	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:55933805-55934122	K562	blood:	n/a	n/a
9	ATF1	chr15:55939036-55939172	K562	blood:	n/a	n/a
10	ATF2	chr15:55977363-55977942	GM12878	blood:	n/a	n/a
11	ATF2	chr15:55986700-55987145	GM12878	blood:	n/a	n/a
12	ATF2	chr15:55977465-55977883	GM12878	blood:	n/a	n/a
13	ATF2	chr15:55986675-55987097	GM12878	blood:	n/a	n/a
14	ATF3	chr15:55818765-55819007	K562	blood:	n/a	n/a
15	ATF3	chr15:55818618-55819080	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr15:55928620-55928792	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr15:56034376-56035496	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr15:55879929-55880216	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr15:55880445-55881363	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr15:55790323-55790739	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr15:55845070-55845357	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr15:55977447-55977812	GM12878	blood:	n/a	n/a
23	BATF	chr15:55986779-55987078	GM12878	blood:	n/a	chr15:55986877-55986886
24	BATF	chr15:55993148-55993363	GM12878	blood:	n/a	chr15:55993286-55993297
25	BATF	chr15:55834598-55834831	GM12878	blood:	n/a	n/a
26	BATF	chr15:55834632-55834829	GM12878	blood:	n/a	n/a
27	BATF	chr15:55993172-55993423	GM12878	blood:	n/a	chr15:55993286-55993297
28	BATF	chr15:55986766-55987079	GM12878	blood:	n/a	chr15:55986877-55986886
29	BATF	chr15:55977485-55977821	GM12878	blood:	n/a	n/a
30	BCL11A	chr15:55977469-55977811	GM12878	blood:	n/a	n/a
31	BCL3	chr15:55790292-55790938	A549	lung:	n/a	n/a
32	BCL3	chr15:55790199-55790921	A549	lung:	n/a	n/a
33	BCL3	chr15:56035153-56035731	A549	lung:	n/a	chr15:56035353-56035366 chr15:56035187-56035196 chr15:56035494-56035507 chr15:56035181-56035194 chr15:56035392-56035405 chr15:56035391-56035404 chr15:56035701-56035714 chr15:56035601-56035610 chr15:56035373-56035382 chr15:56035394-56035407
34	BHLHE40	chr15:56034537-56034723	GM12878	blood:	n/a	chr15:56034581-56034597
35	BHLHE40	chr15:55986825-55987064	GM12878	blood:	n/a	n/a
36	BHLHE40	chr15:55919924-55920203	K562	blood:	n/a	n/a
37	BHLHE40	chr15:56034446-56034746	HepG2	liver:	n/a	chr15:56034581-56034597
38	BHLHE40	chr15:55818801-55818995	K562	blood:	n/a	n/a
39	BHLHE40	chr15:55790520-55790743	K562	blood:	n/a	n/a
40	BHLHE40	chr15:55790404-55790780	HepG2	liver:	n/a	n/a
41	BHLHE40	chr15:55802897-55803042	K562	blood:	n/a	n/a
42	BHLHE40	chr15:55790324-55790820	GM12878	blood:	n/a	n/a
43	BHLHE40	chr15:55830506-55830748	K562	blood:	n/a	n/a
44	BHLHE40	chr15:55919891-55920364	A549	lung:	n/a	n/a
45	BHLHE40	chr15:55791493-55791621	A549	lung:	n/a	n/a
46	BRCA1	chr15:56035121-56035493	H1-hESC	embryonic stem cell:	n/a	chr15:56035306-56035315
47	BRCA1	chr15:56034160-56034637	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr15:56035120-56035618	HepG2	liver:	n/a	chr15:56035306-56035315
49	BRCA1	chr15:55790144-55790756	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr15:55919919-55920523	Hela-S3	cervix:	n/a	n/a

(count:3787 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:55881162-55881212	NT2-D1	testis:	n/a
2	chr15:55881083-55881133	AG09309	skin:	n/a
3	chr15:56038891-56038941	PANC-1	pancreas:	n/a
4	chr15:55881599-55881649	BJ	skin:	n/a
5	chr15:55968637-55968687	HUVEC	blood vessel:	n/a
6	chr15:55881162-55881212	NT2-D1	testis:	n/a
7	chr15:55881083-55881133	AG09309	skin:	n/a
8	chr15:56038891-56038941	PANC-1	pancreas:	n/a
9	chr15:55881599-55881649	BJ	skin:	n/a
10	chr15:55968637-55968687	HUVEC	blood vessel:	n/a
11	chr15:55805949-55805999	LNCaP	prostate:	n/a
12	chr15:56035616-56035666	HCT-116	colon:	n/a
13	chr15:56035476-56035526	HUVEC	blood vessel:	n/a
14	chr15:56031778-56031828	HEK293	kidney:	embryo
15	chr15:55968870-55968920	H1-hESC	embryonic stem cell:	embryo
16	chr15:56035459-56035509	HCM	heart:	n/a
17	chr15:56031778-56031828	HRE	kidney:	n/a
18	chr15:56035371-56035421	HRPEpiC	eye:	n/a
19	chr15:55790571-55790621	RPTEC	kidney:	n/a
20	chr15:55909920-55909970	RPTEC	kidney:	n/a
21	chr15:55881246-55881296	AG10803	skin:	n/a
22	chr15:55968870-55968920	IMR90	lung:	fetal
23	chr15:56036455-56036505	SK-N-MC	brain:	n/a
24	chr15:56034801-56034851	NB4	blood:	n/a
25	chr15:55790675-55790725	AG09309	skin:	n/a
26	chr15:55876513-55876563	GM12891	blood:	n/a
27	chr15:55880997-55881047	SKMC	muscle:	n/a
28	chr15:55805566-55805616	HCPEpiC	choroid plexus:	n/a
29	chr15:56014697-56014747	NH-A	brain:	n/a
30	chr15:55790753-55790803	NT2-D1	testis:	n/a
31	chr15:56035454-56035504	K562	blood:	n/a
32	chr15:55799927-55799977	SK-N-SH	brain:	n/a
33	chr15:55881075-55881125	HIPEpiC	eye:	n/a
34	chr15:55801069-55801119	HRE	kidney:	n/a
35	chr15:55801069-55801119	MCF10A-Er-Src	breast:	n/a
36	chr15:55805566-55805616	GM19239	blood:	n/a
37	chr15:55803008-55803058	HL-60	blood:	n/a
38	chr15:56014697-56014747	Hepatocyte	liver:	n/a
39	chr15:55881706-55881756	HepG2	liver:	n/a
40	chr15:55801378-55801428	HRCEpiC	kidney:	n/a
41	chr15:55790675-55790725	MCF10A-Er-Src	breast:	n/a
42	chr15:55881089-55881139	SAEC	small airway:	n/a
43	chr15:55791821-55791871	BJ	skin:	n/a
44	chr15:55801378-55801428	BJ	skin:	n/a
45	chr15:55791821-55791871	LNCaP	prostate:	n/a
46	chr15:55791821-55791871	AG10803	skin:	n/a
47	chr15:55944483-55944533	PrEC	prostate:	n/a
48	chr15:55790446-55790496	SK-N-MC	brain:	n/a
49	chr15:55806536-55806586	MCF-7	breast:	n/a
50	chr15:56035459-56035509	HRE	kidney:	n/a

(count:108 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:55876611..55879059-chr15:55880096..55882468,2	MCF-7	breast:
2	chr15:56002955..56005054-chr15:56005105..56008036,2	MCF-7	breast:
3	chr14:105942237..105945036-chr15:56032333..56033833,2	MCF-7	breast:
4	chr15:55890024..55892193-chr15:55904346..55906679,2	MCF-7	breast:
5	chr15:55818426..55819436-chr15:55933526..55934353,4	MCF-7	breast:
6	chr15:55940286..55941226-chr15:56189659..56190472,2	MCF-7	breast:
7	chr15:55883057..55885879-chr15:55889260..55891781,2	K562	blood:
8	chr15:55963506..55965782-chr15:55969955..55972854,2	MCF-7	breast:
9	chr15:55818424..55820652-chr15:55918654..55921682,3	MCF-7	breast:
10	chr15:55874660..55876672-chr15:55879383..55881839,2	MCF-7	breast:
11	chr15:55805811..55806979-chr15:55933287..55934076,3	MCF-7	breast:
12	chr15:55940297..55941155-chr15:56138005..56138994,3	K562	blood:
13	chr15:55940663..55943471-chr15:56092171..56094031,2	MCF-7	breast:
14	chr15:56013890..56016353-chr15:56030511..56032311,2	MCF-7	breast:
15	chr15:55790459..55791055-chr21:48054984..48055756,2	HCT-116	colon:
16	chr1:222884982..222885886-chr15:55790504..55791243,2	Hela-S3	cervix:
17	chr15:55818674..55821558-chr15:55828731..55830449,2	MCF-7	breast:
18	chr15:56036934..56038667-chr15:56040692..56043124,2	K562	blood:
19	chr15:55818773..55820947-chr15:55823916..55827475,3	K562	blood:
20	chr15:55881922..55884171-chr15:55889698..55891738,2	MCF-7	breast:
21	chr15:55956127..55957682-chr15:55978986..55980694,2	MCF-7	breast:
22	chr15:56033858..56036761-chr15:56051440..56053715,2	MCF-7	breast:
23	chr15:55940251..55940793-chr15:56189676..56190326,2	K562	blood:
24	chr15:55961153..55963651-chr15:56033694..56036455,3	MCF-7	breast:
25	chr15:55940700..55941248-chr15:56066693..56067247,2	K562	blood:
26	chr15:55808580..55811274-chr15:55928806..55931409,2	MCF-7	breast:
27	chr15:55772415..55774167-chr15:55776745..55778293,2	K562	blood:
28	chr15:55940727..55941250-chr15:56344682..56345231,2	K562	blood:
29	chr15:55984277..55986999-chr15:56034063..56036861,3	MCF-7	breast:
30	chr15:55824404..55826095-chr15:55826140..55828917,2	MCF-7	breast:
31	chr15:56016452..56018726-chr15:56033874..56036297,2	MCF-7	breast:
32	chr15:55832795..55834702-chr15:55836212..55838623,2	MCF-7	breast:
33	chr15:55956127..55957682-chr15:55978986..55980694,2	MCF-7	breast:
34	chr15:55957804..55959845-chr15:56026147..56028031,2	MCF-7	breast:
35	chr15:55939872..55941462-chr15:56091567..56092720,22	MCF-7	breast:
36	chr15:56002613..56005532-chr15:56007469..56010222,2	K562	blood:
37	chr15:55945016..55946690-chr15:55947517..55950057,2	MCF-7	breast:
38	chr15:56031905..56035384-chr15:56036677..56038977,3	MCF-7	breast:
39	chr15:56033691..56036874-chr15:56040601..56044185,4	MCF-7	breast:
40	chr15:55875375..55879008-chr15:55880167..55883388,4	K562	blood:
41	chr15:55871829..55873801-chr15:55877052..55878758,2	K562	blood:
42	chr15:55805811..55806979-chr15:55933287..55934076,3	MCF-7	breast:
43	chr15:55965960..55968011-chr15:56032220..56035162,2	MCF-7	breast:
44	chr15:55957804..55959845-chr15:56026147..56028031,2	MCF-7	breast:
45	chr15:55814401..55816505-chr15:55817575..55819685,2	K562	blood:
46	chr15:55881922..55884171-chr15:55889698..55891738,2	MCF-7	breast:
47	chr15:55999212..56002187-chr15:56002535..56005637,3	K562	blood:
48	chr15:55948243..55950096-chr15:55952230..55953920,2	MCF-7	breast:
49	chr15:55818424..55820652-chr15:55918654..55921682,3	MCF-7	breast:
50	chr15:56002955..56005054-chr15:56005105..56008036,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-178D12.1.1-5	chr15:55881501-55882082	NONHSAT044003
2	lnc-PYGO1-1	chr15:55831082-55834829	NONHSAT044002
3	lnc-NEDD4-2	chr15:56030403-56030857	NONHSAT044007
4	lnc-PYGO1-2	chr15:55904946-55906620	NONHSAT044004
5	lnc-PYGO1-2	chr15:55903750-55904914	NONHSAT044004
6	lnc-RP11-178D12.1.1-5	chr15:55880889-55881017	NONHSAT044003

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PRTG	hsa-let-7b-5p	chr15:55910225-55910219
2	PRTG	hsa-let-7b-5p	chr15:55910219-55910240
3	PRTG	hsa-let-7b-5p	chr15:55911797-55911790
4	PRTG	hsa-let-7b-5p	chr15:55911754-55911748

Variant related genes	Relation type
PRTG	TF binding region
ENSG00000259180	TF binding region
DYX1C1-CCPG1	TF binding region
DYX1C1	TF binding region
PYGO1	TF binding region
ENSG00000259369	TF binding region
PRTG	CpG island
ENSG00000259180	CpG island
DYX1C1-CCPG1	CpG island
DYX1C1	CpG island
PYGO1	CpG island
ENSG00000259369	CpG island
ENSG00000166450	chromatin interactions
ENSG00000182809	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000069943	chromatin interactions
ENSG00000259369	chromatin interactions
ENSG00000171016	chromatin interactions
ENSG00000251484	chromatin interactions
ENSG00000259180	chromatin interactions
ENSG00000221218	chromatin interactions
ENSG00000186063	chromatin interactions
ENSG00000261771	chromatin interactions
ENSG00000256061	chromatin interactions
ENSG00000160310	chromatin interactions
ENSG00000225973	chromatin interactions

Extended variants
information (count: 11676 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:11676 , 50 per page) page: 1 2 3 4 5 6 7 ... 234

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559759120	chr15:55759605-55759606	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540608587	chr15:55759651-55759652	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112691530	chr15:55759656-55759657	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138636678	chr15:55759666-55759667	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542290928	chr15:55759680-55759681	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2290981	chr15:55759688-55759689	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs142338996	chr15:55759742-55759743	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201190531	chr15:55759743-55759744	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534341264	chr15:55759744-55759745	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147806341	chr15:55759757-55759758	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs59329424	chr15:55759767-55759768	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530050117	chr15:55759782-55759783	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550077520	chr15:55759856-55759857	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141175990	chr15:55759899-55759900	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115183389	chr15:55759918-55759919	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs28658029	chr15:55759921-55759922	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs144004096	chr15:55759948-55759949	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs377635238	chr15:55759951-55759952	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565719863	chr15:55760014-55760015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78755396	chr15:55760058-55760059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554818969	chr15:55760077-55760078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7181999	chr15:55760078-55760079	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs144833105	chr15:55760105-55760106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567698970	chr15:55760111-55760112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183061350	chr15:55760138-55760139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187757259	chr15:55760181-55760182	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537372562	chr15:55760207-55760208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200078536	chr15:55760234-55760235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs626248	chr15:55760263-55760264	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs577377170	chr15:55760286-55760287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539976790	chr15:55760297-55760298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571588468	chr15:55760326-55760327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553289183	chr15:55760332-55760333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150742722	chr15:55760365-55760366	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542327765	chr15:55760370-55760371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs137987516	chr15:55760381-55760382	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575680010	chr15:55760444-55760445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs76523753	chr15:55760464-55760465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75407192	chr15:55760480-55760481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532207937	chr15:55760508-55760509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs692690	chr15:55760522-55760523	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs559271010	chr15:55760528-55760529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528203331	chr15:55760543-55760544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs146005748	chr15:55760557-55760558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs692691	chr15:55760575-55760576	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs368894035	chr15:55760680-55760681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370983513	chr15:55760711-55760712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs139953278	chr15:55760740-55760741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs546184228	chr15:55760745-55760746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs628438	chr15:55760755-55760756	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:3035 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55740000-55768400	Weak transcription	Pancreas	Pancrea
2	chr15:55749200-55778800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr15:55749600-55773600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr15:55750200-55778200	Weak transcription	Ovary	ovary
5	chr15:55755600-55759800	Weak transcription	Fetal Intestine Small	intestine
6	chr15:55756200-55790000	Weak transcription	Fetal Kidney	kidney
7	chr15:55757200-55773400	Weak transcription	Fetal Stomach	stomach
8	chr15:55758600-55759600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr15:55758800-55759600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr15:55759000-55759600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr15:55759000-55760000	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr15:55759600-55760000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr15:55759600-55760000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr15:55759800-55760200	Enhancers	H9 Cell Line	embryonic stem cell
15	chr15:55759800-55760400	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr15:55760000-55772600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr15:55760400-55761200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr15:55764400-55767800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr15:55766600-55766800	Enhancers	Primary hematopoietic stem cells	blood
20	chr15:55766800-55767800	Weak transcription	Primary hematopoietic stem cells	blood
21	chr15:55767400-55767600	Enhancers	GM12878-XiMat	blood
22	chr15:55767600-55768200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr15:55767600-55768200	Flanking Active TSS	GM12878-XiMat	blood
24	chr15:55767600-55768600	Enhancers	Primary B cells from peripheral blood	blood
25	chr15:55767600-55769000	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr15:55767800-55768000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr15:55767800-55768600	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr15:55767800-55768600	Enhancers	HSMMtube	muscle
29	chr15:55767800-55768800	Enhancers	Primary B cells from cord blood	blood
30	chr15:55767800-55768800	Enhancers	Primary hematopoietic stem cells	blood
31	chr15:55768000-55768600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr15:55768000-55768600	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr15:55768200-55768600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr15:55768200-55768600	Enhancers	GM12878-XiMat	blood
35	chr15:55768400-55768600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr15:55768400-55768600	Enhancers	Pancreas	Pancrea
37	chr15:55768400-55782800	Weak transcription	Brain Anterior Caudate	brain
38	chr15:55768600-55768800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr15:55768600-55769000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr15:55768600-55771000	Weak transcription	HSMMtube	muscle
41	chr15:55768600-55773600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr15:55769800-55770000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr15:55770200-55773600	Weak transcription	Gastric	stomach
44	chr15:55771000-55771400	Enhancers	HSMMtube	muscle
45	chr15:55771200-55771400	Enhancers	HSMM	muscle
46	chr15:55771400-55790000	Weak transcription	HSMM	muscle
47	chr15:55771600-55790000	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr15:55772000-55773200	Weak transcription	Fetal Brain Female	brain
49	chr15:55772200-55790000	Weak transcription	Brain Angular Gyrus	brain
50	chr15:55772400-55772800	Enhancers	HepG2	liver

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