Variant report

Variant	nsv1018614
Chromosome Location	chr5:59708223-59910308
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1662)
CpG islands
(count:977)
Chromatin interactive
region (count:18)
LncRNA
region (count:35)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1662 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:59882175-59882637	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:59742744-59743990	HepG2	liver:	n/a	chr5:59743535-59743551
3	ARID3A	chr5:59788755-59789293	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:59788058-59788177	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:59769493-59769923	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:59859760-59860115	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:59722961-59722993	K562	blood:	n/a	n/a
8	ARID3A	chr5:59782791-59784363	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:59759049-59759883	HepG2	liver:	n/a	n/a
10	ARID3A	chr5:59837874-59838286	HepG2	liver:	n/a	n/a
11	ARID3A	chr5:59712885-59714270	HepG2	liver:	n/a	n/a
12	ATF1	chr5:59830023-59830183	K562	blood:	n/a	n/a
13	ATF2	chr5:59893349-59893790	GM12878	blood:	n/a	n/a
14	ATF2	chr5:59790377-59790950	GM12878	blood:	n/a	n/a
15	ATF2	chr5:59817730-59818784	GM12878	blood:	n/a	n/a
16	ATF2	chr5:59893333-59893844	GM12878	blood:	n/a	n/a
17	ATF2	chr5:59836756-59838235	GM12878	blood:	n/a	n/a
18	ATF2	chr5:59799603-59800070	GM12878	blood:	n/a	n/a
19	ATF2	chr5:59822280-59822686	GM12878	blood:	n/a	n/a
20	ATF2	chr5:59836891-59837899	GM12878	blood:	n/a	n/a
21	ATF2	chr5:59799554-59800592	GM12878	blood:	n/a	n/a
22	ATF2	chr5:59817180-59818864	GM12878	blood:	n/a	n/a
23	ATF3	chr5:59758895-59759556	A549	lung:	n/a	n/a
24	BACH1	chr5:59788830-59789123	K562	blood:	n/a	n/a
25	BATF	chr5:59817733-59818123	GM12878	blood:	n/a	n/a
26	BATF	chr5:59893451-59893766	GM12878	blood:	n/a	n/a
27	BATF	chr5:59837023-59837632	GM12878	blood:	n/a	n/a
28	BATF	chr5:59837795-59838211	GM12878	blood:	n/a	n/a
29	BATF	chr5:59712137-59712393	GM12878	blood:	n/a	n/a
30	BATF	chr5:59836987-59837677	GM12878	blood:	n/a	n/a
31	BATF	chr5:59818329-59818755	GM12878	blood:	n/a	chr5:59818490-59818501
32	BATF	chr5:59799597-59799997	GM12878	blood:	n/a	n/a
33	BATF	chr5:59879446-59879632	GM12878	blood:	n/a	chr5:59879534-59879545
34	BATF	chr5:59879434-59879689	GM12878	blood:	n/a	chr5:59879534-59879545
35	BATF	chr5:59837857-59838127	GM12878	blood:	n/a	n/a
36	BATF	chr5:59818271-59818769	GM12878	blood:	n/a	chr5:59818490-59818501
37	BATF	chr5:59800210-59800533	GM12878	blood:	n/a	n/a
38	BATF	chr5:59799565-59800001	GM12878	blood:	n/a	n/a
39	BATF	chr5:59831094-59831409	GM12878	blood:	n/a	n/a
40	BCL11A	chr5:59893477-59893730	GM12878	blood:	n/a	n/a
41	BCL11A	chr5:59837051-59837649	GM12878	blood:	n/a	n/a
42	BCL11A	chr5:59837014-59837664	GM12878	blood:	n/a	n/a
43	BCL11A	chr5:59790507-59790809	GM12878	blood:	n/a	n/a
44	BCL11A	chr5:59712066-59712395	GM12878	blood:	n/a	n/a
45	BCL3	chr5:59818298-59818758	GM12878	blood:	n/a	chr5:59818521-59818529
46	BCL3	chr5:59788656-59789391	A549	lung:	n/a	n/a
47	BCL3	chr5:59783314-59783823	A549	lung:	n/a	n/a
48	BCL3	chr5:59822261-59822625	GM12878	blood:	n/a	n/a
49	BCL3	chr5:59758832-59759533	A549	lung:	n/a	n/a
50	BCL3	chr5:59758809-59759695	A549	lung:	n/a	chr5:59759578-59759587

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:59774763-59774813	HL-60	blood:	n/a
2	chr5:59774763-59774813	HL-60	blood:	n/a
3	chr5:59783035-59783085	SK-N-MC	brain:	n/a
4	chr5:59783668-59783718	HPAEpiC	pulmonary alveolar:	n/a
5	chr5:59837426-59837476	AG04449	skin:	fetal
6	chr5:59783035-59783085	ProgFib	skin:	n/a
7	chr5:59784544-59784594	HEEpiC	esophagus:	n/a
8	chr5:59824695-59824745	PANC-1	pancreas:	n/a
9	chr5:59711350-59711400	BJ	skin:	n/a
10	chr5:59837012-59837062	ProgFib	skin:	n/a
11	chr5:59783629-59783679	ProgFib	skin:	n/a
12	chr5:59826471-59826521	ovcar-3	ovarian:	n/a
13	chr5:59824695-59824745	Caco-2	colon:	n/a
14	chr5:59783668-59783718	CMK	blood:	n/a
15	chr5:59893187-59893237	K562	blood:	n/a
16	chr5:59826471-59826521	RPTEC	kidney:	n/a
17	chr5:59824695-59824745	T-47D	breast:	n/a
18	chr5:59837426-59837476	BJ	skin:	n/a
19	chr5:59783906-59783956	SKMC	muscle:	n/a
20	chr5:59784203-59784253	AG09319	gingival:	n/a
21	chr5:59783035-59783085	NB4	blood:	n/a
22	chr5:59783035-59783085	U87	brain:	n/a
23	chr5:59783035-59783085	NHBE	bronchial:	n/a
24	chr5:59711378-59711428	SK-N-SH_RA	brain:	n/a
25	chr5:59782121-59782171	H1-hESC	embryonic stem cell:	embryo
26	chr5:59711350-59711400	NT2-D1	testis:	n/a
27	chr5:59711350-59711400	ProgFib	skin:	n/a
28	chr5:59774763-59774813	A549	lung:	n/a
29	chr5:59782121-59782171	AoSMC	blood vessel:	n/a
30	chr5:59774763-59774813	SK-N-SH	brain:	n/a
31	chr5:59783035-59783085	AG09309	skin:	n/a
32	chr5:59774763-59774813	GM19239	blood:	n/a
33	chr5:59782121-59782171	SKMC	muscle:	n/a
34	chr5:59826471-59826521	BE2_C	brain:	n/a
35	chr5:59784203-59784253	Caco-2	colon:	n/a
36	chr5:59783035-59783085	SK-N-SH	brain:	n/a
37	chr5:59784203-59784253	MCF-7	breast:	n/a
38	chr5:59824695-59824745	HIPEpiC	eye:	n/a
39	chr5:59774763-59774813	Hepatocyte	liver:	n/a
40	chr5:59837426-59837476	HRCEpiC	kidney:	n/a
41	chr5:59783035-59783085	Caco-2	colon:	n/a
42	chr5:59783906-59783956	A549	lung:	n/a
43	chr5:59837426-59837476	MCF-7	breast:	n/a
44	chr5:59837426-59837476	HepG2	liver:	n/a
45	chr5:59783668-59783718	HEEpiC	esophagus:	n/a
46	chr5:59783035-59783085	HUVEC	blood vessel:	n/a
47	chr5:59826471-59826521	CMK	blood:	n/a
48	chr5:59727726-59727776	SK-N-SH	brain:	n/a
49	chr5:59826471-59826521	HPAEpiC	pulmonary alveolar:	n/a
50	chr5:59711350-59711400	ECC-1	luminal epithelium:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:59809546..59811841-chr5:59829888..59832066,2	K562	blood:
2	chr1:114972833..114973619-chr5:59845525..59846067,2	MCF-7	breast:
3	chr5:59801403..59803161-chr5:59818355..59820086,2	MCF-7	breast:
4	chr5:59831215..59833995-chr5:59834537..59838360,3	K562	blood:
5	chr5:59783715..59786154-chr5:59800134..59801883,2	K562	blood:
6	chr5:59880816..59882802-chr5:59924058..59926051,2	K562	blood:
7	chr5:59880816..59882802-chr5:59922734..59926051,3	K562	blood:
8	chr5:59809546..59811841-chr5:59829888..59832066,2	K562	blood:
9	chr5:59784827..59787759-chr5:59790470..59792339,3	K562	blood:
10	chr5:59591035..59591843-chr5:59881984..59882629,2	MCF-7	breast:
11	chr5:59678290..59679528-chr5:59881870..59883189,3	MCF-7	breast:
12	chr5:59109675..59110399-chr5:59882024..59882767,2	MCF-7	breast:
13	chr5:59801403..59803161-chr5:59818355..59820086,2	MCF-7	breast:
14	chr5:59105946..59106527-chr5:59881839..59882378,2	K562	blood:
15	chr5:59750546..59752966-chr5:59754525..59756849,2	K562	blood:
16	chr5:59831215..59833995-chr5:59834537..59838360,3	K562	blood:
17	chr5:59700212..59701783-chr5:59712786..59715237,2	K562	blood:
18	chr5:59784827..59787759-chr5:59790470..59792339,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC109486.1-1	chr5:59841929-59843484	ENSG00000152931
2	lnc-PDE4D-3	chr5:59858392-59858470	NONHSAT101643
3	lnc-AC109486.1-1	chr5:59825231-59825370	ENSG00000152931
4	lnc-AC109486.1-1	chr5:59783540-59784250	NONHSAT101637
5	lnc-AC109486.1-1	chr5:59784031-59784250	XLOC_004399
6	lnc-AC109486.1-1	chr5:59819609-59822275	NONHSAT101640
7	lnc-AC109486.1-1	chr5:59785488-59787092	ENSG00000152931
8	lnc-PDE4D-3	chr5:59851419-59851496	NONHSAT101643
9	lnc-AC109486.1-1	chr5:59829759-59829846	NONHSAT101637
10	lnc-AC109486.1-1	chr5:59783540-59784250	ENSG00000152931
11	lnc-AC109486.1-1	chr5:59783759-59784250	NR_028508
12	lnc-AC109486.1-1	chr5:59785488-59787345	ENSG00000152931.7
13	lnc-AC109486.1-1	chr5:59785488-59787092	NR_028508
14	lnc-AC109486.1-1	chr5:59783967-59784250	ENSG00000152931
15	lnc-AC109486.1-1	chr5:59825231-59825370	NONHSAT101637
16	lnc-AC109486.1-1	chr5:59784034-59784250	ENSG00000152931
17	lnc-AC109486.1-1	chr5:59816847-59817221	ENSG00000152931
18	lnc-AC109486.1-1	chr5:59829759-59829846	ENSG00000152931
19	lnc-AC109486.1-1	chr5:59841929-59843484	NONHSAT101637
20	lnc-AC109486.1-1	chr5:59821245-59821468	l_2924_chr5:59819710-59821457_kidney
21	lnc-AC109486.1-1	chr5:59785488-59785670	XLOC_004399
22	lnc-AC109486.1-1	chr5:59829685-59829846	XLOC_004399
23	lnc-AC109486.1-1	chr5:59783540-59784250	ENSG00000152931.7
24	lnc-AC109486.1-1	chr5:59852604-59852635	l_2924_chr5:59819710-59821457_kidney
25	lnc-AC109486.1-1	chr5:59816847-59822245	NONHSAT101638
26	lnc-AC109486.1-1	chr5:59841928-59843465	NONHSAT101641
27	lnc-PDE4D-3	chr5:59857239-59857357	NONHSAT101643
28	lnc-AC109486.1-1	chr5:59819711-59820007	l_2924_chr5:59819710-59821457_kidney
29	lnc-AC109486.1-1	chr5:59816847-59822245	ENSG00000152931.7
30	lnc-AC109486.1-1	chr5:59784034-59784250	ENSG00000152931.7
31	lnc-PDE4D-1	chr5:59798346-59798489	XLOC_004839
32	lnc-PDE4D-1	chr5:59817878-59822213	XLOC_004839
33	lnc-AC109486.1-1	chr5:59829684-59829846	NONHSAT101641
34	lnc-AC109486.1-1	chr5:59783759-59784250	NONHSAT101638
35	lnc-AC109486.1-1	chr5:59841929-59843465	XLOC_004399

No data

Variant related genes	Relation type
ENSG00000213896	TF binding region
ENSG00000224838	TF binding region
SETP21	TF binding region
PDE4D	TF binding region
PART1	TF binding region
ENSG00000213896	CpG island
ENSG00000224838	CpG island
SETP21	CpG island
PDE4D	CpG island
PART1	CpG island
ENSG00000035499	chromatin interactions
ENSG00000214244	chromatin interactions
ENSG00000152931	chromatin interactions
ENSG00000113448	chromatin interactions
RXRB	miRNA target sites
CSNK1G1	miRNA target sites
NUCB2	miRNA target sites
PRKD3	miRNA target sites
SNAP23	miRNA target sites
FNIP1	miRNA target sites
FNTA	miRNA target sites
ONECUT2	miRNA target sites
WDR33	miRNA target sites
PRUNE2	miRNA target sites

Extended variants
information (count: 6448 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:6448 , 50 per page) page: 1 2 3 4 5 6 7 ... 129

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6449470	chr5:59708223-59708224	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs373912236	chr5:59708244-59708245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs72755119	chr5:59708246-59708247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375809938	chr5:59708266-59708267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs16878032	chr5:59708361-59708362	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs145438099	chr5:59708380-59708381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541093923	chr5:59708496-59708497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189221630	chr5:59708540-59708541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs180703841	chr5:59708575-59708576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574736482	chr5:59708577-59708578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543836781	chr5:59708610-59708611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185953938	chr5:59708624-59708625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572759085	chr5:59708638-59708639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568142793	chr5:59708676-59708677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs367873063	chr5:59708678-59708679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs57558762	chr5:59708701-59708702	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs192485116	chr5:59708770-59708771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370107873	chr5:59708806-59708807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373607793	chr5:59708811-59708812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141125839	chr5:59708854-59708855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528728775	chr5:59708904-59708905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553938870	chr5:59708958-59708959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145629262	chr5:59708962-59708963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115234582	chr5:59708968-59708969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535862091	chr5:59709020-59709021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549709942	chr5:59709031-59709032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368739666	chr5:59709068-59709069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181833737	chr5:59709161-59709162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372677739	chr5:59709196-59709197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374379868	chr5:59709207-59709208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558444319	chr5:59709208-59709209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571896289	chr5:59709237-59709238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147754846	chr5:59709319-59709320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554755234	chr5:59709385-59709386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574832229	chr5:59709458-59709459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185983923	chr5:59709486-59709487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368342853	chr5:59709502-59709503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142517098	chr5:59709517-59709518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368856594	chr5:59709540-59709541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369666018	chr5:59709541-59709542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548683363	chr5:59709542-59709543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74510551	chr5:59709543-59709544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76300439	chr5:59709556-59709557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79424628	chr5:59709558-59709559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115444617	chr5:59709602-59709603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs72755121	chr5:59709609-59709610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs16878035	chr5:59709614-59709615	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs146870724	chr5:59709644-59709645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs16878037	chr5:59709752-59709753	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs148323214	chr5:59709758-59709759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1263 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59695000-59712600	Weak transcription	Primary B cells from cord blood	blood
2	chr5:59696000-59713200	Weak transcription	Aorta	Aorta
3	chr5:59707200-59712400	Weak transcription	HepG2	liver
4	chr5:59712200-59713000	Enhancers	Primary B cells from peripheral blood	blood
5	chr5:59712400-59713000	Enhancers	GM12878-XiMat	blood
6	chr5:59712400-59716800	Enhancers	HepG2	liver
7	chr5:59712600-59713200	Enhancers	Primary B cells from cord blood	blood
8	chr5:59712600-59713200	Enhancers	Primary hematopoietic stem cells	blood
9	chr5:59712800-59713400	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr5:59713000-59713200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
11	chr5:59713200-59713600	Enhancers	Aorta	Aorta
12	chr5:59713200-59716000	Weak transcription	Primary B cells from cord blood	blood
13	chr5:59716000-59716600	ZNF genes & repeats	Primary B cells from cord blood	blood
14	chr5:59716400-59716800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr5:59716400-59716800	ZNF genes & repeats	Pancreas	Pancrea
16	chr5:59716800-59717000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr5:59717000-59730000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr5:59727200-59766600	Weak transcription	Primary B cells from cord blood	blood
19	chr5:59730000-59730400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr5:59730400-59731000	Enhancers	Colon Smooth Muscle	Colon
21	chr5:59730400-59731800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:59730400-59733200	Enhancers	HepG2	liver
23	chr5:59731800-59732000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr5:59732000-59732400	Enhancers	GM12878-XiMat	blood
25	chr5:59732400-59733000	Enhancers	Primary B cells from peripheral blood	blood
26	chr5:59732400-59733400	Flanking Active TSS	GM12878-XiMat	blood
27	chr5:59732800-59733000	Enhancers	Aorta	Aorta
28	chr5:59733000-59742600	Weak transcription	Aorta	Aorta
29	chr5:59733200-59738800	Weak transcription	HepG2	liver
30	chr5:59733400-59733800	Enhancers	GM12878-XiMat	blood
31	chr5:59734000-59734400	Enhancers	Fetal Kidney	kidney
32	chr5:59738800-59742800	Enhancers	HepG2	liver
33	chr5:59740000-59741200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr5:59740000-59741600	Enhancers	Fetal Brain Male	brain
35	chr5:59740200-59740600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr5:59740400-59741000	Enhancers	Fetal Brain Female	brain
37	chr5:59740400-59741000	Enhancers	Hela-S3	cervix
38	chr5:59740600-59740800	Enhancers	Gastric	stomach
39	chr5:59741000-59744200	Weak transcription	Hela-S3	cervix
40	chr5:59741200-59741600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr5:59741600-59741800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr5:59741600-59743200	Enhancers	Stomach Mucosa	stomach
43	chr5:59741600-59744800	Weak transcription	Fetal Brain Male	brain
44	chr5:59741800-59783200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr5:59742600-59743000	Enhancers	Aorta	Aorta
46	chr5:59742600-59743000	Enhancers	A549	lung
47	chr5:59742600-59744400	Enhancers	Gastric	stomach
48	chr5:59742800-59743200	Flanking Active TSS	HepG2	liver
49	chr5:59743000-59743600	Flanking Active TSS	A549	lung
50	chr5:59743000-59743800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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