Variant report

Variant	nsv904263
Chromosome Location	chr15:58340072-58437346
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1605)
CpG islands
(count:1283)
Chromatin interactive
region (count:101)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1605 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:58403141-58404251	K562	blood:	n/a	n/a
2	ARID3A	chr15:58383973-58384116	K562	blood:	n/a	n/a
3	ARID3A	chr15:58354534-58354692	K562	blood:	n/a	n/a
4	ARID3A	chr15:58406982-58407925	K562	blood:	n/a	n/a
5	ARID3A	chr15:58358634-58358800	K562	blood:	n/a	n/a
6	ARID3A	chr15:58354012-58354304	K562	blood:	n/a	chr15:58354220-58354236
7	ARID3A	chr15:58357164-58357177	K562	blood:	n/a	n/a
8	ARID3A	chr15:58356039-58356049	K562	blood:	n/a	n/a
9	ARID3A	chr15:58369703-58370028	K562	blood:	n/a	n/a
10	ARID3A	chr15:58357749-58357751	K562	blood:	n/a	n/a
11	ARID3A	chr15:58363058-58363339	HepG2	liver:	n/a	n/a
12	ARID3A	chr15:58352786-58353110	K562	blood:	n/a	n/a
13	ARID3A	chr15:58395672-58396090	K562	blood:	n/a	n/a
14	ARID3A	chr15:58400308-58400825	K562	blood:	n/a	n/a
15	ARID3A	chr15:58389380-58389410	K562	blood:	n/a	n/a
16	ARID3A	chr15:58363037-58363469	K562	blood:	n/a	n/a
17	ARID3A	chr15:58355252-58355570	K562	blood:	n/a	n/a
18	ARID3A	chr15:58348211-58348512	K562	blood:	n/a	n/a
19	ARID3A	chr15:58409376-58410453	HepG2	liver:	n/a	n/a
20	ARID3A	chr15:58435113-58435606	K562	blood:	n/a	n/a
21	ATF1	chr15:58407006-58407420	K562	blood:	n/a	n/a
22	ATF1	chr15:58395788-58395964	K562	blood:	n/a	n/a
23	ATF1	chr15:58372658-58372910	K562	blood:	n/a	n/a
24	ATF1	chr15:58403177-58404184	K562	blood:	n/a	n/a
25	ATF1	chr15:58435080-58435720	K562	blood:	n/a	n/a
26	ATF1	chr15:58400264-58400665	K562	blood:	n/a	n/a
27	ATF1	chr15:58369690-58370014	K562	blood:	n/a	n/a
28	ATF1	chr15:58357118-58357128	K562	blood:	n/a	n/a
29	ATF3	chr15:58357915-58358171	K562	blood:	n/a	chr15:58358044-58358053
30	ATF3	chr15:58395692-58395981	K562	blood:	n/a	n/a
31	BACH1	chr15:58403538-58403774	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr15:58403096-58404272	K562	blood:	n/a	chr15:58403430-58403444
33	BACH1	chr15:58342067-58342345	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr15:58358059-58358350	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr15:58372631-58372714	K562	blood:	n/a	n/a
36	BCLAF1	chr15:58357508-58358003	K562	blood:	n/a	chr15:58357980-58357993
37	BCLAF1	chr15:58354252-58354873	K562	blood:	n/a	n/a
38	BCLAF1	chr15:58403373-58404330	K562	blood:	n/a	n/a
39	BCLAF1	chr15:58358424-58358973	K562	blood:	n/a	n/a
40	BHLHE40	chr15:58376386-58376443	K562	blood:	n/a	n/a
41	BHLHE40	chr15:58363087-58363540	K562	blood:	n/a	n/a
42	BHLHE40	chr15:58357209-58357396	K562	blood:	n/a	n/a
43	BHLHE40	chr15:58358494-58358828	K562	blood:	n/a	n/a
44	BHLHE40	chr15:58376685-58376686	K562	blood:	n/a	n/a
45	BHLHE40	chr15:58407059-58407207	K562	blood:	n/a	n/a
46	BHLHE40	chr15:58350332-58350550	K562	blood:	n/a	n/a
47	BHLHE40	chr15:58369815-58370046	K562	blood:	n/a	n/a
48	BHLHE40	chr15:58403181-58404269	K562	blood:	n/a	n/a
49	BHLHE40	chr15:58372615-58372750	K562	blood:	n/a	n/a
50	BRCA1	chr15:58369573-58369653	HepG2	liver:	n/a	n/a

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:58357989-58358039	IMR90	lung:	fetal
2	chr15:58358811-58358861	HCT-116	colon:	n/a
3	chr15:58357989-58358039	IMR90	lung:	fetal
4	chr15:58358811-58358861	HCT-116	colon:	n/a
5	chr15:58357319-58357369	Caco-2	colon:	n/a
6	chr15:58358384-58358434	HAEpiC	amniotic membrane:	n/a
7	chr15:58357987-58358037	SK-N-SH_RA	brain:	n/a
8	chr15:58358811-58358861	A549	lung:	n/a
9	chr15:58358775-58358825	SAEC	small airway:	n/a
10	chr15:58429751-58429801	HMEC	breast:	n/a
11	chr15:58410989-58411039	ProgFib	skin:	n/a
12	chr15:58358811-58358861	HCF	heart:	n/a
13	chr15:58357874-58357924	HCF	heart:	n/a
14	chr15:58357891-58357941	HRCEpiC	kidney:	n/a
15	chr15:58357973-58358023	SKMC	muscle:	n/a
16	chr15:58429729-58429779	GM12878	blood:	n/a
17	chr15:58430539-58430589	AG04449	skin:	fetal
18	chr15:58429729-58429779	PFSK-1	brain:	n/a
19	chr15:58361558-58361608	A549	lung:	n/a
20	chr15:58429751-58429801	AoSMC	blood vessel:	n/a
21	chr15:58357319-58357369	GM12892	blood:	n/a
22	chr15:58430682-58430732	GM12878	blood:	n/a
23	chr15:58357987-58358037	HRPEpiC	eye:	n/a
24	chr15:58357319-58357369	BE2_C	brain:	n/a
25	chr15:58361558-58361608	HCT-116	colon:	n/a
26	chr15:58353849-58353899	HCPEpiC	choroid plexus:	n/a
27	chr15:58429751-58429801	MCF10A-Er-Src	breast:	n/a
28	chr15:58357989-58358039	LNCaP	prostate:	n/a
29	chr15:58357973-58358023	GM12878	blood:	n/a
30	chr15:58353849-58353899	PANC-1	pancreas:	n/a
31	chr15:58357879-58357929	MCF10A-Er-Src	breast:	n/a
32	chr15:58358811-58358861	K562	blood:	n/a
33	chr15:58357879-58357929	LNCaP	prostate:	n/a
34	chr15:58357989-58358039	NB4	blood:	n/a
35	chr15:58353849-58353899	GM06990	blood:	n/a
36	chr15:58357879-58357929	HRPEpiC	eye:	n/a
37	chr15:58357879-58357929	Jurkat	blood:	n/a
38	chr15:58430391-58430441	AG04449	skin:	fetal
39	chr15:58357987-58358037	AG09309	skin:	n/a
40	chr15:58429729-58429779	RPTEC	kidney:	n/a
41	chr15:58410989-58411039	NH-A	brain:	n/a
42	chr15:58357204-58357254	AG04449	skin:	fetal
43	chr15:58357204-58357254	NH-A	brain:	n/a
44	chr15:58358879-58358929	HCM	heart:	n/a
45	chr15:58358384-58358434	H1-hESC	embryonic stem cell:	embryo
46	chr15:58357987-58358037	ECC-1	luminal epithelium:	n/a
47	chr15:58353849-58353899	HPAEpiC	pulmonary alveolar:	n/a
48	chr15:58358879-58358929	AG04450	lung:	fetal
49	chr15:58353849-58353899	HEEpiC	esophagus:	n/a
50	chr15:58429729-58429779	U87	brain:	n/a

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:58372097..58374045-chr15:58377092..58379907,3	K562	blood:
2	chr15:58433881..58435963-chr15:58440042..58441729,2	K562	blood:
3	chr15:58387123..58389195-chr15:58391774..58393493,2	K562	blood:
4	chr15:58435593..58437807-chr15:58437844..58439525,2	K562	blood:
5	chr15:58414406..58417362-chr15:58440343..58442016,3	K562	blood:
6	chr15:58361640..58363619-chr15:58378533..58380318,2	K562	blood:
7	chr15:58395080..58396956-chr15:58399631..58401834,2	K562	blood:
8	chr15:58240183..58241922-chr15:58434571..58436348,2	K562	blood:
9	chr15:58354852..58359954-chr15:58398987..58405153,11	K562	blood:
10	chr15:58389052..58391594-chr15:58404567..58406553,2	K562	blood:
11	chr15:58377122..58381403-chr15:58381478..58386444,6	K562	blood:
12	chr15:58407482..58408061-chr15:58513659..58514466,2	MCF-7	breast:
13	chr15:58402876..58406319-chr15:58411755..58414973,3	K562	blood:
14	chr15:58362749..58363649-chr15:58474448..58475386,2	MCF-7	breast:
15	chr15:58389052..58391594-chr15:58404567..58406553,2	K562	blood:
16	chr15:58378945..58381403-chr15:58384396..58386444,2	K562	blood:
17	chr15:58370654..58372424-chr15:58402743..58405731,2	K562	blood:
18	chr15:58402721..58405438-chr15:58406173..58409890,4	K562	blood:
19	chr15:58389670..58391517-chr15:58401775..58404180,2	K562	blood:
20	chr15:58407522..58408442-chr15:58474456..58475377,4	K562	blood:
21	chr15:58369177..58370015-chr15:58513534..58514314,2	K562	blood:
22	chr15:58402749..58406127-chr15:58406949..58409453,4	K562	blood:
23	chr15:58330591..58332432-chr15:58347287..58349860,2	K562	blood:
24	chr15:58339367..58342167-chr15:58342533..58344499,3	K562	blood:
25	chr15:58407591..58408456-chr15:58474477..58475204,2	MCF-7	breast:
26	chr15:58346910..58349954-chr15:58473390..58475572,3	K562	blood:
27	chr15:58398996..58401637-chr15:58416020..58417854,2	K562	blood:
28	chr15:58158121..58158992-chr15:58362976..58363943,6	K562	blood:
29	chr15:58324356..58327238-chr15:58338542..58340895,2	K562	blood:
30	chr15:58372097..58374045-chr15:58377092..58379907,3	K562	blood:
31	chr15:58337253..58339004-chr15:58345727..58347852,2	K562	blood:
32	chr15:58299490..58302063-chr15:58354314..58356908,2	K562	blood:
33	chr15:58361275..58362874-chr15:58371926..58373547,2	K562	blood:
34	chr15:58400220..58402410-chr15:58409775..58411614,2	K562	blood:
35	chr15:58369470..58372316-chr15:58397826..58400720,3	K562	blood:
36	chr15:58337544..58340240-chr15:58358497..58360223,2	K562	blood:
37	chr15:58362436..58364377-chr15:58373826..58376648,2	K562	blood:
38	chr15:58348390..58350453-chr15:58469668..58473033,3	K562	blood:
39	chr15:58358402..58360542-chr15:58406579..58409075,2	K562	blood:
40	chr15:58372779..58375340-chr15:58393313..58395498,2	K562	blood:
41	chr15:58401521..58404295-chr15:58452218..58454934,2	K562	blood:
42	chr15:58369515..58370275-chr15:58474521..58475420,3	MCF-7	breast:
43	chr15:58306217..58308259-chr15:58356597..58358737,2	K562	blood:
44	chr15:58367485..58369030-chr15:58369816..58372224,2	K562	blood:
45	chr15:58395080..58396956-chr15:58399631..58401834,2	K562	blood:
46	chr15:58424607..58427157-chr15:58433686..58435502,2	K562	blood:
47	chr15:58373526..58376880-chr15:58386408..58389932,3	K562	blood:
48	chr15:58402876..58406319-chr15:58411755..58414973,3	K562	blood:
49	chr15:58336832..58338668-chr15:58341480..58343380,2	K562	blood:
50	chr15:58361275..58362874-chr15:58371926..58373547,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AQP9-1	chr15:58363006-58363241	NONHSAT044091
2	lnc-AQP9-1	chr15:58363006-58363241	ENSG00000259285.1
3	lnc-ADAM10-9	chr15:58430646-58430771	NONHSAT044089
4	lnc-AQP9-1	chr15:58363006-58363241	ENSG00000245722
5	lnc-AQP9-1	chr15:58357423-58357940	ENSG00000245722
6	lnc-AQP9-1	chr15:58364020-58364902	ENSG00000245722
7	lnc-AQP9-1	chr15:58357401-58357405	NONHSAT044091
8	lnc-AQP9-1	chr15:58364020-58364903	NONHSAT044091
9	lnc-ADAM10-9	chr15:58399518-58399667	NONHSAT044089
10	lnc-AQP9-1	chr15:58357428-58357940	NONHSAT044091
11	lnc-ADAM10-9	chr15:58399616-58399667	NONHSAT044093
12	lnc-ADAM10-9	chr15:58430646-58430771	NONHSAT044093
13	lnc-AQP9-1	chr15:58359013-58359132	ENSG00000259285.1
14	lnc-AQP9-1	chr15:58359013-58359132	NONHSAT044091
15	lnc-AQP9-1	chr15:58359013-58359132	ENSG00000245722
16	lnc-AQP9-1	chr15:58357423-58357940	ENSG00000259285.1
17	lnc-LIPC-7	chr15:58430462-58430875	NONHSAT044094
18	lnc-ADAM10-9	chr15:58430646-58430771	NONHSAT044095

No data

Variant related genes	Relation type
AQP9	TF binding region
ENSG00000259285	TF binding region
ALDH1A2	TF binding region
AQP9	CpG island
ENSG00000259285	CpG island
ALDH1A2	CpG island
ENSG00000128918	chromatin interactions
ENSG00000259379	chromatin interactions
ENSG00000182718	chromatin interactions
ENSG00000259285	chromatin interactions
CPOX	miRNA target sites
JUN	miRNA target sites
PRDM1	miRNA target sites

Extended variants
information (count: 3185 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3185 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1874158	chr15:58340072-58340073	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576838635	chr15:58340101-58340102	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs556474757	chr15:58340106-58340107	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs576306808	chr15:58340111-58340112	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs575377374	chr15:58340172-58340173	Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs376897334	chr15:58340257-58340258	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs545050732	chr15:58340276-58340277	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs565275360	chr15:58340310-58340311	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs112946582	chr15:58340364-58340365	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs545583436	chr15:58340367-58340368	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs75254177	chr15:58340375-58340376	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs541519581	chr15:58340389-58340390	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs565382069	chr15:58340428-58340429	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs529928704	chr15:58340466-58340467	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs4646574	chr15:58340474-58340475	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs184026809	chr15:58340524-58340525	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs563603579	chr15:58340576-58340577	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs367898128	chr15:58340670-58340671	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs188430146	chr15:58340674-58340675	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs376163881	chr15:58340697-58340698	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs551925846	chr15:58340699-58340700	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs139908902	chr15:58340709-58340710	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs181000040	chr15:58340710-58340711	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs562578526	chr15:58340732-58340733	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs35115757	chr15:58340749-58340750	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs536475581	chr15:58340767-58340768	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs559689151	chr15:58340769-58340770	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs143522789	chr15:58340786-58340787	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs533424665	chr15:58340816-58340817	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs16939727	chr15:58340832-58340833	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs34917541	chr15:58340838-58340839	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs541030019	chr15:58340912-58340913	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs140446962	chr15:58340965-58340966	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs574961421	chr15:58340985-58340986	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs562419285	chr15:58340998-58340999	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs185879884	chr15:58341011-58341012	Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs192469676	chr15:58341020-58341021	Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs532304547	chr15:58341080-58341081	Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs182090194	chr15:58341113-58341114	Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs35152578	chr15:58341121-58341122	Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs375811381	chr15:58341124-58341125	Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs11854019	chr15:58341128-58341129	Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs34575484	chr15:58341271-58341272	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs547855416	chr15:58341328-58341329	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs567862455	chr15:58341342-58341343	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs117382336	chr15:58341361-58341362	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs150391706	chr15:58341415-58341416	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs190668534	chr15:58341454-58341455	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs74018830	chr15:58341458-58341459	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs372959818	chr15:58341465-58341466	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Gastrointestinal stromal cancer	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	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
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
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:625 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58338800-58340400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr15:58339400-58340200	Weak transcription	K562	blood
3	chr15:58339400-58340400	Weak transcription	Fetal Lung	lung
4	chr15:58339400-58342800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr15:58339800-58343800	Weak transcription	Fetal Kidney	kidney
6	chr15:58340000-58340200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
7	chr15:58340200-58340800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr15:58340200-58340800	Enhancers	K562	blood
9	chr15:58340400-58340600	Enhancers	Fetal Lung	lung
10	chr15:58340400-58341000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr15:58340600-58342000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
12	chr15:58340800-58341800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr15:58340800-58341800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
14	chr15:58340800-58341800	Weak transcription	K562	blood
15	chr15:58340800-58342000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
16	chr15:58341400-58341800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
17	chr15:58341400-58342000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
18	chr15:58341400-58342200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr15:58341600-58341800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
20	chr15:58341800-58342000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
21	chr15:58341800-58342000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
22	chr15:58341800-58342200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr15:58341800-58342200	Enhancers	H9 Cell Line	embryonic stem cell
24	chr15:58341800-58342400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
25	chr15:58341800-58342600	Genic enhancers	K562	blood
26	chr15:58341800-58343200	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr15:58342000-58342200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
28	chr15:58342000-58342400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
29	chr15:58342000-58342600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
30	chr15:58342000-58344600	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr15:58342200-58342400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
32	chr15:58342200-58343000	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr15:58342400-58342600	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr15:58342400-58344400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
35	chr15:58342400-58344600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
36	chr15:58342600-58343000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
37	chr15:58342600-58343000	Weak transcription	K562	blood
38	chr15:58342600-58344600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
39	chr15:58342800-58344600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr15:58343000-58343200	Genic enhancers	K562	blood
41	chr15:58343000-58344000	Enhancers	H1 Cell Line	embryonic stem cell
42	chr15:58343200-58343800	Weak transcription	K562	blood
43	chr15:58343800-58344200	Strong transcription	K562	blood
44	chr15:58343800-58344400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
45	chr15:58343800-58347200	Enhancers	Fetal Kidney	kidney
46	chr15:58344000-58344200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
47	chr15:58344200-58344400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
48	chr15:58344200-58349000	Weak transcription	K562	blood
49	chr15:58344800-58346600	Enhancers	Fetal Lung	lung
50	chr15:58347200-58350200	Weak transcription	Fetal Kidney	kidney

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