Variant report

Variant	nsv569596
Chromosome Location	chr15:58355798-58408763
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1306)
CpG islands
(count:855)
Chromatin interactive
region (count:72)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1306 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:58383973-58384116	K562	blood:	n/a	n/a
2	ARID3A	chr15:58358634-58358800	K562	blood:	n/a	n/a
3	ARID3A	chr15:58400308-58400825	K562	blood:	n/a	n/a
4	ARID3A	chr15:58369703-58370028	K562	blood:	n/a	n/a
5	ARID3A	chr15:58406982-58407925	K562	blood:	n/a	n/a
6	ARID3A	chr15:58363037-58363469	K562	blood:	n/a	n/a
7	ARID3A	chr15:58395672-58396090	K562	blood:	n/a	n/a
8	ARID3A	chr15:58363058-58363339	HepG2	liver:	n/a	n/a
9	ARID3A	chr15:58357164-58357177	K562	blood:	n/a	n/a
10	ARID3A	chr15:58389380-58389410	K562	blood:	n/a	n/a
11	ARID3A	chr15:58356039-58356049	K562	blood:	n/a	n/a
12	ARID3A	chr15:58403141-58404251	K562	blood:	n/a	n/a
13	ARID3A	chr15:58357749-58357751	K562	blood:	n/a	n/a
14	ATF1	chr15:58357118-58357128	K562	blood:	n/a	n/a
15	ATF1	chr15:58407006-58407420	K562	blood:	n/a	n/a
16	ATF1	chr15:58400264-58400665	K562	blood:	n/a	n/a
17	ATF1	chr15:58395788-58395964	K562	blood:	n/a	n/a
18	ATF1	chr15:58369690-58370014	K562	blood:	n/a	n/a
19	ATF1	chr15:58372658-58372910	K562	blood:	n/a	n/a
20	ATF1	chr15:58403177-58404184	K562	blood:	n/a	n/a
21	ATF3	chr15:58395692-58395981	K562	blood:	n/a	n/a
22	ATF3	chr15:58357915-58358171	K562	blood:	n/a	chr15:58358044-58358053
23	BACH1	chr15:58358059-58358350	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr15:58403538-58403774	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr15:58372631-58372714	K562	blood:	n/a	n/a
26	BACH1	chr15:58403096-58404272	K562	blood:	n/a	chr15:58403430-58403444
27	BCLAF1	chr15:58358424-58358973	K562	blood:	n/a	n/a
28	BCLAF1	chr15:58357508-58358003	K562	blood:	n/a	chr15:58357980-58357993
29	BCLAF1	chr15:58403373-58404330	K562	blood:	n/a	n/a
30	BHLHE40	chr15:58369815-58370046	K562	blood:	n/a	n/a
31	BHLHE40	chr15:58363087-58363540	K562	blood:	n/a	n/a
32	BHLHE40	chr15:58358494-58358828	K562	blood:	n/a	n/a
33	BHLHE40	chr15:58376685-58376686	K562	blood:	n/a	n/a
34	BHLHE40	chr15:58407059-58407207	K562	blood:	n/a	n/a
35	BHLHE40	chr15:58357209-58357396	K562	blood:	n/a	n/a
36	BHLHE40	chr15:58376386-58376443	K562	blood:	n/a	n/a
37	BHLHE40	chr15:58403181-58404269	K562	blood:	n/a	n/a
38	BHLHE40	chr15:58372615-58372750	K562	blood:	n/a	n/a
39	BRCA1	chr15:58369573-58369653	HepG2	liver:	n/a	n/a
40	CBX3	chr15:58403151-58403875	K562	blood:	n/a	n/a
41	CBX3	chr15:58395620-58396284	K562	blood:	n/a	n/a
42	CBX3	chr15:58358482-58358944	K562	blood:	n/a	n/a
43	CBX3	chr15:58400257-58400701	K562	blood:	n/a	n/a
44	CBX3	chr15:58388708-58389316	K562	blood:	n/a	n/a
45	CCNT2	chr15:58407053-58407406	K562	blood:	n/a	n/a
46	CCNT2	chr15:58405550-58405768	K562	blood:	n/a	n/a
47	CCNT2	chr15:58356876-58358872	K562	blood:	n/a	chr15:58358513-58358522
48	CCNT2	chr15:58400519-58400792	K562	blood:	n/a	chr15:58400740-58400749
49	CCNT2	chr15:58403185-58404272	K562	blood:	n/a	n/a
50	CEBPB	chr15:58406952-58407486	K562	blood:	n/a	chr15:58407295-58407306 chr15:58407294-58407307

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:58357989-58358039	Hela-S3	cervix:	n/a
2	chr15:58357989-58358039	Hela-S3	cervix:	n/a
3	chr15:58358811-58358861	AG09309	skin:	n/a
4	chr15:58358384-58358434	HMEC	breast:	n/a
5	chr15:58357989-58358039	GM12892	blood:	n/a
6	chr15:58358775-58358825	HCF	heart:	n/a
7	chr15:58358775-58358825	HRCEpiC	kidney:	n/a
8	chr15:58357874-58357924	HNPCEpiC	eye:	n/a
9	chr15:58357204-58357254	PFSK-1	brain:	n/a
10	chr15:58357319-58357369	HPAEpiC	pulmonary alveolar:	n/a
11	chr15:58357987-58358037	ProgFib	skin:	n/a
12	chr15:58357973-58358023	AG09319	gingival:	n/a
13	chr15:58357987-58358037	AoSMC	blood vessel:	n/a
14	chr15:58358811-58358861	BE2_C	brain:	n/a
15	chr15:58357874-58357924	GM12878	blood:	n/a
16	chr15:58357874-58357924	BE2_C	brain:	n/a
17	chr15:58357874-58357924	GM06990	blood:	n/a
18	chr15:58357204-58357254	SAEC	small airway:	n/a
19	chr15:58357874-58357924	RPTEC	kidney:	n/a
20	chr15:58361558-58361608	SK-N-MC	brain:	n/a
21	chr15:58357891-58357941	NB4	blood:	n/a
22	chr15:58357891-58357941	Hela-S3	cervix:	n/a
23	chr15:58358811-58358861	LNCaP	prostate:	n/a
24	chr15:58357879-58357929	HCPEpiC	choroid plexus:	n/a
25	chr15:58357891-58357941	MCF10A-Er-Src	breast:	n/a
26	chr15:58357319-58357369	HEEpiC	esophagus:	n/a
27	chr15:58357891-58357941	CMK	blood:	n/a
28	chr15:58357319-58357369	HUVEC	blood vessel:	n/a
29	chr15:58357874-58357924	HRCEpiC	kidney:	n/a
30	chr15:58358879-58358929	NB4	blood:	n/a
31	chr15:58358811-58358861	HCPEpiC	choroid plexus:	n/a
32	chr15:58357204-58357254	HPAEpiC	pulmonary alveolar:	n/a
33	chr15:58357874-58357924	Jurkat	blood:	n/a
34	chr15:58358811-58358861	CMK	blood:	n/a
35	chr15:58361558-58361608	HCM	heart:	n/a
36	chr15:58357879-58357929	Hepatocyte	liver:	n/a
37	chr15:58357874-58357924	HepG2	liver:	n/a
38	chr15:58357874-58357924	NHDF-neo	bronchial:	n/a
39	chr15:58361558-58361608	HUVEC	blood vessel:	n/a
40	chr15:58357922-58357972	SK-N-SH	brain:	n/a
41	chr15:58357989-58358039	NH-A	brain:	n/a
42	chr15:58358384-58358434	T-47D	breast:	n/a
43	chr15:58358775-58358825	BE2_C	brain:	n/a
44	chr15:58358879-58358929	HIPEpiC	eye:	n/a
45	chr15:58357891-58357941	HNPCEpiC	eye:	n/a
46	chr15:58357989-58358039	HRCEpiC	kidney:	n/a
47	chr15:58361558-58361608	BE2_C	brain:	n/a
48	chr15:58358811-58358861	HRE	kidney:	n/a
49	chr15:58358879-58358929	T-47D	breast:	n/a
50	chr15:58358811-58358861	ECC-1	luminal epithelium:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:58261520..58262217-chr15:58362720..58363602,3	MCF-7	breast:
2	chr15:58356974..58359469-chr15:60688408..60691704,3	K562	blood:
3	chr15:58382678..58385376-chr15:58387559..58389345,2	K562	blood:
4	chr15:58362749..58363649-chr15:58474448..58475386,2	MCF-7	breast:
5	chr15:58377122..58381403-chr15:58381478..58386444,6	K562	blood:
6	chr15:58402721..58405438-chr15:58406173..58409890,4	K562	blood:
7	chr15:58354852..58359954-chr15:58398987..58405153,11	K562	blood:
8	chr15:58035424..58036079-chr15:58362751..58363370,2	MCF-7	breast:
9	chr15:58369177..58370015-chr15:58513534..58514314,2	K562	blood:
10	chr15:58361640..58363619-chr15:58378533..58380318,2	K562	blood:
11	chr15:58356241..58358717-chr15:58403285..58405338,4	K562	blood:
12	chr15:58157674..58158877-chr15:58362866..58363674,3	MCF-7	breast:
13	chr15:58387123..58389195-chr15:58391774..58393493,2	K562	blood:
14	chr15:58407482..58408061-chr15:58513659..58514466,2	MCF-7	breast:
15	chr15:58377122..58381403-chr15:58381478..58386444,6	K562	blood:
16	chr15:58395080..58396956-chr15:58399631..58401834,2	K562	blood:
17	chr15:58358402..58360542-chr15:58406579..58409075,2	K562	blood:
18	chr15:58398996..58401637-chr15:58416020..58417854,2	K562	blood:
19	chr15:58395080..58396956-chr15:58399631..58401834,2	K562	blood:
20	chr15:58361275..58362874-chr15:58371926..58373547,2	K562	blood:
21	chr15:58382678..58385376-chr15:58387559..58389345,2	K562	blood:
22	chr15:58368356..58371327-chr15:58469110..58471908,2	K562	blood:
23	chr15:58401521..58404295-chr15:58452218..58454934,2	K562	blood:
24	chr15:58404558..58406881-chr15:58443582..58445148,2	K562	blood:
25	chr15:58358213..58359860-chr15:58377988..58380006,2	K562	blood:
26	chr15:58389670..58391517-chr15:58401775..58404180,2	K562	blood:
27	chr15:58373526..58376880-chr15:58386408..58389932,3	K562	blood:
28	chr15:58362436..58364377-chr15:58373826..58376648,2	K562	blood:
29	chr15:58372097..58374045-chr15:58377092..58379907,3	K562	blood:
30	chr15:58360768..58363074-chr15:58403366..58406297,2	K562	blood:
31	chr15:58402749..58406127-chr15:58406949..58409453,4	K562	blood:
32	chr15:58367485..58369030-chr15:58369816..58372224,2	K562	blood:
33	chr15:58373526..58376880-chr15:58386408..58389932,3	K562	blood:
34	chr15:58402749..58406127-chr15:58406949..58409453,4	K562	blood:
35	chr15:58407522..58408442-chr15:58474456..58475377,4	K562	blood:
36	chr15:58402733..58404852-chr15:58471216..58473457,2	K562	blood:
37	chr15:58407591..58408456-chr15:58474477..58475204,2	MCF-7	breast:
38	chr15:58372779..58375340-chr15:58393313..58395498,2	K562	blood:
39	chr15:58328560..58331091-chr15:58356467..58358929,2	K562	blood:
40	chr15:58369470..58372316-chr15:58397826..58400720,3	K562	blood:
41	chr15:58367485..58369030-chr15:58369816..58372224,2	K562	blood:
42	chr15:58370654..58372424-chr15:58402743..58405731,2	K562	blood:
43	chr15:58357214..58361231-chr15:58369830..58374157,6	K562	blood:
44	chr15:58387123..58389195-chr15:58391774..58393493,2	K562	blood:
45	chr15:58402611..58405043-chr15:58470858..58473947,6	K562	blood:
46	chr15:58378945..58381403-chr15:58384396..58386444,2	K562	blood:
47	chr15:58378945..58381403-chr15:58384396..58386444,2	K562	blood:
48	chr15:58402876..58406319-chr15:58411755..58414973,3	K562	blood:
49	chr15:58369470..58372316-chr15:58397826..58400720,3	K562	blood:
50	chr15:58389052..58391594-chr15:58404567..58406553,2	K562	blood:

(count:14 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 1674 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1674 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4646552	chr15:58355798-58355799	Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs142925538	chr15:58355867-58355868	Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs556069283	chr15:58355873-58355874	Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs192136101	chr15:58355876-58355877	Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs8027466	chr15:58355895-58355896	Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs557731027	chr15:58356045-58356046	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs147427973	chr15:58356089-58356090	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs540346560	chr15:58356097-58356098	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs185713799	chr15:58356101-58356102	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs200259106	chr15:58356175-58356176	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs529116075	chr15:58356180-58356181	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs370845349	chr15:58356198-58356199	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs542454279	chr15:58356254-58356255	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs2414530	chr15:58356362-58356363	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs531648540	chr15:58356368-58356369	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs528144212	chr15:58356369-58356370	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs551656940	chr15:58356422-58356423	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs571278426	chr15:58356429-58356430	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs187603727	chr15:58356430-58356431	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs547543062	chr15:58356438-58356439	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs567246188	chr15:58356439-58356440	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs536084769	chr15:58356456-58356457	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs8032472	chr15:58356457-58356458	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs377357215	chr15:58356473-58356474	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs569385091	chr15:58356499-58356500	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs148521085	chr15:58356565-58356566	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs538167208	chr15:58356620-58356621	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs35862652	chr15:58356621-58356622	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs548326036	chr15:58356632-58356633	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs192177767	chr15:58356745-58356746	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs35710482	chr15:58356746-58356747	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs554288963	chr15:58356765-58356766	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs34972167	chr15:58356784-58356785	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs543069149	chr15:58356787-58356788	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs562545720	chr15:58356800-58356801	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs576269806	chr15:58356803-58356804	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs545354230	chr15:58356817-58356818	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs565155178	chr15:58356819-58356820	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs527329362	chr15:58356820-58356821	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs7171261	chr15:58356855-58356856	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs192897297	chr15:58356874-58356875	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs184537180	chr15:58356911-58356912	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs530504403	chr15:58356946-58356947	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs549818052	chr15:58356953-58356954	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs150644108	chr15:58356954-58356955	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs139743202	chr15:58356959-58356960	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs550352905	chr15:58356970-58356971	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs570716143	chr15:58357036-58357037	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs35270169	chr15:58357044-58357045	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs35365571	chr15:58357048-58357049	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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

Chromatin state (count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58353400-58358800	Active TSS	K562	blood
2	chr15:58353600-58359000	Active TSS	Fetal Kidney	kidney
3	chr15:58354000-58356800	Flanking Active TSS	HUVEC	blood vessel
4	chr15:58354200-58358800	Active TSS	Ovary	ovary
5	chr15:58354400-58358800	Active TSS	Right Atrium	heart
6	chr15:58354800-58355800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr15:58355800-58356000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
8	chr15:58355800-58357200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
9	chr15:58355800-58357200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
10	chr15:58356000-58357400	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
11	chr15:58356200-58356400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
12	chr15:58356400-58356600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
13	chr15:58356400-58356600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
14	chr15:58356400-58356800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
15	chr15:58356400-58357000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
16	chr15:58356600-58356800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
17	chr15:58356600-58356800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
18	chr15:58356600-58357000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
19	chr15:58356600-58357000	Active TSS	Fetal Stomach	stomach
20	chr15:58356800-58357000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
21	chr15:58356800-58357000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
22	chr15:58356800-58357000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
23	chr15:58356800-58357000	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
24	chr15:58356800-58357200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
25	chr15:58356800-58357200	Active TSS	HUVEC	blood vessel
26	chr15:58357000-58357200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
27	chr15:58357000-58357200	Flanking Bivalent TSS/Enh	Fetal Lung	lung
28	chr15:58357000-58357200	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
29	chr15:58357000-58357200	Bivalent/Poised TSS	Fetal Stomach	stomach
30	chr15:58357000-58357200	Enhancers	Pancreas	Pancrea
31	chr15:58357000-58357400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
32	chr15:58357000-58357600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
33	chr15:58357000-58357600	Bivalent/Poised TSS	Primary neutrophils fromperipheralblood	blood
34	chr15:58357000-58357600	Bivalent/Poised TSS	Primary B cells from cord blood	blood
35	chr15:58357000-58358800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
36	chr15:58357200-58357400	Flanking Bivalent TSS/Enh	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr15:58357200-58357400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr15:58357200-58357400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr15:58357200-58357400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
40	chr15:58357200-58357400	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
41	chr15:58357200-58357400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
42	chr15:58357200-58357400	Bivalent Enhancer	Primary T cells from cord blood	blood
43	chr15:58357200-58357400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
44	chr15:58357200-58357400	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
45	chr15:58357200-58357400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
46	chr15:58357200-58357400	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr15:58357200-58357400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr15:58357200-58357400	Bivalent Enhancer	Brain Germinal Matrix	brain
49	chr15:58357200-58357400	Bivalent Enhancer	Colonic Mucosa	Colon
50	chr15:58357200-58357400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum

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