Variant report

Variant	nsv904354
Chromosome Location	chr15:74697084-74722924
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1003)
CpG islands
(count:732)
Chromatin interactive
region (count:77)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1003 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:74715318-74715492	HepG2	liver:	n/a	n/a
2	ATF1	chr15:74718102-74718311	K562	blood:	n/a	n/a
3	ATF2	chr15:74699403-74701453	GM12878	blood:	n/a	n/a
4	ATF2	chr15:74722812-74723350	GM12878	blood:	n/a	n/a
5	ATF2	chr15:74720720-74721192	GM12878	blood:	n/a	n/a
6	ATF2	chr15:74722838-74723267	GM12878	blood:	n/a	n/a
7	ATF2	chr15:74694362-74697167	GM12878	blood:	n/a	n/a
8	BACH1	chr15:74715730-74716028	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr15:74715311-74715511	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr15:74699581-74701359	GM12878	blood:	n/a	n/a
11	BCL3	chr15:74708452-74709073	GM12878	blood:	n/a	n/a
12	BCL3	chr15:74708516-74709009	GM12878	blood:	n/a	n/a
13	BCLAF1	chr15:74717831-74718350	GM12878	blood:	n/a	n/a
14	BCLAF1	chr15:74720588-74721799	GM12878	blood:	n/a	chr15:74720893-74720902
15	BCLAF1	chr15:74699512-74701513	GM12878	blood:	n/a	n/a
16	BCLAF1	chr15:74694242-74697237	GM12878	blood:	n/a	chr15:74695477-74695486 chr15:74694864-74694877
17	BCLAF1	chr15:74695117-74697104	GM12878	blood:	n/a	chr15:74695477-74695486
18	BCLAF1	chr15:74700412-74701555	GM12878	blood:	n/a	n/a
19	BHLHE40	chr15:74699805-74700005	GM12878	blood:	n/a	n/a
20	BHLHE40	chr15:74715185-74715213	K562	blood:	n/a	n/a
21	BHLHE40	chr15:74722829-74723197	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:74701298-74701504	K562	blood:	n/a	n/a
23	BHLHE40	chr15:74717998-74718303	K562	blood:	n/a	n/a
24	BHLHE40	chr15:74701065-74701517	GM12878	blood:	n/a	n/a
25	BHLHE40	chr15:74715011-74715309	GM12878	blood:	n/a	n/a
26	BHLHE40	chr15:74714990-74715773	HepG2	liver:	n/a	chr15:74715008-74715024
27	BHLHE40	chr15:74716460-74716593	K562	blood:	n/a	n/a
28	BRCA1	chr15:74712549-74712574	GM12878	blood:	n/a	n/a
29	BRCA1	chr15:74716073-74716075	HepG2	liver:	n/a	n/a
30	CBX3	chr15:74717996-74718373	K562	blood:	n/a	n/a
31	CCNT2	chr15:74701668-74701968	K562	blood:	n/a	n/a
32	CCNT2	chr15:74702749-74703137	K562	blood:	n/a	n/a
33	CCNT2	chr15:74717925-74718315	K562	blood:	n/a	n/a
34	CEBPB	chr15:74719987-74720199	Hela-S3	cervix:	n/a	chr15:74720069-74720080
35	CEBPB	chr15:74722751-74723767	GM12878	blood:	n/a	n/a
36	CEBPB	chr15:74718109-74718218	K562	blood:	n/a	n/a
37	CEBPB	chr15:74715338-74715511	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr15:74714996-74715499	HepG2	liver:	n/a	chr15:74715131-74715148
39	CEBPB	chr15:74715024-74715461	IMR90	lung:	n/a	chr15:74715131-74715148
40	CEBPB	chr15:74694905-74697085	GM12878	blood:	n/a	n/a
41	CEBPB	chr15:74719897-74720254	HepG2	liver:	n/a	chr15:74720069-74720080
42	CEBPB	chr15:74719920-74720257	HepG2	liver:	n/a	chr15:74720069-74720080
43	CEBPB	chr15:74715316-74715323	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPD	chr15:74713862-74714212	HepG2	liver:	n/a	n/a
45	CHD1	chr15:74718083-74718133	GM12878	blood:	n/a	n/a
46	CHD1	chr15:74722244-74727150	IMR90	lung:	n/a	chr15:74726359-74726369 chr15:74725431-74725441 chr15:74725141-74725151 chr15:74726366-74726376
47	CHD1	chr15:74722765-74723617	GM12878	blood:	n/a	n/a
48	CHD1	chr15:74722168-74722285	GM12878	blood:	n/a	n/a
49	CHD1	chr15:74720735-74721809	GM12878	blood:	n/a	n/a
50	CHD2	chr15:74715354-74715573	HepG2	liver:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:74703101-74703151	HRE	kidney:	n/a
2	chr15:74699653-74699703	A549	lung:	n/a
3	chr15:74715105-74715155	HL-60	blood:	n/a
4	chr15:74709717-74709767	GM12891	blood:	n/a
5	chr15:74704423-74704473	AG10803	skin:	n/a
6	chr15:74715105-74715155	HUVEC	blood vessel:	n/a
7	chr15:74714463-74714513	LNCaP	prostate:	n/a
8	chr15:74702956-74703006	HIPEpiC	eye:	n/a
9	chr15:74706314-74706364	GM06990	blood:	n/a
10	chr15:74703254-74703304	Hela-S3	cervix:	n/a
11	chr15:74715105-74715155	BJ	skin:	n/a
12	chr15:74703141-74703191	AG04449	skin:	fetal
13	chr15:74703141-74703191	HRCEpiC	kidney:	n/a
14	chr15:74703165-74703215	HCT-116	colon:	n/a
15	chr15:74704423-74704473	HRE	kidney:	n/a
16	chr15:74703101-74703151	HepG2	liver:	n/a
17	chr15:74703101-74703151	AG09319	gingival:	n/a
18	chr15:74703101-74703151	AG04449	skin:	fetal
19	chr15:74703141-74703191	HUVEC	blood vessel:	n/a
20	chr15:74703165-74703215	HIPEpiC	eye:	n/a
21	chr15:74703254-74703304	ECC-1	luminal epithelium:	n/a
22	chr15:74709717-74709767	NHBE	bronchial:	n/a
23	chr15:74715105-74715155	RPTEC	kidney:	n/a
24	chr15:74703054-74703104	HCPEpiC	choroid plexus:	n/a
25	chr15:74703165-74703215	HL-60	blood:	n/a
26	chr15:74706314-74706364	MCF-7	breast:	n/a
27	chr15:74702956-74703006	T-47D	breast:	n/a
28	chr15:74704423-74704473	HNPCEpiC	eye:	n/a
29	chr15:74703165-74703215	HMEC	breast:	n/a
30	chr15:74703254-74703304	ovcar-3	ovarian:	n/a
31	chr15:74706314-74706364	Caco-2	colon:	n/a
32	chr15:74702956-74703006	NHDF-neo	bronchial:	n/a
33	chr15:74703165-74703215	HepG2	liver:	n/a
34	chr15:74702956-74703006	Hela-S3	cervix:	n/a
35	chr15:74714463-74714513	AG10803	skin:	n/a
36	chr15:74703254-74703304	HEEpiC	esophagus:	n/a
37	chr15:74702956-74703006	Hepatocyte	liver:	n/a
38	chr15:74703254-74703304	HUVEC	blood vessel:	n/a
39	chr15:74715105-74715155	A549	lung:	n/a
40	chr15:74714463-74714513	NB4	blood:	n/a
41	chr15:74703054-74703104	BJ	skin:	n/a
42	chr15:74709717-74709767	Hela-S3	cervix:	n/a
43	chr15:74703141-74703191	NT2-D1	testis:	n/a
44	chr15:74714463-74714513	U87	brain:	n/a
45	chr15:74699653-74699703	GM19239	blood:	n/a
46	chr15:74714463-74714513	HPAEpiC	pulmonary alveolar:	n/a
47	chr15:74703254-74703304	RPTEC	kidney:	n/a
48	chr15:74714463-74714513	Caco-2	colon:	n/a
49	chr15:74699653-74699703	RPTEC	kidney:	n/a
50	chr15:74703165-74703215	PrEC	prostate:	n/a

(count:77 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:74682079..74683871-chr15:74715405..74717396,2	MCF-7	breast:
2	chr15:74708765..74710665-chr15:74717275..74720280,3	K562	blood:
3	chr15:74703939..74707088-chr15:74707597..74710860,4	K562	blood:
4	chr15:74688222..74690157-chr15:74695368..74697306,2	K562	blood:
5	chr15:74693785..74695419-chr15:74712435..74714990,2	MCF-7	breast:
6	chr15:74698476..74700326-chr15:74700408..74702340,3	MCF-7	breast:
7	chr15:74683786..74686291-chr15:74709517..74711848,2	K562	blood:
8	chr15:74698106..74700226-chr15:74701422..74703511,2	MCF-7	breast:
9	chr15:74712355..74714244-chr15:74719225..74721195,3	K562	blood:
10	chr15:74665724..74666602-chr15:74716103..74717034,2	K562	blood:
11	chr15:74689624..74691251-chr15:74705543..74707714,2	K562	blood:
12	chr15:74706143..74707711-chr15:74709343..74712295,2	K562	blood:
13	chr15:74688657..74691908-chr15:74695060..74698552,3	K562	blood:
14	chr15:74708430..74711665-chr15:74722964..74726115,3	K562	blood:
15	chr15:74706143..74707711-chr15:74709343..74712295,2	K562	blood:
16	chr15:74708765..74710665-chr15:74717275..74720280,3	K562	blood:
17	chr15:74691943..74695030-chr15:74695154..74698186,3	MCF-7	breast:
18	chr15:74709534..74711192-chr15:74725861..74727762,2	MCF-7	breast:
19	chr15:74681656..74683846-chr15:74699710..74701534,2	K562	blood:
20	chr15:74698938..74701316-chr15:74711313..74715118,3	MCF-7	breast:
21	chr15:74700131..74703007-chr15:74725422..74727638,2	MCF-7	breast:
22	chr15:74712692..74714612-chr15:74714775..74716965,2	MCF-7	breast:
23	chr15:74715058..74717919-chr15:74753629..74755415,2	K562	blood:
24	chr15:74687537..74689333-chr15:74700401..74702548,2	MCF-7	breast:
25	chr15:74718075..74720590-chr15:74744935..74747887,2	K562	blood:
26	chr15:74709055..74711069-chr15:74716225..74718265,2	MCF-7	breast:
27	chr15:74696752..74700266-chr15:74701872..74704964,3	K562	blood:
28	chr15:74713352..74715766-chr15:74724000..74726928,3	MCF-7	breast:
29	chr15:74689719..74694435-chr15:74706184..74713253,9	MCF-7	breast:
30	chr15:74712355..74714244-chr15:74719225..74721195,3	K562	blood:
31	chr15:74678579..74680979-chr15:74717975..74720152,2	MCF-7	breast:
32	chr15:74712692..74714612-chr15:74714775..74716965,2	MCF-7	breast:
33	chr15:74710597..74712982-chr15:75051460..75053643,2	K562	blood:
34	chr15:74692372..74694317-chr15:74699188..74700787,2	MCF-7	breast:
35	chr15:74674587..74678748-chr15:74711681..74714409,4	K562	blood:
36	chr15:74698106..74700226-chr15:74701422..74703511,2	MCF-7	breast:
37	chr15:74688261..74689838-chr15:74715380..74717091,2	K562	blood:
38	chr15:74711706..74714244-chr15:74719320..74721195,2	K562	blood:
39	chr15:74690543..74693238-chr15:74721737..74723787,2	MCF-7	breast:
40	chr15:74699281..74701462-chr15:74703798..74706437,2	MCF-7	breast:
41	chr15:74694779..74697327-chr15:74724134..74726269,2	MCF-7	breast:
42	chr15:74692322..74695920-chr15:74711238..74714934,4	K562	blood:
43	chr15:74710571..74713498-chr15:74715208..74717540,3	K562	blood:
44	chr15:74708483..74711346-chr15:74713083..74715062,3	MCF-7	breast:
45	chr15:74715079..74717127-chr15:74720885..74723638,2	MCF-7	breast:
46	chr15:74720298..74721801-chr15:74727091..74728921,2	MCF-7	breast:
47	chr15:74720324..74723910-chr15:74723921..74727050,4	MCF-7	breast:
48	chr15:74673143..74676106-chr15:74720304..74723999,3	K562	blood:
49	chr15:74679411..74681539-chr15:74718072..74720189,2	K562	blood:
50	chr15:74684231..74686824-chr15:74694888..74698763,3	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6881-3p	chr15:74703702-74703723	MIMAT0027663
hsa-miR-6881-5p	chr15:74703747-74703768	MIMAT0027662

No data

Variant related genes	Relation type
SEMA7A	TF binding region
SEMA7A	CpG island
ENSG00000138623	chromatin interactions
ENSG00000260919	chromatin interactions
ENSG00000179335	chromatin interactions
ENSG00000247240	chromatin interactions

Extended variants
information (count: 1093 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1093 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4243086	chr15:74697084-74697085	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs4589509	chr15:74697122-74697123	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs375183983	chr15:74697156-74697157	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs142888136	chr15:74697198-74697199	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs528770112	chr15:74697207-74697208	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs6495100	chr15:74697236-74697237	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs561961613	chr15:74697261-74697262	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs7496188	chr15:74697276-74697277	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs549159226	chr15:74697297-74697298	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs529253277	chr15:74697305-74697306	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs550695179	chr15:74697327-74697328	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs556700625	chr15:74697335-74697336	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs183396695	chr15:74697343-74697344	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs111342540	chr15:74697384-74697385	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs372006597	chr15:74697386-74697387	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs148712894	chr15:74697483-74697484	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs545668051	chr15:74697488-74697489	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs141422290	chr15:74697545-74697546	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs113056846	chr15:74697579-74697580	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs377074255	chr15:74697582-74697583	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs546842743	chr15:74697603-74697604	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs567976046	chr15:74697615-74697616	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs150843275	chr15:74697657-74697658	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
24	rs557120333	chr15:74697675-74697676	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs139306848	chr15:74697722-74697723	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs557261450	chr15:74697741-74697742	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs540077960	chr15:74697784-74697785	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs187291511	chr15:74697818-74697819	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs192177689	chr15:74697852-74697853	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs575511959	chr15:74697853-74697854	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs573358817	chr15:74697864-74697865	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs144355655	chr15:74697865-74697866	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs75052979	chr15:74697949-74697950	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs140155715	chr15:74698003-74698004	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs373523537	chr15:74698080-74698081	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs544199164	chr15:74698104-74698105	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs562684692	chr15:74698161-74698162	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs533262878	chr15:74698172-74698173	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs183856286	chr15:74698219-74698220	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs78872678	chr15:74698312-74698313	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs11854442	chr15:74698331-74698332	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs541452573	chr15:74698332-74698333	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs148815098	chr15:74698334-74698335	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs557973709	chr15:74698353-74698354	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs568321213	chr15:74698440-74698441	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs12911146	chr15:74698441-74698442	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs12911577	chr15:74698442-74698443	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs535489096	chr15:74698472-74698473	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs80339866	chr15:74698498-74698499	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs568829865	chr15:74698535-74698536	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	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
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
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
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:1088 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74685400-74699400	Weak transcription	Brain Substantia Nigra	brain
2	chr15:74688000-74699000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr15:74689400-74702400	Weak transcription	Gastric	stomach
4	chr15:74689600-74698000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr15:74691800-74697200	Flanking Active TSS	GM12878-XiMat	blood
6	chr15:74692000-74701200	Enhancers	Spleen	Spleen
7	chr15:74692800-74698000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr15:74693600-74699200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr15:74693600-74701600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr15:74693800-74698600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr15:74693800-74698800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr15:74693800-74699000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr15:74693800-74700000	Weak transcription	Esophagus	oesophagus
14	chr15:74694000-74698000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr15:74694000-74698800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr15:74694000-74699000	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr15:74694000-74699000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr15:74694000-74699200	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr15:74694000-74699400	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr15:74694200-74698000	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr15:74694200-74699000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr15:74694200-74699000	Weak transcription	Hela-S3	cervix
23	chr15:74694400-74697400	Enhancers	Fetal Brain Male	brain
24	chr15:74694400-74699000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr15:74695000-74697200	Genic enhancers	HSMM	muscle
26	chr15:74695400-74697200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr15:74695800-74699200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr15:74696000-74698800	Weak transcription	NHEK	skin
29	chr15:74696000-74699200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr15:74696000-74700400	Enhancers	Ovary	ovary
31	chr15:74696200-74697200	Genic enhancers	NH-A	brain
32	chr15:74696200-74698600	Weak transcription	HMEC	breast
33	chr15:74696200-74699000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr15:74696200-74700000	Enhancers	Primary B cells from peripheral blood	blood
35	chr15:74696200-74702600	Weak transcription	Lung	lung
36	chr15:74696200-74710400	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr15:74696200-74711400	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr15:74696200-74712600	Weak transcription	Right Atrium	heart
39	chr15:74696400-74697200	Enhancers	Primary hematopoietic stem cells	blood
40	chr15:74696400-74697200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr15:74696400-74697200	Enhancers	Fetal Kidney	kidney
42	chr15:74696400-74699000	Weak transcription	Brain Angular Gyrus	brain
43	chr15:74696400-74700600	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr15:74696400-74702400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr15:74696400-74707000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr15:74696400-74712200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr15:74696600-74698800	Strong transcription	Placenta	Placenta
48	chr15:74696600-74699800	Enhancers	Fetal Thymus	thymus
49	chr15:74696600-74703600	Weak transcription	Rectal Smooth Muscle	rectum
50	chr15:74696600-74706200	Weak transcription	Primary T cells from cord blood	blood

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