Variant report

Variant	nsv471253
Chromosome Location	chr15:74489207-74545148
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1445)
CpG islands
(count:2387)
Chromatin interactive
region (count:69)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1445 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:74507718-74507872	HepG2	liver:	n/a	n/a
2	ATF1	chr15:74502533-74502830	K562	blood:	n/a	n/a
3	ATF2	chr15:74494985-74495663	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr15:74494889-74495592	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr15:74506325-74506657	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr15:74516142-74516531	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr15:74517335-74517547	K562	blood:	n/a	n/a
8	ATF3	chr15:74532206-74532673	A549	lung:	n/a	n/a
9	ATF3	chr15:74492667-74493149	A549	lung:	n/a	n/a
10	BACH1	chr15:74494893-74495685	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr15:74496082-74496694	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr15:74504375-74504439	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr15:74521267-74521353	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr15:74516256-74516452	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr15:74492765-74493061	GM12878	blood:	n/a	chr15:74492924-74492935
16	BCL3	chr15:74492626-74493188	A549	lung:	n/a	chr15:74492969-74492978
17	BCL3	chr15:74492637-74493293	A549	lung:	n/a	chr15:74492969-74492978
18	BCL3	chr15:74532195-74532642	A549	lung:	n/a	chr15:74532509-74532518
19	BHLHE40	chr15:74519595-74519733	K562	blood:	n/a	n/a
20	BHLHE40	chr15:74515777-74516104	K562	blood:	n/a	chr15:74515954-74515963 chr15:74515954-74515963 chr15:74515953-74515962
21	BHLHE40	chr15:74506104-74506388	K562	blood:	n/a	n/a
22	BHLHE40	chr15:74494772-74494865	K562	blood:	n/a	n/a
23	BHLHE40	chr15:74515801-74516117	HepG2	liver:	n/a	chr15:74515954-74515963 chr15:74515954-74515963 chr15:74515953-74515962
24	BRCA1	chr15:74494960-74495467	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr15:74504795-74504804	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr15:74532331-74532656	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr15:74502602-74502839	K562	blood:	n/a	n/a
28	CEBPB	chr15:74507625-74507947	HepG2	liver:	n/a	chr15:74507788-74507799
29	CEBPB	chr15:74495243-74495720	A549	lung:	n/a	n/a
30	CEBPB	chr15:74502519-74503172	IMR90	lung:	n/a	n/a
31	CEBPB	chr15:74507630-74507980	A549	lung:	n/a	chr15:74507788-74507799
32	CEBPB	chr15:74507612-74507975	IMR90	lung:	n/a	chr15:74507788-74507799
33	CEBPB	chr15:74492570-74493235	MCF-7	breast:	n/a	n/a
34	CEBPB	chr15:74507527-74508058	MCF-7	breast:	n/a	chr15:74507788-74507799
35	CEBPB	chr15:74507640-74507911	K562	blood:	n/a	chr15:74507788-74507799
36	CEBPB	chr15:74507456-74508116	MCF-7	breast:	n/a	chr15:74507788-74507799
37	CEBPB	chr15:74492662-74493110	GM12878	blood:	n/a	n/a
38	CEBPB	chr15:74492570-74493268	A549	lung:	n/a	n/a
39	CEBPB	chr15:74507545-74508040	ECC-1	luminal epithelium:	n/a	chr15:74507788-74507799
40	CEBPB	chr15:74492763-74493161	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr15:74492719-74493144	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr15:74507638-74507860	HepG2	liver:	n/a	chr15:74507788-74507799
43	CEBPB	chr15:74507561-74508026	ECC-1	luminal epithelium:	n/a	chr15:74507788-74507799
44	CEBPB	chr15:74507555-74507904	H1-hESC	embryonic stem cell:	n/a	chr15:74507788-74507799
45	CEBPB	chr15:74507631-74507922	A549	lung:	n/a	chr15:74507788-74507799
46	CEBPB	chr15:74496474-74496646	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr15:74492716-74493096	A549	lung:	n/a	n/a
48	CEBPB	chr15:74507314-74508118	Hela-S3	cervix:	n/a	chr15:74507788-74507799
49	CEBPB	chr15:74495012-74495601	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr15:74507426-74508037	A549	lung:	n/a	chr15:74507788-74507799

(count:2387 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:74532450-74532500	SK-N-MC	brain:	n/a
2	chr15:74494900-74494950	BE2_C	brain:	n/a
3	chr15:74495637-74495687	BE2_C	brain:	n/a
4	chr15:74494900-74494950	AG04449	skin:	fetal
5	chr15:74514346-74514396	SK-N-MC	brain:	n/a
6	chr15:74541993-74542043	AG10803	skin:	n/a
7	chr15:74514346-74514396	AG04449	skin:	fetal
8	chr15:74494861-74494911	HCPEpiC	choroid plexus:	n/a
9	chr15:74532450-74532500	SK-N-MC	brain:	n/a
10	chr15:74494900-74494950	BE2_C	brain:	n/a
11	chr15:74495637-74495687	BE2_C	brain:	n/a
12	chr15:74494900-74494950	AG04449	skin:	fetal
13	chr15:74514346-74514396	SK-N-MC	brain:	n/a
14	chr15:74541993-74542043	AG10803	skin:	n/a
15	chr15:74514346-74514396	AG04449	skin:	fetal
16	chr15:74494861-74494911	HCPEpiC	choroid plexus:	n/a
17	chr15:74494854-74494904	A549	lung:	n/a
18	chr15:74501771-74501821	BJ	skin:	n/a
19	chr15:74495384-74495434	H1-hESC	embryonic stem cell:	embryo
20	chr15:74494909-74494959	HAEpiC	amniotic membrane:	n/a
21	chr15:74537819-74537869	AG09319	gingival:	n/a
22	chr15:74496040-74496090	PrEC	prostate:	n/a
23	chr15:74539100-74539150	HPAEpiC	pulmonary alveolar:	n/a
24	chr15:74537514-74537564	BJ	skin:	n/a
25	chr15:74502200-74502250	GM12891	blood:	n/a
26	chr15:74494900-74494950	NB4	blood:	n/a
27	chr15:74495109-74495159	SKMC	muscle:	n/a
28	chr15:74528563-74528613	MCF10A-Er-Src	breast:	n/a
29	chr15:74537514-74537564	LNCaP	prostate:	n/a
30	chr15:74528719-74528769	IMR90	lung:	fetal
31	chr15:74528606-74528656	Hela-S3	cervix:	n/a
32	chr15:74496040-74496090	MCF-7	breast:	n/a
33	chr15:74528522-74528572	PrEC	prostate:	n/a
34	chr15:74501584-74501634	Caco-2	colon:	n/a
35	chr15:74506668-74506718	NHBE	bronchial:	n/a
36	chr15:74501584-74501634	PrEC	prostate:	n/a
37	chr15:74494854-74494904	HRE	kidney:	n/a
38	chr15:74506668-74506718	HCT-116	colon:	n/a
39	chr15:74528243-74528293	NT2-D1	testis:	n/a
40	chr15:74501317-74501367	AG09309	skin:	n/a
41	chr15:74534692-74534742	GM19239	blood:	n/a
42	chr15:74494909-74494959	AG09319	gingival:	n/a
43	chr15:74537963-74538013	HEK293	kidney:	embryo
44	chr15:74494909-74494959	GM19239	blood:	n/a
45	chr15:74495384-74495434	AG09319	gingival:	n/a
46	chr15:74538030-74538080	NT2-D1	testis:	n/a
47	chr15:74502200-74502250	HEEpiC	esophagus:	n/a
48	chr15:74532450-74532500	ovcar-3	ovarian:	n/a
49	chr15:74532450-74532500	LNCaP	prostate:	n/a
50	chr15:74537514-74537564	HEEpiC	esophagus:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:74532021..74532873-chr15:74587892..74588777,3	MCF-7	breast:
2	chr15:74485403..74487595-chr15:74523951..74526382,2	K562	blood:
3	chr15:74497610..74499444-chr15:74504967..74507735,2	K562	blood:
4	chr15:74494443..74497074-chr15:74501503..74504271,2	K562	blood:
5	chr15:74531000..74533096-chr15:74589038..74591277,2	MCF-7	breast:
6	chr15:74522465..74524879-chr15:74525973..74528718,2	K562	blood:
7	chr15:74522433..74524879-chr15:74525973..74529290,3	K562	blood:
8	chr15:74544782..74547040-chr15:74550761..74553089,2	MCF-7	breast:
9	chr15:74519618..74521200-chr15:74525359..74527344,2	K562	blood:
10	chr15:74489028..74490850-chr15:74509672..74512569,2	MCF-7	breast:
11	chr15:74490081..74492588-chr15:74507681..74510665,2	MCF-7	breast:
12	chr15:74489985..74491760-chr15:74513574..74516077,2	MCF-7	breast:
13	chr15:74495538..74499115-chr15:74503082..74506667,3	MCF-7	breast:
14	chr15:74492912..74495035-chr15:74502031..74504562,2	MCF-7	breast:
15	chr15:74516266..74518836-chr15:74583231..74585495,2	MCF-7	breast:
16	chr15:74503151..74507416-chr15:74511304..74513886,3	MCF-7	breast:
17	chr15:74495756..74498011-chr15:74498578..74500648,2	K562	blood:
18	chr15:74513953..74515786-chr15:74517220..74519970,2	K562	blood:
19	chr15:74496432..74499341-chr15:74503073..74505170,2	MCF-7	breast:
20	chr15:74495538..74499115-chr15:74503082..74506667,3	MCF-7	breast:
21	chr15:74209119..74211492-chr15:74491566..74493612,2	MCF-7	breast:
22	chr15:74492912..74495035-chr15:74502031..74504562,2	MCF-7	breast:
23	chr15:74481853..74488513-chr15:74489689..74497281,13	MCF-7	breast:
24	chr15:74525638..74529372-chr15:74534834..74537226,3	K562	blood:
25	chr1:247553460..247553986-chr15:74497052..74497552,2	MCF-7	breast:
26	chr15:74519618..74521200-chr15:74525359..74527344,2	K562	blood:
27	chr15:74516668..74519200-chr15:74524275..74526738,2	MCF-7	breast:
28	chr15:74491398..74493100-chr15:74498606..74500534,2	MCF-7	breast:
29	chr15:74543564..74546354-chr15:74548836..74550787,2	K562	blood:
30	chr15:74535160..74537354-chr15:74542878..74545726,2	K562	blood:
31	chr15:74542391..74545216-chr15:74545436..74547097,2	MCF-7	breast:
32	chr15:74525463..74526963-chr17:41465876..41467879,2	K562	blood:
33	chr15:74515195..74518052-chr15:74528039..74529707,2	K562	blood:
34	chr15:74489985..74491760-chr15:74513574..74516077,2	MCF-7	breast:
35	chr15:74535160..74537354-chr15:74542878..74545726,2	K562	blood:
36	chr15:74514536..74518272-chr15:74526056..74529692,3	MCF-7	breast:
37	chr15:74531319..74532959-chr15:74536975..74539724,2	MCF-7	breast:
38	chr15:74530832..74532774-chr15:74536942..74538994,3	MCF-7	breast:
39	chr15:74488727..74491632-chr15:74492213..74494817,3	MCF-7	breast:
40	chr15:74494443..74497074-chr15:74501503..74504271,2	K562	blood:
41	chr15:74489184..74491442-chr15:74495568..74497527,4	MCF-7	breast:
42	chr15:74502835..74504692-chr15:74505087..74506965,2	MCF-7	breast:
43	chr15:74530832..74532774-chr15:74536942..74538994,3	MCF-7	breast:
44	chr15:74497610..74499444-chr15:74504967..74507735,2	K562	blood:
45	chr15:74532146..74532873-chr15:74594558..74596149,4	MCF-7	breast:
46	chr15:74489028..74490850-chr15:74509672..74512569,2	MCF-7	breast:
47	chr15:74483852..74487473-chr15:74489633..74493518,4	K562	blood:
48	chr15:74531065..74532057-chr7:5566416..5567064,2	Hela-S3	cervix:
49	chr15:74419524..74420135-chr15:74531852..74532605,3	MCF-7	breast:
50	chr15:74419604..74420502-chr15:74495753..74496632,3	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC33-1	chr15:74510838-74511202	ENSG00000259264.1
2	lnc-CCDC33-1	chr15:74501729-74501875	ENSG00000259264.1
3	lnc-CCDC33-1	chr15:74504487-74504618	ENSG00000259264.1
4	lnc-CCDC33-1	chr15:74505609-74505829	ENSG00000259264.1
5	lnc-CCDC33-1	chr15:74504487-74504618	ENSG00000259264.1
6	lnc-CCDC33-1	chr15:74504487-74504618	ENSG00000259264.1
7	lnc-CCDC33-1	chr15:74495351-74495439	ENSG00000259264.1
8	lnc-CCDC33-1	chr15:74501729-74501875	ENSG00000259264.1
9	lnc-CCDC33-1	chr15:74501729-74501875	ENSG00000259264.1
10	lnc-STRA6-2	chr15:74526637-74526886	NONHSAT047220
11	lnc-CCDC33-1	chr15:74504823-74505314	ENSG00000259264.1
12	lnc-CCDC33-1	chr15:74513591-74513896	ENSG00000259264.1
13	lnc-CCDC33-1	chr15:74495391-74495439	ENSG00000259264.1
14	lnc-RP11-247C2.2.1-6	chr15:74494496-74494746	NONHSAT047214
15	lnc-STRA6-2	chr15:74528329-74528543	NONHSAT047220
16	lnc-CCDC33-1	chr15:74495046-74495439	ENSG00000259264.1

No data

Variant related genes	Relation type
ENSG00000259264	TF binding region
CCDC33	TF binding region
STRA6	TF binding region
ENSG00000259264	CpG island
CCDC33	CpG island
STRA6	CpG island
ENSG00000187990	chromatin interactions
ENSG00000248540	chromatin interactions
ENSG00000167178	chromatin interactions
ENSG00000259264	chromatin interactions
ENSG00000140481	chromatin interactions
ENSG00000261384	chromatin interactions
ENSG00000137868	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000168274	chromatin interactions

Extended variants
information (count: 2152 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2152 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs351219	chr15:74489207-74489208	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567197654	chr15:74489219-74489220	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs368410875	chr15:74489231-74489232	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs571571774	chr15:74489242-74489243	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs138374385	chr15:74489251-74489252	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs184387981	chr15:74489305-74489306	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs531263069	chr15:74489319-74489320	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs572558576	chr15:74489342-74489343	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs375572477	chr15:74489368-74489369	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs187275553	chr15:74489383-74489384	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs536565300	chr15:74489386-74489387	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs574026645	chr15:74489388-74489389	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs141348562	chr15:74489412-74489413	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs733163	chr15:74489413-74489414	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs192612522	chr15:74489417-74489418	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs575973106	chr15:74489469-74489470	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs544789824	chr15:74489470-74489471	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs185622850	chr15:74489491-74489492	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs145132123	chr15:74489510-74489511	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs549210198	chr15:74489526-74489527	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs189339136	chr15:74489559-74489560	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs531915753	chr15:74489560-74489561	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs550423009	chr15:74489573-74489574	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs571567311	chr15:74489631-74489632	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs148373434	chr15:74489642-74489643	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs180889966	chr15:74489706-74489707	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs200203042	chr15:74489728-74489729	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs184122828	chr15:74489798-74489799	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs188723297	chr15:74489865-74489866	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs141592072	chr15:74489874-74489875	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs351218	chr15:74489883-74489884	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs556386562	chr15:74489892-74489893	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs150712067	chr15:74489906-74489907	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs181152472	chr15:74489912-74489913	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs572179737	chr15:74489920-74489921	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs559713899	chr15:74489969-74489970	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs571848789	chr15:74489982-74489983	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs542269177	chr15:74490002-74490003	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs561169835	chr15:74490034-74490035	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs531899877	chr15:74490041-74490042	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs186185335	chr15:74490093-74490094	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs377041925	chr15:74490096-74490097	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs142105038	chr15:74490100-74490101	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs370760511	chr15:74490113-74490114	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs547854196	chr15:74490125-74490126	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs151176007	chr15:74490128-74490129	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs200937669	chr15:74490132-74490133	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs140547600	chr15:74490135-74490136	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs79081338	chr15:74490149-74490150	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs369285489	chr15:74490150-74490151	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Gastrointestinal stromal cancer	20877625	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
Bipolar disorder	19114987	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	18458336	CNVD

Chromatin state (count:1798 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74466200-74492800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr15:74469200-74491800	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr15:74469400-74493200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr15:74470800-74492800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr15:74478600-74491400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr15:74480600-74491800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr15:74484000-74490000	Enhancers	HSMM	muscle
8	chr15:74485000-74489800	Enhancers	NH-A	brain
9	chr15:74485400-74493000	Weak transcription	Fetal Thymus	thymus
10	chr15:74485800-74491000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr15:74485800-74492600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr15:74486000-74490200	Enhancers	Esophagus	oesophagus
13	chr15:74486400-74491400	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr15:74487400-74489600	Enhancers	Spleen	Spleen
15	chr15:74487400-74490200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr15:74487400-74491600	Genic enhancers	Placenta	Placenta
17	chr15:74487600-74489400	Enhancers	Lung	lung
18	chr15:74487600-74489600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr15:74487600-74489600	Enhancers	Fetal Muscle Leg	muscle
20	chr15:74487600-74489800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr15:74487600-74489800	Enhancers	Fetal Heart	heart
22	chr15:74487600-74492600	Weak transcription	GM12878-XiMat	blood
23	chr15:74487800-74489400	Enhancers	Fetal Lung	lung
24	chr15:74487800-74489800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr15:74487800-74492600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr15:74488000-74489400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr15:74488000-74491200	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr15:74488000-74492600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr15:74488000-74492800	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr15:74488200-74489400	Enhancers	Right Atrium	heart
31	chr15:74488200-74489400	Enhancers	Osteobl	bone
32	chr15:74488200-74489600	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr15:74488200-74489600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr15:74488200-74489600	Enhancers	Duodenum Mucosa	Duodenum
35	chr15:74488200-74490000	Enhancers	HSMMtube	muscle
36	chr15:74488200-74490400	Enhancers	Fetal Intestine Large	intestine
37	chr15:74488200-74490400	Genic enhancers	Fetal Intestine Small	intestine
38	chr15:74488200-74491600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
39	chr15:74488400-74489400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr15:74488400-74489400	Enhancers	Adipose Nuclei	Adipose
41	chr15:74488400-74489400	Enhancers	Brain Anterior Caudate	brain
42	chr15:74488400-74489400	Enhancers	Fetal Stomach	stomach
43	chr15:74488400-74489400	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr15:74488400-74489600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr15:74488400-74489600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr15:74488400-74489600	Enhancers	Colonic Mucosa	Colon
47	chr15:74488400-74489600	Enhancers	Rectal Mucosa Donor 29	rectum
48	chr15:74488400-74489600	Enhancers	HMEC	breast
49	chr15:74488400-74489600	Enhancers	NHDF-Ad	bronchial
50	chr15:74488400-74492600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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