Variant report

Variant	nsv833011
Chromosome Location	chr15:54226235-54421567
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:817)
CpG islands
(count:549)
Chromatin interactive
region (count:38)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr15:54255417-54255420	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr15:54270443-54270603	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr15:54269100-54269383	GM12878	blood:	n/a	chr15:54269243-54269254
4	BATF	chr15:54406133-54406329	GM12878	blood:	n/a	n/a
5	BCL3	chr15:54375816-54376051	GM12878	blood:	n/a	n/a
6	BHLHE40	chr15:54375171-54375297	GM12878	blood:	n/a	n/a
7	BHLHE40	chr15:54270556-54270727	GM12878	blood:	n/a	n/a
8	BHLHE40	chr15:54267062-54267260	GM12878	blood:	n/a	n/a
9	BHLHE40	chr15:54269065-54269371	GM12878	blood:	n/a	n/a
10	BHLHE40	chr15:54269170-54269333	HepG2	liver:	n/a	n/a
11	BHLHE40	chr15:54358727-54358963	GM12878	blood:	n/a	n/a
12	BRCA1	chr15:54375208-54375398	GM12878	blood:	n/a	n/a
13	BRCA1	chr15:54376140-54376218	GM12878	blood:	n/a	n/a
14	CEBPB	chr15:54335334-54335567	HepG2	liver:	n/a	chr15:54335407-54335420 chr15:54335407-54335420
15	CEBPB	chr15:54405089-54405315	HepG2	liver:	n/a	n/a
16	CEBPB	chr15:54411288-54411565	HepG2	liver:	n/a	n/a
17	CEBPB	chr15:54250286-54250627	MCF-7	breast:	n/a	chr15:54250456-54250467
18	CEBPB	chr15:54264954-54265172	HepG2	liver:	n/a	chr15:54265094-54265107 chr15:54265094-54265105 chr15:54265096-54265107
19	CEBPB	chr15:54254502-54254970	MCF-7	breast:	n/a	chr15:54254727-54254740 chr15:54254727-54254738 chr15:54254729-54254740 chr15:54254727-54254740
20	CEBPB	chr15:54254637-54254932	MCF-7	breast:	n/a	chr15:54254727-54254740 chr15:54254727-54254738 chr15:54254729-54254740 chr15:54254727-54254740
21	CEBPB	chr15:54272984-54273248	HepG2	liver:	n/a	chr15:54273084-54273095
22	CEBPB	chr15:54250295-54250528	HepG2	liver:	n/a	chr15:54250456-54250467
23	CEBPB	chr15:54327914-54328190	A549	lung:	n/a	chr15:54328041-54328052
24	CEBPB	chr15:54327868-54328211	Hela-S3	cervix:	n/a	chr15:54328041-54328052
25	CEBPB	chr15:54254551-54254923	HepG2	liver:	n/a	chr15:54254727-54254740 chr15:54254727-54254738 chr15:54254729-54254740 chr15:54254727-54254740
26	CEBPB	chr15:54250333-54250627	Hela-S3	cervix:	n/a	chr15:54250456-54250467
27	CEBPB	chr15:54334058-54334298	IMR90	lung:	n/a	n/a
28	CEBPB	chr15:54317233-54317453	IMR90	lung:	n/a	n/a
29	CEBPB	chr15:54254557-54254885	A549	lung:	n/a	chr15:54254727-54254740 chr15:54254727-54254738 chr15:54254729-54254740 chr15:54254727-54254740
30	CEBPB	chr15:54254561-54254881	IMR90	lung:	n/a	chr15:54254727-54254740 chr15:54254727-54254738 chr15:54254729-54254740 chr15:54254727-54254740
31	CEBPB	chr15:54338360-54338559	A549	lung:	n/a	n/a
32	CEBPB	chr15:54327869-54328210	HepG2	liver:	n/a	chr15:54328041-54328052
33	CEBPB	chr15:54254620-54254904	K562	blood:	n/a	chr15:54254727-54254740 chr15:54254727-54254738 chr15:54254729-54254740 chr15:54254727-54254740
34	CHD1	chr15:54271429-54271624	GM12878	blood:	n/a	n/a
35	CHD1	chr15:54275962-54276044	GM12878	blood:	n/a	n/a
36	CHD1	chr15:54270369-54270604	GM12878	blood:	n/a	n/a
37	CHD1	chr15:54375292-54375397	GM12878	blood:	n/a	n/a
38	CHD2	chr15:54270395-54270817	GM12878	blood:	n/a	n/a
39	CHD2	chr15:54375231-54375384	GM12878	blood:	n/a	n/a
40	CHD2	chr15:54269281-54269328	HepG2	liver:	n/a	n/a
41	CHD2	chr15:54383047-54383312	GM12878	blood:	n/a	chr15:54383265-54383275
42	CHD2	chr15:54375592-54375770	GM12878	blood:	n/a	n/a
43	CHD2	chr15:54380837-54380897	GM12878	blood:	n/a	n/a
44	CHD2	chr15:54395054-54395191	GM12878	blood:	n/a	n/a
45	CTCF	chr15:54269220-54269370	HA-sp	spinal cord:	n/a	n/a
46	CTCF	chr15:54375180-54375330	NHLF	lung:	n/a	n/a
47	CTCF	chr15:54375125-54375361	GM13977	blood:	n/a	n/a
48	CTCF	chr15:54269140-54269290	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr15:54375126-54375389	K562	blood:	n/a	n/a
50	CTCF	chr15:54255240-54255390	HBMEC	blood vessel:	n/a	chr15:54255322-54255340 chr15:54255323-54255339

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:54304778-54304828	SK-N-SH	brain:	n/a
2	chr15:54304950-54305000	GM12892	blood:	n/a
3	chr15:54270947-54270997	GM12892	blood:	n/a
4	chr15:54270693-54270743	HRCEpiC	kidney:	n/a
5	chr15:54270661-54270711	CMK	blood:	n/a
6	chr15:54304778-54304828	HL-60	blood:	n/a
7	chr15:54271167-54271217	HEEpiC	esophagus:	n/a
8	chr15:54303927-54303977	HRE	kidney:	n/a
9	chr15:54304950-54305000	AG10803	skin:	n/a
10	chr15:54304778-54304828	SAEC	small airway:	n/a
11	chr15:54270661-54270711	BJ	skin:	n/a
12	chr15:54271167-54271217	HCT-116	colon:	n/a
13	chr15:54270557-54270607	MCF10A-Er-Src	breast:	n/a
14	chr15:54303927-54303977	T-47D	breast:	n/a
15	chr15:54270947-54270997	HUVEC	blood vessel:	n/a
16	chr15:54270947-54270997	GM12878	blood:	n/a
17	chr15:54270947-54270997	HRE	kidney:	n/a
18	chr15:54271167-54271217	T-47D	breast:	n/a
19	chr15:54304950-54305000	NH-A	brain:	n/a
20	chr15:54270661-54270711	HCPEpiC	choroid plexus:	n/a
21	chr15:54270661-54270711	HepG2	liver:	n/a
22	chr15:54304950-54305000	HRE	kidney:	n/a
23	chr15:54304950-54305000	AG04449	skin:	fetal
24	chr15:54271167-54271217	ProgFib	skin:	n/a
25	chr15:54270947-54270997	HCM	heart:	n/a
26	chr15:54270557-54270607	PrEC	prostate:	n/a
27	chr15:54270557-54270607	LNCaP	prostate:	n/a
28	chr15:54270693-54270743	SK-N-SH_RA	brain:	n/a
29	chr15:54271167-54271217	Caco-2	colon:	n/a
30	chr15:54270557-54270607	HIPEpiC	eye:	n/a
31	chr15:54305206-54305256	HEK293	kidney:	embryo
32	chr15:54270947-54270997	GM19239	blood:	n/a
33	chr15:54305206-54305256	AG10803	skin:	n/a
34	chr15:54270693-54270743	Hela-S3	cervix:	n/a
35	chr15:54270661-54270711	Caco-2	colon:	n/a
36	chr15:54304778-54304828	HRE	kidney:	n/a
37	chr15:54270947-54270997	HEEpiC	esophagus:	n/a
38	chr15:54271167-54271217	GM06990	blood:	n/a
39	chr15:54303927-54303977	HL-60	blood:	n/a
40	chr15:54304950-54305000	Hela-S3	cervix:	n/a
41	chr15:54270693-54270743	T-47D	breast:	n/a
42	chr15:54271167-54271217	HCPEpiC	choroid plexus:	n/a
43	chr15:54270693-54270743	SAEC	small airway:	n/a
44	chr15:54270661-54270711	HPAEpiC	pulmonary alveolar:	n/a
45	chr15:54270661-54270711	NH-A	brain:	n/a
46	chr15:54270661-54270711	HMEC	breast:	n/a
47	chr15:54305206-54305256	GM06990	blood:	n/a
48	chr15:54270557-54270607	NH-A	brain:	n/a
49	chr15:54270557-54270607	PFSK-1	brain:	n/a
50	chr15:54270693-54270743	HEK293	kidney:	embryo

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:54254831..54255689-chr15:55400781..55401468,2	MCF-7	breast:
2	chr15:54322544..54324113-chr15:54326394..54329349,2	K562	blood:
3	chr15:54323697..54325296-chr15:54326702..54328336,2	MCF-7	breast:
4	chr15:54316286..54318779-chr15:54320377..54322655,2	MCF-7	breast:
5	chr15:54266407..54270072-chr15:55486535..55491034,4	MCF-7	breast:
6	chr15:54254977..54255831-chr15:54374717..54376166,5	MCF-7	breast:
7	chr15:54254685..54255342-chr15:54375170..54375703,2	MCF-7	breast:
8	chr15:54242646..54244179-chr15:54244228..54246313,2	MCF-7	breast:
9	chr15:54307497..54309750-chr15:54313366..54316109,2	K562	blood:
10	chr15:54166967..54168008-chr15:54254966..54255810,4	MCF-7	breast:
11	chr15:54374784..54375687-chr15:55460665..55461171,2	MCF-7	breast:
12	chr15:54298660..54299394-chr15:54317743..54318508,2	MCF-7	breast:
13	chr15:54323697..54325296-chr15:54326702..54328336,2	MCF-7	breast:
14	chr15:54375029..54375976-chr15:55400805..55401778,3	MCF-7	breast:
15	chr15:54166889..54167944-chr15:54254910..54255478,3	MCF-7	breast:
16	chr15:54272577..54275424-chr15:54278207..54281083,2	MCF-7	breast:
17	chr15:54355045..54357590-chr15:54360185..54362187,2	K562	blood:
18	chr15:54254977..54255831-chr15:54374717..54376166,5	MCF-7	breast:
19	chr15:54367693..54370404-chr15:54374986..54376971,2	MCF-7	breast:
20	chr15:54272577..54275424-chr15:54278207..54281083,2	MCF-7	breast:
21	chr15:54316286..54318779-chr15:54320377..54322655,2	MCF-7	breast:
22	chr15:54367693..54370404-chr15:54374986..54376971,2	MCF-7	breast:
23	chr15:54254706..54255764-chr15:54268796..54269699,6	MCF-7	breast:
24	chr15:54242646..54244179-chr15:54244228..54246313,2	MCF-7	breast:
25	chr15:54254851..54255818-chr15:55460244..55461151,4	MCF-7	breast:
26	chr15:54355045..54357590-chr15:54360185..54362187,2	K562	blood:
27	chr15:54268767..54269686-chr15:54375127..54375711,4	MCF-7	breast:
28	chr15:54254908..54255701-chr15:55489106..55489772,3	MCF-7	breast:
29	chr15:54103533..54104375-chr15:54255060..54255801,2	MCF-7	breast:
30	chr15:54322544..54324113-chr15:54326394..54329349,2	K562	blood:
31	chr15:54103478..54104302-chr15:54255062..54255563,2	MCF-7	breast:
32	chr15:54077990..54080956-chr15:54224851..54227112,2	MCF-7	breast:
33	chr15:54307497..54309750-chr15:54313366..54316109,2	K562	blood:
34	chr15:54100067..54100735-chr15:54254841..54255517,2	MCF-7	breast:
35	chr15:54374868..54376175-chr15:55400827..55401744,4	MCF-7	breast:
36	chr15:54254945..54255611-chr15:55399622..55400326,2	MCF-7	breast:
37	chr15:54298660..54299394-chr15:54317743..54318508,2	MCF-7	breast:
38	chr15:54254685..54255342-chr15:54375170..54375703,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR72-1	chr15:54264872-54264981	NONHSAT140240
2	lnc-WDR72-1	chr15:54268965-54269105	ENSG00000259669.1
3	lnc-WDR72-1	chr15:54239821-54240033	ENSG00000259669.1
4	lnc-WDR72-1	chr15:54247966-54248028	ENSG00000259669.1
5	lnc-WDR72-1	chr15:54260199-54260347	ENSG00000259669.1
6	lnc-WDR72-1	chr15:54240686-54240805	ENSG00000259669.1
7	lnc-WDR72-1	chr15:54260199-54260347	ENSG00000259669.1
8	lnc-WDR72-1	chr15:54264867-54264981	ENSG00000259669.1
9	lnc-WDR72-1	chr15:54247966-54248028	ENSG00000259669.1
10	lnc-WDR72-1	chr15:54267015-54267147	ENSG00000259669.1
11	lnc-WDR72-1	chr15:54267015-54267206	NONHSAT140240
12	lnc-WDR72-1	chr15:54247966-54248028	ENSG00000259669.1
13	lnc-WDR72-1	chr15:54267015-54267136	ENSG00000259669.1
14	lnc-WDR72-1	chr15:54264867-54264981	ENSG00000259669.1
15	lnc-WDR72-1	chr15:54267015-54267165	ENSG00000259669.1
16	lnc-WDR72-1	chr15:54240403-54240805	ENSG00000259669.1
17	lnc-WDR72-1	chr15:54264867-54264981	ENSG00000259669.1
18	lnc-WDR72-1	chr15:54240343-54240805	ENSG00000259669.1

No data

Variant related genes	Relation type
ENSG00000259669	TF binding region
UNC13C	TF binding region
ENSG00000259619	TF binding region
ENSG00000259669	CpG island
UNC13C	CpG island
ENSG00000259619	CpG island
ENSG00000137876	chromatin interactions
ENSG00000259669	chromatin interactions

Extended variants
information (count: 5477 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5477 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148659762	chr15:54226268-54226269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs372556901	chr15:54226271-54226272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550928287	chr15:54226273-54226274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566314286	chr15:54226280-54226281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs118094717	chr15:54226288-54226289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs141218182	chr15:54226308-54226309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2019407	chr15:54226311-54226312	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs189139834	chr15:54226330-54226331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs118004626	chr15:54226334-54226335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551744052	chr15:54226339-54226340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371859556	chr15:54226390-54226391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs1824756	chr15:54226400-54226401	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs2019406	chr15:54226413-54226414	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs537237451	chr15:54226421-54226422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs117718399	chr15:54226501-54226502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567486533	chr15:54226534-54226535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576650479	chr15:54226540-54226541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536408908	chr15:54226588-54226589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552997057	chr15:54226594-54226595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs117363190	chr15:54226595-54226596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559431107	chr15:54226629-54226630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182159055	chr15:54226657-54226658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1961238	chr15:54226663-54226664	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs1961236	chr15:54226673-54226674	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs1961237	chr15:54226685-54226686	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs146218597	chr15:54226698-54226699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs116988555	chr15:54226729-54226730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187646224	chr15:54226744-54226745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs74610191	chr15:54226810-54226811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565828416	chr15:54226823-54226824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs60539011	chr15:54226831-54226832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558572201	chr15:54226837-54226838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547914435	chr15:54226841-54226842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs139159017	chr15:54226869-54226870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs117405025	chr15:54226894-54226895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536918995	chr15:54226914-54226915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs557225552	chr15:54226939-54226940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs28657914	chr15:54226992-54226993	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs2725559	chr15:54228247-54228248	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs575262804	chr15:54228361-54228362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543921728	chr15:54228405-54228406	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs563689076	chr15:54228421-54228422	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs190313618	chr15:54228429-54228430	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs373331279	chr15:54228450-54228451	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs546480211	chr15:54228454-54228455	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs147048378	chr15:54228465-54228466	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs182172707	chr15:54228521-54228522	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs2725560	chr15:54228551-54228552	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs34342990	chr15:54228582-54228583	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs568974726	chr15:54228589-54228590	Flanking Active TSS	n/a	n/a	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
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	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
Myelofibrosis	22110671	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:370 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:54225800-54226400	Enhancers	Gastric	stomach
2	chr15:54225800-54226600	Enhancers	Rectal Smooth Muscle	rectum
3	chr15:54226000-54227000	Enhancers	Colon Smooth Muscle	Colon
4	chr15:54226000-54227000	Enhancers	Fetal Stomach	stomach
5	chr15:54226200-54226600	Enhancers	Stomach Mucosa	stomach
6	chr15:54228200-54228400	Enhancers	HepG2	liver
7	chr15:54228400-54228600	Flanking Active TSS	HepG2	liver
8	chr15:54228600-54229000	Enhancers	HepG2	liver
9	chr15:54229400-54232400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr15:54244200-54244600	Enhancers	Fetal Stomach	stomach
11	chr15:54244400-54245200	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr15:54245200-54245800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr15:54245600-54246200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr15:54245800-54246000	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr15:54246200-54246600	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr15:54246600-54250200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr15:54247200-54256000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr15:54247600-54248000	Enhancers	Brain Germinal Matrix	brain
19	chr15:54250000-54250600	Enhancers	HepG2	liver
20	chr15:54250200-54250600	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr15:54250400-54250800	Enhancers	H9 Cell Line	embryonic stem cell
22	chr15:54255000-54257400	Enhancers	Fetal Brain Male	brain
23	chr15:54259600-54260200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr15:54259800-54261200	Enhancers	Fetal Lung	lung
25	chr15:54267000-54267200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr15:54267400-54269600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr15:54269200-54269400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
28	chr15:54269200-54269400	Enhancers	Esophagus	oesophagus
29	chr15:54269200-54269400	Enhancers	Fetal Intestine Small	intestine
30	chr15:54269200-54270000	Enhancers	Fetal Brain Female	brain
31	chr15:54269200-54270000	Enhancers	Fetal Lung	lung
32	chr15:54269200-54277200	Active TSS	Aorta	Aorta
33	chr15:54269400-54270400	Weak transcription	Esophagus	oesophagus
34	chr15:54269600-54269800	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr15:54269800-54270000	Bivalent Enhancer	Brain Hippocampus Middle	brain
36	chr15:54269800-54274800	Active TSS	Skeletal Muscle Male	skeletal muscle
37	chr15:54270000-54270200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
38	chr15:54270000-54270200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr15:54270000-54270200	Bivalent Enhancer	Brain Cingulate Gyrus	brain
40	chr15:54270000-54270200	Enhancers	Brain Germinal Matrix	brain
41	chr15:54270000-54270200	Active TSS	Duodenum Smooth Muscle	Duodenum
42	chr15:54270000-54270200	Active TSS	Fetal Brain Male	brain
43	chr15:54270000-54270400	Flanking Active TSS	Fetal Brain Female	brain
44	chr15:54270000-54270600	Flanking Active TSS	Fetal Lung	lung
45	chr15:54270000-54270800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
46	chr15:54270000-54271600	Active TSS	Stomach Smooth Muscle	stomach
47	chr15:54270200-54270400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
48	chr15:54270200-54270400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr15:54270200-54270400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr15:54270200-54270400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell

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