Variant report

Variant	esv1806890
Chromosome Location	chr15:78744695-78786064
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:616)
CpG islands
(count:122)
Chromatin interactive
region (count:54)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:616 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:78748043-78748291	K562	blood:	n/a	n/a
2	ARID3A	chr15:78774675-78775022	HepG2	liver:	n/a	n/a
3	ATF1	chr15:78748123-78748384	K562	blood:	n/a	n/a
4	BACH1	chr15:78774767-78774789	K562	blood:	n/a	n/a
5	BACH1	chr15:78774755-78775008	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr15:78764544-78764731	GM12878	blood:	n/a	chr15:78764662-78764671
7	BATF	chr15:78764462-78764796	GM12878	blood:	n/a	chr15:78764662-78764671
8	BHLHE40	chr15:78774808-78774966	K562	blood:	n/a	n/a
9	BRCA1	chr15:78766661-78766740	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr15:78770651-78770814	HepG2	liver:	n/a	n/a
11	CEBPB	chr15:78774785-78774895	K562	blood:	n/a	n/a
12	CEBPB	chr15:78785447-78785587	HepG2	liver:	n/a	chr15:78785535-78785546
13	CEBPB	chr15:78770436-78770572	HepG2	liver:	n/a	n/a
14	CEBPB	chr15:78770539-78770793	A549	lung:	n/a	n/a
15	CEBPB	chr15:78770682-78770747	Hela-S3	cervix:	n/a	n/a
16	CHD1	chr15:78784774-78784780	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr15:78748083-78748407	H1-hESC	embryonic stem cell:	n/a	n/a
18	CREB1	chr15:78748185-78748357	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr15:78774820-78774970	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr15:78774740-78774890	HAc	cerebellar:	n/a	n/a
21	CTCF	chr15:78774790-78775004	GM10266	blood:	n/a	n/a
22	CTCF	chr15:78774759-78775015	K562	blood:	n/a	n/a
23	CTCF	chr15:78774780-78774930	HepG2	liver:	n/a	n/a
24	CTCF	chr15:78774805-78774970	GM20000	blood:	n/a	n/a
25	CTCF	chr15:78774690-78775013	T-47D	breast:	n/a	n/a
26	CTCF	chr15:78775332-78775373	GM13976	blood:	n/a	n/a
27	CTCF	chr15:78774840-78774990	AG10803	skin:	n/a	n/a
28	CTCF	chr15:78774454-78775285	A549	lung:	n/a	n/a
29	CTCF	chr15:78774800-78774950	GM12865	blood:	n/a	n/a
30	CTCF	chr15:78774800-78774950	GM12867	blood:	n/a	n/a
31	CTCF	chr15:78774759-78775013	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr15:78774820-78774970	NHEK	skin:	n/a	n/a
33	CTCF	chr15:78774776-78774972	GM12892	blood:	n/a	n/a
34	CTCF	chr15:78774780-78774930	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr15:78774800-78774950	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr15:78774820-78774970	HFF	foreskin:	n/a	n/a
37	CTCF	chr15:78774800-78774950	SAEC	small airway:	n/a	n/a
38	CTCF	chr15:78774800-78774950	HRE	kidney:	n/a	n/a
39	CTCF	chr15:78774780-78774930	HRE	kidney:	n/a	n/a
40	CTCF	chr15:78774780-78774930	GM12864	blood:	n/a	n/a
41	CTCF	chr15:78774820-78774970	GM12864	blood:	n/a	n/a
42	CTCF	chr15:78774742-78775002	Pancreas_OC	pancreas:	n/a	n/a
43	CTCF	chr15:78774820-78774970	MCF-7	breast:	n/a	n/a
44	CTCF	chr15:78774785-78774946	MCF-7	breast:	n/a	n/a
45	CTCF	chr15:78774820-78774970	AG04449	skin:	n/a	n/a
46	CTCF	chr15:78774671-78775060	IMR90	lung:	n/a	n/a
47	CTCF	chr15:78774668-78774942	A549	lung:	n/a	n/a
48	CTCF	chr15:78774820-78774970	HMEC	breast:	n/a	n/a
49	CTCF	chr15:78774800-78774950	GM12871	blood:	n/a	n/a
50	CTCF	chr15:78774677-78775064	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78748272-78748322	HRPEpiC	eye:	n/a
2	chr15:78745427-78745477	Hepatocyte	liver:	n/a
3	chr15:78745427-78745477	HIPEpiC	eye:	n/a
4	chr15:78748272-78748322	HepG2	liver:	n/a
5	chr15:78745427-78745477	HepG2	liver:	n/a
6	chr15:78745427-78745477	RPTEC	kidney:	n/a
7	chr15:78748272-78748322	A549	lung:	n/a
8	chr15:78745427-78745477	SKMC	muscle:	n/a
9	chr15:78745427-78745477	ovcar-3	ovarian:	n/a
10	chr15:78745427-78745477	H1-hESC	embryonic stem cell:	embryo
11	chr15:78748272-78748322	HRCEpiC	kidney:	n/a
12	chr15:78748272-78748322	T-47D	breast:	n/a
13	chr15:78745427-78745477	Hela-S3	cervix:	n/a
14	chr15:78748272-78748322	ECC-1	luminal epithelium:	n/a
15	chr15:78748272-78748322	PrEC	prostate:	n/a
16	chr15:78748272-78748322	HNPCEpiC	eye:	n/a
17	chr15:78748272-78748322	HAEpiC	amniotic membrane:	n/a
18	chr15:78748272-78748322	MCF10A-Er-Src	breast:	n/a
19	chr15:78748272-78748322	IMR90	lung:	fetal
20	chr15:78748272-78748322	HRE	kidney:	n/a
21	chr15:78745427-78745477	HEEpiC	esophagus:	n/a
22	chr15:78748272-78748322	AG09319	gingival:	n/a
23	chr15:78745427-78745477	AoSMC	blood vessel:	n/a
24	chr15:78748272-78748322	HCM	heart:	n/a
25	chr15:78745427-78745477	SK-N-MC	brain:	n/a
26	chr15:78745427-78745477	HEK293	kidney:	embryo
27	chr15:78748272-78748322	Caco-2	colon:	n/a
28	chr15:78748272-78748322	LNCaP	prostate:	n/a
29	chr15:78748272-78748322	Hepatocyte	liver:	n/a
30	chr15:78745427-78745477	HCT-116	colon:	n/a
31	chr15:78745427-78745477	U87	brain:	n/a
32	chr15:78745427-78745477	NHBE	bronchial:	n/a
33	chr15:78745427-78745477	HL-60	blood:	n/a
34	chr15:78745427-78745477	AG04450	lung:	fetal
35	chr15:78748272-78748322	GM12878	blood:	n/a
36	chr15:78748272-78748322	SK-N-SH_RA	brain:	n/a
37	chr15:78748272-78748322	H1-hESC	embryonic stem cell:	embryo
38	chr15:78748272-78748322	GM12892	blood:	n/a
39	chr15:78748272-78748322	CMK	blood:	n/a
40	chr15:78745427-78745477	SAEC	small airway:	n/a
41	chr15:78748272-78748322	PANC-1	pancreas:	n/a
42	chr15:78748272-78748322	RPTEC	kidney:	n/a
43	chr15:78745427-78745477	HPAEpiC	pulmonary alveolar:	n/a
44	chr15:78745427-78745477	HRCEpiC	kidney:	n/a
45	chr15:78748272-78748322	AG10803	skin:	n/a
46	chr15:78748272-78748322	HEEpiC	esophagus:	n/a
47	chr15:78748272-78748322	HL-60	blood:	n/a
48	chr15:78745427-78745477	AG09319	gingival:	n/a
49	chr15:78745427-78745477	GM19239	blood:	n/a
50	chr15:78745427-78745477	IMR90	lung:	fetal

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:78753474..78756837-chr15:78765952..78769081,5	K562	blood:
2	chr15:78775448..78779203-chr15:78783785..78786320,3	MCF-7	breast:
3	chr15:78783856..78786006-chr15:78856773..78858650,2	MCF-7	breast:
4	chr15:78775973..78778928-chr15:78790506..78793354,2	K562	blood:
5	chr15:78591467..78594108-chr15:78749535..78752267,2	K562	blood:
6	chr15:78732336..78734017-chr15:78769375..78771802,2	K562	blood:
7	chr15:78753474..78756837-chr15:78765952..78769081,5	K562	blood:
8	chr15:78743131..78745408-chr15:78751883..78754148,2	K562	blood:
9	chr15:78732279..78734656-chr15:78753816..78756332,3	MCF-7	breast:
10	chr15:78730050..78732098-chr15:78751945..78754976,3	MCF-7	breast:
11	chr15:78735160..78737788-chr15:78742563..78745375,2	MCF-7	breast:
12	chr15:78780872..78783666-chr15:78797179..78800862,3	K562	blood:
13	chr15:78743131..78746223-chr15:78751883..78753767,3	K562	blood:
14	chr15:78761259..78764170-chr15:78766967..78768485,2	MCF-7	breast:
15	chr15:78766300..78768930-chr15:78769580..78772946,4	K562	blood:
16	chr15:78740565..78742425-chr15:78743943..78746196,2	MCF-7	breast:
17	chr15:78728558..78732848-chr15:78754139..78757790,4	K562	blood:
18	chr15:78754951..78757475-chr15:78760395..78762445,2	K562	blood:
19	chr15:78730612..78732522-chr15:78757828..78760111,2	MCF-7	breast:
20	chr15:78728522..78731480-chr15:78746642..78749638,2	K562	blood:
21	chr15:78742068..78744487-chr15:78745696..78748456,2	K562	blood:
22	chr15:78761259..78764170-chr15:78766967..78768485,2	MCF-7	breast:
23	chr15:78774778..78776989-chr15:78777902..78779588,2	MCF-7	breast:
24	chr15:78742068..78744005-chr15:78744591..78747196,2	K562	blood:
25	chr15:78785104..78787346-chr15:78855967..78858154,2	MCF-7	breast:
26	chr15:78743131..78746223-chr15:78751883..78753767,3	K562	blood:
27	chr15:78743131..78745408-chr15:78751883..78754148,2	K562	blood:
28	chr15:78729183..78733288-chr15:78740820..78746070,7	K562	blood:
29	chr15:78730557..78733272-chr15:78761388..78763524,2	MCF-7	breast:
30	chr15:78742361..78745153-chr15:78747081..78749461,2	MCF-7	breast:
31	chr15:78742361..78745153-chr15:78747081..78749461,2	MCF-7	breast:
32	chr15:78730825..78732581-chr15:78754139..78756670,3	K562	blood:
33	chr15:78770581..78772645-chr15:78799903..78802215,2	MCF-7	breast:
34	chr15:78748240..78750749-chr15:78750932..78754713,4	K562	blood:
35	chr15:78773415..78776394-chr15:78857535..78859504,2	MCF-7	breast:
36	chr15:78754951..78757475-chr15:78760395..78762445,2	K562	blood:
37	chr15:78780416..78782021-chr15:78786342..78788190,2	K562	blood:
38	chr15:78766300..78768486-chr15:78771126..78772946,2	K562	blood:
39	chr15:78762628..78765009-chr15:78768296..78770207,2	K562	blood:
40	chr15:78766300..78768486-chr15:78771126..78772946,2	K562	blood:
41	chr15:78753745..78758512-chr15:78765952..78770345,6	K562	blood:
42	chr15:78735474..78739238-chr15:78747549..78750774,3	MCF-7	breast:
43	chr15:78727207..78732074-chr15:78744204..78747986,5	MCF-7	breast:
44	chr15:78766300..78768930-chr15:78769580..78772946,4	K562	blood:
45	chr15:78762628..78765009-chr15:78768296..78770207,2	K562	blood:
46	chr15:78728533..78731605-chr15:78775460..78778377,3	K562	blood:
47	chr15:78785786..78788600-chr15:78798276..78800163,3	K562	blood:
48	chr15:78763504..78765233-chr15:78857709..78859471,2	MCF-7	breast:
49	chr15:78769199..78770172-chr6:27115409..27115983,2	NB4	blood:
50	chr15:78600505..78601404-chr15:78774428..78774961,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHRNA3-2	chr15:78772399-78772602	ENSG00000259474.1
2	lnc-CHRNA3-2	chr15:78774042-78774162	ENSG00000259474.1
3	lnc-AGPHD1-3	chr15:78755264-78755286	NONHSAT047565

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	IREB2	hsa-miR-9-5p	chr15:78766020-78766041

Variant related genes	Relation type
IREB2	TF binding region
ENSG00000259474	TF binding region
IREB2	CpG island
ENSG00000259474	CpG island
ENSG00000188266	chromatin interactions
ENSG00000041357	chromatin interactions
ENSG00000169684	chromatin interactions
ENSG00000140395	chromatin interactions
ENSG00000136381	chromatin interactions

Extended variants
information (count: 1689 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1689 , 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	rs537359867	chr15:78744707-78744708	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs559161407	chr15:78744719-78744720	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs577367035	chr15:78744722-78744723	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs149872059	chr15:78744723-78744724	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs373882892	chr15:78744789-78744790	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs77291732	chr15:78744857-78744858	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs574621752	chr15:78744861-78744862	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs144971079	chr15:78744865-78744866	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs186970343	chr15:78744882-78744883	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs530897683	chr15:78744901-78744902	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs552191563	chr15:78744931-78744932	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs564452590	chr15:78744932-78744933	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs139859316	chr15:78744936-78744937	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs191642202	chr15:78744958-78744959	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs74248578	chr15:78744965-78744966	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs34741376	chr15:78744971-78744972	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs368740504	chr15:78745019-78745020	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs375717783	chr15:78745020-78745021	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs71447202	chr15:78745057-78745058	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs535566033	chr15:78745074-78745075	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs550660774	chr15:78745150-78745151	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs568769571	chr15:78745221-78745222	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs111425925	chr15:78745243-78745244	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs539369576	chr15:78745275-78745276	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs557462286	chr15:78745289-78745290	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs143224577	chr15:78745334-78745335	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs2656071	chr15:78745343-78745344	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs553174334	chr15:78745353-78745354	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs183053186	chr15:78745385-78745386	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs374633069	chr15:78745415-78745416	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs76711744	chr15:78745416-78745417	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs146733852	chr15:78745428-78745429	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs188136289	chr15:78745458-78745459	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs190874879	chr15:78745696-78745697	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs2656069	chr15:78745707-78745708	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs546220158	chr15:78745804-78745805	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs542327766	chr15:78745884-78745885	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs140323929	chr15:78745916-78745917	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs75888429	chr15:78745924-78745925	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs145599495	chr15:78745934-78745935	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs75577625	chr15:78745969-78745970	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs550695555	chr15:78745970-78745971	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs568978367	chr15:78746034-78746035	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs78065488	chr15:78746052-78746053	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs151004592	chr15:78746064-78746065	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs566318563	chr15:78746085-78746086	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs535002892	chr15:78746105-78746106	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs76175644	chr15:78746118-78746119	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs563572330	chr15:78746140-78746141	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs182297202	chr15:78746151-78746152	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:1408 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78731400-78745400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr15:78731600-78756400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr15:78731600-78760200	Weak transcription	Aorta	Aorta
4	chr15:78732200-78747600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr15:78732200-78799400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr15:78732800-78758600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr15:78734000-78747200	Weak transcription	Fetal Brain Male	brain
8	chr15:78738600-78747400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr15:78738800-78747400	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr15:78739200-78745200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr15:78739200-78745600	Weak transcription	Primary hematopoietic stem cells	blood
12	chr15:78739200-78745600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr15:78739200-78747600	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr15:78739200-78748400	Weak transcription	HSMM	muscle
15	chr15:78739200-78748800	Weak transcription	HUVEC	blood vessel
16	chr15:78739200-78749600	Weak transcription	HSMMtube	muscle
17	chr15:78739200-78755200	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr15:78739400-78745600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr15:78739400-78747600	Weak transcription	NHDF-Ad	bronchial
20	chr15:78739400-78747800	Weak transcription	Osteobl	bone
21	chr15:78739600-78746800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr15:78739600-78755200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr15:78740000-78746600	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr15:78740400-78753200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr15:78740600-78748800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr15:78740600-78756000	Weak transcription	Brain Germinal Matrix	brain
27	chr15:78740800-78748200	Weak transcription	Fetal Muscle Trunk	muscle
28	chr15:78741000-78747600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr15:78741200-78747000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr15:78741200-78747000	Weak transcription	Fetal Muscle Leg	muscle
31	chr15:78741200-78755400	Weak transcription	Fetal Stomach	stomach
32	chr15:78741200-78781800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr15:78741800-78745200	Weak transcription	K562	blood
34	chr15:78741800-78745400	Weak transcription	Small Intestine	intestine
35	chr15:78741800-78745600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr15:78741800-78746600	Weak transcription	Brain Hippocampus Middle	brain
37	chr15:78741800-78747400	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr15:78742000-78745600	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr15:78742000-78745600	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr15:78742000-78747200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr15:78742000-78747200	Weak transcription	Brain Cingulate Gyrus	brain
42	chr15:78742000-78747600	Weak transcription	Fetal Lung	lung
43	chr15:78742000-78749000	Weak transcription	NH-A	brain
44	chr15:78742000-78753000	Weak transcription	Dnd41	blood
45	chr15:78742000-78753400	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr15:78742200-78745200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr15:78742200-78745400	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr15:78742200-78747000	Weak transcription	Fetal Thymus	thymus
49	chr15:78742200-78748200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr15:78742400-78745200	Weak transcription	Primary T cells from cord blood	blood

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