Variant report

Variant	nsv519800
Chromosome Location	chr15:99950772-99987109
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:591)
CpG islands
(count:1405)
Chromatin interactive
region (count:52)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:591 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:99961418-99962008	HepG2	liver:	n/a	n/a
2	ATF2	chr15:99965347-99965754	GM12878	blood:	n/a	n/a
3	BATF	chr15:99965364-99965661	GM12878	blood:	n/a	chr15:99965442-99965451
4	BCL3	chr15:99951803-99952015	GM12878	blood:	n/a	n/a
5	BHLHE40	chr15:99973687-99973691	GM12878	blood:	n/a	n/a
6	BHLHE40	chr15:99965453-99965469	K562	blood:	n/a	n/a
7	BHLHE40	chr15:99961440-99962002	HepG2	liver:	n/a	n/a
8	BRCA1	chr15:99975665-99975680	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr15:99961467-99961647	HepG2	liver:	n/a	n/a
10	CEBPB	chr15:99961370-99961725	HepG2	liver:	n/a	n/a
11	CEBPB	chr15:99953257-99953373	IMR90	lung:	n/a	chr15:99953308-99953319
12	CEBPB	chr15:99965381-99965715	IMR90	lung:	n/a	n/a
13	CEBPB	chr15:99961492-99961572	IMR90	lung:	n/a	n/a
14	CEBPB	chr15:99953270-99953426	A549	lung:	n/a	chr15:99953308-99953319
15	CEBPB	chr15:99953294-99953334	HepG2	liver:	n/a	chr15:99953308-99953319
16	CEBPB	chr15:99965407-99965607	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr15:99982704-99983088	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr15:99982646-99983055	IMR90	lung:	n/a	n/a
19	CEBPB	chr15:99961361-99961734	HepG2	liver:	n/a	n/a
20	CEBPB	chr15:99953268-99953329	Hela-S3	cervix:	n/a	chr15:99953308-99953319
21	CEBPB	chr15:99961470-99961726	MCF-7	breast:	n/a	n/a
22	CEBPD	chr15:99961442-99961604	HepG2	liver:	n/a	n/a
23	CHD2	chr15:99975690-99975908	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr15:99973825-99973857	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr15:99973694-99973933	GM12878	blood:	n/a	n/a
26	CHD2	chr15:99965573-99965713	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr15:99961572-99961672	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr15:99982693-99983140	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr15:99961599-99961785	HepG2	liver:	n/a	n/a
30	CTCF	chr15:99975630-99975763	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr15:99975560-99975710	SAEC	small airway:	n/a	n/a
32	CTCF	chr15:99966243-99966391	A549	lung:	n/a	n/a
33	CTCF	chr15:99975580-99975730	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr15:99966280-99966430	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr15:99966241-99966385	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr15:99966220-99966370	GM12870	blood:	n/a	n/a
37	CTCF	chr15:99966240-99966390	GM12878	blood:	n/a	n/a
38	CTCF	chr15:99966260-99966410	HRE	kidney:	n/a	n/a
39	CTCF	chr15:99973260-99973410	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr15:99973240-99973390	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr15:99966280-99966430	HVMF	connective:	n/a	n/a
42	CTCF	chr15:99966240-99966390	HEK293	kidney:	n/a	n/a
43	CTCF	chr15:99966220-99966370	AG10803	skin:	n/a	n/a
44	CTCF	chr15:99966236-99966395	ProgFib	skin:	n/a	n/a
45	CTCF	chr15:99966240-99966390	HCM	heart:	n/a	n/a
46	CTCF	chr15:99966320-99966470	HAc	cerebellar:	n/a	n/a
47	CTCF	chr15:99978300-99978450	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr15:99966193-99966442	MCF-7	breast:	n/a	n/a
49	CTCF	chr15:99966230-99966383	HepG2	liver:	n/a	n/a
50	CTCF	chr15:99966240-99966390	HCPEpiC	choroid plexus:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:99979584-99979634	MCF10A-Er-Src	breast:	n/a
2	chr15:99979059-99979109	GM12891	blood:	n/a
3	chr15:99979584-99979634	MCF10A-Er-Src	breast:	n/a
4	chr15:99979059-99979109	GM12891	blood:	n/a
5	chr15:99966968-99967018	HL-60	blood:	n/a
6	chr15:99974369-99974419	SK-N-SH_RA	brain:	n/a
7	chr15:99979013-99979063	T-47D	breast:	n/a
8	chr15:99979389-99979439	HPAEpiC	pulmonary alveolar:	n/a
9	chr15:99975470-99975520	NT2-D1	testis:	n/a
10	chr15:99974369-99974419	HCM	heart:	n/a
11	chr15:99974369-99974419	NHDF-neo	bronchial:	n/a
12	chr15:99979290-99979340	HCF	heart:	n/a
13	chr15:99979527-99979577	BJ	skin:	n/a
14	chr15:99979527-99979577	HRCEpiC	kidney:	n/a
15	chr15:99979013-99979063	GM06990	blood:	n/a
16	chr15:99982524-99982574	ECC-1	luminal epithelium:	n/a
17	chr15:99979290-99979340	HCT-116	colon:	n/a
18	chr15:99979059-99979109	HCF	heart:	n/a
19	chr15:99975010-99975060	GM06990	blood:	n/a
20	chr15:99966833-99966883	HRE	kidney:	n/a
21	chr15:99979346-99979396	LNCaP	prostate:	n/a
22	chr15:99979013-99979063	HEEpiC	esophagus:	n/a
23	chr15:99979059-99979109	SK-N-SH_RA	brain:	n/a
24	chr15:99979584-99979634	AG09309	skin:	n/a
25	chr15:99971213-99971263	MCF-7	breast:	n/a
26	chr15:99971423-99971473	SK-N-SH	brain:	n/a
27	chr15:99975310-99975360	HCT-116	colon:	n/a
28	chr15:99966833-99966883	HIPEpiC	eye:	n/a
29	chr15:99979527-99979577	Caco-2	colon:	n/a
30	chr15:99982524-99982574	HNPCEpiC	eye:	n/a
31	chr15:99982524-99982574	NHBE	bronchial:	n/a
32	chr15:99971329-99971379	MCF-7	breast:	n/a
33	chr15:99974332-99974382	BE2_C	brain:	n/a
34	chr15:99979059-99979109	NB4	blood:	n/a
35	chr15:99967055-99967105	SKMC	muscle:	n/a
36	chr15:99971213-99971263	AG09309	skin:	n/a
37	chr15:99967055-99967105	SK-N-SH	brain:	n/a
38	chr15:99975470-99975520	NB4	blood:	n/a
39	chr15:99979389-99979439	NT2-D1	testis:	n/a
40	chr15:99974881-99974931	HEK293	kidney:	embryo
41	chr15:99971423-99971473	PFSK-1	brain:	n/a
42	chr15:99975470-99975520	SK-N-MC	brain:	n/a
43	chr15:99971423-99971473	IMR90	lung:	fetal
44	chr15:99974881-99974931	GM12891	blood:	n/a
45	chr15:99974881-99974931	Hepatocyte	liver:	n/a
46	chr15:99966833-99966883	K562	blood:	n/a
47	chr15:99971423-99971473	RPTEC	kidney:	n/a
48	chr15:99975334-99975384	HL-60	blood:	n/a
49	chr15:99975010-99975060	MCF-7	breast:	n/a
50	chr15:99975010-99975060	LNCaP	prostate:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:99947884..99951610-chr15:100057572..100060447,3	MCF-7	breast:
2	chr15:99976374..99976897-chr15:100105314..100105862,2	Hela-S3	cervix:
3	chr15:99985824..99988050-chr15:99992595..99995524,2	MCF-7	breast:
4	chr15:99962979..99964880-chr15:99972892..99975204,2	MCF-7	breast:
5	chr15:99963793..99965594-chr15:99976352..99978718,2	K562	blood:
6	chr15:99960211..99963086-chr15:99964919..99968237,3	MCF-7	breast:
7	chr15:99949443..99953317-chr15:100104194..100106896,3	MCF-7	breast:
8	chr15:99952846..99955288-chr15:100271943..100274389,2	MCF-7	breast:
9	chr15:99973224..99976448-chr15:99991050..99995157,5	MCF-7	breast:
10	chr15:99979583..99981872-chr15:99983556..99985309,2	MCF-7	breast:
11	chr15:99977572..99979807-chr15:99980072..99982815,2	K562	blood:
12	chr15:99975615..99977769-chr15:99978276..99979849,2	MCF-7	breast:
13	chr15:99949149..99950707-chr15:99953216..99956210,2	MCF-7	breast:
14	chr15:99948631..99950805-chr15:100153730..100155690,2	MCF-7	breast:
15	chr15:99964977..99967345-chr15:100103742..100106400,3	MCF-7	breast:
16	chr15:99943334..99944866-chr15:99950624..99952403,2	MCF-7	breast:
17	chr15:99972394..99975109-chr15:99977541..99980166,2	MCF-7	breast:
18	chr15:99975316..99977266-chr15:99981293..99982934,2	K562	blood:
19	chr15:99947710..99950479-chr15:99955909..99957738,2	MCF-7	breast:
20	chr15:99976307..99978594-chr15:100018036..100019822,2	MCF-7	breast:
21	chr15:99981264..99984715-chr15:99985641..99987973,4	MCF-7	breast:
22	chr15:99977572..99979807-chr15:99980072..99982815,2	K562	blood:
23	chr15:99972525..99976931-chr15:99986719..99991606,5	MCF-7	breast:
24	chr15:99960211..99963086-chr15:99964919..99968237,3	MCF-7	breast:
25	chr15:99979674..99981771-chr15:99994725..99997256,2	K562	blood:
26	chr15:99981180..99982961-chr15:99993073..99995315,2	MCF-7	breast:
27	chr15:99974033..99977897-chr15:99978912..99982934,5	K562	blood:
28	chr15:99951575..99954227-chr15:99954620..99956790,2	K562	blood:
29	chr15:99965843..99966811-chr15:100243795..100245106,3	MCF-7	breast:
30	chr15:99949082..99949796-chr15:99965826..99966399,2	MCF-7	breast:
31	chr15:99986076..99989977-chr15:99992374..99995201,3	K562	blood:
32	chr15:99966071..99969014-chr15:100104345..100107384,3	MCF-7	breast:
33	chr15:99965407..99967484-chr15:99969675..99971240,2	K562	blood:
34	chr15:99975316..99977266-chr15:99981293..99982934,2	K562	blood:
35	chr15:99979583..99981872-chr15:99983556..99985309,2	MCF-7	breast:
36	chr15:99975615..99977769-chr15:99978276..99979849,2	MCF-7	breast:
37	chr15:99974033..99977897-chr15:99978912..99982934,5	K562	blood:
38	chr15:99972394..99975109-chr15:99977541..99980166,2	MCF-7	breast:
39	chr15:99981264..99984715-chr15:99985641..99987973,4	MCF-7	breast:
40	chr15:99981781..99983657-chr15:100018041..100019744,2	MCF-7	breast:
41	chr15:99960171..99963200-chr15:100104719..100108193,3	MCF-7	breast:
42	chr15:99962979..99964880-chr15:99972892..99975204,2	MCF-7	breast:
43	chr15:99971316..99975999-chr15:100104042..100107403,7	MCF-7	breast:
44	chr15:99951575..99954227-chr15:99954620..99956790,2	K562	blood:
45	chr15:99966023..99966782-chr15:100243828..100244741,2	MCF-7	breast:
46	chr15:99966102..99966691-chr15:100044817..100045390,2	MCF-7	breast:
47	chr15:99972525..99976931-chr15:99986719..99991606,5	MCF-7	breast:
48	chr15:99962601..99965549-chr15:100104653..100107115,3	MCF-7	breast:
49	chr15:99984466..99986504-chr15:100104174..100107057,2	K562	blood:
50	chr15:99966031..99966539-chr15:100044729..100045649,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTC23-5	chr15:99971676-99972112	l_1247_chr15:99961345-99972053_liver
2	lnc-TTC23-3	chr15:99967214-99967407	ENSG00000259341.1
3	lnc-TTC23-5	chr15:99961346-99963761	l_1247_chr15:99961345-99972053_liver
4	lnc-TTC23-5	chr15:99971261-99971500	l_1247_chr15:99961345-99972053_liver
5	lnc-TTC23-5	chr15:99964546-99965708	l_1247_chr15:99961345-99972053_liver
6	lnc-TTC23-3	chr15:99971033-99971233	ENSG00000259341.1

No data

Variant related genes	Relation type
ENSG00000259341	TF binding region
ENSG00000259341	CpG island
ENSG00000259341	chromatin interactions
ENSG00000068305	chromatin interactions
ENSG00000183060	chromatin interactions

Extended variants
information (count: 1701 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1701 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4393551	chr15:99950772-99950773	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550425989	chr15:99950802-99950803	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs192814950	chr15:99950824-99950825	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs532870820	chr15:99950948-99950949	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs80074279	chr15:99950953-99950954	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs116921100	chr15:99951001-99951002	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs4408522	chr15:99951021-99951022	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs78745568	chr15:99951049-99951050	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs28622986	chr15:99951069-99951070	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs576629184	chr15:99951077-99951078	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs537129009	chr15:99951079-99951080	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs555977219	chr15:99951085-99951086	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs148174428	chr15:99951096-99951097	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs75377573	chr15:99951100-99951101	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs538946711	chr15:99951104-99951105	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs188508693	chr15:99951158-99951159	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs28619298	chr15:99951167-99951168	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs28645177	chr15:99951169-99951170	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs181020962	chr15:99951195-99951196	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs13380154	chr15:99951213-99951214	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs542298740	chr15:99951214-99951215	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs560916641	chr15:99951248-99951249	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs576239144	chr15:99951356-99951357	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs147515650	chr15:99951362-99951363	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs565499674	chr15:99951374-99951375	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs148181664	chr15:99951393-99951394	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs199947639	chr15:99951396-99951397	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs386787187	chr15:99951397-99951398	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs60800535	chr15:99951398-99951399	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs530415328	chr15:99951399-99951400	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs111904827	chr15:99951445-99951446	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs569702182	chr15:99951451-99951452	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs537165737	chr15:99951483-99951484	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs552226998	chr15:99951515-99951516	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs577410870	chr15:99951577-99951578	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs74035721	chr15:99951598-99951599	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs8033502	chr15:99951602-99951603	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs80305960	chr15:99951662-99951663	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs565882418	chr15:99951667-99951668	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs74035722	chr15:99951668-99951669	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs35551422	chr15:99951672-99951673	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs115438110	chr15:99951680-99951681	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs187070780	chr15:99951683-99951684	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs150809488	chr15:99951704-99951705	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs12910304	chr15:99951710-99951711	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs577001302	chr15:99951725-99951726	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs541307286	chr15:99951735-99951736	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs559873413	chr15:99951760-99951761	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs530363004	chr15:99951761-99951762	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs78144987	chr15:99951762-99951763	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Intellectual disability	22102821	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	21147756	CNVD
Hepatocellular carcinoma	16750200	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	20811773	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Emphysema	19352772	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17142309	CNVD
Schizophrenia	23813976	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:1107 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:99944800-99972400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr15:99945000-99954600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:99947400-99951200	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr15:99948000-99951000	Enhancers	Fetal Stomach	stomach
5	chr15:99948200-99951000	Enhancers	Fetal Muscle Trunk	muscle
6	chr15:99948200-99951000	Enhancers	Right Atrium	heart
7	chr15:99948200-99951000	Enhancers	HSMMtube	muscle
8	chr15:99948600-99950800	Weak transcription	Thymus	Thymus
9	chr15:99949000-99952400	Weak transcription	Hela-S3	cervix
10	chr15:99949400-99950800	Weak transcription	Primary T cells from cord blood	blood
11	chr15:99949400-99951400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr15:99949400-99954400	Weak transcription	HMEC	breast
13	chr15:99949600-99950800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr15:99949600-99950800	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr15:99949600-99950800	Weak transcription	Fetal Heart	heart
16	chr15:99949600-99950800	Weak transcription	Spleen	Spleen
17	chr15:99949600-99951200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr15:99949600-99954800	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr15:99949600-99956400	Weak transcription	HepG2	liver
20	chr15:99949800-99954600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr15:99950000-99952600	Weak transcription	Right Ventricle	heart
22	chr15:99950000-99954600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr15:99950000-99954600	Weak transcription	Esophagus	oesophagus
24	chr15:99950000-99964800	Weak transcription	Adipose Nuclei	Adipose
25	chr15:99950200-99950800	Weak transcription	Brain Substantia Nigra	brain
26	chr15:99950200-99954200	Weak transcription	Rectal Smooth Muscle	rectum
27	chr15:99950200-99954600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr15:99950200-99955000	Weak transcription	Left Ventricle	heart
29	chr15:99950200-99956600	Weak transcription	Lung	lung
30	chr15:99950200-99956800	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr15:99950600-99950800	Enhancers	Aorta	Aorta
32	chr15:99950600-99951600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr15:99950600-99951600	Enhancers	Fetal Thymus	thymus
34	chr15:99950800-99951000	Enhancers	Primary T cells from cord blood	blood
35	chr15:99950800-99951000	Enhancers	Brain Substantia Nigra	brain
36	chr15:99950800-99951000	Enhancers	Spleen	Spleen
37	chr15:99950800-99951200	Enhancers	Thymus	Thymus
38	chr15:99950800-99951600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr15:99950800-99951600	Enhancers	Fetal Heart	heart
40	chr15:99950800-99965800	Weak transcription	Aorta	Aorta
41	chr15:99951000-99951200	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr15:99951000-99956800	Weak transcription	Right Atrium	heart
43	chr15:99951000-99965200	Weak transcription	Spleen	Spleen
44	chr15:99951200-99951400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr15:99951200-99954200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr15:99951400-99952600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr15:99951600-99954800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr15:99951600-99955600	Weak transcription	Fetal Heart	heart
49	chr15:99952400-99952600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr15:99952400-99952800	Enhancers	Hela-S3	cervix

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