Variant report

Variant	nsv3798
Chromosome Location	chr3:46778630-46865606
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:341)
CpG islands
(count:1776)
Chromatin interactive
region (count:35)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:341 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr3:46792308-46792631	K562	blood:	n/a	n/a
2	ATF3	chr3:46792267-46792609	K562	blood:	n/a	n/a
3	BACH1	chr3:46853993-46854163	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr3:46834950-46835224	GM12878	blood:	n/a	n/a
5	BATF	chr3:46834909-46835249	GM12878	blood:	n/a	n/a
6	BCL11A	chr3:46834834-46835220	GM12878	blood:	n/a	n/a
7	BHLHE40	chr3:46798309-46798511	K562	blood:	n/a	n/a
8	BHLHE40	chr3:46792161-46792741	K562	blood:	n/a	chr3:46792470-46792479 chr3:46792470-46792479
9	CBX3	chr3:46864817-46865093	K562	blood:	n/a	n/a
10	CBX3	chr3:46805384-46805615	K562	blood:	n/a	n/a
11	CBX3	chr3:46853564-46854307	K562	blood:	n/a	n/a
12	CBX3	chr3:46792069-46792673	K562	blood:	n/a	n/a
13	CBX3	chr3:46862333-46862734	K562	blood:	n/a	n/a
14	CBX3	chr3:46798157-46798548	K562	blood:	n/a	n/a
15	CBX3	chr3:46862397-46862721	K562	blood:	n/a	n/a
16	CCNT2	chr3:46853838-46854110	K562	blood:	n/a	chr3:46854080-46854089
17	CCNT2	chr3:46792259-46792508	K562	blood:	n/a	n/a
18	CEBPB	chr3:46780721-46781004	HepG2	liver:	n/a	n/a
19	CEBPB	chr3:46780720-46780724	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr3:46839064-46839245	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr3:46853890-46853892	GM12878	blood:	n/a	n/a
22	CHD2	chr3:46798208-46798651	K562	blood:	n/a	n/a
23	CHD2	chr3:46853361-46853740	H1-hESC	embryonic stem cell:	n/a	chr3:46853514-46853524
24	CHD2	chr3:46798433-46798503	HepG2	liver:	n/a	n/a
25	CTCF	chr3:46798034-46798529	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
26	CTCF	chr3:46846160-46846310	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr3:46792287-46792555	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792394-46792407
28	CTCF	chr3:46798359-46798450	LNCaP	prostate:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
29	CTCF	chr3:46792209-46792538	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792234-46792247 chr3:46792394-46792407
30	CTCF	chr3:46854876-46854950	GM20000	blood:	n/a	n/a
31	CTCF	chr3:46794500-46794650	GM12873	blood:	n/a	n/a
32	CTCF	chr3:46792356-46792487	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792394-46792407
33	CTCF	chr3:46850100-46850250	GM12864	blood:	n/a	chr3:46850217-46850226
34	CTCF	chr3:46792360-46792510	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792394-46792407
35	CTCF	chr3:46798136-46798509	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
36	CTCF	chr3:46798280-46798435	HepG2	liver:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
37	CTCF	chr3:46801730-46801825	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr3:46794520-46794670	GM12864	blood:	n/a	n/a
39	CTCF	chr3:46794460-46794610	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr3:46850200-46850350	GM12864	blood:	n/a	chr3:46850217-46850226
41	CTCF	chr3:46850080-46850230	GM12873	blood:	n/a	chr3:46850217-46850226
42	CTCF	chr3:46798156-46798539	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
43	CTCF	chr3:46792152-46792625	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792234-46792247 chr3:46792394-46792407
44	CTCF	chr3:46853580-46853730	SAEC	small airway:	n/a	n/a
45	CTCF	chr3:46865442-46865496	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr3:46794560-46794710	HCT-116	colon:	n/a	n/a
47	CTCF	chr3:46854325-46854386	GM20000	blood:	n/a	n/a
48	CTCF	chr3:46798400-46798550	HVMF	connective:	n/a	n/a
49	CTCF	chr3:46798280-46798430	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
50	CTCF	chr3:46798300-46798450	HepG2	liver:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396

(count:1776 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46785957-46786007	HIPEpiC	eye:	n/a
2	chr3:46854311-46854361	HMEC	breast:	n/a
3	chr3:46853986-46854036	BE2_C	brain:	n/a
4	chr3:46786238-46786288	SK-N-SH_RA	brain:	n/a
5	chr3:46850588-46850638	NHBE	bronchial:	n/a
6	chr3:46799010-46799060	LNCaP	prostate:	n/a
7	chr3:46856803-46856853	HEEpiC	esophagus:	n/a
8	chr3:46785957-46786007	HIPEpiC	eye:	n/a
9	chr3:46854311-46854361	HMEC	breast:	n/a
10	chr3:46853986-46854036	BE2_C	brain:	n/a
11	chr3:46786238-46786288	SK-N-SH_RA	brain:	n/a
12	chr3:46850588-46850638	NHBE	bronchial:	n/a
13	chr3:46799010-46799060	LNCaP	prostate:	n/a
14	chr3:46856803-46856853	HEEpiC	esophagus:	n/a
15	chr3:46792364-46792414	HNPCEpiC	eye:	n/a
16	chr3:46853986-46854036	MCF10A-Er-Src	breast:	n/a
17	chr3:46796026-46796076	H1-hESC	embryonic stem cell:	embryo
18	chr3:46796026-46796076	MCF10A-Er-Src	breast:	n/a
19	chr3:46792462-46792512	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:46799010-46799060	HUVEC	blood vessel:	n/a
21	chr3:46796026-46796076	NHDF-neo	bronchial:	n/a
22	chr3:46792357-46792407	U87	brain:	n/a
23	chr3:46792023-46792073	HMEC	breast:	n/a
24	chr3:46853910-46853960	PANC-1	pancreas:	n/a
25	chr3:46854173-46854223	LNCaP	prostate:	n/a
26	chr3:46786387-46786437	ECC-1	luminal epithelium:	n/a
27	chr3:46792192-46792242	GM12891	blood:	n/a
28	chr3:46787073-46787123	SKMC	muscle:	n/a
29	chr3:46786238-46786288	HL-60	blood:	n/a
30	chr3:46854231-46854281	AG09309	skin:	n/a
31	chr3:46792357-46792407	HCT-116	colon:	n/a
32	chr3:46854173-46854223	AoSMC	blood vessel:	n/a
33	chr3:46854231-46854281	HAEpiC	amniotic membrane:	n/a
34	chr3:46856803-46856853	ECC-1	luminal epithelium:	n/a
35	chr3:46792462-46792512	HRE	kidney:	n/a
36	chr3:46790182-46790232	AG09319	gingival:	n/a
37	chr3:46787073-46787123	PrEC	prostate:	n/a
38	chr3:46792364-46792414	CMK	blood:	n/a
39	chr3:46854297-46854347	Hepatocyte	liver:	n/a
40	chr3:46856803-46856853	SKMC	muscle:	n/a
41	chr3:46778871-46778921	IMR90	lung:	fetal
42	chr3:46853986-46854036	PrEC	prostate:	n/a
43	chr3:46797928-46797978	AG04449	skin:	fetal
44	chr3:46853910-46853960	BJ	skin:	n/a
45	chr3:46798240-46798290	AG04450	lung:	fetal
46	chr3:46853986-46854036	HUVEC	blood vessel:	n/a
47	chr3:46796026-46796076	K562	blood:	n/a
48	chr3:46792357-46792407	Hepatocyte	liver:	n/a
49	chr3:46791477-46791527	T-47D	breast:	n/a
50	chr3:46854311-46854361	NH-A	brain:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:
2	chr3:46864966..46867284-chr3:46873787..46876389,2	K562	blood:
3	chr3:46774758..46775741-chr3:46797694..46798443,2	K562	blood:
4	chr3:46858188..46860125-chr3:46939783..46942119,2	K562	blood:
5	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
6	chr3:46792775..46794351-chr3:46906387..46908133,2	K562	blood:
7	chr3:46720178..46722487-chr3:46787613..46789601,2	K562	blood:
8	chr3:46746227..46747136-chr3:46797879..46798830,2	K562	blood:
9	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
10	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
11	chr3:46796598..46799185-chr3:46799676..46801957,2	MCF-7	breast:
12	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
13	chr3:46789741..46793223-chr3:46794604..46798425,5	K562	blood:
14	chr3:46780314..46782174-chr3:46791450..46793098,2	K562	blood:
15	chr3:46853522..46855564-chr3:46864841..46866780,2	K562	blood:
16	chr3:46789981..46792010-chr3:46794604..46797550,3	K562	blood:
17	chr3:46776204..46778019-chr3:46778181..46780158,2	K562	blood:
18	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
19	chr3:46847486..46849953-chr3:46878692..46880394,2	K562	blood:
20	chr3:46789981..46792010-chr3:46794604..46797550,3	K562	blood:
21	chr3:46788120..46791042-chr3:46798895..46800766,2	K562	blood:
22	chr3:46780631..46782178-chr3:46786371..46787877,2	K562	blood:
23	chr3:46788120..46791042-chr3:46798895..46800766,2	K562	blood:
24	chr3:46780631..46782178-chr3:46786371..46787877,2	K562	blood:
25	chr3:46764632..46767218-chr3:46782393..46785331,2	K562	blood:
26	chr3:46796598..46799185-chr3:46799676..46801957,2	MCF-7	breast:
27	chr3:46783774..46785518-chr3:46915413..46918248,2	MCF-7	breast:
28	chr3:46798748..46799515-chr3:46907913..46908649,2	K562	blood:
29	chr3:46783977..46786592-chr3:46791856..46793997,2	MCF-7	breast:
30	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:
31	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
32	chr3:46789741..46793223-chr3:46794604..46798425,5	K562	blood:
33	chr3:46785802..46787615-chr3:46790135..46792444,2	K562	blood:
34	chr3:46780314..46782174-chr3:46791450..46793098,2	K562	blood:
35	chr3:46819637..46822469-chr3:46912934..46914923,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRSS50-1	chr3:46853712-46854064	NONHSAT089457
2	lnc-PRSS50-1	chr3:46797532-46798119	NONHSAT089457
3	lnc-PRSS50-1	chr3:46795974-46796138	NONHSAT089457
4	lnc-PTH1R-2	chr3:46839613-46839880	NONHSAT089458

No data

Variant related genes	Relation type
ENSG00000238013	TF binding region
PRSS50	TF binding region
PRSS44	TF binding region
PRSS45	TF binding region
PRSS46	TF binding region
ENSG00000238013	CpG island
PRSS50	CpG island
PRSS44	CpG island
PRSS45	CpG island
PRSS46	CpG island
ENSG00000261603	chromatin interactions
ENSG00000178055	chromatin interactions
ENSG00000188086	chromatin interactions
ENSG00000206549	chromatin interactions

Extended variants
information (count: 1770 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1770 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545250875	chr3:46778635-46778636	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs58800070	chr3:46778636-46778637	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs141872981	chr3:46778637-46778638	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs397955121	chr3:46778643-46778644	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs138077659	chr3:46778677-46778678	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs60410557	chr3:46778678-46778679	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs563916604	chr3:46778680-46778681	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs531197638	chr3:46778695-46778696	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs368620641	chr3:46778696-46778697	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs542640343	chr3:46778701-46778702	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs12493158	chr3:46778842-46778843	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs528592088	chr3:46778871-46778872	Enhancers Weak transcription Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs373381065	chr3:46778881-46778882	Enhancers Weak transcription Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs79770858	chr3:46778885-46778886	Enhancers Weak transcription Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs145209976	chr3:46778886-46778887	Enhancers Weak transcription Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs112372064	chr3:46778904-46778905	Enhancers Weak transcription Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs6763438	chr3:46778988-46778989	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs535944554	chr3:46779054-46779055	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs35708476	chr3:46779109-46779110	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs180992711	chr3:46779113-46779114	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs59711990	chr3:46779114-46779115	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs569846501	chr3:46779186-46779187	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs6772081	chr3:46779187-46779188	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs149199405	chr3:46779192-46779193	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs145020563	chr3:46779224-46779225	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs576414420	chr3:46779228-46779229	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs148530966	chr3:46779237-46779238	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs372263019	chr3:46779271-46779272	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs574409054	chr3:46779286-46779287	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs531617920	chr3:46779357-46779358	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs541925160	chr3:46779391-46779392	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs6414431	chr3:46779410-46779411	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs531154941	chr3:46779413-46779414	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs6414432	chr3:46779431-46779432	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs564807952	chr3:46779433-46779434	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs528489293	chr3:46779446-46779447	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs113211508	chr3:46779503-46779504	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs546628302	chr3:46779504-46779505	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs534129001	chr3:46779506-46779507	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs6442025	chr3:46779547-46779548	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs529336868	chr3:46779573-46779574	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs551077323	chr3:46779584-46779585	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs6797059	chr3:46779654-46779655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs62246229	chr3:46779689-46779690	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs557449798	chr3:46779733-46779734	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs558421087	chr3:46779765-46779766	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs6442026	chr3:46779799-46779800	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs185374875	chr3:46779832-46779833	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs6794689	chr3:46779846-46779847	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs574395090	chr3:46779847-46779848	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Recurrent pregnancy loss	19789632	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46744000-46792200	Weak transcription	Right Atrium	heart
2	chr3:46769000-46792400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr3:46776600-46778800	Weak transcription	Pancreas	Pancrea
4	chr3:46777000-46779800	Enhancers	Thymus	Thymus
5	chr3:46778000-46780000	Enhancers	Fetal Thymus	thymus
6	chr3:46778200-46778800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr3:46778400-46779200	Enhancers	Fetal Muscle Trunk	muscle
8	chr3:46778600-46779200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr3:46778600-46779200	Enhancers	Fetal Muscle Leg	muscle
10	chr3:46778800-46779000	Bivalent Enhancer	HSMM	muscle
11	chr3:46778800-46779200	Enhancers	Left Ventricle	heart
12	chr3:46778800-46779400	Enhancers	Pancreas	Pancrea
13	chr3:46779000-46779200	Enhancers	Spleen	Spleen
14	chr3:46779000-46779400	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
15	chr3:46779200-46782000	Weak transcription	Left Ventricle	heart
16	chr3:46779400-46795400	Weak transcription	Spleen	Spleen
17	chr3:46779400-46799600	Weak transcription	Pancreas	Pancrea
18	chr3:46779600-46780400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr3:46779800-46792800	Weak transcription	Thymus	Thymus
20	chr3:46780800-46785000	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr3:46784400-46785200	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr3:46784400-46785200	Enhancers	Fetal Stomach	stomach
23	chr3:46784600-46785000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr3:46784600-46785000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr3:46784600-46785000	Enhancers	Placenta	Placenta
26	chr3:46784600-46785200	Enhancers	Fetal Lung	lung
27	chr3:46784600-46785200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr3:46784800-46785200	Enhancers	Fetal Intestine Small	intestine
29	chr3:46785000-46785200	Weak transcription	Placenta	Placenta
30	chr3:46785000-46785800	Strong transcription	Skeletal Muscle Male	skeletal muscle
31	chr3:46785000-46786200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr3:46785000-46789800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr3:46785200-46785600	Enhancers	Placenta	Placenta
34	chr3:46785200-46799800	Weak transcription	Fetal Intestine Small	intestine
35	chr3:46785600-46789800	Weak transcription	Placenta	Placenta
36	chr3:46785800-46786200	Enhancers	GM12878-XiMat	blood
37	chr3:46785800-46795600	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr3:46786200-46787800	Weak transcription	GM12878-XiMat	blood
39	chr3:46786400-46786600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr3:46787800-46789200	Enhancers	GM12878-XiMat	blood
41	chr3:46789200-46794200	Weak transcription	GM12878-XiMat	blood
42	chr3:46789600-46789800	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr3:46789600-46790400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr3:46789600-46790400	Enhancers	Fetal Muscle Leg	muscle
45	chr3:46789800-46790000	Enhancers	Fetal Stomach	stomach
46	chr3:46789800-46790200	Enhancers	H9 Cell Line	embryonic stem cell
47	chr3:46789800-46790400	Enhancers	Placenta	Placenta
48	chr3:46789800-46790600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr3:46790600-46791800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr3:46791800-46792400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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