Variant report

Variant	esv3486129
Chromosome Location	chr2:231175581-231265831
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1078)
CpG islands
(count:489)
Chromatin interactive
region (count:42)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1078 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:231200089-231200926	K562	blood:	n/a	n/a
2	ARID3A	chr2:231195481-231195828	K562	blood:	n/a	n/a
3	ARID3A	chr2:231263535-231263838	K562	blood:	n/a	n/a
4	ARID3A	chr2:231193785-231193842	K562	blood:	n/a	n/a
5	ARID3A	chr2:231220790-231221227	HepG2	liver:	n/a	n/a
6	ATF1	chr2:231200164-231200933	K562	blood:	n/a	n/a
7	ATF1	chr2:231263609-231263884	K562	blood:	n/a	n/a
8	ATF1	chr2:231195509-231195828	K562	blood:	n/a	n/a
9	ATF2	chr2:231212671-231213120	GM12878	blood:	n/a	n/a
10	ATF2	chr2:231212653-231213056	GM12878	blood:	n/a	n/a
11	ATF2	chr2:231191449-231192490	GM12878	blood:	n/a	n/a
12	ATF2	chr2:231183218-231184347	GM12878	blood:	n/a	n/a
13	ATF2	chr2:231191499-231192552	GM12878	blood:	n/a	n/a
14	ATF3	chr2:231191653-231192040	K562	blood:	n/a	n/a
15	ATF3	chr2:231195446-231195770	K562	blood:	n/a	n/a
16	ATF3	chr2:231187989-231188190	K562	blood:	n/a	n/a
17	BACH1	chr2:231246869-231247136	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr2:231195688-231195715	K562	blood:	n/a	n/a
19	BACH1	chr2:231212939-231212941	K562	blood:	n/a	n/a
20	BATF	chr2:231192119-231192378	GM12878	blood:	n/a	n/a
21	BATF	chr2:231191613-231192080	GM12878	blood:	n/a	chr2:231191862-231191873
22	BATF	chr2:231212475-231213126	GM12878	blood:	n/a	n/a
23	BATF	chr2:231212698-231213095	GM12878	blood:	n/a	n/a
24	BATF	chr2:231183939-231184211	GM12878	blood:	n/a	n/a
25	BATF	chr2:231223054-231223350	GM12878	blood:	n/a	chr2:231223160-231223171
26	BCL11A	chr2:231183914-231184198	GM12878	blood:	n/a	n/a
27	BCL11A	chr2:231212720-231213098	GM12878	blood:	n/a	n/a
28	BCL3	chr2:231183905-231184420	GM12878	blood:	n/a	n/a
29	BCLAF1	chr2:231183804-231184388	GM12878	blood:	n/a	n/a
30	BCLAF1	chr2:231183163-231183628	GM12878	blood:	n/a	n/a
31	BCLAF1	chr2:231191490-231192616	GM12878	blood:	n/a	n/a
32	BHLHE40	chr2:231195575-231195864	K562	blood:	n/a	n/a
33	BHLHE40	chr2:231183871-231184059	GM12878	blood:	n/a	n/a
34	BHLHE40	chr2:231212896-231213138	GM12878	blood:	n/a	n/a
35	BHLHE40	chr2:231191646-231192075	K562	blood:	n/a	n/a
36	BHLHE40	chr2:231187972-231188245	K562	blood:	n/a	n/a
37	BHLHE40	chr2:231191722-231192202	GM12878	blood:	n/a	n/a
38	BHLHE40	chr2:231200051-231200459	K562	blood:	n/a	n/a
39	BRCA1	chr2:231188205-231188381	HepG2	liver:	n/a	n/a
40	CBX3	chr2:231207951-231208212	K562	blood:	n/a	n/a
41	CBX3	chr2:231187268-231187635	K562	blood:	n/a	n/a
42	CBX3	chr2:231206580-231206982	K562	blood:	n/a	n/a
43	CBX3	chr2:231187908-231188441	K562	blood:	n/a	n/a
44	CBX3	chr2:231211141-231211548	K562	blood:	n/a	n/a
45	CBX3	chr2:231191548-231192096	K562	blood:	n/a	n/a
46	CBX3	chr2:231263346-231263876	K562	blood:	n/a	n/a
47	CBX3	chr2:231195454-231195813	K562	blood:	n/a	n/a
48	CEBPB	chr2:231264789-231264989	HepG2	liver:	n/a	n/a
49	CEBPB	chr2:231262251-231262496	HepG2	liver:	n/a	chr2:231262353-231262364 chr2:231262351-231262362 chr2:231262351-231262364
50	CEBPB	chr2:231190427-231190706	H1-hESC	embryonic stem cell:	n/a	chr2:231190563-231190572 chr2:231190561-231190574 chr2:231190563-231190572 chr2:231190562-231190573 chr2:231190563-231190572 chr2:231190563-231190572

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:231191727-231191777	HRCEpiC	kidney:	n/a
2	chr2:231191727-231191777	HRCEpiC	kidney:	n/a
3	chr2:231191916-231191966	HRE	kidney:	n/a
4	chr2:231191662-231191712	HCF	heart:	n/a
5	chr2:231177866-231177916	HCF	heart:	n/a
6	chr2:231235574-231235624	AoSMC	blood vessel:	n/a
7	chr2:231235574-231235624	HRPEpiC	eye:	n/a
8	chr2:231191727-231191777	PFSK-1	brain:	n/a
9	chr2:231191893-231191943	K562	blood:	n/a
10	chr2:231177866-231177916	HCT-116	colon:	n/a
11	chr2:231191876-231191926	NB4	blood:	n/a
12	chr2:231191893-231191943	T-47D	breast:	n/a
13	chr2:231191916-231191966	AG10803	skin:	n/a
14	chr2:231191916-231191966	Hepatocyte	liver:	n/a
15	chr2:231235574-231235624	PrEC	prostate:	n/a
16	chr2:231235574-231235624	ECC-1	luminal epithelium:	n/a
17	chr2:231190414-231190464	U87	brain:	n/a
18	chr2:231191662-231191712	HEEpiC	esophagus:	n/a
19	chr2:231191916-231191966	A549	lung:	n/a
20	chr2:231235574-231235624	GM12892	blood:	n/a
21	chr2:231191662-231191712	GM12878	blood:	n/a
22	chr2:231235574-231235624	Hepatocyte	liver:	n/a
23	chr2:231191916-231191966	NB4	blood:	n/a
24	chr2:231177866-231177916	HRCEpiC	kidney:	n/a
25	chr2:231191876-231191926	MCF10A-Er-Src	breast:	n/a
26	chr2:231191727-231191777	AoSMC	blood vessel:	n/a
27	chr2:231191893-231191943	SKMC	muscle:	n/a
28	chr2:231191876-231191926	PANC-1	pancreas:	n/a
29	chr2:231177866-231177916	HepG2	liver:	n/a
30	chr2:231190414-231190464	AoSMC	blood vessel:	n/a
31	chr2:231177866-231177916	HCPEpiC	choroid plexus:	n/a
32	chr2:231191916-231191966	Hela-S3	cervix:	n/a
33	chr2:231191662-231191712	A549	lung:	n/a
34	chr2:231191893-231191943	HRCEpiC	kidney:	n/a
35	chr2:231191893-231191943	HAEpiC	amniotic membrane:	n/a
36	chr2:231191916-231191966	AG09309	skin:	n/a
37	chr2:231177866-231177916	GM12891	blood:	n/a
38	chr2:231235574-231235624	AG10803	skin:	n/a
39	chr2:231235574-231235624	GM19239	blood:	n/a
40	chr2:231177866-231177916	HL-60	blood:	n/a
41	chr2:231191876-231191926	HRCEpiC	kidney:	n/a
42	chr2:231191662-231191712	Hela-S3	cervix:	n/a
43	chr2:231191916-231191966	K562	blood:	n/a
44	chr2:231177866-231177916	HRPEpiC	eye:	n/a
45	chr2:231191876-231191926	HCT-116	colon:	n/a
46	chr2:231190414-231190464	SK-N-MC	brain:	n/a
47	chr2:231235574-231235624	MCF-7	breast:	n/a
48	chr2:231235574-231235624	RPTEC	kidney:	n/a
49	chr2:231191662-231191712	PFSK-1	brain:	n/a
50	chr2:231191893-231191943	NHDF-neo	bronchial:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:231187675..231188630-chr2:231663234..231663815,2	K562	blood:
2	chr2:231194037..231196548-chr2:231226140..231228040,2	K562	blood:
3	chr2:231225373..231227509-chr2:231238018..231240508,2	MCF-7	breast:
4	chr2:231250673..231252951-chr2:231254109..231256319,2	K562	blood:
5	chr2:231235932..231237817-chr2:231243056..231245722,2	K562	blood:
6	chr2:231195214..231197850-chr2:231199409..231202103,3	K562	blood:
7	chr2:231192831..231194646-chr2:231195490..231197463,2	K562	blood:
8	chr2:231176097..231178034-chr2:231181270..231184101,2	MCF-7	breast:
9	chr2:231211181..231213107-chr2:231272080..231274624,2	K562	blood:
10	chr2:231191754..231192275-chr2:231280477..231281313,4	HCT-116	colon:
11	chr2:231245270..231247001-chr2:231250596..231253585,2	K562	blood:
12	chr2:231225373..231227509-chr2:231238018..231240508,2	MCF-7	breast:
13	chr2:231187646..231188478-chr2:231276184..231277085,2	HCT-116	colon:
14	chr2:231232811..231234963-chr2:231243502..231245395,2	K562	blood:
15	chr2:231250470..231252017-chr2:231286033..231287832,2	K562	blood:
16	chr2:231191663..231192385-chr2:231280228..231281288,3	Hela-S3	cervix:
17	chr2:231245270..231247001-chr2:231250596..231253585,2	K562	blood:
18	chr2:231187795..231189523-chr2:231196681..231199404,2	MCF-7	breast:
19	chr2:231182687..231184963-chr2:231663131..231665649,2	K562	blood:
20	chr2:231177190..231178996-chr2:231181299..231183714,2	K562	blood:
21	chr2:231187795..231189523-chr2:231196681..231199404,2	MCF-7	breast:
22	chr2:231177190..231178996-chr2:231181299..231183714,2	K562	blood:
23	chr2:231183815..231186331-chr2:231189683..231191890,3	MCF-7	breast:
24	chr2:231208083..231209786-chr2:231217678..231219607,2	K562	blood:
25	chr2:231211608..231214034-chr2:231214766..231217419,2	K562	blood:
26	chr2:231232811..231234963-chr2:231243502..231245395,2	K562	blood:
27	chr2:231187450..231190323-chr2:231192038..231194221,2	K562	blood:
28	chr2:231191400..231192273-chr2:231280039..231281003,2	MCF-7	breast:
29	chr2:231187450..231190323-chr2:231192038..231194221,2	K562	blood:
30	chr2:231211608..231214034-chr2:231214766..231217419,2	K562	blood:
31	chr2:231208083..231209786-chr2:231217678..231219607,2	K562	blood:
32	chr2:231176097..231178034-chr2:231181270..231184101,2	MCF-7	breast:
33	chr2:231194037..231196548-chr2:231226140..231228040,2	K562	blood:
34	chr2:231211208..231214034-chr2:231215264..231217419,2	K562	blood:
35	chr2:231211208..231214034-chr2:231215264..231217419,2	K562	blood:
36	chr2:231199506..231201405-chr2:231206253..231208187,2	K562	blood:
37	chr2:231195214..231197850-chr2:231199409..231202103,3	K562	blood:
38	chr2:231183815..231186331-chr2:231189683..231191890,3	MCF-7	breast:
39	chr2:231192831..231194646-chr2:231195490..231197463,2	K562	blood:
40	chr16:17916509..17917287-chr2:231255356..231256048,2	MCF-7	breast:
41	chr2:231250673..231252951-chr2:231254109..231256319,2	K562	blood:
42	chr2:231235932..231237817-chr2:231243056..231245722,2	K562	blood:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SP140-5	chr2:231264842-231264957	NONHSAT077280
2	lnc-SP110-5	chr2:231263880-231265192	ucscGeneNc_uc002vqw_1
3	lnc-SP140-5	chr2:231254634-231254738	NONHSAT077278
4	lnc-SP110-4	chr2:231174307-231176000	NONHSAT077276
5	lnc-SP140-5	chr2:231265670-231265768	NONHSAT077280
6	lnc-SP140-5	chr2:231256802-231256944	NONHSAT077280
7	lnc-SP140-5	chr2:231249956-231250019	NONHSAT077279
8	lnc-SP140-5	chr2:231248225-231248290	NONHSAT077278
9	lnc-SP140-5	chr2:231261472-231261513	NONHSAT077280
10	lnc-SP140-5	chr2:231256430-231256522	NONHSAT077280
11	lnc-SP140-5	chr2:231264536-231264957	NONHSAT077281
12	lnc-SP140-5	chr2:231261472-231261513	NONHSAT077278
13	lnc-SP140-5	chr2:231253274-231253501	NONHSAT077279
14	lnc-SP140L-1	chr2:231175869-231176238	NONHSAT077277
15	lnc-SP140-5	chr2:231265049-231265128	NONHSAT077280
16	lnc-SP140-5	chr2:231258129-231258176	NONHSAT077280
17	lnc-SP140-5	chr2:231264842-231266158	NONHSAT077278
18	lnc-SP140-5	chr2:231258129-231258176	NONHSAT077278
19	lnc-SP140-5	chr2:231249939-231250019	NONHSAT077278
20	lnc-SP140-5	chr2:231235621-231235682	NONHSAT077278
21	lnc-SP140-5	chr2:231265049-231265192	NONHSAT077281
22	lnc-SP140-5	chr2:231253274-231253348	NONHSAT077278
23	lnc-SP140-5	chr2:231256802-231256944	NONHSAT077278
24	lnc-SP140-5	chr2:231236313-231236366	NONHSAT077278

No data

Variant related genes	Relation type
SP140L	TF binding region
SP140L	CpG island
ENSG00000067066	chromatin interactions
ENSG00000185404	chromatin interactions

Extended variants
information (count: 3493 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3493 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533963773	chr2:231175615-231175616	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs558487113	chr2:231175618-231175619	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs577142533	chr2:231175629-231175630	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs544459118	chr2:231175636-231175637	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs377093921	chr2:231175660-231175661	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs562952349	chr2:231175671-231175672	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs575020961	chr2:231175720-231175721	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs112512464	chr2:231175723-231175724	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs542054946	chr2:231175761-231175762	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs66642167	chr2:231175763-231175764	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs192345800	chr2:231175784-231175785	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs148480087	chr2:231175795-231175796	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs145316306	chr2:231175796-231175797	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs545831658	chr2:231175813-231175814	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs368697917	chr2:231175819-231175820	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs564023168	chr2:231175834-231175835	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs200628836	chr2:231175916-231175917	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs531645900	chr2:231175978-231175979	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs139570354	chr2:231176040-231176041	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs550138621	chr2:231176053-231176054	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs568261031	chr2:231176054-231176055	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs183455734	chr2:231176059-231176060	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs547256613	chr2:231176063-231176064	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs201588897	chr2:231176155-231176156	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs199837567	chr2:231176163-231176164	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs533999979	chr2:231176175-231176176	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs374525484	chr2:231176177-231176178	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs558534066	chr2:231176178-231176179	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs570474295	chr2:231176190-231176191	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs377705244	chr2:231176194-231176195	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs201144938	chr2:231176196-231176197	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs369678024	chr2:231176238-231176239	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs376122291	chr2:231176295-231176296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187832648	chr2:231176349-231176350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554039896	chr2:231176388-231176389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572194368	chr2:231176470-231176471	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192352422	chr2:231176482-231176483	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184640374	chr2:231176487-231176488	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190096102	chr2:231176549-231176550	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531380397	chr2:231176580-231176581	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543028982	chr2:231176601-231176602	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181853430	chr2:231176607-231176608	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369026063	chr2:231176616-231176617	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529139000	chr2:231176633-231176634	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557317388	chr2:231176648-231176649	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547588805	chr2:231176652-231176653	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573885419	chr2:231176666-231176667	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565489831	chr2:231176759-231176760	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372670383	chr2:231176796-231176797	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527791462	chr2:231176837-231176838	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	22429812	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
prenatal diagnosis	22389664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mental retardation	20152051	CNVD
Cancer	21183584	CNVD
Albright''s disease	22277900	CNVD
Brachydactyly-Mental Retardation Syndrome	22470819	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2237 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231147800-231182400	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr2:231153800-231183400	Weak transcription	Duodenum Mucosa	Duodenum
3	chr2:231162600-231180800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr2:231165400-231180200	Weak transcription	Primary T cells from cord blood	blood
5	chr2:231165400-231181600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr2:231165800-231181000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr2:231170200-231175600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr2:231172400-231180800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr2:231174000-231175600	Strong transcription	Primary T cells fromperipheralblood	blood
10	chr2:231174200-231179600	Strong transcription	Primary T helper cells PMA-I stimulated	--
11	chr2:231174400-231182000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr2:231175000-231177400	Weak transcription	Primary B cells from cord blood	blood
13	chr2:231175000-231177400	Weak transcription	Spleen	Spleen
14	chr2:231175000-231183800	Weak transcription	HMEC	breast
15	chr2:231175200-231175600	Strong transcription	Primary B cells from peripheral blood	blood
16	chr2:231175200-231177200	Weak transcription	GM12878-XiMat	blood
17	chr2:231175400-231176800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr2:231175400-231177200	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr2:231175400-231177200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr2:231175400-231177400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr2:231175400-231177400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr2:231175400-231180200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr2:231175400-231182000	Weak transcription	Lung	lung
24	chr2:231175600-231176000	Weak transcription	Primary B cells from peripheral blood	blood
25	chr2:231175600-231177200	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr2:231175600-231177200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr2:231176000-231181000	Strong transcription	Primary B cells from peripheral blood	blood
28	chr2:231176400-231177400	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr2:231176600-231177000	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr2:231176600-231177200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr2:231176800-231177400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr2:231176800-231179000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr2:231177200-231177600	Enhancers	HSMMtube	muscle
34	chr2:231177200-231177800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr2:231177200-231177800	Enhancers	HSMM	muscle
36	chr2:231177200-231177800	Enhancers	NH-A	brain
37	chr2:231177200-231177800	Enhancers	NHEK	skin
38	chr2:231177200-231178000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr2:231177200-231178800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr2:231177200-231178800	Strong transcription	GM12878-XiMat	blood
41	chr2:231177200-231179200	Strong transcription	Primary T helper cells fromperipheralblood	blood
42	chr2:231177200-231179800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr2:231177200-231180400	Strong transcription	Primary T cells fromperipheralblood	blood
44	chr2:231177400-231177800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr2:231177400-231177800	Enhancers	Muscle Satellite Cultured Cells	--
46	chr2:231177400-231177800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr2:231177400-231177800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr2:231177400-231177800	Strong transcription	Spleen	Spleen
49	chr2:231177400-231177800	Enhancers	Osteobl	bone
50	chr2:231177400-231178200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood

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