Variant report

Variant	esv33628
Chromosome Location	chr2:33257484-33455355
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2613)
CpG islands
(count:1283)
Chromatin interactive
region (count:174)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2613 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:33285574-33285673	K562	blood:	n/a	n/a
2	ARID3A	chr2:33434537-33434706	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:33289402-33289458	K562	blood:	n/a	n/a
4	ARID3A	chr2:33422362-33423050	HepG2	liver:	n/a	chr2:33423023-33423039
5	ARID3A	chr2:33359413-33359619	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:33437224-33437416	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:33437278-33437465	K562	blood:	n/a	n/a
8	ARID3A	chr2:33333652-33334321	K562	blood:	n/a	n/a
9	ARID3A	chr2:33258718-33258942	K562	blood:	n/a	n/a
10	ARID3A	chr2:33287152-33287157	K562	blood:	n/a	n/a
11	ARID3A	chr2:33343824-33343996	K562	blood:	n/a	n/a
12	ARID3A	chr2:33366668-33366820	K562	blood:	n/a	n/a
13	ATF1	chr2:33296225-33296352	K562	blood:	n/a	n/a
14	ATF1	chr2:33347733-33348203	K562	blood:	n/a	n/a
15	ATF1	chr2:33444884-33445120	K562	blood:	n/a	n/a
16	ATF1	chr2:33294897-33295215	K562	blood:	n/a	n/a
17	ATF1	chr2:33333227-33334393	K562	blood:	n/a	n/a
18	ATF1	chr2:33435158-33435389	K562	blood:	n/a	n/a
19	ATF1	chr2:33437243-33437663	K562	blood:	n/a	n/a
20	ATF2	chr2:33430981-33431571	GM12878	blood:	n/a	n/a
21	ATF2	chr2:33430993-33431496	GM12878	blood:	n/a	n/a
22	ATF3	chr2:33276577-33277518	A549	lung:	n/a	n/a
23	ATF3	chr2:33294808-33295592	A549	lung:	n/a	n/a
24	ATF3	chr2:33294806-33295714	A549	lung:	n/a	n/a
25	ATF3	chr2:33333639-33334249	K562	blood:	n/a	n/a
26	ATF3	chr2:33276601-33277556	A549	lung:	n/a	n/a
27	ATF3	chr2:33444854-33445162	K562	blood:	n/a	n/a
28	BACH1	chr2:33329783-33330049	K562	blood:	n/a	chr2:33329934-33329948
29	BACH1	chr2:33329593-33330080	H1-hESC	embryonic stem cell:	n/a	chr2:33329934-33329948
30	BACH1	chr2:33333738-33333858	K562	blood:	n/a	n/a
31	BATF	chr2:33431021-33431435	GM12878	blood:	n/a	n/a
32	BATF	chr2:33431034-33431436	GM12878	blood:	n/a	n/a
33	BATF	chr2:33294981-33295180	GM12878	blood:	n/a	n/a
34	BCL11A	chr2:33431084-33431417	GM12878	blood:	n/a	n/a
35	BCL11A	chr2:33431036-33431509	GM12878	blood:	n/a	n/a
36	BCL3	chr2:33294764-33295617	A549	lung:	n/a	n/a
37	BCL3	chr2:33276536-33277655	A549	lung:	n/a	chr2:33276828-33276837 chr2:33276960-33276969
38	BCL3	chr2:33276548-33277522	A549	lung:	n/a	chr2:33276828-33276837 chr2:33276960-33276969
39	BCL3	chr2:33294735-33295709	A549	lung:	n/a	n/a
40	BCLAF1	chr2:33431038-33431502	GM12878	blood:	n/a	n/a
41	BHLHE40	chr2:33358791-33358805	K562	blood:	n/a	n/a
42	BHLHE40	chr2:33336056-33336315	HepG2	liver:	n/a	n/a
43	BHLHE40	chr2:33431113-33431490	GM12878	blood:	n/a	n/a
44	BHLHE40	chr2:33439553-33439834	HepG2	liver:	n/a	n/a
45	BHLHE40	chr2:33431901-33431908	GM12878	blood:	n/a	n/a
46	BHLHE40	chr2:33289555-33289569	K562	blood:	n/a	n/a
47	BHLHE40	chr2:33314483-33314612	K562	blood:	n/a	n/a
48	BHLHE40	chr2:33437240-33437442	K562	blood:	n/a	n/a
49	BHLHE40	chr2:33333586-33334367	K562	blood:	n/a	n/a
50	BRCA1	chr2:33315537-33315669	GM12878	blood:	n/a	n/a

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:33295138-33295188	AG10803	skin:	n/a
2	chr2:33372733-33372783	H1-hESC	embryonic stem cell:	embryo
3	chr2:33295138-33295188	AG10803	skin:	n/a
4	chr2:33372733-33372783	H1-hESC	embryonic stem cell:	embryo
5	chr2:33428629-33428679	ovcar-3	ovarian:	n/a
6	chr2:33359356-33359406	AG09309	skin:	n/a
7	chr2:33342294-33342344	NHBE	bronchial:	n/a
8	chr2:33368461-33368511	HAEpiC	amniotic membrane:	n/a
9	chr2:33436054-33436104	RPTEC	kidney:	n/a
10	chr2:33342294-33342344	HUVEC	blood vessel:	n/a
11	chr2:33368461-33368511	AG09309	skin:	n/a
12	chr2:33415906-33415956	SK-N-SH	brain:	n/a
13	chr2:33359550-33359600	AG04449	skin:	fetal
14	chr2:33384367-33384417	SK-N-SH	brain:	n/a
15	chr2:33368461-33368511	ovcar-3	ovarian:	n/a
16	chr2:33276281-33276331	HNPCEpiC	eye:	n/a
17	chr2:33282816-33282866	HepG2	liver:	n/a
18	chr2:33348262-33348312	AG04450	lung:	fetal
19	chr2:33295138-33295188	PANC-1	pancreas:	n/a
20	chr2:33372733-33372783	HAEpiC	amniotic membrane:	n/a
21	chr2:33348262-33348312	IMR90	lung:	fetal
22	chr2:33433039-33433089	GM19239	blood:	n/a
23	chr2:33436054-33436104	HEEpiC	esophagus:	n/a
24	chr2:33415906-33415956	A549	lung:	n/a
25	chr2:33359356-33359406	HCPEpiC	choroid plexus:	n/a
26	chr2:33295138-33295188	AG04449	skin:	fetal
27	chr2:33359529-33359579	NH-A	brain:	n/a
28	chr2:33348262-33348312	Caco-2	colon:	n/a
29	chr2:33342294-33342344	IMR90	lung:	fetal
30	chr2:33428629-33428679	HNPCEpiC	eye:	n/a
31	chr2:33372733-33372783	HEEpiC	esophagus:	n/a
32	chr2:33359281-33359331	GM12892	blood:	n/a
33	chr2:33282816-33282866	H1-hESC	embryonic stem cell:	embryo
34	chr2:33436054-33436104	NHBE	bronchial:	n/a
35	chr2:33359198-33359248	NB4	blood:	n/a
36	chr2:33359198-33359248	SK-N-MC	brain:	n/a
37	chr2:33311428-33311478	U87	brain:	n/a
38	chr2:33359356-33359406	HUVEC	blood vessel:	n/a
39	chr2:33372733-33372783	K562	blood:	n/a
40	chr2:33433039-33433089	GM06990	blood:	n/a
41	chr2:33391915-33391965	LNCaP	prostate:	n/a
42	chr2:33384367-33384417	NHBE	bronchial:	n/a
43	chr2:33359198-33359248	IMR90	lung:	fetal
44	chr2:33359198-33359248	Caco-2	colon:	n/a
45	chr2:33359688-33359738	BE2_C	brain:	n/a
46	chr2:33428629-33428679	Hepatocyte	liver:	n/a
47	chr2:33348262-33348312	HRE	kidney:	n/a
48	chr2:33391915-33391965	GM12891	blood:	n/a
49	chr2:33359281-33359331	HEEpiC	esophagus:	n/a
50	chr2:33391915-33391965	HPAEpiC	pulmonary alveolar:	n/a

(count:174 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr2:33382825..33385246-chr2:33385612..33388538,2	K562	blood:
2	chr2:33289501..33292346-chr2:33293436..33295716,3	MCF-7	breast:
3	chr2:33352861..33355600-chr2:33385791..33387865,2	MCF-7	breast:
4	chr2:33269061..33270926-chr2:33275558..33277502,2	MCF-7	breast:
5	chr2:33320811..33323465-chr2:33327393..33329847,2	K562	blood:
6	chr2:33294964..33297126-chr2:33297596..33299242,2	MCF-7	breast:
7	chr2:33257210..33260008-chr2:33260500..33262252,2	MCF-7	breast:
8	chr2:33256831..33258647-chr2:33264636..33267150,2	K562	blood:
9	chr2:33294991..33295910-chr2:33416929..33417799,3	MCF-7	breast:
10	chr2:33321965..33324050-chr2:33326516..33328893,2	K562	blood:
11	chr2:33276038..33279091-chr2:33288680..33292519,3	MCF-7	breast:
12	chr2:33369700..33371935-chr2:33440247..33441794,2	K562	blood:
13	chr2:33433433..33434972-chr2:33439448..33441761,2	MCF-7	breast:
14	chr2:33341850..33346633-chr2:33347912..33351586,5	K562	blood:
15	chr2:33383408..33387314-chr2:33391651..33394582,3	K562	blood:
16	chr2:33321965..33324050-chr2:33326516..33328893,2	K562	blood:
17	chr2:33289501..33292346-chr2:33293436..33295716,3	MCF-7	breast:
18	chr2:33260304..33260822-chr2:33495358..33496007,2	MCF-7	breast:
19	chr2:33372580..33375286-chr2:33379288..33381912,2	MCF-7	breast:
20	chr2:33372580..33375286-chr2:33379288..33381912,2	MCF-7	breast:
21	chr2:33294735..33295813-chr2:33311218..33312090,5	MCF-7	breast:
22	chr2:33319782..33321597-chr2:33324862..33327252,2	K562	blood:
23	chr2:33256831..33258647-chr2:33264636..33267150,2	K562	blood:
24	chr2:33325545..33328306-chr2:33331227..33333844,3	K562	blood:
25	chr2:33260407..33262474-chr2:33263325..33265020,2	MCF-7	breast:
26	chr1:22780784..22781462-chr2:33294993..33295833,2	MCF-7	breast:
27	chr2:33295235..33295963-chr8:129153954..129154573,2	MCF-7	breast:
28	chr2:33346676..33349370-chr2:33351753..33353323,2	MCF-7	breast:
29	chr2:33170909..33171727-chr2:33294922..33295425,2	MCF-7	breast:
30	chr2:33387130..33389156-chr2:33413071..33415726,2	K562	blood:
31	chr2:33284687..33288170-chr2:33293184..33297507,4	K562	blood:
32	chr2:33320811..33323465-chr2:33327393..33329847,2	K562	blood:
33	chr2:33259319..33260252-chr2:33597390..33598654,4	MCF-7	breast:
34	chr2:33295214..33297626-chr2:33299821..33301525,2	K562	blood:
35	chr2:33295016..33295604-chr2:33594643..33595514,3	MCF-7	breast:
36	chr2:33342989..33344574-chr2:33349726..33351939,2	K562	blood:
37	chr2:33357374..33360115-chr2:33361788..33364595,2	K562	blood:
38	chr2:32997330..32998373-chr2:33258363..33259384,12	MCF-7	breast:
39	chr2:33325612..33327794-chr2:33340279..33342950,2	MCF-7	breast:
40	chr2:33440018..33441970-chr2:33445005..33447288,2	K562	blood:
41	chr2:33259613..33260414-chr2:33495403..33496285,3	MCF-7	breast:
42	chr2:33293451..33296755-chr2:33301954..33305143,4	MCF-7	breast:
43	chr2:33171020..33173389-chr2:33256999..33258641,3	MCF-7	breast:
44	chr2:33360506..33363015-chr2:33369952..33372450,2	K562	blood:
45	chr2:33430736..33432934-chr2:33471410..33474169,2	MCF-7	breast:
46	chr2:33319782..33321597-chr2:33324862..33327252,2	K562	blood:
47	chr2:33295981..33298155-chr2:33304588..33306275,2	K562	blood:
48	chr2:33259746..33260329-chr2:33311629..33312361,2	MCF-7	breast:
49	chr2:33293451..33296755-chr2:33301954..33305143,4	MCF-7	breast:
50	chr2:33428794..33433443-chr2:33434852..33438418,7	K562	blood:

No data

Variant related genes	Relation type
ENSG00000223951	TF binding region
LTBP1	TF binding region
ENSG00000223951	CpG island
LTBP1	CpG island
ENSG00000206951	chromatin interactions
ENSG00000049323	chromatin interactions
ENSG00000223951	chromatin interactions

Extended variants
information (count: 8822 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:8822 , 50 per page) page: 1 2 3 4 5 6 7 ... 177

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534457405	chr2:33257499-33257500	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs17324731	chr2:33257502-33257503	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs574326160	chr2:33257503-33257504	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs537126870	chr2:33257518-33257519	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs543329435	chr2:33257586-33257587	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs147517947	chr2:33257664-33257665	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs577072391	chr2:33257679-33257680	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs545340787	chr2:33257686-33257687	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs552200338	chr2:33257689-33257690	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs115386192	chr2:33257708-33257709	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs116662751	chr2:33257889-33257890	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs188262734	chr2:33257923-33257924	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs534976550	chr2:33258038-33258039	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs561447576	chr2:33258043-33258044	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs530289995	chr2:33258047-33258048	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs140081163	chr2:33258049-33258050	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs369222147	chr2:33258080-33258081	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs570286566	chr2:33258090-33258091	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs13391477	chr2:33258134-33258135	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs192785026	chr2:33258144-33258145	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs551751443	chr2:33258145-33258146	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs13417308	chr2:33258202-33258203	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs534397424	chr2:33258276-33258277	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs554272065	chr2:33258282-33258283	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs568085073	chr2:33258285-33258286	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs143523431	chr2:33258286-33258287	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs547052523	chr2:33258368-33258369	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs144139524	chr2:33258378-33258379	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs577065519	chr2:33258407-33258408	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs545821157	chr2:33258484-33258485	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs558978189	chr2:33258485-33258486	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs113692001	chr2:33258488-33258489	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs144369252	chr2:33258522-33258523	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs374487146	chr2:33258531-33258532	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs148613262	chr2:33258543-33258544	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs561330183	chr2:33258555-33258556	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs530143880	chr2:33258582-33258583	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs543947170	chr2:33258669-33258670	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs558994331	chr2:33258681-33258682	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs71407493	chr2:33258682-33258683	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs386389873	chr2:33258693-33258694	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs36113954	chr2:33258695-33258696	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs80152417	chr2:33258775-33258776	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs369831007	chr2:33258781-33258782	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs565314983	chr2:33258823-33258824	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs528049794	chr2:33258932-33258933	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs184821069	chr2:33258962-33258963	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs2236266	chr2:33258969-33258970	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs142047927	chr2:33258976-33258977	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs372100009	chr2:33258979-33258980	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3159 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33246400-33258800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:33246400-33262800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr2:33247400-33258400	Weak transcription	Stomach Smooth Muscle	stomach
4	chr2:33247600-33258600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr2:33249400-33258800	Weak transcription	Colon Smooth Muscle	Colon
6	chr2:33249400-33258800	Weak transcription	Fetal Lung	lung
7	chr2:33249600-33258800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr2:33250200-33258400	Weak transcription	Liver	Liver
9	chr2:33250200-33258800	Weak transcription	Fetal Muscle Leg	muscle
10	chr2:33250200-33263200	Weak transcription	Left Ventricle	heart
11	chr2:33250200-33265600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:33250600-33273000	Weak transcription	K562	blood
13	chr2:33254800-33258800	Weak transcription	NHLF	lung
14	chr2:33255200-33258800	Weak transcription	A549	lung
15	chr2:33255400-33258400	Weak transcription	Brain Germinal Matrix	brain
16	chr2:33255400-33258600	Weak transcription	Brain Cingulate Gyrus	brain
17	chr2:33255400-33258800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:33255400-33258800	Weak transcription	HUVEC	blood vessel
19	chr2:33255600-33258800	Weak transcription	Brain Anterior Caudate	brain
20	chr2:33255600-33259000	Weak transcription	Small Intestine	intestine
21	chr2:33255800-33259000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr2:33256200-33258800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr2:33256800-33257600	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr2:33257000-33257600	Enhancers	Stomach Mucosa	stomach
25	chr2:33257000-33258600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr2:33257000-33258800	Weak transcription	Fetal Intestine Large	intestine
27	chr2:33257200-33258400	Weak transcription	Fetal Heart	heart
28	chr2:33257200-33258800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr2:33257200-33258800	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr2:33257200-33259000	Weak transcription	Right Atrium	heart
31	chr2:33257600-33258800	Weak transcription	Stomach Mucosa	stomach
32	chr2:33257600-33259000	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr2:33258000-33258200	Enhancers	Fetal Kidney	kidney
34	chr2:33258200-33258800	Weak transcription	Fetal Kidney	kidney
35	chr2:33258400-33258800	Enhancers	Brain Germinal Matrix	brain
36	chr2:33258400-33258800	Enhancers	Brain Hippocampus Middle	brain
37	chr2:33258400-33258800	Enhancers	Duodenum Smooth Muscle	Duodenum
38	chr2:33258400-33258800	Enhancers	Stomach Smooth Muscle	stomach
39	chr2:33258400-33259200	Enhancers	Liver	Liver
40	chr2:33258400-33262200	Enhancers	Fetal Heart	heart
41	chr2:33258600-33258800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr2:33258600-33258800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr2:33258600-33258800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr2:33258600-33258800	Enhancers	Brain Cingulate Gyrus	brain
45	chr2:33258600-33258800	Enhancers	HMEC	breast
46	chr2:33258600-33258800	Enhancers	HSMM	muscle
47	chr2:33258600-33259400	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr2:33258800-33259000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr2:33258800-33259000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr2:33258800-33259000	Active TSS	Muscle Satellite Cultured Cells	--

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