Variant report

Variant	nsv581485
Chromosome Location	chr2:38839323-38893660
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1207)
CpG islands
(count:793)
Chromatin interactive
region (count:90)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1207 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:38892880-38893239	K562	blood:	n/a	n/a
2	ARID3A	chr2:38853526-38853744	K562	blood:	n/a	n/a
3	ARID3A	chr2:38842209-38842783	K562	blood:	n/a	n/a
4	ARID3A	chr2:38842122-38842215	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:38840174-38840596	K562	blood:	n/a	n/a
6	ARID3A	chr2:38861740-38862106	K562	blood:	n/a	n/a
7	ARID3A	chr2:38847372-38847870	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:38880715-38881014	K562	blood:	n/a	n/a
9	ARID3A	chr2:38892806-38893881	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:38879587-38880043	K562	blood:	n/a	n/a
11	ARID3A	chr2:38881524-38881720	HepG2	liver:	n/a	n/a
12	ARID3A	chr2:38863497-38863532	K562	blood:	n/a	n/a
13	ARID3A	chr2:38870825-38871318	K562	blood:	n/a	n/a
14	ARID3A	chr2:38840796-38841448	K562	blood:	n/a	n/a
15	ARID3A	chr2:38854643-38854940	HepG2	liver:	n/a	n/a
16	ATF1	chr2:38840955-38841435	K562	blood:	n/a	n/a
17	ATF1	chr2:38870842-38871367	K562	blood:	n/a	n/a
18	ATF1	chr2:38881066-38882442	K562	blood:	n/a	n/a
19	ATF1	chr2:38849416-38849660	K562	blood:	n/a	n/a
20	ATF1	chr2:38861864-38862095	K562	blood:	n/a	n/a
21	ATF1	chr2:38879564-38879931	K562	blood:	n/a	n/a
22	ATF2	chr2:38880502-38881325	GM12878	blood:	n/a	n/a
23	ATF2	chr2:38846580-38846892	GM12878	blood:	n/a	n/a
24	ATF2	chr2:38890859-38891427	GM12878	blood:	n/a	n/a
25	ATF2	chr2:38892876-38893286	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr2:38892778-38893287	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr2:38861690-38862196	GM12878	blood:	n/a	n/a
28	ATF2	chr2:38861670-38862301	GM12878	blood:	n/a	n/a
29	ATF2	chr2:38842329-38842820	GM12878	blood:	n/a	n/a
30	ATF2	chr2:38846498-38847085	GM12878	blood:	n/a	n/a
31	ATF2	chr2:38842193-38842915	GM12878	blood:	n/a	n/a
32	ATF3	chr2:38870859-38871314	K562	blood:	n/a	n/a
33	ATF3	chr2:38842450-38842769	K562	blood:	n/a	n/a
34	ATF3	chr2:38892941-38893712	A549	lung:	n/a	n/a
35	BACH1	chr2:38840872-38840956	K562	blood:	n/a	n/a
36	BATF	chr2:38846621-38846911	GM12878	blood:	n/a	n/a
37	BATF	chr2:38890987-38891390	GM12878	blood:	n/a	n/a
38	BATF	chr2:38846612-38847030	GM12878	blood:	n/a	n/a
39	BATF	chr2:38842488-38842803	GM12878	blood:	n/a	chr2:38842612-38842623
40	BATF	chr2:38859186-38859514	GM12878	blood:	n/a	n/a
41	BATF	chr2:38880553-38881370	GM12878	blood:	n/a	n/a
42	BATF	chr2:38842431-38842723	GM12878	blood:	n/a	chr2:38842612-38842623
43	BCL11A	chr2:38846711-38846949	GM12878	blood:	n/a	n/a
44	BCL11A	chr2:38861720-38862141	GM12878	blood:	n/a	n/a
45	BCL11A	chr2:38842474-38842809	GM12878	blood:	n/a	chr2:38842615-38842624 chr2:38842616-38842625
46	BCL11A	chr2:38846562-38846974	GM12878	blood:	n/a	n/a
47	BCL11A	chr2:38890965-38891338	GM12878	blood:	n/a	n/a
48	BCL11A	chr2:38880543-38881471	GM12878	blood:	n/a	n/a
49	BCL3	chr2:38890959-38891353	GM12878	blood:	n/a	n/a
50	BCL3	chr2:38861808-38862179	GM12878	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:38893161-38893211	NT2-D1	testis:	n/a
2	chr2:38892887-38892937	AG10803	skin:	n/a
3	chr2:38870290-38870340	NH-A	brain:	n/a
4	chr2:38893251-38893301	AG10803	skin:	n/a
5	chr2:38870535-38870585	AoSMC	blood vessel:	n/a
6	chr2:38870535-38870585	HRE	kidney:	n/a
7	chr2:38847451-38847501	AG04449	skin:	fetal
8	chr2:38892365-38892415	GM12892	blood:	n/a
9	chr2:38892365-38892415	HRPEpiC	eye:	n/a
10	chr2:38893237-38893287	CMK	blood:	n/a
11	chr2:38893237-38893287	AoSMC	blood vessel:	n/a
12	chr2:38870535-38870585	GM12891	blood:	n/a
13	chr2:38847451-38847501	Hela-S3	cervix:	n/a
14	chr2:38892958-38893008	NH-A	brain:	n/a
15	chr2:38892958-38893008	HPAEpiC	pulmonary alveolar:	n/a
16	chr2:38892309-38892359	HEK293	kidney:	embryo
17	chr2:38892901-38892951	SK-N-MC	brain:	n/a
18	chr2:38892365-38892415	HRCEpiC	kidney:	n/a
19	chr2:38870535-38870585	HPAEpiC	pulmonary alveolar:	n/a
20	chr2:38870290-38870340	HPAEpiC	pulmonary alveolar:	n/a
21	chr2:38892846-38892896	GM19239	blood:	n/a
22	chr2:38892365-38892415	PANC-1	pancreas:	n/a
23	chr2:38892846-38892896	ECC-1	luminal epithelium:	n/a
24	chr2:38893237-38893287	GM19239	blood:	n/a
25	chr2:38892309-38892359	AG04450	lung:	fetal
26	chr2:38893251-38893301	HCF	heart:	n/a
27	chr2:38893161-38893211	HRPEpiC	eye:	n/a
28	chr2:38893251-38893301	NT2-D1	testis:	n/a
29	chr2:38893237-38893287	SK-N-MC	brain:	n/a
30	chr2:38893251-38893301	HCM	heart:	n/a
31	chr2:38892365-38892415	ovcar-3	ovarian:	n/a
32	chr2:38892958-38893008	HCF	heart:	n/a
33	chr2:38892958-38893008	BJ	skin:	n/a
34	chr2:38893251-38893301	NHBE	bronchial:	n/a
35	chr2:38892846-38892896	PANC-1	pancreas:	n/a
36	chr2:38870535-38870585	HEK293	kidney:	embryo
37	chr2:38893519-38893569	NHDF-neo	bronchial:	n/a
38	chr2:38870290-38870340	HepG2	liver:	n/a
39	chr2:38893161-38893211	PFSK-1	brain:	n/a
40	chr2:38892846-38892896	SK-N-SH	brain:	n/a
41	chr2:38870535-38870585	HNPCEpiC	eye:	n/a
42	chr2:38847451-38847501	GM12878	blood:	n/a
43	chr2:38892887-38892937	GM19239	blood:	n/a
44	chr2:38892887-38892937	K562	blood:	n/a
45	chr2:38892901-38892951	SK-N-SH	brain:	n/a
46	chr2:38893237-38893287	AG09309	skin:	n/a
47	chr2:38892901-38892951	BE2_C	brain:	n/a
48	chr2:38847451-38847501	NH-A	brain:	n/a
49	chr2:38892365-38892415	HCF	heart:	n/a
50	chr2:38892365-38892415	A549	lung:	n/a

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:38844900..38847632-chr2:38892837..38895832,2	K562	blood:
2	chr2:38857535..38860181-chr2:38880883..38883565,2	K562	blood:
3	chr2:38823810..38825373-chr2:38867072..38871026,3	K562	blood:
4	chr2:38827420..38830831-chr2:38879840..38883102,4	K562	blood:
5	chr2:38856981..38859644-chr2:38870744..38873095,2	K562	blood:
6	chr2:38838640..38841229-chr2:38869315..38872620,3	K562	blood:
7	chr2:38826349..38827886-chr2:38868902..38871204,2	K562	blood:
8	chr2:38828087..38831042-chr2:38842947..38845050,2	MCF-7	breast:
9	chr2:38876173..38878521-chr2:38919650..38921533,2	MCF-7	breast:
10	chr2:38828271..38831581-chr2:38848960..38853344,4	K562	blood:
11	chr2:38829011..38830871-chr2:38864426..38867339,2	MCF-7	breast:
12	chr2:38850355..38852366-chr2:38854447..38858679,3	K562	blood:
13	chr2:38861872..38863650-chr2:38976891..38979789,2	K562	blood:
14	chr2:38862386..38864039-chr2:38870726..38872820,2	K562	blood:
15	chr2:38850355..38852366-chr2:38854447..38858679,3	K562	blood:
16	chr2:38818005..38820191-chr2:38893287..38895221,2	K562	blood:
17	chr2:38887947..38890064-chr2:38891296..38894559,3	K562	blood:
18	chr2:38842870..38845739-chr2:38968254..38970613,2	K562	blood:
19	chr2:38862386..38864039-chr2:38870726..38872820,2	K562	blood:
20	chr2:38884843..38887789-chr2:38891442..38893148,3	K562	blood:
21	chr2:38829210..38832278-chr2:38859055..38864456,6	K562	blood:
22	chr2:38830024..38832660-chr2:38864551..38867364,2	K562	blood:
23	chr2:38828302..38829916-chr2:38889127..38891080,2	K562	blood:
24	chr2:38869520..38871191-chr2:38897792..38900773,2	K562	blood:
25	chr2:38892007..38895113-chr2:38976994..38979857,4	K562	blood:
26	chr2:38826787..38828390-chr2:38864612..38866971,2	K562	blood:
27	chr2:38852070..38854007-chr2:38978194..38979843,2	MCF-7	breast:
28	chr2:38881069..38883433-chr2:38890460..38892656,2	K562	blood:
29	chr2:38885587..38887853-chr2:38899789..38902113,2	K562	blood:
30	chr2:38868989..38871119-chr2:38916647..38918525,3	K562	blood:
31	chr2:38841845..38846119-chr2:38859783..38862280,3	K562	blood:
32	chr2:38846799..38849062-chr2:38862889..38864827,2	K562	blood:
33	chr2:38884282..38886148-chr2:38894534..38896833,2	K562	blood:
34	chr2:38838600..38841339-chr2:38925326..38927602,2	K562	blood:
35	chr2:38857535..38860181-chr2:38880883..38883565,2	K562	blood:
36	chr2:38831260..38832784-chr2:38845014..38847198,2	MCF-7	breast:
37	chr2:38837653..38839575-chr2:38845023..38848760,3	MCF-7	breast:
38	chr2:38888499..38891196-chr2:38892046..38897483,5	K562	blood:
39	chr2:38826731..38830931-chr2:38855127..38860520,4	MCF-7	breast:
40	chr2:38891821..38893324-chr2:38896247..38899182,2	K562	blood:
41	chr2:38841845..38846119-chr2:38859783..38862280,3	K562	blood:
42	chr2:38827470..38830831-chr2:38880188..38882467,3	K562	blood:
43	chr2:38826787..38832652-chr2:38859055..38867252,11	K562	blood:
44	chr2:38845035..38846915-chr2:38976457..38978947,3	K562	blood:
45	chr2:38866346..38869051-chr2:38869593..38871787,4	K562	blood:
46	chr2:38822264..38824489-chr2:38870337..38872562,2	K562	blood:
47	chr2:38880141..38882510-chr2:38904571..38906681,2	K562	blood:
48	chr2:38861742..38863889-chr2:38865469..38867826,3	K562	blood:
49	chr2:38827906..38831148-chr2:38849873..38855053,6	K562	blood:
50	chr2:38841845..38843703-chr2:38858739..38861283,2	K562	blood:

No data

Variant related genes	Relation type
GALM	TF binding region
GALM	CpG island
ENSG00000152147	chromatin interactions
ENSG00000143889	chromatin interactions
ENSG00000235586	chromatin interactions
ENSG00000143891	chromatin interactions
ENSG00000115875	chromatin interactions
ENSG00000232518	chromatin interactions

Extended variants
information (count: 2613 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2613 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372139	chr2:38839323-38839324	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs72907929	chr2:38839339-38839340	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs145239182	chr2:38839352-38839353	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs75432923	chr2:38839372-38839373	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs137857684	chr2:38839396-38839397	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs568545633	chr2:38839440-38839441	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs76960027	chr2:38839444-38839445	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs149114034	chr2:38839455-38839456	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs115285058	chr2:38839463-38839464	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs187357529	chr2:38839480-38839481	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs558448018	chr2:38839491-38839492	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs576628246	chr2:38839511-38839512	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs73929101	chr2:38839528-38839529	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs555014473	chr2:38839531-38839532	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs565115004	chr2:38839545-38839546	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs13011896	chr2:38839569-38839570	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs552632905	chr2:38839572-38839573	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs536710437	chr2:38839574-38839575	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs143165722	chr2:38839598-38839599	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs527536933	chr2:38839599-38839600	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs576509845	chr2:38839617-38839618	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs192786005	chr2:38839660-38839661	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs563610330	chr2:38839663-38839664	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs537245947	chr2:38839772-38839773	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs111473337	chr2:38839808-38839809	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs542905869	chr2:38839937-38839938	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs561983228	chr2:38839980-38839981	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs184920848	chr2:38840026-38840027	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs529292155	chr2:38840049-38840050	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs6710613	chr2:38840068-38840069	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs189381946	chr2:38840076-38840077	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs192757182	chr2:38840079-38840080	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs184165079	chr2:38840098-38840099	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs189592708	chr2:38840149-38840150	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs537388637	chr2:38840159-38840160	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs181845384	chr2:38840187-38840188	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs570028496	chr2:38840189-38840190	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs566956237	chr2:38840202-38840203	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs79123424	chr2:38840206-38840207	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs552671574	chr2:38840224-38840225	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs577283425	chr2:38840230-38840231	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs545192807	chr2:38840271-38840272	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs556923157	chr2:38840286-38840287	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs575387669	chr2:38840322-38840323	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs577080934	chr2:38840323-38840324	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs17022967	chr2:38840339-38840340	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs371066751	chr2:38840418-38840419	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs561146584	chr2:38840427-38840428	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs368071792	chr2:38840493-38840494	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs531094443	chr2:38840562-38840563	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 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
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	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
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	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
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Colorectal cancer	16272173	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:965 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:38831200-38840400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:38831200-38840600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:38831400-38840000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr2:38831400-38840800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr2:38832800-38839400	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr2:38835200-38839400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr2:38835200-38840000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr2:38835200-38840000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr2:38835200-38840000	Weak transcription	NHLF	lung
10	chr2:38835200-38840400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr2:38835200-38843400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr2:38835400-38842000	Weak transcription	HMEC	breast
13	chr2:38835400-38842200	Weak transcription	NHEK	skin
14	chr2:38835400-38843400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr2:38835400-38862400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr2:38837800-38839800	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr2:38837800-38842400	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr2:38838200-38840200	Enhancers	Primary T cells fromperipheralblood	blood
19	chr2:38838600-38840600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr2:38838600-38840600	Enhancers	K562	blood
21	chr2:38838600-38842200	Enhancers	Stomach Mucosa	stomach
22	chr2:38838600-38845000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr2:38838800-38840000	Weak transcription	Duodenum Mucosa	Duodenum
24	chr2:38839000-38839800	Weak transcription	Lung	lung
25	chr2:38839000-38839800	Weak transcription	HSMMtube	muscle
26	chr2:38839000-38839800	Weak transcription	Osteobl	bone
27	chr2:38839000-38840000	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr2:38839000-38840200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr2:38839000-38842000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr2:38839000-38847200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr2:38839200-38839600	Weak transcription	HSMM	muscle
32	chr2:38839200-38839800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr2:38839200-38840200	Enhancers	GM12878-XiMat	blood
34	chr2:38839200-38841800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr2:38839200-38842600	Enhancers	HepG2	liver
36	chr2:38839400-38839800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr2:38839400-38841200	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr2:38839400-38842200	Enhancers	Primary hematopoietic stem cells	blood
39	chr2:38839600-38840200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr2:38839600-38841000	Enhancers	HSMM	muscle
41	chr2:38839600-38841400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr2:38839800-38840000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
43	chr2:38839800-38840000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr2:38839800-38840000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr2:38839800-38840000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
46	chr2:38839800-38840000	Enhancers	Adipose Nuclei	Adipose
47	chr2:38839800-38840000	Enhancers	Lung	lung
48	chr2:38839800-38840400	Enhancers	Osteobl	bone
49	chr2:38839800-38840600	Enhancers	NHDF-Ad	bronchial
50	chr2:38839800-38841000	Enhancers	HSMMtube	muscle

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