Variant report

Variant	nsv873778
Chromosome Location	chr2:32297984-32409007
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1177)
CpG islands
(count:611)
Chromatin interactive
region (count:113)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1177 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:32360552-32360797	K562	blood:	n/a	n/a
2	ARID3A	chr2:32390529-32391251	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:32390598-32391244	K562	blood:	n/a	n/a
4	ARID3A	chr2:32392464-32392760	K562	blood:	n/a	n/a
5	ARID3A	chr2:32389782-32389936	K562	blood:	n/a	n/a
6	ARID3A	chr2:32393621-32394178	K562	blood:	n/a	n/a
7	ARID3A	chr2:32360503-32360792	HepG2	liver:	n/a	n/a
8	ATF1	chr2:32390651-32391070	K562	blood:	n/a	n/a
9	ATF2	chr2:32390618-32391071	GM12878	blood:	n/a	n/a
10	ATF2	chr2:32390497-32390875	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr2:32390433-32391263	GM12878	blood:	n/a	n/a
12	ATF2	chr2:32390517-32391098	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr2:32360364-32360955	A549	lung:	n/a	n/a
14	ATF3	chr2:32390421-32391132	A549	lung:	n/a	n/a
15	ATF3	chr2:32390403-32391347	A549	lung:	n/a	n/a
16	ATF3	chr2:32397983-32398246	K562	blood:	n/a	n/a
17	ATF3	chr2:32360411-32360813	K562	blood:	n/a	n/a
18	BACH1	chr2:32391979-32392030	K562	blood:	n/a	n/a
19	BACH1	chr2:32389737-32389990	K562	blood:	n/a	n/a
20	BACH1	chr2:32391093-32391254	K562	blood:	n/a	n/a
21	BACH1	chr2:32390650-32391341	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr2:32310696-32310874	GM12878	blood:	n/a	n/a
23	BATF	chr2:32393573-32393937	GM12878	blood:	n/a	n/a
24	BATF	chr2:32390571-32390976	GM12878	blood:	n/a	n/a
25	BATF	chr2:32347277-32347502	GM12878	blood:	n/a	n/a
26	BATF	chr2:32393529-32393893	GM12878	blood:	n/a	n/a
27	BCL11A	chr2:32393546-32393929	GM12878	blood:	n/a	chr2:32393681-32393690
28	BCL3	chr2:32390413-32391403	A549	lung:	n/a	chr2:32390948-32390956
29	BCL3	chr2:32390636-32391175	GM12878	blood:	n/a	chr2:32390948-32390956
30	BCL3	chr2:32390387-32391574	A549	lung:	n/a	chr2:32390948-32390956
31	BCLAF1	chr2:32390415-32391205	K562	blood:	n/a	chr2:32390948-32390956
32	BCLAF1	chr2:32390437-32391295	GM12878	blood:	n/a	chr2:32390948-32390956
33	BCLAF1	chr2:32390501-32391336	GM12878	blood:	n/a	chr2:32390948-32390956
34	BCLAF1	chr2:32390429-32391412	K562	blood:	n/a	chr2:32390948-32390956
35	BCLAF1	chr2:32393509-32393876	GM12878	blood:	n/a	chr2:32393681-32393690
36	BHLHE40	chr2:32393691-32393966	K562	blood:	n/a	n/a
37	BHLHE40	chr2:32391572-32391712	GM12878	blood:	n/a	n/a
38	BHLHE40	chr2:32390575-32391190	HepG2	liver:	n/a	n/a
39	BHLHE40	chr2:32390556-32391689	K562	blood:	n/a	n/a
40	BHLHE40	chr2:32390520-32391173	GM12878	blood:	n/a	n/a
41	BRCA1	chr2:32390621-32391028	HepG2	liver:	n/a	n/a
42	BRCA1	chr2:32390598-32391441	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr2:32390578-32391196	H1-hESC	embryonic stem cell:	n/a	n/a
44	CBX3	chr2:32393663-32394072	K562	blood:	n/a	n/a
45	CBX3	chr2:32392334-32393217	K562	blood:	n/a	n/a
46	CBX3	chr2:32384802-32385274	K562	blood:	n/a	n/a
47	CBX3	chr2:32331394-32331669	K562	blood:	n/a	n/a
48	CBX3	chr2:32390359-32391179	K562	blood:	n/a	n/a
49	CBX3	chr2:32390170-32391291	K562	blood:	n/a	n/a
50	CCNT2	chr2:32393666-32393873	K562	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:32386706-32386756	Jurkat	blood:	n/a
2	chr2:32386706-32386756	Jurkat	blood:	n/a
3	chr2:32390673-32390723	HEEpiC	esophagus:	n/a
4	chr2:32394762-32394812	NB4	blood:	n/a
5	chr2:32381397-32381447	U87	brain:	n/a
6	chr2:32390678-32390728	T-47D	breast:	n/a
7	chr2:32394762-32394812	SAEC	small airway:	n/a
8	chr2:32394762-32394812	MCF10A-Er-Src	breast:	n/a
9	chr2:32390791-32390841	AG09319	gingival:	n/a
10	chr2:32390937-32390987	PANC-1	pancreas:	n/a
11	chr2:32390673-32390723	BJ	skin:	n/a
12	chr2:32390678-32390728	IMR90	lung:	fetal
13	chr2:32381397-32381447	HCT-116	colon:	n/a
14	chr2:32391091-32391141	SK-N-MC	brain:	n/a
15	chr2:32390924-32390974	SKMC	muscle:	n/a
16	chr2:32391091-32391141	HRCEpiC	kidney:	n/a
17	chr2:32390678-32390728	HPAEpiC	pulmonary alveolar:	n/a
18	chr2:32394762-32394812	HepG2	liver:	n/a
19	chr2:32390791-32390841	BJ	skin:	n/a
20	chr2:32390924-32390974	GM12878	blood:	n/a
21	chr2:32381397-32381447	NB4	blood:	n/a
22	chr2:32390673-32390723	GM12878	blood:	n/a
23	chr2:32390937-32390987	HEK293	kidney:	embryo
24	chr2:32381397-32381447	GM12892	blood:	n/a
25	chr2:32390791-32390841	NB4	blood:	n/a
26	chr2:32390937-32390987	SK-N-SH	brain:	n/a
27	chr2:32390937-32390987	ECC-1	luminal epithelium:	n/a
28	chr2:32390924-32390974	AG09319	gingival:	n/a
29	chr2:32390673-32390723	LNCaP	prostate:	n/a
30	chr2:32390678-32390728	U87	brain:	n/a
31	chr2:32386706-32386756	BE2_C	brain:	n/a
32	chr2:32394762-32394812	AG10803	skin:	n/a
33	chr2:32386706-32386756	SK-N-MC	brain:	n/a
34	chr2:32390924-32390974	HAEpiC	amniotic membrane:	n/a
35	chr2:32386706-32386756	PANC-1	pancreas:	n/a
36	chr2:32391091-32391141	H1-hESC	embryonic stem cell:	embryo
37	chr2:32381397-32381447	K562	blood:	n/a
38	chr2:32391091-32391141	AG10803	skin:	n/a
39	chr2:32394762-32394812	NT2-D1	testis:	n/a
40	chr2:32386706-32386756	Hela-S3	cervix:	n/a
41	chr2:32390791-32390841	HCM	heart:	n/a
42	chr2:32390924-32390974	PANC-1	pancreas:	n/a
43	chr2:32381397-32381447	HIPEpiC	eye:	n/a
44	chr2:32386706-32386756	HEEpiC	esophagus:	n/a
45	chr2:32390791-32390841	CMK	blood:	n/a
46	chr2:32390678-32390728	CMK	blood:	n/a
47	chr2:32381397-32381447	PANC-1	pancreas:	n/a
48	chr2:32386706-32386756	Hepatocyte	liver:	n/a
49	chr2:32391035-32391085	PANC-1	pancreas:	n/a
50	chr2:32390937-32390987	HCPEpiC	choroid plexus:	n/a

(count:113 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:32288016..32290061-chr2:32304327..32306371,3	MCF-7	breast:
2	chr2:32236441..32237946-chr2:32298713..32301695,2	K562	blood:
3	chr2:32390281..32391012-chr9:96213301..96214069,2	Hela-S3	cervix:
4	chr2:27434377..27435229-chr2:32390388..32391013,2	Hela-S3	cervix:
5	chr2:32241277..32243768-chr2:32387990..32389632,2	K562	blood:
6	chr2:32393475..32396085-chr2:32440047..32443005,2	K562	blood:
7	chr2:32296316..32299145-chr2:32301569..32303768,2	K562	blood:
8	chr2:32347290..32350052-chr2:32351484..32354177,3	K562	blood:
9	chr2:32389277..32392458-chr2:32500839..32506003,6	K562	blood:
10	chr2:32112402..32115115-chr2:32387877..32390821,4	K562	blood:
11	chr2:32404294..32406231-chr2:32406780..32408474,2	K562	blood:
12	chr2:32391365..32393354-chr2:32406873..32408474,2	K562	blood:
13	chr2:32368464..32370560-chr2:32386203..32388440,2	K562	blood:
14	chr2:32405594..32407741-chr2:32408500..32410420,2	K562	blood:
15	chr2:32362766..32364698-chr2:32390702..32392991,2	K562	blood:
16	chr2:32107600..32109917-chr2:32388289..32390102,3	K562	blood:
17	chr2:32232439..32235784-chr2:32380849..32383379,3	K562	blood:
18	chr2:32368107..32369829-chr2:32378343..32381333,2	K562	blood:
19	chr2:32347290..32350643-chr2:32351484..32354177,5	K562	blood:
20	chr2:32389694..32394396-chr2:32399001..32405946,7	MCF-7	breast:
21	chr2:32294649..32296576-chr2:32297962..32299990,3	K562	blood:
22	chr2:32397197..32398862-chr2:32406291..32408481,2	K562	blood:
23	chr2:32309929..32311662-chr2:32314588..32316321,2	K562	blood:
24	chr2:32299913..32303134-chr2:32303836..32306094,3	MCF-7	breast:
25	chr2:32234641..32236375-chr2:32389314..32391737,5	MCF-7	breast:
26	chr2:32338831..32341439-chr2:32391344..32393556,2	K562	blood:
27	chr2:32368107..32369829-chr2:32378343..32381333,2	K562	blood:
28	chr2:32347290..32350052-chr2:32351484..32354177,3	K562	blood:
29	chr2:32113177..32115838-chr2:32349330..32352082,2	K562	blood:
30	chr2:32347290..32350643-chr2:32351484..32354177,5	K562	blood:
31	chr2:32233185..32238105-chr2:32388775..32395245,11	K562	blood:
32	chr2:32295719..32297694-chr2:32389118..32390763,2	K562	blood:
33	chr2:32338831..32341439-chr2:32391344..32393556,2	K562	blood:
34	chr2:32286904..32290628-chr2:32293788..32299321,9	MCF-7	breast:
35	chr2:32351379..32353037-chr2:32389504..32392021,2	K562	blood:
36	chr2:32296316..32299145-chr2:32301569..32303768,2	K562	blood:
37	chr2:32397197..32398862-chr2:32406291..32408481,2	K562	blood:
38	chr2:32388347..32391315-chr6:27100140..27102328,2	MCF-7	breast:
39	chr2:32264101..32266985-chr2:32387828..32391332,6	K562	blood:
40	chr2:32382124..32388019-chr2:32388107..32392393,6	MCF-7	breast:
41	chr2:32287339..32289467-chr2:32389793..32392170,2	MCF-7	breast:
42	chr2:32299913..32303134-chr2:32303836..32306094,3	MCF-7	breast:
43	chr2:32314303..32316677-chr2:32317500..32319718,2	K562	blood:
44	chr2:32349609..32353037-chr2:32390063..32392021,3	K562	blood:
45	chr2:32401110..32403653-chr2:32405850..32408293,2	K562	blood:
46	chr2:32389583..32392652-chr2:32503120..32506003,3	K562	blood:
47	chr2:32263395..32265602-chr2:32389530..32391691,2	MCF-7	breast:
48	chr13:111365513..111366041-chr2:32390122..32390862,2	Hela-S3	cervix:
49	chr2:32296494..32298709-chr2:32308097..32310088,3	K562	blood:
50	chr2:32401411..32403653-chr2:32405930..32408293,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NLRC4-3	chr2:32390115-32390826	ENSG00000272716.1
2	lnc-NLRC4-3	chr2:32390542-32390783	NONHSAT069968

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SPAST	hsa-miR-132-3p	chr2:32380354-32380375
2	SPAST	hsa-miR-132-3p	chr2:32380368-32380375

Variant related genes	Relation type
ENSG00000263802	TF binding region
ENSG00000272716	TF binding region
SLC30A6	TF binding region
ENSG00000263802	CpG island
ENSG00000272716	CpG island
SLC30A6	CpG island
ENSG00000184557	chromatin interactions
ENSG00000115760	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000123472	chromatin interactions
ENSG00000124635	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000091106	chromatin interactions
ENSG00000188938	chromatin interactions
ENSG00000162959	chromatin interactions
ENSG00000272716	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000138085	chromatin interactions
ENSG00000048828	chromatin interactions
ENSG00000100462	chromatin interactions
ENSG00000152683	chromatin interactions
ENSG00000138074	chromatin interactions
ENSG00000169710	chromatin interactions
ENSG00000162961	chromatin interactions
ENSG00000230046	chromatin interactions
ENSG00000119820	chromatin interactions
ENSG00000021574	chromatin interactions
ENSG00000173894	chromatin interactions

Extended variants
information (count: 4688 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:4688 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10084280	chr2:32297984-32297985	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535793949	chr2:32298020-32298021	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs538986554	chr2:32298030-32298031	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs575899591	chr2:32298036-32298037	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs17011801	chr2:32298072-32298073	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs141231755	chr2:32298077-32298078	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs538478780	chr2:32298087-32298088	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs147406809	chr2:32298091-32298092	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs578163798	chr2:32298099-32298100	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs75983502	chr2:32298150-32298151	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs34899667	chr2:32298151-32298152	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs540605259	chr2:32298156-32298157	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs386389861	chr2:32298158-32298159	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs397688843	chr2:32298160-32298161	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs113080319	chr2:32298273-32298274	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs372293791	chr2:32298307-32298308	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs573046828	chr2:32298342-32298343	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs139728227	chr2:32298382-32298383	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs113491435	chr2:32298389-32298390	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs530616664	chr2:32298432-32298433	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs180796799	chr2:32298454-32298455	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs374648074	chr2:32298466-32298467	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs34050087	chr2:32298493-32298494	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs145308019	chr2:32298530-32298531	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs376400812	chr2:32298533-32298534	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs532902564	chr2:32298565-32298566	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs75732934	chr2:32298571-32298572	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs566345839	chr2:32298580-32298581	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs185416663	chr2:32298599-32298600	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188365543	chr2:32298611-32298612	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs116039450	chr2:32298638-32298639	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs181145445	chr2:32298658-32298659	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs558422815	chr2:32298717-32298718	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs369675678	chr2:32298721-32298722	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs534038527	chr2:32298729-32298730	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs554096572	chr2:32298734-32298735	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs573942512	chr2:32298760-32298761	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs559558176	chr2:32298771-32298772	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs555223002	chr2:32298779-32298780	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs147870696	chr2:32298791-32298792	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs543970801	chr2:32298800-32298801	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs530241391	chr2:32298819-32298820	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs563963546	chr2:32298850-32298851	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs548658380	chr2:32298994-32298995	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs539959809	chr2:32299052-32299053	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs560232519	chr2:32299113-32299114	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs576346351	chr2:32299175-32299176	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs549027516	chr2:32299246-32299247	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs139235518	chr2:32299269-32299270	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs532059215	chr2:32299277-32299278	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Neurocytoma	17123091	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2581 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:32289600-32330800	Weak transcription	Spleen	Spleen
2	chr2:32289800-32298400	Weak transcription	Small Intestine	intestine
3	chr2:32289800-32304000	Weak transcription	Ovary	ovary
4	chr2:32289800-32313800	Weak transcription	Stomach Smooth Muscle	stomach
5	chr2:32289800-32314600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr2:32289800-32315800	Weak transcription	Colon Smooth Muscle	Colon
7	chr2:32289800-32319400	Weak transcription	Aorta	Aorta
8	chr2:32289800-32319400	Weak transcription	Pancreas	Pancrea
9	chr2:32289800-32330800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr2:32290000-32299600	Weak transcription	Thymus	Thymus
11	chr2:32290000-32315800	Weak transcription	Fetal Kidney	kidney
12	chr2:32290000-32315800	Weak transcription	HSMM	muscle
13	chr2:32290000-32316600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr2:32290000-32318600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr2:32290200-32313800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr2:32290200-32330800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr2:32290400-32298200	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr2:32290400-32304000	Weak transcription	Adipose Nuclei	Adipose
19	chr2:32290400-32313400	Weak transcription	Fetal Thymus	thymus
20	chr2:32290400-32313800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr2:32290400-32315000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr2:32290400-32315000	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr2:32290400-32315000	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr2:32290400-32331000	Weak transcription	Rectal Smooth Muscle	rectum
25	chr2:32290400-32353400	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr2:32290600-32314800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr2:32290600-32330800	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr2:32290800-32299000	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr2:32290800-32313600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr2:32290800-32313800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr2:32290800-32317200	Weak transcription	Brain Hippocampus Middle	brain
32	chr2:32290800-32330200	Weak transcription	Primary hematopoietic stem cells	blood
33	chr2:32291000-32298400	Weak transcription	Primary T cells from cord blood	blood
34	chr2:32291000-32299000	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr2:32291000-32301600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:32291000-32304200	Weak transcription	GM12878-XiMat	blood
37	chr2:32291000-32314800	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr2:32291000-32330400	Weak transcription	Brain Anterior Caudate	brain
39	chr2:32291000-32330800	Weak transcription	Brain Angular Gyrus	brain
40	chr2:32291000-32332600	Weak transcription	A549	lung
41	chr2:32291200-32301200	Weak transcription	HMEC	breast
42	chr2:32291400-32298000	Weak transcription	HepG2	liver
43	chr2:32291400-32299000	Weak transcription	Duodenum Mucosa	Duodenum
44	chr2:32291400-32327600	Weak transcription	Hela-S3	cervix
45	chr2:32291400-32331000	Weak transcription	Brain Cingulate Gyrus	brain
46	chr2:32291600-32322000	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr2:32291600-32330800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr2:32291600-32330800	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr2:32291600-32332200	Weak transcription	HUVEC	blood vessel
50	chr2:32291800-32313200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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