Variant report

Variant	nsv833670
Chromosome Location	chr2:32295778-32481857
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1645)
CpG islands
(count:855)
Chromatin interactive
region (count:174)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1645 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:32393621-32394178	K562	blood:	n/a	n/a
2	ARID3A	chr2:32360552-32360797	K562	blood:	n/a	n/a
3	ARID3A	chr2:32360503-32360792	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:32457044-32457343	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:32392464-32392760	K562	blood:	n/a	n/a
6	ARID3A	chr2:32390529-32391251	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:32475495-32475784	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:32390598-32391244	K562	blood:	n/a	n/a
9	ARID3A	chr2:32389782-32389936	K562	blood:	n/a	n/a
10	ATF1	chr2:32390651-32391070	K562	blood:	n/a	n/a
11	ATF2	chr2:32390618-32391071	GM12878	blood:	n/a	n/a
12	ATF2	chr2:32390497-32390875	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr2:32390517-32391098	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr2:32390433-32391263	GM12878	blood:	n/a	n/a
15	ATF2	chr2:32414742-32415251	GM12878	blood:	n/a	n/a
16	ATF2	chr2:32414734-32415268	GM12878	blood:	n/a	n/a
17	ATF3	chr2:32397983-32398246	K562	blood:	n/a	n/a
18	ATF3	chr2:32360364-32360955	A549	lung:	n/a	n/a
19	ATF3	chr2:32390403-32391347	A549	lung:	n/a	n/a
20	ATF3	chr2:32390421-32391132	A549	lung:	n/a	n/a
21	ATF3	chr2:32360411-32360813	K562	blood:	n/a	n/a
22	BACH1	chr2:32391979-32392030	K562	blood:	n/a	n/a
23	BACH1	chr2:32391093-32391254	K562	blood:	n/a	n/a
24	BACH1	chr2:32389737-32389990	K562	blood:	n/a	n/a
25	BACH1	chr2:32390650-32391341	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr2:32414876-32415227	GM12878	blood:	n/a	n/a
27	BATF	chr2:32414676-32415451	GM12878	blood:	n/a	n/a
28	BATF	chr2:32347277-32347502	GM12878	blood:	n/a	n/a
29	BATF	chr2:32310696-32310874	GM12878	blood:	n/a	n/a
30	BATF	chr2:32393573-32393937	GM12878	blood:	n/a	n/a
31	BATF	chr2:32390571-32390976	GM12878	blood:	n/a	n/a
32	BATF	chr2:32393529-32393893	GM12878	blood:	n/a	n/a
33	BCL11A	chr2:32414740-32415480	GM12878	blood:	n/a	n/a
34	BCL11A	chr2:32414792-32415134	GM12878	blood:	n/a	n/a
35	BCL11A	chr2:32393546-32393929	GM12878	blood:	n/a	chr2:32393681-32393690
36	BCL3	chr2:32390413-32391403	A549	lung:	n/a	chr2:32390948-32390956
37	BCL3	chr2:32390636-32391175	GM12878	blood:	n/a	chr2:32390948-32390956
38	BCL3	chr2:32390387-32391574	A549	lung:	n/a	chr2:32390948-32390956
39	BCLAF1	chr2:32390415-32391205	K562	blood:	n/a	chr2:32390948-32390956
40	BCLAF1	chr2:32390501-32391336	GM12878	blood:	n/a	chr2:32390948-32390956
41	BCLAF1	chr2:32393509-32393876	GM12878	blood:	n/a	chr2:32393681-32393690
42	BCLAF1	chr2:32390437-32391295	GM12878	blood:	n/a	chr2:32390948-32390956
43	BCLAF1	chr2:32390429-32391412	K562	blood:	n/a	chr2:32390948-32390956
44	BCLAF1	chr2:32414663-32415276	GM12878	blood:	n/a	n/a
45	BHLHE40	chr2:32390575-32391190	HepG2	liver:	n/a	n/a
46	BHLHE40	chr2:32390556-32391689	K562	blood:	n/a	n/a
47	BHLHE40	chr2:32455336-32455552	HepG2	liver:	n/a	n/a
48	BHLHE40	chr2:32414817-32415252	GM12878	blood:	n/a	n/a
49	BHLHE40	chr2:32390520-32391173	GM12878	blood:	n/a	n/a
50	BHLHE40	chr2:32455457-32455536	K562	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:32381397-32381447	AG04449	skin:	fetal
2	chr2:32381397-32381447	AG04449	skin:	fetal
3	chr2:32391091-32391141	GM12878	blood:	n/a
4	chr2:32381397-32381447	PrEC	prostate:	n/a
5	chr2:32449528-32449578	HCM	heart:	n/a
6	chr2:32391035-32391085	SAEC	small airway:	n/a
7	chr2:32390678-32390728	AG09319	gingival:	n/a
8	chr2:32391035-32391085	GM06990	blood:	n/a
9	chr2:32390924-32390974	AG04449	skin:	fetal
10	chr2:32386706-32386756	AG09309	skin:	n/a
11	chr2:32386706-32386756	AG09319	gingival:	n/a
12	chr2:32381397-32381447	Hela-S3	cervix:	n/a
13	chr2:32386706-32386756	PFSK-1	brain:	n/a
14	chr2:32446172-32446222	ovcar-3	ovarian:	n/a
15	chr2:32391091-32391141	NHBE	bronchial:	n/a
16	chr2:32381397-32381447	K562	blood:	n/a
17	chr2:32391091-32391141	HepG2	liver:	n/a
18	chr2:32391035-32391085	HepG2	liver:	n/a
19	chr2:32390937-32390987	GM12891	blood:	n/a
20	chr2:32390673-32390723	SAEC	small airway:	n/a
21	chr2:32446172-32446222	LNCaP	prostate:	n/a
22	chr2:32464513-32464563	K562	blood:	n/a
23	chr2:32449528-32449578	GM06990	blood:	n/a
24	chr2:32391035-32391085	Caco-2	colon:	n/a
25	chr2:32390791-32390841	H1-hESC	embryonic stem cell:	embryo
26	chr2:32390791-32390841	NHDF-neo	bronchial:	n/a
27	chr2:32391035-32391085	PFSK-1	brain:	n/a
28	chr2:32390924-32390974	SK-N-MC	brain:	n/a
29	chr2:32391035-32391085	H1-hESC	embryonic stem cell:	embryo
30	chr2:32394762-32394812	Hela-S3	cervix:	n/a
31	chr2:32446172-32446222	NT2-D1	testis:	n/a
32	chr2:32390673-32390723	SK-N-MC	brain:	n/a
33	chr2:32391035-32391085	NB4	blood:	n/a
34	chr2:32446172-32446222	AG09309	skin:	n/a
35	chr2:32390678-32390728	HPAEpiC	pulmonary alveolar:	n/a
36	chr2:32394762-32394812	GM19239	blood:	n/a
37	chr2:32381397-32381447	U87	brain:	n/a
38	chr2:32390673-32390723	HCT-116	colon:	n/a
39	chr2:32446172-32446222	HEK293	kidney:	embryo
40	chr2:32381397-32381447	RPTEC	kidney:	n/a
41	chr2:32386706-32386756	GM12892	blood:	n/a
42	chr2:32394762-32394812	IMR90	lung:	fetal
43	chr2:32391091-32391141	HCPEpiC	choroid plexus:	n/a
44	chr2:32390673-32390723	NHBE	bronchial:	n/a
45	chr2:32381397-32381447	SK-N-MC	brain:	n/a
46	chr2:32386706-32386756	HIPEpiC	eye:	n/a
47	chr2:32464513-32464563	AoSMC	blood vessel:	n/a
48	chr2:32465387-32465437	HRPEpiC	eye:	n/a
49	chr2:32390924-32390974	ECC-1	luminal epithelium:	n/a
50	chr2:32390791-32390841	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:32351514..32353019-chr2:32390044..32392430,2	MCF-7	breast:
2	chr2:32264868..32267001-chr2:32389298..32391324,2	K562	blood:
3	chr2:32391365..32393354-chr2:32406873..32408474,2	K562	blood:
4	chr2:32463297..32465974-chr2:32475784..32478393,2	K562	blood:
5	chr2:32360874..32363843-chr2:32386760..32389149,2	K562	blood:
6	chr2:32234641..32236375-chr2:32389314..32391737,5	MCF-7	breast:
7	chr2:32395858..32398697-chr2:32406981..32409057,2	K562	blood:
8	chr2:32377730..32381004-chr2:32388156..32391396,4	MCF-7	breast:
9	chr2:32474270..32479271-chr2:32479320..32483848,6	K562	blood:
10	chr2:32294423..32296947-chr2:32389682..32392119,3	K562	blood:
11	chr2:32296494..32298709-chr2:32308097..32310088,3	K562	blood:
12	chr2:32390601..32392270-chr2:32450948..32453894,2	MCF-7	breast:
13	chr2:32462083..32465466-chr2:32467498..32469177,3	K562	blood:
14	chr2:32264101..32266985-chr2:32387828..32391332,6	K562	blood:
15	chr2:32456174..32459090-chr2:32459159..32461418,3	MCF-7	breast:
16	chr17:77751563..77752252-chr2:32390356..32391194,2	HCT-116	colon:
17	chr2:32469608..32472298-chr2:32474844..32477443,2	K562	blood:
18	chr2:32388440..32390986-chr2:32579691..32583834,6	K562	blood:
19	chr2:32462083..32465466-chr2:32467498..32469177,3	K562	blood:
20	chr2:32367367..32371154-chr2:32378343..32385071,6	K562	blood:
21	chr2:32474270..32479271-chr2:32479320..32483848,6	K562	blood:
22	chr2:32419509..32422064-chr2:32580659..32583571,2	K562	blood:
23	chr2:32435157..32437239-chr2:32449933..32452199,2	K562	blood:
24	chr2:32372239..32374198-chr2:32394451..32396644,2	K562	blood:
25	chr2:32365815..32368775-chr2:32370522..32372496,2	K562	blood:
26	chr2:32417565..32420186-chr2:32581197..32583774,2	MCF-7	breast:
27	chr2:32263820..32266854-chr2:32389080..32393861,5	MCF-7	breast:
28	chr2:32394761..32396480-chr2:32583676..32585697,2	K562	blood:
29	chr2:32233185..32238105-chr2:32388775..32395245,11	K562	blood:
30	chr2:32286352..32290626-chr2:32388602..32393371,12	K562	blood:
31	chr2:32347290..32350052-chr2:32351484..32354177,3	K562	blood:
32	chr2:27434377..27435229-chr2:32390388..32391013,2	Hela-S3	cervix:
33	chr1:47133479..47134274-chr2:32390536..32391142,2	HCT-116	colon:
34	chr2:32368107..32369829-chr2:32378343..32381333,2	K562	blood:
35	chr2:32445227..32449129-chr2:32451328..32453997,4	K562	blood:
36	chr2:32397197..32398862-chr2:32406291..32408481,2	K562	blood:
37	chr2:32425954..32428808-chr2:32433525..32435175,2	K562	blood:
38	chr2:32443634..32446548-chr2:32446914..32449802,2	K562	blood:
39	chr2:32388347..32391315-chr6:27100140..27102328,2	MCF-7	breast:
40	chr2:32372239..32374198-chr2:32394451..32396644,2	K562	blood:
41	chr2:32389104..32394341-chr2:32415587..32422183,9	K562	blood:
42	chr2:32107600..32109917-chr2:32388289..32390102,3	K562	blood:
43	chr2:32394949..32397744-chr2:32404684..32406566,2	MCF-7	breast:
44	chr2:32459736..32462357-chr2:32463296..32464848,2	K562	blood:
45	chr2:32456174..32459090-chr2:32459159..32461418,3	MCF-7	breast:
46	chr2:32314303..32316677-chr2:32317500..32319718,2	K562	blood:
47	chr2:32450716..32453123-chr2:32453250..32456033,3	MCF-7	breast:
48	chr2:32388385..32389940-chr2:32579717..32581806,2	K562	blood:
49	chr13:111365513..111366041-chr2:32390122..32390862,2	Hela-S3	cervix:
50	chr2:32465425..32467029-chr2:32470034..32472157,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NLRC4-3	chr2:32390115-32390826	ENSG00000272716.1
2	lnc-SPAST-1	chr2:32426669-32429068	NONHSAT069969
3	lnc-NLRC4-2	chr2:32435291-32436600	ncRnaDb_ncrna_FR119451_1
4	lnc-NLRC4-3	chr2:32390542-32390783	NONHSAT069968

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	SLC30A6	hsa-miR-196a-5p	chr2:32448664-32448670
2	SPAST	hsa-miR-132-3p	chr2:32380354-32380375
3	SPAST	hsa-miR-132-3p	chr2:32380368-32380375
4	SLC30A6	hsa-let-7d-5p	chr2:32448665-32448672

Variant related genes	Relation type
ENSG00000263802	TF binding region
ENSG00000272716	TF binding region
RNU6-647P	TF binding region
SLC30A6	TF binding region
DDX50P1	TF binding region
ENSG00000263802	CpG island
ENSG00000272716	CpG island
RNU6-647P	CpG island
SLC30A6	CpG island
DDX50P1	CpG island
ENSG00000123472	chromatin interactions
ENSG00000184557	chromatin interactions
ENSG00000169710	chromatin interactions
ENSG00000138074	chromatin interactions
ENSG00000119820	chromatin interactions
ENSG00000124635	chromatin interactions
ENSG00000115760	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000091106	chromatin interactions
ENSG00000162959	chromatin interactions
ENSG00000173894	chromatin interactions
ENSG00000272716	chromatin interactions
ENSG00000230046	chromatin interactions
ENSG00000188938	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000162961	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000152683	chromatin interactions
ENSG00000021574	chromatin interactions
ENSG00000100462	chromatin interactions
ENSG00000138085	chromatin interactions
ENSG00000048828	chromatin interactions
ENSG00000229816	chromatin interactions

Extended variants
information (count: 7782 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:7782 , 50 per page) page: 1 2 3 4 5 6 7 ... 156

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567417230	chr2:32295790-32295791	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs542242707	chr2:32295791-32295792	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs370263567	chr2:32295811-32295812	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs556347253	chr2:32295838-32295839	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs372878096	chr2:32295871-32295872	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs72862257	chr2:32295880-32295881	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs114749627	chr2:32295892-32295893	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs377321188	chr2:32295918-32295919	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs572133194	chr2:32295959-32295960	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs540652874	chr2:32295975-32295976	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs560953493	chr2:32296035-32296036	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs78605745	chr2:32296039-32296040	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs113253271	chr2:32296040-32296041	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs563497189	chr2:32296052-32296053	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs141065805	chr2:32296076-32296077	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs536248465	chr2:32296088-32296089	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs10084410	chr2:32296099-32296100	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs190373721	chr2:32296117-32296118	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs78871913	chr2:32296134-32296135	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs377754020	chr2:32296147-32296148	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs183331888	chr2:32296161-32296162	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs536116637	chr2:32296171-32296172	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs550091267	chr2:32296190-32296191	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs374729686	chr2:32296205-32296206	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs186852506	chr2:32296222-32296223	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs191642582	chr2:32296243-32296244	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs72862258	chr2:32296248-32296249	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs183894622	chr2:32296250-32296251	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs188787977	chr2:32296266-32296267	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs10490360	chr2:32296268-32296269	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs543052427	chr2:32296314-32296315	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs201602478	chr2:32296321-32296322	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs563634472	chr2:32296347-32296348	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs577144780	chr2:32296354-32296355	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs545955310	chr2:32296355-32296356	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs571421090	chr2:32296379-32296380	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs150270490	chr2:32296400-32296401	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs542318645	chr2:32296412-32296413	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs374732177	chr2:32296436-32296437	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs530932345	chr2:32296508-32296509	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs368803814	chr2:32296512-32296513	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs559768038	chr2:32296669-32296670	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs191270149	chr2:32296673-32296674	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs569948140	chr2:32296720-32296721	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs532463315	chr2:32296721-32296722	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs554588943	chr2:32296736-32296737	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs552372416	chr2:32296747-32296748	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs182337551	chr2:32296751-32296752	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs372581504	chr2:32296772-32296773	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs566222116	chr2:32296782-32296783	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 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:3911 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:32289600-32330800	Weak transcription	Spleen	Spleen
2	chr2:32289800-32297000	Weak transcription	Psoas Muscle	Psoas
3	chr2:32289800-32298400	Weak transcription	Small Intestine	intestine
4	chr2:32289800-32304000	Weak transcription	Ovary	ovary
5	chr2:32289800-32313800	Weak transcription	Stomach Smooth Muscle	stomach
6	chr2:32289800-32314600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:32289800-32315800	Weak transcription	Colon Smooth Muscle	Colon
8	chr2:32289800-32319400	Weak transcription	Aorta	Aorta
9	chr2:32289800-32319400	Weak transcription	Pancreas	Pancrea
10	chr2:32289800-32330800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr2:32290000-32297400	Weak transcription	Osteobl	bone
12	chr2:32290000-32299600	Weak transcription	Thymus	Thymus
13	chr2:32290000-32315800	Weak transcription	Fetal Kidney	kidney
14	chr2:32290000-32315800	Weak transcription	HSMM	muscle
15	chr2:32290000-32316600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr2:32290000-32318600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr2:32290200-32313800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr2:32290200-32330800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr2:32290400-32297400	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr2:32290400-32298200	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr2:32290400-32304000	Weak transcription	Adipose Nuclei	Adipose
22	chr2:32290400-32313400	Weak transcription	Fetal Thymus	thymus
23	chr2:32290400-32313800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr2:32290400-32315000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr2:32290400-32315000	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr2:32290400-32315000	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr2:32290400-32331000	Weak transcription	Rectal Smooth Muscle	rectum
28	chr2:32290400-32353400	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr2:32290600-32314800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr2:32290600-32330800	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr2:32290800-32295800	Strong transcription	Fetal Stomach	stomach
32	chr2:32290800-32299000	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr2:32290800-32313600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:32290800-32313800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr2:32290800-32317200	Weak transcription	Brain Hippocampus Middle	brain
36	chr2:32290800-32330200	Weak transcription	Primary hematopoietic stem cells	blood
37	chr2:32291000-32298400	Weak transcription	Primary T cells from cord blood	blood
38	chr2:32291000-32299000	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr2:32291000-32301600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:32291000-32304200	Weak transcription	GM12878-XiMat	blood
41	chr2:32291000-32314800	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr2:32291000-32330400	Weak transcription	Brain Anterior Caudate	brain
43	chr2:32291000-32330800	Weak transcription	Brain Angular Gyrus	brain
44	chr2:32291000-32332600	Weak transcription	A549	lung
45	chr2:32291200-32301200	Weak transcription	HMEC	breast
46	chr2:32291400-32296600	Weak transcription	Fetal Intestine Large	intestine
47	chr2:32291400-32296800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr2:32291400-32297800	Weak transcription	Brain Germinal Matrix	brain
49	chr2:32291400-32298000	Weak transcription	HepG2	liver
50	chr2:32291400-32299000	Weak transcription	Duodenum Mucosa	Duodenum

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