Variant report

Variant	nsv874001
Chromosome Location	chr2:48534363-48624007
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2084)
CpG islands
(count:671)
Chromatin interactive
region (count:88)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:13)

(count:2084 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:48574979-48575185	K562	blood:	n/a	n/a
2	ARID3A	chr2:48572216-48572796	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:48570947-48571931	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:48541410-48541598	K562	blood:	n/a	n/a
5	ARID3A	chr2:48582705-48582882	K562	blood:	n/a	n/a
6	ARID3A	chr2:48539414-48539593	HepG2	liver:	n/a	chr2:48539471-48539487
7	ARID3A	chr2:48584022-48584395	K562	blood:	n/a	n/a
8	ARID3A	chr2:48573086-48573910	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:48550653-48550822	K562	blood:	n/a	n/a
10	ARID3A	chr2:48567436-48567451	K562	blood:	n/a	n/a
11	ARID3A	chr2:48574923-48575175	HepG2	liver:	n/a	n/a
12	ARID3A	chr2:48541115-48541924	HepG2	liver:	n/a	n/a
13	ATF1	chr2:48541246-48541966	K562	blood:	n/a	n/a
14	ATF2	chr2:48541076-48541516	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr2:48540729-48541627	GM12878	blood:	n/a	n/a
16	ATF2	chr2:48540569-48542082	GM12878	blood:	n/a	n/a
17	ATF2	chr2:48541096-48541755	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr2:48542597-48543257	GM12878	blood:	n/a	n/a
19	ATF2	chr2:48542416-48543255	GM12878	blood:	n/a	n/a
20	ATF2	chr2:48543862-48544398	GM12878	blood:	n/a	n/a
21	ATF3	chr2:48541711-48542216	K562	blood:	n/a	chr2:48542122-48542131
22	ATF3	chr2:48540896-48541754	A549	lung:	n/a	chr2:48541387-48541396 chr2:48541418-48541427
23	ATF3	chr2:48541076-48542041	A549	lung:	n/a	chr2:48541387-48541396 chr2:48541418-48541427
24	BACH1	chr2:48541206-48541571	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr2:48542894-48543055	K562	blood:	n/a	n/a
26	BACH1	chr2:48541997-48542279	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr2:48541114-48541423	GM12878	blood:	n/a	n/a
28	BATF	chr2:48540708-48541073	GM12878	blood:	n/a	n/a
29	BCL3	chr2:48570810-48571714	A549	lung:	n/a	n/a
30	BCL3	chr2:48541360-48542139	GM12878	blood:	n/a	chr2:48541528-48541536 chr2:48542004-48542017 chr2:48542023-48542032 chr2:48541430-48541439 chr2:48542061-48542070 chr2:48541387-48541400
31	BCL3	chr2:48542537-48543218	A549	lung:	n/a	chr2:48542645-48542654
32	BCL3	chr2:48542300-48543515	A549	lung:	n/a	chr2:48542645-48542654
33	BCL3	chr2:48541041-48542176	A549	lung:	n/a	chr2:48541528-48541536 chr2:48542004-48542017 chr2:48542023-48542032 chr2:48541430-48541439 chr2:48542061-48542070 chr2:48541387-48541400
34	BCL3	chr2:48540922-48541794	A549	lung:	n/a	chr2:48541528-48541536 chr2:48541430-48541439 chr2:48541387-48541400
35	BCLAF1	chr2:48580177-48580745	GM12878	blood:	n/a	n/a
36	BCLAF1	chr2:48541027-48542258	GM12878	blood:	n/a	chr2:48541528-48541536 chr2:48542004-48542017 chr2:48542023-48542032 chr2:48541430-48541439 chr2:48542061-48542070 chr2:48541387-48541400
37	BCLAF1	chr2:48541729-48542114	GM12878	blood:	n/a	chr2:48542004-48542017 chr2:48542023-48542032 chr2:48542061-48542070
38	BCLAF1	chr2:48542393-48543366	GM12878	blood:	n/a	chr2:48542645-48542654
39	BCLAF1	chr2:48541047-48541725	GM12878	blood:	n/a	chr2:48541528-48541536 chr2:48541430-48541439 chr2:48541387-48541400
40	BCLAF1	chr2:48574818-48575241	GM12878	blood:	n/a	n/a
41	BHLHE40	chr2:48540988-48543349	GM12878	blood:	n/a	chr2:48541996-48542012 chr2:48541814-48541830 chr2:48542765-48542781 chr2:48541804-48541820
42	BHLHE40	chr2:48584174-48584447	K562	blood:	n/a	n/a
43	BHLHE40	chr2:48556596-48556820	HepG2	liver:	n/a	n/a
44	BHLHE40	chr2:48572468-48572678	HepG2	liver:	n/a	n/a
45	BHLHE40	chr2:48555477-48555585	GM12878	blood:	n/a	n/a
46	BHLHE40	chr2:48589554-48589602	GM12878	blood:	n/a	n/a
47	BHLHE40	chr2:48584258-48584478	GM12878	blood:	n/a	n/a
48	BHLHE40	chr2:48541091-48543199	K562	blood:	n/a	chr2:48541996-48542012 chr2:48541814-48541830 chr2:48542765-48542781 chr2:48541804-48541820
49	BHLHE40	chr2:48541181-48542335	HepG2	liver:	n/a	chr2:48541996-48542012 chr2:48541814-48541830 chr2:48541804-48541820
50	BHLHE40	chr2:48574997-48575123	GM12878	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:48542335-48542385	SK-N-MC	brain:	n/a
2	chr2:48545621-48545671	GM19239	blood:	n/a
3	chr2:48545621-48545671	MCF10A-Er-Src	breast:	n/a
4	chr2:48541532-48541582	ECC-1	luminal epithelium:	n/a
5	chr2:48584360-48584410	SK-N-SH_RA	brain:	n/a
6	chr2:48545621-48545671	NHDF-neo	bronchial:	n/a
7	chr2:48541532-48541582	NH-A	brain:	n/a
8	chr2:48543191-48543241	AG10803	skin:	n/a
9	chr2:48543191-48543241	SKMC	muscle:	n/a
10	chr2:48543165-48543215	HUVEC	blood vessel:	n/a
11	chr2:48543165-48543215	HCM	heart:	n/a
12	chr2:48541921-48541971	AoSMC	blood vessel:	n/a
13	chr2:48543191-48543241	HMEC	breast:	n/a
14	chr2:48604775-48604825	HUVEC	blood vessel:	n/a
15	chr2:48541921-48541971	K562	blood:	n/a
16	chr2:48543165-48543215	PANC-1	pancreas:	n/a
17	chr2:48541532-48541582	MCF10A-Er-Src	breast:	n/a
18	chr2:48541532-48541582	HEEpiC	esophagus:	n/a
19	chr2:48541532-48541582	HRE	kidney:	n/a
20	chr2:48543165-48543215	HPAEpiC	pulmonary alveolar:	n/a
21	chr2:48543165-48543215	CMK	blood:	n/a
22	chr2:48543165-48543215	SK-N-SH_RA	brain:	n/a
23	chr2:48541532-48541582	MCF-7	breast:	n/a
24	chr2:48604775-48604825	HCT-116	colon:	n/a
25	chr2:48543165-48543215	HCPEpiC	choroid plexus:	n/a
26	chr2:48540671-48540721	AG04449	skin:	fetal
27	chr2:48545621-48545671	SK-N-SH_RA	brain:	n/a
28	chr2:48541264-48541314	LNCaP	prostate:	n/a
29	chr2:48541532-48541582	AG09319	gingival:	n/a
30	chr2:48543191-48543241	Hepatocyte	liver:	n/a
31	chr2:48541532-48541582	AG04450	lung:	fetal
32	chr2:48541264-48541314	AG10803	skin:	n/a
33	chr2:48545621-48545671	ProgFib	skin:	n/a
34	chr2:48541921-48541971	HepG2	liver:	n/a
35	chr2:48545621-48545671	Hela-S3	cervix:	n/a
36	chr2:48584360-48584410	SK-N-SH	brain:	n/a
37	chr2:48540671-48540721	BE2_C	brain:	n/a
38	chr2:48542335-48542385	HAEpiC	amniotic membrane:	n/a
39	chr2:48542335-48542385	BJ	skin:	n/a
40	chr2:48540671-48540721	AoSMC	blood vessel:	n/a
41	chr2:48541532-48541582	GM06990	blood:	n/a
42	chr2:48604775-48604825	NHDF-neo	bronchial:	n/a
43	chr2:48542674-48542724	ECC-1	luminal epithelium:	n/a
44	chr2:48584360-48584410	HepG2	liver:	n/a
45	chr2:48541532-48541582	SK-N-SH	brain:	n/a
46	chr2:48541921-48541971	PFSK-1	brain:	n/a
47	chr2:48541921-48541971	T-47D	breast:	n/a
48	chr2:48541532-48541582	NHBE	bronchial:	n/a
49	chr2:48540671-48540721	SKMC	muscle:	n/a
50	chr2:48542335-48542385	Caco-2	colon:	n/a

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:48589573..48591686-chr2:48594924..48597026,2	K562	blood:
2	chr2:48551728..48554180-chr2:48555389..48557801,2	MCF-7	breast:
3	chr2:48532704..48536258-chr2:48538581..48541257,5	K562	blood:
4	chr2:48542159..48543116-chr6:26158101..26158766,2	Hela-S3	cervix:
5	chr2:48559522..48562446-chr2:48563870..48566960,3	MCF-7	breast:
6	chr2:48568928..48571039-chr2:48579815..48581773,2	MCF-7	breast:
7	chr2:48598202..48600856-chr2:48603158..48604738,2	K562	blood:
8	chr2:48592285..48594588-chr2:48601399..48603499,2	MCF-7	breast:
9	chr2:48617829..48620871-chr2:48622412..48626412,3	K562	blood:
10	chr2:48133540..48135075-chr2:48540885..48543276,2	K562	blood:
11	chr2:48341598..48344591-chr2:48542825..48544946,2	K562	blood:
12	chr2:48541080..48542668-chr2:48550192..48552132,2	MCF-7	breast:
13	chr2:48568069..48570400-chr2:48600787..48602390,2	K562	blood:
14	chr2:48492137..48494411-chr2:48542775..48545328,2	K562	blood:
15	chr2:48342619..48344591-chr2:48541998..48544325,2	K562	blood:
16	chr2:48583541..48585248-chr2:48599640..48601828,2	MCF-7	breast:
17	chr2:48536558..48539555-chr2:48539697..48542040,2	K562	blood:
18	chr2:48010207..48012260-chr2:48541505..48544232,2	K562	blood:
19	chr2:48551728..48554180-chr2:48555389..48557801,2	MCF-7	breast:
20	chr2:48578681..48582388-chr2:48582784..48586647,4	K562	blood:
21	chr2:48539557..48542081-chr2:48666297..48668955,4	MCF-7	breast:
22	chr2:48578681..48582388-chr2:48582784..48586647,4	K562	blood:
23	chr2:48550065..48552046-chr2:48557575..48559707,2	MCF-7	breast:
24	chr2:48536399..48538424-chr2:48545720..48548096,2	K562	blood:
25	chr2:48515255..48518583-chr2:48539283..48541492,3	K562	blood:
26	chr2:48558442..48561276-chr2:48561458..48563692,2	K562	blood:
27	chr2:48559522..48562446-chr2:48563870..48566960,3	MCF-7	breast:
28	chr2:48534472..48536847-chr2:48541135..48543354,2	MCF-7	breast:
29	chr2:48532704..48536258-chr2:48538581..48541257,5	K562	blood:
30	chr2:48549627..48551864-chr2:48552790..48555987,3	K562	blood:
31	chr2:48552083..48554152-chr2:48555088..48558115,3	K562	blood:
32	chr2:48549627..48551864-chr2:48552790..48555987,3	K562	blood:
33	chr2:48550065..48552046-chr2:48557575..48559707,2	MCF-7	breast:
34	chr2:48337910..48340125-chr2:48569442..48571000,2	MCF-7	breast:
35	chr2:48517525..48519074-chr2:48557962..48560768,2	K562	blood:
36	chr2:48618125..48619641-chr2:48666426..48668080,2	K562	blood:
37	chr2:48558442..48561276-chr2:48561458..48563692,2	K562	blood:
38	chr2:48337775..48340265-chr2:48597214..48600170,2	MCF-7	breast:
39	chr2:48568928..48571039-chr2:48579815..48581773,2	MCF-7	breast:
40	chr2:48496037..48498281-chr2:48536801..48539296,2	K562	blood:
41	chr2:48545774..48548252-chr2:48556563..48558332,2	K562	blood:
42	chr2:48542620..48544627-chr2:48553697..48556453,2	K562	blood:
43	chr2:48492280..48493854-chr2:48539785..48541732,2	K562	blood:
44	chr2:48598202..48600856-chr2:48603158..48604738,2	K562	blood:
45	chr17:40610255..40611147-chr2:48541967..48542604,2	HCT-116	colon:
46	chr2:48568069..48570400-chr2:48600787..48602390,2	K562	blood:
47	chr2:48568770..48570498-chr2:48574091..48575734,2	MCF-7	breast:
48	chr2:48541852..48543622-chr2:48550647..48553258,3	MCF-7	breast:
49	chr2:48601929..48604341-chr2:48608996..48611918,2	MCF-7	breast:
50	chr2:48604176..48606531-chr2:48606806..48608312,2	K562	blood:

No data

(count:13 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	FOXN2	hsa-miR-183-5p	chr2:48603740-48603746
2	FOXN2	hsa-miR-32-5p	chr2:48605322-48605342
3	FOXN2	hsa-miR-32-5p	chr2:48605335-48605342
4	FOXN2	hsa-miR-186-5p	chr2:48604712-48604733
5	FOXN2	hsa-miR-183-5p	chr2:48603727-48603747
6	FOXN2	hsa-miR-186-5p	chr2:48602617-48602624
7	FOXN2	hsa-miR-186-5p	chr2:48605960-48605980
8	FOXN2	hsa-miR-32-5p	chr2:48602583-48602604
9	FOXN2	hsa-miR-183-5p	chr2:48605994-48606000
10	FOXN2	hsa-miR-186-5p	chr2:48603298-48603319
11	FOXN2	hsa-miR-186-5p	chr2:48605973-48605979
12	FOXN2	hsa-miR-186-5p	chr2:48602603-48602624
13	FOXN2	hsa-miR-183-5p	chr2:48605980-48606001

Variant related genes	Relation type
RNU4-49P	TF binding region
FOXN2	TF binding region
RNU4-49P	CpG island
FOXN2	CpG island
ENSG00000158373	chromatin interactions
ENSG00000170802	chromatin interactions
ENSG00000033627	chromatin interactions
ENSG00000115840	chromatin interactions
ENSG00000172878	chromatin interactions
ENSG00000138081	chromatin interactions
ENSG00000272663	chromatin interactions
ENSG00000116062	chromatin interactions
ENSG00000251889	chromatin interactions
ENSG00000233230	chromatin interactions
ENSG00000162869	chromatin interactions
ENSG00000202538	chromatin interactions

Extended variants
information (count: 3843 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3843 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4455210	chr2:48534363-48534364	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs142048756	chr2:48534442-48534443	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570346979	chr2:48534456-48534457	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs62138805	chr2:48534487-48534488	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs552894197	chr2:48534495-48534496	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs192045860	chr2:48534525-48534526	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs151151707	chr2:48534544-48534545	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs556929990	chr2:48534546-48534547	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs140159630	chr2:48534553-48534554	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs182828422	chr2:48534570-48534571	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs564656534	chr2:48534575-48534576	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs186108811	chr2:48534606-48534607	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs191255061	chr2:48534621-48534622	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs562198039	chr2:48534623-48534624	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs571239672	chr2:48534667-48534668	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs145152415	chr2:48534676-48534677	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs78852182	chr2:48534694-48534695	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs182760509	chr2:48534696-48534697	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs533235258	chr2:48534823-48534824	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs551500154	chr2:48534884-48534885	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs113711256	chr2:48534902-48534903	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs377384214	chr2:48534923-48534924	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs142176440	chr2:48534924-48534925	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs146052704	chr2:48534979-48534980	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs10186237	chr2:48535012-48535013	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs34531134	chr2:48535030-48535031	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs535765253	chr2:48535049-48535050	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs556665288	chr2:48535069-48535070	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs575232422	chr2:48535081-48535082	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs545907372	chr2:48535082-48535083	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs557932745	chr2:48535087-48535088	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs568648957	chr2:48535091-48535092	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs375419179	chr2:48535105-48535106	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs576412334	chr2:48535111-48535112	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs545318952	chr2:48535113-48535114	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs187406803	chr2:48535126-48535127	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs572978310	chr2:48535156-48535157	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs540789579	chr2:48535188-48535189	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs200519812	chr2:48535261-48535262	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs560408475	chr2:48535266-48535267	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs145606569	chr2:48535282-48535283	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs527917874	chr2:48535304-48535305	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs544924049	chr2:48535311-48535312	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs562728225	chr2:48535421-48535422	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs72818489	chr2:48535453-48535454	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs533107675	chr2:48535455-48535456	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs566583651	chr2:48535457-48535458	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs527793300	chr2:48535469-48535470	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs546446714	chr2:48535506-48535507	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs143638095	chr2:48535581-48535582	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
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
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	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
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3339 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:48506000-48539000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:48528000-48539200	Weak transcription	Primary T cells from cord blood	blood
3	chr2:48530200-48540200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:48532200-48535000	Enhancers	HepG2	liver
5	chr2:48532800-48534600	Enhancers	HSMMtube	muscle
6	chr2:48533000-48534600	Enhancers	Adipose Nuclei	Adipose
7	chr2:48533000-48534800	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr2:48533000-48539800	Weak transcription	Primary B cells from cord blood	blood
9	chr2:48533200-48534800	Enhancers	Placenta	Placenta
10	chr2:48533600-48534400	Enhancers	Fetal Muscle Leg	muscle
11	chr2:48533600-48534800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr2:48533800-48534400	Enhancers	Right Atrium	heart
13	chr2:48533800-48534400	Enhancers	NHEK	skin
14	chr2:48533800-48534600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
15	chr2:48533800-48534600	Enhancers	Hela-S3	cervix
16	chr2:48533800-48534800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:48533800-48534800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr2:48534000-48534400	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr2:48534000-48534400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr2:48534000-48534400	Enhancers	Stomach Smooth Muscle	stomach
21	chr2:48534000-48534600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr2:48534200-48534400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr2:48534200-48534600	Enhancers	NHDF-Ad	bronchial
24	chr2:48534400-48534800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr2:48534400-48538800	Weak transcription	NHEK	skin
26	chr2:48534400-48540200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr2:48534600-48534800	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr2:48534600-48539200	Weak transcription	Hela-S3	cervix
29	chr2:48534600-48540200	Weak transcription	Adipose Nuclei	Adipose
30	chr2:48534600-48540200	Weak transcription	NHDF-Ad	bronchial
31	chr2:48534800-48539600	Weak transcription	Placenta	Placenta
32	chr2:48534800-48539600	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr2:48534800-48539600	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr2:48535000-48538400	Weak transcription	HepG2	liver
35	chr2:48535400-48535800	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr2:48535400-48535800	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr2:48535600-48535800	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr2:48535600-48540400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr2:48535800-48539400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr2:48535800-48539600	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr2:48535800-48539600	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr2:48536400-48539400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr2:48537400-48539200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr2:48537600-48537800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr2:48538400-48540400	Enhancers	HepG2	liver
46	chr2:48538400-48540600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr2:48538600-48540400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr2:48538600-48540800	Enhancers	Fetal Intestine Large	intestine
49	chr2:48538800-48540200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr2:48538800-48541200	Enhancers	NHEK	skin

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