Variant report

Variant	esv17182
Chromosome Location	chr2:133011474-133047633
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7054)
CpG islands
(count:3357)
Chromatin interactive
region (count:256)
LncRNA
region (count:10)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:7054 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:133041164-133041233	K562	blood:	n/a	n/a
2	ARID3A	chr2:133021777-133024659	K562	blood:	n/a	n/a
3	ARID3A	chr2:133024999-133028006	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:133044459-133044810	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:133015019-133015747	K562	blood:	n/a	n/a
6	ARID3A	chr2:133032280-133033731	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:133035680-133036126	K562	blood:	n/a	n/a
8	ARID3A	chr2:133032461-133033743	K562	blood:	n/a	n/a
9	ARID3A	chr2:133024878-133031935	K562	blood:	n/a	n/a
10	ARID3A	chr2:133011761-133013355	K562	blood:	n/a	n/a
11	ARID3A	chr2:133037976-133039294	K562	blood:	n/a	n/a
12	ATF1	chr2:133032469-133033732	K562	blood:	n/a	n/a
13	ATF1	chr2:133044238-133044806	K562	blood:	n/a	n/a
14	ATF1	chr2:133021765-133024691	K562	blood:	n/a	n/a
15	ATF1	chr2:133024991-133031933	K562	blood:	n/a	n/a
16	ATF1	chr2:133018613-133021289	K562	blood:	n/a	n/a
17	ATF1	chr2:133011772-133013346	K562	blood:	n/a	n/a
18	ATF1	chr2:133016237-133017446	K562	blood:	n/a	n/a
19	ATF2	chr2:133011825-133013352	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr2:133011836-133012126	GM12878	blood:	n/a	n/a
21	ATF2	chr2:133012312-133013340	GM12878	blood:	n/a	n/a
22	ATF2	chr2:133012462-133013089	GM12878	blood:	n/a	n/a
23	ATF2	chr2:133011789-133012265	GM12878	blood:	n/a	n/a
24	ATF2	chr2:133011823-133013332	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr2:133028916-133031075	GM12878	blood:	n/a	n/a
26	ATF3	chr2:133028832-133029372	HepG2	liver:	n/a	n/a
27	ATF3	chr2:133026094-133026523	K562	blood:	n/a	n/a
28	ATF3	chr2:133015927-133017546	K562	blood:	n/a	n/a
29	ATF3	chr2:133020043-133020233	K562	blood:	n/a	n/a
30	ATF3	chr2:133012465-133013223	K562	blood:	n/a	n/a
31	ATF3	chr2:133016628-133016997	K562	blood:	n/a	n/a
32	ATF3	chr2:133016618-133017347	HepG2	liver:	n/a	n/a
33	ATF3	chr2:133031168-133031383	K562	blood:	n/a	n/a
34	ATF3	chr2:133012415-133012641	K562	blood:	n/a	n/a
35	ATF3	chr2:133032559-133032768	HepG2	liver:	n/a	n/a
36	ATF3	chr2:133034363-133034795	K562	blood:	n/a	n/a
37	ATF3	chr2:133025549-133026035	HepG2	liver:	n/a	n/a
38	ATF3	chr2:133011752-133013354	A549	lung:	n/a	n/a
39	ATF3	chr2:133011829-133012122	HepG2	liver:	n/a	n/a
40	ATF3	chr2:133032785-133033604	HepG2	liver:	n/a	n/a
41	ATF3	chr2:133031489-133031880	HepG2	liver:	n/a	n/a
42	ATF3	chr2:133028279-133028662	HepG2	liver:	n/a	n/a
43	ATF3	chr2:133018720-133019129	K562	blood:	n/a	n/a
44	ATF3	chr2:133025667-133026458	K562	blood:	n/a	n/a
45	ATF3	chr2:133018709-133019159	HepG2	liver:	n/a	n/a
46	ATF3	chr2:133033300-133033492	K562	blood:	n/a	n/a
47	ATF3	chr2:133026082-133027274	HepG2	liver:	n/a	n/a
48	ATF3	chr2:133025728-133025957	K562	blood:	n/a	n/a
49	ATF3	chr2:133015084-133015367	K562	blood:	n/a	n/a
50	ATF3	chr2:133012465-133012990	GM12878	blood:	n/a	n/a

(count:3357 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133037057-133037107	PFSK-1	brain:	n/a
2	chr2:133015670-133015720	AoSMC	blood vessel:	n/a
3	chr2:133037057-133037107	PFSK-1	brain:	n/a
4	chr2:133015670-133015720	AoSMC	blood vessel:	n/a
5	chr2:133036548-133036598	GM06990	blood:	n/a
6	chr2:133013048-133013098	NT2-D1	testis:	n/a
7	chr2:133033202-133033252	H1-hESC	embryonic stem cell:	embryo
8	chr2:133014684-133014734	MCF10A-Er-Src	breast:	n/a
9	chr2:133036873-133036923	PrEC	prostate:	n/a
10	chr2:133014640-133014690	AG04449	skin:	fetal
11	chr2:133016453-133016503	HCT-116	colon:	n/a
12	chr2:133030701-133030751	HMEC	breast:	n/a
13	chr2:133039779-133039829	U87	brain:	n/a
14	chr2:133016799-133016849	SK-N-SH	brain:	n/a
15	chr2:133014640-133014690	HPAEpiC	pulmonary alveolar:	n/a
16	chr2:133011643-133011693	HCPEpiC	choroid plexus:	n/a
17	chr2:133039152-133039202	HCT-116	colon:	n/a
18	chr2:133022980-133023030	MCF-7	breast:	n/a
19	chr2:133036695-133036745	HCT-116	colon:	n/a
20	chr2:133033270-133033320	HUVEC	blood vessel:	n/a
21	chr2:133036695-133036745	AoSMC	blood vessel:	n/a
22	chr2:133038098-133038148	ProgFib	skin:	n/a
23	chr2:133015639-133015689	PANC-1	pancreas:	n/a
24	chr2:133038261-133038311	GM12891	blood:	n/a
25	chr2:133037153-133037203	LNCaP	prostate:	n/a
26	chr2:133037006-133037056	GM12891	blood:	n/a
27	chr2:133039143-133039193	NB4	blood:	n/a
28	chr2:133013489-133013539	AG09309	skin:	n/a
29	chr2:133011643-133011693	Jurkat	blood:	n/a
30	chr2:133038836-133038886	A549	lung:	n/a
31	chr2:133012182-133012232	PFSK-1	brain:	n/a
32	chr2:133022980-133023030	NHDF-neo	bronchial:	n/a
33	chr2:133011643-133011693	HepG2	liver:	n/a
34	chr2:133014765-133014815	HNPCEpiC	eye:	n/a
35	chr2:133038098-133038148	HUVEC	blood vessel:	n/a
36	chr2:133016799-133016849	HNPCEpiC	eye:	n/a
37	chr2:133038927-133038977	HIPEpiC	eye:	n/a
38	chr2:133023100-133023150	Hepatocyte	liver:	n/a
39	chr2:133039083-133039133	AG04449	skin:	fetal
40	chr2:133014765-133014815	IMR90	lung:	fetal
41	chr2:133037153-133037203	HIPEpiC	eye:	n/a
42	chr2:133025835-133025885	HCF	heart:	n/a
43	chr2:133022807-133022857	CMK	blood:	n/a
44	chr2:133038098-133038148	Caco-2	colon:	n/a
45	chr2:133033202-133033252	GM12878	blood:	n/a
46	chr2:133036073-133036123	Hela-S3	cervix:	n/a
47	chr2:133033202-133033252	AG09319	gingival:	n/a
48	chr2:133011643-133011693	NT2-D1	testis:	n/a
49	chr2:133015670-133015720	PANC-1	pancreas:	n/a
50	chr2:133014784-133014834	GM19239	blood:	n/a

(count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr16:33963139..33963772-chr2:133012277..133013465,4	MCF-7	breast:
2	chr12:20702911..20705964-chr2:133010767..133014432,7	K562	blood:
3	chr12:20703902..20704952-chr2:133011967..133012812,14	MCF-7	breast:
4	chr12:38447143..38447662-chr2:133026232..133026787,2	MCF-7	breast:
5	chr2:133036040..133038933-chr8:70602384..70604113,2	K562	blood:
6	chr2:133011277..133016757-chr20:26187363..26191986,20	K562	blood:
7	chr16:33964145..33964938-chr2:133011953..133012475,2	MCF-7	breast:
8	chr17:31149683..31150297-chr2:133036002..133036512,3	MCF-7	breast:
9	chr2:133021735..133023570-chr2:133028674..133030666,2	K562	blood:
10	chr2:133034721..133036011-chr6:119558119..119559094,3	MCF-7	breast:
11	chr2:133023726..133025567-chr2:133036787..133038950,2	K562	blood:
12	chr16:33954432..33957320-chr2:133023311..133028999,7	MCF-7	breast:
13	chr2:133034372..133035957-chr6:119557078..119558627,2	K562	blood:
14	chr2:133026305..133027045-chr20:54154213..54154785,2	MCF-7	breast:
15	chr16:33965082..33965599-chr2:133012112..133012771,2	MCF-7	breast:
16	chr16:33952012..33953185-chr2:133030483..133031473,5	MCF-7	breast:
17	chr2:133012152..133012832-chr4:183777693..183778673,2	MCF-7	breast:
18	chr2:133033298..133034623-chrX:136519950..136520939,4	MCF-7	breast:
19	chr2:133038177..133039677-chr2:230044041..230045609,2	MCF-7	breast:
20	chr16:33953270..33954082-chr2:133026230..133026906,2	MCF-7	breast:
21	chr16:33962974..33964644-chr2:133011974..133013442,13	MCF-7	breast:
22	chr17:45221257..45221782-chr2:133016917..133017640,2	MCF-7	breast:
23	chr2:133038137..133038973-chr2:230045043..230045602,2	MCF-7	breast:
24	chr2:133026098..133026689-chr2:133106836..133107370,2	MCF-7	breast:
25	chr2:133010317..133016704-chr21:9824094..9829011,32	MCF-7	breast:
26	chr2:133010455..133013497-chrX:108295941..108299311,5	K562	blood:
27	chr2:133034513..133038165-chr21:9824366..9827688,5	K562	blood:
28	chr17:31149781..31150380-chr2:133035854..133036526,6	MCF-7	breast:
29	chr11:85193628..85196531-chr2:133032953..133034631,2	K562	blood:
30	chr2:133015187..133015799-chr21:9825605..9826185,2	K562	blood:
31	chr2:133038935..133039656-chr8:56754719..56755312,2	MCF-7	breast:
32	chr17:31149448..31151294-chr2:133036023..133039051,5	K562	blood:
33	chr2:133032278..133034990-chr21:9826150..9828910,2	MCF-7	breast:
34	chr2:133012862..133013586-chr21:9827253..9827981,2	MCF-7	breast:
35	chr16:33951094..33954926-chr2:133029316..133031796,4	K562	blood:
36	chr2:133036012..133038474-chr20:26188735..26191734,4	K562	blood:
37	chr1:108113044..108113591-chr2:133038209..133039151,2	MCF-7	breast:
38	chr16:33948058..33954885-chr2:133028801..133034197,14	MCF-7	breast:
39	chr19:7635601..7636121-chr2:133015921..133016809,2	MCF-7	breast:
40	chr2:133011942..133012809-chr21:27228141..27228643,3	MCF-7	breast:
41	chr2:133014709..133015762-chr20:26188882..26190143,12	MCF-7	breast:
42	chr2:133013667..133017081-chr20:26187658..26190834,11	MCF-7	breast:
43	chr2:133036040..133038933-chr8:70602384..70604113,3	K562	blood:
44	chr2:133011920..133013710-chr21:9825482..9828043,33	MCF-7	breast:
45	chr16:14579456..14582439-chr2:133031887..133034194,4	MCF-7	breast:
46	chr2:1599670..1601170-chr2:133031746..133033249,2	MCF-7	breast:
47	chr2:133012736..133013451-chr7:80963085..80963599,2	MCF-7	breast:
48	chr2:133011942..133013448-chr2:133036648..133038896,2	K562	blood:
49	chr16:14580936..14581468-chr2:133032924..133033512,2	MCF-7	breast:
50	chr2:133033211..133034907-chrX:136519062..136521940,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR39-7	chr2:133038656-133038732	NONHSAT074524
2	lnc-GPR39-10	chr2:133013340-133013485	NONHSAT074516
3	lnc-GPR39-10	chr2:133013066-133013266	NONHSAT074516
4	lnc-GPR39-7	chr2:133036673-133036713	NONHSAT074524
5	lnc-GPR39-7	chr2:133037726-133037732	NONHSAT074524
6	lnc-ANKRD30BL-1	chr2:133046475-133046638	XLOC_002329
7	lnc-ANKRD30BL-3	chr2:133015102-133015542	NONHSAT074513
8	lnc-GPR39-7	chr2:133038981-133039086	NONHSAT074524
9	lnc-GPR39-9	chr2:133019901-133020615	NONHSAT074520
10	lnc-ANKRD30BL-1	chr2:133043368-133043465	XLOC_002329

miRNA name	Chromosome Location	mirBase accession
hsa-miR-663b	chr2:133014543-133014564	MIMAT0005867

No data

Variant related genes	Relation type
ANKRD30BL	TF binding region
CDC27P1	TF binding region
MIR663B	TF binding region
RNA5-8SP5	TF binding region
ANKRD30BL	CpG island
CDC27P1	CpG island
MIR663B	CpG island
RNA5-8SP5	CpG island
ENSG00000206737	chromatin interactions
ENSG00000140538	chromatin interactions
ENSG00000256663	chromatin interactions
ENSG00000256642	chromatin interactions
ENSG00000264462	chromatin interactions
ENSG00000198133	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000207986	chromatin interactions
ENSG00000104497	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000256616	chromatin interactions
ENSG00000226958	chromatin interactions
ENSG00000227195	chromatin interactions
ENSG00000168056	chromatin interactions
ENSG00000161888	chromatin interactions
ENSG00000239776	chromatin interactions
ENSG00000107968	chromatin interactions
ENSG00000200434	chromatin interactions
ENSG00000004897	chromatin interactions
HRASLS5	Mature miRNA region

Extended variants
information (count: 6162 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:6162 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72869417	chr2:133011476-133011477	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs72869418	chr2:133011483-133011484	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs74543495	chr2:133011486-133011487	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs75492935	chr2:133011487-133011488	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs571825871	chr2:133011503-133011504	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs80118839	chr2:133011504-133011505	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs538827940	chr2:133011505-133011506	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs74669878	chr2:133011525-133011526	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs79147981	chr2:133011526-133011527	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs78522957	chr2:133011528-133011529	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs77689863	chr2:133011534-133011535	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs78562309	chr2:133011539-133011540	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs547949234	chr2:133011541-133011542	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs79109914	chr2:133011549-133011550	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs77917735	chr2:133011550-133011551	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs76502450	chr2:133011551-133011552	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs2060742	chr2:133011557-133011558	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs80288152	chr2:133011559-133011560	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs75557324	chr2:133011564-133011565	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs114529703	chr2:133011569-133011570	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs200792804	chr2:133011571-133011572	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs75993859	chr2:133011576-133011577	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs72869420	chr2:133011596-133011597	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs536338331	chr2:133011597-133011598	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs554718381	chr2:133011602-133011603	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs76041760	chr2:133011604-133011605	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs200490158	chr2:133011605-133011606	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs72869421	chr2:133011614-133011615	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs201213923	chr2:133011615-133011616	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs375335833	chr2:133011618-133011619	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs36033889	chr2:133011619-133011620	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs189270445	chr2:133011621-133011622	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs537759672	chr2:133011622-133011623	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs556151844	chr2:133011628-133011629	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs113713710	chr2:133011629-133011630	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs577791995	chr2:133011634-133011635	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs544905397	chr2:133011635-133011636	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs553920864	chr2:133011636-133011637	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs113299228	chr2:133011641-133011642	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs572089168	chr2:133011642-133011643	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs542696195	chr2:133011644-133011645	ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs79098821	chr2:133011646-133011647	ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs72869422	chr2:133011647-133011648	ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs201889731	chr2:133011653-133011654	ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs565459834	chr2:133011655-133011656	ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs368339774	chr2:133011664-133011665	ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs372929804	chr2:133011665-133011666	ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs374435626	chr2:133011670-133011671	ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs531297727	chr2:133011673-133011674	ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs72869424	chr2:133011674-133011675	ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2168 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133004400-133012000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:133008400-133013200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
3	chr2:133008400-133017400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
4	chr2:133009600-133012000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr2:133009600-133012000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr2:133009800-133011800	Weak transcription	Stomach Smooth Muscle	stomach
7	chr2:133009800-133017400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr2:133009800-133017600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:133010000-133012000	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
10	chr2:133010400-133017400	ZNF genes & repeats	Colonic Mucosa	Colon
11	chr2:133010400-133017400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
12	chr2:133010400-133017600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
13	chr2:133010600-133012600	ZNF genes & repeats	Fetal Stomach	stomach
14	chr2:133010600-133017400	ZNF genes & repeats	Dnd41	blood
15	chr2:133010800-133012000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr2:133011000-133011800	Weak transcription	Adipose Nuclei	Adipose
17	chr2:133011000-133017600	ZNF genes & repeats	Fetal Intestine Large	intestine
18	chr2:133011400-133017400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
19	chr2:133011600-133017400	ZNF genes & repeats	Fetal Thymus	thymus
20	chr2:133011800-133012000	ZNF genes & repeats	Adipose Nuclei	Adipose
21	chr2:133011800-133012200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr2:133011800-133012600	ZNF genes & repeats	Fetal Muscle Leg	muscle
23	chr2:133011800-133013200	Flanking Bivalent TSS/Enh	Gastric	stomach
24	chr2:133011800-133013200	Flanking Bivalent TSS/Enh	Psoas Muscle	Psoas
25	chr2:133011800-133013400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:133011800-133013400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr2:133011800-133013400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
28	chr2:133011800-133013400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
29	chr2:133011800-133013400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
30	chr2:133011800-133013400	ZNF genes & repeats	Primary T cells from cord blood	blood
31	chr2:133011800-133013400	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
32	chr2:133011800-133013400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
33	chr2:133011800-133013400	ZNF genes & repeats	Ovary	ovary
34	chr2:133011800-133013400	ZNF genes & repeats	Rectal Smooth Muscle	rectum
35	chr2:133011800-133013400	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
36	chr2:133011800-133013400	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
37	chr2:133011800-133013800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr2:133011800-133013800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr2:133011800-133014400	ZNF genes & repeats	Brain Germinal Matrix	brain
40	chr2:133011800-133016000	ZNF genes & repeats	Fetal Brain Male	brain
41	chr2:133011800-133016600	ZNF genes & repeats	Pancreas	Pancrea
42	chr2:133011800-133017400	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
43	chr2:133011800-133017400	ZNF genes & repeats	Esophagus	oesophagus
44	chr2:133011800-133017400	ZNF genes & repeats	Fetal Brain Female	brain
45	chr2:133011800-133017400	ZNF genes & repeats	Small Intestine	intestine
46	chr2:133011800-133017400	ZNF genes & repeats	Thymus	Thymus
47	chr2:133011800-133017400	ZNF genes & repeats	Spleen	Spleen
48	chr2:133012000-133012200	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
49	chr2:133012000-133012200	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
50	chr2:133012000-133012200	Bivalent/Poised TSS	Primary T killer naive cells fromperipheralblood	blood

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