Variant report

Variant	nsv1004194
Chromosome Location	chr3:195864466-195919077
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1889)
CpG islands
(count:915)
Chromatin interactive
region (count:111)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1889 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:195874788-195875071	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:195906289-195906522	K562	blood:	n/a	n/a
3	ARID3A	chr3:195908711-195909109	K562	blood:	n/a	n/a
4	ARID3A	chr3:195867000-195867390	K562	blood:	n/a	n/a
5	ARID3A	chr3:195872724-195872995	K562	blood:	n/a	n/a
6	ARID3A	chr3:195870111-195870710	K562	blood:	n/a	n/a
7	ARID3A	chr3:195898904-195899274	HepG2	liver:	n/a	n/a
8	ATF1	chr3:195872777-195873075	K562	blood:	n/a	n/a
9	ATF1	chr3:195908745-195909160	K562	blood:	n/a	n/a
10	ATF2	chr3:195913315-195914251	GM12878	blood:	n/a	n/a
11	ATF2	chr3:195905963-195907220	GM12878	blood:	n/a	n/a
12	ATF2	chr3:195908514-195909189	GM12878	blood:	n/a	n/a
13	ATF2	chr3:195918798-195920402	GM12878	blood:	n/a	n/a
14	ATF2	chr3:195910195-195910849	GM12878	blood:	n/a	n/a
15	ATF2	chr3:195886598-195887269	GM12878	blood:	n/a	n/a
16	ATF2	chr3:195908567-195909161	GM12878	blood:	n/a	n/a
17	ATF2	chr3:195913609-195914179	GM12878	blood:	n/a	n/a
18	ATF2	chr3:195918896-195919717	GM12878	blood:	n/a	n/a
19	ATF2	chr3:195910206-195910875	GM12878	blood:	n/a	n/a
20	ATF2	chr3:195905969-195907085	GM12878	blood:	n/a	n/a
21	ATF3	chr3:195869970-195870664	K562	blood:	n/a	n/a
22	ATF3	chr3:195869536-195869963	K562	blood:	n/a	n/a
23	ATF3	chr3:195876240-195876553	K562	blood:	n/a	n/a
24	BACH1	chr3:195913660-195913791	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr3:195918941-195919475	GM12878	blood:	n/a	n/a
26	BATF	chr3:195910182-195910723	GM12878	blood:	n/a	chr3:195910516-195910527
27	BATF	chr3:195887294-195887716	GM12878	blood:	n/a	n/a
28	BATF	chr3:195906144-195906417	GM12878	blood:	n/a	n/a
29	BATF	chr3:195906139-195907164	GM12878	blood:	n/a	chr3:195906691-195906702
30	BATF	chr3:195908565-195909036	GM12878	blood:	n/a	n/a
31	BATF	chr3:195906480-195906892	GM12878	blood:	n/a	chr3:195906691-195906702
32	BATF	chr3:195910177-195910836	GM12878	blood:	n/a	chr3:195910516-195910527
33	BATF	chr3:195908690-195909060	GM12878	blood:	n/a	n/a
34	BCL11A	chr3:195910286-195910721	GM12878	blood:	n/a	chr3:195910349-195910358
35	BCL11A	chr3:195910211-195910812	GM12878	blood:	n/a	chr3:195910349-195910358
36	BCL11A	chr3:195906145-195907011	GM12878	blood:	n/a	chr3:195906843-195906852
37	BCL11A	chr3:195906459-195907031	GM12878	blood:	n/a	chr3:195906843-195906852
38	BCL11A	chr3:195908618-195909029	GM12878	blood:	n/a	n/a
39	BCL11A	chr3:195908670-195909026	GM12878	blood:	n/a	n/a
40	BCL11A	chr3:195897675-195897914	GM12878	blood:	n/a	n/a
41	BCL3	chr3:195918807-195919898	GM12878	blood:	n/a	n/a
42	BCL3	chr3:195906245-195907130	GM12878	blood:	n/a	chr3:195906843-195906852
43	BCL3	chr3:195910171-195910805	GM12878	blood:	n/a	chr3:195910349-195910358
44	BCL3	chr3:195908562-195909101	GM12878	blood:	n/a	n/a
45	BCL3	chr3:195918286-195918598	GM12878	blood:	n/a	n/a
46	BCLAF1	chr3:195910245-195910870	GM12878	blood:	n/a	chr3:195910349-195910358
47	BCLAF1	chr3:195886628-195887361	GM12878	blood:	n/a	n/a
48	BCLAF1	chr3:195908597-195909569	GM12878	blood:	n/a	n/a
49	BCLAF1	chr3:195913384-195914248	GM12878	blood:	n/a	n/a
50	BCLAF1	chr3:195913353-195914171	GM12878	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195897904-195897954	ECC-1	luminal epithelium:	n/a
2	chr3:195906436-195906486	SK-N-MC	brain:	n/a
3	chr3:195897833-195897883	Jurkat	blood:	n/a
4	chr3:195907142-195907192	GM12892	blood:	n/a
5	chr3:195914017-195914067	AG10803	skin:	n/a
6	chr3:195897912-195897962	HCT-116	colon:	n/a
7	chr3:195897912-195897962	HRCEpiC	kidney:	n/a
8	chr3:195886898-195886948	AG04449	skin:	fetal
9	chr3:195907142-195907192	AG09319	gingival:	n/a
10	chr3:195870092-195870142	HAEpiC	amniotic membrane:	n/a
11	chr3:195870009-195870059	AG10803	skin:	n/a
12	chr3:195886898-195886948	HRPEpiC	eye:	n/a
13	chr3:195914092-195914142	HRPEpiC	eye:	n/a
14	chr3:195914113-195914163	HCT-116	colon:	n/a
15	chr3:195870249-195870299	HIPEpiC	eye:	n/a
16	chr3:195869691-195869741	SAEC	small airway:	n/a
17	chr3:195870249-195870299	SKMC	muscle:	n/a
18	chr3:195914017-195914067	NT2-D1	testis:	n/a
19	chr3:195897904-195897954	LNCaP	prostate:	n/a
20	chr3:195886898-195886948	HEK293	kidney:	embryo
21	chr3:195897833-195897883	BJ	skin:	n/a
22	chr3:195870092-195870142	NB4	blood:	n/a
23	chr3:195870249-195870299	SK-N-MC	brain:	n/a
24	chr3:195897833-195897883	HUVEC	blood vessel:	n/a
25	chr3:195870009-195870059	NT2-D1	testis:	n/a
26	chr3:195914113-195914163	AG04450	lung:	fetal
27	chr3:195897912-195897962	IMR90	lung:	fetal
28	chr3:195897912-195897962	PrEC	prostate:	n/a
29	chr3:195870092-195870142	IMR90	lung:	fetal
30	chr3:195886898-195886948	NB4	blood:	n/a
31	chr3:195897912-195897962	GM12892	blood:	n/a
32	chr3:195914092-195914142	T-47D	breast:	n/a
33	chr3:195914113-195914163	ECC-1	luminal epithelium:	n/a
34	chr3:195914113-195914163	H1-hESC	embryonic stem cell:	embryo
35	chr3:195907142-195907192	GM06990	blood:	n/a
36	chr3:195870009-195870059	CMK	blood:	n/a
37	chr3:195914092-195914142	SK-N-SH	brain:	n/a
38	chr3:195914113-195914163	AG04449	skin:	fetal
39	chr3:195907142-195907192	AoSMC	blood vessel:	n/a
40	chr3:195868640-195868690	GM12891	blood:	n/a
41	chr3:195897833-195897883	A549	lung:	n/a
42	chr3:195886898-195886948	ovcar-3	ovarian:	n/a
43	chr3:195897912-195897962	HRPEpiC	eye:	n/a
44	chr3:195897912-195897962	HNPCEpiC	eye:	n/a
45	chr3:195870009-195870059	HAEpiC	amniotic membrane:	n/a
46	chr3:195870009-195870059	GM12892	blood:	n/a
47	chr3:195886898-195886948	HRE	kidney:	n/a
48	chr3:195897912-195897962	HCF	heart:	n/a
49	chr3:195897912-195897962	U87	brain:	n/a
50	chr3:195886898-195886948	HCT-116	colon:	n/a

(count:111 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:195865561..195866107-chr3:195873941..195874769,3	MCF-7	breast:
2	chr3:195806798..195809921-chr3:195918894..195921572,5	MCF-7	breast:
3	chr3:195854158..195855690-chr3:195863445..195865120,2	MCF-7	breast:
4	chr3:195865618..195868542-chr3:195904431..195907406,2	MCF-7	breast:
5	chr3:195858633..195860716-chr3:195871946..195874804,2	K562	blood:
6	chr3:195862933..195865516-chr3:195916637..195919200,2	MCF-7	breast:
7	chr3:195807091..195810537-chr3:195867675..195869638,3	MCF-7	breast:
8	chr3:195853339..195855440-chr3:195917765..195919794,2	K562	blood:
9	chr3:195918010..195921527-chr3:195922088..195925554,4	K562	blood:
10	chr3:195871243..195872835-chr3:195903079..195904769,2	K562	blood:
11	chr3:195871532..195873508-chr3:195933763..195935660,2	K562	blood:
12	chr3:195793504..195812987-chr3:195901613..195938073,113	K562	blood:
13	chr3:195871413..195873461-chr3:195905965..195908112,2	K562	blood:
14	chr3:195869552..195872825-chr3:195874431..195876682,3	K562	blood:
15	chr3:195792851..195794855-chr3:195871353..195874189,2	K562	blood:
16	chr3:195837558..195842265-chr3:195869775..195872800,4	K562	blood:
17	chr3:195840247..195843702-chr3:195870905..195872821,3	K562	blood:
18	chr3:195861753..195863466-chr3:195918246..195921048,2	K562	blood:
19	chr3:195821883..195824753-chr3:195869631..195872398,2	K562	blood:
20	chr3:195901978..195904372-chr3:195908307..195910643,2	MCF-7	breast:
21	chr3:195871327..195874118-chr3:195876962..195879289,2	K562	blood:
22	chr3:195806936..195809950-chr3:195876209..195879769,3	K562	blood:
23	chr3:195894083..195898677-chr3:195900136..195905272,5	K562	blood:
24	chr3:195800491..195804775-chr3:195913481..195918135,5	MCF-7	breast:
25	chr3:195866591..195868218-chr3:195877200..195880044,2	K562	blood:
26	chr3:195876196..195878053-chr3:195879575..195881077,2	K562	blood:
27	chr3:195823642..195825667-chr3:195890214..195892220,2	K562	blood:
28	chr3:195854603..195857572-chr3:195905057..195907261,2	K562	blood:
29	chr3:195903618..195905705-chr3:195906197..195908381,3	K562	blood:
30	chr3:195885531..195888308-chr3:195908401..195910834,2	K562	blood:
31	chr3:195808310..195809179-chr3:195876922..195877750,2	MCF-7	breast:
32	chr3:195868011..195869690-chr3:195889023..195890635,2	MCF-7	breast:
33	chr3:195890135..195892758-chr3:195896649..195899546,2	K562	blood:
34	chr3:195807106..195808985-chr3:195881023..195882640,2	MCF-7	breast:
35	chr3:195895053..195896578-chr6:7190290..7192717,2	K562	blood:
36	chr3:195866882..195869334-chr3:195921149..195922972,2	K562	blood:
37	chr3:195840398..195842445-chr3:195874732..195876479,2	K562	blood:
38	chr3:195796942..195799374-chr3:195862059..195864559,2	K562	blood:
39	chr3:195854415..195856195-chr3:195888995..195891354,2	K562	blood:
40	chr3:195890392..195892758-chr3:195896649..195898282,2	K562	blood:
41	chr3:195813315..195814867-chr3:195884701..195886737,2	K562	blood:
42	chr3:195807237..195809801-chr3:195891488..195894845,3	MCF-7	breast:
43	chr3:195901978..195904372-chr3:195908307..195910643,2	MCF-7	breast:
44	chr3:195903618..195905705-chr3:195906197..195908381,3	K562	blood:
45	chr3:195806658..195811369-chr3:195865432..195872361,14	MCF-7	breast:
46	chr3:195884789..195887031-chr3:195907240..195909901,2	K562	blood:
47	chr3:195900051..195902109-chr3:195908917..195911441,2	K562	blood:
48	chr3:195868179..195870899-chr3:195889538..195893919,5	K562	blood:
49	chr3:195871413..195873461-chr3:195905965..195908112,2	K562	blood:
50	chr3:195799311..195801331-chr3:195903536..195907265,3	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC069257.9.1-2	chr3:195869519-195869871	NONHSAT094297
2	lnc-AC069257.9.1-8	chr3:195911292-195911606	l_2563_chr3:195910484-195920505_testes
3	lnc-AC069257.9.1-2	chr3:195870150-195870193	XLOC_003002
4	lnc-AC069257.9.1-2	chr3:195871048-195871248	XLOC_003002
5	lnc-AC069257.9.1-2	chr3:195869507-195869871	ENSG00000224652
6	lnc-AC069257.9.1-2	chr3:195886771-195887761	ENSG00000224652
7	lnc-AC069257.9.1-2	chr3:195870777-195870822	XLOC_003002
8	lnc-AC069257.9.1-2	chr3:195886771-195886896	XLOC_003002
9	lnc-AC069257.9.1-2	chr3:195871048-195871249	XLOC_003002
10	lnc-AC069257.9.1-2	chr3:195869671-195869871	XLOC_003002
11	lnc-AC069257.9.1-2	chr3:195886771-195886851	XLOC_003002
12	lnc-AC069257.9.1-2	chr3:195871048-195871248	NONHSAT094297
13	lnc-AC069257.9.1-2	chr3:195870915-195871248	XLOC_003002
14	lnc-AC069257.9.1-2	chr3:195886771-195887593	NONHSAT094297
15	lnc-AC069257.9.1-2	chr3:195869626-195870280	XLOC_003002
16	lnc-AC069257.9.1-8	chr3:195916991-195917200	l_2563_chr3:195910484-195920505_testes
17	lnc-AC069257.9.1-9	chr3:195904190-195904502	NONHSAT094301
18	lnc-AC069257.9.1-2	chr3:195871048-195871248	XLOC_003002
19	lnc-AC069257.9.1-2	chr3:195870777-195871248	ENSG00000224652
20	lnc-AC069257.9.1-2	chr3:195869677-195869871	XLOC_003002
21	lnc-AC069257.9.1-2	chr3:195886771-195886841	XLOC_003002
22	lnc-AC069257.9.1-8	chr3:195910485-195911165	l_2563_chr3:195910484-195920505_testes

No data

Variant related genes	Relation type
LINC00885	TF binding region
LINC00885	CpG island
ENSG00000061938	chromatin interactions
ENSG00000072274	chromatin interactions
ENSG00000252174	chromatin interactions
ENSG00000224652	chromatin interactions
YKT6	miRNA target sites
AKT3	miRNA target sites
WLS	miRNA target sites
WDR26	miRNA target sites
SC4MOL	miRNA target sites
WDFY3	miRNA target sites
NCDN	miRNA target sites
SLC35D2	miRNA target sites

Extended variants
information (count: 2565 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2565 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145286832	chr3:195864471-195864472	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs549088346	chr3:195864510-195864511	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs567350953	chr3:195864522-195864523	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs534667627	chr3:195864553-195864554	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs553625304	chr3:195864578-195864579	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs578182447	chr3:195864587-195864588	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs188511981	chr3:195864606-195864607	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs557360395	chr3:195864699-195864700	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs575642399	chr3:195864700-195864701	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs76937886	chr3:195864709-195864710	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs542636313	chr3:195864722-195864723	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs561079630	chr3:195864727-195864728	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs191989834	chr3:195864735-195864736	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs554580102	chr3:195864744-195864745	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs540304303	chr3:195864760-195864761	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs559128166	chr3:195864781-195864782	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs532944855	chr3:195864876-195864877	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs551696581	chr3:195864892-195864893	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs375844337	chr3:195864900-195864901	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs367807702	chr3:195864907-195864908	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs576155584	chr3:195864915-195864916	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs548715843	chr3:195864917-195864918	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs567240982	chr3:195864974-195864975	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs377641069	chr3:195864990-195864991	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs111229215	chr3:195864995-195864996	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs4927887	chr3:195865023-195865024	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs550601347	chr3:195865076-195865077	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs571908315	chr3:195865087-195865088	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs538853232	chr3:195865119-195865120	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs201216281	chr3:195865168-195865169	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs141027711	chr3:195865169-195865170	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs184229547	chr3:195865190-195865191	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs557664530	chr3:195865246-195865247	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs11419136	chr3:195865270-195865271	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs397786656	chr3:195865273-195865274	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs569434008	chr3:195865309-195865310	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs536916914	chr3:195865319-195865320	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs577415154	chr3:195865326-195865327	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs554568228	chr3:195865364-195865365	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs572857200	chr3:195865373-195865374	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs7634650	chr3:195865387-195865388	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs189378253	chr3:195865532-195865533	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs539463453	chr3:195865534-195865535	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs181736730	chr3:195865535-195865536	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs146421369	chr3:195865540-195865541	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs375475984	chr3:195865572-195865573	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs75179937	chr3:195865582-195865583	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs112666411	chr3:195865584-195865585	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs530055853	chr3:195865656-195865657	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs369720754	chr3:195865801-195865802	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1556 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195860400-195869000	Enhancers	Placenta	Placenta
2	chr3:195861600-195867200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:195861800-195865800	Weak transcription	Fetal Lung	lung
4	chr3:195862000-195868800	Weak transcription	Fetal Muscle Leg	muscle
5	chr3:195862600-195864600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr3:195862600-195864800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr3:195863000-195865400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr3:195863000-195868000	Weak transcription	Spleen	Spleen
9	chr3:195863000-195868600	Weak transcription	Esophagus	oesophagus
10	chr3:195863000-195869200	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr3:195863200-195865400	Weak transcription	Pancreas	Pancrea
12	chr3:195863200-195865400	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr3:195863200-195865400	Weak transcription	HSMMtube	muscle
14	chr3:195863200-195869000	Weak transcription	Gastric	stomach
15	chr3:195863200-195869600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr3:195863400-195864800	Enhancers	HMEC	breast
17	chr3:195863400-195865400	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr3:195863400-195865400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr3:195863400-195866200	Weak transcription	Fetal Thymus	thymus
20	chr3:195863400-195869000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr3:195863400-195869000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr3:195863400-195869200	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr3:195863600-195865200	Weak transcription	Liver	Liver
24	chr3:195863600-195865400	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr3:195863600-195867200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr3:195863600-195869200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr3:195863800-195865000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr3:195863800-195865200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr3:195863800-195866200	Enhancers	NHEK	skin
30	chr3:195864000-195865200	Enhancers	Hela-S3	cervix
31	chr3:195864000-195865400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr3:195864000-195869600	Weak transcription	Ovary	ovary
33	chr3:195864200-195865400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr3:195864400-195864600	Enhancers	Primary hematopoietic stem cells	blood
35	chr3:195864400-195865400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr3:195864400-195865400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr3:195864400-195865600	Enhancers	K562	blood
38	chr3:195864600-195866400	Weak transcription	Primary hematopoietic stem cells	blood
39	chr3:195864600-195867000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr3:195864800-195865200	Weak transcription	HMEC	breast
41	chr3:195864800-195866800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr3:195865000-195866600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr3:195865200-195866400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr3:195865200-195866400	Enhancers	Liver	Liver
45	chr3:195865200-195866400	Enhancers	HMEC	breast
46	chr3:195865200-195866600	Flanking Active TSS	Hela-S3	cervix
47	chr3:195865400-195865800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr3:195865400-195865800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr3:195865400-195866000	Enhancers	H9 Cell Line	embryonic stem cell
50	chr3:195865400-195866000	Enhancers	HUES48 Cell Line	embryonic stem cell

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