Variant report

Variant	nsv1000927
Chromosome Location	chr3:138423543-138632596
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2849)
CpG islands
(count:1405)
Chromatin interactive
region (count:202)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2849 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:138465588-138465752	K562	blood:	n/a	n/a
2	ARID3A	chr3:138445097-138445297	K562	blood:	n/a	n/a
3	ARID3A	chr3:138568361-138568735	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:138542664-138543186	K562	blood:	n/a	n/a
5	ARID3A	chr3:138542527-138543276	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:138617451-138617764	K562	blood:	n/a	n/a
7	ARID3A	chr3:138609961-138610392	K562	blood:	n/a	n/a
8	ARID3A	chr3:138522011-138522401	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:138572981-138573417	HepG2	liver:	n/a	n/a
10	ARID3A	chr3:138553811-138554115	HepG2	liver:	n/a	n/a
11	ARID3A	chr3:138501609-138502054	K562	blood:	n/a	n/a
12	ARID3A	chr3:138594268-138595377	K562	blood:	n/a	n/a
13	ARID3A	chr3:138564641-138565358	HepG2	liver:	n/a	n/a
14	ARID3A	chr3:138630689-138631330	K562	blood:	n/a	n/a
15	ARID3A	chr3:138598754-138598832	HepG2	liver:	n/a	n/a
16	ARID3A	chr3:138551179-138551208	K562	blood:	n/a	n/a
17	ARID3A	chr3:138553348-138553595	HepG2	liver:	n/a	n/a
18	ARID3A	chr3:138597287-138597298	K562	blood:	n/a	n/a
19	ARID3A	chr3:138609977-138610292	HepG2	liver:	n/a	n/a
20	ARID3A	chr3:138581261-138582347	K562	blood:	n/a	n/a
21	ARID3A	chr3:138581282-138582578	HepG2	liver:	n/a	n/a
22	ARID3A	chr3:138445956-138445960	K562	blood:	n/a	n/a
23	ARID3A	chr3:138551687-138551841	K562	blood:	n/a	n/a
24	ATF1	chr3:138551530-138551860	K562	blood:	n/a	n/a
25	ATF1	chr3:138610130-138610387	K562	blood:	n/a	n/a
26	ATF1	chr3:138594439-138595145	K562	blood:	n/a	n/a
27	ATF1	chr3:138444959-138445226	K562	blood:	n/a	n/a
28	ATF1	chr3:138501467-138501905	K562	blood:	n/a	n/a
29	ATF1	chr3:138542619-138542957	K562	blood:	n/a	n/a
30	ATF1	chr3:138436534-138436682	K562	blood:	n/a	n/a
31	ATF2	chr3:138509814-138510628	GM12878	blood:	n/a	n/a
32	ATF2	chr3:138607390-138607749	GM12878	blood:	n/a	n/a
33	ATF2	chr3:138553809-138554162	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF2	chr3:138510165-138510623	GM12878	blood:	n/a	n/a
35	ATF2	chr3:138542541-138543170	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF2	chr3:138561204-138561757	GM12878	blood:	n/a	n/a
37	ATF2	chr3:138607348-138607780	GM12878	blood:	n/a	n/a
38	ATF2	chr3:138516289-138516751	GM12878	blood:	n/a	n/a
39	ATF2	chr3:138436122-138436716	GM12878	blood:	n/a	n/a
40	ATF2	chr3:138542557-138543202	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF3	chr3:138542582-138542931	K562	blood:	n/a	n/a
42	ATF3	chr3:138493312-138493595	K562	blood:	n/a	n/a
43	ATF3	chr3:138594328-138595139	K562	blood:	n/a	n/a
44	ATF3	chr3:138581585-138582572	K562	blood:	n/a	n/a
45	ATF3	chr3:138486887-138487303	K562	blood:	n/a	n/a
46	BACH1	chr3:138553568-138553687	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr3:138581420-138582029	H1-hESC	embryonic stem cell:	n/a	chr3:138581961-138581975
48	BACH1	chr3:138542613-138543119	K562	blood:	n/a	n/a
49	BACH1	chr3:138552962-138553282	H1-hESC	embryonic stem cell:	n/a	n/a
50	BACH1	chr3:138561623-138561922	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:138617437-138617487	HEEpiC	esophagus:	n/a
2	chr3:138478129-138478179	SK-N-MC	brain:	n/a
3	chr3:138617437-138617487	HEEpiC	esophagus:	n/a
4	chr3:138478129-138478179	SK-N-MC	brain:	n/a
5	chr3:138553528-138553578	ovcar-3	ovarian:	n/a
6	chr3:138553528-138553578	BE2_C	brain:	n/a
7	chr3:138479285-138479335	HPAEpiC	pulmonary alveolar:	n/a
8	chr3:138487881-138487931	NT2-D1	testis:	n/a
9	chr3:138553760-138553810	PFSK-1	brain:	n/a
10	chr3:138494226-138494276	HCF	heart:	n/a
11	chr3:138494226-138494276	RPTEC	kidney:	n/a
12	chr3:138479125-138479175	HRE	kidney:	n/a
13	chr3:138543076-138543126	PFSK-1	brain:	n/a
14	chr3:138552844-138552894	HCM	heart:	n/a
15	chr3:138581702-138581752	HNPCEpiC	eye:	n/a
16	chr3:138478129-138478179	A549	lung:	n/a
17	chr3:138479392-138479442	AG04449	skin:	fetal
18	chr3:138522351-138522401	ECC-1	luminal epithelium:	n/a
19	chr3:138631456-138631506	HRE	kidney:	n/a
20	chr3:138552648-138552698	HCT-116	colon:	n/a
21	chr3:138557288-138557338	AG04449	skin:	fetal
22	chr3:138479125-138479175	HCT-116	colon:	n/a
23	chr3:138617437-138617487	H1-hESC	embryonic stem cell:	embryo
24	chr3:138553774-138553824	NHBE	bronchial:	n/a
25	chr3:138581702-138581752	NHBE	bronchial:	n/a
26	chr3:138631456-138631506	HRCEpiC	kidney:	n/a
27	chr3:138617437-138617487	SAEC	small airway:	n/a
28	chr3:138487881-138487931	HCT-116	colon:	n/a
29	chr3:138553528-138553578	Jurkat	blood:	n/a
30	chr3:138553170-138553220	ovcar-3	ovarian:	n/a
31	chr3:138553760-138553810	HCM	heart:	n/a
32	chr3:138617437-138617487	SK-N-MC	brain:	n/a
33	chr3:138581702-138581752	AG04449	skin:	fetal
34	chr3:138554516-138554566	NT2-D1	testis:	n/a
35	chr3:138478129-138478179	NHBE	bronchial:	n/a
36	chr3:138552648-138552698	HepG2	liver:	n/a
37	chr3:138553170-138553220	SK-N-SH	brain:	n/a
38	chr3:138479392-138479442	HEK293	kidney:	embryo
39	chr3:138479392-138479442	GM12892	blood:	n/a
40	chr3:138552891-138552941	HCF	heart:	n/a
41	chr3:138522351-138522401	ovcar-3	ovarian:	n/a
42	chr3:138479125-138479175	Hela-S3	cervix:	n/a
43	chr3:138553528-138553578	Hepatocyte	liver:	n/a
44	chr3:138552648-138552698	NT2-D1	testis:	n/a
45	chr3:138631456-138631506	SAEC	small airway:	n/a
46	chr3:138631456-138631506	HMEC	breast:	n/a
47	chr3:138543076-138543126	BE2_C	brain:	n/a
48	chr3:138553760-138553810	Caco-2	colon:	n/a
49	chr3:138617437-138617487	AG04450	lung:	fetal
50	chr3:138552844-138552894	SKMC	muscle:	n/a

(count:202 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr3:138603808..138606375-chr3:138611752..138614261,2	K562	blood:
2	chr3:138575224..138576892-chr3:138580105..138582108,2	K562	blood:
3	chr3:138541276..138545209-chr3:138550830..138554565,5	MCF-7	breast:
4	chr3:138446350..138448726-chr3:138452813..138454889,2	K562	blood:
5	chr3:138427248..138429921-chr3:138433122..138435175,2	K562	blood:
6	chr3:138472857..138474633-chr3:138553666..138555234,2	MCF-7	breast:
7	chr3:138539146..138542013-chr3:138544348..138547069,3	K562	blood:
8	chr3:138421817..138424189-chr3:138551922..138554097,3	MCF-7	breast:
9	chr3:138447382..138449925-chr3:138453457..138455253,2	MCF-7	breast:
10	chr3:138439627..138441502-chr3:138475761..138477385,2	K562	blood:
11	chr3:138459994..138462249-chr3:138507589..138510165,2	K562	blood:
12	chr3:138532061..138535019-chr3:138545611..138549640,3	K562	blood:
13	chr3:138514134..138516251-chr3:138522655..138525070,2	MCF-7	breast:
14	chr3:138532061..138535019-chr3:138545611..138549640,3	K562	blood:
15	chr3:138593690..138596327-chr3:138610684..138613648,2	K562	blood:
16	chr14:105143562..105144379-chr3:138553432..138553985,2	HCT-116	colon:
17	chr3:138515862..138518056-chr3:138520254..138523440,3	K562	blood:
18	chr3:138628286..138631050-chr3:138632993..138634639,2	MCF-7	breast:
19	chr3:138312690..138314858-chr3:138552284..138553853,2	K562	blood:
20	chr3:137891312..137893819-chr3:138582385..138585243,2	K562	blood:
21	chr3:138549301..138556465-chr3:138628994..138637084,25	K562	blood:
22	chr3:138415770..138417345-chr3:138421498..138424319,2	K562	blood:
23	chr3:138446030..138450160-chr3:138450548..138454889,4	K562	blood:
24	chr3:138530180..138531865-chr3:138606061..138609027,2	K562	blood:
25	chr3:138541276..138545209-chr3:138550830..138554565,5	MCF-7	breast:
26	chr3:138624955..138627737-chr3:138631788..138633518,2	K562	blood:
27	chr3:138551460..138555147-chr3:138627528..138630688,3	MCF-7	breast:
28	chr3:138580257..138585634-chr3:138593415..138596528,8	K562	blood:
29	chr3:138615801..138617614-chr3:138617709..138619376,2	K562	blood:
30	chr3:138586530..138588929-chr3:138592253..138594819,3	K562	blood:
31	chr3:138617072..138618761-chr3:138627916..138629568,2	K562	blood:
32	chr3:138572929..138574739-chr3:138578967..138582635,3	K562	blood:
33	chr3:138453648..138456326-chr3:138462764..138465635,2	K562	blood:
34	chr3:138570386..138571941-chr3:138575382..138577524,2	K562	blood:
35	chr3:138593490..138596609-chr3:138597250..138600269,4	K562	blood:
36	chr3:138497639..138499838-chr3:138521505..138523466,2	K562	blood:
37	chr3:138553429..138554961-chr3:138609413..138611787,2	K562	blood:
38	chr3:138548916..138550963-chr3:138596429..138598640,2	K562	blood:
39	chr3:138552112..138555391-chr3:138593368..138596315,4	K562	blood:
40	chr3:138477863..138479769-chr3:138480027..138482650,2	K562	blood:
41	chr3:138552568..138555141-chr3:138666105..138668600,2	K562	blood:
42	chr3:138475304..138477689-chr3:138484977..138487664,2	K562	blood:
43	chr3:138547576..138550266-chr3:138633999..138636358,2	MCF-7	breast:
44	chr3:138491707..138493497-chr3:138496731..138499014,2	K562	blood:
45	chr3:138433313..138434820-chr3:138553042..138555465,2	MCF-7	breast:
46	chr3:138419957..138424581-chr3:138425428..138429195,4	K562	blood:
47	chr3:138581629..138583620-chr3:138597045..138599792,2	K562	blood:
48	chr3:138553512..138555191-chr3:138558686..138560524,2	MCF-7	breast:
49	chr3:138548916..138550963-chr3:138596429..138598640,2	K562	blood:
50	chr3:138497768..138501036-chr3:138504474..138507070,3	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXL2-3	chr3:138551007-138551271	uc_125_-
2	lnc-C3orf72-4	chr3:138544770-138544844	NONHSAT092342
3	lnc-FAIM-4	chr3:138466234-138466725	uc_123_+
4	lnc-C3orf72-2	chr3:138608338-138608608	uc_126_+
5	lnc-C3orf72-4	chr3:138544653-138544666	NONHSAT092342
6	lnc-C3orf72-4	chr3:138543905-138545171	NONHSAT092341
7	lnc-C3orf72-4	chr3:138544861-138545200	NONHSAT092342
8	lnc-FOXL2-2	chr3:138608548-138608799	NONHSAT092343
9	lnc-FOXL2-4	chr3:138531134-138531420	uc_124_-
10	lnc-CEP70-2	chr3:138466234-138466725	uc_123_-
11	lnc-C3orf72-3	chr3:138551007-138551271	uc_125_+
12	lnc-C3orf72-5	chr3:138531134-138531420	uc_124_+
13	lnc-FOXL2-2	chr3:138608338-138608608	uc_126_-
14	lnc-FOXL2-2	chr3:138608097-138608254	NONHSAT092343
15	lnc-C3orf72-6	chr3:138515693-138516082	NONHSAT092340

No data

Variant related genes	Relation type
EEF1A1P25	TF binding region
RPL23AP40	TF binding region
GAPDHP39	TF binding region
PIK3CB	TF binding region
ATP5G1P3	TF binding region
EEF1A1P25	CpG island
RPL23AP40	CpG island
GAPDHP39	CpG island
PIK3CB	CpG island
ATP5G1P3	CpG island
ENSG00000252245	chromatin interactions
ENSG00000051382	chromatin interactions
ENSG00000158234	chromatin interactions
ENSG00000222724	chromatin interactions
ENSG00000138231	chromatin interactions
ENSG00000244578	chromatin interactions
ENSG00000242321	chromatin interactions
ENSG00000241429	chromatin interactions
ENSG00000104613	chromatin interactions
ENSG00000103126	chromatin interactions
ENSG00000242244	chromatin interactions
ENSG00000183770	chromatin interactions
ENSG00000239207	chromatin interactions
ENSG00000114107	chromatin interactions
ENSG00000265291	chromatin interactions
ENSG00000206262	chromatin interactions

Extended variants
information (count: 7800 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:7800 , 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	rs374874290	chr3:138423559-138423560	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs564984613	chr3:138423599-138423600	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs554572089	chr3:138423603-138423604	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs57112316	chr3:138423616-138423617	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs189242898	chr3:138423625-138423626	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs147472980	chr3:138423745-138423746	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs182031245	chr3:138423755-138423756	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs567251162	chr3:138423799-138423800	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs536374813	chr3:138423804-138423805	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs574459116	chr3:138423830-138423831	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs569446928	chr3:138423834-138423835	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs185042999	chr3:138423843-138423844	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs558329310	chr3:138423943-138423944	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs395666	chr3:138423961-138423962	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs387579	chr3:138423964-138423965	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs191063582	chr3:138423984-138423985	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs73864485	chr3:138424009-138424010	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs563614217	chr3:138424016-138424017	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs553775557	chr3:138424019-138424020	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs12631204	chr3:138424023-138424024	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs201997168	chr3:138424028-138424029	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs60660285	chr3:138424032-138424033	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs576188072	chr3:138424033-138424034	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs544921455	chr3:138424036-138424037	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs1449361	chr3:138424049-138424050	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs112685597	chr3:138424058-138424059	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs143959804	chr3:138424110-138424111	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs527614926	chr3:138424158-138424159	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs606536	chr3:138424159-138424160	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs182783641	chr3:138424183-138424184	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs186647642	chr3:138424187-138424188	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs529676363	chr3:138424216-138424217	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs439720	chr3:138424217-138424218	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs569699321	chr3:138424248-138424249	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs536211226	chr3:138424296-138424297	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs191437496	chr3:138424321-138424322	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs529671571	chr3:138424329-138424330	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs977489	chr3:138424369-138424370	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs146878714	chr3:138424393-138424394	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs371368225	chr3:138424442-138424443	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs571484111	chr3:138424551-138424552	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs75656025	chr3:138424553-138424554	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs534241176	chr3:138424563-138424564	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs140746544	chr3:138424600-138424601	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76778888	chr3:138424679-138424680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536198085	chr3:138424743-138424744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556517180	chr3:138424749-138424750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191713	chr3:138424857-138424858	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs9876610	chr3:138424936-138424937	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552923531	chr3:138424941-138424942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	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
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	23813976	CNVD
Cancer	20164919	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4049 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:138364400-138459200	Weak transcription	Psoas Muscle	Psoas
2	chr3:138369000-138493000	Weak transcription	Fetal Lung	lung
3	chr3:138369200-138428800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr3:138369200-138435600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr3:138375200-138429000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr3:138383200-138448200	Weak transcription	Gastric	stomach
7	chr3:138383400-138426400	Weak transcription	Spleen	Spleen
8	chr3:138383400-138443000	Weak transcription	Brain Cingulate Gyrus	brain
9	chr3:138390800-138459600	Weak transcription	Right Ventricle	heart
10	chr3:138393800-138515000	Weak transcription	Aorta	Aorta
11	chr3:138395200-138436800	Weak transcription	Brain Germinal Matrix	brain
12	chr3:138395800-138444800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr3:138395800-138459800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr3:138395800-138480200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr3:138396000-138436400	Weak transcription	Fetal Brain Female	brain
16	chr3:138396000-138469200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr3:138396200-138443200	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr3:138396200-138469200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr3:138396200-138486400	Weak transcription	Rectal Smooth Muscle	rectum
20	chr3:138396200-138487000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr3:138397200-138434400	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr3:138399600-138443400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:138400600-138442800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr3:138401600-138436600	Weak transcription	Brain Hippocampus Middle	brain
25	chr3:138401800-138442800	Weak transcription	Brain Angular Gyrus	brain
26	chr3:138402000-138442800	Weak transcription	Brain Substantia Nigra	brain
27	chr3:138402200-138431000	Weak transcription	Stomach Smooth Muscle	stomach
28	chr3:138404800-138442200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr3:138406000-138432600	Weak transcription	Fetal Kidney	kidney
30	chr3:138406800-138442200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr3:138408000-138479800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr3:138408200-138427200	Weak transcription	GM12878-XiMat	blood
33	chr3:138408200-138443200	Weak transcription	Brain Anterior Caudate	brain
34	chr3:138408400-138426000	Weak transcription	Primary B cells from peripheral blood	blood
35	chr3:138408400-138499200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr3:138409800-138427000	Strong transcription	Primary neutrophils fromperipheralblood	blood
37	chr3:138412000-138432000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr3:138412600-138432000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr3:138413600-138430800	Weak transcription	Stomach Mucosa	stomach
40	chr3:138413800-138426000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr3:138413800-138445400	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr3:138413800-138445400	Weak transcription	Ovary	ovary
43	chr3:138413800-138458400	Weak transcription	Thymus	Thymus
44	chr3:138413800-138487600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr3:138414000-138426400	Weak transcription	HSMM	muscle
46	chr3:138414000-138432600	Weak transcription	NHEK	skin
47	chr3:138414200-138453400	Weak transcription	HMEC	breast
48	chr3:138414400-138436200	Weak transcription	NHDF-Ad	bronchial
49	chr3:138415600-138428800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr3:138415800-138445800	Weak transcription	NH-A	brain

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