Variant report

Variant	nsv831762
Chromosome Location	chr9:140338779-140514107
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:8747)
CpG islands
(count:6781)
Chromatin interactive
region (count:519)
LncRNA
region (count:9)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:8747 , 50 per page) page: 1 2 3 4 5 6 7 ... 175

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:140476767-140476847	K562	blood:	n/a	n/a
2	ARID3A	chr9:140397266-140397473	K562	blood:	n/a	n/a
3	ARID3A	chr9:140339716-140339973	K562	blood:	n/a	n/a
4	ARID3A	chr9:140476704-140476869	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:140349264-140349724	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:140349505-140349575	K562	blood:	n/a	n/a
7	ARID3A	chr9:140473269-140473545	K562	blood:	n/a	n/a
8	ARID3A	chr9:140455523-140455741	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:140353775-140353946	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:140429317-140429674	K562	blood:	n/a	n/a
11	ARID3A	chr9:140339748-140340324	HepG2	liver:	n/a	n/a
12	ARID3A	chr9:140388745-140388839	K562	blood:	n/a	n/a
13	ARID3A	chr9:140512995-140513194	K562	blood:	n/a	n/a
14	ARID3A	chr9:140406300-140406534	K562	blood:	n/a	n/a
15	ARID3A	chr9:140431001-140431055	K562	blood:	n/a	n/a
16	ARID3A	chr9:140473271-140473827	HepG2	liver:	n/a	n/a
17	ATF1	chr9:140385237-140385607	K562	blood:	n/a	n/a
18	ATF1	chr9:140512908-140513272	K562	blood:	n/a	n/a
19	ATF1	chr9:140386077-140386838	K562	blood:	n/a	n/a
20	ATF1	chr9:140376674-140377053	K562	blood:	n/a	n/a
21	ATF1	chr9:140406110-140406643	K562	blood:	n/a	n/a
22	ATF1	chr9:140485031-140485339	K562	blood:	n/a	n/a
23	ATF1	chr9:140413661-140413862	K562	blood:	n/a	n/a
24	ATF1	chr9:140353686-140354042	K562	blood:	n/a	n/a
25	ATF1	chr9:140469909-140470724	K562	blood:	n/a	n/a
26	ATF2	chr9:140356259-140356799	GM12878	blood:	n/a	n/a
27	ATF2	chr9:140473015-140473621	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr9:140512882-140513291	GM12878	blood:	n/a	n/a
29	ATF2	chr9:140339754-140340081	GM12878	blood:	n/a	n/a
30	ATF2	chr9:140376547-140376853	GM12878	blood:	n/a	n/a
31	ATF2	chr9:140512846-140513342	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr9:140473265-140473580	GM12878	blood:	n/a	n/a
33	ATF2	chr9:140513019-140513356	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF2	chr9:140353700-140354020	GM12878	blood:	n/a	n/a
35	ATF2	chr9:140473133-140473657	GM12878	blood:	n/a	n/a
36	ATF2	chr9:140339651-140340225	GM12878	blood:	n/a	n/a
37	ATF2	chr9:140512599-140513361	GM12878	blood:	n/a	n/a
38	ATF3	chr9:140473135-140473716	A549	lung:	n/a	n/a
39	ATF3	chr9:140473017-140473719	A549	lung:	n/a	chr9:140473065-140473074
40	ATF3	chr9:140512666-140513485	A549	lung:	n/a	chr9:140513400-140513409
41	ATF3	chr9:140353730-140354018	K562	blood:	n/a	chr9:140353933-140353942
42	ATF3	chr9:140473293-140473650	K562	blood:	n/a	n/a
43	ATF3	chr9:140500314-140500576	K562	blood:	n/a	n/a
44	ATF3	chr9:140429242-140429797	HepG2	liver:	n/a	n/a
45	ATF3	chr9:140376711-140377025	K562	blood:	n/a	n/a
46	ATF3	chr9:140473254-140473601	K562	blood:	n/a	n/a
47	ATF3	chr9:140429268-140429655	H1-hESC	embryonic stem cell:	n/a	n/a
48	ATF3	chr9:140406167-140406614	K562	blood:	n/a	n/a
49	ATF3	chr9:140429357-140429545	GM12878	blood:	n/a	n/a
50	ATF3	chr9:140429318-140429660	HepG2	liver:	n/a	n/a

(count:6781 , 50 per page) page: 1 2 3 4 5 6 7 ... 136

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140389750-140389800	SK-N-SH	brain:	n/a
2	chr9:140374285-140374335	GM12892	blood:	n/a
3	chr9:140353134-140353184	MCF-7	breast:	n/a
4	chr9:140501305-140501355	RPTEC	kidney:	n/a
5	chr9:140343617-140343667	SK-N-MC	brain:	n/a
6	chr9:140500037-140500087	GM12891	blood:	n/a
7	chr9:140471399-140471449	A549	lung:	n/a
8	chr9:140418776-140418826	AoSMC	blood vessel:	n/a
9	chr9:140354043-140354093	HUVEC	blood vessel:	n/a
10	chr9:140343854-140343904	Caco-2	colon:	n/a
11	chr9:140389750-140389800	SK-N-SH	brain:	n/a
12	chr9:140374285-140374335	GM12892	blood:	n/a
13	chr9:140353134-140353184	MCF-7	breast:	n/a
14	chr9:140501305-140501355	RPTEC	kidney:	n/a
15	chr9:140343617-140343667	SK-N-MC	brain:	n/a
16	chr9:140500037-140500087	GM12891	blood:	n/a
17	chr9:140471399-140471449	A549	lung:	n/a
18	chr9:140418776-140418826	AoSMC	blood vessel:	n/a
19	chr9:140354043-140354093	HUVEC	blood vessel:	n/a
20	chr9:140343854-140343904	Caco-2	colon:	n/a
21	chr9:140418776-140418826	SK-N-MC	brain:	n/a
22	chr9:140394139-140394189	PANC-1	pancreas:	n/a
23	chr9:140512455-140512505	MCF-7	breast:	n/a
24	chr9:140355318-140355368	AG10803	skin:	n/a
25	chr9:140485596-140485646	ovcar-3	ovarian:	n/a
26	chr9:140361383-140361433	HPAEpiC	pulmonary alveolar:	n/a
27	chr9:140473606-140473656	A549	lung:	n/a
28	chr9:140359339-140359389	SK-N-SH_RA	brain:	n/a
29	chr9:140417551-140417601	GM12878	blood:	n/a
30	chr9:140512513-140512563	AG04449	skin:	fetal
31	chr9:140473875-140473925	HEEpiC	esophagus:	n/a
32	chr9:140473184-140473234	T-47D	breast:	n/a
33	chr9:140446823-140446873	AG10803	skin:	n/a
34	chr9:140473545-140473595	GM19239	blood:	n/a
35	chr9:140425395-140425445	RPTEC	kidney:	n/a
36	chr9:140377789-140377839	RPTEC	kidney:	n/a
37	chr9:140355163-140355213	HEK293	kidney:	embryo
38	chr9:140343617-140343667	AG09309	skin:	n/a
39	chr9:140484847-140484897	HRPEpiC	eye:	n/a
40	chr9:140418776-140418826	NHDF-neo	bronchial:	n/a
41	chr9:140500037-140500087	GM06990	blood:	n/a
42	chr9:140400693-140400743	K562	blood:	n/a
43	chr9:140354241-140354291	GM06990	blood:	n/a
44	chr9:140408634-140408684	HAEpiC	amniotic membrane:	n/a
45	chr9:140499397-140499447	AG09309	skin:	n/a
46	chr9:140369012-140369062	HAEpiC	amniotic membrane:	n/a
47	chr9:140349969-140350019	NHBE	bronchial:	n/a
48	chr9:140357706-140357756	AG09319	gingival:	n/a
49	chr9:140441854-140441904	Jurkat	blood:	n/a
50	chr9:140473606-140473656	NH-A	brain:	n/a

(count:519 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Distal block	Cell Line	Cell type
1	chr9:140427985..140429515-chr9:140431192..140432744,2	K562	blood:
2	chr9:140470766..140479486-chr9:140497266..140502997,13	MCF-7	breast:
3	chr9:140487259..140491195-chr9:140511184..140515704,4	K562	blood:
4	chr11:57101757..57103257-chr9:140397098..140398604,2	MCF-7	breast:
5	chr9:140513748..140516192-chr9:140572995..140575836,2	MCF-7	breast:
6	chr9:140192004..140196032-chr9:140413457..140417425,3	MCF-7	breast:
7	chr17:62502544..62503507-chr9:140352975..140353583,2	Hela-S3	cervix:
8	chr9:140431100..140433802-chr9:140474645..140476543,2	K562	blood:
9	chr9:140195671..140196210-chr9:140339702..140340361,2	MCF-7	breast:
10	chr9:140320912..140322713-chr9:140405258..140407507,2	MCF-7	breast:
11	chr9:140356011..140357682-chr9:140374580..140376240,2	K562	blood:
12	chr9:140414450..140416350-chr9:140433102..140436050,2	MCF-7	breast:
13	chr9:140473011..140477060-chr9:140511720..140517022,6	K562	blood:
14	chr9:140332776..140334313-chr9:140412829..140415749,2	MCF-7	breast:
15	chr9:140445002..140446703-chr9:140512317..140515053,2	MCF-7	breast:
16	chr9:140209677..140212013-chr9:140385479..140387034,2	K562	blood:
17	chr9:140331075..140334517-chr9:140343053..140345567,3	K562	blood:
18	chr9:140482066..140484246-chr9:140508462..140511181,2	K562	blood:
19	chr9:140443475..140446294-chr9:140484220..140486836,3	MCF-7	breast:
20	chr9:140463229..140465776-chr9:140474685..140477530,2	MCF-7	breast:
21	chr9:140457953..140460745-chr9:140471921..140474546,2	K562	blood:
22	chr9:140481402..140486615-chr9:140511490..140514947,5	K562	blood:
23	chr9:140420711..140423726-chr9:140426984..140429291,3	K562	blood:
24	chr9:140347379..140350027-chr9:140394775..140397563,4	K562	blood:
25	chr9:140352137..140355481-chr9:140359120..140360959,3	MCF-7	breast:
26	chr9:140444243..140447461-chr9:140473220..140477204,4	MCF-7	breast:
27	chr17:80817947..80820292-chr9:140513382..140515787,2	MCF-7	breast:
28	chr9:140509926..140512200-chr9:140526442..140528104,2	MCF-7	breast:
29	chr9:140470139..140471923-chr9:140487419..140488929,2	MCF-7	breast:
30	chr9:140402660..140405211-chr9:140405983..140408009,2	MCF-7	breast:
31	chr9:140469278..140479132-chr9:140503165..140510984,27	MCF-7	breast:
32	chr9:140142023..140145002-chr9:140350817..140354805,3	K562	blood:
33	chr9:140470445..140476327-chr9:140498022..140503450,9	K562	blood:
34	chr9:140189070..140190708-chr9:140435043..140436758,2	K562	blood:
35	chr9:140245725..140246694-chr9:140339428..140340337,3	MCF-7	breast:
36	chr9:140470852..140475352-chr9:140511735..140515041,9	MCF-7	breast:
37	chr9:140470852..140475352-chr9:140511735..140515041,9	MCF-7	breast:
38	chr9:140116174..140118873-chr9:140338820..140340591,2	MCF-7	breast:
39	chr9:140335850..140343594-chr9:140351085..140357770,13	MCF-7	breast:
40	chr9:140432353..140434549-chr9:140437572..140440082,2	K562	blood:
41	chr14:36295481..36295998-chr9:140513118..140513972,2	Hela-S3	cervix:
42	chr9:140317349..140318505-chr9:140339431..140340433,7	K562	blood:
43	chr9:140413558..140415139-chr9:140438109..140439773,2	MCF-7	breast:
44	chr9:140444557..140448587-chr9:140470804..140473699,6	MCF-7	breast:
45	chr9:140189163..140189728-chr9:140339137..140339973,2	MCF-7	breast:
46	chr9:140472065..140474628-chr9:140492745..140495141,2	MCF-7	breast:
47	chr17:41464701..41468607-chr9:140403951..140406971,9	K562	blood:
48	chr9:140500723..140503070-chr9:140566116..140568927,3	K562	blood:
49	chr9:140189560..140193480-chr9:140384679..140388476,4	K562	blood:
50	chr9:140511122..140512699-chr9:140559780..140561959,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NOXA1-2	chr9:140383507-140383567	NONHSAT135732
2	lnc-WDR85-1	chr9:140412889-140412899	NONHSAT135734
3	lnc-NOXA1-2	chr9:140383224-140383341	NONHSAT135733
4	lnc-ARRDC1-1	chr9:140477241-140479475	NONHSAT135743
5	lnc-NELF-2	chr9:140385913-140386550	NONHSAT135731
6	lnc-NOXA1-2	chr9:140383407-140384391	NONHSAT135733
7	lnc-NELF-2	chr9:140382990-140383726	NONHSAT135731
8	lnc-NOXA1-2	chr9:140383003-140383341	NONHSAT135732
9	lnc-WDR85-1	chr9:140411319-140412418	NONHSAT135734

miRNA name	Chromosome Location	mirBase accession
hsa-miR-7114-3p	chr9:140344478-140344498	MIMAT0028126
hsa-miR-7114-5p	chr9:140344513-140344533	MIMAT0028125

No data

Variant related genes	Relation type
ENSG00000263933	TF binding region
ZMYND19	TF binding region
PNPLA7	TF binding region
ARRDC1	TF binding region
DPH7	TF binding region
ENTPD8	TF binding region
MRPL41	TF binding region
EHMT1	TF binding region
C9orf37	TF binding region
NSMF	TF binding region
ENSG00000263933	CpG island
ZMYND19	CpG island
PNPLA7	CpG island
ARRDC1	CpG island
DPH7	CpG island
ENTPD8	CpG island
MRPL41	CpG island
EHMT1	CpG island
C9orf37	CpG island
NSMF	CpG island
ENSG00000258890	chromatin interactions
ENSG00000124216	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000259642	chromatin interactions
ENSG00000113594	chromatin interactions
ENSG00000134825	chromatin interactions
ENSG00000143570	chromatin interactions
ENSG00000087087	chromatin interactions
ENSG00000260806	chromatin interactions
ENSG00000179094	chromatin interactions
ENSG00000044574	chromatin interactions
ENSG00000108654	chromatin interactions
ENSG00000258938	chromatin interactions
ENSG00000244968	chromatin interactions
ENSG00000198113	chromatin interactions
ENSG00000130653	chromatin interactions
ENSG00000165724	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000134001	chromatin interactions
ENSG00000006125	chromatin interactions
ENSG00000245080	chromatin interactions
ENSG00000141556	chromatin interactions
ENSG00000188229	chromatin interactions
ENSG00000233296	chromatin interactions
ENSG00000180953	chromatin interactions
ENSG00000197070	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000198435	chromatin interactions
ENSG00000203993	chromatin interactions
ENSG00000239705	chromatin interactions
ENSG00000090060	chromatin interactions
ENSG00000260996	chromatin interactions
ENSG00000151353	chromatin interactions
ENSG00000263933	chromatin interactions
ENSG00000165716	chromatin interactions
ENSG00000168209	chromatin interactions
ENSG00000072401	chromatin interactions
ENSG00000177239	chromatin interactions
ENSG00000143578	chromatin interactions
ENSG00000188747	chromatin interactions
ENSG00000165417	chromatin interactions
ENSG00000188986	chromatin interactions
ENSG00000144580	chromatin interactions
ENSG00000259332	chromatin interactions
ENSG00000197191	chromatin interactions
ENSG00000100916	chromatin interactions
ENSG00000199753	chromatin interactions
ENSG00000181090	chromatin interactions
ENSG00000169957	chromatin interactions
ENSG00000100554	chromatin interactions
ENSG00000188833	chromatin interactions
ENSG00000187609	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000135829	chromatin interactions
ENSG00000182154	chromatin interactions
ENSG00000258498	chromatin interactions
ENSG00000257028	chromatin interactions
ENSG00000226308	chromatin interactions
ENSG00000268996	chromatin interactions
ENSG00000203987	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000176058	chromatin interactions
ENSG00000178980	chromatin interactions
ENSG00000188163	chromatin interactions
ENSG00000198961	chromatin interactions
ENSG00000169714	chromatin interactions
ENSG00000133858	chromatin interactions
ENSG00000165802	chromatin interactions
ENSG00000167716	chromatin interactions
ENSG00000176101	chromatin interactions
ENSG00000132475	chromatin interactions
ENSG00000207601	chromatin interactions
ENSG00000176248	chromatin interactions
ENSG00000176623	chromatin interactions
ENSG00000100664	chromatin interactions
ENSG00000266402	chromatin interactions
ENSG00000134824	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000120889	chromatin interactions
ENSG00000148399	chromatin interactions
ENSG00000149136	chromatin interactions
ENSG00000168496	chromatin interactions

Extended variants
information (count: 8481 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:8481 , 50 per page) page: 1 2 3 4 5 6 7 ... 170

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570328925	chr9:140338815-140338816	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs535814332	chr9:140338816-140338817	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs28395258	chr9:140338913-140338914	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs556036157	chr9:140338921-140338922	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs148571847	chr9:140338926-140338927	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs185221844	chr9:140338932-140338933	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs553417543	chr9:140338936-140338937	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs116562468	chr9:140338958-140338959	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs545761354	chr9:140339008-140339009	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs555933087	chr9:140339010-140339011	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs142917620	chr9:140339038-140339039	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs369789103	chr9:140339071-140339072	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs150642936	chr9:140339077-140339078	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs11516129	chr9:140339091-140339092	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs560382053	chr9:140339145-140339146	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs377580589	chr9:140339153-140339154	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs561964061	chr9:140339194-140339195	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs188557914	chr9:140339223-140339224	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs560450416	chr9:140339278-140339279	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs541241242	chr9:140339333-140339334	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs140050373	chr9:140339340-140339341	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs533314306	chr9:140339343-140339344	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs143610889	chr9:140339360-140339361	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs181375503	chr9:140339376-140339377	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs529291935	chr9:140339377-140339378	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs7867154	chr9:140339386-140339387	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs7862271	chr9:140339430-140339431	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs368227468	chr9:140339440-140339441	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs532395189	chr9:140339480-140339481	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs534873802	chr9:140339522-140339523	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs146798358	chr9:140339538-140339539	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs183735518	chr9:140339593-140339594	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs74723367	chr9:140339617-140339618	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs556232528	chr9:140339619-140339620	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs575899391	chr9:140339625-140339626	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs541829206	chr9:140339678-140339679	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs574182509	chr9:140339717-140339718	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs112882115	chr9:140339728-140339729	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs188449408	chr9:140339759-140339760	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs182103555	chr9:140339768-140339769	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs187204033	chr9:140339786-140339787	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs564317053	chr9:140339790-140339791	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs577779413	chr9:140339812-140339813	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs116312862	chr9:140339813-140339814	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs563827331	chr9:140339816-140339817	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs529238703	chr9:140339827-140339828	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs549001277	chr9:140339846-140339847	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs140490411	chr9:140339893-140339894	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs76432244	chr9:140339898-140339899	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs149758425	chr9:140339900-140339901	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:20)

Disease	PMID	Source
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Mantle cell lymphoma	19029149	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:8281 , 50 per page) page: 1 2 3 4 5 6 7 ... 166

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140336000-140339600	Weak transcription	Placenta	Placenta
2	chr9:140336200-140339400	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr9:140336200-140339600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr9:140336200-140340000	Weak transcription	Lung	lung
5	chr9:140336200-140340000	Weak transcription	Pancreas	Pancrea
6	chr9:140336200-140342600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr9:140336200-140343000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr9:140336200-140347800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr9:140336400-140339600	Weak transcription	HMEC	breast
10	chr9:140336400-140339800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr9:140336400-140348200	Weak transcription	Right Atrium	heart
12	chr9:140336600-140339400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr9:140336600-140339400	Weak transcription	NHEK	skin
14	chr9:140336600-140339600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr9:140336600-140339600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr9:140336600-140340000	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr9:140336600-140340000	Weak transcription	Colonic Mucosa	Colon
18	chr9:140336600-140343600	Weak transcription	Right Ventricle	heart
19	chr9:140336600-140348600	Weak transcription	Left Ventricle	heart
20	chr9:140336800-140339400	Weak transcription	Duodenum Mucosa	Duodenum
21	chr9:140336800-140339600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr9:140336800-140339600	Weak transcription	Primary B cells from cord blood	blood
23	chr9:140336800-140339600	Weak transcription	Primary T helper cells fromperipheralblood	blood
24	chr9:140336800-140339800	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr9:140336800-140340000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr9:140336800-140340000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr9:140336800-140343200	Weak transcription	Ovary	ovary
28	chr9:140336800-140343400	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr9:140336800-140343600	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr9:140336800-140343600	Weak transcription	Aorta	Aorta
31	chr9:140336800-140352400	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr9:140337000-140339200	Weak transcription	Hela-S3	cervix
33	chr9:140337000-140339400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr9:140337000-140339400	Weak transcription	Fetal Intestine Large	intestine
35	chr9:140337000-140339400	Weak transcription	Fetal Intestine Small	intestine
36	chr9:140337000-140339400	Weak transcription	K562	blood
37	chr9:140337000-140339600	Weak transcription	Liver	Liver
38	chr9:140337000-140339600	Weak transcription	A549	lung
39	chr9:140337000-140339600	Weak transcription	HepG2	liver
40	chr9:140337000-140340000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr9:140338200-140346600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr9:140339200-140339600	Enhancers	Hela-S3	cervix
43	chr9:140339400-140340200	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chr9:140339400-140340200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr9:140339400-140340200	Enhancers	Fetal Intestine Small	intestine
46	chr9:140339400-140340400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr9:140339400-140340400	Enhancers	Muscle Satellite Cultured Cells	--
48	chr9:140339400-140340600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr9:140339400-140340600	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr9:140339400-140340600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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