Variant report

Variant	nsv537435
Chromosome Location	chr4:187332658-187525542
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1604)
CpG islands
(count:4155)
Chromatin interactive
region (count:80)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1604 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:187508653-187508797	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:187393967-187394511	K562	blood:	n/a	n/a
3	ARID3A	chr4:187394041-187394370	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:187508528-187509011	K562	blood:	n/a	n/a
5	ATF1	chr4:187421894-187422344	K562	blood:	n/a	n/a
6	ATF1	chr4:187420491-187420916	K562	blood:	n/a	n/a
7	ATF3	chr4:187394371-187394479	GM12878	blood:	n/a	n/a
8	ATF3	chr4:187421950-187422165	K562	blood:	n/a	n/a
9	BACH1	chr4:187356907-187357919	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:187476293-187476945	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:187459112-187459482	K562	blood:	n/a	n/a
12	BACH1	chr4:187487248-187487849	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr4:187487400-187487517	K562	blood:	n/a	n/a
14	BACH1	chr4:187392859-187392959	K562	blood:	n/a	n/a
15	BATF	chr4:187467939-187468156	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:187354074-187354310	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:187422808-187423008	K562	blood:	n/a	n/a
18	BHLHE40	chr4:187475724-187475895	HepG2	liver:	n/a	n/a
19	BHLHE40	chr4:187421756-187422525	K562	blood:	n/a	n/a
20	BHLHE40	chr4:187362735-187362783	K562	blood:	n/a	n/a
21	BHLHE40	chr4:187442068-187442244	K562	blood:	n/a	n/a
22	BHLHE40	chr4:187491598-187491621	K562	blood:	n/a	n/a
23	BHLHE40	chr4:187475701-187476008	K562	blood:	n/a	n/a
24	BHLHE40	chr4:187458935-187459776	K562	blood:	n/a	n/a
25	BRCA1	chr4:187346073-187346283	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr4:187520434-187520442	HepG2	liver:	n/a	n/a
27	BRCA1	chr4:187511473-187511598	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr4:187475689-187475898	H1-hESC	embryonic stem cell:	n/a	n/a
29	CBX3	chr4:187373146-187373490	K562	blood:	n/a	n/a
30	CBX3	chr4:187373086-187373652	HCT-116	colon:	n/a	n/a
31	CBX3	chr4:187373072-187373601	HCT-116	colon:	n/a	n/a
32	CBX3	chr4:187354461-187354780	K562	blood:	n/a	n/a
33	CBX3	chr4:187459280-187459848	K562	blood:	n/a	n/a
34	CBX3	chr4:187411097-187411357	K562	blood:	n/a	n/a
35	CBX3	chr4:187503228-187503597	K562	blood:	n/a	n/a
36	CBX3	chr4:187421712-187422622	K562	blood:	n/a	n/a
37	CBX3	chr4:187458876-187459841	K562	blood:	n/a	n/a
38	CBX3	chr4:187503291-187503563	K562	blood:	n/a	n/a
39	CBX3	chr4:187373144-187373570	K562	blood:	n/a	n/a
40	CBX3	chr4:187457484-187457861	K562	blood:	n/a	n/a
41	CBX3	chr4:187421797-187422410	K562	blood:	n/a	n/a
42	CCNT2	chr4:187362847-187363236	K562	blood:	n/a	n/a
43	CCNT2	chr4:187459142-187459761	K562	blood:	n/a	n/a
44	CCNT2	chr4:187421964-187422263	K562	blood:	n/a	n/a
45	CEBPB	chr4:187463000-187463285	IMR90	lung:	n/a	chr4:187463129-187463140
46	CEBPB	chr4:187371144-187371490	HepG2	liver:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
47	CEBPB	chr4:187375483-187375595	HepG2	liver:	n/a	chr4:187375528-187375539
48	CEBPB	chr4:187371179-187371335	K562	blood:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
49	CEBPB	chr4:187506056-187506356	HepG2	liver:	n/a	chr4:187506188-187506199
50	CEBPB	chr4:187460389-187460582	K562	blood:	n/a	chr4:187460425-187460436

(count:4155 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187455559-187455609	AG09319	gingival:	n/a
2	chr4:187459415-187459465	Caco-2	colon:	n/a
3	chr4:187509603-187509653	PrEC	prostate:	n/a
4	chr4:187404988-187405038	Caco-2	colon:	n/a
5	chr4:187507476-187507526	Hela-S3	cervix:	n/a
6	chr4:187517847-187517897	K562	blood:	n/a
7	chr4:187455532-187455582	HepG2	liver:	n/a
8	chr4:187455559-187455609	AG09319	gingival:	n/a
9	chr4:187459415-187459465	Caco-2	colon:	n/a
10	chr4:187509603-187509653	PrEC	prostate:	n/a
11	chr4:187404988-187405038	Caco-2	colon:	n/a
12	chr4:187507476-187507526	Hela-S3	cervix:	n/a
13	chr4:187517847-187517897	K562	blood:	n/a
14	chr4:187455532-187455582	HepG2	liver:	n/a
15	chr4:187475784-187475834	HRCEpiC	kidney:	n/a
16	chr4:187476543-187476593	NT2-D1	testis:	n/a
17	chr4:187459415-187459465	Hepatocyte	liver:	n/a
18	chr4:187394380-187394430	Caco-2	colon:	n/a
19	chr4:187422119-187422169	GM12878	blood:	n/a
20	chr4:187499458-187499508	HEEpiC	esophagus:	n/a
21	chr4:187459449-187459499	BJ	skin:	n/a
22	chr4:187454891-187454941	PrEC	prostate:	n/a
23	chr4:187510100-187510150	SKMC	muscle:	n/a
24	chr4:187510183-187510233	HEK293	kidney:	embryo
25	chr4:187518154-187518204	HCM	heart:	n/a
26	chr4:187459415-187459465	HRCEpiC	kidney:	n/a
27	chr4:187454891-187454941	A549	lung:	n/a
28	chr4:187475784-187475834	NT2-D1	testis:	n/a
29	chr4:187491428-187491478	NHDF-neo	bronchial:	n/a
30	chr4:187422114-187422164	HCT-116	colon:	n/a
31	chr4:187491362-187491412	MCF-7	breast:	n/a
32	chr4:187507476-187507526	GM06990	blood:	n/a
33	chr4:187517847-187517897	AG09309	skin:	n/a
34	chr4:187517794-187517844	HIPEpiC	eye:	n/a
35	chr4:187404958-187405008	HUVEC	blood vessel:	n/a
36	chr4:187517794-187517844	HL-60	blood:	n/a
37	chr4:187517939-187517989	MCF10A-Er-Src	breast:	n/a
38	chr4:187517847-187517897	HEEpiC	esophagus:	n/a
39	chr4:187455532-187455582	HIPEpiC	eye:	n/a
40	chr4:187476953-187477003	NHBE	bronchial:	n/a
41	chr4:187349714-187349764	ovcar-3	ovarian:	n/a
42	chr4:187524686-187524736	BE2_C	brain:	n/a
43	chr4:187524750-187524800	HCT-116	colon:	n/a
44	chr4:187459449-187459499	ECC-1	luminal epithelium:	n/a
45	chr4:187422005-187422055	Hela-S3	cervix:	n/a
46	chr4:187517847-187517897	GM12891	blood:	n/a
47	chr4:187422035-187422085	SK-N-SH	brain:	n/a
48	chr4:187499358-187499408	AG04450	lung:	fetal
49	chr4:187517794-187517844	NHBE	bronchial:	n/a
50	chr4:187455532-187455582	MCF10A-Er-Src	breast:	n/a

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:187516733..187519515-chr4:187519671..187523118,3	K562	blood:
2	chr4:187217859..187218927-chr4:187508295..187509239,10	K562	blood:
3	chr4:187332246..187335061-chr4:187336434..187338116,2	K562	blood:
4	chr4:187402656..187405583-chr4:187422037..187423656,2	K562	blood:
5	chr4:187336442..187338955-chr4:187341117..187342706,2	K562	blood:
6	chr4:187393992..187394694-chr4:187476207..187476860,2	MCF-7	breast:
7	chr4:187394154..187394722-chr4:187508267..187509221,2	K562	blood:
8	chr4:187500135..187502809-chr4:187503552..187505975,2	MCF-7	breast:
9	chr4:187414357..187416175-chr4:187420876..187423477,2	MCF-7	breast:
10	chr4:187332850..187335061-chr4:187335595..187338116,3	K562	blood:
11	chr4:187450978..187452522-chr4:187454014..187456071,2	K562	blood:
12	chr4:187394722..187395443-chr4:187508309..187509281,2	MCF-7	breast:
13	chr4:187327492..187329160-chr4:187332412..187335274,2	K562	blood:
14	chr4:187458318..187460106-chr4:187464822..187466767,2	K562	blood:
15	chr4:187371013..187372540-chr4:187375746..187378339,2	K562	blood:
16	chr4:187393785..187394637-chr4:187475328..187475950,2	MCF-7	breast:
17	chr4:187448150..187450256-chr4:187458216..187460408,2	K562	blood:
18	chr4:187332850..187335061-chr4:187335595..187338116,3	K562	blood:
19	chr11:62608697..62609221-chr4:187449246..187449766,2	Hela-S3	cervix:
20	chr4:187464736..187466287-chr4:187469928..187471897,2	K562	blood:
21	chr4:187507521..187509715-chr4:187510958..187513013,2	K562	blood:
22	chr4:187378015..187379794-chr4:187381538..187383252,2	K562	blood:
23	chr4:187512892..187514461-chr4:187519314..187520852,2	MCF-7	breast:
24	chr4:187339945..187342685-chr4:187344135..187346623,2	K562	blood:
25	chr4:187500880..187503976-chr4:187505788..187508799,3	K562	blood:
26	chr4:187424618..187426617-chr4:187440828..187442815,2	MCF-7	breast:
27	chr4:187448150..187450256-chr4:187458216..187460408,2	K562	blood:
28	chr4:187458318..187460106-chr4:187464822..187466767,2	K562	blood:
29	chr4:187500135..187502809-chr4:187503552..187505975,2	MCF-7	breast:
30	chr4:187121686..187123375-chr4:187456206..187458817,2	K562	blood:
31	chr4:187458073..187459669-chr4:187489557..187491261,2	K562	blood:
32	chr4:187507521..187509715-chr4:187510958..187513013,2	K562	blood:
33	chr4:187477233..187480575-chr4:187481254..187484237,4	K562	blood:
34	chr4:187378015..187379794-chr4:187381538..187383252,2	K562	blood:
35	chr4:187420835..187422454-chr4:187508241..187510216,2	K562	blood:
36	chr4:187425444..187427113-chr4:187432314..187434673,2	K562	blood:
37	chr4:187216645..187219482-chr4:187510341..187512353,2	K562	blood:
38	chr4:187394348..187396815-chr4:187456742..187459587,2	K562	blood:
39	chr4:187365176..187367106-chr4:187368874..187370492,2	K562	blood:
40	chr4:187400808..187402522-chr4:187420720..187422452,2	MCF-7	breast:
41	chr4:187394348..187396815-chr4:187456742..187459587,2	K562	blood:
42	chr4:187500880..187503976-chr4:187505788..187508799,3	K562	blood:
43	chr4:187418143..187425298-chr4:187427395..187434877,12	K562	blood:
44	chr17:41464198..41466205-chr4:187449246..187450766,2	MCF-7	breast:
45	chr4:187463972..187466236-chr4:187470397..187471997,2	K562	blood:
46	chr4:187454593..187456201-chr4:187457410..187459187,2	K562	blood:
47	chr4:187421685..187424267-chr4:187426709..187429265,2	MCF-7	breast:
48	chr4:187419835..187422222-chr4:187436024..187437802,2	K562	blood:
49	chr4:187394154..187394722-chr4:187508267..187509221,2	K562	blood:
50	chr4:187458073..187459669-chr4:187489557..187491261,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTNR1A-1	chr4:187337280-187337490	NONHSAT099658
2	lnc-MTNR1A-1	chr4:187347391-187348252	NONHSAT099658
3	lnc-MTNR1A-1	chr4:187353299-187353392	ENSG00000251165.1
4	lnc-MTNR1A-1	chr4:187344882-187344986	ENSG00000251165.1
5	lnc-MTNR1A-1	chr4:187421999-187422151	ENSG00000251165.1
6	lnc-MTNR1A-1	chr4:187353299-187353392	ENSG00000251165.1
7	lnc-MTNR1A-1	chr4:187421999-187422151	ENSG00000251165.1
8	lnc-MTNR1A-1	chr4:187347391-187348252	ENSG00000251165.1
9	lnc-MTNR1A-1	chr4:187352772-187352922	NONHSAT099658
10	lnc-MTNR1A-1	chr4:187345244-187345390	ENSG00000251165.1
11	lnc-F11-8	chr4:187500098-187503339	NONHSAT099666
12	lnc-MTNR1A-1	chr4:187347391-187347447	ENSG00000251165.1
13	lnc-MTNR1A-1	chr4:187352772-187352922	ENSG00000251165.1
14	lnc-MTNR1A-1	chr4:187421999-187422212	NONHSAT099658
15	lnc-MTNR1A-1	chr4:187349859-187350004	ENSG00000251165.1
16	lnc-MTNR1A-1	chr4:187344882-187344986	ENSG00000251165.1
17	lnc-MTNR1A-1	chr4:187344883-187344986	NONHSAT099658
18	lnc-MTNR1A-1	chr4:187353299-187353392	NONHSAT099658
19	lnc-MTNR1A-1	chr4:187348128-187348252	ENSG00000251165.1
20	lnc-FAT1-5	chr4:187409184-187409778	predAs_chen_AV690772_1
21	lnc-MTNR1A-1	chr4:187345244-187345390	NONHSAT099658
22	lnc-MTNR1A-1	chr4:187352772-187352922	ENSG00000251165.1

No data

Variant related genes	Relation type
F11-AS1	TF binding region
RNU6-1055P	TF binding region
ENSG00000272297	TF binding region
FAT1	TF binding region
MTNR1A	TF binding region
F11-AS1	CpG island
RNU6-1055P	CpG island
ENSG00000272297	CpG island
FAT1	CpG island
MTNR1A	CpG island
ENSG00000251165	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000212387	chromatin interactions
ENSG00000272297	chromatin interactions
ENSG00000168412	chromatin interactions
ENSG00000083857	chromatin interactions

Extended variants
information (count: 7999 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:7999 , 50 per page) page: 1 2 3 4 5 6 7 ... 160

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540869772	chr4:187334612-187334613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs147350648	chr4:187334643-187334644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs115264858	chr4:187334655-187334656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554851793	chr4:187334656-187334657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576385664	chr4:187334705-187334706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543776964	chr4:187334710-187334711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545930865	chr4:187334740-187334741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189755297	chr4:187334744-187334745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558960321	chr4:187334764-187334765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs722128	chr4:187334793-187334794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561978116	chr4:187334819-187334820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530062557	chr4:187334831-187334832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs115268758	chr4:187334854-187334855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566902642	chr4:187334860-187334861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181412717	chr4:187334872-187334873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs6552981	chr4:187334888-187334889	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs569089888	chr4:187334936-187334937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538074055	chr4:187334969-187334970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554809638	chr4:187334986-187334987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184993540	chr4:187334995-187334996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs377163036	chr4:187335014-187335015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs372335487	chr4:187335040-187335041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs36046954	chr4:187335049-187335050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148020904	chr4:187335051-187335052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79593472	chr4:187335084-187335085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576813554	chr4:187335114-187335115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189165122	chr4:187335119-187335120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141671205	chr4:187335187-187335188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs576269800	chr4:187335191-187335192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115342528	chr4:187335217-187335218	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs181823534	chr4:187335274-187335275	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs527586071	chr4:187335365-187335366	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs547707930	chr4:187335386-187335387	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs115865236	chr4:187335401-187335402	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs114553635	chr4:187335407-187335408	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs574921740	chr4:187335450-187335451	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs552226977	chr4:187335452-187335453	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs28678859	chr4:187335462-187335463	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs150887387	chr4:187335519-187335520	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs11941175	chr4:187335534-187335535	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs568685500	chr4:187335542-187335543	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs369221454	chr4:187335576-187335577	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs376837323	chr4:187335589-187335590	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs534216417	chr4:187335622-187335623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs554476737	chr4:187335636-187335637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576735022	chr4:187335679-187335680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539454896	chr4:187335680-187335681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556252931	chr4:187335728-187335729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576207026	chr4:187335769-187335770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs75326755	chr4:187335770-187335771	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
XY gonadal dysgenesis	20685758	CNVD

Chromatin state (count:1318 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187334600-187336200	Enhancers	Sigmoid Colon	Sigmoid Colon
2	chr4:187334800-187335200	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr4:187334800-187335400	Enhancers	Small Intestine	intestine
4	chr4:187334800-187336200	Enhancers	Duodenum Mucosa	Duodenum
5	chr4:187334800-187336200	Enhancers	Fetal Intestine Large	intestine
6	chr4:187334800-187336200	Enhancers	Fetal Intestine Small	intestine
7	chr4:187335000-187335200	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr4:187335000-187336200	Enhancers	Pancreas	Pancrea
9	chr4:187335200-187335600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
10	chr4:187335200-187335600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
11	chr4:187335600-187336200	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr4:187335600-187336400	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr4:187335800-187336400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:187336200-187339200	Weak transcription	Fetal Intestine Small	intestine
15	chr4:187337800-187338200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr4:187339200-187340000	Enhancers	Fetal Intestine Small	intestine
17	chr4:187340800-187342400	Enhancers	Fetal Lung	lung
18	chr4:187342400-187343400	Weak transcription	Fetal Lung	lung
19	chr4:187343400-187343600	Enhancers	Fetal Stomach	stomach
20	chr4:187343400-187345400	Enhancers	Fetal Lung	lung
21	chr4:187343600-187343800	Enhancers	Sigmoid Colon	Sigmoid Colon
22	chr4:187344400-187344600	Enhancers	Fetal Stomach	stomach
23	chr4:187347200-187353200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr4:187353200-187353400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr4:187353200-187354000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr4:187354000-187354400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr4:187354000-187357000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:187354400-187357000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr4:187357000-187357200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:187357000-187357800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr4:187357000-187357800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr4:187357000-187357800	ZNF genes & repeats	Gastric	stomach
33	chr4:187357600-187357800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr4:187362600-187363400	Enhancers	K562	blood
35	chr4:187365800-187366000	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr4:187366000-187366800	Active TSS	Rectal Mucosa Donor 31	rectum
37	chr4:187366200-187366800	Active TSS	Rectal Mucosa Donor 29	rectum
38	chr4:187366800-187367000	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr4:187369800-187371000	Weak transcription	Pancreas	Pancrea
40	chr4:187372400-187375600	ZNF genes & repeats	Liver	Liver
41	chr4:187372800-187374400	ZNF genes & repeats	Adipose Nuclei	Adipose
42	chr4:187373200-187374400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:187374400-187382200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:187375200-187375400	ZNF genes & repeats	K562	blood
45	chr4:187375400-187392600	Weak transcription	K562	blood
46	chr4:187375800-187376400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr4:187378600-187381400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr4:187381400-187382600	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr4:187381800-187383000	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr4:187382000-187382400	Enhancers	Fetal Lung	lung

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