Variant report

Variant	esv3386469
Chromosome Location	chr2:112215911-112447472
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3681)
CpG islands
(count:733)
Chromatin interactive
region (count:94)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3681 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112286629-112286892	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:112421055-112421554	K562	blood:	n/a	n/a
3	ARID3A	chr2:112279969-112280556	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:112407331-112407538	K562	blood:	n/a	n/a
5	ARID3A	chr2:112374864-112376031	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:112376535-112377049	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:112382440-112382785	K562	blood:	n/a	n/a
8	ARID3A	chr2:112221794-112221988	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:112400566-112400827	K562	blood:	n/a	n/a
10	ARID3A	chr2:112383691-112384719	K562	blood:	n/a	n/a
11	ARID3A	chr2:112377103-112377411	K562	blood:	n/a	n/a
12	ATF1	chr2:112383432-112384030	K562	blood:	n/a	n/a
13	ATF1	chr2:112252616-112252812	K562	blood:	n/a	n/a
14	ATF1	chr2:112251003-112251203	K562	blood:	n/a	n/a
15	ATF1	chr2:112409614-112409887	K562	blood:	n/a	n/a
16	ATF1	chr2:112400419-112400917	K562	blood:	n/a	n/a
17	ATF1	chr2:112382410-112382671	K562	blood:	n/a	n/a
18	ATF1	chr2:112391689-112391967	K562	blood:	n/a	n/a
19	ATF2	chr2:112390081-112390607	GM12878	blood:	n/a	n/a
20	ATF2	chr2:112390137-112390517	GM12878	blood:	n/a	n/a
21	ATF2	chr2:112236677-112236938	GM12878	blood:	n/a	n/a
22	ATF3	chr2:112292952-112293475	HepG2	liver:	n/a	chr2:112293252-112293272 chr2:112293263-112293272
23	ATF3	chr2:112383692-112384042	K562	blood:	n/a	n/a
24	BACH1	chr2:112251425-112251440	K562	blood:	n/a	n/a
25	BACH1	chr2:112409768-112409943	K562	blood:	n/a	n/a
26	BACH1	chr2:112425190-112425427	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr2:112434807-112435070	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr2:112400397-112400730	K562	blood:	n/a	n/a
29	BACH1	chr2:112436147-112436481	H1-hESC	embryonic stem cell:	n/a	n/a
30	BATF	chr2:112220893-112221142	GM12878	blood:	n/a	n/a
31	BATF	chr2:112290692-112291073	GM12878	blood:	n/a	chr2:112290906-112290916 chr2:112290905-112290916
32	BATF	chr2:112264445-112264864	GM12878	blood:	n/a	n/a
33	BATF	chr2:112221520-112221892	GM12878	blood:	n/a	n/a
34	BATF	chr2:112250963-112251779	GM12878	blood:	n/a	chr2:112251535-112251545 chr2:112251573-112251582
35	BATF	chr2:112236428-112237126	GM12878	blood:	n/a	n/a
36	BATF	chr2:112251898-112252984	GM12878	blood:	n/a	chr2:112252692-112252702 chr2:112252678-112252688
37	BATF	chr2:112236417-112237152	GM12878	blood:	n/a	n/a
38	BATF	chr2:112248667-112249139	GM12878	blood:	n/a	n/a
39	BATF	chr2:112303348-112304091	GM12878	blood:	n/a	chr2:112303735-112303744
40	BATF	chr2:112240605-112241034	GM12878	blood:	n/a	chr2:112240788-112240798
41	BATF	chr2:112290657-112291078	GM12878	blood:	n/a	chr2:112290906-112290916 chr2:112290905-112290916
42	BATF	chr2:112251972-112252940	GM12878	blood:	n/a	chr2:112252692-112252702 chr2:112252678-112252688
43	BATF	chr2:112327786-112328223	GM12878	blood:	n/a	n/a
44	BATF	chr2:112303521-112304031	GM12878	blood:	n/a	chr2:112303735-112303744
45	BATF	chr2:112238764-112238956	GM12878	blood:	n/a	n/a
46	BATF	chr2:112282643-112283006	GM12878	blood:	n/a	n/a
47	BATF	chr2:112221408-112221914	GM12878	blood:	n/a	n/a
48	BATF	chr2:112327815-112328182	GM12878	blood:	n/a	n/a
49	BATF	chr2:112391706-112392054	GM12878	blood:	n/a	n/a
50	BATF	chr2:112264388-112264857	GM12878	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112430423-112430473	IMR90	lung:	fetal
2	chr2:112430423-112430473	IMR90	lung:	fetal
3	chr2:112440678-112440728	AG09309	skin:	n/a
4	chr2:112383396-112383446	A549	lung:	n/a
5	chr2:112417362-112417412	NHBE	bronchial:	n/a
6	chr2:112391213-112391263	ovcar-3	ovarian:	n/a
7	chr2:112417362-112417412	H1-hESC	embryonic stem cell:	embryo
8	chr2:112430423-112430473	HRE	kidney:	n/a
9	chr2:112435953-112436003	HPAEpiC	pulmonary alveolar:	n/a
10	chr2:112420098-112420148	HCT-116	colon:	n/a
11	chr2:112440678-112440728	SK-N-MC	brain:	n/a
12	chr2:112383396-112383446	BE2_C	brain:	n/a
13	chr2:112375854-112375904	HRPEpiC	eye:	n/a
14	chr2:112280286-112280336	SAEC	small airway:	n/a
15	chr2:112435953-112436003	MCF-7	breast:	n/a
16	chr2:112439582-112439632	HAEpiC	amniotic membrane:	n/a
17	chr2:112435953-112436003	AG04449	skin:	fetal
18	chr2:112252254-112252304	Hela-S3	cervix:	n/a
19	chr2:112391213-112391263	HIPEpiC	eye:	n/a
20	chr2:112439582-112439632	AG04449	skin:	fetal
21	chr2:112435953-112436003	HMEC	breast:	n/a
22	chr2:112420098-112420148	RPTEC	kidney:	n/a
23	chr2:112375854-112375904	IMR90	lung:	fetal
24	chr2:112280286-112280336	HCM	heart:	n/a
25	chr2:112375854-112375904	A549	lung:	n/a
26	chr2:112293267-112293317	AG10803	skin:	n/a
27	chr2:112391213-112391263	HMEC	breast:	n/a
28	chr2:112417362-112417412	HNPCEpiC	eye:	n/a
29	chr2:112439582-112439632	HCT-116	colon:	n/a
30	chr2:112439582-112439632	SK-N-MC	brain:	n/a
31	chr2:112252254-112252304	HRPEpiC	eye:	n/a
32	chr2:112440678-112440728	NHBE	bronchial:	n/a
33	chr2:112435953-112436003	U87	brain:	n/a
34	chr2:112252254-112252304	SKMC	muscle:	n/a
35	chr2:112383396-112383446	AG09309	skin:	n/a
36	chr2:112420098-112420148	SAEC	small airway:	n/a
37	chr2:112440678-112440728	NH-A	brain:	n/a
38	chr2:112417362-112417412	HEEpiC	esophagus:	n/a
39	chr2:112252254-112252304	GM12892	blood:	n/a
40	chr2:112420098-112420148	HPAEpiC	pulmonary alveolar:	n/a
41	chr2:112391213-112391263	SAEC	small airway:	n/a
42	chr2:112383396-112383446	Caco-2	colon:	n/a
43	chr2:112293267-112293317	HRPEpiC	eye:	n/a
44	chr2:112439582-112439632	NHDF-neo	bronchial:	n/a
45	chr2:112430423-112430473	HRCEpiC	kidney:	n/a
46	chr2:112439582-112439632	A549	lung:	n/a
47	chr2:112391213-112391263	HEK293	kidney:	embryo
48	chr2:112252254-112252304	PFSK-1	brain:	n/a
49	chr2:112435953-112436003	Jurkat	blood:	n/a
50	chr2:112383396-112383446	HEK293	kidney:	embryo

(count:94 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:112376861..112378670-chr2:112458387..112460460,2	K562	blood:
2	chr2:112391627..112394097-chr2:112402013..112403917,2	K562	blood:
3	chr2:112404521..112406276-chr2:112418863..112420984,2	MCF-7	breast:
4	chr2:112443707..112446597-chr2:112448656..112451342,3	K562	blood:
5	chr2:112422912..112424543-chr2:112435057..112437624,2	K562	blood:
6	chr2:112415503..112417633-chr2:112463417..112464976,2	MCF-7	breast:
7	chr2:112413487..112415634-chr2:112416547..112421397,4	MCF-7	breast:
8	chr2:112239413..112241217-chr2:112461159..112463413,2	MCF-7	breast:
9	chr1:182808366..182808884-chr2:112383326..112383826,2	NB4	blood:
10	chr2:112391627..112394432-chr2:112401597..112404973,3	K562	blood:
11	chr2:112374742..112377562-chr2:112458693..112461036,2	MCF-7	breast:
12	chr2:112420650..112422209-chr2:112446178..112448541,2	MCF-7	breast:
13	chr2:112412317..112414698-chr2:112415444..112417727,2	K562	blood:
14	chr2:112412317..112414698-chr2:112415444..112417727,2	K562	blood:
15	chr2:112418934..112421688-chr2:112422273..112424750,2	K562	blood:
16	chr2:112416973..112418721-chr2:112421428..112423715,2	MCF-7	breast:
17	chr2:112374024..112376697-chr2:112377578..112380485,2	K562	blood:
18	chr2:112416973..112418721-chr2:112421428..112423715,2	MCF-7	breast:
19	chr2:112407508..112410822-chr2:112413499..112416205,3	MCF-7	breast:
20	chr2:112407508..112410822-chr2:112413499..112416205,3	MCF-7	breast:
21	chr2:112404706..112406626-chr2:112415850..112417469,2	MCF-7	breast:
22	chr2:112395688..112397342-chr2:112404915..112406866,2	K562	blood:
23	chr2:112426158..112428552-chr2:112435022..112436930,2	MCF-7	breast:
24	chr2:112415609..112418598-chr2:112432941..112434486,2	MCF-7	breast:
25	chr2:111878764..111880387-chr2:112231090..112233888,2	MCF-7	breast:
26	chr2:112375556..112378419-chr2:112378851..112380695,2	MCF-7	breast:
27	chr2:112382780..112385327-chr2:112409728..112411247,2	MCF-7	breast:
28	chr17:56708659..56709602-chr2:112416534..112417109,2	MCF-7	breast:
29	chr2:112374024..112376697-chr2:112377578..112380485,2	K562	blood:
30	chr2:112395623..112398484-chr2:112400861..112402821,2	K562	blood:
31	chr2:112376815..112377394-chr2:112421087..112421873,3	MCF-7	breast:
32	chr2:112418934..112421688-chr2:112422273..112424750,2	K562	blood:
33	chr2:112419168..112422098-chr2:112423722..112426374,3	MCF-7	breast:
34	chr2:112391627..112394097-chr2:112402013..112403917,2	K562	blood:
35	chr2:112376832..112377622-chr2:112493675..112494396,3	MCF-7	breast:
36	chr2:112402419..112406237-chr2:112407904..112411161,4	MCF-7	breast:
37	chr2:112395623..112398484-chr2:112400861..112402821,2	K562	blood:
38	chr2:112420650..112422209-chr2:112446178..112448541,2	MCF-7	breast:
39	chr2:112415374..112417265-chr2:112463686..112465545,2	MCF-7	breast:
40	chr2:112392219..112395501-chr2:112398954..112401482,3	K562	blood:
41	chr2:112415314..112417347-chr2:112459623..112461902,2	MCF-7	breast:
42	chr2:112375556..112378419-chr2:112378851..112380695,2	MCF-7	breast:
43	chr2:112377428..112379190-chr2:112425946..112427813,2	MCF-7	breast:
44	chr2:112391627..112394432-chr2:112401597..112404973,3	K562	blood:
45	chr2:112402711..112405515-chr2:112410229..112412374,2	K562	blood:
46	chr2:112397541..112399746-chr2:112416589..112418149,2	MCF-7	breast:
47	chr2:112409243..112412120-chr2:112414450..112416738,2	K562	blood:
48	chr2:112389816..112391811-chr2:112392544..112394680,2	MCF-7	breast:
49	chr2:112444088..112447481-chr2:112453009..112458135,6	K562	blood:
50	chr2:112395688..112397342-chr2:112404915..112406866,2	K562	blood:

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC108463.1-2	chr2:112252134-112252388	ENSG00000224959
2	lnc-BCL2L11-3	chr2:112248850-112249239	XLOC_001625
3	lnc-AC108463.1-3	chr2:112252462-112252692	NONHSAT073622
4	lnc-AC108463.1-3	chr2:112237484-112237657	NONHSAT073639
5	lnc-AC108463.1-3	chr2:112237484-112237638	ENSG00000172965.6
6	lnc-AC108463.1-3	chr2:112252462-112252611	ENSG00000172965.6
7	lnc-AC108463.1-3	chr2:112237484-112237638	ENSG00000172965.6
8	lnc-AC108463.1-2	chr2:112249520-112250145	ENSG00000224959
9	lnc-AC108463.1-3	chr2:112252462-112252677	ENSG00000172965.6
10	lnc-MERTK-1	chr2:112369479-112370095	XLOC_001626
11	lnc-AC108463.1-3	chr2:112252462-112252540	NONHSAT073639
12	lnc-AC108463.1-3	chr2:112227180-112227564	ENSG00000172965.6
13	lnc-AC108463.1-3	chr2:112252462-112252692	NONHSAT073640
14	lnc-AC108463.1-3	chr2:112252462-112252625	ENSG00000172965.6
15	lnc-AC108463.1-3	chr2:112229566-112229674	ENSG00000172965.6
16	lnc-MERTK-1	chr2:112365418-112365592	XLOC_001626
17	lnc-AC108463.1-3	chr2:112227364-112227564	ENSG00000172965.6
18	lnc-MERTK-4	chr2:112432603-112432920	NONHSAT073661
19	lnc-BCL2L11-3	chr2:112257365-112258585	NONHSAT073656
20	lnc-AC108463.1-3	chr2:112252462-112252692	NONHSAT073642
21	lnc-BCL2L11-3	chr2:112268201-112268567	XLOC_001625
22	lnc-AC108463.1-3	chr2:112237746-112237838	ENSG00000172965.6
23	lnc-AC108463.1-3	chr2:112252462-112252625	ENSG00000172965.6
24	lnc-AC108463.1-3	chr2:112252462-112252597	ENSG00000172965.6
25	lnc-MERTK-1	chr2:112365277-112365592	NONHSAT073660
26	lnc-BCL2L11-3	chr2:112249107-112249838	NONHSAT073654
27	lnc-AC108463.1-3	chr2:112252462-112252610	ENSG00000172965.6
28	lnc-MERTK-1	chr2:112369479-112369982	NONHSAT073660
29	lnc-AC108463.1-3	chr2:112227095-112227564	ENSG00000172965.6
30	lnc-AC108463.1-3	chr2:112252462-112252602	ENSG00000172965.6
31	lnc-AC108463.1-3	chr2:112237746-112237838	ENSG00000172965.6
32	lnc-BCL2L11-3	chr2:112257365-112258585	NONHSAT073658
33	lnc-ANAPC1-3	chr2:112315990-112317514	NONHSAT073659
34	lnc-AC108463.1-3	chr2:112227364-112227376	NONHSAT073639
35	lnc-BCL2L11-3	chr2:112249107-112249838	NONHSAT073656
36	lnc-AC108463.1-3	chr2:112229566-112229674	ENSG00000172965.6
37	lnc-AC108463.1-3	chr2:112252462-112252631	ENSG00000172965.6
38	lnc-AC108463.1-3	chr2:112227215-112227564	ENSG00000172965.6

No data

Variant related genes	Relation type
ENSG00000240350	TF binding region
ENSG00000224959	TF binding region
ENSG00000225744	TF binding region
ENSG00000237583	TF binding region
MIR4435-1HG	TF binding region
ENSG00000271635	TF binding region
ENSG00000240350	CpG island
ENSG00000224959	CpG island
ENSG00000225744	CpG island
ENSG00000237583	CpG island
MIR4435-1HG	CpG island
ENSG00000271635	CpG island
ENSG00000237583	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000135829	chromatin interactions
ENSG00000153094	chromatin interactions

Extended variants
information (count: 6863 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:6863 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192702268	chr2:112215961-112215962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs374899365	chr2:112215962-112215963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563696270	chr2:112215966-112215967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs57685432	chr2:112215995-112215996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184502585	chr2:112216001-112216002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546117684	chr2:112216003-112216004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200700116	chr2:112216005-112216006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145261999	chr2:112216073-112216074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189775172	chr2:112216097-112216098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192756853	chr2:112216105-112216106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184406783	chr2:112216213-112216214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs367909664	chr2:112216219-112216220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189118526	chr2:112216239-112216240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527326759	chr2:112216249-112216250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11889011	chr2:112216253-112216254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535139031	chr2:112216261-112216262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547240120	chr2:112216285-112216286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567438242	chr2:112216428-112216429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs62161390	chr2:112216447-112216448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142093749	chr2:112216452-112216453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556493803	chr2:112216469-112216470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs62161391	chr2:112216657-112216658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372805368	chr2:112216730-112216731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200609533	chr2:112216758-112216759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576413830	chr2:112216771-112216772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538591977	chr2:112216787-112216788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558546803	chr2:112216941-112216942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572013178	chr2:112216985-112216986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541107020	chr2:112216986-112216987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560849959	chr2:112216987-112216988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374453504	chr2:112217126-112217127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377293517	chr2:112217137-112217138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs58354454	chr2:112217188-112217189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374677901	chr2:112217190-112217191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543652324	chr2:112217192-112217193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563597082	chr2:112217194-112217195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370247345	chr2:112217196-112217197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112276394	chr2:112217228-112217229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552259190	chr2:112217311-112217312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559710770	chr2:112217333-112217334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112154200	chr2:112217372-112217373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528509502	chr2:112217403-112217404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548641628	chr2:112217505-112217506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568507982	chr2:112217537-112217538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529875611	chr2:112217563-112217564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550004271	chr2:112217598-112217599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569939574	chr2:112217656-112217657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538951669	chr2:112217687-112217688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558615365	chr2:112217719-112217720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs62161392	chr2:112217721-112217722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2651 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112185400-112220200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr2:112209600-112219400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:112209800-112220400	Weak transcription	HSMMtube	muscle
4	chr2:112210600-112220600	Weak transcription	NH-A	brain
5	chr2:112211000-112220400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr2:112211200-112217800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr2:112211200-112225200	Weak transcription	HSMM	muscle
8	chr2:112213200-112218800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr2:112213400-112219400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr2:112213400-112223000	Weak transcription	A549	lung
11	chr2:112213400-112227200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr2:112213600-112218200	Weak transcription	K562	blood
13	chr2:112213600-112219600	Weak transcription	Hela-S3	cervix
14	chr2:112213600-112220000	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr2:112213600-112220400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr2:112217800-112218600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr2:112218200-112218400	Enhancers	H9 Cell Line	embryonic stem cell
18	chr2:112218200-112218800	Enhancers	K562	blood
19	chr2:112218200-112221000	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr2:112218600-112220200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr2:112218600-112224400	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr2:112218800-112219600	Weak transcription	K562	blood
23	chr2:112218800-112219800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
24	chr2:112219200-112219400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr2:112219200-112219600	Weak transcription	NHDF-Ad	bronchial
26	chr2:112219400-112219600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr2:112219400-112219600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr2:112219400-112219600	Enhancers	Duodenum Mucosa	Duodenum
29	chr2:112219400-112219600	Weak transcription	HUVEC	blood vessel
30	chr2:112219400-112219800	Enhancers	Fetal Intestine Small	intestine
31	chr2:112219400-112220400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr2:112219400-112221400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr2:112219600-112219800	Enhancers	Colonic Mucosa	Colon
34	chr2:112219600-112219800	Enhancers	Fetal Intestine Large	intestine
35	chr2:112219600-112219800	Enhancers	Rectal Mucosa Donor 29	rectum
36	chr2:112219600-112219800	Enhancers	K562	blood
37	chr2:112219600-112220000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr2:112219600-112220400	Weak transcription	Duodenum Mucosa	Duodenum
39	chr2:112219600-112220800	Enhancers	NHDF-Ad	bronchial
40	chr2:112219600-112221200	Enhancers	Hela-S3	cervix
41	chr2:112219600-112221400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr2:112219600-112221400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr2:112219600-112221600	Enhancers	HMEC	breast
44	chr2:112219600-112221600	Enhancers	HUVEC	blood vessel
45	chr2:112219600-112222400	Enhancers	Fetal Thymus	thymus
46	chr2:112219600-112222400	Enhancers	NHEK	skin
47	chr2:112219600-112223400	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr2:112219800-112220400	Weak transcription	K562	blood
49	chr2:112219800-112220600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr2:112219800-112221200	Weak transcription	Rectal Mucosa Donor 29	rectum

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