Variant report

Variant	nsv948878
Chromosome Location	chr2:213345197-213534298
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:213401997-213402263	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr2:213368330-213368485	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:213400803-213401775	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:213402946-213403789	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:213430555-213430591	K562	blood:	n/a	n/a
6	BACH1	chr2:213414514-213414697	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr2:213370363-213370703	GM12878	blood:	n/a	chr2:213370531-213370542
8	BATF	chr2:213370321-213370680	GM12878	blood:	n/a	chr2:213370531-213370542
9	BATF	chr2:213354672-213355022	GM12878	blood:	n/a	chr2:213354879-213354890
10	BATF	chr2:213354721-213355083	GM12878	blood:	n/a	chr2:213354879-213354890
11	BHLHE40	chr2:213461390-213461740	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:213354751-213354946	GM12878	blood:	n/a	n/a
13	BRCA1	chr2:213402263-213402279	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:213474237-213474570	MCF-7	breast:	n/a	chr2:213474442-213474453 chr2:213474443-213474452 chr2:213474440-213474457 chr2:213474443-213474452 chr2:213474443-213474452
15	CEBPB	chr2:213464981-213465770	IMR90	lung:	n/a	chr2:213465622-213465633 chr2:213465621-213465632 chr2:213465269-213465282 chr2:213465739-213465752 chr2:213465086-213465103
16	CEBPB	chr2:213474331-213474643	A549	lung:	n/a	chr2:213474442-213474453 chr2:213474443-213474452 chr2:213474440-213474457 chr2:213474443-213474452 chr2:213474443-213474452
17	CEBPB	chr2:213461995-213462190	HepG2	liver:	n/a	chr2:213462139-213462150
18	CEBPB	chr2:213477932-213478812	Hela-S3	cervix:	n/a	chr2:213478645-213478656
19	CEBPB	chr2:213462447-213462733	A549	lung:	n/a	chr2:213462556-213462567 chr2:213462555-213462566 chr2:213462555-213462568 chr2:213462554-213462571
20	CEBPB	chr2:213474268-213474623	A549	lung:	n/a	chr2:213474442-213474453 chr2:213474443-213474452 chr2:213474440-213474457 chr2:213474443-213474452 chr2:213474443-213474452
21	CEBPB	chr2:213413184-213413476	HepG2	liver:	n/a	chr2:213413325-213413336
22	CEBPB	chr2:213465083-213465789	HepG2	liver:	n/a	chr2:213465622-213465633 chr2:213465621-213465632 chr2:213465269-213465282 chr2:213465739-213465752 chr2:213465086-213465103
23	CEBPB	chr2:213474364-213474590	K562	blood:	n/a	chr2:213474442-213474453 chr2:213474443-213474452 chr2:213474440-213474457 chr2:213474443-213474452 chr2:213474443-213474452
24	CEBPB	chr2:213478489-213479039	HepG2	liver:	n/a	chr2:213478645-213478656
25	CEBPB	chr2:213483331-213483808	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr2:213403563-213404207	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr2:213432387-213432623	MCF-7	breast:	n/a	n/a
28	CEBPB	chr2:213499789-213500081	A549	lung:	n/a	chr2:213499932-213499941 chr2:213499930-213499943 chr2:213499930-213499941 chr2:213499931-213499942 chr2:213499930-213499943
29	CEBPB	chr2:213474263-213474610	H1-hESC	embryonic stem cell:	n/a	chr2:213474442-213474453 chr2:213474443-213474452 chr2:213474440-213474457 chr2:213474443-213474452 chr2:213474443-213474452
30	CEBPB	chr2:213457895-213458175	A549	lung:	n/a	chr2:213458017-213458028 chr2:213458015-213458028 chr2:213458015-213458026 chr2:213458015-213458028 chr2:213458015-213458028
31	CEBPB	chr2:213350659-213350945	IMR90	lung:	n/a	chr2:213350800-213350811 chr2:213350802-213350811
32	CEBPB	chr2:213511399-213511765	IMR90	lung:	n/a	n/a
33	CEBPB	chr2:213518974-213518996	IMR90	lung:	n/a	n/a
34	CEBPB	chr2:213401039-213401263	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr2:213511467-213511797	MCF-7	breast:	n/a	n/a
36	CEBPB	chr2:213359368-213359588	HepG2	liver:	n/a	chr2:213359423-213359434
37	CEBPB	chr2:213478515-213478995	A549	lung:	n/a	chr2:213478645-213478656
38	CEBPB	chr2:213457847-213458183	HepG2	liver:	n/a	chr2:213458017-213458028 chr2:213458015-213458028 chr2:213458015-213458026 chr2:213458015-213458028 chr2:213458015-213458028
39	CEBPB	chr2:213474265-213474628	Hela-S3	cervix:	n/a	chr2:213474442-213474453 chr2:213474443-213474452 chr2:213474440-213474457 chr2:213474443-213474452 chr2:213474443-213474452
40	CEBPB	chr2:213462389-213462747	Hela-S3	cervix:	n/a	chr2:213462556-213462567 chr2:213462555-213462566 chr2:213462555-213462568 chr2:213462554-213462571
41	CEBPB	chr2:213402488-213402825	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr2:213457861-213458151	IMR90	lung:	n/a	chr2:213458017-213458028 chr2:213458015-213458028 chr2:213458015-213458026 chr2:213458015-213458028 chr2:213458015-213458028
43	CEBPB	chr2:213499772-213500059	HepG2	liver:	n/a	chr2:213499932-213499941 chr2:213499930-213499943 chr2:213499930-213499941 chr2:213499931-213499942 chr2:213499930-213499943
44	CEBPB	chr2:213359062-213359665	ECC-1	luminal epithelium:	n/a	chr2:213359423-213359434
45	CEBPB	chr2:213474260-213474613	HepG2	liver:	n/a	chr2:213474442-213474453 chr2:213474443-213474452 chr2:213474440-213474457 chr2:213474443-213474452 chr2:213474443-213474452
46	CEBPB	chr2:213374901-213375173	IMR90	lung:	n/a	chr2:213375009-213375018 chr2:213375009-213375020 chr2:213375009-213375018 chr2:213375007-213375018 chr2:213375009-213375018 chr2:213375009-213375018 chr2:213375007-213375020
47	CEBPB	chr2:213474275-213474607	MCF-7	breast:	n/a	chr2:213474442-213474453 chr2:213474443-213474452 chr2:213474440-213474457 chr2:213474443-213474452 chr2:213474443-213474452
48	CEBPB	chr2:213474261-213474631	IMR90	lung:	n/a	chr2:213474442-213474453 chr2:213474443-213474452 chr2:213474440-213474457 chr2:213474443-213474452 chr2:213474443-213474452
49	CEBPB	chr2:213359220-213360036	Hela-S3	cervix:	n/a	chr2:213359423-213359434
50	CEBPB	chr2:213462410-213462743	HepG2	liver:	n/a	chr2:213462556-213462567 chr2:213462555-213462566 chr2:213462555-213462568 chr2:213462554-213462571

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:213401195-213401245	GM12892	blood:	n/a
2	chr2:213401801-213401851	SK-N-MC	brain:	n/a
3	chr2:213401195-213401245	GM12892	blood:	n/a
4	chr2:213401801-213401851	SK-N-MC	brain:	n/a
5	chr2:213400869-213400919	HEK293	kidney:	embryo
6	chr2:213401996-213402046	HIPEpiC	eye:	n/a
7	chr2:213401801-213401851	HRE	kidney:	n/a
8	chr2:213403519-213403569	H1-hESC	embryonic stem cell:	embryo
9	chr2:213400869-213400919	AoSMC	blood vessel:	n/a
10	chr2:213403734-213403784	PFSK-1	brain:	n/a
11	chr2:213401544-213401594	SK-N-SH	brain:	n/a
12	chr2:213400697-213400747	Caco-2	colon:	n/a
13	chr2:213402433-213402483	SK-N-SH_RA	brain:	n/a
14	chr2:213403212-213403262	HIPEpiC	eye:	n/a
15	chr2:213401544-213401594	HCPEpiC	choroid plexus:	n/a
16	chr2:213402433-213402483	HRPEpiC	eye:	n/a
17	chr2:213406960-213407010	GM12878	blood:	n/a
18	chr2:213401333-213401383	GM12891	blood:	n/a
19	chr2:213403859-213403909	Jurkat	blood:	n/a
20	chr2:213401544-213401594	Hela-S3	cervix:	n/a
21	chr2:213403519-213403569	PrEC	prostate:	n/a
22	chr2:213400697-213400747	GM12892	blood:	n/a
23	chr2:213401056-213401106	GM19239	blood:	n/a
24	chr2:213403212-213403262	SAEC	small airway:	n/a
25	chr2:213401544-213401594	PFSK-1	brain:	n/a
26	chr2:213403859-213403909	CMK	blood:	n/a
27	chr2:213403519-213403569	SAEC	small airway:	n/a
28	chr2:213406960-213407010	Caco-2	colon:	n/a
29	chr2:213406960-213407010	HCM	heart:	n/a
30	chr2:213401565-213401615	GM12891	blood:	n/a
31	chr2:213406960-213407010	K562	blood:	n/a
32	chr2:213400869-213400919	HRPEpiC	eye:	n/a
33	chr2:213402815-213402865	GM19239	blood:	n/a
34	chr2:213403859-213403909	ovcar-3	ovarian:	n/a
35	chr2:213401565-213401615	SK-N-MC	brain:	n/a
36	chr2:213400869-213400919	ECC-1	luminal epithelium:	n/a
37	chr2:213403960-213404010	A549	lung:	n/a
38	chr2:213403519-213403569	HRE	kidney:	n/a
39	chr2:213400697-213400747	ProgFib	skin:	n/a
40	chr2:213403321-213403371	HCF	heart:	n/a
41	chr2:213401333-213401383	T-47D	breast:	n/a
42	chr2:213401996-213402046	HEEpiC	esophagus:	n/a
43	chr2:213403519-213403569	HMEC	breast:	n/a
44	chr2:213403859-213403909	LNCaP	prostate:	n/a
45	chr2:213401801-213401851	HCT-116	colon:	n/a
46	chr2:213406960-213407010	ECC-1	luminal epithelium:	n/a
47	chr2:213401056-213401106	SK-N-SH_RA	brain:	n/a
48	chr2:213400869-213400919	AG09309	skin:	n/a
49	chr2:213401056-213401106	AoSMC	blood vessel:	n/a
50	chr2:213400697-213400747	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:213457818..213459698-chr2:214016202..214018755,2	MCF-7	breast:
2	chr2:213476033..213477807-chr2:213483623..213485149,2	MCF-7	breast:
3	chr2:213476033..213477807-chr2:213483623..213485149,2	MCF-7	breast:
4	chr2:213511589..213513226-chr2:213513298..213514802,2	MCF-7	breast:
5	chr2:213042144..213043012-chr2:213382544..213383068,2	MCF-7	breast:
6	chr2:213460436..213462639-chr2:213462830..213465484,2	MCF-7	breast:
7	chr2:213489595..213491555-chr2:213494161..213496417,2	MCF-7	breast:
8	chr17:57924251..57926616-chr2:213401786..213403830,2	MCF-7	breast:
9	chr2:213401536..213403038-chr2:213405253..213408127,2	MCF-7	breast:
10	chr2:213370671..213373168-chr2:213375734..213377389,2	MCF-7	breast:
11	chr2:213392043..213394903-chr2:213396609..213399566,4	MCF-7	breast:
12	chr2:213511589..213513226-chr2:213513298..213514802,2	MCF-7	breast:
13	chr2:213338459..213340893-chr2:213342035..213345641,3	MCF-7	breast:
14	chr2:213394025..213397226-chr2:213401428..213405238,3	MCF-7	breast:
15	chr2:213392919..213394585-chr2:213396394..213398532,2	K562	blood:
16	chr2:211949622..211950636-chr2:213412760..213413513,3	MCF-7	breast:
17	chr2:213459447..213460444-chr2:213641393..213642336,2	MCF-7	breast:
18	chr2:213346530..213348548-chr2:213350642..213352540,2	MCF-7	breast:
19	chr2:213489595..213491555-chr2:213494161..213496417,2	MCF-7	breast:
20	chr2:213353950..213356217-chr2:213359072..213360969,2	MCF-7	breast:
21	chr2:212099679..212101187-chr2:213398262..213400932,2	MCF-7	breast:
22	chr2:213401917..213403622-chr2:213408443..213409958,2	MCF-7	breast:
23	chr2:213401536..213403038-chr2:213405253..213408127,2	MCF-7	breast:
24	chr2:213460436..213462639-chr2:213462830..213465484,2	MCF-7	breast:
25	chr2:213470074..213472529-chr2:213472625..213475028,3	MCF-7	breast:
26	chr16:57053938..57054564-chr2:213523534..213524034,2	Hela-S3	cervix:
27	chr2:213392043..213394903-chr2:213396609..213399566,4	MCF-7	breast:
28	chr2:213346530..213348548-chr2:213350642..213352540,2	MCF-7	breast:
29	chr2:213457758..213459954-chr2:213549287..213551027,2	MCF-7	breast:
30	chr2:213392919..213394585-chr2:213396394..213398532,2	K562	blood:
31	chr2:213370671..213373168-chr2:213375734..213377389,2	MCF-7	breast:
32	chr2:213463640..213465923-chr2:214016038..214018642,2	MCF-7	breast:
33	chr2:213353950..213356217-chr2:213359072..213360969,2	MCF-7	breast:
34	chr2:212742372..212744206-chr2:213400637..213402216,2	MCF-7	breast:
35	chr2:213470074..213472529-chr2:213472625..213475028,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPAG16-10	chr2:213368289-213368358	l_2023_chr2:213368288-213390223_testes
2	lnc-IKZF2-4	chr2:213446081-213446132	ENSG00000225332.2
3	lnc-SPAG16-10	chr2:213389892-213390223	l_2023_chr2:213368288-213390223_testes
4	lnc-SPAG16-10	chr2:213384075-213384142	l_2023_chr2:213368288-213390223_testes

Variant related genes	Relation type
ERBB4	TF binding region
ERBB4	CpG island
ENSG00000030419	chromatin interactions
ENSG00000178568	chromatin interactions
ENSG00000270659	chromatin interactions
ENSG00000201524	chromatin interactions

Extended variants
information (count: 5341 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:5341 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16848665	chr2:213345197-213345198	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557824260	chr2:213345200-213345201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138689078	chr2:213345210-213345211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182306912	chr2:213345260-213345261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561686807	chr2:213345290-213345291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575007920	chr2:213345318-213345319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141140162	chr2:213345328-213345329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540424817	chr2:213345332-213345333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150804405	chr2:213345377-213345378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562777040	chr2:213345420-213345421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7603379	chr2:213345437-213345438	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs115603642	chr2:213345510-213345511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185749343	chr2:213345532-213345533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs527732427	chr2:213345613-213345614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528555750	chr2:213345650-213345651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549464646	chr2:213345652-213345653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs567695563	chr2:213345653-213345654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs73063172	chr2:213345667-213345668	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs58520119	chr2:213345686-213345687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370708543	chr2:213345698-213345699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373387366	chr2:213345747-213345748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377487272	chr2:213345750-213345751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556508566	chr2:213345790-213345791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs113815038	chr2:213345816-213345817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs114078782	chr2:213345842-213345843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs72050730	chr2:213345889-213345890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189427227	chr2:213345906-213345907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs572881120	chr2:213345928-213345929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539911598	chr2:213345990-213345991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530409807	chr2:213346007-213346008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555436264	chr2:213346124-213346125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574262666	chr2:213346129-213346130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544376643	chr2:213346193-213346194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562557146	chr2:213346286-213346287	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs138069295	chr2:213346300-213346301	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs13385257	chr2:213346358-213346359	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs560074643	chr2:213346392-213346393	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs527670756	chr2:213346489-213346490	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs370319101	chr2:213346516-213346517	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs549157275	chr2:213346517-213346518	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs374853800	chr2:213346518-213346519	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs571590294	chr2:213346528-213346529	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs180888119	chr2:213346591-213346592	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs114353805	chr2:213346607-213346608	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs185510160	chr2:213346616-213346617	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs571893940	chr2:213346648-213346649	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs111376338	chr2:213346752-213346753	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs76849460	chr2:213346757-213346758	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs566420130	chr2:213346759-213346760	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs533758398	chr2:213346797-213346798	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	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
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	21147756	CNVD
Schizophrenia	18990708	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:898 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213342800-213345400	Weak transcription	Brain Cingulate Gyrus	brain
2	chr2:213343400-213348000	Enhancers	Fetal Heart	heart
3	chr2:213343600-213345800	Enhancers	Fetal Brain Female	brain
4	chr2:213344000-213346200	Enhancers	Fetal Brain Male	brain
5	chr2:213345200-213345400	Enhancers	Brain Anterior Caudate	brain
6	chr2:213345200-213345600	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr2:213345200-213345800	Enhancers	Brain Hippocampus Middle	brain
8	chr2:213345200-213346600	Enhancers	Brain Substantia Nigra	brain
9	chr2:213345400-213345600	Enhancers	Brain Cingulate Gyrus	brain
10	chr2:213345400-213345600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr2:213345400-213346400	Weak transcription	Brain Anterior Caudate	brain
12	chr2:213345600-213346400	Weak transcription	Brain Cingulate Gyrus	brain
13	chr2:213345600-213346600	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr2:213345600-213350600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr2:213345800-213346200	Weak transcription	Brain Hippocampus Middle	brain
16	chr2:213345800-213347200	Weak transcription	Fetal Brain Female	brain
17	chr2:213346200-213346800	Enhancers	Brain Hippocampus Middle	brain
18	chr2:213346200-213347000	Bivalent Enhancer	Fetal Brain Male	brain
19	chr2:213346400-213346800	Enhancers	Brain Cingulate Gyrus	brain
20	chr2:213346400-213347000	Enhancers	Brain Anterior Caudate	brain
21	chr2:213346600-213346800	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr2:213346600-213347000	Flanking Active TSS	Brain Substantia Nigra	brain
23	chr2:213346800-213347000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr2:213346800-213347200	Weak transcription	Brain Hippocampus Middle	brain
25	chr2:213346800-213349600	Weak transcription	Brain Cingulate Gyrus	brain
26	chr2:213346800-213352400	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr2:213347000-213347400	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr2:213347000-213347400	Enhancers	Brain Substantia Nigra	brain
29	chr2:213347000-213347800	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr2:213347000-213349400	Weak transcription	Brain Anterior Caudate	brain
31	chr2:213347000-213350000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr2:213347200-213347400	Enhancers	Brain Hippocampus Middle	brain
33	chr2:213347200-213347400	Enhancers	Fetal Brain Female	brain
34	chr2:213347400-213349400	Weak transcription	Brain Substantia Nigra	brain
35	chr2:213347400-213349600	Weak transcription	Brain Hippocampus Middle	brain
36	chr2:213348000-213349400	Weak transcription	Fetal Heart	heart
37	chr2:213349200-213352400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr2:213349400-213349800	Enhancers	Aorta	Aorta
39	chr2:213349400-213350400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr2:213349400-213350800	Enhancers	Brain Anterior Caudate	brain
41	chr2:213349400-213350800	Enhancers	Fetal Heart	heart
42	chr2:213349400-213351400	Enhancers	Brain Substantia Nigra	brain
43	chr2:213349600-213349800	Enhancers	Psoas Muscle	Psoas
44	chr2:213349600-213350200	Active TSS	Brain Cingulate Gyrus	brain
45	chr2:213349600-213350200	Enhancers	Brain Hippocampus Middle	brain
46	chr2:213349800-213350400	Weak transcription	Psoas Muscle	Psoas
47	chr2:213349800-213350600	Weak transcription	Aorta	Aorta
48	chr2:213350000-213351000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr2:213350200-213352800	Weak transcription	Brain Hippocampus Middle	brain
50	chr2:213350200-213353400	Weak transcription	Brain Cingulate Gyrus	brain

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