Variant report

Variant	esv1816787
Chromosome Location	chr1:144620079-144830258
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:840)
CpG islands
(count:366)
Chromatin interactive
region (count:5)
LncRNA
region (count:44)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:840 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr1:144679564-144679880	GM12878	blood:	n/a	n/a
2	BATF	chr1:144816815-144817082	GM12878	blood:	n/a	n/a
3	BATF	chr1:144828481-144829126	GM12878	blood:	n/a	n/a
4	BATF	chr1:144816769-144817077	GM12878	blood:	n/a	n/a
5	BATF	chr1:144811689-144812035	GM12878	blood:	n/a	n/a
6	BATF	chr1:144828408-144829114	GM12878	blood:	n/a	n/a
7	BATF	chr1:144679543-144679819	GM12878	blood:	n/a	n/a
8	BATF	chr1:144690283-144690581	GM12878	blood:	n/a	chr1:144690289-144690297 chr1:144690402-144690411
9	BATF	chr1:144621396-144621792	GM12878	blood:	n/a	n/a
10	BATF	chr1:144822457-144822900	GM12878	blood:	n/a	n/a
11	BATF	chr1:144829153-144829560	GM12878	blood:	n/a	n/a
12	BATF	chr1:144822461-144822911	GM12878	blood:	n/a	n/a
13	BATF	chr1:144672666-144672904	GM12878	blood:	n/a	n/a
14	BATF	chr1:144829689-144829978	GM12878	blood:	n/a	n/a
15	BATF	chr1:144811804-144812040	GM12878	blood:	n/a	n/a
16	BATF	chr1:144829180-144829396	GM12878	blood:	n/a	n/a
17	BATF	chr1:144690796-144691031	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:144828457-144828809	GM12878	blood:	n/a	n/a
19	BCL11A	chr1:144828835-144829095	GM12878	blood:	n/a	n/a
20	BCL11A	chr1:144621190-144621435	GM12878	blood:	n/a	n/a
21	BCL11A	chr1:144816834-144816993	GM12878	blood:	n/a	n/a
22	BCL11A	chr1:144690657-144691064	GM12878	blood:	n/a	n/a
23	BCL11A	chr1:144620110-144620305	GM12878	blood:	n/a	n/a
24	BCL11A	chr1:144687719-144687979	GM12878	blood:	n/a	n/a
25	BCL11A	chr1:144829792-144829953	GM12878	blood:	n/a	n/a
26	BCL11A	chr1:144690673-144690958	GM12878	blood:	n/a	n/a
27	BCL11A	chr1:144811376-144811736	GM12878	blood:	n/a	n/a
28	BCL11A	chr1:144829265-144829496	GM12878	blood:	n/a	n/a
29	BCL11A	chr1:144829682-144829901	GM12878	blood:	n/a	n/a
30	BCL11A	chr1:144672707-144672942	GM12878	blood:	n/a	n/a
31	BCL11A	chr1:144822517-144822688	GM12878	blood:	n/a	n/a
32	BCL11A	chr1:144690359-144690638	GM12878	blood:	n/a	n/a
33	BCL11A	chr1:144828446-144828898	GM12878	blood:	n/a	n/a
34	BHLHE40	chr1:144811752-144811972	HepG2	liver:	n/a	n/a
35	BHLHE40	chr1:144621538-144621780	HepG2	liver:	n/a	n/a
36	CEBPB	chr1:144679661-144679667	IMR90	lung:	n/a	n/a
37	CEBPD	chr1:144690310-144690706	K562	blood:	n/a	n/a
38	CEBPD	chr1:144706674-144707423	K562	blood:	n/a	n/a
39	CEBPD	chr1:144825427-144825748	K562	blood:	n/a	n/a
40	CTCF	chr1:144621555-144621610	Lung_OC	lung:	n/a	n/a
41	CTCF	chr1:144697640-144697790	RPTEC	kidney:	n/a	n/a
42	CTCF	chr1:144692743-144692821	K562	blood:	n/a	n/a
43	CTCF	chr1:144697600-144697750	SAEC	small airway:	n/a	n/a
44	CTCF	chr1:144697620-144697770	GM12875	blood:	n/a	n/a
45	CTCF	chr1:144815338-144815368	GM10248	blood:	n/a	n/a
46	CTCF	chr1:144811603-144812012	A549	lung:	n/a	n/a
47	CTCF	chr1:144812081-144812180	GM10248	blood:	n/a	n/a
48	CTCF	chr1:144697648-144697743	ProgFib	skin:	n/a	n/a
49	CTCF	chr1:144811774-144811990	LNCaP	prostate:	n/a	n/a
50	CTCF	chr1:144621387-144621708	K562	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144815302-144815352	U87	brain:	n/a
2	chr1:144692074-144692124	IMR90	lung:	fetal
3	chr1:144811373-144811423	A549	lung:	n/a
4	chr1:144815915-144815965	HRCEpiC	kidney:	n/a
5	chr1:144814628-144814678	HRCEpiC	kidney:	n/a
6	chr1:144815915-144815965	H1-hESC	embryonic stem cell:	embryo
7	chr1:144815915-144815965	RPTEC	kidney:	n/a
8	chr1:144814628-144814678	NT2-D1	testis:	n/a
9	chr1:144815302-144815352	SK-N-SH	brain:	n/a
10	chr1:144815915-144815965	AG04450	lung:	fetal
11	chr1:144815915-144815965	HPAEpiC	pulmonary alveolar:	n/a
12	chr1:144811373-144811423	ProgFib	skin:	n/a
13	chr1:144811373-144811423	HMEC	breast:	n/a
14	chr1:144814628-144814678	GM12878	blood:	n/a
15	chr1:144692074-144692124	HMEC	breast:	n/a
16	chr1:144692074-144692124	HCM	heart:	n/a
17	chr1:144814628-144814678	SKMC	muscle:	n/a
18	chr1:144815915-144815965	ECC-1	luminal epithelium:	n/a
19	chr1:144814628-144814678	ProgFib	skin:	n/a
20	chr1:144814628-144814678	PFSK-1	brain:	n/a
21	chr1:144815915-144815965	BE2_C	brain:	n/a
22	chr1:144815302-144815352	ECC-1	luminal epithelium:	n/a
23	chr1:144620428-144620478	AG10803	skin:	n/a
24	chr1:144692074-144692124	AG09319	gingival:	n/a
25	chr1:144620428-144620478	HRE	kidney:	n/a
26	chr1:144811373-144811423	LNCaP	prostate:	n/a
27	chr1:144692074-144692124	PFSK-1	brain:	n/a
28	chr1:144620428-144620478	PFSK-1	brain:	n/a
29	chr1:144815915-144815965	HCM	heart:	n/a
30	chr1:144692074-144692124	Caco-2	colon:	n/a
31	chr1:144620428-144620478	GM12892	blood:	n/a
32	chr1:144814628-144814678	SK-N-SH	brain:	n/a
33	chr1:144815915-144815965	HIPEpiC	eye:	n/a
34	chr1:144815302-144815352	HCPEpiC	choroid plexus:	n/a
35	chr1:144815915-144815965	GM12878	blood:	n/a
36	chr1:144620428-144620478	HEK293	kidney:	embryo
37	chr1:144815915-144815965	ovcar-3	ovarian:	n/a
38	chr1:144814628-144814678	HCT-116	colon:	n/a
39	chr1:144815302-144815352	HRE	kidney:	n/a
40	chr1:144815302-144815352	NHBE	bronchial:	n/a
41	chr1:144811373-144811423	BJ	skin:	n/a
42	chr1:144814628-144814678	ovcar-3	ovarian:	n/a
43	chr1:144815915-144815965	Hepatocyte	liver:	n/a
44	chr1:144620428-144620478	HPAEpiC	pulmonary alveolar:	n/a
45	chr1:144811373-144811423	HUVEC	blood vessel:	n/a
46	chr1:144811373-144811423	HCPEpiC	choroid plexus:	n/a
47	chr1:144620428-144620478	SKMC	muscle:	n/a
48	chr1:144620428-144620478	HRCEpiC	kidney:	n/a
49	chr1:144692074-144692124	ProgFib	skin:	n/a
50	chr1:144620428-144620478	AG04449	skin:	fetal

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:144708092..144711018-chr1:144989311..144991763,2	K562	blood:
2	chr1:144535050..144535880-chr1:144697650..144698167,2	MCF-7	breast:
3	chr1:144696978..144697597-chr1:144972550..144973477,2	MCF-7	breast:
4	chr1:144687969..144690729-chr1:144930762..144933228,2	MCF-7	breast:
5	chr1:144709036..144711011-chr1:144986149..144988620,2	K562	blood:

(count:44 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL592284.1-1	chr1:144619883-144620094	ENSG00000225241
2	lnc-AL592284.1-1	chr1:144828541-144830407	NR_102404
3	lnc-AL592284.1-1	chr1:144816473-144816678	NR_102405
4	lnc-AL592284.1-1	chr1:144619883-144620094	ENSG00000225241
5	lnc-AL592284.1-1	chr1:144619883-144620094	NR_102405
6	lnc-AL592284.1-1	chr1:144826933-144827105	NR_102405
7	lnc-AL592284.1-1	chr1:144817966-144818017	NR_102405
8	lnc-AL592284.1-1	chr1:144814683-144814894	NONHSAT005838
9	lnc-AL592284.1-1	chr1:144823128-144823179	NR_102404
10	lnc-AL592284.1-1	chr1:144825353-144825525	NR_102405
11	lnc-AL592284.1-1	chr1:144814560-144814894	NONHSAT005837
12	lnc-AL592284.1-1	chr1:144826933-144827105	NR_102404
13	lnc-AL592284.1-1	chr1:144824705-144824756	NR_102404
14	lnc-AL592284.1-1	chr1:144823128-144823179	NR_102405
15	lnc-AL592284.1-1	chr1:144827820-144827928	NR_102405
16	lnc-AL592284.1-1	chr1:144814680-144814894	NR_102405
17	lnc-AL592284.1-1	chr1:144828973-144830389	NONHSAT005839
18	lnc-AL592284.1-1	chr1:144815936-144816049	NONHSAT005837
19	lnc-AL592284.1-1	chr1:144621447-144621655	ENSG00000225241
20	lnc-AL592284.1-1	chr1:144621447-144621656	NR_102405
21	lnc-AL592284.1-1	chr1:144826235-144826286	NR_102405
22	lnc-AL592284.1-1	chr1:144813742-144813844	NR_102405
23	lnc-AL592284.1-1	chr1:144621447-144621656	ENSG00000225241
24	lnc-AL592284.1-1	chr1:144619883-144620094	ENSG00000225241
25	lnc-AL592284.1-1	chr1:144816473-144816678	NR_102404
26	lnc-AL592284.1-1	chr1:144816316-144816795	NONHSAT005838
27	lnc-AL592284.1-1	chr1:144815936-144816008	NR_102404
28	lnc-AL592284.1-1	chr1:144621447-144621656	ENSG00000225241
29	lnc-AL592284.1-1	chr1:144825353-144825525	NR_102404
30	lnc-AL592284.1-1	chr1:144826235-144826286	NR_102404
31	lnc-AL592284.1-1	chr1:144813742-144813844	NR_102404
32	lnc-AL592284.1-1	chr1:144823813-144823985	NR_102405
33	lnc-AL592284.1-1	chr1:144823813-144823985	NR_102404
34	lnc-AL592284.1-1	chr1:144828541-144830407	NR_102405
35	lnc-AL592284.1-1	chr1:144814680-144814894	NR_102404
36	lnc-AL592284.1-1	chr1:144815936-144816008	NONHSAT005838
37	lnc-AL592284.1-1	chr1:144824705-144824756	NR_102405
38	lnc-AL592284.1-1	chr1:144817966-144818017	NR_102404
39	lnc-AL592284.1-1	chr1:144621447-144621656	NR_102404
40	lnc-AL592284.1-1	chr1:144619883-144620094	ENSG00000225241
41	lnc-AL592284.1-1	chr1:144827820-144827928	NR_102404
42	lnc-AL592284.1-1	chr1:144619883-144620094	ENSG00000225241
43	lnc-AL592284.1-1	chr1:144619883-144620094	NR_102404
44	lnc-AL592284.1-1	chr1:144815936-144816008	NR_102405

No data

Variant related genes	Relation type
NBPF9	TF binding region
ENSG00000215861	TF binding region
NBPF9	CpG island
ENSG00000215861	CpG island
ENSG00000178104	chromatin interactions

Extended variants
information (count: 2538 )
Associated
traits (count: 167 )

Variant overlapped rSNPs/rCNVs (count:2538 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199575725	chr1:144620085-144620086	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs61810898	chr1:144620091-144620092	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs587624931	chr1:144620098-144620099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs587666838	chr1:144620111-144620112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs587745030	chr1:144620113-144620114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs587620332	chr1:144620133-144620134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs28464134	chr1:144620144-144620145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs28503226	chr1:144620146-144620147	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369101760	chr1:144620149-144620150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs587704034	chr1:144620185-144620186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs587761985	chr1:144620189-144620190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs28645653	chr1:144620201-144620202	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs587632294	chr1:144620206-144620207	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200739982	chr1:144620230-144620231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376230665	chr1:144620233-144620234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs61810899	chr1:144620265-144620266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs587685103	chr1:144620269-144620270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs587761499	chr1:144620277-144620278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201444196	chr1:144620332-144620333	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs587631164	chr1:144620344-144620345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs587735976	chr1:144620354-144620355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs75742396	chr1:144620361-144620362	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs587770810	chr1:144620364-144620365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs587672869	chr1:144620369-144620370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188133961	chr1:144620397-144620398	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs61810900	chr1:144620404-144620405	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs200925988	chr1:144620409-144620410	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs202246663	chr1:144620411-144620412	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs61810901	chr1:144620413-144620414	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs61810902	chr1:144620425-144620426	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs61810903	chr1:144620429-144620430	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs587729796	chr1:144620430-144620431	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs61810904	chr1:144620436-144620437	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs61810905	chr1:144620439-144620440	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs144789499	chr1:144620440-144620441	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191280260	chr1:144620477-144620478	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs201154502	chr1:144620502-144620503	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369929363	chr1:144620505-144620506	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs61810906	chr1:144620508-144620509	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs61810907	chr1:144620513-144620514	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs61810908	chr1:144620520-144620521	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs61810909	chr1:144620550-144620551	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs587705723	chr1:144620562-144620563	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs148150478	chr1:144620567-144620568	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373046422	chr1:144620578-144620579	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs587665215	chr1:144620595-144620596	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs587745153	chr1:144620606-144620607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372054070	chr1:144620624-144620625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587624243	chr1:144620651-144620652	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs587681658	chr1:144620653-144620654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:167)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Williams Syndrome	20824207	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD

Chromatin state (count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144594600-144621200	Weak transcription	Gastric	stomach
2	chr1:144594600-144622000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:144594600-144622000	Weak transcription	Placenta	Placenta
4	chr1:144594800-144620200	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr1:144594800-144620600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr1:144594800-144621200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr1:144594800-144621200	Weak transcription	Fetal Lung	lung
8	chr1:144594800-144621200	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr1:144594800-144621400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:144594800-144621400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr1:144594800-144621600	Weak transcription	HSMM	muscle
12	chr1:144594800-144621800	Weak transcription	Brain Germinal Matrix	brain
13	chr1:144594800-144621800	Weak transcription	HSMMtube	muscle
14	chr1:144594800-144622000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr1:144594800-144622000	Weak transcription	Duodenum Mucosa	Duodenum
16	chr1:144594800-144623400	Weak transcription	Primary T cells from cord blood	blood
17	chr1:144594800-144623400	Weak transcription	HUVEC	blood vessel
18	chr1:144594800-144624000	Weak transcription	Right Ventricle	heart
19	chr1:144595800-144623200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr1:144596200-144621400	Weak transcription	Pancreas	Pancrea
21	chr1:144596400-144622000	Weak transcription	NH-A	brain
22	chr1:144598800-144621400	Weak transcription	Colon Smooth Muscle	Colon
23	chr1:144598800-144623600	Weak transcription	Hela-S3	cervix
24	chr1:144599000-144621200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr1:144599200-144621600	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr1:144599400-144620400	Weak transcription	Fetal Muscle Trunk	muscle
27	chr1:144599400-144621600	Weak transcription	HMEC	breast
28	chr1:144599400-144621800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr1:144599400-144622000	Weak transcription	Fetal Stomach	stomach
30	chr1:144599400-144623400	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr1:144599800-144623800	Weak transcription	Fetal Intestine Small	intestine
32	chr1:144600000-144620200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr1:144601600-144621000	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr1:144604400-144620200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:144604400-144621600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr1:144607800-144621400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr1:144607800-144622000	Weak transcription	Fetal Intestine Large	intestine
38	chr1:144607800-144622000	Weak transcription	Left Ventricle	heart
39	chr1:144607800-144622000	Weak transcription	Ovary	ovary
40	chr1:144607800-144623600	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr1:144608000-144621000	Weak transcription	NHLF	lung
42	chr1:144609600-144620400	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr1:144615000-144620400	Weak transcription	HepG2	liver
44	chr1:144615200-144621400	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr1:144615600-144620800	Weak transcription	Brain Anterior Caudate	brain
46	chr1:144615600-144620800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr1:144615800-144620400	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr1:144616600-144620200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr1:144617000-144620600	Strong transcription	Primary monocytes fromperipheralblood	blood
50	chr1:144617200-144620600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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