Variant report

Variant	nsv875812
Chromosome Location	chr2:213395507-213434856
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	chr2:213430555-213430591	K562	blood:	n/a	n/a
2	BACH1	chr2:213401997-213402263	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	chr2:213414514-213414697	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr2:213402263-213402279	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:213432341-213432683	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr2:213432387-213432623	MCF-7	breast:	n/a	n/a
9	CEBPB	chr2:213413184-213413476	HepG2	liver:	n/a	chr2:213413325-213413336
10	CEBPB	chr2:213402488-213402825	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr2:213401039-213401263	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr2:213403563-213404207	Hela-S3	cervix:	n/a	n/a
13	CHD1	chr2:213402626-213402790	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr2:213402257-213402830	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr2:213402431-213402438	HepG2	liver:	n/a	n/a
16	CHD2	chr2:213403694-213404221	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr2:213403476-213404207	Hela-S3	cervix:	n/a	n/a
18	CTBP2	chr2:213400916-213404322	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr2:213413264-213413435	GM12878	blood:	n/a	chr2:213413330-213413351
20	CTCF	chr2:213401480-213401630	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr2:213397400-213397550	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr2:213397380-213397530	GM12873	blood:	n/a	n/a
23	CTCF	chr2:213413280-213413430	A549	lung:	n/a	chr2:213413330-213413351
24	CTCF	chr2:213397462-213397521	NHEK	skin:	n/a	n/a
25	CTCF	chr2:213413260-213413410	MCF-7	breast:	n/a	chr2:213413330-213413351
26	CTCF	chr2:213432500-213432650	GM12869	blood:	n/a	chr2:213432516-213432537 chr2:213432522-213432538 chr2:213432523-213432536 chr2:213432527-213432536 chr2:213432521-213432539
27	CTCF	chr2:213432338-213432629	K562	blood:	n/a	chr2:213432516-213432537 chr2:213432522-213432538 chr2:213432523-213432536 chr2:213432527-213432536 chr2:213432521-213432539
28	CTCF	chr2:213397491-213397552	LNCaP	prostate:	n/a	n/a
29	CTCF	chr2:213432460-213432610	GM12865	blood:	n/a	chr2:213432516-213432537 chr2:213432522-213432538 chr2:213432523-213432536 chr2:213432527-213432536 chr2:213432521-213432539
30	CTCF	chr2:213413156-213413518	GM12878	blood:	n/a	chr2:213413330-213413351
31	CTCF	chr2:213432440-213432590	BE2_C	brain:	n/a	chr2:213432516-213432537 chr2:213432522-213432538 chr2:213432523-213432536 chr2:213432527-213432536 chr2:213432521-213432539
32	CTCF	chr2:213413254-213413443	LNCaP	prostate:	n/a	chr2:213413330-213413351
33	CTCF	chr2:213402520-213402670	GM12875	blood:	n/a	chr2:213402588-213402601
34	CTCF	chr2:213432440-213432590	K562	blood:	n/a	chr2:213432516-213432537 chr2:213432522-213432538 chr2:213432523-213432536 chr2:213432527-213432536 chr2:213432521-213432539
35	CTCF	chr2:213432440-213432590	HRPEpiC	eye:	n/a	chr2:213432516-213432537 chr2:213432522-213432538 chr2:213432523-213432536 chr2:213432527-213432536 chr2:213432521-213432539
36	CTCF	chr2:213432420-213432570	Hela-S3	cervix:	n/a	chr2:213432516-213432537 chr2:213432522-213432538 chr2:213432523-213432536 chr2:213432527-213432536 chr2:213432521-213432539
37	CTCF	chr2:213401360-213401510	HRE	kidney:	n/a	n/a
38	CTCF	chr2:213432440-213432590	AG09319	gingival:	n/a	chr2:213432516-213432537 chr2:213432522-213432538 chr2:213432523-213432536 chr2:213432527-213432536 chr2:213432521-213432539
39	CTCF	chr2:213432440-213432590	GM12875	blood:	n/a	chr2:213432516-213432537 chr2:213432522-213432538 chr2:213432523-213432536 chr2:213432527-213432536 chr2:213432521-213432539
40	CTCF	chr2:213432440-213432590	HA-sp	spinal cord:	n/a	chr2:213432516-213432537 chr2:213432522-213432538 chr2:213432523-213432536 chr2:213432527-213432536 chr2:213432521-213432539
41	CTCF	chr2:213413271-213413439	HepG2	liver:	n/a	chr2:213413330-213413351
42	CTCF	chr2:213413244-213413445	Gliobla	brain:	n/a	chr2:213413330-213413351
43	CTCF	chr2:213413280-213413430	HepG2	liver:	n/a	chr2:213413330-213413351
44	CTCF	chr2:213432397-213432649	GM12878	blood:	n/a	chr2:213432516-213432537 chr2:213432522-213432538 chr2:213432523-213432536 chr2:213432527-213432536 chr2:213432521-213432539
45	CTCF	chr2:213432460-213432610	K562	blood:	n/a	chr2:213432516-213432537 chr2:213432522-213432538 chr2:213432523-213432536 chr2:213432527-213432536 chr2:213432521-213432539
46	CTCF	chr2:213432408-213432656	Kidney_OC	kidney:	n/a	chr2:213432516-213432537 chr2:213432522-213432538 chr2:213432523-213432536 chr2:213432527-213432536 chr2:213432521-213432539
47	CTCF	chr2:213432421-213432574	NHEK	skin:	n/a	chr2:213432516-213432537 chr2:213432522-213432538 chr2:213432523-213432536 chr2:213432527-213432536 chr2:213432521-213432539
48	CTCF	chr2:213432520-213432670	RPTEC	kidney:	n/a	chr2:213432522-213432538 chr2:213432523-213432536 chr2:213432527-213432536 chr2:213432521-213432539
49	CTCF	chr2:213401920-213402070	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr2:213413240-213413390	GM12873	blood:	n/a	chr2:213413330-213413351

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:213403321-213403371	Hela-S3	cervix:	n/a
2	chr2:213402181-213402231	MCF10A-Er-Src	breast:	n/a
3	chr2:213403321-213403371	Hela-S3	cervix:	n/a
4	chr2:213402181-213402231	MCF10A-Er-Src	breast:	n/a
5	chr2:213401565-213401615	MCF10A-Er-Src	breast:	n/a
6	chr2:213403859-213403909	A549	lung:	n/a
7	chr2:213403734-213403784	AG09319	gingival:	n/a
8	chr2:213403929-213403979	SKMC	muscle:	n/a
9	chr2:213403859-213403909	HIPEpiC	eye:	n/a
10	chr2:213401565-213401615	AG10803	skin:	n/a
11	chr2:213403960-213404010	HIPEpiC	eye:	n/a
12	chr2:213403734-213403784	SK-N-MC	brain:	n/a
13	chr2:213403859-213403909	HCT-116	colon:	n/a
14	chr2:213401195-213401245	NHDF-neo	bronchial:	n/a
15	chr2:213401565-213401615	GM19239	blood:	n/a
16	chr2:213402433-213402483	HEEpiC	esophagus:	n/a
17	chr2:213402433-213402483	MCF-7	breast:	n/a
18	chr2:213403929-213403979	SAEC	small airway:	n/a
19	chr2:213403321-213403371	SK-N-MC	brain:	n/a
20	chr2:213406960-213407010	GM06990	blood:	n/a
21	chr2:213401565-213401615	Hepatocyte	liver:	n/a
22	chr2:213401195-213401245	MCF10A-Er-Src	breast:	n/a
23	chr2:213403734-213403784	AG10803	skin:	n/a
24	chr2:213401544-213401594	HMEC	breast:	n/a
25	chr2:213403212-213403262	HCF	heart:	n/a
26	chr2:213403859-213403909	HEEpiC	esophagus:	n/a
27	chr2:213406960-213407010	Jurkat	blood:	n/a
28	chr2:213401565-213401615	HUVEC	blood vessel:	n/a
29	chr2:213400869-213400919	SK-N-SH_RA	brain:	n/a
30	chr2:213403212-213403262	NH-A	brain:	n/a
31	chr2:213403519-213403569	HL-60	blood:	n/a
32	chr2:213400697-213400747	GM06990	blood:	n/a
33	chr2:213403519-213403569	Hela-S3	cervix:	n/a
34	chr2:213403859-213403909	PANC-1	pancreas:	n/a
35	chr2:213402181-213402231	AG09309	skin:	n/a
36	chr2:213403734-213403784	NT2-D1	testis:	n/a
37	chr2:213401996-213402046	HUVEC	blood vessel:	n/a
38	chr2:213403321-213403371	CMK	blood:	n/a
39	chr2:213400869-213400919	GM12892	blood:	n/a
40	chr2:213401333-213401383	HCPEpiC	choroid plexus:	n/a
41	chr2:213403212-213403262	HAEpiC	amniotic membrane:	n/a
42	chr2:213401544-213401594	Caco-2	colon:	n/a
43	chr2:213401565-213401615	SK-N-SH	brain:	n/a
44	chr2:213403960-213404010	HEK293	kidney:	embryo
45	chr2:213400697-213400747	PrEC	prostate:	n/a
46	chr2:213401195-213401245	A549	lung:	n/a
47	chr2:213401333-213401383	SK-N-MC	brain:	n/a
48	chr2:213401195-213401245	PANC-1	pancreas:	n/a
49	chr2:213401333-213401383	NHDF-neo	bronchial:	n/a
50	chr2:213402815-213402865	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr2:212742372..212744206-chr2:213400637..213402216,2	MCF-7	breast:
2	chr2:213394025..213397226-chr2:213401428..213405238,3	MCF-7	breast:
3	chr2:213401536..213403038-chr2:213405253..213408127,2	MCF-7	breast:
4	chr17:57924251..57926616-chr2:213401786..213403830,2	MCF-7	breast:
5	chr2:212099679..212101187-chr2:213398262..213400932,2	MCF-7	breast:
6	chr2:213401536..213403038-chr2:213405253..213408127,2	MCF-7	breast:
7	chr2:211949622..211950636-chr2:213412760..213413513,3	MCF-7	breast:
8	chr2:213392043..213394903-chr2:213396609..213399566,4	MCF-7	breast:
9	chr2:213392919..213394585-chr2:213396394..213398532,2	K562	blood:
10	chr2:213401917..213403622-chr2:213408443..213409958,2	MCF-7	breast:

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

Extended variants
information (count: 824 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:824 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7598042	chr2:213395507-213395508	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554072437	chr2:213395540-213395541	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs7598055	chr2:213395548-213395549	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs7571642	chr2:213395552-213395553	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs554945751	chr2:213395567-213395568	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs13397864	chr2:213395569-213395570	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs149299077	chr2:213395673-213395674	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs565042909	chr2:213395721-213395722	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs532541160	chr2:213395727-213395728	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs144574449	chr2:213395732-213395733	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs148453699	chr2:213395734-213395735	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs16848787	chr2:213395746-213395747	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs142075207	chr2:213395828-213395829	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs531219992	chr2:213395858-213395859	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs549818174	chr2:213395871-213395872	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs192795709	chr2:213395896-213395897	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs544694414	chr2:213395899-213395900	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs564647788	chr2:213395917-213395918	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs182789180	chr2:213395978-213395979	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs188349305	chr2:213395979-213395980	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs552476622	chr2:213395985-213395986	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs74897819	chr2:213395986-213395987	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs536536904	chr2:213396009-213396010	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs73989049	chr2:213396029-213396030	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs146326585	chr2:213396039-213396040	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs543475835	chr2:213396046-213396047	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs558593812	chr2:213396049-213396050	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs17262059	chr2:213396059-213396060	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs541155270	chr2:213396061-213396062	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs367901886	chr2:213396065-213396066	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs559520890	chr2:213396076-213396077	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs530272993	chr2:213396077-213396078	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs542470004	chr2:213396078-213396079	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs563846731	chr2:213396090-213396091	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs531300831	chr2:213396111-213396112	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs549784062	chr2:213396157-213396158	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs6724920	chr2:213396169-213396170	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs112794414	chr2:213396187-213396188	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs191949547	chr2:213396221-213396222	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs529929368	chr2:213396222-213396223	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs547555275	chr2:213396249-213396250	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs565838407	chr2:213396254-213396255	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs144184951	chr2:213396318-213396319	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs554822216	chr2:213396328-213396329	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs569868232	chr2:213396333-213396334	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs537386137	chr2:213396343-213396344	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs558507541	chr2:213396383-213396384	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs576876048	chr2:213396435-213396436	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs534786539	chr2:213396444-213396445	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs367727845	chr2:213396472-213396473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

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

Chromatin state (count:595 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213391600-213399200	Enhancers	Fetal Heart	heart
2	chr2:213393000-213399000	Weak transcription	Psoas Muscle	Psoas
3	chr2:213393000-213400800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr2:213393200-213396000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:213393200-213399000	Weak transcription	Brain Angular Gyrus	brain
6	chr2:213393200-213400600	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr2:213395200-213399600	Enhancers	Brain Substantia Nigra	brain
8	chr2:213395400-213396000	Active TSS	Aorta	Aorta
9	chr2:213395400-213397000	Weak transcription	Brain Hippocampus Middle	brain
10	chr2:213395400-213397400	Enhancers	Brain Anterior Caudate	brain
11	chr2:213395400-213398200	Weak transcription	Brain Cingulate Gyrus	brain
12	chr2:213395400-213398800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr2:213396000-213396200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:213396000-213399000	Weak transcription	Aorta	Aorta
15	chr2:213396200-213396600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:213396600-213397000	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr2:213396600-213400000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:213397000-213397600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:213397000-213397600	Enhancers	Brain Hippocampus Middle	brain
20	chr2:213397000-213398200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr2:213397000-213399000	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr2:213397400-213397600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr2:213397400-213397600	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr2:213397400-213397600	Flanking Active TSS	Brain Anterior Caudate	brain
25	chr2:213397400-213397600	Bivalent Enhancer	Left Ventricle	heart
26	chr2:213397600-213398600	Weak transcription	Brain Hippocampus Middle	brain
27	chr2:213397600-213400200	Enhancers	Brain Anterior Caudate	brain
28	chr2:213398200-213398600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr2:213398200-213398600	Enhancers	Brain Cingulate Gyrus	brain
30	chr2:213398400-213400000	Active TSS	Brain Germinal Matrix	brain
31	chr2:213398600-213398800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr2:213398600-213399000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr2:213398600-213399000	Active TSS	Brain Cingulate Gyrus	brain
34	chr2:213398600-213399600	Enhancers	Brain Hippocampus Middle	brain
35	chr2:213398800-213399800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr2:213398800-213401000	Bivalent/Poised TSS	Fetal Brain Female	brain
37	chr2:213398800-213402600	Bivalent/Poised TSS	Fetal Kidney	kidney
38	chr2:213399000-213399200	Enhancers	Brain Angular Gyrus	brain
39	chr2:213399000-213399200	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr2:213399000-213399400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr2:213399000-213399400	Flanking Active TSS	Aorta	Aorta
42	chr2:213399000-213399400	Enhancers	Psoas Muscle	Psoas
43	chr2:213399000-213400800	Bivalent/Poised TSS	Fetal Brain Male	brain
44	chr2:213399200-213400200	Weak transcription	Brain Angular Gyrus	brain
45	chr2:213399200-213400400	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr2:213399200-213403800	Active TSS	Fetal Heart	heart
47	chr2:213399400-213399600	Active TSS	Aorta	Aorta
48	chr2:213399400-213399600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
49	chr2:213399400-213399800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr2:213399400-213400800	Weak transcription	Psoas Muscle	Psoas

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