Variant report

Variant	nsv432024
Chromosome Location	chr2:213314899-213446726
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	ARID3A	chr2:213316375-213316996	HepG2	liver:	n/a	n/a
2	ATF3	chr2:213316506-213316722	HepG2	liver:	n/a	n/a
3	ATF3	chr2:213316396-213316830	HepG2	liver:	n/a	n/a
4	ATF3	chr2:213316535-213316821	HCT-116	colon:	n/a	n/a
5	BACH1	chr2:213414514-213414697	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:213402946-213403789	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr2:213342070-213342161	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr2:213400803-213401775	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:213430555-213430591	K562	blood:	n/a	n/a
10	BACH1	chr2:213401997-213402263	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:213368330-213368485	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr2:213330212-213330484	GM12878	blood:	n/a	chr2:213330364-213330375
13	BATF	chr2:213370321-213370680	GM12878	blood:	n/a	chr2:213370531-213370542
14	BATF	chr2:213370363-213370703	GM12878	blood:	n/a	chr2:213370531-213370542
15	BATF	chr2:213354721-213355083	GM12878	blood:	n/a	chr2:213354879-213354890
16	BATF	chr2:213354672-213355022	GM12878	blood:	n/a	chr2:213354879-213354890
17	BHLHE40	chr2:213316508-213316845	HepG2	liver:	n/a	n/a
18	BHLHE40	chr2:213354751-213354946	GM12878	blood:	n/a	n/a
19	BRCA1	chr2:213402263-213402279	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:213341543-213341622	K562	blood:	n/a	chr2:213341572-213341583
21	CEBPB	chr2:213341421-213341739	IMR90	lung:	n/a	chr2:213341572-213341583
22	CEBPB	chr2:213401039-213401263	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr2:213403563-213404207	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr2:213359368-213359588	HepG2	liver:	n/a	chr2:213359423-213359434
25	CEBPB	chr2:213316471-213316823	IMR90	lung:	n/a	chr2:213316636-213316647
26	CEBPB	chr2:213375009-213375063	H1-hESC	embryonic stem cell:	n/a	chr2:213375009-213375018 chr2:213375009-213375020 chr2:213375009-213375018 chr2:213375009-213375018 chr2:213375009-213375018
27	CEBPB	chr2:213341473-213341740	A549	lung:	n/a	chr2:213341572-213341583
28	CEBPB	chr2:213316512-213316739	HepG2	liver:	n/a	chr2:213316636-213316647
29	CEBPB	chr2:213341412-213341751	HepG2	liver:	n/a	chr2:213341572-213341583
30	CEBPB	chr2:213432387-213432623	MCF-7	breast:	n/a	n/a
31	CEBPB	chr2:213316478-213316816	H1-hESC	embryonic stem cell:	n/a	chr2:213316636-213316647
32	CEBPB	chr2:213432341-213432683	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr2:213359062-213359665	ECC-1	luminal epithelium:	n/a	chr2:213359423-213359434
34	CEBPB	chr2:213316394-213316953	ECC-1	luminal epithelium:	n/a	chr2:213316636-213316647
35	CEBPB	chr2:213316431-213316834	HepG2	liver:	n/a	chr2:213316636-213316647
36	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
37	CEBPB	chr2:213359220-213360036	Hela-S3	cervix:	n/a	chr2:213359423-213359434
38	CEBPB	chr2:213402488-213402825	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr2:213350632-213350977	HepG2	liver:	n/a	chr2:213350800-213350811 chr2:213350802-213350811
40	CEBPB	chr2:213316493-213316769	HepG2	liver:	n/a	chr2:213316636-213316647
41	CEBPB	chr2:213316458-213317006	A549	lung:	n/a	chr2:213316636-213316647
42	CEBPB	chr2:213316503-213316868	ECC-1	luminal epithelium:	n/a	chr2:213316636-213316647
43	CEBPB	chr2:213340349-213340389	HepG2	liver:	n/a	chr2:213340367-213340378
44	CEBPB	chr2:213413184-213413476	HepG2	liver:	n/a	chr2:213413325-213413336
45	CEBPB	chr2:213359155-213359722	ECC-1	luminal epithelium:	n/a	chr2:213359423-213359434
46	CEBPB	chr2:213316456-213317006	Hela-S3	cervix:	n/a	chr2:213316636-213316647
47	CEBPB	chr2:213350659-213350945	IMR90	lung:	n/a	chr2:213350800-213350811 chr2:213350802-213350811
48	CEBPB	chr2:213316458-213316869	HepG2	liver:	n/a	chr2:213316636-213316647
49	CEBPB	chr2:213374877-213375196	HepG2	liver:	n/a	chr2:213375009-213375018 chr2:213375009-213375020 chr2:213375009-213375018 chr2:213375007-213375018 chr2:213375009-213375018 chr2:213375009-213375018 chr2:213375007-213375020
50	CEBPD	chr2:213316501-213316725	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:213403734-213403784	Caco-2	colon:	n/a
2	chr2:213403212-213403262	HEEpiC	esophagus:	n/a
3	chr2:213403734-213403784	Caco-2	colon:	n/a
4	chr2:213403212-213403262	HEEpiC	esophagus:	n/a
5	chr2:213401565-213401615	NHDF-neo	bronchial:	n/a
6	chr2:213401195-213401245	HCM	heart:	n/a
7	chr2:213406960-213407010	A549	lung:	n/a
8	chr2:213403859-213403909	HRPEpiC	eye:	n/a
9	chr2:213403519-213403569	HCT-116	colon:	n/a
10	chr2:213406960-213407010	AG04449	skin:	fetal
11	chr2:213402433-213402483	HepG2	liver:	n/a
12	chr2:213401544-213401594	HAEpiC	amniotic membrane:	n/a
13	chr2:213403212-213403262	SK-N-SH	brain:	n/a
14	chr2:213401565-213401615	GM12891	blood:	n/a
15	chr2:213403960-213404010	HRPEpiC	eye:	n/a
16	chr2:213401333-213401383	RPTEC	kidney:	n/a
17	chr2:213403960-213404010	Hepatocyte	liver:	n/a
18	chr2:213406960-213407010	HIPEpiC	eye:	n/a
19	chr2:213403960-213404010	HCF	heart:	n/a
20	chr2:213401195-213401245	AG09319	gingival:	n/a
21	chr2:213403212-213403262	SK-N-SH_RA	brain:	n/a
22	chr2:213400869-213400919	BJ	skin:	n/a
23	chr2:213402181-213402231	ovcar-3	ovarian:	n/a
24	chr2:213403734-213403784	IMR90	lung:	fetal
25	chr2:213401544-213401594	PrEC	prostate:	n/a
26	chr2:213401056-213401106	MCF10A-Er-Src	breast:	n/a
27	chr2:213401565-213401615	SKMC	muscle:	n/a
28	chr2:213406960-213407010	CMK	blood:	n/a
29	chr2:213406960-213407010	PANC-1	pancreas:	n/a
30	chr2:213401801-213401851	HCPEpiC	choroid plexus:	n/a
31	chr2:213402433-213402483	HEEpiC	esophagus:	n/a
32	chr2:213401056-213401106	RPTEC	kidney:	n/a
33	chr2:213403734-213403784	AG09319	gingival:	n/a
34	chr2:213401333-213401383	AG04450	lung:	fetal
35	chr2:213402815-213402865	IMR90	lung:	fetal
36	chr2:213403321-213403371	Hela-S3	cervix:	n/a
37	chr2:213401056-213401106	Caco-2	colon:	n/a
38	chr2:213403929-213403979	Hela-S3	cervix:	n/a
39	chr2:213403960-213404010	HCM	heart:	n/a
40	chr2:213400697-213400747	HCPEpiC	choroid plexus:	n/a
41	chr2:213401056-213401106	K562	blood:	n/a
42	chr2:213403960-213404010	ovcar-3	ovarian:	n/a
43	chr2:213403212-213403262	U87	brain:	n/a
44	chr2:213406960-213407010	MCF-7	breast:	n/a
45	chr2:213401544-213401594	AG04449	skin:	fetal
46	chr2:213401544-213401594	A549	lung:	n/a
47	chr2:213401195-213401245	AG10803	skin:	n/a
48	chr2:213400869-213400919	AG09309	skin:	n/a
49	chr2:213401195-213401245	HEEpiC	esophagus:	n/a
50	chr2:213401996-213402046	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:213401917..213403622-chr2:213408443..213409958,2	MCF-7	breast:
2	chr2:213401536..213403038-chr2:213405253..213408127,2	MCF-7	breast:
3	chr2:213394025..213397226-chr2:213401428..213405238,3	MCF-7	breast:
4	chr2:213353950..213356217-chr2:213359072..213360969,2	MCF-7	breast:
5	chr2:213370671..213373168-chr2:213375734..213377389,2	MCF-7	breast:
6	chr2:23609593..23610480-chr2:213341871..213342572,2	MCF-7	breast:
7	chr2:213392919..213394585-chr2:213396394..213398532,2	K562	blood:
8	chr2:213392043..213394903-chr2:213396609..213399566,4	MCF-7	breast:
9	chr17:57924251..57926616-chr2:213401786..213403830,2	MCF-7	breast:
10	chr2:213338459..213340893-chr2:213342035..213345641,3	MCF-7	breast:
11	chr2:213346530..213348548-chr2:213350642..213352540,2	MCF-7	breast:
12	chr2:213392919..213394585-chr2:213396394..213398532,2	K562	blood:
13	chr2:213338459..213340893-chr2:213342035..213345641,3	MCF-7	breast:
14	chr2:212742372..212744206-chr2:213400637..213402216,2	MCF-7	breast:
15	chr2:213370671..213373168-chr2:213375734..213377389,2	MCF-7	breast:
16	chr2:213392043..213394903-chr2:213396609..213399566,4	MCF-7	breast:
17	chr2:211949622..211950636-chr2:213412760..213413513,3	MCF-7	breast:
18	chr2:213346530..213348548-chr2:213350642..213352540,2	MCF-7	breast:
19	chr2:213401536..213403038-chr2:213405253..213408127,2	MCF-7	breast:
20	chr2:213353950..213356217-chr2:213359072..213360969,2	MCF-7	breast:
21	chr2:213042144..213043012-chr2:213382544..213383068,2	MCF-7	breast:
22	chr2:212099679..212101187-chr2:213398262..213400932,2	MCF-7	breast:

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

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

Extended variants
information (count: 3806 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3806 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1283312	chr2:213314899-213314900	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538478719	chr2:213314920-213314921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547243018	chr2:213314925-213314926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565649512	chr2:213314939-213314940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527779071	chr2:213314944-213314945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs536189593	chr2:213314974-213314975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550044183	chr2:213315017-213315018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569980139	chr2:213315020-213315021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6435705	chr2:213315099-213315100	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs13420607	chr2:213315100-213315101	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs188573800	chr2:213315138-213315139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571415593	chr2:213315200-213315201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541644531	chr2:213315240-213315241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554193980	chr2:213315278-213315279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553662317	chr2:213315303-213315304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527304105	chr2:213315361-213315362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575200398	chr2:213315393-213315394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192995167	chr2:213315419-213315420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs140749510	chr2:213315463-213315464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185638904	chr2:213315542-213315543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571989010	chr2:213315545-213315546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs57931477	chr2:213315564-213315565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs377123495	chr2:213315565-213315566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142976602	chr2:213315606-213315607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534794034	chr2:213315656-213315657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547402436	chr2:213315701-213315702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190411896	chr2:213315783-213315784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs180675867	chr2:213315792-213315793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs111840650	chr2:213315801-213315802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112753493	chr2:213315838-213315839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs565588379	chr2:213315839-213315840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150036405	chr2:213315841-213315842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551520860	chr2:213315844-213315845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548111753	chr2:213315878-213315879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569997836	chr2:213315897-213315898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs537070540	chr2:213315994-213315995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs16848583	chr2:213316034-213316035	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs570866148	chr2:213316064-213316065	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs183865324	chr2:213316099-213316100	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs537295789	chr2:213316135-213316136	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs557613298	chr2:213316154-213316155	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs78247957	chr2:213316169-213316170	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs535397428	chr2:213316212-213316213	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs575112541	chr2:213316213-213316214	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs115335172	chr2:213316217-213316218	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs561685709	chr2:213316236-213316237	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs369335418	chr2:213316298-213316299	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs188425515	chr2:213316306-213316307	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs73989006	chr2:213316320-213316321	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs181191569	chr2:213316327-213316328	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Breast cancer	22522925	CNVD

Chromatin state (count:863 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213312200-213320400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:213312600-213315400	Enhancers	Fetal Heart	heart
3	chr2:213312600-213316000	Enhancers	HepG2	liver
4	chr2:213313200-213316400	Weak transcription	Brain Substantia Nigra	brain
5	chr2:213313800-213315400	Enhancers	Fetal Kidney	kidney
6	chr2:213314000-213316400	Weak transcription	Brain Hippocampus Middle	brain
7	chr2:213314000-213316600	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr2:213314200-213316600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:213314800-213315000	Enhancers	A549	lung
10	chr2:213315000-213315200	Enhancers	Brain Cingulate Gyrus	brain
11	chr2:213315000-213315200	Enhancers	NHEK	skin
12	chr2:213315000-213316000	Weak transcription	A549	lung
13	chr2:213315200-213315400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr2:213315200-213315800	Weak transcription	NHEK	skin
15	chr2:213315400-213315800	Weak transcription	Fetal Heart	heart
16	chr2:213315400-213316200	Weak transcription	Fetal Kidney	kidney
17	chr2:213315400-213316400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr2:213315400-213316400	Weak transcription	Brain Cingulate Gyrus	brain
19	chr2:213315800-213316600	Enhancers	Fetal Heart	heart
20	chr2:213315800-213317200	Enhancers	NHEK	skin
21	chr2:213315800-213317400	Enhancers	Muscle Satellite Cultured Cells	--
22	chr2:213316000-213316200	Flanking Active TSS	A549	lung
23	chr2:213316000-213316200	Flanking Active TSS	HepG2	liver
24	chr2:213316000-213316400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr2:213316200-213316400	Enhancers	HepG2	liver
26	chr2:213316200-213316600	Active TSS	A549	lung
27	chr2:213316200-213317000	Enhancers	Fetal Kidney	kidney
28	chr2:213316400-213316600	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr2:213316400-213316600	Flanking Active TSS	HepG2	liver
30	chr2:213316400-213316800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr2:213316400-213316800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr2:213316400-213316800	Enhancers	Brain Hippocampus Middle	brain
33	chr2:213316400-213317000	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr2:213316400-213317000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr2:213316400-213317000	Enhancers	Brain Cingulate Gyrus	brain
36	chr2:213316400-213317000	Enhancers	Brain Substantia Nigra	brain
37	chr2:213316400-213317000	Enhancers	HMEC	breast
38	chr2:213316400-213317000	Enhancers	HSMMtube	muscle
39	chr2:213316400-213317200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr2:213316400-213317200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr2:213316400-213317200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr2:213316400-213317200	Enhancers	NHDF-Ad	bronchial
43	chr2:213316600-213316800	Enhancers	Colon Smooth Muscle	Colon
44	chr2:213316600-213316800	Flanking Active TSS	Fetal Heart	heart
45	chr2:213316600-213316800	Flanking Active TSS	A549	lung
46	chr2:213316600-213317000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr2:213316600-213317000	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr2:213316600-213317000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr2:213316600-213317000	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr2:213316600-213317000	Enhancers	Rectal Smooth Muscle	rectum

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