Variant report

Variant	nsv834527
Chromosome Location	chr2:213115966-213334308
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:714)
CpG islands
(count:183)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:213313548-213313878	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:213224153-213224545	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:213316375-213316996	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:213288860-213289080	HepG2	liver:	n/a	n/a
5	ATF2	chr2:213164628-213165033	GM12878	blood:	n/a	n/a
6	ATF3	chr2:213316506-213316722	HepG2	liver:	n/a	n/a
7	ATF3	chr2:213316396-213316830	HepG2	liver:	n/a	n/a
8	ATF3	chr2:213316535-213316821	HCT-116	colon:	n/a	n/a
9	BATF	chr2:213330212-213330484	GM12878	blood:	n/a	chr2:213330364-213330375
10	BCL11A	chr2:213293765-213294070	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr2:213164643-213165029	GM12878	blood:	n/a	chr2:213164727-213164736
12	BCL11A	chr2:213164602-213165058	GM12878	blood:	n/a	chr2:213164727-213164736
13	BHLHE40	chr2:213164655-213165134	GM12878	blood:	n/a	n/a
14	BHLHE40	chr2:213316508-213316845	HepG2	liver:	n/a	n/a
15	BHLHE40	chr2:213224318-213224388	HepG2	liver:	n/a	n/a
16	CCNT2	chr2:213167804-213168004	K562	blood:	n/a	n/a
17	CEBPB	chr2:213316458-213316869	HepG2	liver:	n/a	chr2:213316636-213316647
18	CEBPB	chr2:213316512-213316739	HepG2	liver:	n/a	chr2:213316636-213316647
19	CEBPB	chr2:213209329-213209566	A549	lung:	n/a	chr2:213209437-213209454 chr2:213209442-213209453 chr2:213209440-213209451
20	CEBPB	chr2:213316458-213317006	A549	lung:	n/a	chr2:213316636-213316647
21	CEBPB	chr2:213309343-213309393	HepG2	liver:	n/a	chr2:213309366-213309377
22	CEBPB	chr2:213316431-213316834	HepG2	liver:	n/a	chr2:213316636-213316647
23	CEBPB	chr2:213123445-213123723	HepG2	liver:	n/a	chr2:213123586-213123597 chr2:213123588-213123599
24	CEBPB	chr2:213316471-213316823	IMR90	lung:	n/a	chr2:213316636-213316647
25	CEBPB	chr2:213316478-213316816	H1-hESC	embryonic stem cell:	n/a	chr2:213316636-213316647
26	CEBPB	chr2:213271036-213271238	HepG2	liver:	n/a	chr2:213271134-213271147
27	CEBPB	chr2:213192916-213193235	IMR90	lung:	n/a	chr2:213193066-213193077
28	CEBPB	chr2:213316503-213316868	ECC-1	luminal epithelium:	n/a	chr2:213316636-213316647
29	CEBPB	chr2:213316394-213316953	ECC-1	luminal epithelium:	n/a	chr2:213316636-213316647
30	CEBPB	chr2:213240595-213240973	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr2:213155653-213155877	HepG2	liver:	n/a	chr2:213155792-213155803 chr2:213155790-213155801 chr2:213155790-213155803
32	CEBPB	chr2:213240458-213240973	A549	lung:	n/a	n/a
33	CEBPB	chr2:213165459-213165613	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr2:213302550-213302702	HepG2	liver:	n/a	chr2:213302635-213302646
35	CEBPB	chr2:213192901-213193253	HepG2	liver:	n/a	chr2:213193066-213193077
36	CEBPB	chr2:213192968-213193202	A549	lung:	n/a	chr2:213193066-213193077
37	CEBPB	chr2:213209433-213209436	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr2:213224251-213224578	HepG2	liver:	n/a	chr2:213224544-213224556
39	CEBPB	chr2:213165371-213165600	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:213316456-213317006	Hela-S3	cervix:	n/a	chr2:213316636-213316647
41	CEBPB	chr2:213286777-213287045	A549	lung:	n/a	n/a
42	CEBPB	chr2:213253278-213253564	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:213240564-213240940	IMR90	lung:	n/a	n/a
44	CEBPB	chr2:213209362-213209592	HepG2	liver:	n/a	chr2:213209437-213209454 chr2:213209442-213209453 chr2:213209440-213209451
45	CEBPB	chr2:213209262-213209565	IMR90	lung:	n/a	chr2:213209320-213209329 chr2:213209437-213209454 chr2:213209320-213209329 chr2:213209442-213209453 chr2:213209440-213209451
46	CEBPB	chr2:213240450-213241002	HepG2	liver:	n/a	n/a
47	CEBPB	chr2:213316493-213316769	HepG2	liver:	n/a	chr2:213316636-213316647
48	CEBPD	chr2:213316501-213316725	HepG2	liver:	n/a	n/a
49	CHD2	chr2:213164541-213165145	GM12878	blood:	n/a	n/a
50	CTCF	chr2:213332420-213332570	AG09319	gingival:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:213228956-213229006	HIPEpiC	eye:	n/a
2	chr2:213248884-213248934	Jurkat	blood:	n/a
3	chr2:213248884-213248934	ovcar-3	ovarian:	n/a
4	chr2:213228956-213229006	GM19239	blood:	n/a
5	chr2:213228956-213229006	RPTEC	kidney:	n/a
6	chr2:213248884-213248934	NHDF-neo	bronchial:	n/a
7	chr2:213292541-213292591	GM12891	blood:	n/a
8	chr2:213248884-213248934	GM12891	blood:	n/a
9	chr2:213228956-213229006	CMK	blood:	n/a
10	chr2:213292541-213292591	GM19239	blood:	n/a
11	chr2:213228956-213229006	Jurkat	blood:	n/a
12	chr2:213292541-213292591	SK-N-MC	brain:	n/a
13	chr2:213292541-213292591	HCM	heart:	n/a
14	chr2:213228956-213229006	HRCEpiC	kidney:	n/a
15	chr2:213228956-213229006	H1-hESC	embryonic stem cell:	embryo
16	chr2:213292541-213292591	A549	lung:	n/a
17	chr2:213228956-213229006	PFSK-1	brain:	n/a
18	chr2:213248884-213248934	Hepatocyte	liver:	n/a
19	chr2:213228956-213229006	AoSMC	blood vessel:	n/a
20	chr2:213292541-213292591	HIPEpiC	eye:	n/a
21	chr2:213292541-213292591	H1-hESC	embryonic stem cell:	embryo
22	chr2:213228956-213229006	ECC-1	luminal epithelium:	n/a
23	chr2:213248884-213248934	NB4	blood:	n/a
24	chr2:213228956-213229006	AG04450	lung:	fetal
25	chr2:213292541-213292591	PFSK-1	brain:	n/a
26	chr2:213292541-213292591	HPAEpiC	pulmonary alveolar:	n/a
27	chr2:213292541-213292591	AG10803	skin:	n/a
28	chr2:213292541-213292591	HUVEC	blood vessel:	n/a
29	chr2:213228956-213229006	T-47D	breast:	n/a
30	chr2:213228956-213229006	AG04449	skin:	fetal
31	chr2:213228956-213229006	GM12892	blood:	n/a
32	chr2:213248884-213248934	PANC-1	pancreas:	n/a
33	chr2:213228956-213229006	GM12891	blood:	n/a
34	chr2:213248884-213248934	HCT-116	colon:	n/a
35	chr2:213228956-213229006	ProgFib	skin:	n/a
36	chr2:213248884-213248934	HL-60	blood:	n/a
37	chr2:213292541-213292591	HCT-116	colon:	n/a
38	chr2:213228956-213229006	NB4	blood:	n/a
39	chr2:213292541-213292591	HepG2	liver:	n/a
40	chr2:213248884-213248934	BJ	skin:	n/a
41	chr2:213228956-213229006	PrEC	prostate:	n/a
42	chr2:213292541-213292591	MCF10A-Er-Src	breast:	n/a
43	chr2:213228956-213229006	SAEC	small airway:	n/a
44	chr2:213292541-213292591	PANC-1	pancreas:	n/a
45	chr2:213228956-213229006	HRPEpiC	eye:	n/a
46	chr2:213292541-213292591	GM12878	blood:	n/a
47	chr2:213248884-213248934	K562	blood:	n/a
48	chr2:213248884-213248934	SK-N-MC	brain:	n/a
49	chr2:213292541-213292591	Jurkat	blood:	n/a
50	chr2:213228956-213229006	HepG2	liver:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:213280702..213283541-chr2:213286415..213289040,2	MCF-7	breast:
2	chr2:213202563..213204297-chr2:213206010..213208677,2	K562	blood:
3	chr2:213223218..213224821-chr2:213227410..213229033,2	MCF-7	breast:
4	chr2:213133438..213135317-chr2:213137687..213139229,2	K562	blood:
5	chr2:213294886..213296406-chrX:142860992..142862514,2	K562	blood:
6	chr2:213213790..213216008-chr2:213223245..213225984,2	MCF-7	breast:
7	chr2:213217638..213221383-chr2:213223310..213226579,3	MCF-7	breast:
8	chr2:213213790..213216008-chr2:213223245..213225984,2	MCF-7	breast:
9	chr2:213145552..213149044-chr2:213151103..213154081,3	MCF-7	breast:
10	chr2:213252657..213254943-chr2:213260775..213262754,2	K562	blood:
11	chr2:213108853..213110992-chr2:213114605..213117467,2	MCF-7	breast:
12	chr2:213169267..213171740-chr2:213191721..213193864,2	MCF-7	breast:
13	chr2:213169330..213171305-chr2:213174705..213177385,2	MCF-7	breast:
14	chr2:213223218..213224821-chr2:213227410..213229033,2	MCF-7	breast:
15	chr2:212824327..212826321-chr2:213119385..213121248,2	MCF-7	breast:
16	chr2:213217638..213221383-chr2:213223310..213226579,3	MCF-7	breast:
17	chr2:213280702..213283541-chr2:213286415..213289040,2	MCF-7	breast:
18	chr2:213202563..213204297-chr2:213206010..213208677,2	K562	blood:
19	chr2:213145552..213149044-chr2:213151103..213154081,3	MCF-7	breast:
20	chr2:213169267..213171740-chr2:213191721..213193864,2	MCF-7	breast:
21	chr2:213165115..213165752-chr21:42883583..42884373,2	MCF-7	breast:
22	chr2:213169330..213171305-chr2:213174705..213177385,2	MCF-7	breast:
23	chr2:213252657..213254943-chr2:213260775..213262754,2	K562	blood:
24	chr2:213133438..213135317-chr2:213137687..213139229,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548f-3p	chr2:213291008-213291026	MIMAT0005895_1

No data

Variant related genes	Relation type
MIR548F2	TF binding region
ERBB4	TF binding region
MIR548F2	CpG island
ERBB4	CpG island
ENSG00000178568	chromatin interactions

Extended variants
information (count: 8089 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:8089 , 50 per page) page: 1 2 3 4 5 6 7 ... 162

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567679137	chr2:213115995-213115996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs143034178	chr2:213116005-213116006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs80019179	chr2:213116007-213116008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561028967	chr2:213116023-213116024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556007835	chr2:213116026-213116027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574396791	chr2:213116033-213116034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7587246	chr2:213116085-213116086	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs138897101	chr2:213116136-213116137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372876840	chr2:213116144-213116145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs13426487	chr2:213116181-213116182	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs552074507	chr2:213116183-213116184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113831758	chr2:213116196-213116197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531087138	chr2:213116197-213116198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572441757	chr2:213116300-213116301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146979041	chr2:213116351-213116352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs138149649	chr2:213116367-213116368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536276132	chr2:213116393-213116394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs56395249	chr2:213116401-213116402	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs201208341	chr2:213116416-213116417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566726661	chr2:213116422-213116423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs11885830	chr2:213116423-213116424	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs558392362	chr2:213116432-213116433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs575137037	chr2:213116497-213116498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs6709743	chr2:213116503-213116504	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs554398120	chr2:213116510-213116511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs143105369	chr2:213116528-213116529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs10644810	chr2:213116537-213116538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192636671	chr2:213116555-213116556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372684540	chr2:213116633-213116634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560114116	chr2:213116722-213116723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs536705972	chr2:213116726-213116727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183502892	chr2:213116815-213116816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs56388911	chr2:213116827-213116828	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs114150191	chr2:213116835-213116836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs531176199	chr2:213116842-213116843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs116974503	chr2:213116844-213116845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561259142	chr2:213116849-213116850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187946875	chr2:213116865-213116866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs6728429	chr2:213116916-213116917	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs549739313	chr2:213116941-213116942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567949290	chr2:213116954-213116955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs35184022	chr2:213116976-213116977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114538677	chr2:213116989-213116990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532363247	chr2:213117002-213117003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs12466094	chr2:213117008-213117009	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs150838583	chr2:213117029-213117030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537686748	chr2:213117068-213117069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554766976	chr2:213117092-213117093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs568132332	chr2:213117127-213117128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs149998015	chr2:213117185-213117186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Pancreatic cancer	17952125	CNVD
Schizophrenia	18990708	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:791 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213107800-213134000	Weak transcription	Aorta	Aorta
2	chr2:213114200-213116600	Weak transcription	Fetal Heart	heart
3	chr2:213114600-213130400	Weak transcription	Brain Hippocampus Middle	brain
4	chr2:213115200-213119000	Weak transcription	Brain Angular Gyrus	brain
5	chr2:213115400-213121800	Weak transcription	Brain Substantia Nigra	brain
6	chr2:213115400-213134000	Weak transcription	Brain Cingulate Gyrus	brain
7	chr2:213116200-213117400	Enhancers	Fetal Kidney	kidney
8	chr2:213116600-213117400	Enhancers	Fetal Heart	heart
9	chr2:213117400-213117600	Weak transcription	Fetal Kidney	kidney
10	chr2:213117600-213118800	Enhancers	Fetal Kidney	kidney
11	chr2:213119000-213119400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:213119000-213119400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr2:213119000-213119400	Enhancers	Brain Angular Gyrus	brain
14	chr2:213119400-213122400	Weak transcription	Brain Angular Gyrus	brain
15	chr2:213121800-213122800	Enhancers	Brain Substantia Nigra	brain
16	chr2:213122400-213122600	Enhancers	Brain Angular Gyrus	brain
17	chr2:213122400-213122800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr2:213122800-213131200	Weak transcription	Brain Substantia Nigra	brain
19	chr2:213127400-213127600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr2:213127600-213128000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr2:213128000-213130800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr2:213128600-213128800	Enhancers	Brain Anterior Caudate	brain
23	chr2:213128600-213129400	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr2:213128800-213129200	Flanking Active TSS	Brain Anterior Caudate	brain
25	chr2:213128800-213129200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr2:213128800-213129800	Enhancers	Skeletal Muscle Male	skeletal muscle
27	chr2:213128800-213130800	Enhancers	Brain Germinal Matrix	brain
28	chr2:213129000-213129200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr2:213129000-213129800	Enhancers	Psoas Muscle	Psoas
30	chr2:213129200-213141000	Weak transcription	Brain Anterior Caudate	brain
31	chr2:213129400-213130800	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr2:213129400-213131000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr2:213129600-213130000	Weak transcription	Brain Angular Gyrus	brain
34	chr2:213129600-213133000	Enhancers	Fetal Heart	heart
35	chr2:213129800-213135400	Weak transcription	Psoas Muscle	Psoas
36	chr2:213130400-213130800	Active TSS	Brain Hippocampus Middle	brain
37	chr2:213130800-213131600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr2:213131000-213131200	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr2:213131000-213131200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr2:213131000-213131600	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr2:213131200-213132000	Enhancers	Brain Substantia Nigra	brain
42	chr2:213131200-213133400	Weak transcription	Brain Angular Gyrus	brain
43	chr2:213131600-213133600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr2:213132000-213134000	Weak transcription	Brain Substantia Nigra	brain
45	chr2:213133000-213135400	Weak transcription	Fetal Heart	heart
46	chr2:213133400-213134200	Enhancers	Brain Angular Gyrus	brain
47	chr2:213133600-213133800	Enhancers	Brain Hippocampus Middle	brain
48	chr2:213133600-213134400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:213133600-213134600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr2:213134000-213134200	Enhancers	Aorta	Aorta

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