Variant report

Variant	esv2757142
Chromosome Location	chr5:146429843-146539500
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	chr5:146520206-146520486	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:146477848-146478079	HepG2	liver:	n/a	n/a
3	BACH1	chr5:146435481-146435711	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr5:146451905-146452198	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr5:146510404-146510527	H1-hESC	embryonic stem cell:	n/a	chr5:146510426-146510437
6	CEBPB	chr5:146510268-146510550	A549	lung:	n/a	chr5:146510426-146510437
7	CEBPB	chr5:146472717-146473114	HepG2	liver:	n/a	chr5:146473010-146473018 chr5:146472899-146472910
8	CEBPB	chr5:146513915-146513976	HepG2	liver:	n/a	n/a
9	CEBPB	chr5:146520139-146520338	HepG2	liver:	n/a	n/a
10	CEBPB	chr5:146510331-146510513	Hela-S3	cervix:	n/a	chr5:146510426-146510437
11	CEBPB	chr5:146510315-146510506	HepG2	liver:	n/a	chr5:146510426-146510437
12	CEBPB	chr5:146524877-146525014	HepG2	liver:	n/a	chr5:146524982-146524995
13	CEBPB	chr5:146472652-146473133	A549	lung:	n/a	chr5:146473010-146473018 chr5:146472899-146472910
14	CEBPB	chr5:146472763-146473074	MCF-7	breast:	n/a	chr5:146473010-146473018 chr5:146472899-146472910
15	CEBPB	chr5:146472752-146473025	ECC-1	luminal epithelium:	n/a	chr5:146473010-146473018 chr5:146472899-146472910
16	CEBPB	chr5:146510291-146510568	IMR90	lung:	n/a	chr5:146510426-146510437
17	CEBPB	chr5:146472736-146473063	MCF-7	breast:	n/a	chr5:146473010-146473018 chr5:146472899-146472910
18	CEBPB	chr5:146472733-146473099	Hela-S3	cervix:	n/a	chr5:146473010-146473018 chr5:146472899-146472910
19	CEBPB	chr5:146441724-146441958	HepG2	liver:	n/a	chr5:146441852-146441863
20	CEBPB	chr5:146472695-146472966	A549	lung:	n/a	chr5:146472899-146472910
21	CEBPB	chr5:146435983-146436296	IMR90	lung:	n/a	chr5:146436039-146436050 chr5:146436190-146436201
22	CEBPB	chr5:146472721-146473094	IMR90	lung:	n/a	chr5:146473010-146473018 chr5:146472899-146472910
23	CEBPB	chr5:146510243-146510610	HepG2	liver:	n/a	chr5:146510426-146510437
24	CEBPB	chr5:146472717-146473102	H1-hESC	embryonic stem cell:	n/a	chr5:146473010-146473018 chr5:146472899-146472910
25	CEBPB	chr5:146457335-146457561	HepG2	liver:	n/a	chr5:146457417-146457428 chr5:146457336-146457348
26	CEBPB	chr5:146472730-146473090	A549	lung:	n/a	chr5:146473010-146473018 chr5:146472899-146472910
27	CEBPB	chr5:146435943-146436224	H1-hESC	embryonic stem cell:	n/a	chr5:146436039-146436050 chr5:146436190-146436201
28	CEBPB	chr5:146472761-146473058	K562	blood:	n/a	chr5:146473010-146473018 chr5:146472899-146472910
29	CEBPB	chr5:146435908-146436307	HepG2	liver:	n/a	chr5:146436039-146436050 chr5:146436190-146436201
30	CREB1	chr5:146520102-146520447	HepG2	liver:	n/a	n/a
31	CTCF	chr5:146477814-146477995	MCF-7	breast:	n/a	n/a
32	CTCF	chr5:146477820-146477970	GM12864	blood:	n/a	n/a
33	CTCF	chr5:146477820-146477970	GM12875	blood:	n/a	n/a
34	CTCF	chr5:146478160-146478310	GM12864	blood:	n/a	chr5:146478249-146478265
35	CTCF	chr5:146477840-146477990	NB4	blood:	n/a	n/a
36	CTCF	chr5:146477780-146477930	GM12872	blood:	n/a	n/a
37	CTCF	chr5:146477777-146477961	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr5:146477667-146478096	IMR90	lung:	n/a	n/a
39	CTCF	chr5:146477800-146477950	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr5:146477500-146477650	HRE	kidney:	n/a	n/a
41	CTCF	chr5:146477880-146478030	GM12869	blood:	n/a	n/a
42	CTCF	chr5:146477838-146478039	GM13976	blood:	n/a	n/a
43	CTCF	chr5:146477830-146477951	GM19239	blood:	n/a	n/a
44	CTCF	chr5:146478040-146478190	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr5:146477880-146478030	GM12875	blood:	n/a	n/a
46	CTCF	chr5:146477754-146478039	GM12878	blood:	n/a	n/a
47	CTCF	chr5:146461040-146461190	GM12869	blood:	n/a	n/a
48	CTCF	chr5:146501438-146501504	GM10248	blood:	n/a	n/a
49	CTCF	chr5:146478180-146478330	GM12872	blood:	n/a	chr5:146478249-146478265
50	CTCF	chr5:146477800-146477950	GM06990	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:146453021-146453071	Caco-2	colon:	n/a
2	chr5:146453021-146453071	Caco-2	colon:	n/a
3	chr5:146435656-146435706	HMEC	breast:	n/a
4	chr5:146436805-146436855	AoSMC	blood vessel:	n/a
5	chr5:146472905-146472955	HL-60	blood:	n/a
6	chr5:146461855-146461905	MCF10A-Er-Src	breast:	n/a
7	chr5:146435656-146435706	HL-60	blood:	n/a
8	chr5:146436093-146436143	RPTEC	kidney:	n/a
9	chr5:146435967-146436017	H1-hESC	embryonic stem cell:	embryo
10	chr5:146461045-146461095	AG04450	lung:	fetal
11	chr5:146435967-146436017	GM12892	blood:	n/a
12	chr5:146453021-146453071	HEK293	kidney:	embryo
13	chr5:146453021-146453071	HAEpiC	amniotic membrane:	n/a
14	chr5:146435967-146436017	BJ	skin:	n/a
15	chr5:146435967-146436017	HepG2	liver:	n/a
16	chr5:146436805-146436855	T-47D	breast:	n/a
17	chr5:146435656-146435706	HPAEpiC	pulmonary alveolar:	n/a
18	chr5:146461785-146461835	AG04449	skin:	fetal
19	chr5:146435656-146435706	HNPCEpiC	eye:	n/a
20	chr5:146436093-146436143	PrEC	prostate:	n/a
21	chr5:146436805-146436855	NHBE	bronchial:	n/a
22	chr5:146436093-146436143	PFSK-1	brain:	n/a
23	chr5:146435656-146435706	GM12878	blood:	n/a
24	chr5:146435967-146436017	HPAEpiC	pulmonary alveolar:	n/a
25	chr5:146461811-146461861	BE2_C	brain:	n/a
26	chr5:146436093-146436143	HMEC	breast:	n/a
27	chr5:146461855-146461905	Hela-S3	cervix:	n/a
28	chr5:146461785-146461835	HL-60	blood:	n/a
29	chr5:146435967-146436017	SK-N-SH	brain:	n/a
30	chr5:146472905-146472955	HRPEpiC	eye:	n/a
31	chr5:146461045-146461095	AG04449	skin:	fetal
32	chr5:146460987-146461037	ovcar-3	ovarian:	n/a
33	chr5:146436093-146436143	A549	lung:	n/a
34	chr5:146461811-146461861	GM12878	blood:	n/a
35	chr5:146461811-146461861	SK-N-SH_RA	brain:	n/a
36	chr5:146461855-146461905	HL-60	blood:	n/a
37	chr5:146436805-146436855	CMK	blood:	n/a
38	chr5:146436093-146436143	SAEC	small airway:	n/a
39	chr5:146453021-146453071	NT2-D1	testis:	n/a
40	chr5:146460987-146461037	AG10803	skin:	n/a
41	chr5:146461785-146461835	HCT-116	colon:	n/a
42	chr5:146435967-146436017	AG04449	skin:	fetal
43	chr5:146436093-146436143	SK-N-SH_RA	brain:	n/a
44	chr5:146435656-146435706	Hepatocyte	liver:	n/a
45	chr5:146460987-146461037	AG09309	skin:	n/a
46	chr5:146436805-146436855	Caco-2	colon:	n/a
47	chr5:146461045-146461095	U87	brain:	n/a
48	chr5:146461045-146461095	BE2_C	brain:	n/a
49	chr5:146472905-146472955	HAEpiC	amniotic membrane:	n/a
50	chr5:146461855-146461905	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:146534524..146536364-chr5:146537043..146540039,2	MCF-7	breast:
2	chr5:146477605..146478292-chr5:146957723..146958313,2	MCF-7	breast:
3	chr5:146438427..146440767-chr5:146443761..146445468,2	K562	blood:
4	chr5:146534524..146536364-chr5:146537043..146540039,2	MCF-7	breast:
5	chr5:146438427..146440767-chr5:146443761..146445468,2	K562	blood:
6	chr5:146454924..146457427-chr5:146463228..146465855,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR151-4	chr5:146460622-146460699	NONHSAT104414
2	lnc-GPR151-4	chr5:146464146-146464347	NONHSAT104414

Variant related genes	Relation type
PPP2R2B	TF binding region
PPP2R2B	CpG island
ENSG00000156475	chromatin interactions

Extended variants
information (count: 3284 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3284 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1031915	chr5:146429843-146429844	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556969617	chr5:146429885-146429886	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576930676	chr5:146429902-146429903	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs539304235	chr5:146429942-146429943	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528285599	chr5:146429950-146429951	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559015950	chr5:146429958-146429959	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572600455	chr5:146429984-146429985	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541307117	chr5:146430040-146430041	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145573029	chr5:146430047-146430048	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574547697	chr5:146430077-146430078	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572278916	chr5:146430118-146430119	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs190379288	chr5:146430123-146430124	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532502790	chr5:146430126-146430127	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs373112657	chr5:146430143-146430144	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146484140	chr5:146430147-146430148	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs193283356	chr5:146430151-146430152	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559435438	chr5:146430195-146430196	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs185110527	chr5:146430210-146430211	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs4705125	chr5:146430224-146430225	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs10631399	chr5:146430234-146430235	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34991825	chr5:146430235-146430236	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs34893993	chr5:146430236-146430237	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs397810071	chr5:146430252-146430253	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs373348657	chr5:146430253-146430254	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537109972	chr5:146430281-146430282	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs77111274	chr5:146430311-146430312	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112134373	chr5:146430388-146430389	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550731564	chr5:146430391-146430392	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561450601	chr5:146430425-146430426	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144649302	chr5:146430429-146430430	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539108722	chr5:146430452-146430453	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148228646	chr5:146430453-146430454	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376726440	chr5:146430489-146430490	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs116139214	chr5:146430599-146430600	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572614063	chr5:146430683-146430684	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189003648	chr5:146430691-146430692	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs554717436	chr5:146430752-146430753	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181094048	chr5:146430765-146430766	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543493521	chr5:146430794-146430795	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs141211761	chr5:146430873-146430874	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs150289334	chr5:146430874-146430875	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541342535	chr5:146430881-146430882	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs368563037	chr5:146430884-146430885	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545917189	chr5:146430889-146430890	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs559706353	chr5:146430934-146430935	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528326108	chr5:146430949-146430950	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548524203	chr5:146430990-146430991	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs185485285	chr5:146430994-146430995	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530755034	chr5:146431019-146431020	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs188702395	chr5:146431062-146431063	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	16864856	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	20864512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:146426000-146434400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr5:146426400-146434200	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr5:146426400-146435600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:146428400-146430000	Enhancers	Brain Substantia Nigra	brain
5	chr5:146428600-146430000	Enhancers	Brain Cingulate Gyrus	brain
6	chr5:146428800-146430400	Enhancers	Brain Angular Gyrus	brain
7	chr5:146429000-146430000	Genic enhancers	Brain Inferior Temporal Lobe	brain
8	chr5:146429000-146430200	Enhancers	Brain Hippocampus Middle	brain
9	chr5:146429000-146430200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
10	chr5:146429000-146431200	Enhancers	Brain Anterior Caudate	brain
11	chr5:146429400-146430200	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr5:146430000-146430600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr5:146430000-146431800	Weak transcription	Brain Cingulate Gyrus	brain
14	chr5:146430000-146431800	Weak transcription	Brain Substantia Nigra	brain
15	chr5:146430200-146430600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr5:146430200-146430800	Weak transcription	Brain Hippocampus Middle	brain
17	chr5:146430200-146432800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:146430400-146432000	Weak transcription	Brain Angular Gyrus	brain
19	chr5:146430600-146430800	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr5:146430600-146433200	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr5:146430800-146431000	Genic enhancers	Brain Hippocampus Middle	brain
22	chr5:146430800-146431600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr5:146431000-146432000	Weak transcription	Brain Hippocampus Middle	brain
24	chr5:146431200-146433200	Weak transcription	Brain Anterior Caudate	brain
25	chr5:146431600-146433400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr5:146431800-146432200	Enhancers	Brain Cingulate Gyrus	brain
27	chr5:146431800-146434600	Enhancers	Brain Substantia Nigra	brain
28	chr5:146432000-146433000	Enhancers	Brain Angular Gyrus	brain
29	chr5:146432000-146433800	Enhancers	Brain Hippocampus Middle	brain
30	chr5:146432200-146432800	Weak transcription	Brain Cingulate Gyrus	brain
31	chr5:146432800-146433200	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:146432800-146433200	Enhancers	Brain Cingulate Gyrus	brain
33	chr5:146433000-146433400	Active TSS	Brain Angular Gyrus	brain
34	chr5:146433200-146433400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
35	chr5:146433200-146433600	Flanking Active TSS	Brain Cingulate Gyrus	brain
36	chr5:146433200-146434400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr5:146433200-146434400	Enhancers	Brain Anterior Caudate	brain
38	chr5:146433400-146433600	Flanking Active TSS	Brain Angular Gyrus	brain
39	chr5:146433400-146434000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr5:146433400-146434200	Active TSS	Brain Inferior Temporal Lobe	brain
41	chr5:146433600-146434000	Enhancers	Brain Angular Gyrus	brain
42	chr5:146433600-146434200	Enhancers	Brain Cingulate Gyrus	brain
43	chr5:146433800-146434200	Active TSS	Brain Hippocampus Middle	brain
44	chr5:146434000-146434200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr5:146434000-146434200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr5:146434000-146434800	Flanking Active TSS	Brain Angular Gyrus	brain
47	chr5:146434200-146434600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
48	chr5:146434200-146434600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
49	chr5:146434200-146434800	Flanking Active TSS	Brain Cingulate Gyrus	brain
50	chr5:146434200-146435200	Enhancers	Fetal Brain Female	brain

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