Variant report

Variant	nsv882760
Chromosome Location	chr5:117087858-117292268
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	chr5:117188782-117188783	K562	blood:	n/a	n/a
2	BRCA1	chr5:117192690-117192791	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr5:117225271-117225273	GM12878	blood:	n/a	n/a
4	CCNT2	chr5:117264356-117264536	K562	blood:	n/a	n/a
5	CCNT2	chr5:117173830-117173997	K562	blood:	n/a	n/a
6	CEBPB	chr5:117168511-117168821	IMR90	lung:	n/a	chr5:117168641-117168652
7	CEBPB	chr5:117139138-117139638	IMR90	lung:	n/a	n/a
8	CEBPB	chr5:117225285-117225673	IMR90	lung:	n/a	n/a
9	CEBPB	chr5:117228871-117229261	IMR90	lung:	n/a	n/a
10	CEBPB	chr5:117291421-117291633	HepG2	liver:	n/a	n/a
11	CEBPB	chr5:117172356-117172719	HepG2	liver:	n/a	chr5:117172536-117172547
12	CEBPB	chr5:117122720-117122726	K562	blood:	n/a	n/a
13	CEBPB	chr5:117172423-117172650	H1-hESC	embryonic stem cell:	n/a	chr5:117172536-117172547
14	CEBPB	chr5:117172935-117173233	HepG2	liver:	n/a	chr5:117173066-117173079 chr5:117173067-117173078
15	CEBPB	chr5:117278900-117279161	HepG2	liver:	n/a	chr5:117279029-117279040
16	CEBPB	chr5:117172354-117172704	A549	lung:	n/a	chr5:117172536-117172547
17	CEBPB	chr5:117265625-117265899	HepG2	liver:	n/a	chr5:117265754-117265765
18	CEBPB	chr5:117265654-117265907	IMR90	lung:	n/a	chr5:117265754-117265765
19	CEBPB	chr5:117168507-117168774	A549	lung:	n/a	chr5:117168641-117168652
20	CEBPB	chr5:117172347-117172719	IMR90	lung:	n/a	chr5:117172536-117172547
21	CEBPB	chr5:117291423-117291720	IMR90	lung:	n/a	n/a
22	CEBPB	chr5:117168502-117168804	HepG2	liver:	n/a	chr5:117168641-117168652
23	CEBPB	chr5:117238164-117238250	A549	lung:	n/a	n/a
24	CTCF	chr5:117124432-117124541	Medullo	brain:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
25	CTCF	chr5:117124400-117124550	HRPEpiC	eye:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
26	CTCF	chr5:117124380-117124530	BJ	skin:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
27	CTCF	chr5:117123767-117123833	GM13976	blood:	n/a	n/a
28	CTCF	chr5:117165720-117165870	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr5:117267736-117267849	GM20000	blood:	n/a	n/a
30	CTCF	chr5:117124300-117124450	NHDF-neo	bronchial:	n/a	n/a
31	CTCF	chr5:117158477-117158527	GM10248	blood:	n/a	n/a
32	CTCF	chr5:117105540-117105630	GM13976	blood:	n/a	n/a
33	CTCF	chr5:117124340-117124490	NB4	blood:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
34	CTCF	chr5:117124440-117124590	BJ	skin:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
35	CTCF	chr5:117124380-117124530	WERI-Rb-1	eye:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
36	CTCF	chr5:117124400-117124550	Caco-2	colon:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
37	CTCF	chr5:117124300-117124450	MCF-7	breast:	n/a	n/a
38	CTCF	chr5:117124478-117124500	GM12878	blood:	n/a	n/a
39	CTCF	chr5:117124217-117124730	MCF-7	breast:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
40	CTCF	chr5:117109043-117109065	MCF-7	breast:	n/a	n/a
41	CTCF	chr5:117124439-117124487	ProgFib	skin:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
42	CTCF	chr5:117124360-117124510	HPAF	blood vessel:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
43	CTCF	chr5:117103172-117103228	K562	blood:	n/a	n/a
44	CTCF	chr5:117124300-117124450	RPTEC	kidney:	n/a	n/a
45	CTCF	chr5:117124340-117124490	AG09319	gingival:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
46	CTCF	chr5:117124393-117124550	MCF-7	breast:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
47	CTCF	chr5:117124326-117124647	IMR90	lung:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
48	CTCF	chr5:117124460-117124610	AG09309	skin:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
49	CTCF	chr5:117124360-117124510	NHEK	skin:	n/a	chr5:117124461-117124482 chr5:117124466-117124484
50	CTCF	chr5:117124420-117124570	AG04449	skin:	n/a	chr5:117124461-117124482 chr5:117124466-117124484

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:117098484-117098534	NB4	blood:	n/a
2	chr5:117098484-117098534	Hepatocyte	liver:	n/a
3	chr5:117098484-117098534	SAEC	small airway:	n/a
4	chr5:117098484-117098534	SK-N-SH	brain:	n/a
5	chr5:117098484-117098534	HIPEpiC	eye:	n/a
6	chr5:117098484-117098534	IMR90	lung:	fetal
7	chr5:117098484-117098534	NHDF-neo	bronchial:	n/a
8	chr5:117098484-117098534	GM12878	blood:	n/a
9	chr5:117098484-117098534	H1-hESC	embryonic stem cell:	embryo
10	chr5:117098484-117098534	K562	blood:	n/a
11	chr5:117098484-117098534	HUVEC	blood vessel:	n/a
12	chr5:117098484-117098534	HCT-116	colon:	n/a
13	chr5:117098484-117098534	PFSK-1	brain:	n/a
14	chr5:117098484-117098534	AG04450	lung:	fetal
15	chr5:117098484-117098534	PANC-1	pancreas:	n/a
16	chr5:117098484-117098534	CMK	blood:	n/a
17	chr5:117098484-117098534	BJ	skin:	n/a
18	chr5:117098484-117098534	T-47D	breast:	n/a
19	chr5:117098484-117098534	HAEpiC	amniotic membrane:	n/a
20	chr5:117098484-117098534	RPTEC	kidney:	n/a
21	chr5:117098484-117098534	HPAEpiC	pulmonary alveolar:	n/a
22	chr5:117098484-117098534	LNCaP	prostate:	n/a
23	chr5:117098484-117098534	BE2_C	brain:	n/a
24	chr5:117098484-117098534	AG09319	gingival:	n/a
25	chr5:117098484-117098534	PrEC	prostate:	n/a
26	chr5:117098484-117098534	GM19239	blood:	n/a
27	chr5:117098484-117098534	SKMC	muscle:	n/a
28	chr5:117098484-117098534	HRE	kidney:	n/a
29	chr5:117098484-117098534	GM06990	blood:	n/a
30	chr5:117098484-117098534	NT2-D1	testis:	n/a
31	chr5:117098484-117098534	ovcar-3	ovarian:	n/a
32	chr5:117098484-117098534	HNPCEpiC	eye:	n/a
33	chr5:117098484-117098534	AG04449	skin:	fetal
34	chr5:117098484-117098534	AG09309	skin:	n/a
35	chr5:117098484-117098534	HepG2	liver:	n/a
36	chr5:117098484-117098534	HCM	heart:	n/a
37	chr5:117098484-117098534	SK-N-SH_RA	brain:	n/a
38	chr5:117098484-117098534	NH-A	brain:	n/a
39	chr5:117098484-117098534	HMEC	breast:	n/a
40	chr5:117098484-117098534	Jurkat	blood:	n/a
41	chr5:117098484-117098534	HRCEpiC	kidney:	n/a
42	chr5:117098484-117098534	HEEpiC	esophagus:	n/a
43	chr5:117098484-117098534	SK-N-MC	brain:	n/a
44	chr5:117098484-117098534	HRPEpiC	eye:	n/a
45	chr5:117098484-117098534	NHBE	bronchial:	n/a
46	chr5:117098484-117098534	AG10803	skin:	n/a
47	chr5:117098484-117098534	A549	lung:	n/a
48	chr5:117098484-117098534	AoSMC	blood vessel:	n/a
49	chr5:117098484-117098534	HL-60	blood:	n/a
50	chr5:117098484-117098534	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:117089885..117092759-chr5:117093000..117095939,2	MCF-7	breast:
2	chr5:117268408..117270558-chr5:117281285..117282851,2	MCF-7	breast:
3	chr5:117112749..117115394-chr5:117119190..117122198,3	K562	blood:
4	chr5:117290251..117292922-chr5:117295708..117298452,2	K562	blood:
5	chr5:117281554..117282055-chr5:117345500..117346273,2	MCF-7	breast:
6	chr5:117201656..117203414-chr5:117208664..117210271,2	MCF-7	breast:
7	chr5:117089885..117092759-chr5:117093000..117095939,2	MCF-7	breast:
8	chr5:117125890..117127438-chr5:117130783..117133189,2	MCF-7	breast:
9	chr5:117201656..117203414-chr5:117208664..117210271,2	MCF-7	breast:
10	chr5:117149206..117151782-chr5:117152643..117155518,2	MCF-7	breast:
11	chr5:117268408..117270558-chr5:117281285..117282851,2	MCF-7	breast:
12	chr5:117125890..117127438-chr5:117130783..117133189,2	MCF-7	breast:
13	chr5:117149206..117151782-chr5:117152643..117155518,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMXL1-4	chr5:117260703-117260826	XLOC_004524
2	lnc-DMXL1-4	chr5:117260715-117260826	XLOC_004524
3	lnc-DTWD2-12	chr5:117114521-117115227	NONHSAT103390
4	lnc-DMXL1-4	chr5:117260705-117260826	NR_104997

Variant related genes	Relation type
RPL7L1P4	TF binding region
ENSG00000249797	TF binding region
RPL7L1P4	CpG island
ENSG00000249797	CpG island
ENSG00000249582	chromatin interactions

Extended variants
information (count: 2770 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:2770 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554748736	chr5:117095004-117095005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370590379	chr5:117095005-117095006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147013195	chr5:117095044-117095045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537150331	chr5:117095054-117095055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73270993	chr5:117095077-117095078	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs576926865	chr5:117095093-117095094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545799446	chr5:117095170-117095171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560115768	chr5:117095197-117095198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113825969	chr5:117095285-117095286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542097872	chr5:117095320-117095321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547530535	chr5:117095323-117095324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs12188743	chr5:117095332-117095333	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs372735306	chr5:117095339-117095340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551077186	chr5:117095389-117095390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564208256	chr5:117095391-117095392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568176518	chr5:117095449-117095450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533190992	chr5:117095478-117095479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114313974	chr5:117095484-117095485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35843265	chr5:117095495-117095496	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs534911561	chr5:117095506-117095507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs78386818	chr5:117095659-117095660	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs187154483	chr5:117095687-117095688	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs568264775	chr5:117095694-117095695	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs115512946	chr5:117095699-117095700	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs79544656	chr5:117095728-117095729	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs576990768	chr5:117095739-117095740	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs192651207	chr5:117095745-117095746	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs200984625	chr5:117095770-117095771	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs372226193	chr5:117095772-117095773	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs552995350	chr5:117095773-117095774	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs61259806	chr5:117095776-117095777	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs542513026	chr5:117095777-117095778	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs555757689	chr5:117095814-117095815	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs184446836	chr5:117095824-117095825	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs551648548	chr5:117095886-117095887	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs369066750	chr5:117095898-117095899	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs188929000	chr5:117095902-117095903	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs540273977	chr5:117095906-117095907	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs560115158	chr5:117095907-117095908	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs529240844	chr5:117095908-117095909	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs548477457	chr5:117095910-117095911	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs4304103	chr5:117095928-117095929	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs193097622	chr5:117095962-117095963	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs550791096	chr5:117095968-117095969	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs74487913	chr5:117096038-117096039	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs556416556	chr5:117096064-117096065	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs539548476	chr5:117096108-117096109	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs577634750	chr5:117096135-117096136	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs544965520	chr5:117096176-117096177	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs571490967	chr5:117096232-117096233	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	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
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	21509527	CNVD
Autism	22543975	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:236 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:117095000-117095600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr5:117095000-117099000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr5:117095600-117095800	Enhancers	Small Intestine	intestine
4	chr5:117095600-117096200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr5:117095600-117098800	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr5:117096200-117098800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr5:117097000-117097600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr5:117097600-117097800	Enhancers	Brain Hippocampus Middle	brain
9	chr5:117097600-117098000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr5:117097600-117098000	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr5:117097800-117098400	Weak transcription	Brain Hippocampus Middle	brain
12	chr5:117098000-117098400	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr5:117098000-117098800	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr5:117098400-117098600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr5:117098400-117099200	Enhancers	Brain Hippocampus Middle	brain
16	chr5:117098600-117099600	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr5:117098800-117105000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr5:117099600-117100000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr5:117103000-117105600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr5:117105600-117105800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr5:117105800-117114800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr5:117113800-117114200	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
23	chr5:117122400-117123000	Enhancers	Fetal Lung	lung
24	chr5:117127800-117128200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr5:117127800-117128200	Enhancers	Fetal Intestine Small	intestine
26	chr5:117128200-117129400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr5:117129200-117130000	Active TSS	Ovary	ovary
28	chr5:117129400-117129600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr5:117129400-117129600	Active TSS	Brain Angular Gyrus	brain
30	chr5:117129400-117129600	Enhancers	Brain Hippocampus Middle	brain
31	chr5:117129400-117129600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
32	chr5:117129400-117129800	Enhancers	Fetal Brain Female	brain
33	chr5:117129400-117130000	Active TSS	Brain Cingulate Gyrus	brain
34	chr5:117129400-117130200	Active TSS	Brain Anterior Caudate	brain
35	chr5:117129400-117130200	Active TSS	Brain Inferior Temporal Lobe	brain
36	chr5:117129400-117130400	Enhancers	Brain Germinal Matrix	brain
37	chr5:117129400-117130400	Enhancers	Brain Substantia Nigra	brain
38	chr5:117129600-117129800	Flanking Active TSS	Brain Angular Gyrus	brain
39	chr5:117129600-117130000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr5:117129600-117130000	Active TSS	Right Atrium	heart
41	chr5:117129600-117130200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr5:117129600-117130200	Flanking Active TSS	Brain Hippocampus Middle	brain
43	chr5:117129800-117130000	Active TSS	Brain Angular Gyrus	brain
44	chr5:117130000-117130400	Enhancers	Brain Angular Gyrus	brain
45	chr5:117130200-117130400	Enhancers	Brain Hippocampus Middle	brain
46	chr5:117130200-117131200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr5:117131200-117136000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr5:117132600-117133000	Enhancers	Fetal Intestine Large	intestine
49	chr5:117136000-117136400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr5:117136000-117136400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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