Variant report

Variant	nsv537880
Chromosome Location	chr5:117900051-118027895
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	BATF	chr5:117966281-117966527	GM12878	blood:	n/a	chr5:117966409-117966419 chr5:117966408-117966419
2	BCL3	chr5:118025299-118025601	GM12878	blood:	n/a	n/a
3	BHLHE40	chr5:117934828-117934953	GM12878	blood:	n/a	n/a
4	BRCA1	chr5:117968451-117968509	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr5:117980648-117980924	HepG2	liver:	n/a	n/a
6	CEBPB	chr5:118016169-118016299	IMR90	lung:	n/a	n/a
7	CEBPB	chr5:118016144-118016302	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr5:118001014-118001180	K562	blood:	n/a	n/a
9	CEBPB	chr5:117980695-117980854	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr5:117980712-117980912	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr5:117980631-117980944	IMR90	lung:	n/a	n/a
12	CEBPB	chr5:117932289-117932583	A549	lung:	n/a	n/a
13	CEBPB	chr5:117932234-117932584	HepG2	liver:	n/a	n/a
14	CEBPB	chr5:117980697-117980954	MCF-7	breast:	n/a	n/a
15	CEBPB	chr5:117966977-117967267	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr5:117947180-117947330	HCT-116	colon:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
17	CTCF	chr5:117947158-117947327	GM20000	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
18	CTCF	chr5:117947160-117947310	SAEC	small airway:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
19	CTCF	chr5:117947034-117947399	HepG2	liver:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
20	CTCF	chr5:117947146-117947328	GM10266	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
21	CTCF	chr5:117947180-117947330	WERI-Rb-1	eye:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
22	CTCF	chr5:117942819-117942875	MCF-7	breast:	n/a	n/a
23	CTCF	chr5:117947360-117947510	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr5:117928760-117928910	GM12878	blood:	n/a	chr5:117928819-117928828
25	CTCF	chr5:117947180-117947330	HRPEpiC	eye:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
26	CTCF	chr5:117947160-117947310	GM12867	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
27	CTCF	chr5:117947128-117947363	HUVEC	blood vessel:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
28	CTCF	chr5:117947180-117947330	HEK293	kidney:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
29	CTCF	chr5:117928760-117928910	GM12867	blood:	n/a	chr5:117928819-117928828
30	CTCF	chr5:117947034-117947445	GM12878	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
31	CTCF	chr5:117928760-117928910	HPAF	blood vessel:	n/a	chr5:117928819-117928828
32	CTCF	chr5:117964680-117964830	MCF-7	breast:	n/a	n/a
33	CTCF	chr5:117928770-117928862	GM10266	blood:	n/a	chr5:117928819-117928828
34	CTCF	chr5:117928740-117928890	HRPEpiC	eye:	n/a	chr5:117928819-117928828
35	CTCF	chr5:117928760-117928910	AG09319	gingival:	n/a	chr5:117928819-117928828
36	CTCF	chr5:117928780-117928930	AG09309	skin:	n/a	chr5:117928819-117928828
37	CTCF	chr5:117947148-117947345	Kidney_OC	kidney:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
38	CTCF	chr5:117947040-117947190	WI-38	lung:	n/a	n/a
39	CTCF	chr5:117928760-117928910	BE2_C	brain:	n/a	chr5:117928819-117928828
40	CTCF	chr5:117947160-117947310	RPTEC	kidney:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
41	CTCF	chr5:117928760-117929010	HA-sp	spinal cord:	n/a	chr5:117928819-117928828
42	CTCF	chr5:117928780-117928930	K562	blood:	n/a	chr5:117928819-117928828
43	CTCF	chr5:117928740-117928890	HBMEC	blood vessel:	n/a	chr5:117928819-117928828
44	CTCF	chr5:117928720-117928870	Caco-2	colon:	n/a	chr5:117928819-117928828
45	CTCF	chr5:117928820-117928970	HAc	cerebellar:	n/a	n/a
46	CTCF	chr5:117947160-117947310	HCT-116	colon:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
47	CTCF	chr5:117947160-117947310	HUVEC	blood vessel:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
48	CTCF	chr5:117947140-117947290	GM12875	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
49	CTCF	chr5:117947180-117947330	GM12871	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
50	CTCF	chr5:117928747-117928890	Medullo	brain:	n/a	chr5:117928819-117928828

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:117964718-117964768	Jurkat	blood:	n/a
2	chr5:117964718-117964768	HCM	heart:	n/a
3	chr5:117964718-117964768	HCT-116	colon:	n/a
4	chr5:117964718-117964768	GM12878	blood:	n/a
5	chr5:117964718-117964768	A549	lung:	n/a
6	chr5:117964718-117964768	NB4	blood:	n/a
7	chr5:117964718-117964768	Hepatocyte	liver:	n/a
8	chr5:117964718-117964768	NHDF-neo	bronchial:	n/a
9	chr5:117964718-117964768	HL-60	blood:	n/a
10	chr5:117964718-117964768	SKMC	muscle:	n/a
11	chr5:117964718-117964768	SK-N-SH_RA	brain:	n/a
12	chr5:117964718-117964768	HEK293	kidney:	embryo
13	chr5:117964718-117964768	AG10803	skin:	n/a
14	chr5:117964718-117964768	K562	blood:	n/a
15	chr5:117964718-117964768	AG04450	lung:	fetal
16	chr5:117964718-117964768	AG04449	skin:	fetal
17	chr5:117964718-117964768	BJ	skin:	n/a
18	chr5:117964718-117964768	LNCaP	prostate:	n/a
19	chr5:117964718-117964768	BE2_C	brain:	n/a
20	chr5:117964718-117964768	Hela-S3	cervix:	n/a
21	chr5:117964718-117964768	NH-A	brain:	n/a
22	chr5:117964718-117964768	Caco-2	colon:	n/a
23	chr5:117964718-117964768	MCF-7	breast:	n/a
24	chr5:117964718-117964768	U87	brain:	n/a
25	chr5:117964718-117964768	HIPEpiC	eye:	n/a
26	chr5:117964718-117964768	SK-N-SH	brain:	n/a
27	chr5:117964718-117964768	PANC-1	pancreas:	n/a
28	chr5:117964718-117964768	HNPCEpiC	eye:	n/a
29	chr5:117964718-117964768	GM19239	blood:	n/a
30	chr5:117964718-117964768	CMK	blood:	n/a
31	chr5:117964718-117964768	SAEC	small airway:	n/a
32	chr5:117964718-117964768	T-47D	breast:	n/a
33	chr5:117964718-117964768	SK-N-MC	brain:	n/a
34	chr5:117964718-117964768	HMEC	breast:	n/a
35	chr5:117964718-117964768	H1-hESC	embryonic stem cell:	embryo
36	chr5:117964718-117964768	ECC-1	luminal epithelium:	n/a
37	chr5:117964718-117964768	AG09319	gingival:	n/a
38	chr5:117964718-117964768	HRPEpiC	eye:	n/a
39	chr5:117964718-117964768	HepG2	liver:	n/a
40	chr5:117964718-117964768	HPAEpiC	pulmonary alveolar:	n/a
41	chr5:117964718-117964768	PFSK-1	brain:	n/a
42	chr5:117964718-117964768	MCF10A-Er-Src	breast:	n/a
43	chr5:117964718-117964768	HCF	heart:	n/a
44	chr5:117964718-117964768	HRE	kidney:	n/a
45	chr5:117964718-117964768	PrEC	prostate:	n/a
46	chr5:117964718-117964768	HRCEpiC	kidney:	n/a
47	chr5:117964718-117964768	ProgFib	skin:	n/a
48	chr5:117964718-117964768	HUVEC	blood vessel:	n/a
49	chr5:117964718-117964768	IMR90	lung:	fetal
50	chr5:117964718-117964768	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:117989069..117990852-chr5:117992183..117994675,2	K562	blood:
2	chr5:117989069..117990852-chr5:117992183..117994675,2	K562	blood:
3	chr5:117923008..117924830-chr5:117927973..117929496,2	MCF-7	breast:
4	chr5:117892457..117896152-chr5:117898946..117902524,3	MCF-7	breast:
5	chr5:117893334..117895634-chr5:117899247..117902608,3	K562	blood:
6	chr5:117911515..117913042-chr5:117914826..117917481,2	MCF-7	breast:
7	chr5:117946766..117947670-chr5:118127610..118128249,2	MCF-7	breast:
8	chr5:117930634..117932935-chr5:117933519..117935108,2	MCF-7	breast:
9	chr5:117911515..117913042-chr5:117914826..117917481,2	MCF-7	breast:
10	chr5:117997413..117999188-chr5:118002983..118004523,2	MCF-7	breast:
11	chr3:161088409..161090897-chr5:117945115..117947573,2	MCF-7	breast:
12	chr5:117997413..117999188-chr5:118002983..118004523,2	MCF-7	breast:
13	chr5:117953386..117954146-chr5:118127518..118128022,2	MCF-7	breast:
14	chr5:117923008..117924830-chr5:117927973..117929496,2	MCF-7	breast:
15	chr5:117947053..117948753-chr5:118127871..118130563,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMXL1-2	chr5:117915349-117915489	XLOC_004526
2	lnc-DMXL1-2	chr5:117911270-117911381	XLOC_004526
3	lnc-DTWD2-10	chr5:117925515-117925717	l_3002_chr5:117837955-117925717_heart
4	lnc-DMXL1-2	chr5:117912735-117912889	XLOC_004526
5	lnc-DMXL1-2	chr5:117916227-117916343	XLOC_004526
6	lnc-DMXL1-1	chr5:117947055-117947122	XLOC_004527
7	lnc-DMXL1-1	chr5:117945434-117945572	XLOC_004527
8	lnc-DMXL1-1	chr5:117931883-117931916	XLOC_004527
9	lnc-DMXL1-1	chr5:117963545-117963787	XLOC_004527
10	lnc-DMXL1-1	chr5:117949988-117950046	XLOC_004527
11	lnc-DTWD2-10	chr5:117909342-117909743	l_3002_chr5:117837955-117925717_heart
12	lnc-DMXL1-2	chr5:117916964-117917019	XLOC_004526
13	lnc-DTWD2-10	chr5:117918641-117918733	l_3002_chr5:117837955-117925717_heart

Variant related genes	Relation type
ENSG00000249551	TF binding region
ENSG00000249128	TF binding region
ENSG00000250891	TF binding region
ENSG00000249551	CpG island
ENSG00000249128	CpG island
ENSG00000250891	CpG island
ENSG00000196542	chromatin interactions
ENSG00000249128	chromatin interactions
DIABLO	miRNA target sites
DICER1	miRNA target sites
MARS2	miRNA target sites
MARK2	miRNA target sites
MAT2A	miRNA target sites
MATR3	miRNA target sites
DHX57	miRNA target sites

Extended variants
information (count: 3627 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:3627 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150681947	chr5:117900075-117900076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs6867635	chr5:117900115-117900116	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs78196960	chr5:117900116-117900117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138900427	chr5:117900166-117900167	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs528899794	chr5:117900169-117900170	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs542292748	chr5:117900181-117900182	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs149396110	chr5:117900194-117900195	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs531553576	chr5:117900212-117900213	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs79062475	chr5:117900226-117900227	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs147385748	chr5:117900238-117900239	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs533421392	chr5:117900246-117900247	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs547140257	chr5:117900348-117900349	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs550670406	chr5:117900355-117900356	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs139680188	chr5:117900412-117900413	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs77959314	chr5:117900515-117900516	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs74659045	chr5:117900521-117900522	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs192721688	chr5:117900526-117900527	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs72780306	chr5:117900527-117900528	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs550863020	chr5:117900571-117900572	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs557890189	chr5:117900613-117900614	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs577817970	chr5:117900614-117900615	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs537659341	chr5:117900623-117900624	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs6868251	chr5:117900654-117900655	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs76474764	chr5:117900666-117900667	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs570263062	chr5:117900672-117900673	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs553817112	chr5:117900707-117900708	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs73251234	chr5:117900742-117900743	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs80327831	chr5:117900770-117900771	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs76829259	chr5:117900777-117900778	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs577167218	chr5:117900793-117900794	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs201797357	chr5:117900794-117900795	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs200595578	chr5:117900802-117900803	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs202008715	chr5:117900806-117900807	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs70982438	chr5:117900839-117900840	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs373585505	chr5:117900841-117900842	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs75481452	chr5:117900851-117900852	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs546717735	chr5:117900884-117900885	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs545327360	chr5:117900902-117900903	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs534965888	chr5:117900904-117900905	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs565047673	chr5:117900925-117900926	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs527495733	chr5:117900969-117900970	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs189475852	chr5:117900987-117900988	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs74320559	chr5:117900999-117901000	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs375506610	chr5:117901000-117901001	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs6872719	chr5:117901006-117901007	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs147219599	chr5:117901026-117901027	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs569167083	chr5:117901042-117901043	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs538101433	chr5:117901046-117901047	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs80047665	chr5:117901066-117901067	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs571642972	chr5:117901069-117901070	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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	17122850	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:209 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:117895200-117901200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:117895800-117900600	Weak transcription	Brain Germinal Matrix	brain
3	chr5:117896000-117901000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr5:117897400-117900200	Enhancers	Fetal Heart	heart
5	chr5:117898000-117900600	Weak transcription	Fetal Brain Male	brain
6	chr5:117900600-117900800	Enhancers	Brain Germinal Matrix	brain
7	chr5:117900600-117901000	Enhancers	Fetal Brain Male	brain
8	chr5:117900600-117901600	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr5:117900800-117901200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr5:117900800-117901200	Weak transcription	Brain Germinal Matrix	brain
11	chr5:117901000-117902000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr5:117901200-117902000	Enhancers	Brain Germinal Matrix	brain
13	chr5:117901200-117902200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr5:117901400-117902200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr5:117901400-117902200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr5:117901600-117901800	Weak transcription	HMEC	breast
17	chr5:117901800-117902000	Enhancers	HMEC	breast
18	chr5:117902000-117904400	Weak transcription	HMEC	breast
19	chr5:117902200-117904400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr5:117904400-117904800	ZNF genes & repeats	Aorta	Aorta
21	chr5:117904400-117906400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr5:117904400-117906400	Enhancers	HMEC	breast
23	chr5:117904800-117905600	Weak transcription	Aorta	Aorta
24	chr5:117907200-117907600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr5:117907400-117915800	Weak transcription	Ovary	ovary
26	chr5:117911600-117912200	Enhancers	Aorta	Aorta
27	chr5:117912200-117913400	Weak transcription	Aorta	Aorta
28	chr5:117913200-117914600	Enhancers	Right Atrium	heart
29	chr5:117913200-117914800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr5:117913200-117914800	Enhancers	Fetal Muscle Leg	muscle
31	chr5:117913200-117915600	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr5:117913400-117914600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr5:117913400-117914600	Enhancers	Aorta	Aorta
34	chr5:117913400-117915600	Enhancers	HSMMtube	muscle
35	chr5:117913600-117914800	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr5:117913800-117914400	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr5:117913800-117914600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr5:117914000-117914400	Enhancers	Brain Substantia Nigra	brain
39	chr5:117914000-117914600	Enhancers	Brain Hippocampus Middle	brain
40	chr5:117914000-117914600	Enhancers	Fetal Lung	lung
41	chr5:117914200-117914800	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr5:117914400-117914800	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr5:117914400-117916000	Enhancers	Psoas Muscle	Psoas
44	chr5:117914600-117915800	Weak transcription	Right Atrium	heart
45	chr5:117914600-117916000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr5:117914600-117916000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr5:117914600-117916200	Weak transcription	Fetal Lung	lung
48	chr5:117914800-117915800	Weak transcription	Fetal Muscle Leg	muscle
49	chr5:117915600-117916000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr5:117915600-117916400	Weak transcription	HSMMtube	muscle

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