Variant report

Variant	esv2757134
Chromosome Location	chr5:115578810-115633474
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:342)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:115614176-115614178	K562	blood:	n/a	n/a
2	BATF	chr5:115609200-115609492	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
3	BATF	chr5:115609206-115609493	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
4	CBX3	chr5:115612612-115613059	HCT-116	colon:	n/a	n/a
5	CBX3	chr5:115612653-115612965	K562	blood:	n/a	n/a
6	CBX3	chr5:115612735-115612979	K562	blood:	n/a	n/a
7	CEBPB	chr5:115615956-115616164	HepG2	liver:	n/a	n/a
8	CEBPB	chr5:115601292-115601498	HepG2	liver:	n/a	n/a
9	CEBPB	chr5:115608269-115608767	MCF-7	breast:	n/a	chr5:115608483-115608494
10	CEBPB	chr5:115584135-115584482	HepG2	liver:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
11	CEBPB	chr5:115584254-115584389	K562	blood:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
12	CEBPB	chr5:115608311-115608872	IMR90	lung:	n/a	chr5:115608483-115608494
13	CEBPB	chr5:115608381-115608622	HepG2	liver:	n/a	chr5:115608483-115608494
14	CEBPB	chr5:115632480-115632726	HepG2	liver:	n/a	n/a
15	CEBPB	chr5:115584119-115584488	MCF-7	breast:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
16	CEBPB	chr5:115612611-115612811	A549	lung:	n/a	n/a
17	CEBPB	chr5:115584226-115584373	HepG2	liver:	n/a	chr5:115584298-115584309 chr5:115584300-115584311
18	CEBPB	chr5:115608357-115608659	A549	lung:	n/a	chr5:115608483-115608494
19	CEBPB	chr5:115608227-115608718	MCF-7	breast:	n/a	chr5:115608483-115608494
20	CHD2	chr5:115608466-115608624	GM12878	blood:	n/a	n/a
21	CHD2	chr5:115609186-115609453	GM12878	blood:	n/a	n/a
22	CTCF	chr5:115608420-115608570	GM12873	blood:	n/a	n/a
23	CTCF	chr5:115625080-115625230	MCF-7	breast:	n/a	chr5:115625169-115625182
24	CTCF	chr5:115608360-115608510	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr5:115625072-115625269	MCF-7	breast:	n/a	chr5:115625169-115625182
26	CTCF	chr5:115625080-115625230	HAc	cerebellar:	n/a	chr5:115625169-115625182
27	CTCF	chr5:115608387-115608561	MCF-7	breast:	n/a	n/a
28	CTCF	chr5:115625080-115625230	GM12873	blood:	n/a	chr5:115625169-115625182
29	CTCF	chr5:115625120-115625270	MCF-7	breast:	n/a	chr5:115625169-115625182
30	CTCF	chr5:115608380-115608530	BE2_C	brain:	n/a	n/a
31	CTCF	chr5:115625080-115625230	NHEK	skin:	n/a	chr5:115625169-115625182
32	CTCF	chr5:115608340-115608490	BJ	skin:	n/a	n/a
33	CTCF	chr5:115608320-115608470	HMEC	breast:	n/a	n/a
34	CTCF	chr5:115625060-115625210	SAEC	small airway:	n/a	chr5:115625169-115625182
35	CTCF	chr5:115625120-115625270	GM12864	blood:	n/a	chr5:115625169-115625182
36	CTCF	chr5:115608434-115608519	HepG2	liver:	n/a	n/a
37	CTCF	chr5:115633240-115633390	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr5:115627143-115627204	GM10248	blood:	n/a	n/a
39	CTCF	chr5:115625040-115625190	HMF	breast:	n/a	chr5:115625169-115625182
40	CTCF	chr5:115625088-115625282	H1-hESC	embryonic stem cell:	n/a	chr5:115625169-115625182
41	CTCF	chr5:115625080-115625230	GM12872	blood:	n/a	chr5:115625169-115625182
42	CTCF	chr5:115625133-115625254	MCF-7	breast:	n/a	chr5:115625169-115625182
43	CTCF	chr5:115608340-115608490	BE2_C	brain:	n/a	n/a
44	CTCF	chr5:115633069-115633549	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:115608320-115608470	RPTEC	kidney:	n/a	n/a
46	CTCF	chr5:115625100-115625250	HCFaa	heart:	n/a	chr5:115625169-115625182
47	CTCF	chr5:115608320-115608470	HCM	heart:	n/a	n/a
48	CTCF	chr5:115625060-115625210	Caco-2	colon:	n/a	chr5:115625169-115625182
49	CTCF	chr5:115608380-115608530	HMF	breast:	n/a	n/a
50	CTCF	chr5:115608380-115608530	AoAF	blood vessel:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:115599680-115599730	AG04449	skin:	fetal
2	chr5:115599680-115599730	ovcar-3	ovarian:	n/a
3	chr5:115599680-115599730	NT2-D1	testis:	n/a
4	chr5:115599680-115599730	HPAEpiC	pulmonary alveolar:	n/a
5	chr5:115599680-115599730	GM12892	blood:	n/a
6	chr5:115599680-115599730	AG09309	skin:	n/a
7	chr5:115599680-115599730	HRE	kidney:	n/a
8	chr5:115599680-115599730	Jurkat	blood:	n/a
9	chr5:115599680-115599730	HRCEpiC	kidney:	n/a
10	chr5:115599680-115599730	RPTEC	kidney:	n/a
11	chr5:115599680-115599730	HCPEpiC	choroid plexus:	n/a
12	chr5:115599680-115599730	SK-N-SH_RA	brain:	n/a
13	chr5:115599680-115599730	AoSMC	blood vessel:	n/a
14	chr5:115599680-115599730	NB4	blood:	n/a
15	chr5:115599680-115599730	HepG2	liver:	n/a
16	chr5:115599680-115599730	HRPEpiC	eye:	n/a
17	chr5:115599680-115599730	ECC-1	luminal epithelium:	n/a
18	chr5:115599680-115599730	T-47D	breast:	n/a
19	chr5:115599680-115599730	HAEpiC	amniotic membrane:	n/a
20	chr5:115599680-115599730	IMR90	lung:	fetal
21	chr5:115599680-115599730	SAEC	small airway:	n/a
22	chr5:115599680-115599730	HIPEpiC	eye:	n/a
23	chr5:115599680-115599730	MCF-7	breast:	n/a
24	chr5:115599680-115599730	GM06990	blood:	n/a
25	chr5:115599680-115599730	LNCaP	prostate:	n/a
26	chr5:115599680-115599730	NHDF-neo	bronchial:	n/a
27	chr5:115599680-115599730	NHBE	bronchial:	n/a
28	chr5:115599680-115599730	BJ	skin:	n/a
29	chr5:115599680-115599730	HEEpiC	esophagus:	n/a
30	chr5:115599680-115599730	Caco-2	colon:	n/a
31	chr5:115599680-115599730	PFSK-1	brain:	n/a
32	chr5:115599680-115599730	HCF	heart:	n/a
33	chr5:115599680-115599730	AG04450	lung:	fetal
34	chr5:115599680-115599730	HCT-116	colon:	n/a
35	chr5:115599680-115599730	HEK293	kidney:	embryo
36	chr5:115599680-115599730	MCF10A-Er-Src	breast:	n/a
37	chr5:115599680-115599730	A549	lung:	n/a
38	chr5:115599680-115599730	BE2_C	brain:	n/a
39	chr5:115599680-115599730	ProgFib	skin:	n/a
40	chr5:115599680-115599730	CMK	blood:	n/a
41	chr5:115599680-115599730	SK-N-SH	brain:	n/a
42	chr5:115599680-115599730	GM12878	blood:	n/a
43	chr5:115599680-115599730	Hela-S3	cervix:	n/a
44	chr5:115599680-115599730	SKMC	muscle:	n/a
45	chr5:115599680-115599730	HNPCEpiC	eye:	n/a
46	chr5:115599680-115599730	GM12891	blood:	n/a
47	chr5:115599680-115599730	AG10803	skin:	n/a
48	chr5:115599680-115599730	SK-N-MC	brain:	n/a
49	chr5:115599680-115599730	HCM	heart:	n/a
50	chr5:115599680-115599730	HUVEC	blood vessel:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:115630950..115633524-chr5:115633964..115636710,2	MCF-7	breast:
2	chr20:47537809..47538621-chr5:115628215..115629028,2	MCF-7	breast:
3	chr5:115573428..115574084-chr5:115607901..115608709,2	MCF-7	breast:
4	chr5:115607181..115609929-chr5:115613382..115615949,2	K562	blood:
5	chr5:115632385..115634405-chr5:115635053..115637473,2	K562	blood:
6	chr5:115473058..115473763-chr5:115624723..115625238,2	MCF-7	breast:
7	chr5:115473639..115474170-chr5:115607611..115608509,2	MCF-7	breast:
8	chr5:115611187..115613784-chr5:115614610..115617269,2	MCF-7	breast:
9	chr5:115611187..115613784-chr5:115614610..115617269,2	MCF-7	breast:
10	chr5:115607181..115609929-chr5:115613382..115615949,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LVRN.1-4	chr5:115632111-115632653	NONHSAT103359
2	lnc-LVRN.1-4	chr5:115628154-115628257	NONHSAT103358

No data

Variant related genes	Relation type
COMMD10	TF binding region
COMMD10	CpG island
ENSG00000124198	chromatin interactions

Extended variants
information (count: 2866 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2866 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17139265	chr5:115578810-115578811	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559569946	chr5:115578817-115578818	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs6884520	chr5:115578832-115578833	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs548356741	chr5:115578850-115578851	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs17139268	chr5:115578852-115578853	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs113396435	chr5:115578856-115578857	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551027712	chr5:115578864-115578865	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532249718	chr5:115578886-115578887	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187981655	chr5:115578903-115578904	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs17139272	chr5:115578932-115578933	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs147345003	chr5:115578938-115578939	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs567110783	chr5:115578953-115578954	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535677111	chr5:115579042-115579043	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181242579	chr5:115579047-115579048	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577586710	chr5:115579056-115579057	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543413765	chr5:115579059-115579060	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183868207	chr5:115579068-115579069	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139485590	chr5:115579077-115579078	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149953010	chr5:115579089-115579090	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545751051	chr5:115579102-115579103	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs114251019	chr5:115579110-115579111	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs117835789	chr5:115579114-115579115	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs569619190	chr5:115579137-115579138	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573087713	chr5:115579174-115579175	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs374633245	chr5:115579200-115579201	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368591619	chr5:115579231-115579232	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542084981	chr5:115579234-115579235	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561849540	chr5:115579251-115579252	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531054564	chr5:115579267-115579268	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188496207	chr5:115579291-115579292	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558355617	chr5:115579331-115579332	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564566675	chr5:115579334-115579335	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs11241380	chr5:115579358-115579359	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs12332489	chr5:115579386-115579387	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs567099732	chr5:115579389-115579390	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs576950360	chr5:115579437-115579438	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs554207891	chr5:115579474-115579475	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545515717	chr5:115579487-115579488	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181684622	chr5:115579507-115579508	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149112868	chr5:115579513-115579514	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs142145816	chr5:115579604-115579605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186964808	chr5:115579607-115579608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556655576	chr5:115579631-115579632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6890192	chr5:115579647-115579648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539108358	chr5:115579662-115579663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552922564	chr5:115579671-115579672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111752974	chr5:115579672-115579673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542123717	chr5:115579689-115579690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555669616	chr5:115579713-115579714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs146730399	chr5:115579726-115579727	Weak transcription	n/a	n/a	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
Sezary syndrome	18413736	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115557400-115580800	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr5:115557400-115583200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr5:115560400-115581000	Weak transcription	Primary T cells from cord blood	blood
4	chr5:115560400-115610600	Weak transcription	Left Ventricle	heart
5	chr5:115561400-115580000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr5:115561800-115586400	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr5:115562400-115589000	Weak transcription	Ovary	ovary
8	chr5:115569800-115582200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr5:115572000-115580400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr5:115574000-115580000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr5:115577600-115579600	Enhancers	Fetal Kidney	kidney
12	chr5:115578200-115579000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr5:115578800-115579000	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr5:115578800-115579600	Strong transcription	Primary B cells from cord blood	blood
15	chr5:115578800-115586000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr5:115579600-115581800	Weak transcription	Fetal Intestine Large	intestine
17	chr5:115579600-115610600	Weak transcription	Primary B cells from cord blood	blood
18	chr5:115580400-115580800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr5:115581000-115581200	Strong transcription	Primary T cells from cord blood	blood
20	chr5:115581200-115581400	ZNF genes & repeats	Primary T cells from cord blood	blood
21	chr5:115581400-115591600	Weak transcription	Primary T cells from cord blood	blood
22	chr5:115581800-115582600	ZNF genes & repeats	Fetal Intestine Large	intestine
23	chr5:115582600-115594600	Weak transcription	Fetal Intestine Large	intestine
24	chr5:115583000-115583200	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
25	chr5:115583600-115589000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr5:115583800-115586200	Weak transcription	Brain Hippocampus Middle	brain
27	chr5:115584200-115586200	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr5:115584800-115603600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr5:115585200-115587800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr5:115585600-115586400	Weak transcription	Dnd41	blood
31	chr5:115585800-115586000	Weak transcription	Primary hematopoietic stem cells	blood
32	chr5:115585800-115601200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr5:115586000-115587000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr5:115586200-115586600	Strong transcription	Duodenum Smooth Muscle	Duodenum
35	chr5:115586200-115586800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
36	chr5:115586200-115586800	Strong transcription	Brain Hippocampus Middle	brain
37	chr5:115586400-115586600	Enhancers	Aorta	Aorta
38	chr5:115586400-115586600	ZNF genes & repeats	Dnd41	blood
39	chr5:115586400-115586800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
40	chr5:115586600-115586800	ZNF genes & repeats	Adipose Nuclei	Adipose
41	chr5:115586600-115586800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
42	chr5:115586600-115586800	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
43	chr5:115586600-115595600	Weak transcription	Aorta	Aorta
44	chr5:115586600-115603000	Weak transcription	Dnd41	blood
45	chr5:115586800-115587200	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr5:115586800-115588400	Weak transcription	Brain Hippocampus Middle	brain
47	chr5:115586800-115597000	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr5:115586800-115608000	Weak transcription	Adipose Nuclei	Adipose
49	chr5:115586800-115609800	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr5:115586800-115610800	Weak transcription	Primary hematopoietic stem cells	blood

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