Variant report

Variant	esv2422101
Chromosome Location	chr5:115594144-115625228
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:278)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:278 , 50 per page) page: 1 2 3 4 5 6

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	chr5:115609206-115609493	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
3	BATF	chr5:115609200-115609492	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	chr5:115612611-115612811	A549	lung:	n/a	n/a
8	CEBPB	chr5:115608227-115608718	MCF-7	breast:	n/a	chr5:115608483-115608494
9	CEBPB	chr5:115608311-115608872	IMR90	lung:	n/a	chr5:115608483-115608494
10	CEBPB	chr5:115601292-115601498	HepG2	liver:	n/a	n/a
11	CEBPB	chr5:115615956-115616164	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:115608357-115608659	A549	lung:	n/a	chr5:115608483-115608494
13	CEBPB	chr5:115608381-115608622	HepG2	liver:	n/a	chr5:115608483-115608494
14	CEBPB	chr5:115608269-115608767	MCF-7	breast:	n/a	chr5:115608483-115608494
15	CHD2	chr5:115608466-115608624	GM12878	blood:	n/a	n/a
16	CHD2	chr5:115609186-115609453	GM12878	blood:	n/a	n/a
17	CTCF	chr5:115625160-115625310	GM06990	blood:	n/a	chr5:115625169-115625182
18	CTCF	chr5:115614780-115614930	BJ	skin:	n/a	n/a
19	CTCF	chr5:115608411-115608564	GM12878	blood:	n/a	n/a
20	CTCF	chr5:115625140-115625290	RPTEC	kidney:	n/a	chr5:115625169-115625182
21	CTCF	chr5:115625129-115625224	HUVEC	blood vessel:	n/a	chr5:115625169-115625182
22	CTCF	chr5:115608420-115608517	LNCaP	prostate:	n/a	n/a
23	CTCF	chr5:115625040-115625190	AG09319	gingival:	n/a	chr5:115625169-115625182
24	CTCF	chr5:115608400-115608550	NHLF	lung:	n/a	n/a
25	CTCF	chr5:115625060-115625210	HVMF	connective:	n/a	chr5:115625169-115625182
26	CTCF	chr5:115608372-115608591	MCF-7	breast:	n/a	n/a
27	CTCF	chr5:115605340-115605490	AG10803	skin:	n/a	n/a
28	CTCF	chr5:115608420-115608570	HMEC	breast:	n/a	n/a
29	CTCF	chr5:115625140-115625290	WI-38	lung:	n/a	chr5:115625169-115625182
30	CTCF	chr5:115622300-115622450	AG09319	gingival:	n/a	n/a
31	CTCF	chr5:115608400-115608550	GM12871	blood:	n/a	n/a
32	CTCF	chr5:115608420-115608570	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr5:115625120-115625270	GM12864	blood:	n/a	chr5:115625169-115625182
34	CTCF	chr5:115608380-115608530	GM12866	blood:	n/a	n/a
35	CTCF	chr5:115608440-115608590	AG04450	lung:	n/a	n/a
36	CTCF	chr5:115625140-115625290	HA-sp	spinal cord:	n/a	chr5:115625169-115625182
37	CTCF	chr5:115608400-115608550	AG04450	lung:	n/a	n/a
38	CTCF	chr5:115608355-115608631	MCF-7	breast:	n/a	n/a
39	CTCF	chr5:115625120-115625270	HVMF	connective:	n/a	chr5:115625169-115625182
40	CTCF	chr5:115624962-115625365	H1-hESC	embryonic stem cell:	n/a	chr5:115625169-115625182
41	CTCF	chr5:115625060-115625210	HBMEC	blood vessel:	n/a	chr5:115625169-115625182
42	CTCF	chr5:115625120-115625270	MCF-7	breast:	n/a	chr5:115625169-115625182
43	CTCF	chr5:115625040-115625190	HCPEpiC	choroid plexus:	n/a	chr5:115625169-115625182
44	CTCF	chr5:115625040-115625190	HPF	lung:	n/a	chr5:115625169-115625182
45	CTCF	chr5:115625100-115625250	BE2_C	brain:	n/a	chr5:115625169-115625182
46	CTCF	chr5:115608300-115608651	GM12878	blood:	n/a	n/a
47	CTCF	chr5:115608434-115608519	HepG2	liver:	n/a	n/a
48	CTCF	chr5:115608420-115608570	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr5:115608400-115608550	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr5:115625100-115625250	HEK293	kidney:	n/a	chr5:115625169-115625182

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:115599680-115599730	PFSK-1	brain:	n/a
2	chr5:115599680-115599730	MCF10A-Er-Src	breast:	n/a
3	chr5:115599680-115599730	PrEC	prostate:	n/a
4	chr5:115599680-115599730	HRCEpiC	kidney:	n/a
5	chr5:115599680-115599730	NHBE	bronchial:	n/a
6	chr5:115599680-115599730	IMR90	lung:	fetal
7	chr5:115599680-115599730	U87	brain:	n/a
8	chr5:115599680-115599730	SK-N-SH	brain:	n/a
9	chr5:115599680-115599730	HCM	heart:	n/a
10	chr5:115599680-115599730	H1-hESC	embryonic stem cell:	embryo
11	chr5:115599680-115599730	Hela-S3	cervix:	n/a
12	chr5:115599680-115599730	CMK	blood:	n/a
13	chr5:115599680-115599730	MCF-7	breast:	n/a
14	chr5:115599680-115599730	K562	blood:	n/a
15	chr5:115599680-115599730	HAEpiC	amniotic membrane:	n/a
16	chr5:115599680-115599730	HL-60	blood:	n/a
17	chr5:115599680-115599730	AoSMC	blood vessel:	n/a
18	chr5:115599680-115599730	SKMC	muscle:	n/a
19	chr5:115599680-115599730	ProgFib	skin:	n/a
20	chr5:115599680-115599730	Caco-2	colon:	n/a
21	chr5:115599680-115599730	GM12891	blood:	n/a
22	chr5:115599680-115599730	AG09319	gingival:	n/a
23	chr5:115599680-115599730	GM06990	blood:	n/a
24	chr5:115599680-115599730	GM12892	blood:	n/a
25	chr5:115599680-115599730	HMEC	breast:	n/a
26	chr5:115599680-115599730	NB4	blood:	n/a
27	chr5:115599680-115599730	Hepatocyte	liver:	n/a
28	chr5:115599680-115599730	HIPEpiC	eye:	n/a
29	chr5:115599680-115599730	PANC-1	pancreas:	n/a
30	chr5:115599680-115599730	Jurkat	blood:	n/a
31	chr5:115599680-115599730	HEK293	kidney:	embryo
32	chr5:115599680-115599730	HRPEpiC	eye:	n/a
33	chr5:115599680-115599730	HNPCEpiC	eye:	n/a
34	chr5:115599680-115599730	SK-N-SH_RA	brain:	n/a
35	chr5:115599680-115599730	ovcar-3	ovarian:	n/a
36	chr5:115599680-115599730	HCF	heart:	n/a
37	chr5:115599680-115599730	RPTEC	kidney:	n/a
38	chr5:115599680-115599730	HPAEpiC	pulmonary alveolar:	n/a
39	chr5:115599680-115599730	ECC-1	luminal epithelium:	n/a
40	chr5:115599680-115599730	SK-N-MC	brain:	n/a
41	chr5:115599680-115599730	SAEC	small airway:	n/a
42	chr5:115599680-115599730	AG04450	lung:	fetal
43	chr5:115599680-115599730	HRE	kidney:	n/a
44	chr5:115599680-115599730	A549	lung:	n/a
45	chr5:115599680-115599730	GM12878	blood:	n/a
46	chr5:115599680-115599730	BE2_C	brain:	n/a
47	chr5:115599680-115599730	AG09309	skin:	n/a
48	chr5:115599680-115599730	HepG2	liver:	n/a
49	chr5:115599680-115599730	HEEpiC	esophagus:	n/a
50	chr5:115599680-115599730	AG10803	skin:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:115473639..115474170-chr5:115607611..115608509,2	MCF-7	breast:
2	chr5:115473058..115473763-chr5:115624723..115625238,2	MCF-7	breast:
3	chr5:115573428..115574084-chr5:115607901..115608709,2	MCF-7	breast:
4	chr5:115611187..115613784-chr5:115614610..115617269,2	MCF-7	breast:
5	chr5:115611187..115613784-chr5:115614610..115617269,2	MCF-7	breast:
6	chr5:115607181..115609929-chr5:115613382..115615949,2	K562	blood:
7	chr5:115607181..115609929-chr5:115613382..115615949,2	K562	blood:

No data

Variant related genes	Relation type
COMMD10	TF binding region
COMMD10	CpG island

Extended variants
information (count: 1640 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1640 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs37183	chr5:115594144-115594145	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs58266995	chr5:115594146-115594147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs199663234	chr5:115594150-115594151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs397701612	chr5:115594155-115594156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574159201	chr5:115594178-115594179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563323048	chr5:115594185-115594186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543194954	chr5:115594190-115594191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555545022	chr5:115594193-115594194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139909237	chr5:115594228-115594229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544292774	chr5:115594240-115594241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564095008	chr5:115594246-115594247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538238946	chr5:115594255-115594256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532896642	chr5:115594258-115594259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554677701	chr5:115594324-115594325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185291342	chr5:115594329-115594330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142971714	chr5:115594334-115594335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529124496	chr5:115594338-115594339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190292463	chr5:115594369-115594370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574846275	chr5:115594370-115594371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569043628	chr5:115594389-115594390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182843432	chr5:115594413-115594414	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs551432525	chr5:115594419-115594420	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs571552633	chr5:115594457-115594458	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs534155734	chr5:115594471-115594472	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs554207854	chr5:115594487-115594488	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs567944082	chr5:115594501-115594502	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs4566828	chr5:115594505-115594506	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs151129852	chr5:115594552-115594553	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs187062335	chr5:115594566-115594567	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs13355348	chr5:115594586-115594587	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs544329442	chr5:115594603-115594604	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs73261010	chr5:115594610-115594611	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs577608251	chr5:115594618-115594619	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs532606130	chr5:115594625-115594626	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs540222272	chr5:115594630-115594631	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs560217288	chr5:115594649-115594650	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs529171367	chr5:115594654-115594655	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs77099426	chr5:115594665-115594666	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs141100845	chr5:115594669-115594670	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs191711178	chr5:115594705-115594706	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs551467699	chr5:115594706-115594707	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs149814832	chr5:115594725-115594726	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs527729943	chr5:115594750-115594751	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs36082006	chr5:115594760-115594761	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs77516388	chr5:115594783-115594784	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs183604452	chr5:115594790-115594791	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs187923321	chr5:115594801-115594802	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs192481614	chr5:115594810-115594811	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs191512941	chr5:115594814-115594815	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs34105005	chr5:115594817-115594818	Weak transcription ZNF genes & repeats	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:194 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115560400-115610600	Weak transcription	Left Ventricle	heart
2	chr5:115579600-115610600	Weak transcription	Primary B cells from cord blood	blood
3	chr5:115582600-115594600	Weak transcription	Fetal Intestine Large	intestine
4	chr5:115584800-115603600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr5:115585800-115601200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr5:115586600-115595600	Weak transcription	Aorta	Aorta
7	chr5:115586600-115603000	Weak transcription	Dnd41	blood
8	chr5:115586800-115597000	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr5:115586800-115608000	Weak transcription	Adipose Nuclei	Adipose
10	chr5:115586800-115609800	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr5:115586800-115610800	Weak transcription	Primary hematopoietic stem cells	blood
12	chr5:115587000-115599800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr5:115590800-115610200	Weak transcription	Primary B cells from peripheral blood	blood
14	chr5:115591000-115607200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr5:115592000-115599600	Weak transcription	Primary T cells from cord blood	blood
16	chr5:115592000-115607800	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr5:115593000-115601400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr5:115594400-115595400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr5:115595000-115601200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr5:115595200-115595400	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr5:115595200-115597800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr5:115595400-115597000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr5:115595600-115596600	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr5:115595800-115603800	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr5:115596200-115596400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr5:115596200-115596800	Enhancers	Colon Smooth Muscle	Colon
27	chr5:115596400-115598400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr5:115596600-115597600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr5:115596800-115597800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr5:115597000-115597400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr5:115597000-115597600	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr5:115597000-115599000	Strong transcription	Monocytes-CD14+_RO01746	blood
33	chr5:115597000-115608200	Weak transcription	NHDF-Ad	bronchial
34	chr5:115597400-115599600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr5:115597600-115599800	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr5:115597800-115599800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr5:115597800-115603400	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr5:115598400-115598600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr5:115598600-115598800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr5:115599000-115601400	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr5:115599200-115612600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr5:115599600-115600400	Enhancers	H1 Cell Line	embryonic stem cell
43	chr5:115599600-115600400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr5:115599600-115600400	Strong transcription	Primary T cells from cord blood	blood
45	chr5:115599600-115600600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr5:115599600-115602200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr5:115599800-115600400	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr5:115599800-115600400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr5:115599800-115600400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr5:115599800-115600600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links