Variant report

Variant	nsv1015300
Chromosome Location	chr5:115597953-115629523
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:284)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:284 , 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	chr5:115612653-115612965	K562	blood:	n/a	n/a
5	CBX3	chr5:115612612-115613059	HCT-116	colon:	n/a	n/a
6	CBX3	chr5:115612735-115612979	K562	blood:	n/a	n/a
7	CEBPB	chr5:115608381-115608622	HepG2	liver:	n/a	chr5:115608483-115608494
8	CEBPB	chr5:115608311-115608872	IMR90	lung:	n/a	chr5:115608483-115608494
9	CEBPB	chr5:115615956-115616164	HepG2	liver:	n/a	n/a
10	CEBPB	chr5:115612611-115612811	A549	lung:	n/a	n/a
11	CEBPB	chr5:115601292-115601498	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:115608227-115608718	MCF-7	breast:	n/a	chr5:115608483-115608494
13	CEBPB	chr5:115608357-115608659	A549	lung:	n/a	chr5:115608483-115608494
14	CEBPB	chr5:115608269-115608767	MCF-7	breast:	n/a	chr5:115608483-115608494
15	CHD2	chr5:115609186-115609453	GM12878	blood:	n/a	n/a
16	CHD2	chr5:115608466-115608624	GM12878	blood:	n/a	n/a
17	CTCF	chr5:115608380-115608530	HCFaa	heart:	n/a	n/a
18	CTCF	chr5:115625080-115625230	K562	blood:	n/a	chr5:115625169-115625182
19	CTCF	chr5:115608380-115608530	MCF-7	breast:	n/a	n/a
20	CTCF	chr5:115608440-115608590	HVMF	connective:	n/a	n/a
21	CTCF	chr5:115625120-115625270	GM12864	blood:	n/a	chr5:115625169-115625182
22	CTCF	chr5:115625119-115625254	Gliobla	brain:	n/a	chr5:115625169-115625182
23	CTCF	chr5:115608360-115608510	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr5:115608080-115608230	BE2_C	brain:	n/a	n/a
25	CTCF	chr5:115625060-115625210	HepG2	liver:	n/a	chr5:115625169-115625182
26	CTCF	chr5:115608400-115608550	HPF	lung:	n/a	n/a
27	CTCF	chr5:115608340-115608490	HA-sp	spinal cord:	n/a	n/a
28	CTCF	chr5:115624940-115625090	GM12866	blood:	n/a	n/a
29	CTCF	chr5:115625060-115625210	GM12865	blood:	n/a	chr5:115625169-115625182
30	CTCF	chr5:115608380-115608530	AG10803	skin:	n/a	n/a
31	CTCF	chr5:115614780-115614930	BJ	skin:	n/a	n/a
32	CTCF	chr5:115605340-115605490	AG10803	skin:	n/a	n/a
33	CTCF	chr5:115625000-115625150	GM12872	blood:	n/a	n/a
34	CTCF	chr5:115625111-115625252	MCF-7	breast:	n/a	chr5:115625169-115625182
35	CTCF	chr5:115625120-115625270	AG04450	lung:	n/a	chr5:115625169-115625182
36	CTCF	chr5:115608400-115608550	GM06990	blood:	n/a	n/a
37	CTCF	chr5:115624980-115625130	NHEK	skin:	n/a	n/a
38	CTCF	chr5:115625080-115625230	HMF	breast:	n/a	chr5:115625169-115625182
39	CTCF	chr5:115622300-115622450	AG09319	gingival:	n/a	n/a
40	CTCF	chr5:115608440-115608590	AG04450	lung:	n/a	n/a
41	CTCF	chr5:115625088-115625282	H1-hESC	embryonic stem cell:	n/a	chr5:115625169-115625182
42	CTCF	chr5:115625040-115625190	HUVEC	blood vessel:	n/a	chr5:115625169-115625182
43	CTCF	chr5:115608320-115608470	HFF	foreskin:	n/a	n/a
44	CTCF	chr5:115625160-115625310	HEK293	kidney:	n/a	chr5:115625169-115625182
45	CTCF	chr5:115625171-115625218	MCF-7	breast:	n/a	n/a
46	CTCF	chr5:115625180-115625330	GM06990	blood:	n/a	n/a
47	CTCF	chr5:115608380-115608530	AG04449	skin:	n/a	n/a
48	CTCF	chr5:115608300-115608651	GM12878	blood:	n/a	n/a
49	CTCF	chr5:115608320-115608470	GM12872	blood:	n/a	n/a
50	CTCF	chr5:115608355-115608631	MCF-7	breast:	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	HAEpiC	amniotic membrane:	n/a
2	chr5:115599680-115599730	HCM	heart:	n/a
3	chr5:115599680-115599730	GM12878	blood:	n/a
4	chr5:115599680-115599730	HRE	kidney:	n/a
5	chr5:115599680-115599730	PFSK-1	brain:	n/a
6	chr5:115599680-115599730	H1-hESC	embryonic stem cell:	embryo
7	chr5:115599680-115599730	GM12892	blood:	n/a
8	chr5:115599680-115599730	HMEC	breast:	n/a
9	chr5:115599680-115599730	HPAEpiC	pulmonary alveolar:	n/a
10	chr5:115599680-115599730	MCF-7	breast:	n/a
11	chr5:115599680-115599730	SK-N-MC	brain:	n/a
12	chr5:115599680-115599730	SKMC	muscle:	n/a
13	chr5:115599680-115599730	NT2-D1	testis:	n/a
14	chr5:115599680-115599730	HCF	heart:	n/a
15	chr5:115599680-115599730	T-47D	breast:	n/a
16	chr5:115599680-115599730	HCPEpiC	choroid plexus:	n/a
17	chr5:115599680-115599730	Caco-2	colon:	n/a
18	chr5:115599680-115599730	HCT-116	colon:	n/a
19	chr5:115599680-115599730	NHDF-neo	bronchial:	n/a
20	chr5:115599680-115599730	HIPEpiC	eye:	n/a
21	chr5:115599680-115599730	RPTEC	kidney:	n/a
22	chr5:115599680-115599730	HEEpiC	esophagus:	n/a
23	chr5:115599680-115599730	IMR90	lung:	fetal
24	chr5:115599680-115599730	HRCEpiC	kidney:	n/a
25	chr5:115599680-115599730	MCF10A-Er-Src	breast:	n/a
26	chr5:115599680-115599730	BE2_C	brain:	n/a
27	chr5:115599680-115599730	AG04449	skin:	fetal
28	chr5:115599680-115599730	AoSMC	blood vessel:	n/a
29	chr5:115599680-115599730	PANC-1	pancreas:	n/a
30	chr5:115599680-115599730	HRPEpiC	eye:	n/a
31	chr5:115599680-115599730	AG10803	skin:	n/a
32	chr5:115599680-115599730	HL-60	blood:	n/a
33	chr5:115599680-115599730	U87	brain:	n/a
34	chr5:115599680-115599730	ProgFib	skin:	n/a
35	chr5:115599680-115599730	AG09309	skin:	n/a
36	chr5:115599680-115599730	K562	blood:	n/a
37	chr5:115599680-115599730	GM12891	blood:	n/a
38	chr5:115599680-115599730	SK-N-SH_RA	brain:	n/a
39	chr5:115599680-115599730	HNPCEpiC	eye:	n/a
40	chr5:115599680-115599730	AG09319	gingival:	n/a
41	chr5:115599680-115599730	GM06990	blood:	n/a
42	chr5:115599680-115599730	HepG2	liver:	n/a
43	chr5:115599680-115599730	Jurkat	blood:	n/a
44	chr5:115599680-115599730	NHBE	bronchial:	n/a
45	chr5:115599680-115599730	NB4	blood:	n/a
46	chr5:115599680-115599730	HEK293	kidney:	embryo
47	chr5:115599680-115599730	LNCaP	prostate:	n/a
48	chr5:115599680-115599730	HUVEC	blood vessel:	n/a
49	chr5:115599680-115599730	Hepatocyte	liver:	n/a
50	chr5:115599680-115599730	AG04450	lung:	fetal

(count:8 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	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: 1649 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1649 , 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	rs186724881	chr5:115597954-115597955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs190887304	chr5:115597965-115597966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554307503	chr5:115597995-115597996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182761537	chr5:115598014-115598015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535494244	chr5:115598044-115598045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555360123	chr5:115598060-115598061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572514770	chr5:115598069-115598070	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78888713	chr5:115598086-115598087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538152457	chr5:115598116-115598117	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146840003	chr5:115598118-115598119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554903658	chr5:115598122-115598123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576686147	chr5:115598124-115598125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540816879	chr5:115598152-115598153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552819279	chr5:115598172-115598173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537000682	chr5:115598178-115598179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572958422	chr5:115598245-115598246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556820443	chr5:115598252-115598253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs202194525	chr5:115598253-115598254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201519595	chr5:115598254-115598255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544060103	chr5:115598259-115598260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530468349	chr5:115598268-115598269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558913401	chr5:115598274-115598275	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139722605	chr5:115598311-115598312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564394002	chr5:115598313-115598314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577019103	chr5:115598326-115598327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs77521383	chr5:115598333-115598334	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188134800	chr5:115598349-115598350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540766698	chr5:115598376-115598377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113568671	chr5:115598380-115598381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111250915	chr5:115598383-115598384	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192901290	chr5:115598385-115598386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556944002	chr5:115598420-115598421	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146469958	chr5:115598469-115598470	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184536122	chr5:115598511-115598512	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558212437	chr5:115598539-115598540	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572849914	chr5:115598584-115598585	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140778725	chr5:115598630-115598631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs375288464	chr5:115598646-115598647	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187407971	chr5:115598649-115598650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554422047	chr5:115598692-115598693	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574254592	chr5:115598707-115598708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376735251	chr5:115598724-115598725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113053744	chr5:115598756-115598757	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112232465	chr5:115598783-115598784	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555459571	chr5:115598813-115598814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150077039	chr5:115598816-115598817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544175232	chr5:115598817-115598818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564259497	chr5:115598842-115598843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577887247	chr5:115598876-115598877	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540130979	chr5:115598891-115598892	Weak transcription Strong 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:269 , 50 per page) page: 1 2 3 4 5 6

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	chr5:115584800-115603600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr5:115585800-115601200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr5:115586600-115603000	Weak transcription	Dnd41	blood
6	chr5:115586800-115608000	Weak transcription	Adipose Nuclei	Adipose
7	chr5:115586800-115609800	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr5:115586800-115610800	Weak transcription	Primary hematopoietic stem cells	blood
9	chr5:115587000-115599800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr5:115590800-115610200	Weak transcription	Primary B cells from peripheral blood	blood
11	chr5:115591000-115607200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr5:115592000-115599600	Weak transcription	Primary T cells from cord blood	blood
13	chr5:115592000-115607800	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr5:115593000-115601400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr5:115595000-115601200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr5:115595800-115603800	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr5:115596400-115598400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr5:115597000-115599000	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr5:115597000-115608200	Weak transcription	NHDF-Ad	bronchial
20	chr5:115597400-115599600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr5:115597600-115599800	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr5:115597800-115599800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr5:115597800-115603400	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr5:115598400-115598600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr5:115598600-115598800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr5:115599000-115601400	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr5:115599200-115612600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr5:115599600-115600400	Enhancers	H1 Cell Line	embryonic stem cell
29	chr5:115599600-115600400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr5:115599600-115600400	Strong transcription	Primary T cells from cord blood	blood
31	chr5:115599600-115600600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr5:115599600-115602200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr5:115599800-115600400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr5:115599800-115600400	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr5:115599800-115600400	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr5:115599800-115600600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr5:115600000-115600400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr5:115600200-115601000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr5:115600400-115601000	ZNF genes & repeats	Primary T cells from cord blood	blood
40	chr5:115600600-115611400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr5:115600800-115601600	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr5:115601000-115601800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr5:115601000-115606200	Weak transcription	Primary T cells from cord blood	blood
44	chr5:115601200-115601600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr5:115601400-115601600	ZNF genes & repeats	Fetal Lung	lung
46	chr5:115601400-115601800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
47	chr5:115601600-115604600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr5:115601600-115608000	Weak transcription	Fetal Lung	lung
49	chr5:115601800-115602000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr5:115602200-115603600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links