Variant report

Variant	nsv969021
Chromosome Location	chr5:177060702-177111251
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:238)
CpG islands
(count:611)
Chromatin interactive
region (count:2)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:238 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:177099131-177099156	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr5:177075765-177076001	GM12878	blood:	n/a	n/a
3	BATF	chr5:177097054-177097393	GM12878	blood:	n/a	n/a
4	BATF	chr5:177084755-177084988	GM12878	blood:	n/a	chr5:177084851-177084862
5	BCL11A	chr5:177097155-177097449	GM12878	blood:	n/a	n/a
6	CEBPB	chr5:177084874-177085247	K562	blood:	n/a	chr5:177085047-177085058
7	CEBPB	chr5:177103493-177103545	K562	blood:	n/a	n/a
8	CEBPB	chr5:177085035-177085201	Hela-S3	cervix:	n/a	chr5:177085047-177085058
9	CEBPB	chr5:177085014-177085213	HepG2	liver:	n/a	chr5:177085047-177085058
10	CEBPB	chr5:177084865-177085231	IMR90	lung:	n/a	chr5:177085047-177085058
11	CEBPB	chr5:177085019-177085215	H1-hESC	embryonic stem cell:	n/a	chr5:177085047-177085058
12	CEBPD	chr5:177072941-177073293	K562	blood:	n/a	n/a
13	CTCF	chr5:177085303-177085362	Medullo	brain:	n/a	n/a
14	CTCF	chr5:177102278-177102430	MCF-7	breast:	n/a	n/a
15	CTCF	chr5:177085087-177085135	A549	lung:	n/a	n/a
16	CTCF	chr5:177083506-177083547	GM10248	blood:	n/a	n/a
17	CTCF	chr5:177102279-177102438	NHEK	skin:	n/a	n/a
18	CTCF	chr5:177098926-177099013	GM19239	blood:	n/a	n/a
19	CTCF	chr5:177098901-177099025	Fibrobl	skin:	n/a	n/a
20	CTCF	chr5:177098901-177098990	GM12892	blood:	n/a	n/a
21	CTCF	chr5:177085077-177085162	GM12878	blood:	n/a	n/a
22	CTCF	chr5:177085060-177085210	HEEpiC	esophagus:	n/a	n/a
23	CTCF	chr5:177102287-177102424	ProgFib	skin:	n/a	n/a
24	CTCF	chr5:177085071-177085174	Pancreas_OC	pancreas:	n/a	n/a
25	CTCF	chr5:177102350-177102370	Pancreas_OC	pancreas:	n/a	n/a
26	CTCF	chr5:177074278-177074337	Lung_OC	lung:	n/a	n/a
27	CTCF	chr5:177111186-177111252	ProgFib	skin:	n/a	n/a
28	CTCF	chr5:177085089-177085106	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr5:177102324-177102426	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr5:177102288-177102433	GM12892	blood:	n/a	n/a
31	CTCF	chr5:177102263-177102459	GM12878	blood:	n/a	n/a
32	CTCF	chr5:177102291-177102422	Fibrobl	skin:	n/a	n/a
33	CTCF	chr5:177085039-177085170	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr5:177085100-177085250	BJ	skin:	n/a	n/a
35	CTCF	chr5:177102198-177102433	A549	lung:	n/a	n/a
36	CTCF	chr5:177098971-177098999	NHEK	skin:	n/a	n/a
37	CTCF	chr5:177084900-177085050	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr5:177102258-177102450	GM19238	blood:	n/a	n/a
39	CTCF	chr5:177084942-177085274	A549	lung:	n/a	n/a
40	CTCF	chr5:177085140-177085290	Caco-2	colon:	n/a	n/a
41	CTCF	chr5:177085089-177085164	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr5:177102283-177102439	GM19240	blood:	n/a	n/a
43	CTCF	chr5:177102109-177102470	A549	lung:	n/a	n/a
44	CTCF	chr5:177102393-177102434	Medullo	brain:	n/a	n/a
45	CTCF	chr5:177098921-177099028	MCF-7	breast:	n/a	n/a
46	CTCF	chr5:177102259-177102440	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr5:177102286-177102442	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr5:177102294-177102414	Lung_OC	lung:	n/a	n/a
49	CTCF	chr5:177085008-177085178	MCF-7	breast:	n/a	n/a
50	CTCF	chr5:177102363-177102390	MCF-7	breast:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177099102-177099152	AG09309	skin:	n/a
2	chr5:177099102-177099152	AG09309	skin:	n/a
3	chr5:177100448-177100498	MCF-7	breast:	n/a
4	chr5:177100448-177100498	HCM	heart:	n/a
5	chr5:177100428-177100478	SK-N-MC	brain:	n/a
6	chr5:177097760-177097810	GM06990	blood:	n/a
7	chr5:177097760-177097810	HCM	heart:	n/a
8	chr5:177103100-177103150	AoSMC	blood vessel:	n/a
9	chr5:177099378-177099428	NH-A	brain:	n/a
10	chr5:177099373-177099423	ProgFib	skin:	n/a
11	chr5:177099378-177099428	GM06990	blood:	n/a
12	chr5:177095013-177095063	HNPCEpiC	eye:	n/a
13	chr5:177097760-177097810	SK-N-SH_RA	brain:	n/a
14	chr5:177100428-177100478	HMEC	breast:	n/a
15	chr5:177099373-177099423	CMK	blood:	n/a
16	chr5:177100428-177100478	HRPEpiC	eye:	n/a
17	chr5:177099378-177099428	GM12878	blood:	n/a
18	chr5:177099373-177099423	NH-A	brain:	n/a
19	chr5:177099378-177099428	AG10803	skin:	n/a
20	chr5:177099378-177099428	MCF10A-Er-Src	breast:	n/a
21	chr5:177099102-177099152	HPAEpiC	pulmonary alveolar:	n/a
22	chr5:177099251-177099301	GM06990	blood:	n/a
23	chr5:177097760-177097810	AG04449	skin:	fetal
24	chr5:177099102-177099152	PFSK-1	brain:	n/a
25	chr5:177099644-177099694	ProgFib	skin:	n/a
26	chr5:177095013-177095063	HCT-116	colon:	n/a
27	chr5:177103100-177103150	AG10803	skin:	n/a
28	chr5:177095013-177095063	AoSMC	blood vessel:	n/a
29	chr5:177099378-177099428	HMEC	breast:	n/a
30	chr5:177097760-177097810	AoSMC	blood vessel:	n/a
31	chr5:177099378-177099428	SK-N-SH	brain:	n/a
32	chr5:177103100-177103150	HepG2	liver:	n/a
33	chr5:177103100-177103150	NH-A	brain:	n/a
34	chr5:177095013-177095063	T-47D	breast:	n/a
35	chr5:177099102-177099152	HL-60	blood:	n/a
36	chr5:177099373-177099423	HPAEpiC	pulmonary alveolar:	n/a
37	chr5:177099644-177099694	CMK	blood:	n/a
38	chr5:177099251-177099301	SAEC	small airway:	n/a
39	chr5:177099378-177099428	HL-60	blood:	n/a
40	chr5:177095013-177095063	Hela-S3	cervix:	n/a
41	chr5:177099251-177099301	HIPEpiC	eye:	n/a
42	chr5:177099644-177099694	GM12892	blood:	n/a
43	chr5:177099644-177099694	HPAEpiC	pulmonary alveolar:	n/a
44	chr5:177097760-177097810	HUVEC	blood vessel:	n/a
45	chr5:177095013-177095063	A549	lung:	n/a
46	chr5:177099644-177099694	HEEpiC	esophagus:	n/a
47	chr5:177103100-177103150	MCF-7	breast:	n/a
48	chr5:177097760-177097810	GM19239	blood:	n/a
49	chr5:177099644-177099694	NT2-D1	testis:	n/a
50	chr5:177099373-177099423	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:177033397..177036154-chr5:177060023..177062974,2	K562	blood:
2	chr5:177034192..177034791-chr5:177084697..177085207,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1026M7.2.1-2	chr5:177109295-177109372	ENSG00000249849.1
2	lnc-B4GALT7-3	chr5:177077160-177077324	l_3073_chr5:177076081-177077324_testes
3	lnc-B4GALT7-3	chr5:177076082-177076209	l_3073_chr5:177076081-177077324_testes

No data

Variant related genes	Relation type
ENSG00000249849	TF binding region
ENSG00000246596	TF binding region
ENSG00000249849	CpG island
ENSG00000246596	CpG island
ENSG00000027847	chromatin interactions

Extended variants
information (count: 1307 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1307 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116039744	chr5:177060788-177060789	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs554215649	chr5:177060791-177060792	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs572421448	chr5:177060815-177060816	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs546297974	chr5:177060848-177060849	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs145993295	chr5:177060854-177060855	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs557935306	chr5:177060913-177060914	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs576462466	chr5:177060924-177060925	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs543706991	chr5:177060952-177060953	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs113576213	chr5:177060961-177060962	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs561939821	chr5:177061058-177061059	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs201811187	chr5:177061077-177061078	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs529554992	chr5:177061082-177061083	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs541279984	chr5:177061219-177061220	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs558946468	chr5:177061221-177061222	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs113637573	chr5:177061231-177061232	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs532759614	chr5:177061232-177061233	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs551342083	chr5:177061245-177061246	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs569677615	chr5:177061270-177061271	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs530625848	chr5:177061332-177061333	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs73804379	chr5:177061334-177061335	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs143089696	chr5:177061344-177061345	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs551004137	chr5:177061417-177061418	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs13171038	chr5:177061452-177061453	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs534917115	chr5:177061505-177061506	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs13166526	chr5:177061508-177061509	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs183720711	chr5:177061522-177061523	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs566093364	chr5:177061537-177061538	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs148084435	chr5:177061575-177061576	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs186895329	chr5:177061582-177061583	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs13159087	chr5:177061598-177061599	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs576503152	chr5:177061624-177061625	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543860850	chr5:177061644-177061645	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs150681014	chr5:177061670-177061671	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs34327383	chr5:177061708-177061709	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs541341801	chr5:177061711-177061712	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs566571721	chr5:177061755-177061756	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs549057612	chr5:177061778-177061779	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs13166915	chr5:177061789-177061790	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs13170705	chr5:177061806-177061807	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs578179726	chr5:177061836-177061837	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs544723630	chr5:177061865-177061866	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs563285834	chr5:177061919-177061920	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs10479521	chr5:177061936-177061937	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs549049916	chr5:177061959-177061960	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs561086402	chr5:177061969-177061970	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs528259885	chr5:177061991-177061992	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs546799266	chr5:177062038-177062039	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs571616921	chr5:177062042-177062043	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs538917729	chr5:177062044-177062045	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs143762518	chr5:177062058-177062059	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Autism	20841430	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177044400-177061800	Weak transcription	Small Intestine	intestine
2	chr5:177046600-177068400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr5:177046600-177069200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr5:177046600-177069600	Weak transcription	Esophagus	oesophagus
5	chr5:177046800-177060800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr5:177046800-177065800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr5:177046800-177084000	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr5:177047000-177079000	Weak transcription	Colon Smooth Muscle	Colon
9	chr5:177047200-177061000	Weak transcription	Brain Hippocampus Middle	brain
10	chr5:177047200-177064000	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr5:177047200-177070800	Weak transcription	Pancreas	Pancrea
12	chr5:177047400-177075000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr5:177047800-177068200	Weak transcription	Fetal Intestine Large	intestine
14	chr5:177047800-177069000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr5:177047800-177080200	Weak transcription	Primary B cells from cord blood	blood
16	chr5:177048000-177061200	Weak transcription	Brain Germinal Matrix	brain
17	chr5:177048000-177069000	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr5:177048400-177066800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr5:177048800-177063200	Weak transcription	Fetal Brain Female	brain
20	chr5:177048800-177083600	Weak transcription	Fetal Lung	lung
21	chr5:177049400-177060800	Weak transcription	Fetal Muscle Trunk	muscle
22	chr5:177051600-177069000	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr5:177051800-177080200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr5:177052000-177083200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr5:177052000-177085600	Weak transcription	Gastric	stomach
26	chr5:177052200-177070000	Weak transcription	Primary T cells from cord blood	blood
27	chr5:177052400-177065200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr5:177052800-177060800	Weak transcription	Fetal Muscle Leg	muscle
29	chr5:177052800-177068200	Weak transcription	Spleen	Spleen
30	chr5:177052800-177070200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr5:177052800-177070200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr5:177052800-177070400	Weak transcription	Adipose Nuclei	Adipose
33	chr5:177052800-177076400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr5:177054000-177084600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr5:177054200-177062000	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr5:177054200-177066600	Weak transcription	Dnd41	blood
37	chr5:177054200-177069200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr5:177054200-177070000	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr5:177054400-177068200	Weak transcription	Ovary	ovary
40	chr5:177054400-177068200	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr5:177054400-177096000	Weak transcription	Primary B cells from peripheral blood	blood
42	chr5:177054600-177062000	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr5:177058000-177066400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr5:177059000-177068400	Weak transcription	Aorta	Aorta
45	chr5:177059200-177062200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr5:177059400-177067600	Weak transcription	Thymus	Thymus
47	chr5:177059600-177068200	Weak transcription	Lung	lung
48	chr5:177059800-177066000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr5:177063600-177065800	Weak transcription	Fetal Brain Female	brain
50	chr5:177065200-177067000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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