Variant report

Variant	nsv830408
Chromosome Location	chr5:94894032-94915995
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:39)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:39 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:94899136-94899384	K562	blood:	n/a	n/a
2	CCNT2	chr5:94899183-94899383	K562	blood:	n/a	n/a
3	CCNT2	chr5:94902108-94902191	K562	blood:	n/a	n/a
4	CTCF	chr5:94900909-94900991	Medullo	brain:	n/a	n/a
5	CTCF	chr5:94897367-94897410	Pancreas_OC	pancreas:	n/a	n/a
6	CTCF	chr5:94912760-94912910	RPTEC	kidney:	n/a	n/a
7	CUX1	chr5:94899105-94899499	K562	blood:	n/a	n/a
8	CUX1	chr5:94897176-94897190	GM12878	blood:	n/a	n/a
9	E2F4	chr5:94902497-94902743	MCF10A-Er-Src	breast:	n/a	n/a
10	IRF1	chr5:94898605-94898731	K562	blood:	n/a	n/a
11	IRF1	chr5:94902698-94902864	K562	blood:	n/a	n/a
12	IRF1	chr5:94914211-94914369	K562	blood:	n/a	n/a
13	IRF1	chr5:94913543-94913617	K562	blood:	n/a	n/a
14	JUN	chr5:94899161-94899409	K562	blood:	n/a	n/a
15	JUND	chr5:94899098-94899534	K562	blood:	n/a	n/a
16	KAP1	chr5:94897096-94897359	K562	blood:	n/a	n/a
17	MAFF	chr5:94894226-94894362	HepG2	liver:	n/a	n/a
18	MAFF	chr5:94898022-94898359	K562	blood:	n/a	n/a
19	MAFF	chr5:94898010-94898367	HepG2	liver:	n/a	n/a
20	MAFK	chr5:94898131-94898220	H1-hESC	embryonic stem cell:	n/a	n/a
21	MAFK	chr5:94898013-94898353	K562	blood:	n/a	chr5:94898057-94898068 chr5:94898057-94898068
22	MAFK	chr5:94894155-94894366	HepG2	liver:	n/a	n/a
23	MAFK	chr5:94898035-94898358	Hela-S3	cervix:	n/a	chr5:94898057-94898068 chr5:94898057-94898068
24	MAFK	chr5:94898016-94898345	HepG2	liver:	n/a	chr5:94898057-94898068 chr5:94898057-94898068
25	MAFK	chr5:94898010-94898371	IMR90	lung:	n/a	chr5:94898057-94898068 chr5:94898057-94898068
26	MAFK	chr5:94898005-94898369	HepG2	liver:	n/a	chr5:94898057-94898068 chr5:94898057-94898068
27	MAZ	chr5:94899084-94899408	K562	blood:	n/a	n/a
28	MXI1	chr5:94904008-94904012	K562	blood:	n/a	n/a
29	MXI1	chr5:94898353-94898374	K562	blood:	n/a	n/a
30	POLR2A	chr5:94907427-94907453	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr5:94908639-94908730	GM12878	blood:	n/a	n/a
32	POLR2A	chr5:94914376-94914521	ProgFib	skin:	n/a	n/a
33	POLR2A	chr5:94912944-94912992	MCF10A-Er-Src	breast:	n/a	n/a
34	POLR2A	chr5:94900295-94900451	A549	lung:	n/a	n/a
35	RAD21	chr5:94902742-94902779	A549	lung:	n/a	n/a
36	RCOR1	chr5:94901186-94901201	K562	blood:	n/a	n/a
37	STAT3	chr5:94910771-94910971	MCF10A-Er-Src	breast:	n/a	n/a
38	TAL1	chr5:94899241-94899489	K562	blood:	n/a	n/a
39	ZNF384	chr5:94899468-94899841	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:94901279-94901329	HNPCEpiC	eye:	n/a
2	chr5:94901279-94901329	BE2_C	brain:	n/a
3	chr5:94901279-94901329	HRE	kidney:	n/a
4	chr5:94901279-94901329	HCF	heart:	n/a
5	chr5:94901279-94901329	AG10803	skin:	n/a
6	chr5:94901279-94901329	Jurkat	blood:	n/a
7	chr5:94901279-94901329	GM12891	blood:	n/a
8	chr5:94901279-94901329	NH-A	brain:	n/a
9	chr5:94901279-94901329	Hela-S3	cervix:	n/a
10	chr5:94901279-94901329	NB4	blood:	n/a
11	chr5:94901279-94901329	ProgFib	skin:	n/a
12	chr5:94901279-94901329	A549	lung:	n/a
13	chr5:94901279-94901329	LNCaP	prostate:	n/a
14	chr5:94901279-94901329	HCPEpiC	choroid plexus:	n/a
15	chr5:94901279-94901329	T-47D	breast:	n/a
16	chr5:94901279-94901329	NT2-D1	testis:	n/a
17	chr5:94901279-94901329	NHBE	bronchial:	n/a
18	chr5:94901279-94901329	AG09309	skin:	n/a
19	chr5:94901279-94901329	HRPEpiC	eye:	n/a
20	chr5:94901279-94901329	PANC-1	pancreas:	n/a
21	chr5:94901279-94901329	HMEC	breast:	n/a
22	chr5:94901279-94901329	U87	brain:	n/a
23	chr5:94901279-94901329	ovcar-3	ovarian:	n/a
24	chr5:94901279-94901329	NHDF-neo	bronchial:	n/a
25	chr5:94901279-94901329	HL-60	blood:	n/a
26	chr5:94901279-94901329	CMK	blood:	n/a
27	chr5:94901279-94901329	IMR90	lung:	fetal
28	chr5:94901279-94901329	SK-N-MC	brain:	n/a
29	chr5:94901279-94901329	Caco-2	colon:	n/a
30	chr5:94901279-94901329	PFSK-1	brain:	n/a
31	chr5:94901279-94901329	RPTEC	kidney:	n/a
32	chr5:94901279-94901329	HEK293	kidney:	embryo
33	chr5:94901279-94901329	GM12878	blood:	n/a
34	chr5:94901279-94901329	GM19239	blood:	n/a
35	chr5:94901279-94901329	MCF10A-Er-Src	breast:	n/a
36	chr5:94901279-94901329	HUVEC	blood vessel:	n/a
37	chr5:94901279-94901329	SAEC	small airway:	n/a
38	chr5:94901279-94901329	Hepatocyte	liver:	n/a
39	chr5:94901279-94901329	AG09319	gingival:	n/a
40	chr5:94901279-94901329	SK-N-SH	brain:	n/a
41	chr5:94901279-94901329	HCT-116	colon:	n/a
42	chr5:94901279-94901329	HPAEpiC	pulmonary alveolar:	n/a
43	chr5:94901279-94901329	K562	blood:	n/a
44	chr5:94901279-94901329	HEEpiC	esophagus:	n/a
45	chr5:94901279-94901329	PrEC	prostate:	n/a
46	chr5:94901279-94901329	HAEpiC	amniotic membrane:	n/a
47	chr5:94901279-94901329	SK-N-SH_RA	brain:	n/a
48	chr5:94901279-94901329	AG04449	skin:	fetal
49	chr5:94901279-94901329	H1-hESC	embryonic stem cell:	embryo
50	chr5:94901279-94901329	GM12892	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:94893117..94894866-chr5:94974664..94977618,2	K562	blood:
2	chr5:94892921..94894446-chr5:94936701..94939146,2	K562	blood:
3	chr5:94895692..94898424-chr5:94902068..94903763,2	K562	blood:
4	chr5:94889255..94892254-chr5:94902983..94905843,2	K562	blood:
5	chr5:94856136..94858059-chr5:94897199..94899043,2	K562	blood:
6	chr5:94897161..94899128-chr5:94900453..94902701,3	K562	blood:
7	chr5:94910804..94914424-chr5:94915690..94919110,3	K562	blood:
8	chr5:94889492..94895025-chr5:94981557..94985063,8	K562	blood:
9	chr5:94907342..94909603-chr5:94913208..94915224,2	K562	blood:
10	chr5:94890271..94892404-chr5:94906433..94908089,2	K562	blood:
11	chr5:94897161..94899128-chr5:94900453..94902701,3	K562	blood:
12	chr5:94907342..94909603-chr5:94913208..94915224,2	K562	blood:
13	chr5:94892616..94895050-chr5:95181504..95183040,2	MCF-7	breast:
14	chr5:94895692..94898424-chr5:94902068..94903763,2	K562	blood:
15	chr5:94910804..94914424-chr5:94915690..94919110,3	K562	blood:
16	chr5:94889576..94892057-chr5:94893383..94894937,2	MCF-7	breast:

No data

Variant related genes	Relation type
TTC37	TF binding region
TTC37	CpG island
ENSG00000164291	chromatin interactions
ENSG00000175449	chromatin interactions
ENSG00000198677	chromatin interactions
ENSG00000212259	chromatin interactions

Extended variants
information (count: 744 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:744 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192346051	chr5:94894039-94894040	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs376693816	chr5:94894074-94894075	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs75474586	chr5:94894079-94894080	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs112837730	chr5:94894102-94894103	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs538283870	chr5:94894193-94894194	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs184836034	chr5:94894333-94894334	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs578168117	chr5:94894381-94894382	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs2545842	chr5:94894404-94894405	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs560442056	chr5:94894431-94894432	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs538710916	chr5:94894438-94894439	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs543141224	chr5:94894452-94894453	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs563004576	chr5:94894454-94894455	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs531715347	chr5:94894474-94894475	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs189609641	chr5:94894567-94894568	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs180744964	chr5:94894574-94894575	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs138927498	chr5:94894583-94894584	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs184427789	chr5:94894593-94894594	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs370567929	chr5:94894602-94894603	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs567343700	chr5:94894610-94894611	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs536079434	chr5:94894624-94894625	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs189659635	chr5:94894631-94894632	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs367707297	chr5:94894642-94894643	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs536298537	chr5:94894655-94894656	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs538369842	chr5:94894666-94894667	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs558234767	chr5:94894706-94894707	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs181300705	chr5:94894737-94894738	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs534181299	chr5:94894761-94894762	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs554497143	chr5:94894799-94894800	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs370159154	chr5:94894805-94894806	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs186716716	chr5:94894818-94894819	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs574336550	chr5:94894823-94894824	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs377554483	chr5:94894827-94894828	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs141470388	chr5:94894834-94894835	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs35311126	chr5:94894857-94894858	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs191563988	chr5:94894871-94894872	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs576569980	chr5:94894890-94894891	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs181628439	chr5:94894892-94894893	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs565084338	chr5:94894899-94894900	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs186190652	chr5:94894988-94894989	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs558757160	chr5:94895014-94895015	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs61133215	chr5:94895039-94895040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190984529	chr5:94895049-94895050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182055808	chr5:94895065-94895066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187628246	chr5:94895108-94895109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532039079	chr5:94895114-94895115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552253946	chr5:94895119-94895120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565538238	chr5:94895124-94895125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534653889	chr5:94895196-94895197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556140215	chr5:94895388-94895389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs75484440	chr5:94895430-94895431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	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
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Williams Syndrome	20824207	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	20967226	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:271 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94891400-94900200	Weak transcription	Gastric	stomach
2	chr5:94891800-94900200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr5:94891800-94902800	Weak transcription	Fetal Muscle Trunk	muscle
4	chr5:94892000-94906200	Weak transcription	Brain Hippocampus Middle	brain
5	chr5:94892200-94894200	Enhancers	Osteobl	bone
6	chr5:94892200-94900200	Weak transcription	Fetal Brain Female	brain
7	chr5:94892200-94902000	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr5:94892200-94902400	Weak transcription	Adipose Nuclei	Adipose
9	chr5:94892200-94903000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:94892200-94904400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr5:94892200-94904400	Weak transcription	Aorta	Aorta
12	chr5:94892200-94906000	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr5:94892200-94906800	Weak transcription	Fetal Kidney	kidney
14	chr5:94892200-94907200	Weak transcription	Rectal Smooth Muscle	rectum
15	chr5:94892200-94907400	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr5:94892200-94934400	Weak transcription	Fetal Stomach	stomach
17	chr5:94892200-94936600	Weak transcription	Fetal Lung	lung
18	chr5:94892400-94897000	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr5:94892400-94900200	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr5:94892400-94900400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr5:94892400-94901400	Weak transcription	Primary T cells from cord blood	blood
22	chr5:94892400-94902000	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr5:94892400-94902000	Weak transcription	Liver	Liver
24	chr5:94892400-94902200	Weak transcription	Primary T cells fromperipheralblood	blood
25	chr5:94892400-94902400	Weak transcription	Primary hematopoietic stem cells	blood
26	chr5:94892400-94902400	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr5:94892400-94902400	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr5:94892400-94902600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr5:94892400-94902600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr5:94892400-94902600	Weak transcription	Primary B cells from cord blood	blood
31	chr5:94892400-94902600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr5:94892400-94902800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr5:94892400-94902800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr5:94892400-94902800	Weak transcription	Left Ventricle	heart
35	chr5:94892400-94902800	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr5:94892400-94902800	Weak transcription	GM12878-XiMat	blood
37	chr5:94892400-94903000	Weak transcription	Primary B cells from peripheral blood	blood
38	chr5:94892400-94903000	Weak transcription	Primary T helper cells PMA-I stimulated	--
39	chr5:94892400-94903000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr5:94892400-94903400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr5:94892400-94903400	Weak transcription	Fetal Intestine Large	intestine
42	chr5:94892400-94904200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr5:94892400-94904400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr5:94892400-94904400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr5:94892400-94905600	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr5:94892400-94905800	Weak transcription	Brain Cingulate Gyrus	brain
47	chr5:94892400-94906000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr5:94892400-94906600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr5:94892400-94907600	Weak transcription	Colon Smooth Muscle	Colon
50	chr5:94892400-94908800	Weak transcription	HepG2	liver

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