Variant report

Variant	nsv981576
Chromosome Location	chr7:128036949-128041507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr7:128038739-128038896	GM12878	blood:	n/a	n/a
2	BHLHE40	chr7:128038134-128038400	HepG2	liver:	n/a	n/a
3	BHLHE40	chr7:128038678-128038998	K562	blood:	n/a	n/a
4	BRCA1	chr7:128038725-128038925	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr7:128038798-128038880	K562	blood:	n/a	n/a
6	CEBPB	chr7:128038697-128038943	Hela-S3	cervix:	n/a	n/a
7	CHD1	chr7:128038662-128039072	IMR90	lung:	n/a	n/a
8	CHD2	chr7:128038763-128038916	GM12878	blood:	n/a	n/a
9	CHD2	chr7:128038687-128038918	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr7:128038620-128038770	A549	lung:	n/a	n/a
11	CTCF	chr7:128038641-128038927	HUVEC	blood vessel:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883
12	CTCF	chr7:128038567-128038972	A549	lung:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883 chr7:128038951-128038959
13	CTCF	chr7:128038626-128038930	NHEK	skin:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883
14	CTCF	chr7:128038666-128038902	ProgFib	skin:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883
15	CTCF	chr7:128038740-128038890	HAc	cerebellar:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883
16	CTCF	chr7:128038680-128038830	GM12872	blood:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796
17	CTCF	chr7:128038619-128038928	MCF-7	breast:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883
18	CTCF	chr7:128039318-128039426	LNCaP	prostate:	n/a	n/a
19	CTCF	chr7:128038720-128038870	HPAF	blood vessel:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796
20	CTCF	chr7:128038700-128038850	GM12869	blood:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796
21	CTCF	chr7:128038575-128039031	MCF-7	breast:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883 chr7:128038951-128038959
22	CTCF	chr7:128038457-128039263	A549	lung:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883 chr7:128038951-128038959
23	CTCF	chr7:128038591-128038982	IMR90	lung:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883 chr7:128038951-128038959
24	CTCF	chr7:128038720-128038870	HAc	cerebellar:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796
25	CTCF	chr7:128038740-128038890	MCF-7	breast:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883
26	CTCF	chr7:128038611-128038953	Spleen_OC	spleen:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883
27	CTCF	chr7:128038180-128038330	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr7:128038700-128038850	HCM	heart:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796
29	CTCF	chr7:128038502-128039016	A549	lung:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883 chr7:128038951-128038959
30	CTCF	chr7:128038720-128038870	GM12873	blood:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796
31	CTCF	chr7:128038612-128038944	GM19240	blood:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883
32	CTCF	chr7:128038720-128038870	NHEK	skin:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796
33	CTCF	chr7:128038720-128038870	NHDF-neo	bronchial:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796
34	CTCF	chr7:128038740-128038890	HMEC	breast:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883
35	CTCF	chr7:128038700-128038850	HCPEpiC	choroid plexus:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796
36	CTCF	chr7:128038700-128038850	GM06990	blood:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796
37	CTCF	chr7:128038609-128038611	GM12892	blood:	n/a	n/a
38	CTCF	chr7:128038700-128038850	GM12864	blood:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796
39	CTCF	chr7:128038240-128038390	NHEK	skin:	n/a	chr7:128038322-128038340
40	CTCF	chr7:128038546-128038950	HepG2	liver:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883
41	CTCF	chr7:128038649-128038939	MCF-7	breast:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883
42	CTCF	chr7:128038760-128038910	WI-38	lung:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883
43	CTCF	chr7:128038680-128038830	Hela-S3	cervix:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796
44	CTCF	chr7:128038720-128038870	Caco-2	colon:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796
45	CTCF	chr7:128038700-128038850	SAEC	small airway:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796
46	CTCF	chr7:128037720-128037870	AG09319	gingival:	n/a	n/a
47	CTCF	chr7:128038720-128038870	GM12871	blood:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796
48	CTCF	chr7:128038720-128038870	GM12878	blood:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796
49	CTCF	chr7:128038720-128038870	HVMF	connective:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796
50	CTCF	chr7:128038560-128039010	H1-hESC	embryonic stem cell:	n/a	chr7:128038785-128038803 chr7:128038787-128038808 chr7:128038789-128038796 chr7:128038875-128038883 chr7:128038951-128038959

No.	Distal block	Cell Line	Cell type
1	chr7:128038254..128039329-chr7:128065492..128067551,10	K562	blood:
2	chr7:128033560..128036202-chr7:128037168..128039895,3	MCF-7	breast:
3	chr7:127982050..127985267-chr7:128038524..128041227,4	K562	blood:
4	chr7:127982483..127985267-chr7:128038524..128041227,3	K562	blood:
5	chr7:128038309..128039271-chr7:128065515..128066612,14	MCF-7	breast:
6	chr7:128038860..128040622-chr7:128170673..128172607,2	MCF-7	breast:
7	chr7:128036870..128039033-chr7:128045766..128047569,2	MCF-7	breast:
8	chr7:128038366..128039235-chr7:128099168..128099837,2	K562	blood:
9	chr7:128038292..128039254-chr7:128066985..128067767,3	MCF-7	breast:
10	chr7:128040454..128042949-chr7:128095892..128097636,2	MCF-7	breast:
11	chr7:128036587..128038762-chr7:128050918..128052447,2	MCF-7	breast:
12	chr7:128038276..128039228-chr7:128065303..128066760,7	MCF-7	breast:
13	chr7:128038192..128041556-chr7:128094283..128098008,3	MCF-7	breast:

Variant related genes	Relation type
IMPDH1	TF binding region
ENSG00000135245	chromatin interactions
ENSG00000238750	chromatin interactions
ENSG00000106344	chromatin interactions
ENSG00000106348	chromatin interactions
ENSG00000273184	chromatin interactions
ENSG00000240758	chromatin interactions
ENSG00000273270	chromatin interactions
ENSG00000242588	chromatin interactions

Extended variants
information (count: 211 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:211 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373129667	chr7:128036959-128036960	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs182215710	chr7:128036960-128036961	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs377241514	chr7:128036961-128036962	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs200085694	chr7:128036970-128036971	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs544315308	chr7:128036971-128036972	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs72624962	chr7:128036972-128036973	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs369316633	chr7:128036977-128036978	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs577834994	chr7:128036978-128036979	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs149603914	chr7:128036987-128036988	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs373276383	chr7:128036994-128036995	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs61751223	chr7:128037009-128037010	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs148736020	chr7:128037011-128037012	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs72624961	chr7:128037043-128037044	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs200729507	chr7:128037044-128037045	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs376271750	chr7:128037048-128037049	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs374594472	chr7:128037050-128037051	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs371337802	chr7:128037056-128037057	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs147491964	chr7:128037057-128037058	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs72624960	chr7:128037072-128037073	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs374310214	chr7:128037099-128037100	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs138738090	chr7:128037181-128037182	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs138020240	chr7:128037205-128037206	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs397889755	chr7:128037206-128037207	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs549843482	chr7:128037213-128037214	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs571382355	chr7:128037215-128037216	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs370795168	chr7:128037219-128037220	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs573448556	chr7:128037221-128037222	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs377440501	chr7:128037222-128037223	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs547433988	chr7:128037226-128037227	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs566068478	chr7:128037242-128037243	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs539158808	chr7:128037280-128037281	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs533843977	chr7:128037331-128037332	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs555740605	chr7:128037363-128037364	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs191702901	chr7:128037458-128037459	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs141858269	chr7:128037481-128037482	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs183102805	chr7:128037518-128037519	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs577624594	chr7:128037531-128037532	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs545088227	chr7:128037559-128037560	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs7802305	chr7:128037627-128037628	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs146168341	chr7:128037656-128037657	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs541620942	chr7:128037663-128037664	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs137880459	chr7:128037705-128037706	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs555673050	chr7:128037747-128037748	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs145250164	chr7:128037793-128037794	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs186928537	chr7:128037795-128037796	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs531906357	chr7:128037855-128037856	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs543579040	chr7:128037862-128037863	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs372761432	chr7:128037895-128037896	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs374247128	chr7:128037910-128037911	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs375988596	chr7:128037930-128037931	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:260 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:128002400-128044400	Weak transcription	Right Atrium	heart
2	chr7:128027800-128042800	Weak transcription	Fetal Brain Male	brain
3	chr7:128028000-128045200	Weak transcription	Small Intestine	intestine
4	chr7:128028200-128037000	Weak transcription	Liver	Liver
5	chr7:128028400-128044600	Weak transcription	Fetal Heart	heart
6	chr7:128028800-128037200	Weak transcription	Primary B cells from cord blood	blood
7	chr7:128029200-128037400	Weak transcription	Fetal Kidney	kidney
8	chr7:128029400-128037000	Weak transcription	HSMM	muscle
9	chr7:128029400-128037000	Weak transcription	NH-A	brain
10	chr7:128029600-128044400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:128029800-128037200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr7:128030000-128043800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr7:128030200-128037000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr7:128030200-128037200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr7:128030200-128040000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr7:128030400-128037200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr7:128030400-128037400	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr7:128030400-128038400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr7:128031000-128043800	Strong transcription	Fetal Stomach	stomach
20	chr7:128031200-128037200	Weak transcription	Hela-S3	cervix
21	chr7:128031200-128038400	Strong transcription	Primary T cells from cord blood	blood
22	chr7:128031200-128039000	Strong transcription	Thymus	Thymus
23	chr7:128031200-128043200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr7:128031200-128043200	Strong transcription	A549	lung
25	chr7:128031200-128043600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr7:128031200-128043600	Strong transcription	Lung	lung
27	chr7:128031200-128044200	Strong transcription	Spleen	Spleen
28	chr7:128031400-128041800	Strong transcription	Muscle Satellite Cultured Cells	--
29	chr7:128031400-128043200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr7:128031400-128043200	Strong transcription	Gastric	stomach
31	chr7:128031400-128043600	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr7:128031400-128044000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr7:128031400-128044200	Strong transcription	Fetal Muscle Leg	muscle
34	chr7:128031600-128038400	Strong transcription	Fetal Muscle Trunk	muscle
35	chr7:128031600-128038600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:128031600-128040800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr7:128031600-128041400	Strong transcription	Stomach Smooth Muscle	stomach
38	chr7:128031600-128041600	Strong transcription	Brain Germinal Matrix	brain
39	chr7:128031600-128041800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr7:128031600-128042000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr7:128031600-128042000	Strong transcription	Right Ventricle	heart
42	chr7:128031600-128042200	Strong transcription	Fetal Brain Female	brain
43	chr7:128031600-128043200	Strong transcription	Primary T helper cells fromperipheralblood	blood
44	chr7:128031600-128043800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr7:128031600-128043800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr7:128031600-128043800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr7:128031600-128043800	Strong transcription	Adipose Nuclei	Adipose
48	chr7:128031600-128044400	Strong transcription	Fetal Intestine Small	intestine
49	chr7:128031800-128037400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr7:128031800-128038200	Weak transcription	Stomach Mucosa	stomach

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