Variant report

Variant	nsv528122
Chromosome Location	chr7:2955097-2976767
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:390)
CpG islands
(count:1160)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:390 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:2973742-2974089	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr7:2973786-2974076	A549	lung:	n/a	n/a
3	CEBPB	chr7:2973811-2974021	IMR90	lung:	n/a	n/a
4	CEBPB	chr7:2973631-2974175	A549	lung:	n/a	n/a
5	CEBPB	chr7:2970586-2970758	HepG2	liver:	n/a	chr7:2970723-2970734
6	CEBPD	chr7:2959971-2960680	K562	blood:	n/a	n/a
7	CEBPD	chr7:2960051-2960504	K562	blood:	n/a	n/a
8	CHD1	chr7:2959808-2959815	GM12878	blood:	n/a	n/a
9	CHD2	chr7:2974010-2974011	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr7:2955080-2955230	GM12864	blood:	n/a	chr7:2955118-2955127 chr7:2955168-2955176 chr7:2955165-2955183 chr7:2955168-2955181
11	CTCF	chr7:2968500-2968650	SK-N-SH_RA	brain:	n/a	chr7:2968635-2968643
12	CTCF	chr7:2974020-2974170	AoAF	blood vessel:	n/a	n/a
13	CTCF	chr7:2961580-2961730	BE2_C	brain:	n/a	n/a
14	CTCF	chr7:2961380-2961530	HAc	cerebellar:	n/a	n/a
15	CTCF	chr7:2961520-2961670	GM06990	blood:	n/a	n/a
16	CTCF	chr7:2973900-2974050	RPTEC	kidney:	n/a	chr7:2974018-2974031
17	CTCF	chr7:2961552-2961675	MCF-7	breast:	n/a	n/a
18	CTCF	chr7:2961340-2961490	A549	lung:	n/a	n/a
19	CTCF	chr7:2974020-2974170	NHEK	skin:	n/a	n/a
20	CTCF	chr7:2973960-2974110	HCPEpiC	choroid plexus:	n/a	chr7:2974018-2974031
21	CTCF	chr7:2973900-2974050	HCT-116	colon:	n/a	chr7:2974018-2974031
22	CTCF	chr7:2961500-2961650	HCFaa	heart:	n/a	n/a
23	CTCF	chr7:2961549-2961679	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr7:2961520-2961670	HMF	breast:	n/a	n/a
25	CTCF	chr7:2966939-2967005	GM19240	blood:	n/a	n/a
26	CTCF	chr7:2961520-2961670	GM12875	blood:	n/a	n/a
27	CTCF	chr7:2961540-2961690	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr7:2961500-2961650	HCM	heart:	n/a	n/a
29	CTCF	chr7:2966896-2966957	GM19238	blood:	n/a	chr7:2966932-2966945 chr7:2966930-2966948
30	CTCF	chr7:2961520-2961670	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr7:2961540-2961690	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr7:2966800-2966950	GM12868	blood:	n/a	chr7:2966932-2966945 chr7:2966930-2966948
33	CTCF	chr7:2961550-2961683	GM12878	blood:	n/a	n/a
34	CTCF	chr7:2973940-2974090	RPTEC	kidney:	n/a	chr7:2974018-2974031
35	CTCF	chr7:2961520-2961670	RPTEC	kidney:	n/a	n/a
36	CTCF	chr7:2974000-2974150	HMEC	breast:	n/a	chr7:2974018-2974031
37	CTCF	chr7:2961520-2961670	NHEK	skin:	n/a	n/a
38	CTCF	chr7:2973960-2974110	AG04450	lung:	n/a	chr7:2974018-2974031
39	CTCF	chr7:2961481-2961680	K562	blood:	n/a	n/a
40	CTCF	chr7:2961525-2961704	A549	lung:	n/a	n/a
41	CTCF	chr7:2960660-2960810	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr7:2961340-2961490	AG04450	lung:	n/a	n/a
43	CTCF	chr7:2961505-2961719	A549	lung:	n/a	n/a
44	CTCF	chr7:2973940-2974090	HBMEC	blood vessel:	n/a	chr7:2974018-2974031
45	CTCF	chr7:2961540-2961690	AG04449	skin:	n/a	n/a
46	CTCF	chr7:2973820-2973970	HCT-116	colon:	n/a	n/a
47	CTCF	chr7:2961493-2961709	IMR90	lung:	n/a	n/a
48	CTCF	chr7:2961420-2961570	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr7:2974020-2974170	AG09309	skin:	n/a	n/a
50	CTCF	chr7:2973960-2974110	HPF	lung:	n/a	chr7:2974018-2974031

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:2968316-2968366	HAEpiC	amniotic membrane:	n/a
2	chr7:2968316-2968366	HAEpiC	amniotic membrane:	n/a
3	chr7:2968627-2968677	RPTEC	kidney:	n/a
4	chr7:2962845-2962895	HIPEpiC	eye:	n/a
5	chr7:2968627-2968677	MCF-7	breast:	n/a
6	chr7:2958317-2958367	SK-N-SH_RA	brain:	n/a
7	chr7:2962240-2962290	HepG2	liver:	n/a
8	chr7:2972392-2972442	HEK293	kidney:	embryo
9	chr7:2962795-2962845	ECC-1	luminal epithelium:	n/a
10	chr7:2967973-2968023	T-47D	breast:	n/a
11	chr7:2959121-2959171	PrEC	prostate:	n/a
12	chr7:2958284-2958334	HMEC	breast:	n/a
13	chr7:2972073-2972123	SAEC	small airway:	n/a
14	chr7:2968627-2968677	Hepatocyte	liver:	n/a
15	chr7:2968595-2968645	CMK	blood:	n/a
16	chr7:2968627-2968677	T-47D	breast:	n/a
17	chr7:2967973-2968023	NH-A	brain:	n/a
18	chr7:2962373-2962423	AG09309	skin:	n/a
19	chr7:2958284-2958334	HepG2	liver:	n/a
20	chr7:2962795-2962845	HPAEpiC	pulmonary alveolar:	n/a
21	chr7:2962845-2962895	BE2_C	brain:	n/a
22	chr7:2962240-2962290	ovcar-3	ovarian:	n/a
23	chr7:2959105-2959155	ECC-1	luminal epithelium:	n/a
24	chr7:2962304-2962354	AG04449	skin:	fetal
25	chr7:2972392-2972442	SKMC	muscle:	n/a
26	chr7:2968559-2968609	PrEC	prostate:	n/a
27	chr7:2968595-2968645	NH-A	brain:	n/a
28	chr7:2959067-2959117	SKMC	muscle:	n/a
29	chr7:2972073-2972123	HCPEpiC	choroid plexus:	n/a
30	chr7:2968595-2968645	GM19239	blood:	n/a
31	chr7:2968316-2968366	HNPCEpiC	eye:	n/a
32	chr7:2971898-2971948	AG04449	skin:	fetal
33	chr7:2959105-2959155	SK-N-SH	brain:	n/a
34	chr7:2972073-2972123	HRPEpiC	eye:	n/a
35	chr7:2971898-2971948	GM12892	blood:	n/a
36	chr7:2967973-2968023	HepG2	liver:	n/a
37	chr7:2959067-2959117	NHDF-neo	bronchial:	n/a
38	chr7:2959105-2959155	SK-N-SH_RA	brain:	n/a
39	chr7:2967973-2968023	AoSMC	blood vessel:	n/a
40	chr7:2962373-2962423	GM12891	blood:	n/a
41	chr7:2958317-2958367	HepG2	liver:	n/a
42	chr7:2962845-2962895	HRE	kidney:	n/a
43	chr7:2959121-2959171	SK-N-SH_RA	brain:	n/a
44	chr7:2962304-2962354	NHBE	bronchial:	n/a
45	chr7:2959105-2959155	MCF10A-Er-Src	breast:	n/a
46	chr7:2972073-2972123	HepG2	liver:	n/a
47	chr7:2959067-2959117	MCF-7	breast:	n/a
48	chr7:2972392-2972442	A549	lung:	n/a
49	chr7:2958284-2958334	GM19239	blood:	n/a
50	chr7:2958317-2958367	GM06990	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:2961215..2963886-chr7:2968624..2970785,2	K562	blood:
2	chr7:2958335..2961015-chr7:2975473..2978226,3	MCF-7	breast:
3	chr7:2956076..2958556-chr7:2973835..2976275,2	K562	blood:
4	chr7:2912565..2914175-chr7:2952368..2955309,3	MCF-7	breast:
5	chr7:2963250..2965630-chr7:2965961..2967966,2	MCF-7	breast:
6	chr7:2953518..2955325-chr7:2956793..2958637,3	K562	blood:
7	chr7:2951702..2953400-chr7:2956754..2958330,2	K562	blood:
8	chr7:2961215..2963886-chr7:2968624..2971671,3	K562	blood:
9	chr7:2912665..2915404-chr7:2954032..2956544,2	MCF-7	breast:
10	chr7:2963250..2965630-chr7:2965961..2967966,2	MCF-7	breast:
11	chr7:2961215..2963886-chr7:2968624..2970785,2	K562	blood:
12	chr7:2956076..2958556-chr7:2973835..2976275,2	K562	blood:
13	chr7:2975475..2978008-chr7:2979225..2981624,2	K562	blood:
14	chr7:2958335..2961015-chr7:2975473..2978226,3	MCF-7	breast:
15	chr7:2968286..2971132-chr7:2974565..2976842,2	MCF-7	breast:
16	chr7:2961215..2963886-chr7:2968624..2971671,3	K562	blood:
17	chr7:2950966..2953401-chr7:2956155..2958518,2	MCF-7	breast:
18	chr7:2953518..2955325-chr7:2956793..2958637,3	K562	blood:

No data

Variant related genes	Relation type
CARD11	TF binding region
CARD11	CpG island
ENSG00000198286	chromatin interactions

Extended variants
information (count: 1262 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1262 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2301920	chr7:2955097-2955098	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs41458744	chr7:2955151-2955152	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs41455246	chr7:2955221-2955222	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs535894771	chr7:2955229-2955230	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185130640	chr7:2955241-2955242	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143366390	chr7:2955257-2955258	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537226552	chr7:2955267-2955268	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575698967	chr7:2955268-2955269	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs41435148	chr7:2955281-2955282	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs147538088	chr7:2955290-2955291	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs578128389	chr7:2955291-2955292	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs41456244	chr7:2955307-2955308	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560453413	chr7:2955340-2955341	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529540897	chr7:2955445-2955446	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540282430	chr7:2955451-2955452	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112084056	chr7:2955471-2955472	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs41336352	chr7:2955476-2955477	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs551699660	chr7:2955529-2955530	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570863308	chr7:2955535-2955536	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538200237	chr7:2955567-2955568	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562304126	chr7:2955619-2955620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556399214	chr7:2955624-2955625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs116370285	chr7:2955648-2955649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115670241	chr7:2955679-2955680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571298927	chr7:2955699-2955700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs41509646	chr7:2955709-2955710	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs145576104	chr7:2955758-2955759	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372393459	chr7:2955821-2955822	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147582399	chr7:2955826-2955827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536505153	chr7:2955843-2955844	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139534344	chr7:2955897-2955898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192164496	chr7:2955916-2955917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538214911	chr7:2955940-2955941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149663802	chr7:2955948-2955949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs145484095	chr7:2955950-2955951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148824917	chr7:2955975-2955976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183886591	chr7:2955990-2955991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574001908	chr7:2956001-2956002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145517250	chr7:2956022-2956023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs76151260	chr7:2956023-2956024	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146521906	chr7:2956036-2956037	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs57846608	chr7:2956056-2956057	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs2679261	chr7:2956085-2956086	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs527382451	chr7:2956096-2956097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547619391	chr7:2956111-2956112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561026390	chr7:2956205-2956206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140980013	chr7:2956214-2956215	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs6461700	chr7:2956217-2956218	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs186809948	chr7:2956218-2956219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558699252	chr7:2956224-2956225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:401 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:2926800-2968000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:2933400-2987200	Weak transcription	Gastric	stomach
3	chr7:2943400-2961200	Weak transcription	Duodenum Mucosa	Duodenum
4	chr7:2943800-2988200	Strong transcription	Primary T cells from cord blood	blood
5	chr7:2944000-2988200	Strong transcription	Primary T helper cells fromperipheralblood	blood
6	chr7:2944200-2981800	Strong transcription	Primary T cells fromperipheralblood	blood
7	chr7:2944200-2987400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr7:2944400-2986800	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr7:2944400-2987400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr7:2944400-2988400	Strong transcription	Primary T helper cells PMA-I stimulated	--
11	chr7:2944800-2964200	Strong transcription	Primary T helper naive cells from peripheral blood	blood
12	chr7:2944800-2987400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr7:2944800-2987600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr7:2944800-2987600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr7:2945400-2961800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:2945400-2961800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr7:2945400-2987400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr7:2945800-2959400	Weak transcription	HUVEC	blood vessel
19	chr7:2947600-2964200	Strong transcription	Thymus	Thymus
20	chr7:2948400-2961600	Weak transcription	Rectal Smooth Muscle	rectum
21	chr7:2948400-2980600	Strong transcription	Primary B cells from peripheral blood	blood
22	chr7:2948800-2959000	Weak transcription	Esophagus	oesophagus
23	chr7:2948800-2961000	Weak transcription	Right Atrium	heart
24	chr7:2949000-2966400	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr7:2949400-2956800	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr7:2949400-2957400	Strong transcription	Primary B cells from cord blood	blood
27	chr7:2949800-2958400	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr7:2949800-2977400	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr7:2951000-2955400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr7:2951000-2988400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr7:2951400-2960600	Weak transcription	Brain Hippocampus Middle	brain
32	chr7:2951800-2956000	Weak transcription	Primary hematopoietic stem cells	blood
33	chr7:2952000-2955200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr7:2952200-2955800	Weak transcription	GM12878-XiMat	blood
35	chr7:2952600-2956400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr7:2953200-2957000	Strong transcription	Fetal Thymus	thymus
37	chr7:2953400-2962800	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr7:2953600-2955600	Strong transcription	Fetal Intestine Small	intestine
39	chr7:2954000-2984800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr7:2954600-2955400	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chr7:2954600-2956600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr7:2954600-2959600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr7:2954800-2955200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr7:2954800-2955800	Strong transcription	Primary T killer memory cells from peripheral blood	blood
45	chr7:2955000-2955400	Genic enhancers	Spleen	Spleen
46	chr7:2955200-2955600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr7:2955200-2957000	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr7:2955200-2960600	Weak transcription	NHEK	skin
49	chr7:2955400-2955600	Strong transcription	Spleen	Spleen
50	chr7:2955400-2957800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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