Variant report

Variant	esv19065
Chromosome Location	chr7:100634661-100635236
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 82 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:82 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61749518	chr7:100634667-100634668	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554591399	chr7:100634670-100634671	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576103280	chr7:100634677-100634678	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140854690	chr7:100634681-100634682	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs61742922	chr7:100634692-100634693	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1790	chr7:100634699-100634700	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs202009257	chr7:100634700-100634701	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs61742928	chr7:100634708-100634709	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530244792	chr7:100634721-100634722	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548382145	chr7:100634739-100634740	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs61742939	chr7:100634742-100634743	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs61742940	chr7:100634744-100634745	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs61742942	chr7:100634756-100634757	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs61742944	chr7:100634763-100634764	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570037739	chr7:100634781-100634782	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11770526	chr7:100634783-100634784	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs376756468	chr7:100634809-100634810	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs576749793	chr7:100634812-100634813	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs571182207	chr7:100634814-100634815	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs79178035	chr7:100634816-100634817	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs112140367	chr7:100634821-100634822	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs370655474	chr7:100634822-100634823	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs61745822	chr7:100634838-100634839	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs547605277	chr7:100634859-100634860	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs565728518	chr7:100634871-100634872	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs372917744	chr7:100634876-100634877	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs61745827	chr7:100634877-100634878	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs61745828	chr7:100634879-100634880	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs376044971	chr7:100634881-100634882	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs73168377	chr7:100634882-100634883	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs182230578	chr7:100634886-100634887	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs117387753	chr7:100634887-100634888	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs186796962	chr7:100634891-100634892	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs201384124	chr7:100634892-100634893	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs200985690	chr7:100634893-100634894	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs201915926	chr7:100634901-100634902	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs61747424	chr7:100634905-100634906	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs200343829	chr7:100634907-100634908	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs201081908	chr7:100634921-100634922	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs199720463	chr7:100634922-100634923	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs182707377	chr7:100634933-100634934	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs371038165	chr7:100634943-100634944	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs375071799	chr7:100634949-100634950	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs4370452	chr7:100634964-100634965	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs541344353	chr7:100634965-100634966	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs368399966	chr7:100634972-100634973	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs559934901	chr7:100634989-100634990	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs372552928	chr7:100634991-100634992	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs375207510	chr7:100635007-100635008	ZNF genes & repeats Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs542320663	chr7:100635014-100635015	ZNF genes & repeats Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100625000-100634800	Weak transcription	Spleen	Spleen
2	chr7:100625600-100635000	Weak transcription	Right Atrium	heart
3	chr7:100633200-100637800	Strong transcription	Rectal Mucosa Donor 31	rectum
4	chr7:100633400-100635400	Strong transcription	Rectal Mucosa Donor 29	rectum
5	chr7:100633400-100636400	Strong transcription	Sigmoid Colon	Sigmoid Colon
6	chr7:100634200-100635000	Weak transcription	Rectal Smooth Muscle	rectum
7	chr7:100634200-100635600	Strong transcription	Colonic Mucosa	Colon
8	chr7:100634800-100635800	ZNF genes & repeats	Spleen	Spleen
9	chr7:100635000-100635200	Bivalent Enhancer	Fetal Stomach	stomach
10	chr7:100635000-100635400	ZNF genes & repeats	Gastric	stomach
11	chr7:100635000-100635800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr7:100635000-100635800	ZNF genes & repeats	Rectal Smooth Muscle	rectum
13	chr7:100635000-100635800	ZNF genes & repeats	Right Atrium	heart

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