Variant report

Variant	esv1810142
Chromosome Location	chr18:14784020-14815826
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD30B-8	chr18:14797660-14797688	NONHSAT058529
2	lnc-ANKRD30B-8	chr18:14808550-14808578	NONHSAT058529
3	lnc-ANKRD30B-8	chr18:14797781-14797853	NONHSAT058529
4	lnc-ANKRD30B-8	chr18:14808671-14808730	NONHSAT058529

Variant related genes	Relation type
GNPTAB	miRNA target sites
GNS	miRNA target sites
GOLGA3	miRNA target sites

Extended variants
information (count: 1402 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1402 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535936078	chr18:14784046-14784047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73427593	chr18:14784054-14784055	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs558353816	chr18:14784108-14784109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575813087	chr18:14784201-14784202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138530619	chr18:14784218-14784219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144059624	chr18:14784223-14784224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150693597	chr18:14784251-14784252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374442391	chr18:14784259-14784260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138681355	chr18:14784279-14784280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561097864	chr18:14784280-14784281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs367794933	chr18:14784319-14784320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574891466	chr18:14784341-14784342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201255823	chr18:14784360-14784361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563934770	chr18:14784362-14784363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374013941	chr18:14784405-14784406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs367855859	chr18:14784407-14784408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189761972	chr18:14784423-14784424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552944155	chr18:14784433-14784434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181736144	chr18:14784467-14784468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149361065	chr18:14784468-14784469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182059135	chr18:14784489-14784490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547387773	chr18:14784492-14784493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567138508	chr18:14784543-14784544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144730951	chr18:14784563-14784564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs187187107	chr18:14784593-14784594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139638843	chr18:14784608-14784609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191647321	chr18:14784621-14784622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561939260	chr18:14784650-14784651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143357191	chr18:14784659-14784660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565659740	chr18:14784666-14784667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377674891	chr18:14784722-14784723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112922655	chr18:14784723-14784724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554980767	chr18:14784742-14784743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188292117	chr18:14784767-14784768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543940934	chr18:14784768-14784769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12969951	chr18:14784793-14784794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577367732	chr18:14784798-14784799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546419548	chr18:14784811-14784812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs71176076	chr18:14784842-14784843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146811520	chr18:14784843-14784844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559954757	chr18:14784876-14784877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528818168	chr18:14784896-14784897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542139105	chr18:14784915-14784916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560987955	chr18:14784929-14784930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529648601	chr18:14784937-14784938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs193041051	chr18:14784945-14784946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374178455	chr18:14784958-14784959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532051060	chr18:14784959-14784960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73427594	chr18:14784975-14784976	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs565523089	chr18:14785019-14785020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:14779400-14796600	Weak transcription	Osteobl	bone
2	chr18:14796600-14798200	ZNF genes & repeats	Osteobl	bone
3	chr18:14797000-14797400	Enhancers	Placenta	Placenta
4	chr18:14797400-14798600	Weak transcription	Placenta	Placenta
5	chr18:14798200-14817600	Weak transcription	Osteobl	bone
6	chr18:14798600-14799000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr18:14798600-14799000	Enhancers	Placenta	Placenta
8	chr18:14799000-14817600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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