Variant report

Variant	nsv961032
Chromosome Location	chr18:14815108-14815933
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:45 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs578080584	chr18:14815153-14815154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540923347	chr18:14815155-14815156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560594893	chr18:14815162-14815163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113396131	chr18:14815166-14815167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528107695	chr18:14815172-14815173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372051104	chr18:14815202-14815203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541831815	chr18:14815222-14815223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113916490	chr18:14815275-14815276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34294835	chr18:14815302-14815303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561795041	chr18:14815304-14815305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34105185	chr18:14815326-14815327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530620177	chr18:14815339-14815340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550543151	chr18:14815345-14815346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs35343525	chr18:14815349-14815350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs34350627	chr18:14815351-14815352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35473967	chr18:14815369-14815370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570638661	chr18:14815376-14815377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532938969	chr18:14815391-14815392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546897613	chr18:14815446-14815447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566396572	chr18:14815450-14815451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35507615	chr18:14815460-14815461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535483822	chr18:14815473-14815474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555336046	chr18:14815489-14815490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114267641	chr18:14815491-14815492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144588563	chr18:14815522-14815523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35591265	chr18:14815527-14815528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192515128	chr18:14815536-14815537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183753958	chr18:14815548-14815549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540437165	chr18:14815564-14815565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35857040	chr18:14815576-14815577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs60767930	chr18:14815577-14815578	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs574366572	chr18:14815579-14815580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150924573	chr18:14815683-14815684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188781540	chr18:14815701-14815702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs11872871	chr18:14815713-14815714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544302146	chr18:14815723-14815724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563999474	chr18:14815726-14815727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533170146	chr18:14815733-14815734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546454571	chr18:14815759-14815760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560060660	chr18:14815801-14815802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140302490	chr18:14815819-14815820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144267187	chr18:14815838-14815839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566995279	chr18:14815866-14815867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534150400	chr18:14815867-14815868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568914954	chr18:14815900-14815901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:14798200-14817600	Weak transcription	Osteobl	bone
2	chr18:14799000-14817600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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