Variant report

Variant	esv3459837
Chromosome Location	chr2:152798478-152799263
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:152793920..152795775-chr2:152797022..152799069,2	K562	blood:
2	chr2:152683465..152686102-chr2:152798913..152801976,3	MCF-7	breast:
3	chr2:152789335..152791707-chr2:152796780..152799093,2	K562	blood:

Variant related genes	Relation type
ENSG00000162980	chromatin interactions

Extended variants
information (count: 22 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561675572	chr2:152798529-152798530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs544326736	chr2:152798666-152798667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138938706	chr2:152798717-152798718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556400612	chr2:152798743-152798744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547338749	chr2:152798751-152798752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562063943	chr2:152798777-152798778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573733158	chr2:152798778-152798779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112324492	chr2:152798816-152798817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146317856	chr2:152798830-152798831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs189832158	chr2:152798831-152798832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs138369117	chr2:152798871-152798872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113055027	chr2:152798899-152798900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566246110	chr2:152798910-152798911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535351591	chr2:152798929-152798930	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs369686975	chr2:152799040-152799041	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs533036969	chr2:152799080-152799081	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs144251461	chr2:152799120-152799121	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs537039966	chr2:152799129-152799130	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs182520691	chr2:152799141-152799142	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs185643451	chr2:152799232-152799233	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs541656053	chr2:152799233-152799234	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs190350247	chr2:152799261-152799262	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:48)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19156171	CNVD
Acute myeloid leukemia	18000384	CNVD
Autism	20808228	CNVD

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:152792800-152803200	Weak transcription	Brain Angular Gyrus	brain
2	chr2:152793600-152800000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr2:152794400-152803600	Weak transcription	Psoas Muscle	Psoas
4	chr2:152796400-152799800	Weak transcription	HepG2	liver
5	chr2:152797200-152803000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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