Variant report

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5902757	chrX:77230978-77230979	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:39)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Astrocytoma	17387387	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	21979893	CNVD
Schizophrenia	23904455	CNVD
Olfactory neuroblastoma	18408657	CNVD
infertile	22614455	CNVD
Acute myeloid leukemia	20729466	CNVD
Autism	22495311	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Follicular lymphoma	20505157	CNVD
primary effusion lymphomas	17116491	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	22429812	CNVD
Cancer	16751803	CNVD
Breast cancer	21611746	CNVD
Premature ovarian failure	20952765	CNVD
Astrocytoma	22246337	CNVD
Mental retardation	17339581	CNVD
Breast cancer	21364760	CNVD
Alcoholism	21790672	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:77209800-77236400	Weak transcription	Primary hematopoietic stem cells	blood
2	chrX:77217400-77240200	Weak transcription	Primary B cells from peripheral blood	blood
3	chrX:77218000-77253800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chrX:77218200-77240400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chrX:77218200-77289000	Weak transcription	Primary T cells fromperipheralblood	blood
6	chrX:77220400-77232800	Weak transcription	Primary B cells from cord blood	blood
7	chrX:77220400-77237400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chrX:77223600-77238800	Weak transcription	Fetal Intestine Small	intestine
9	chrX:77224000-77268200	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chrX:77228200-77231000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chrX:77228800-77231400	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chrX:77228800-77231400	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chrX:77228800-77231600	Weak transcription	Stomach Smooth Muscle	stomach
14	chrX:77229200-77302200	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chrX:77230600-77233800	Enhancers	Hela-S3	cervix

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