Variant report
Variant | esv2762213 |
---|---|
Chromosome Location | chr1:196455365-196455824 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:4)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:4 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:196450695..196453991-chr1:196455427..196457877,3 | K562 | blood: | |
2 | chr1:196448595..196456381-chr1:196458214..196462920,9 | K562 | blood: | |
3 | chr1:196448856..196453298-chr1:196454594..196458706,6 | K562 | blood: | |
4 | chr1:196440873..196444078-chr1:196452789..196457047,3 | K562 | blood: |
No data |
No data |
No data |
No data |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs7531491 | chr1:196455365-196455366 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
2 | rs540049201 | chr1:196455433-196455434 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
3 | rs533333288 | chr1:196455465-196455466 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
4 | rs182800818 | chr1:196455497-196455498 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
5 | rs551078082 | chr1:196455560-196455561 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
6 | rs75573585 | chr1:196455578-196455579 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
7 | rs550294645 | chr1:196455641-196455642 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
8 | rs187087736 | chr1:196455644-196455645 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
9 | rs10922073 | chr1:196455696-196455697 | Weak transcription Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | mRNA abundance |
10 | rs190139228 | chr1:196455705-196455706 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
11 | rs535832420 | chr1:196455723-196455724 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
12 | rs182883150 | chr1:196455769-196455770 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
13 | rs75219798 | chr1:196455808-196455809 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
14 | rs533548326 | chr1:196455816-196455817 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs10737671 | chr1:196455824-196455825 | Weak transcription Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
Disease | PMID | Source |
---|---|---|
Breast cancer | 17603634 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
HIV/AIDS | 22032296 | CNVD |
Schizophrenia | 19415332 | CNVD |
Autism | 22495311 | CNVD |
Liposarcoma | 21253554 | CNVD |
Burkitt''s lymphoma | 18698080 | CNVD |
Melanoma | 18172304 | CNVD |
Rett syndrome | 21593744 | CNVD |
Cancer | 20164919 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Acute lymphoblastic leukemia | 17443227 | CNVD |
Wilms tumour | 21544195 | CNVD |
Breast cancer | 17133270 | CNVD |
Carcinoma ex pleomorphic adenoma | 18828159 | CNVD |
Non-small cell lung cancer | 21044232 | CNVD |
Cervical cancer | 21063398 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Astrocytoma | 17387387 | CNVD |
Breast cancer | 20632083 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Gastrointestinal stromal cancer | 20470368 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Hepatocellular carcinoma | 22174799 | CNVD |
Medulloblastoma | 21292688 | CNVD |
Phyllodes tumor | 17334353 | CNVD |
Breast cancer | 21264507 | CNVD |
Multiple myeloma | 21628407 | CNVD |
Cancer | 16751803 | CNVD |
Prostate cancer | 16705090 | CNVD |
Neuroblastoma | 19435921 | CNVD |
Breast cancer | 17850661 | CNVD |
Breast cancer | 16461572 | CNVD |
Intracranial tumor | 16823260 | CNVD |
Medulloblastoma | 18056178 | CNVD |
Monoclonal gammopathy of undetermined significance | 17077331 | CNVD |
Primary mediastinal b-cell lymphoma | 17728785 | CNVD |
Colorectal cancer | 16272173 | CNVD |
Acute lymphoblastic leukemia | 21098271 | CNVD |
Neuroblastoma | 21899760 | CNVD |
Ovarian neoplasms | 16753589 | CNVD |
Glioblastoma multiforme | 17002787 | CNVD |
Breast cancer | 21858162 | CNVD |
Non-small cell lung cancer | 21385341 | CNVD |
Acute lymphoblastic leukemia | 21980252 | CNVD |
Breast cancer | 16608533 | CNVD |
Ewing''s sarcoma | 22429812 | CNVD |
Acute promyelocytic leukemia | 19109227 | CNVD |
Hepatocellular carcinoma | 18803288 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Breast cancer | 17001317 | CNVD |
Acute myeloid leukemia | 21251322 | CNVD |
Multiple myeloma | 17550852 | CNVD |
Prostate cancer | 18632612 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Testicular germ cell tumor | 18059402 | CNVD |
Ependymoma | 18628472 | CNVD |
Leukemia | 18628472 | CNVD |
Neuroblastoma | 18923191 | CNVD |
Acute lymphoblastic leukemia | 19100363 | CNVD |
Breast cancer | 21509527 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Lung cancer | 18438408 | CNVD |
Metanephric adenoma | 20802469 | CNVD |
Breast cancer | 21611746 | CNVD |
primary effusion lymphomas | 17116491 | CNVD |
Breast cancer | 17393978 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Acute lymphoblastic leukemia | 22237106 | CNVD |
Non-small cell lung cancer | 19010865 | CNVD |
Mental retardation | 17847001 | CNVD |
Basal cell lymphoma | 17170743 | CNVD |
Follicular lymphoma | 17170743 | CNVD |
Trisomy 5 syndrome | 21098271 | CNVD |
Glioblastoma multiforme | 22286061 | CNVD |
Urothelial carcinoma | 21177765 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Breast cancer | 16272173 | CNVD |
Mental retardation | 21062444 | CNVD |
Liver carcinoma | 19366792 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Chordoma | 18071362 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Neuroblastoma | 20406844 | CNVD |
Non-syndromic sensorineural hearing loss | 21987784 | CNVD |
Breast cancer | 22522925 | CNVD |
Intellectual disability | 21811512 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:196420000-196460800 | Weak transcription | H1 Cell Line | embryonic stem cell |
2 | chr1:196434200-196459200 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
3 | chr1:196434600-196459600 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
4 | chr1:196436400-196485200 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
5 | chr1:196437400-196467800 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
6 | chr1:196447400-196458200 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
7 | chr1:196447800-196468000 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
8 | chr1:196448400-196457600 | Weak transcription | Fetal Kidney | kidney |
9 | chr1:196450000-196459800 | Weak transcription | Fetal Muscle Trunk | muscle |
10 | chr1:196450600-196462200 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
11 | chr1:196451200-196462200 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
12 | chr1:196451400-196467600 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
13 | chr1:196452800-196471200 | Weak transcription | Liver | Liver |
14 | chr1:196454400-196467400 | Weak transcription | Ovary | ovary |
15 | chr1:196455600-196456200 | Enhancers | HUVEC | blood vessel |