Variant report
Variant | nsv1041927 |
---|---|
Chromosome Location | chr11:55376486-55497053 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:552)
- CpG islands (count:367)
- Chromatin interactive region (count:1)
- LncRNA region (count:2)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr11:55431152-55431202 | NB4 | blood: | n/a |
2 | chr11:55431152-55431202 | NB4 | blood: | n/a |
3 | chr11:55431584-55431634 | IMR90 | lung: | fetal |
4 | chr11:55417018-55417068 | BE2_C | brain: | n/a |
5 | chr11:55431152-55431202 | HCT-116 | colon: | n/a |
6 | chr11:55418816-55418866 | GM12891 | blood: | n/a |
7 | chr11:55417018-55417068 | HNPCEpiC | eye: | n/a |
8 | chr11:55418816-55418866 | HRPEpiC | eye: | n/a |
9 | chr11:55431584-55431634 | GM12878 | blood: | n/a |
10 | chr11:55431152-55431202 | MCF10A-Er-Src | breast: | n/a |
11 | chr11:55433005-55433055 | Hela-S3 | cervix: | n/a |
12 | chr11:55406191-55406241 | LNCaP | prostate: | n/a |
13 | chr11:55406191-55406241 | SK-N-SH_RA | brain: | n/a |
14 | chr11:55431584-55431634 | NH-A | brain: | n/a |
15 | chr11:55417018-55417068 | LNCaP | prostate: | n/a |
16 | chr11:55417018-55417068 | AG09309 | skin: | n/a |
17 | chr11:55417018-55417068 | MCF-7 | breast: | n/a |
18 | chr11:55431152-55431202 | SK-N-MC | brain: | n/a |
19 | chr11:55433005-55433055 | CMK | blood: | n/a |
20 | chr11:55418816-55418866 | AG09309 | skin: | n/a |
21 | chr11:55418816-55418866 | ECC-1 | luminal epithelium: | n/a |
22 | chr11:55418816-55418866 | CMK | blood: | n/a |
23 | chr11:55431584-55431634 | SKMC | muscle: | n/a |
24 | chr11:55433005-55433055 | U87 | brain: | n/a |
25 | chr11:55418816-55418866 | HCM | heart: | n/a |
26 | chr11:55431152-55431202 | HIPEpiC | eye: | n/a |
27 | chr11:55433005-55433055 | RPTEC | kidney: | n/a |
28 | chr11:55417018-55417068 | HL-60 | blood: | n/a |
29 | chr11:55431152-55431202 | BJ | skin: | n/a |
30 | chr11:55418816-55418866 | ProgFib | skin: | n/a |
31 | chr11:55433005-55433055 | AG04450 | lung: | fetal |
32 | chr11:55431584-55431634 | ovcar-3 | ovarian: | n/a |
33 | chr11:55406191-55406241 | MCF10A-Er-Src | breast: | n/a |
34 | chr11:55433005-55433055 | HCT-116 | colon: | n/a |
35 | chr11:55431152-55431202 | SKMC | muscle: | n/a |
36 | chr11:55431584-55431634 | HCF | heart: | n/a |
37 | chr11:55406191-55406241 | Caco-2 | colon: | n/a |
38 | chr11:55431152-55431202 | SK-N-SH | brain: | n/a |
39 | chr11:55431152-55431202 | SK-N-SH_RA | brain: | n/a |
40 | chr11:55431584-55431634 | HCT-116 | colon: | n/a |
41 | chr11:55431584-55431634 | SK-N-SH_RA | brain: | n/a |
42 | chr11:55418816-55418866 | NHBE | bronchial: | n/a |
43 | chr11:55406191-55406241 | HCF | heart: | n/a |
44 | chr11:55418816-55418866 | Hela-S3 | cervix: | n/a |
45 | chr11:55433005-55433055 | AoSMC | blood vessel: | n/a |
46 | chr11:55418816-55418866 | SK-N-MC | brain: | n/a |
47 | chr11:55431584-55431634 | HEEpiC | esophagus: | n/a |
48 | chr11:55417018-55417068 | NT2-D1 | testis: | n/a |
49 | chr11:55406191-55406241 | NHBE | bronchial: | n/a |
50 | chr11:55418816-55418866 | T-47D | breast: | n/a |
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr11:55491735..55492235-chr19:6736783..6737284,2 | NB4 | blood: |
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-OR4C11-1 | chr11:55451617-55451701 | ENSG00000254804 |
2 | lnc-OR4C11-1 | chr11:55453377-55453636 | ENSG00000254804 |
No data |
No data |
Variant related genes | Relation type |
---|---|
OR4S2 | TF binding region |
OR4P4 | TF binding region |
OR4C6 | TF binding region |
ENSG00000254804 | TF binding region |
OR4C11 | TF binding region |
OR5D2P | TF binding region |
OR4V1P | TF binding region |
OR4P1P | TF binding region |
OR5D3P | TF binding region |
OR4S2 | CpG island |
OR4P4 | CpG island |
OR4C6 | CpG island |
ENSG00000254804 | CpG island |
OR4C11 | CpG island |
OR5D2P | CpG island |
OR4V1P | CpG island |
OR4P1P | CpG island |
OR5D3P | CpG island |
ENSG00000125734 | chromatin interactions |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs542294519 | chr11:55395828-55395829 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
2 | rs112479002 | chr11:55395846-55395847 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
3 | rs113205148 | chr11:55395860-55395861 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
4 | rs36062315 | chr11:55395886-55395887 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
5 | rs531353248 | chr11:55395899-55395900 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
6 | rs12364838 | chr11:55395922-55395923 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
7 | rs145473853 | chr11:55395935-55395936 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
8 | rs557751521 | chr11:55395939-55395940 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
9 | rs532821177 | chr11:55395941-55395942 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
10 | rs544127405 | chr11:55395948-55395949 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
11 | rs189955667 | chr11:55395966-55395967 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
12 | rs373896490 | chr11:55395970-55395971 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
13 | rs116162984 | chr11:55396018-55396019 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
14 | rs368155909 | chr11:55396031-55396032 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
15 | rs180804020 | chr11:55396040-55396041 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
16 | rs10897108 | chr11:55396041-55396042 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
17 | rs12361051 | chr11:55396055-55396056 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
18 | rs537149724 | chr11:55396061-55396062 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
19 | rs148842153 | chr11:55396079-55396080 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
20 | rs143517164 | chr11:55396080-55396081 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
21 | rs111341928 | chr11:55396107-55396108 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
22 | rs34553202 | chr11:55396184-55396185 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
23 | rs571186755 | chr11:55396195-55396196 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
24 | rs572293421 | chr11:55396207-55396208 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
25 | rs77038864 | chr11:55396235-55396236 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
26 | rs560725717 | chr11:55396238-55396239 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
27 | rs12421157 | chr11:55396301-55396302 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
28 | rs570626053 | chr11:55396302-55396303 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
29 | rs543560110 | chr11:55396343-55396344 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
30 | rs565449607 | chr11:55396368-55396369 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
31 | rs532729301 | chr11:55396378-55396379 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
32 | rs76794057 | chr11:55396399-55396400 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
33 | rs559985094 | chr11:55396426-55396427 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
34 | rs113279056 | chr11:55396470-55396471 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
35 | rs567012179 | chr11:55396487-55396488 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
36 | rs142219064 | chr11:55396507-55396508 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
37 | rs569957781 | chr11:55396527-55396528 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
38 | rs201168152 | chr11:55396536-55396537 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
39 | rs76788391 | chr11:55396545-55396546 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
40 | rs386373835 | chr11:55396546-55396547 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
41 | rs199776545 | chr11:55396547-55396548 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
42 | rs398115399 | chr11:55396551-55396552 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
43 | rs371343350 | chr11:55396552-55396553 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
44 | rs371169330 | chr11:55396555-55396556 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
45 | rs374139389 | chr11:55396556-55396557 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
46 | rs111406656 | chr11:55396575-55396576 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
47 | rs73469471 | chr11:55396613-55396614 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
48 | rs185170426 | chr11:55396622-55396623 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
49 | rs11230461 | chr11:55396672-55396673 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
50 | rs542192790 | chr11:55396673-55396674 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Wilms tumour | 21544195 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Gastric cancer | 17908304 | CNVD |
Multiple myeloma | 20724749 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Autism | 22495311 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
Non-small cell lung cancer | 21385341 | CNVD |
Intellectual disability | 22102821 | CNVD |
Renal cell carcinoma | 18194544 | CNVD |
Glioblastoma multiforme | 21138945 | CNVD |
Prostate cancer | 18632612 | CNVD |
Breast cancer | 21990379 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Lung cancer | 18438408 | CNVD |
Esophageal cancer | 21851588 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Breast cancer | 17142309 | CNVD |
Cancer | 20164919 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Non-syndromic sensorineural hearing loss | 15273396 | CNVD |
Glioblastoma multiforme | 22286061 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Cancer | 21637783 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Chronic lymphocytic leukemia | 21795749 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Neuroblastoma | 21484798 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Oral cancer | 21386901 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Breast cancer | 20837533 | CNVD |
Breast cancer | 21264507 | CNVD |
Cervical cancer | 21063398 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Liposarcoma | 21253554 | CNVD |
Neuroblastoma | 18923524 | CNVD |
Multiple myeloma | 16616336 | CNVD |
Neuroblastoma | 18664255 | CNVD |
Monoclonal gammopathy of undetermined significance | 17077331 | CNVD |
Multiple myeloma | 17077331 | CNVD |
Neuroblastoma | 17533364 | CNVD |
Breast cancer | 21364760 | CNVD |
Schizophrenia | 20967226 | CNVD |
Non-syndromic sensorineural hearing loss | 17122850 | CNVD |
Schizophrenia | 23813976 | CNVD |
Breast cancer | 22522925 | CNVD |
Melanoma | 20877625 | CNVD |
Pancreatic cancer | 17952125 | CNVD |
Non-syndromic sensorineural hearing loss | 21293372 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:55395800-55397000 | ZNF genes & repeats | HUES48 Cell Line | embryonic stem cell |
2 | chr11:55411800-55412000 | Active TSS | Fetal Brain Male | brain |
3 | chr11:55412000-55421200 | Weak transcription | Fetal Brain Male | brain |
4 | chr11:55414600-55415000 | ZNF genes & repeats | Rectal Mucosa Donor 29 | rectum |
5 | chr11:55415000-55416200 | Weak transcription | Rectal Mucosa Donor 29 | rectum |
6 | chr11:55416200-55416400 | ZNF genes & repeats | Rectal Mucosa Donor 29 | rectum |
7 | chr11:55421200-55421600 | Active TSS | Fetal Brain Male | brain |
8 | chr11:55425800-55426600 | Enhancers | GM12878-XiMat | blood |
9 | chr11:55426200-55426400 | Enhancers | Rectal Mucosa Donor 29 | rectum |
10 | chr11:55451200-55453000 | ZNF genes & repeats | HUES48 Cell Line | embryonic stem cell |
11 | chr11:55453400-55454000 | Active TSS | ES-I3 Cell Line | embryonic stem cell |