Variant report
Variant | nsv1016387 |
---|---|
Chromosome Location | chr8:104578389-104931853 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:2018)
- CpG islands (count:366)
- Chromatin interactive region (count:79)
- LncRNA region (count:3)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | ARID3A | chr8:104714631-104714831 | HepG2 | liver: | n/a | n/a |
2 | ATF1 | chr8:104664474-104664793 | K562 | blood: | n/a | n/a |
3 | ATF2 | chr8:104777901-104778321 | GM12878 | blood: | n/a | n/a |
4 | ATF2 | chr8:104636282-104636690 | H1-hESC | embryonic stem cell: | n/a | n/a |
5 | ATF2 | chr8:104719487-104719890 | H1-hESC | embryonic stem cell: | n/a | n/a |
6 | ATF2 | chr8:104777947-104778349 | GM12878 | blood: | n/a | n/a |
7 | ATF2 | chr8:104636219-104636718 | H1-hESC | embryonic stem cell: | n/a | n/a |
8 | ATF2 | chr8:104719616-104720089 | H1-hESC | embryonic stem cell: | n/a | n/a |
9 | BACH1 | chr8:104844129-104844147 | H1-hESC | embryonic stem cell: | n/a | n/a |
10 | BACH1 | chr8:104663267-104663670 | H1-hESC | embryonic stem cell: | n/a | n/a |
11 | BATF | chr8:104876181-104876506 | GM12878 | blood: | n/a | n/a |
12 | BCL11A | chr8:104636318-104636561 | H1-hESC | embryonic stem cell: | n/a | n/a |
13 | BCL11A | chr8:104876148-104876465 | GM12878 | blood: | n/a | n/a |
14 | BHLHE40 | chr8:104719659-104719866 | GM12878 | blood: | n/a | n/a |
15 | BRCA1 | chr8:104746860-104746969 | GM12878 | blood: | n/a | n/a |
16 | BRCA1 | chr8:104807784-104807882 | Hela-S3 | cervix: | n/a | n/a |
17 | CCNT2 | chr8:104642639-104642732 | K562 | blood: | n/a | n/a |
18 | CEBPB | chr8:104927395-104927644 | HepG2 | liver: | n/a | chr8:104927479-104927490 chr8:104927478-104927491 |
19 | CEBPB | chr8:104736433-104736529 | K562 | blood: | n/a | chr8:104736467-104736478 |
20 | CEBPB | chr8:104641266-104641578 | A549 | lung: | n/a | chr8:104641422-104641433 |
21 | CEBPB | chr8:104580718-104581322 | HepG2 | liver: | n/a | chr8:104581148-104581159 chr8:104581150-104581161 |
22 | CEBPB | chr8:104639188-104639406 | H1-hESC | embryonic stem cell: | n/a | n/a |
23 | CEBPB | chr8:104664331-104664976 | HCT-116 | colon: | n/a | chr8:104664408-104664421 |
24 | CEBPB | chr8:104636348-104636622 | A549 | lung: | n/a | chr8:104636479-104636490 |
25 | CEBPB | chr8:104782475-104782536 | HepG2 | liver: | n/a | n/a |
26 | CEBPB | chr8:104611455-104611561 | H1-hESC | embryonic stem cell: | n/a | n/a |
27 | CEBPB | chr8:104665413-104665942 | Hela-S3 | cervix: | n/a | n/a |
28 | CEBPB | chr8:104860442-104860768 | HepG2 | liver: | n/a | chr8:104860601-104860612 |
29 | CEBPB | chr8:104636279-104636686 | H1-hESC | embryonic stem cell: | n/a | chr8:104636479-104636490 |
30 | CEBPB | chr8:104826507-104826606 | IMR90 | lung: | n/a | n/a |
31 | CEBPB | chr8:104778041-104778270 | HepG2 | liver: | n/a | chr8:104778153-104778164 |
32 | CEBPB | chr8:104778054-104778242 | IMR90 | lung: | n/a | chr8:104778153-104778164 |
33 | CEBPB | chr8:104784262-104784541 | HepG2 | liver: | n/a | chr8:104784282-104784294 chr8:104784395-104784406 |
34 | CEBPB | chr8:104641255-104641574 | HepG2 | liver: | n/a | chr8:104641422-104641433 |
35 | CEBPB | chr8:104641341-104641477 | IMR90 | lung: | n/a | chr8:104641422-104641433 |
36 | CEBPB | chr8:104664293-104664961 | HCT-116 | colon: | n/a | chr8:104664408-104664421 |
37 | CEBPB | chr8:104812455-104812680 | A549 | lung: | n/a | chr8:104812488-104812499 |
38 | CEBPB | chr8:104664470-104664779 | IMR90 | lung: | n/a | n/a |
39 | CEBPB | chr8:104688092-104688156 | H1-hESC | embryonic stem cell: | n/a | n/a |
40 | CEBPB | chr8:104812325-104812713 | HepG2 | liver: | n/a | chr8:104812488-104812499 |
41 | CEBPB | chr8:104641308-104641534 | H1-hESC | embryonic stem cell: | n/a | chr8:104641422-104641433 |
42 | CEBPB | chr8:104778114-104778170 | K562 | blood: | n/a | chr8:104778153-104778164 |
43 | CEBPB | chr8:104636334-104636653 | HepG2 | liver: | n/a | chr8:104636479-104636490 |
44 | CEBPB | chr8:104784296-104784488 | H1-hESC | embryonic stem cell: | n/a | chr8:104784395-104784406 |
45 | CEBPB | chr8:104736455-104736486 | HepG2 | liver: | n/a | chr8:104736467-104736478 |
46 | CEBPB | chr8:104661210-104661279 | A549 | lung: | n/a | n/a |
47 | CEBPB | chr8:104664429-104664802 | Hela-S3 | cervix: | n/a | n/a |
48 | CEBPB | chr8:104812458-104812528 | K562 | blood: | n/a | chr8:104812488-104812499 |
49 | CEBPB | chr8:104812418-104812687 | IMR90 | lung: | n/a | chr8:104812488-104812499 |
50 | CEBPB | chr8:104664433-104664798 | H1-hESC | embryonic stem cell: | n/a | n/a |
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr8:104709583-104709633 | SK-N-MC | brain: | n/a |
2 | chr8:104897908-104897958 | U87 | brain: | n/a |
3 | chr8:104926570-104926620 | PrEC | prostate: | n/a |
4 | chr8:104897908-104897958 | ProgFib | skin: | n/a |
5 | chr8:104831516-104831566 | SK-N-SH_RA | brain: | n/a |
6 | chr8:104831516-104831566 | HNPCEpiC | eye: | n/a |
7 | chr8:104926570-104926620 | NHDF-neo | bronchial: | n/a |
8 | chr8:104897821-104897871 | HMEC | breast: | n/a |
9 | chr8:104709583-104709633 | HCT-116 | colon: | n/a |
10 | chr8:104605535-104605585 | NHDF-neo | bronchial: | n/a |
11 | chr8:104709583-104709633 | HL-60 | blood: | n/a |
12 | chr8:104709583-104709633 | Jurkat | blood: | n/a |
13 | chr8:104897821-104897871 | MCF10A-Er-Src | breast: | n/a |
14 | chr8:104831516-104831566 | BJ | skin: | n/a |
15 | chr8:104897908-104897958 | SK-N-MC | brain: | n/a |
16 | chr8:104897821-104897871 | GM12878 | blood: | n/a |
17 | chr8:104831516-104831566 | GM19239 | blood: | n/a |
18 | chr8:104605535-104605585 | HCPEpiC | choroid plexus: | n/a |
19 | chr8:104831516-104831566 | HCPEpiC | choroid plexus: | n/a |
20 | chr8:104605535-104605585 | H1-hESC | embryonic stem cell: | embryo |
21 | chr8:104605535-104605585 | SK-N-SH | brain: | n/a |
22 | chr8:104926570-104926620 | ovcar-3 | ovarian: | n/a |
23 | chr8:104709583-104709633 | CMK | blood: | n/a |
24 | chr8:104605535-104605585 | HepG2 | liver: | n/a |
25 | chr8:104897908-104897958 | AG04450 | lung: | fetal |
26 | chr8:104709583-104709633 | Caco-2 | colon: | n/a |
27 | chr8:104709583-104709633 | HepG2 | liver: | n/a |
28 | chr8:104709583-104709633 | H1-hESC | embryonic stem cell: | embryo |
29 | chr8:104831516-104831566 | K562 | blood: | n/a |
30 | chr8:104831516-104831566 | LNCaP | prostate: | n/a |
31 | chr8:104897908-104897958 | AG10803 | skin: | n/a |
32 | chr8:104897908-104897958 | HCPEpiC | choroid plexus: | n/a |
33 | chr8:104926570-104926620 | HUVEC | blood vessel: | n/a |
34 | chr8:104605535-104605585 | NT2-D1 | testis: | n/a |
35 | chr8:104709583-104709633 | HPAEpiC | pulmonary alveolar: | n/a |
36 | chr8:104926570-104926620 | HIPEpiC | eye: | n/a |
37 | chr8:104709583-104709633 | HMEC | breast: | n/a |
38 | chr8:104897908-104897958 | LNCaP | prostate: | n/a |
39 | chr8:104897821-104897871 | AG10803 | skin: | n/a |
40 | chr8:104605535-104605585 | HL-60 | blood: | n/a |
41 | chr8:104709583-104709633 | ECC-1 | luminal epithelium: | n/a |
42 | chr8:104897821-104897871 | ECC-1 | luminal epithelium: | n/a |
43 | chr8:104831516-104831566 | U87 | brain: | n/a |
44 | chr8:104605535-104605585 | BJ | skin: | n/a |
45 | chr8:104709583-104709633 | T-47D | breast: | n/a |
46 | chr8:104831516-104831566 | MCF10A-Er-Src | breast: | n/a |
47 | chr8:104709583-104709633 | HRPEpiC | eye: | n/a |
48 | chr8:104897908-104897958 | HAEpiC | amniotic membrane: | n/a |
49 | chr8:104926570-104926620 | PANC-1 | pancreas: | n/a |
50 | chr8:104897908-104897958 | BE2_C | brain: | n/a |
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr8:104776210..104777349-chr8:105503586..105504992,8 | MCF-7 | breast: | |
2 | chr8:104807373..104809649-chr8:105142104..105143087,16 | MCF-7 | breast: | |
3 | chr8:104776370..104777203-chr8:105504141..105505133,3 | K562 | blood: | |
4 | chr8:104775998..104777146-chr8:105142053..105143087,6 | MCF-7 | breast: | |
5 | chr8:104775882..104776978-chr8:105142360..105143119,4 | MCF-7 | breast: | |
6 | chr8:104814198..104817108-chr8:104820828..104822548,2 | K562 | blood: | |
7 | chr8:104810348..104810984-chr9:83669356..83670326,2 | MCF-7 | breast: | |
8 | chr8:104776221..104777249-chr8:104883194..104884184,4 | MCF-7 | breast: | |
9 | chr6:57541185..57543919-chr8:104728155..104729992,2 | MCF-7 | breast: | |
10 | chr8:104580782..104582976-chr8:104583223..104586612,3 | K562 | blood: | |
11 | chr8:104852211..104853787-chr8:104853794..104855362,2 | MCF-7 | breast: | |
12 | chr8:104808701..104809570-chr8:105504240..105505101,3 | MCF-7 | breast: | |
13 | chr8:104776566..104777114-chr8:105430021..105430537,3 | MCF-7 | breast: | |
14 | chr8:104777366..104779965-chr8:104782082..104783839,2 | K562 | blood: | |
15 | chr8:104807426..104808073-chr8:105429965..105430856,2 | MCF-7 | breast: | |
16 | chr8:104788534..104789141-chr8:105431338..105432088,2 | MCF-7 | breast: | |
17 | chr8:104807751..104808509-chr8:105454443..105455336,3 | MCF-7 | breast: | |
18 | chr8:104718542..104720324-chr8:104722213..104725013,2 | K562 | blood: | |
19 | chr8:104776048..104778695-chr8:104778794..104781400,2 | MCF-7 | breast: | |
20 | chr8:104719474..104720086-chr8:104883273..104884095,3 | MCF-7 | breast: | |
21 | chr8:104776254..104776779-chr8:105454273..105455160,2 | MCF-7 | breast: | |
22 | chr8:104689628..104692491-chr8:104693906..104695801,3 | K562 | blood: | |
23 | chr13:20694205..20697000-chr8:104874403..104876084,2 | MCF-7 | breast: | |
24 | chr8:104808150..104809735-chr8:105454257..105455293,5 | MCF-7 | breast: | |
25 | chr8:104689628..104692491-chr8:104693906..104695801,3 | K562 | blood: | |
26 | chr8:104776352..104776927-chr8:105454295..105454814,2 | K562 | blood: | |
27 | chr8:104808630..104809156-chr8:105326849..105327637,2 | MCF-7 | breast: | |
28 | chr8:104852211..104853787-chr8:104853794..104855362,2 | MCF-7 | breast: | |
29 | chr8:104807400..104808548-chr8:105454246..105455175,3 | K562 | blood: | |
30 | chr8:104720101..104721082-chr8:104883258..104883794,2 | MCF-7 | breast: | |
31 | chr8:104719466..104720176-chr8:104807477..104808353,2 | MCF-7 | breast: | |
32 | chr8:104761856..104762718-chr8:105142470..105143058,2 | MCF-7 | breast: | |
33 | chr8:104663504..104665710-chr8:104666809..104669182,2 | MCF-7 | breast: | |
34 | chr8:104719269..104720167-chr8:104776138..104776892,2 | MCF-7 | breast: | |
35 | chr8:104807876..104808412-chr8:105142129..105143128,2 | K562 | blood: | |
36 | chr8:104586754..104589959-chr8:104592462..104594425,3 | K562 | blood: | |
37 | chr8:104776697..104777502-chr8:105142088..105142615,2 | K562 | blood: | |
38 | chr8:104929972..104931758-chr8:104936150..104938844,2 | MCF-7 | breast: | |
39 | chr8:104719466..104720176-chr8:104807477..104808353,2 | MCF-7 | breast: | |
40 | chr8:104718542..104720324-chr8:104722213..104725013,2 | K562 | blood: | |
41 | chr8:104716978..104719256-chr8:104723133..104725914,2 | MCF-7 | breast: | |
42 | chr8:104719474..104720086-chr8:104883273..104884095,3 | MCF-7 | breast: | |
43 | chr8:104668501..104671183-chr8:104672665..104675173,2 | K562 | blood: | |
44 | chr8:104718269..104720075-chr8:105140265..105142046,2 | MCF-7 | breast: | |
45 | chr8:104776221..104777249-chr8:104883194..104884184,4 | MCF-7 | breast: | |
46 | chr8:104668501..104671183-chr8:104672665..104675173,2 | K562 | blood: | |
47 | chr8:104776128..104776788-chr8:105430212..105430820,2 | MCF-7 | breast: | |
48 | chr8:104776641..104777197-chr8:105504360..105505105,2 | MCF-7 | breast: | |
49 | chr8:104689628..104692134-chr8:104693906..104695603,2 | K562 | blood: | |
50 | chr8:104808988..104809567-chr8:105142388..105143010,2 | MCF-7 | breast: |
(count:3 , 50 per page) page:
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-SLC25A32-7 | chr8:104580374-104580934 | l_3665_chr8:104562639-104580934_testes |
2 | lnc-SLC25A32-7 | chr8:104580831-104581206 | NONHSAT128196 |
3 | lnc-SLC25A32-7 | chr8:104579493-104579658 | l_3665_chr8:104562639-104580934_testes |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000239344 | TF binding region |
ENSG00000216113 | TF binding region |
RIMS2 | TF binding region |
ENSG00000238687 | TF binding region |
ENSG00000254644 | TF binding region |
ENSG00000239344 | CpG island |
ENSG00000216113 | CpG island |
RIMS2 | CpG island |
ENSG00000238687 | CpG island |
ENSG00000254644 | CpG island |
ENSG00000176406 | chromatin interactions |
ENSG00000112394 | chromatin interactions |
ENSG00000254644 | chromatin interactions |
ENSG00000216113 | chromatin interactions |
ENSG00000239344 | chromatin interactions |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs192685899 | chr8:104578394-104578395 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
2 | rs376320498 | chr8:104578411-104578412 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
3 | rs113063895 | chr8:104578432-104578433 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
4 | rs537767884 | chr8:104578446-104578447 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
5 | rs529601196 | chr8:104578460-104578461 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
6 | rs184385088 | chr8:104578463-104578464 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
7 | rs1426288 | chr8:104578464-104578465 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
8 | rs533476256 | chr8:104578470-104578471 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
9 | rs551549403 | chr8:104578484-104578485 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
10 | rs550467855 | chr8:104578512-104578513 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
11 | rs563781703 | chr8:104578521-104578522 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
12 | rs111825087 | chr8:104578527-104578528 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
13 | rs530844236 | chr8:104578588-104578589 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
14 | rs548956677 | chr8:104578605-104578606 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs13272442 | chr8:104578609-104578610 | Weak transcription Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
16 | rs35908590 | chr8:104578656-104578657 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
17 | rs535320481 | chr8:104578691-104578692 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
18 | rs189280939 | chr8:104578695-104578696 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
19 | rs150928098 | chr8:104578698-104578699 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
20 | rs142974608 | chr8:104578726-104578727 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
21 | rs539538020 | chr8:104578740-104578741 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
22 | rs181979339 | chr8:104578750-104578751 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
23 | rs184391566 | chr8:104578778-104578779 | Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
24 | rs189002766 | chr8:104578855-104578856 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
25 | rs555398171 | chr8:104578900-104578901 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
26 | rs140661439 | chr8:104578961-104578962 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
27 | rs574388017 | chr8:104578966-104578967 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
28 | rs541704934 | chr8:104579007-104579008 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
29 | rs61151860 | chr8:104579070-104579071 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
30 | rs578131249 | chr8:104579079-104579080 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
31 | rs559086196 | chr8:104579108-104579109 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
32 | rs563673772 | chr8:104579132-104579133 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
33 | rs531031835 | chr8:104579133-104579134 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
34 | rs150088427 | chr8:104579165-104579166 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
35 | rs560908619 | chr8:104579206-104579207 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
36 | rs529169533 | chr8:104579210-104579211 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
37 | rs558278038 | chr8:104579274-104579275 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
38 | rs57067672 | chr8:104579278-104579279 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
39 | rs371931028 | chr8:104579307-104579308 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
40 | rs74782448 | chr8:104579308-104579309 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
41 | rs539287219 | chr8:104579324-104579325 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
42 | rs535110873 | chr8:104579330-104579331 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
43 | rs78249450 | chr8:104579337-104579338 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
44 | rs145497422 | chr8:104579341-104579342 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
45 | rs537095643 | chr8:104579375-104579376 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
46 | rs35142991 | chr8:104579376-104579377 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
47 | rs369107350 | chr8:104579378-104579379 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
48 | rs76299147 | chr8:104579394-104579395 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
49 | rs573645795 | chr8:104579401-104579402 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
50 | rs141243638 | chr8:104579539-104579540 | Weak transcription | lncRNA | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Wilms tumour | 21544195 | CNVD |
Gastric cancer | 17908304 | CNVD |
Melanoma | 18172304 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Autism | 19415332 | CNVD |
Malaria | 21533027 | CNVD |
Non-syndromic sensorineural hearing loss | 22037309 | CNVD |
Esophageal cancer | 21851588 | CNVD |
Acute promyelocytic leukemia | 19109227 | CNVD |
Breast cancer | 21245420 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Liver carcinoma | 19366792 | CNVD |
Seminomas | 18059402 | CNVD |
Acute lymphoblastic leukemia | 21390130 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Pancreatic cancer | 21811587 | CNVD |
Thyroid cancer | 19087340 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Breast cancer | 17603634 | CNVD |
Testicular cancer | 18059402 | CNVD |
Breast cancer | 17133270 | CNVD |
Breast cancer | 21509527 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Breast cancer | 21858162 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Acute lymphoblastic leukemia | 21248843 | CNVD |
Cancer | 20164919 | CNVD |
abnormal development | 18461090 | CNVD |
Oral cancer | 21386901 | CNVD |
Uveal melanoma | 21693616 | CNVD |
Langer-Giedion syndrome | 22283845 | CNVD |
Cancer | 21637783 | CNVD |
Splenic marginal zone lymphoma | 21957467 | CNVD |
Breast cancer | 20632083 | CNVD |
Breast cancer | 19602461 | CNVD |
Cancer | 22429812 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Hepatocellular carcinoma | 22174799 | CNVD |
Oral cancer | 19627613 | CNVD |
Prostate cancer | 21088497 | CNVD |
colon cancer | 17210682 | CNVD |
Breast cancer | 21264507 | CNVD |
Breast cancer | 22028636 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Cancer | 16751803 | CNVD |
Esophageal squamous carcinoma | 18350619 | CNVD |
Gastric cancer | 17167181 | CNVD |
Colorectal cancer | 19359472 | CNVD |
Breast cancer | 16461572 | CNVD |
Human rectal carcinomas | 16397240 | CNVD |
Medulloblastoma | 16968546 | CNVD |
head and neck squamous cell carcinoma | 18028549 | CNVD |
Breast cancer | 17001317 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
Ewing''s sarcoma | 17952124 | CNVD |
Urothelial carcinoma | 21177765 | CNVD |
Lung cancer | 18438408 | CNVD |
Breast cancer | 16608533 | CNVD |
Metanephric adenoma | 20802469 | CNVD |
Hepatocellular carcinoma | 18803288 | CNVD |
Prostate cancer | 18632612 | CNVD |
Glioblastoma multiforme | 18628472 | CNVD |
Ovarian cancer | 22174824 | CNVD |
Prostate cancer | 16573809 | CNVD |
Malignant peripheral nerve sheath tumor | 18522746 | CNVD |
Cancer | 21949371 | CNVD |
Non-small cell lung cancer | 21829676 | CNVD |
Multiple myeloma | 16461302 | CNVD |
Myeloproliferative neoplasm | 20015882 | CNVD |
Non-syndromic sensorineural hearing loss | 15273396 | CNVD |
Acute myeloid leukemia | 21358987 | CNVD |
Carcinoma ex pleomorphic adenoma | 18828159 | CNVD |
Adenocarcinoma | 21044232 | CNVD |
Squamous cell cancer | 20885788 | CNVD |
T-cell prolymphocytic leukemia | 17713554 | CNVD |
Prostate cancer | 16461572 | CNVD |
Breast cancer | 21399628 | CNVD |
small cell lung cancer | 20016488 | CNVD |
High-grade prostatic intraepithelial neoplasia | 16573809 | CNVD |
Acute lymphoblastic leukemia | 17690704 | CNVD |
Breast cancer | 17393978 | CNVD |
Burkitt''s lymphoma | 18698080 | CNVD |
Non-syndromic sensorineural hearing loss | 20606397 | CNVD |
Bladder cancer | 19088036 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Breast cancer | 17899364 | CNVD |
Acute myeloid leukemia | 21251322 | CNVD |
Renal cell carcinoma | 18765545 | CNVD |
Basal cell lymphoma | 17170743 | CNVD |
Colorectal cancer | 16774939 | CNVD |
Autosomal-dominant progressive external ophthalmoplegia | 19664747 | CNVD |
Congenital diaphragmatic hernia | 21085971 | CNVD |
Malignant melanoma | 17260012 | CNVD |
Sezary syndrome | 18413736 | CNVD |
Urothelial cell carcinoma | 18451213 | CNVD |
Colorectal cancer | 21645411 | CNVD |
Barrett''s adenocarcinoma | 18663352 | CNVD |
Ovarian cancer | 20844748 | CNVD |
Colorectal cancer | 16912164 | CNVD |
Breast cancer | 20409316 | CNVD |
Congenital anomalies of the kidney and urinary tract | 20467480 | CNVD |
Breast cancer | 21611746 | CNVD |
Developmental delay | 21147756 | CNVD |
Autism | 20531469 | CNVD |
Oral squamous cell carcinoma | 21853135 | CNVD |
Congenital diaphragmatic hernia | 21525063 | CNVD |
Prostate cancer | 22341455 | CNVD |
Pancreatic cancer | 17952125 | CNVD |
Breast cancer | 22522925 | CNVD |
Pancreatic ductal adenocarcinoma | 19077451 | CNVD |
Renal cell carcinoma | 21215367 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:104576000-104594000 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
2 | chr8:104576400-104588400 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
3 | chr8:104576400-104592200 | Weak transcription | H1 Cell Line | embryonic stem cell |
4 | chr8:104576600-104589600 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
5 | chr8:104578000-104578600 | ZNF genes & repeats | Pancreatic Islets | Pancreatic Islet |
6 | chr8:104578200-104578600 | Enhancers | Primary neutrophils fromperipheralblood | blood |
7 | chr8:104578200-104578800 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
8 | chr8:104578600-104580600 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
9 | chr8:104578800-104595600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
10 | chr8:104580600-104582400 | Enhancers | Primary neutrophils fromperipheralblood | blood |
11 | chr8:104580800-104581200 | Enhancers | HepG2 | liver |
12 | chr8:104583000-104592000 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
13 | chr8:104586200-104587200 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
14 | chr8:104586400-104586800 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
15 | chr8:104586400-104587200 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
16 | chr8:104586600-104587000 | Enhancers | Fetal Lung | lung |
17 | chr8:104586600-104587200 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
18 | chr8:104586800-104587400 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
19 | chr8:104586800-104588200 | Enhancers | Muscle Satellite Cultured Cells | -- |
20 | chr8:104587200-104588000 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
21 | chr8:104588000-104588600 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
22 | chr8:104588200-104588600 | ZNF genes & repeats | Pancreatic Islets | Pancreatic Islet |
23 | chr8:104588200-104588800 | ZNF genes & repeats | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
24 | chr8:104588600-104592000 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
25 | chr8:104589600-104590200 | ZNF genes & repeats | iPS-20b Cell Line | embryonic stem cell |
26 | chr8:104590400-104590800 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
27 | chr8:104590800-104595000 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
28 | chr8:104592000-104592600 | ZNF genes & repeats | Pancreatic Islets | Pancreatic Islet |
29 | chr8:104592000-104593000 | ZNF genes & repeats | HUES48 Cell Line | embryonic stem cell |
30 | chr8:104592000-104593000 | ZNF genes & repeats | iPS-20b Cell Line | embryonic stem cell |
31 | chr8:104592000-104596000 | Enhancers | Primary neutrophils fromperipheralblood | blood |
32 | chr8:104592200-104592800 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |
33 | chr8:104592200-104593000 | ZNF genes & repeats | H1 Cell Line | embryonic stem cell |
34 | chr8:104592600-104594800 | Weak transcription | ES-WA7 Cell Line | embryonic stem cell |
35 | chr8:104593000-104594000 | Weak transcription | H1 Cell Line | embryonic stem cell |
36 | chr8:104593200-104595000 | Weak transcription | H9 Cell Line | embryonic stem cell |
37 | chr8:104594000-104594200 | ZNF genes & repeats | H1 Cell Line | embryonic stem cell |
38 | chr8:104594200-104595000 | Weak transcription | H1 Cell Line | embryonic stem cell |
39 | chr8:104595000-104595400 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
40 | chr8:104595200-104595400 | ZNF genes & repeats | H1 Cell Line | embryonic stem cell |
41 | chr8:104605600-104605800 | Enhancers | HUES64 Cell Line | embryonic stem cell |
42 | chr8:104605800-104606800 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
43 | chr8:104606200-104607800 | Enhancers | HUES48 Cell Line | embryonic stem cell |
44 | chr8:104606200-104611400 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
45 | chr8:104606600-104607800 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
46 | chr8:104606800-104608200 | Enhancers | HUES6 Cell Line | embryonic stem cell |
47 | chr8:104606800-104610000 | Enhancers | HUES64 Cell Line | embryonic stem cell |
48 | chr8:104606800-104611000 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
49 | chr8:104607600-104608800 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
50 | chr8:104607600-104610000 | Enhancers | ES-I3 Cell Line | embryonic stem cell |