Variant report
Variant | nsv897461 |
---|---|
Chromosome Location | chr11:48939960-49003921 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:624)
- CpG islands (count:672)
- Chromatin interactive region (count:1)
- LncRNA region (count:4)
- 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 | ATF1 | chr11:48940082-48940286 | K562 | blood: | n/a | n/a |
2 | BACH1 | chr11:48961635-48962346 | K562 | blood: | n/a | n/a |
3 | BACH1 | chr11:48956270-48956471 | K562 | blood: | n/a | n/a |
4 | BATF | chr11:48953209-48953631 | GM12878 | blood: | n/a | n/a |
5 | BATF | chr11:48985116-48985352 | GM12878 | blood: | n/a | n/a |
6 | BATF | chr11:48946780-48947152 | GM12878 | blood: | n/a | n/a |
7 | BATF | chr11:48985042-48985405 | GM12878 | blood: | n/a | n/a |
8 | BATF | chr11:48945011-48945390 | GM12878 | blood: | n/a | n/a |
9 | BATF | chr11:48953227-48953611 | GM12878 | blood: | n/a | n/a |
10 | BATF | chr11:48955305-48955628 | GM12878 | blood: | n/a | n/a |
11 | BATF | chr11:48976068-48976336 | GM12878 | blood: | n/a | n/a |
12 | BATF | chr11:48945095-48945310 | GM12878 | blood: | n/a | n/a |
13 | BATF | chr11:48940420-48940720 | GM12878 | blood: | n/a | n/a |
14 | BATF | chr11:48946385-48946719 | GM12878 | blood: | n/a | n/a |
15 | BATF | chr11:48976038-48976262 | GM12878 | blood: | n/a | n/a |
16 | BATF | chr11:48943793-48944288 | GM12878 | blood: | n/a | n/a |
17 | BCL11A | chr11:48953316-48953636 | GM12878 | blood: | n/a | n/a |
18 | BCL11A | chr11:48946416-48947156 | GM12878 | blood: | n/a | n/a |
19 | BCL11A | chr11:48955311-48955544 | GM12878 | blood: | n/a | n/a |
20 | BCL11A | chr11:48945083-48945411 | GM12878 | blood: | n/a | n/a |
21 | BCL11A | chr11:48953233-48953595 | GM12878 | blood: | n/a | n/a |
22 | BCL11A | chr11:48955295-48955655 | GM12878 | blood: | n/a | n/a |
23 | BCL11A | chr11:48943783-48944180 | GM12878 | blood: | n/a | n/a |
24 | BCL11A | chr11:48976050-48976264 | GM12878 | blood: | n/a | n/a |
25 | BCL11A | chr11:48945083-48945369 | GM12878 | blood: | n/a | n/a |
26 | BCL3 | chr11:48990838-48991105 | GM12878 | blood: | n/a | n/a |
27 | BHLHE40 | chr11:48958418-48958674 | HepG2 | liver: | n/a | n/a |
28 | BHLHE40 | chr11:48953193-48953630 | HepG2 | liver: | n/a | n/a |
29 | BHLHE40 | chr11:48948266-48948511 | HepG2 | liver: | n/a | n/a |
30 | BRCA1 | chr11:48956098-48956483 | Hela-S3 | cervix: | n/a | n/a |
31 | BRCA1 | chr11:48942120-48942457 | GM12878 | blood: | n/a | n/a |
32 | BRCA1 | chr11:48956269-48956471 | GM12878 | blood: | n/a | n/a |
33 | BRCA1 | chr11:48960588-48960655 | Hela-S3 | cervix: | n/a | n/a |
34 | CEBPB | chr11:48960415-48960521 | K562 | blood: | n/a | n/a |
35 | CEBPB | chr11:48994051-48994082 | HepG2 | liver: | n/a | n/a |
36 | CEBPB | chr11:48956269-48956469 | K562 | blood: | n/a | n/a |
37 | CEBPD | chr11:48953317-48953723 | K562 | blood: | n/a | n/a |
38 | CHD1 | chr11:48953549-48953581 | GM12878 | blood: | n/a | n/a |
39 | CHD2 | chr11:48959212-48959412 | K562 | blood: | n/a | n/a |
40 | CHD2 | chr11:48958911-48958925 | GM12878 | blood: | n/a | n/a |
41 | CHD2 | chr11:48956269-48956470 | Hela-S3 | cervix: | n/a | n/a |
42 | CTCF | chr11:48966784-48966963 | LNCaP | prostate: | n/a | n/a |
43 | CTCF | chr11:48983139-48983172 | GM13976 | blood: | n/a | n/a |
44 | CTCF | chr11:48973716-48973764 | Pancreas_OC | pancreas: | n/a | n/a |
45 | CTCF | chr11:48966763-48966883 | LNCaP | prostate: | n/a | n/a |
46 | CTCF | chr11:48953254-48953804 | K562 | blood: | n/a | n/a |
47 | CTCF | chr11:48961499-48961663 | K562 | blood: | n/a | n/a |
48 | CTCF | chr11:48995522-48995576 | GM20000 | blood: | n/a | n/a |
49 | CTCF | chr11:48943841-48944139 | K562 | blood: | n/a | n/a |
50 | CTCF | chr11:48940508-48940695 | K562 | blood: | n/a | n/a |
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr11:48990484-48990534 | HepG2 | liver: | n/a |
2 | chr11:48990484-48990534 | HepG2 | liver: | n/a |
3 | chr11:49003527-49003577 | SAEC | small airway: | n/a |
4 | chr11:48994113-48994163 | RPTEC | kidney: | n/a |
5 | chr11:49003361-49003411 | NH-A | brain: | n/a |
6 | chr11:48989769-48989819 | PrEC | prostate: | n/a |
7 | chr11:48994113-48994163 | GM12892 | blood: | n/a |
8 | chr11:48977527-48977577 | HPAEpiC | pulmonary alveolar: | n/a |
9 | chr11:48987265-48987315 | U87 | brain: | n/a |
10 | chr11:49003361-49003411 | HL-60 | blood: | n/a |
11 | chr11:48977527-48977577 | HEK293 | kidney: | embryo |
12 | chr11:48994113-48994163 | NHBE | bronchial: | n/a |
13 | chr11:48990484-48990534 | ovcar-3 | ovarian: | n/a |
14 | chr11:48990484-48990534 | LNCaP | prostate: | n/a |
15 | chr11:48977834-48977884 | H1-hESC | embryonic stem cell: | embryo |
16 | chr11:48990330-48990380 | GM19239 | blood: | n/a |
17 | chr11:48990484-48990534 | HCF | heart: | n/a |
18 | chr11:48987265-48987315 | MCF-7 | breast: | n/a |
19 | chr11:48991619-48991669 | AG09309 | skin: | n/a |
20 | chr11:48977527-48977577 | RPTEC | kidney: | n/a |
21 | chr11:49003527-49003577 | NB4 | blood: | n/a |
22 | chr11:48990484-48990534 | HUVEC | blood vessel: | n/a |
23 | chr11:48987265-48987315 | HCF | heart: | n/a |
24 | chr11:48987265-48987315 | GM12878 | blood: | n/a |
25 | chr11:48987265-48987315 | RPTEC | kidney: | n/a |
26 | chr11:48991619-48991669 | HRE | kidney: | n/a |
27 | chr11:48994113-48994163 | T-47D | breast: | n/a |
28 | chr11:48994113-48994163 | AoSMC | blood vessel: | n/a |
29 | chr11:48987265-48987315 | Jurkat | blood: | n/a |
30 | chr11:48994113-48994163 | PANC-1 | pancreas: | n/a |
31 | chr11:48991619-48991669 | NT2-D1 | testis: | n/a |
32 | chr11:48990211-48990261 | IMR90 | lung: | fetal |
33 | chr11:48991619-48991669 | SKMC | muscle: | n/a |
34 | chr11:48989769-48989819 | GM12878 | blood: | n/a |
35 | chr11:49003361-49003411 | T-47D | breast: | n/a |
36 | chr11:49003527-49003577 | K562 | blood: | n/a |
37 | chr11:48987265-48987315 | MCF10A-Er-Src | breast: | n/a |
38 | chr11:48987265-48987315 | GM12892 | blood: | n/a |
39 | chr11:48990211-48990261 | GM12878 | blood: | n/a |
40 | chr11:48990211-48990261 | HEK293 | kidney: | embryo |
41 | chr11:49003527-49003577 | NHBE | bronchial: | n/a |
42 | chr11:49003361-49003411 | AG09309 | skin: | n/a |
43 | chr11:48990484-48990534 | SKMC | muscle: | n/a |
44 | chr11:48990330-48990380 | GM12878 | blood: | n/a |
45 | chr11:48990211-48990261 | K562 | blood: | n/a |
46 | chr11:48977527-48977577 | NT2-D1 | testis: | n/a |
47 | chr11:48987265-48987315 | HEEpiC | esophagus: | n/a |
48 | chr11:48991619-48991669 | NHBE | bronchial: | n/a |
49 | chr11:48977527-48977577 | Caco-2 | colon: | n/a |
50 | chr11:48977834-48977884 | CMK | blood: | n/a |
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:121484902..121485419-chr11:48946286..48946806,2 | MCF-7 | breast: |
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-AC084851.1-2 | chr11:48983254-48983362 | NONHSAT021303 |
2 | lnc-AC084851.1-2 | chr11:48981480-48981636 | NONHSAT021303 |
3 | lnc-AC084851.1-2 | chr11:48982485-48982577 | NONHSAT021303 |
4 | lnc-AC084851.1-2 | chr11:48981775-48981855 | NONHSAT021303 |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000254517 | TF binding region |
TRIM51CP | TF binding region |
TRIM51GP | TF binding region |
ENSG00000254517 | CpG island |
TRIM51CP | CpG island |
TRIM51GP | CpG island |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs111688298 | chr11:48939960-48939961 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
2 | rs577579841 | chr11:48939970-48939971 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
3 | rs545794153 | chr11:48939975-48939976 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
4 | rs201096100 | chr11:48940033-48940034 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
5 | rs377491844 | chr11:48940036-48940037 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
6 | rs184019439 | chr11:48940045-48940046 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
7 | rs576135796 | chr11:48940046-48940047 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
8 | rs541554489 | chr11:48940049-48940050 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
9 | rs190197989 | chr11:48940059-48940060 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
10 | rs11517696 | chr11:48940073-48940074 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
11 | rs148177948 | chr11:48940077-48940078 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
12 | rs36162981 | chr11:48940087-48940088 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
13 | rs564053477 | chr11:48940098-48940099 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
14 | rs370776553 | chr11:48940157-48940158 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
15 | rs533036317 | chr11:48940162-48940163 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
16 | rs11517697 | chr11:48940164-48940165 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
17 | rs112641135 | chr11:48940172-48940173 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
18 | rs113858726 | chr11:48940177-48940178 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
19 | rs528736847 | chr11:48940183-48940184 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
20 | rs199710826 | chr11:48940193-48940194 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
21 | rs111493008 | chr11:48940201-48940202 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
22 | rs200594292 | chr11:48940207-48940208 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
23 | rs559120732 | chr11:48940217-48940218 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
24 | rs201057791 | chr11:48940226-48940227 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
25 | rs112534546 | chr11:48940241-48940242 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
26 | rs199535872 | chr11:48940257-48940258 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
27 | rs149778650 | chr11:48940264-48940265 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
28 | rs111375823 | chr11:48940267-48940268 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
29 | rs146607692 | chr11:48940277-48940278 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
30 | rs200654612 | chr11:48940290-48940291 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
31 | rs147815543 | chr11:48940294-48940295 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
32 | rs538376770 | chr11:48940295-48940296 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
33 | rs181910871 | chr11:48940301-48940302 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
34 | rs568539925 | chr11:48940313-48940314 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
35 | rs145084868 | chr11:48940317-48940318 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
36 | rs554368792 | chr11:48940319-48940320 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
37 | rs577470519 | chr11:48940341-48940342 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
38 | rs539743668 | chr11:48940350-48940351 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
39 | rs558447425 | chr11:48940378-48940379 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
40 | rs556167229 | chr11:48940390-48940391 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
41 | rs575935682 | chr11:48940392-48940393 | ZNF genes & repeats Active TSS Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
42 | rs12360694 | chr11:48940420-48940421 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
43 | rs144117134 | chr11:48940425-48940426 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
44 | rs74731332 | chr11:48940430-48940431 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
45 | rs78340646 | chr11:48940433-48940434 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
46 | rs561465856 | chr11:48940437-48940438 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
47 | rs375623256 | chr11:48940441-48940442 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
48 | rs376200261 | chr11:48940448-48940449 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
49 | rs571772091 | chr11:48940453-48940454 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
50 | rs75295086 | chr11:48940460-48940461 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Chordoma | 21602918 | CNVD |
Breast cancer | 21949216 | CNVD |
Cancer | 21637783 | CNVD |
Non-syndromic sensorineural hearing loss | 19222835 | CNVD |
T-cell acute lymphoblastic leukemia | 20065082 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Astrocytoma | 17387387 | CNVD |
Breast cancer | 21264507 | CNVD |
Beckwith-Wiedemann syndrome | 21518781 | CNVD |
Wilms tumour | 21518781 | CNVD |
Hepatoblastoma | 21518781 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Gastrointestinal stromal cancer | 17535989 | CNVD |
Paraganglioma | 17535989 | CNVD |
Pulmonary chondroma | 17535989 | CNVD |
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 |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Potocki-Shaffer syndrome | 19222835 | CNVD |
WAGR syndrome | 19222835 | CNVD |
Lung cancer | 18438408 | CNVD |
Breast cancer | 16608533 | CNVD |
Hirschsprung''s Disease | 21712996 | CNVD |
Follicular lymphoma | 20505157 | CNVD |
Colorectal cancer | 21128281 | CNVD |
Glioblastoma multiforme | 21138945 | CNVD |
Breast cancer | 21364760 | CNVD |
Prostate cancer | 18632612 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Acute lymphoblastic leukemia | 22581003 | CNVD |
Breast cancer | 21990379 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Intellectual disability | 22045946 | CNVD |
Non-syndromic sensorineural hearing loss | 17122850 | CNVD |
small cell lung cancer | 17426248 | CNVD |
Breast cancer | 22522925 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:48935200-48947600 | ZNF genes & repeats | HUES48 Cell Line | embryonic stem cell |
2 | chr11:48935600-48943800 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
3 | chr11:48935800-48942400 | ZNF genes & repeats | iPS-18 Cell Line | embryonic stem cell |
4 | chr11:48936400-48949200 | Weak transcription | K562 | blood |
5 | chr11:48936600-48940600 | Weak transcription | NH-A | brain |
6 | chr11:48938000-48949200 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |
7 | chr11:48940000-48940400 | Active TSS | Small Intestine | intestine |
8 | chr11:48943200-48944000 | ZNF genes & repeats | iPS-20b Cell Line | embryonic stem cell |
9 | chr11:48947600-48948400 | ZNF genes & repeats | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
10 | chr11:48947600-48948400 | ZNF genes & repeats | HUVEC | blood vessel |
11 | chr11:48949000-48949200 | Enhancers | Primary T helper naive cells fromperipheralblood | blood |
12 | chr11:48953000-48954400 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
13 | chr11:48953000-48959800 | ZNF genes & repeats | HUES48 Cell Line | embryonic stem cell |
14 | chr11:48953200-48959800 | Weak transcription | K562 | blood |
15 | chr11:48955000-48959000 | ZNF genes & repeats | iPS-18 Cell Line | embryonic stem cell |
16 | chr11:48955200-48955600 | ZNF genes & repeats | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
17 | chr11:48956200-48963400 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |
18 | chr11:48956600-48964400 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
19 | chr11:48957400-48958800 | ZNF genes & repeats | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
20 | chr11:48957800-48958400 | ZNF genes & repeats | HUVEC | blood vessel |
21 | chr11:48957800-48959000 | ZNF genes & repeats | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
22 | chr11:48958000-48958200 | ZNF genes & repeats | Pancreatic Islets | Pancreatic Islet |
23 | chr11:48958000-48958400 | ZNF genes & repeats | ES-I3 Cell Line | embryonic stem cell |
24 | chr11:48958400-48959000 | ZNF genes & repeats | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
25 | chr11:48959000-48960200 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
26 | chr11:48959200-48959600 | ZNF genes & repeats | HUVEC | blood vessel |
27 | chr11:48959400-48960400 | ZNF genes & repeats | iPS-20b Cell Line | embryonic stem cell |
28 | chr11:48961600-48962000 | ZNF genes & repeats | ES-I3 Cell Line | embryonic stem cell |
29 | chr11:48966800-48967600 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |