Variant report
Variant | esv34690 |
---|---|
Chromosome Location | chr11:48346202-48930132 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:3237)
- CpG islands (count:1160)
- Chromatin interactive region (count:8)
- LncRNA region (count:7)
- 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 | chr11:48880376-48880748 | HepG2 | liver: | n/a | n/a |
2 | ARID3A | chr11:48892892-48893269 | HepG2 | liver: | n/a | n/a |
3 | ARID3A | chr11:48600198-48600306 | K562 | blood: | n/a | n/a |
4 | ARID3A | chr11:48895975-48896341 | HepG2 | liver: | n/a | n/a |
5 | ATF1 | chr11:48896850-48897050 | K562 | blood: | n/a | n/a |
6 | ATF1 | chr11:48867583-48867993 | K562 | blood: | n/a | n/a |
7 | ATF1 | chr11:48796111-48796444 | K562 | blood: | n/a | n/a |
8 | ATF1 | chr11:48849264-48849333 | K562 | blood: | n/a | n/a |
9 | ATF1 | chr11:48356437-48356637 | K562 | blood: | n/a | n/a |
10 | ATF1 | chr11:48845364-48845733 | K562 | blood: | n/a | n/a |
11 | ATF1 | chr11:48880374-48880748 | K562 | blood: | n/a | n/a |
12 | ATF1 | chr11:48895825-48896343 | K562 | blood: | n/a | n/a |
13 | ATF1 | chr11:48892890-48893270 | K562 | blood: | n/a | n/a |
14 | ATF1 | chr11:48859189-48859770 | K562 | blood: | n/a | n/a |
15 | ATF1 | chr11:48883351-48883720 | K562 | blood: | n/a | n/a |
16 | ATF3 | chr11:48845439-48845653 | H1-hESC | embryonic stem cell: | n/a | n/a |
17 | ATF3 | chr11:48892858-48893151 | H1-hESC | embryonic stem cell: | n/a | n/a |
18 | BACH1 | chr11:48814467-48814498 | K562 | blood: | n/a | n/a |
19 | BACH1 | chr11:48356973-48356986 | K562 | blood: | n/a | n/a |
20 | BACH1 | chr11:48881669-48882080 | K562 | blood: | n/a | n/a |
21 | BATF | chr11:48861796-48862105 | GM12878 | blood: | n/a | n/a |
22 | BATF | chr11:48834286-48834608 | GM12878 | blood: | n/a | n/a |
23 | BATF | chr11:48877440-48877803 | GM12878 | blood: | n/a | n/a |
24 | BATF | chr11:48844664-48844887 | GM12878 | blood: | n/a | n/a |
25 | BATF | chr11:48885664-48885889 | GM12878 | blood: | n/a | n/a |
26 | BATF | chr11:48895948-48896327 | GM12878 | blood: | n/a | n/a |
27 | BATF | chr11:48867136-48868238 | GM12878 | blood: | n/a | n/a |
28 | BATF | chr11:48883213-48883919 | GM12878 | blood: | n/a | n/a |
29 | BATF | chr11:48906491-48906775 | GM12878 | blood: | n/a | chr11:48906618-48906628 |
30 | BATF | chr11:48810174-48810367 | GM12878 | blood: | n/a | n/a |
31 | BATF | chr11:48892880-48893156 | GM12878 | blood: | n/a | n/a |
32 | BATF | chr11:48810469-48810756 | GM12878 | blood: | n/a | n/a |
33 | BATF | chr11:48916618-48916954 | GM12878 | blood: | n/a | chr11:48916904-48916914 |
34 | BATF | chr11:48916722-48917006 | GM12878 | blood: | n/a | chr11:48916904-48916914 |
35 | BATF | chr11:48805015-48805320 | GM12878 | blood: | n/a | n/a |
36 | BATF | chr11:48741581-48741798 | GM12878 | blood: | n/a | n/a |
37 | BATF | chr11:48898958-48899437 | GM12878 | blood: | n/a | n/a |
38 | BATF | chr11:48894608-48895288 | GM12878 | blood: | n/a | n/a |
39 | BATF | chr11:48877878-48878291 | GM12878 | blood: | n/a | n/a |
40 | BATF | chr11:48888085-48888631 | GM12878 | blood: | n/a | n/a |
41 | BATF | chr11:48775372-48775512 | GM12878 | blood: | n/a | n/a |
42 | BATF | chr11:48859171-48859730 | GM12878 | blood: | n/a | n/a |
43 | BATF | chr11:48810099-48810738 | GM12878 | blood: | n/a | n/a |
44 | BATF | chr11:48886811-48887099 | GM12878 | blood: | n/a | n/a |
45 | BATF | chr11:48854717-48855191 | GM12878 | blood: | n/a | n/a |
46 | BATF | chr11:48898982-48899252 | GM12878 | blood: | n/a | n/a |
47 | BATF | chr11:48894524-48895290 | GM12878 | blood: | n/a | n/a |
48 | BATF | chr11:48877883-48878085 | GM12878 | blood: | n/a | n/a |
49 | BATF | chr11:48885554-48885939 | GM12878 | blood: | n/a | n/a |
50 | BATF | chr11:48834403-48834545 | GM12878 | blood: | n/a | n/a |
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr11:48509778-48509828 | HCF | heart: | n/a |
2 | chr11:48509778-48509828 | HCF | heart: | n/a |
3 | chr11:48509488-48509538 | HRPEpiC | eye: | n/a |
4 | chr11:48922271-48922321 | CMK | blood: | n/a |
5 | chr11:48901914-48901964 | HEEpiC | esophagus: | n/a |
6 | chr11:48922271-48922321 | HCF | heart: | n/a |
7 | chr11:48902014-48902064 | T-47D | breast: | n/a |
8 | chr11:48922269-48922319 | Hela-S3 | cervix: | n/a |
9 | chr11:48922035-48922085 | HMEC | breast: | n/a |
10 | chr11:48923668-48923718 | HL-60 | blood: | n/a |
11 | chr11:48902014-48902064 | K562 | blood: | n/a |
12 | chr11:48901705-48901755 | HUVEC | blood vessel: | n/a |
13 | chr11:48901914-48901964 | GM12891 | blood: | n/a |
14 | chr11:48922271-48922321 | HL-60 | blood: | n/a |
15 | chr11:48922674-48922724 | T-47D | breast: | n/a |
16 | chr11:48922271-48922321 | AG09319 | gingival: | n/a |
17 | chr11:48923577-48923627 | GM12878 | blood: | n/a |
18 | chr11:48901705-48901755 | AG04449 | skin: | fetal |
19 | chr11:48922741-48922791 | NHDF-neo | bronchial: | n/a |
20 | chr11:48922269-48922319 | Caco-2 | colon: | n/a |
21 | chr11:48346680-48346730 | CMK | blood: | n/a |
22 | chr11:48509778-48509828 | AoSMC | blood vessel: | n/a |
23 | chr11:48922271-48922321 | AG04450 | lung: | fetal |
24 | chr11:48374446-48374496 | PrEC | prostate: | n/a |
25 | chr11:48924804-48924854 | HAEpiC | amniotic membrane: | n/a |
26 | chr11:48346680-48346730 | T-47D | breast: | n/a |
27 | chr11:48901914-48901964 | HepG2 | liver: | n/a |
28 | chr11:48901914-48901964 | HCF | heart: | n/a |
29 | chr11:48901914-48901964 | K562 | blood: | n/a |
30 | chr11:48924804-48924854 | PFSK-1 | brain: | n/a |
31 | chr11:48922271-48922321 | HepG2 | liver: | n/a |
32 | chr11:48922674-48922724 | Hela-S3 | cervix: | n/a |
33 | chr11:48924804-48924854 | Hela-S3 | cervix: | n/a |
34 | chr11:48923392-48923442 | HL-60 | blood: | n/a |
35 | chr11:48922035-48922085 | HEEpiC | esophagus: | n/a |
36 | chr11:48346680-48346730 | GM12892 | blood: | n/a |
37 | chr11:48901914-48901964 | SAEC | small airway: | n/a |
38 | chr11:48923392-48923442 | BJ | skin: | n/a |
39 | chr11:48509778-48509828 | NB4 | blood: | n/a |
40 | chr11:48922035-48922085 | HRCEpiC | kidney: | n/a |
41 | chr11:48374446-48374496 | NHDF-neo | bronchial: | n/a |
42 | chr11:48509778-48509828 | PANC-1 | pancreas: | n/a |
43 | chr11:48510647-48510697 | HAEpiC | amniotic membrane: | n/a |
44 | chr11:48922271-48922321 | HCPEpiC | choroid plexus: | n/a |
45 | chr11:48922271-48922321 | PrEC | prostate: | n/a |
46 | chr11:48902014-48902064 | HNPCEpiC | eye: | n/a |
47 | chr11:48901705-48901755 | GM19239 | blood: | n/a |
48 | chr11:48922674-48922724 | HNPCEpiC | eye: | n/a |
49 | chr11:48346680-48346730 | NH-A | brain: | n/a |
50 | chr11:48923577-48923627 | HCT-116 | colon: | n/a |
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:121484496..121485051-chr11:48865024..48865528,2 | K562 | blood: | |
2 | chr1:121484040..121484766-chr11:48865024..48865526,2 | MCF-7 | breast: | |
3 | chr11:48862246..48863766-chr12:38036979..38038502,2 | MCF-7 | breast: | |
4 | chr11:48811378..48811898-chr8:46850618..46851141,2 | MCF-7 | breast: | |
5 | chr11:48361908..48364233-chr11:48365831..48368223,2 | MCF-7 | breast: | |
6 | chr11:48478071..48478587-chr11:49191267..49191777,2 | MCF-7 | breast: | |
7 | chr11:48366878..48368914-chr11:48372533..48375413,2 | MCF-7 | breast: | |
8 | chr11:48361908..48364233-chr11:48365831..48368223,2 | MCF-7 | breast: |
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-AC084851.1-5 | chr11:48919940-48920255 | NONHSAT021301 |
2 | lnc-OR4C5-1 | chr11:48507915-48508377 | NONHSAT021297 |
3 | lnc-AC084851.1-5 | chr11:48914808-48914900 | NONHSAT021301 |
4 | lnc-AC084851.1-5 | chr11:48916513-48916636 | NONHSAT021301 |
5 | lnc-AC084851.1-5 | chr11:48919540-48919822 | NONHSAT021301 |
6 | lnc-AC084851.1-4 | chr11:48928655-48928750 | NONHSAT021302 |
7 | lnc-AC084851.1-4 | chr11:48929840-48930498 | NONHSAT021302 |
No data |
No data |
Variant related genes | Relation type |
---|---|
OR4C9P | TF binding region |
OR4C5 | TF binding region |
OR4C4P | TF binding region |
ENSG00000255527 | TF binding region |
OR4C10P | TF binding region |
OR4A47 | TF binding region |
OR4C2P | TF binding region |
OR4A41P | TF binding region |
OR4A40P | TF binding region |
OR4A46P | TF binding region |
OR4A44P | TF binding region |
ENSG00000255551 | TF binding region |
OR4A45P | TF binding region |
OR4A48P | TF binding region |
ENSG00000254920 | TF binding region |
ENSG00000254728 | TF binding region |
OR4R1P | TF binding region |
OR4C3 | TF binding region |
OR4A42P | TF binding region |
OR4A43P | TF binding region |
OR4C9P | CpG island |
OR4C5 | CpG island |
OR4C4P | CpG island |
ENSG00000255527 | CpG island |
OR4C10P | CpG island |
OR4A47 | CpG island |
OR4C2P | CpG island |
OR4A41P | CpG island |
OR4A40P | CpG island |
OR4A46P | CpG island |
OR4A44P | CpG island |
ENSG00000255551 | CpG island |
OR4A45P | CpG island |
OR4A48P | CpG island |
ENSG00000254920 | CpG island |
ENSG00000254728 | CpG island |
OR4R1P | CpG island |
OR4C3 | CpG island |
OR4A42P | CpG island |
OR4A43P | CpG island |
ENSG00000197161 | chromatin interactions |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs7949865 | chr11:48346202-48346203 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | mRNA abundance |
2 | rs79598002 | chr11:48346204-48346205 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
3 | rs78456867 | chr11:48346215-48346216 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
4 | rs76082925 | chr11:48346216-48346217 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
5 | rs61915355 | chr11:48346229-48346230 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
6 | rs573031034 | chr11:48346243-48346244 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
7 | rs118019472 | chr11:48346244-48346245 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
8 | rs564960984 | chr11:48346274-48346275 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
9 | rs61915356 | chr11:48346280-48346281 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
10 | rs375663699 | chr11:48346285-48346286 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
11 | rs530507845 | chr11:48346286-48346287 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
12 | rs550579167 | chr11:48346287-48346288 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
13 | rs560719620 | chr11:48346294-48346295 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
14 | rs540500434 | chr11:48346297-48346298 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
15 | rs530367198 | chr11:48346298-48346299 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
16 | rs546843367 | chr11:48346333-48346334 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
17 | rs566745231 | chr11:48346361-48346362 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
18 | rs7949320 | chr11:48346389-48346390 | Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
19 | rs538812312 | chr11:48346422-48346423 | Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
20 | rs75646016 | chr11:48346423-48346424 | Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
21 | rs74892148 | chr11:48346427-48346428 | Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
22 | rs79776366 | chr11:48346450-48346451 | Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
23 | rs552478400 | chr11:48346455-48346456 | Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
24 | rs77295176 | chr11:48346458-48346459 | Weak transcription | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
25 | rs375287578 | chr11:48346474-48346475 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
26 | rs377664238 | chr11:48346478-48346479 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
27 | rs370867853 | chr11:48346482-48346483 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
28 | rs569359425 | chr11:48346483-48346484 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
29 | rs537948366 | chr11:48346487-48346488 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
30 | rs33950768 | chr11:48346488-48346489 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
31 | rs139736329 | chr11:48346495-48346496 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
32 | rs574848654 | chr11:48346499-48346500 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
33 | rs112494506 | chr11:48346501-48346502 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
34 | rs142518450 | chr11:48346506-48346507 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
35 | rs78206553 | chr11:48346513-48346514 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
36 | rs140779640 | chr11:48346522-48346523 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
37 | rs72911451 | chr11:48346523-48346524 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
38 | rs76964780 | chr11:48346535-48346536 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
39 | rs75498992 | chr11:48346541-48346542 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
40 | rs368414015 | chr11:48346544-48346545 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
41 | rs145098801 | chr11:48346546-48346547 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
42 | rs79042268 | chr11:48346547-48346548 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
43 | rs77470587 | chr11:48346551-48346552 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
44 | rs371838945 | chr11:48346552-48346553 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
45 | rs72911452 | chr11:48346579-48346580 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
46 | rs373669304 | chr11:48346585-48346586 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
47 | rs75900655 | chr11:48346588-48346589 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
48 | rs75647397 | chr11:48346604-48346605 | ZNF genes & repeats Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
49 | rs267602915 | chr11:48346606-48346607 | ZNF genes & repeats Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
50 | rs553277724 | chr11:48346608-48346609 | ZNF genes & repeats Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Parathyroid adenoma | 22454399 | CNVD |
Medulloblastoma | 21979893 | CNVD |
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 |
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 |
Breast cancer | 17603634 | CNVD |
Chordoma | 18071362 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Potocki-Shaffer syndrome | 19222835 | CNVD |
WAGR syndrome | 19222835 | CNVD |
Lung cancer | 18438408 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Melanoma | 18172304 | CNVD |
Intracranial ependymoma | 16609018 | CNVD |
Myxofibrosarcoma | 16751306 | CNVD |
Potocki-Shaffer syndrome | 22470819 | CNVD |
Neurodevelopmental disorder | 22521361 | CNVD |
Breast cancer | 16608533 | CNVD |
Hirschsprung''s Disease | 21712996 | CNVD |
Follicular lymphoma | 20505157 | CNVD |
Colorectal cancer | 21128281 | CNVD |
Breast cancer | 20409316 | CNVD |
Neurocytoma | 17123091 | CNVD |
Central neurocytomas | 17123091 | CNVD |
Multiple myeloma | 16616336 | CNVD |
Cancer | 17160897 | CNVD |
Mantle cell lymphoma | 19029149 | 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 |
Non-syndromic sensorineural hearing loss | 17122850 | CNVD |
Non-syndromic sensorineural hearing loss | 18451855 | CNVD |
Schizophrenia | 20967226 | CNVD |
Breast cancer | 22522925 | CNVD |
Pancreatic cancer | 17952125 | CNVD |
Non-syndromic sensorineural hearing loss | 21293372 | CNVD |
Glioma | 20126413 | CNVD |
Ovarian clear cell carcinoma | 21343371 | CNVD |
Medulloblastoma | 21163964 | CNVD |
Non-syndromic sensorineural hearing loss | 19587683 | CNVD |
early-passage human iPS cells | 21368824 | CNVD |
Intellectual disability | 22045946 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:48344800-48349800 | Weak transcription | Stomach Mucosa | stomach |
2 | chr11:48346600-48346800 | Enhancers | Primary T helper memory cells from peripheral blood 2 | blood |
3 | chr11:48346600-48347000 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |
4 | chr11:48346600-48347400 | Enhancers | Primary Natural Killer cells fromperipheralblood | blood |
5 | chr11:48346600-48348600 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |
6 | chr11:48346800-48347400 | ZNF genes & repeats | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
7 | chr11:48348800-48350000 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
8 | chr11:48350000-48355600 | Weak transcription | Stomach Mucosa | stomach |
9 | chr11:48352400-48353400 | ZNF genes & repeats | HUES48 Cell Line | embryonic stem cell |
10 | chr11:48352400-48353800 | ZNF genes & repeats | iPS-20b Cell Line | embryonic stem cell |
11 | chr11:48353000-48359800 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |
12 | chr11:48355200-48363800 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |
13 | chr11:48355600-48357000 | Enhancers | Stomach Mucosa | stomach |
14 | chr11:48357000-48358000 | Weak transcription | Stomach Mucosa | stomach |
15 | chr11:48358000-48358200 | Enhancers | Stomach Mucosa | stomach |
16 | chr11:48362000-48362200 | Enhancers | Primary T helper naive cells from peripheral blood | blood |
17 | chr11:48362400-48362800 | Weak transcription | Primary T helper naive cells from peripheral blood | blood |
18 | chr11:48362800-48363200 | Enhancers | Primary T helper naive cells from peripheral blood | blood |
19 | chr11:48362800-48363200 | Enhancers | Primary T cells effector/memory enriched fromperipheralblood | blood |
20 | chr11:48362800-48363600 | Enhancers | Primary T killer naive cells fromperipheralblood | blood |
21 | chr11:48362800-48363800 | Enhancers | Primary T helper memory cells from peripheral blood 2 | blood |
22 | chr11:48363000-48363200 | Enhancers | Primary T helper memory cells from peripheral blood 1 | blood |
23 | chr11:48363000-48363400 | Enhancers | Primary T helper 17 cells PMA-I stimulated | -- |
24 | chr11:48363000-48363400 | Active TSS | A549 | lung |
25 | chr11:48363000-48363600 | Active TSS | Hela-S3 | cervix |
26 | chr11:48363000-48363800 | Enhancers | Primary T helper naive cells fromperipheralblood | blood |
27 | chr11:48363000-48363800 | Enhancers | Primary T helper cells PMA-I stimulated | -- |
28 | chr11:48363200-48363600 | Flanking Active TSS | Primary T helper naive cells from peripheral blood | blood |
29 | chr11:48363200-48363600 | Flanking Active TSS | Primary T helper memory cells from peripheral blood 1 | blood |
30 | chr11:48363200-48363600 | Enhancers | Primary T helper cells fromperipheralblood | blood |
31 | chr11:48363200-48363600 | Enhancers | Primary T killer memory cells from peripheral blood | blood |
32 | chr11:48363200-48363600 | Enhancers | Liver | Liver |
33 | chr11:48363200-48363600 | Enhancers | Dnd41 | blood |
34 | chr11:48363200-48363800 | Enhancers | Primary T cells fromperipheralblood | blood |
35 | chr11:48363200-48366400 | Weak transcription | Primary T cells effector/memory enriched fromperipheralblood | blood |
36 | chr11:48363600-48363800 | Enhancers | Primary T helper naive cells from peripheral blood | blood |
37 | chr11:48363600-48363800 | Enhancers | Primary T helper memory cells from peripheral blood 1 | blood |
38 | chr11:48363600-48363800 | Enhancers | Hela-S3 | cervix |
39 | chr11:48363600-48366800 | Weak transcription | Primary T killer memory cells from peripheral blood | blood |
40 | chr11:48363600-48367000 | Weak transcription | Primary T killer naive cells fromperipheralblood | blood |
41 | chr11:48363800-48366600 | Weak transcription | Primary T helper memory cells from peripheral blood 1 | blood |
42 | chr11:48363800-48366800 | Weak transcription | Primary T helper naive cells from peripheral blood | blood |
43 | chr11:48363800-48367000 | Weak transcription | Primary T helper memory cells from peripheral blood 2 | blood |
44 | chr11:48364200-48364600 | Weak transcription | Primary T helper 17 cells PMA-I stimulated | -- |
45 | chr11:48364800-48367400 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |
46 | chr11:48365000-48366400 | Weak transcription | Primary T helper 17 cells PMA-I stimulated | -- |
47 | chr11:48365200-48365600 | Weak transcription | Primary T helper cells PMA-I stimulated | -- |
48 | chr11:48366400-48366600 | Enhancers | Primary T helper 17 cells PMA-I stimulated | -- |
49 | chr11:48366400-48366800 | Weak transcription | Primary T helper cells PMA-I stimulated | -- |
50 | chr11:48366400-48367400 | ZNF genes & repeats | Primary T cells effector/memory enriched fromperipheralblood | blood |