| Tag | Content |
|---|
EnhancerAtlas ID | HS024-09625 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr2:128164760-128165990 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr2:128165606-128165624 | GCGTCCTTCCCGCCTTCC | - | 6.01 | | KLF16 | MA0741.1 | chr2:128165572-128165583 | GCCCCGCCCCC | + | 6.02 | | KLF16 | MA0741.1 | chr2:128165812-128165823 | GGGGGCGTGGC | - | 6.62 | | KLF5 | MA0599.1 | chr2:128165572-128165582 | GCCCCGCCCC | + | 6.02 | | SP3 | MA0746.2 | chr2:128165811-128165824 | TGGGGGCGTGGCG | - | 6.57 | | SP8 | MA0747.1 | chr2:128165811-128165823 | TGGGGGCGTGGC | - | 6.11 | | TFAP2A | MA0003.3 | chr2:128165379-128165390 | AGCCTCAGGCA | + | 6.32 | | ZNF263 | MA0528.1 | chr2:128165526-128165547 | TCCTCCTCCTCCTCCCCCACC | - | 6.27 | | ZNF263 | MA0528.1 | chr2:128165532-128165553 | TCCTCCTCCCCCACCACCTCT | - | 6.49 | | ZNF263 | MA0528.1 | chr2:128165472-128165493 | CTCCCTCCCTCCTTCTGCTCC | - | 6.59 | | ZNF263 | MA0528.1 | chr2:128165529-128165550 | TCCTCCTCCTCCCCCACCACC | - | 7.31 | | ZNF263 | MA0528.1 | chr2:128165580-128165601 | CCCTCCTCTTCCCCCTGCCCC | - | 7.81 | | ZNF263 | MA0528.1 | chr2:128165523-128165544 | GCCTCCTCCTCCTCCTCCCCC | - | 8.62 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_09644 | chr2:128164535-128166940 | CD14 | | SE_23461 | chr2:128165153-128165765 | Colon_Crypt_1 | | SE_23461 | chr2:128165766-128166677 | Colon_Crypt_1 | | SE_24012 | chr2:128165266-128166623 | Colon_Crypt_2 | | SE_24894 | chr2:128165065-128166599 | Colon_Crypt_3 | | SE_28345 | chr2:128164776-128166852 | Fetal_Intestine | | SE_29146 | chr2:128164682-128166773 | Fetal_Intestine_Large | | SE_43376 | chr2:128165019-128166813 | Lung | | SE_50833 | chr2:128165107-128166882 | Sigmoid_Colon | | SE_52838 | chr2:128165093-128165615 | Small_Intestine | | SE_52838 | chr2:128165639-128166869 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I127406 | chr2 | 128164514 | 128166975 |
|
Enhancer Sequence | TCTCTACAAA AAATTAAAAA ATTAGCCAGG TGTGGCGGTC CATGCCGGTA GTCCCAGCTA 60
CTTGGGAGGC TGAGGCAGGA TGATCACTTG CACCTGGGAC GTTGAGGCGG CAGTGAGCCG 120
TGTTCGCGCC ACTGCACTCC AGCCTGGGTG ACACTGCAAG ACCCTGTCTC AAAAAAAGTA 180
GTCAAGGAGG CTGAGAGCCA GGAAGCCTCT GGCCAGCAGG TGAGCAGGCC CTTTCCTGCT 240
GCTGTGCATT GTATTTAAGA GAAAAGACAG ATACGTCTGA TACCTTCAAA GGTGTTCTTC 300
ATACAGCAGG TTGCAACCTA TTAATAGATC ATAAAATCAG TTTAGTGTTT CATCATCATC 360
ATCAAAAACC ACCACCAACA ACAAAAAGAC CCAGAACAGA TAGTGTAAAG AGTGCATCCC 420
TGCATTCCTG TATAGGGAGA AATATGGTTT TGTGGAACCT TGTTGCGATG TAAAGTGTAC 480
TTCTTAAGAT AAATACAGGG TTGAGGTTTT TGAAATAAAG TTTGAACAGG ACCACCTTAA 540
GCCACAGTGT AGACTTTCCA TAGGCCAAAA CCTGGATCAC CAAGACAGTG TGCCCCAGGC 600
TGCAGGCCAC ACTCCTGGGA GCCTCAGGCA ACCTTGTGCA GGCCTGACTT CGAGACACTC 660
TGAGCATGAG CTGGTTCCTG GGTAGCCTCC CCTCTACCTC TCCCCGCTTG CCCTCCCTCC 720
CTCCTTCTGC TCCTGTCTCT CCTCATCCCC TCCCCGAGTT GCTGCCTCCT CCTCCTCCTC 780
CCCCACCACC TCTCCCCGTC TCCGAGTTGC CTGCCCCGCC CCCTCCTCTT CCCCCTGCCC 840
CTCTCCGCGT CCTTCCCGCC TTCCCCCTCC TCGTCTCCCC CCTCCCCGCC CGCGCCGTCT 900
GCGTCCCTCC CGGGCCCAGA CGCGGCGCGG TCAGGGGGCG CTGACTCACA GGCTGACTCA 960
GCTGCAGGCG CGCTGCCAGG CGACGCAGCG GGCGGGTGGC CGGGCGCCGG CGGGCTCGCA 1020
GCCGGGCTGC TGGCAACGGT GCCGGCGGAG GTGGGGGCGT GGCGCGGGAT GGGCGGCGCG 1080
GGCCCTGCCG TGGTACCGCC TGGCAGCGTC CACCCCGCCG CTGGGGCGCC CTGGAGGCTC 1140
CTGGCCCTCC GTGGGGCCGT GACACCGGCG CTGCGGGGAG CGGTGGCCTC GCAGAGGCTG 1200
GGCATGGGAG GACGGCCGCC CCGGGTAAAG 1230
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