| Tag | Content |
|---|
EnhancerAtlas ID | HS133-17573 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:128164860-128165990 |
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 | GTTGAGGCGG CAGTGAGCCG TGTTCGCGCC ACTGCACTCC AGCCTGGGTG ACACTGCAAG 60
ACCCTGTCTC AAAAAAAGTA GTCAAGGAGG CTGAGAGCCA GGAAGCCTCT GGCCAGCAGG 120
TGAGCAGGCC CTTTCCTGCT GCTGTGCATT GTATTTAAGA GAAAAGACAG ATACGTCTGA 180
TACCTTCAAA GGTGTTCTTC ATACAGCAGG TTGCAACCTA TTAATAGATC ATAAAATCAG 240
TTTAGTGTTT CATCATCATC ATCAAAAACC ACCACCAACA ACAAAAAGAC CCAGAACAGA 300
TAGTGTAAAG AGTGCATCCC TGCATTCCTG TATAGGGAGA AATATGGTTT TGTGGAACCT 360
TGTTGCGATG TAAAGTGTAC TTCTTAAGAT AAATACAGGG TTGAGGTTTT TGAAATAAAG 420
TTTGAACAGG ACCACCTTAA GCCACAGTGT AGACTTTCCA TAGGCCAAAA CCTGGATCAC 480
CAAGACAGTG TGCCCCAGGC TGCAGGCCAC ACTCCTGGGA GCCTCAGGCA ACCTTGTGCA 540
GGCCTGACTT CGAGACACTC TGAGCATGAG CTGGTTCCTG GGTAGCCTCC CCTCTACCTC 600
TCCCCGCTTG CCCTCCCTCC CTCCTTCTGC TCCTGTCTCT CCTCATCCCC TCCCCGAGTT 660
GCTGCCTCCT CCTCCTCCTC CCCCACCACC TCTCCCCGTC TCCGAGTTGC CTGCCCCGCC 720
CCCTCCTCTT CCCCCTGCCC CTCTCCGCGT CCTTCCCGCC TTCCCCCTCC TCGTCTCCCC 780
CCTCCCCGCC CGCGCCGTCT GCGTCCCTCC CGGGCCCAGA CGCGGCGCGG TCAGGGGGCG 840
CTGACTCACA GGCTGACTCA GCTGCAGGCG CGCTGCCAGG CGACGCAGCG GGCGGGTGGC 900
CGGGCGCCGG CGGGCTCGCA GCCGGGCTGC TGGCAACGGT GCCGGCGGAG GTGGGGGCGT 960
GGCGCGGGAT GGGCGGCGCG GGCCCTGCCG TGGTACCGCC TGGCAGCGTC CACCCCGCCG 1020
CTGGGGCGCC CTGGAGGCTC CTGGCCCTCC GTGGGGCCGT GACACCGGCG CTGCGGGGAG 1080
CGGTGGCCTC GCAGAGGCTG GGCATGGGAG GACGGCCGCC CCGGGTAAAG 1130
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