| Tag | Content |
|---|
EnhancerAtlas ID | HS179-16798 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr2:128164710-128165990 |
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 | TGAGCCCAGG AGTTTTTTGA GACCAGCTTG AACAACATAG TGAGACCCCA TCTCTACAAA 60
AAATTAAAAA ATTAGCCAGG TGTGGCGGTC CATGCCGGTA GTCCCAGCTA CTTGGGAGGC 120
TGAGGCAGGA TGATCACTTG CACCTGGGAC GTTGAGGCGG CAGTGAGCCG TGTTCGCGCC 180
ACTGCACTCC AGCCTGGGTG ACACTGCAAG ACCCTGTCTC AAAAAAAGTA GTCAAGGAGG 240
CTGAGAGCCA GGAAGCCTCT GGCCAGCAGG TGAGCAGGCC CTTTCCTGCT GCTGTGCATT 300
GTATTTAAGA GAAAAGACAG ATACGTCTGA TACCTTCAAA GGTGTTCTTC ATACAGCAGG 360
TTGCAACCTA TTAATAGATC ATAAAATCAG TTTAGTGTTT CATCATCATC ATCAAAAACC 420
ACCACCAACA ACAAAAAGAC CCAGAACAGA TAGTGTAAAG AGTGCATCCC TGCATTCCTG 480
TATAGGGAGA AATATGGTTT TGTGGAACCT TGTTGCGATG TAAAGTGTAC TTCTTAAGAT 540
AAATACAGGG TTGAGGTTTT TGAAATAAAG TTTGAACAGG ACCACCTTAA GCCACAGTGT 600
AGACTTTCCA TAGGCCAAAA CCTGGATCAC CAAGACAGTG TGCCCCAGGC TGCAGGCCAC 660
ACTCCTGGGA GCCTCAGGCA ACCTTGTGCA GGCCTGACTT CGAGACACTC TGAGCATGAG 720
CTGGTTCCTG GGTAGCCTCC CCTCTACCTC TCCCCGCTTG CCCTCCCTCC CTCCTTCTGC 780
TCCTGTCTCT CCTCATCCCC TCCCCGAGTT GCTGCCTCCT CCTCCTCCTC CCCCACCACC 840
TCTCCCCGTC TCCGAGTTGC CTGCCCCGCC CCCTCCTCTT CCCCCTGCCC CTCTCCGCGT 900
CCTTCCCGCC TTCCCCCTCC TCGTCTCCCC CCTCCCCGCC CGCGCCGTCT GCGTCCCTCC 960
CGGGCCCAGA CGCGGCGCGG TCAGGGGGCG CTGACTCACA GGCTGACTCA GCTGCAGGCG 1020
CGCTGCCAGG CGACGCAGCG GGCGGGTGGC CGGGCGCCGG CGGGCTCGCA GCCGGGCTGC 1080
TGGCAACGGT GCCGGCGGAG GTGGGGGCGT GGCGCGGGAT GGGCGGCGCG GGCCCTGCCG 1140
TGGTACCGCC TGGCAGCGTC CACCCCGCCG CTGGGGCGCC CTGGAGGCTC CTGGCCCTCC 1200
GTGGGGCCGT GACACCGGCG CTGCGGGGAG CGGTGGCCTC GCAGAGGCTG GGCATGGGAG 1260
GACGGCCGCC CCGGGTAAAG 1280
|
