| Tag | Content |
|---|
EnhancerAtlas ID | HS180-00927 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:26196550-26197090 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr1:26196869-26196879 | GGGGCGGGGC | - | 6.02 | | SP1 | MA0079.4 | chr1:26196867-26196882 | TAGGGGCGGGGCTTC | - | 6.18 | | SP4 | MA0685.1 | chr1:26196865-26196882 | ACTAGGGGCGGGGCTTC | - | 6 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_28529 | chr1:26196677-26199042 | Fetal_Intestine | | SE_29553 | chr1:26196600-26198887 | Fetal_Intestine_Large | | SE_32243 | chr1:26195910-26197358 | Gastric |
|
| | 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 |
| GH01I025870 | chr1 | 26196774 | 26203398 |
|
Enhancer Sequence | TGGAAAGGGA CTCTGATCCA GGGGAAAGGA AAAAGCAGGG GCAGGGGTCA AGCCTGAGCC 60
AGCAGGATGA GGATGGATAT CCGGAGGGCA CCATCAGGGC ATCCTCTGAG TGGTCAGCCT 120
CTGAGTCGTG TGCCCACCAG GCTGCTGGGC CCTGTCTATT CAGGCAGCTC AGCCCAGCCC 180
ACCTCCATGG GCCCCTCCAA GTCTGGCAAA TTGCACTGGG TACCTGGGGG TTTCTCTCAA 240
GCCTGGGGGC TGGTGACCTC TACTATGGGA CTGGGCAAAT TCACCAGATG CTGAGCACTT 300
CCACAGATGA GGGGCACTAG GGGCGGGGCT TCCAGGGACT GGGGGTGTCT TGTGTGATGT 360
CACCAGAGGG TGGGGCTAAA GACAACCTCC CACACCTCTC CTCCCCAACT TCACCACTCC 420
CATAGTGGTG AAATCCATGC TAAACTGTGT GCCTTCCTAG CCAGGCCTCT GCTGCAGCAA 480
GCAGCTCACC ATTCACCTCT GCATGAGACT TACGGGGAAA CCGAGGGCCA GCTGAAAAGT 540
|
