| Tag | Content |
|---|
EnhancerAtlas ID | HS048-11080 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr14:24861260-24862360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr14:24862312-24862323 | CATGAGTCACT | - | 6.14 | | ZNF263 | MA0528.1 | chr14:24862198-24862219 | TTGTTCTCCTTCTCCTCCTCC | - | 6.54 | | ZNF263 | MA0528.1 | chr14:24862204-24862225 | TCCTTCTCCTCCTCCTCTTCT | - | 6.89 | | ZNF263 | MA0528.1 | chr14:24862201-24862222 | TTCTCCTTCTCCTCCTCCTCT | - | 8.79 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27433 | chr14:24861191-24861631 | Esophagus | | SE_27433 | chr14:24861749-24862401 | Esophagus | | SE_28220 | chr14:24861145-24862567 | Fetal_Intestine | | SE_29548 | chr14:24861142-24862388 | Fetal_Intestine_Large |
|
| | 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 |
| GH14I024391 | chr14 | 24860598 | 24862364 |
|
Enhancer Sequence | ACTCCGTCTC AAAAAAAAAA AAAAGAAGGG CTGGAAATAT GCCAGCACTG AGGCAAGGCA 60
GAAATCACCG TATCTGGTGT GATGTCGGGG GCAGACTCTC TTTGCCAGCT CAAGCCAAGA 120
TAAACAGTAA TTCTAAAGTC CCGGGGATAA TGTTTGTTTC AGAAACAAGT CCCAGAGAGA 180
GGTGGGACCA GCCTCTTCAT GTAAAGTTAG AACATTCCTG ATAACAGAAG AAGAATTTCT 240
CCTGTAAGTA TTGATATAGT TGTGTAACAA CAGGTGTACC TTCTTTCTCT TAATATTAAA 300
AAATTATAAT GATAGTTTCT GCTTATTTTT AAAATTCTGA AAAAAATTAA AGGACTCTGA 360
AGCAGGAAGT GGAAGCCTTC TCTTGTACTC CCTACTCACT CTCATCTTAA AGGCATGCCA 420
TATATCTTGT TTTGCAGCCT GTGCTCTTGT GCTCCTTACC GCCCCCCTCC TTTAGGAATT 480
GCTCTATCCT CTACTTCATT ATTTTTATTG GCCACATAAT TTACCATGGT ACGGGTGCAC 540
CATAACACTG GAGAACAATC TTTAATGCCA TCATTCTGCT TCTAGGAATC TGTCCTACAG 600
AAACACCTGG CACTAGCGTG AAACACTGCA CGTACATAAA TGTTCATGAT AGGATTGTTT 660
GCCAATAGTG AAACACTAGA GACAATCTGT TCATTTGTAA TATAATTGAA GAGAGATGAG 720
GAGCGAACCA CTAAGGTATA TATGAGAAGC TCTGACTCTG AGGACTCTGC AGAGGAGACA 780
AAAGGCCACT ATAAAATACT GAACATGAGT TTTCTACCAA TAAAAGTCTC CCCTTTGCGG 840
GGGCAAGCAG GGTAGTATCA GGTTACCTGT CCTCTAACCT GGACTCCAGT GATCTAAAAC 900
AATCGGAAGG ACACTCCTGA CAGTAGTAGT CTCTGTTGTT GTTCTCCTTC TCCTCCTCCT 960
CTTCTCTCTC TCTCTCTCTC TGTTTTATAG AGACGAGGTC TCACTATGTT GCCCAGGTCC 1020
CACCTTGGCC TCTCAAAGTG GTGGATTATG GGCATGAGTC ACTGTGTCAG GTCTTTTTTT 1080
TTTTCTTTTT AATTAAAGAC 1100
|
