| Tag | Content |
|---|
EnhancerAtlas ID | HS012-00951 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr1:209964230-209965610 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr1:209965457-209965468 | GGTGACTCATG | + | 6.62 | | HNF4G | MA0484.1 | chr1:209964431-209964446 | ACAGTTCAAAGTCCA | + | 6.75 | | Hnf4a | MA0114.3 | chr1:209964432-209964448 | CAGTTCAAAGTCCATC | + | 6.35 | | JUND | MA0491.1 | chr1:209965457-209965468 | GGTGACTCATG | + | 6.02 | | NFYA | MA0060.3 | chr1:209965083-209965094 | AACCAATCAGA | + | 6.62 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27309 | chr1:209965418-209966066 | Esophagus | | SE_27823 | chr1:209962589-209967032 | Fetal_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 209964574 | 209965039 | | chr1 | 209965069 | 209965258 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I209789 | chr1 | 209962777 | 209966655 |
|
Enhancer Sequence | CACTGCAAGG TTAGAGATGA CAGTGAGAGT CCTGCTTCAC TGCTCTGCCT GTTCATCCCT 60
GTGACTCATG CAAGTCCATT AAGATCAAGC CACCTTTCAA CCAGCATTCA GGAAGGCCAC 120
TGCCATAGTT ATCCTTCCTG CAATAAAGGG AGACATCAAC ATATCCCTGG AATATTCACT 180
CAAAAGGCTG CCTGAAAGCA AACAGTTCAA AGTCCATCTC AACTATTTCT GTTCAATCAC 240
CACACCCCAA AGGCTACAAT TGCATCAAGT AAAGTGGTCC TGGTGTCCCC ACGCTATACT 300
GACTGAGTCT TCACACCAAT GGTCATTGGA AGGAGCTAAA AACTAAGGTA TCTTGTTTGT 360
GTATCATTTT TAGCTTATTG TTTAAAGAAA CTTGAGGAAG AAGAAGCAAT ACCAAACAAT 420
TTTTCTGAAA ATGACATGTG AACACACACA CTGGGGATCT GCTCTAATAA TATACCATAA 480
AAGGACACAG TTCACATCAA AGTTAATTTT TACTCAGCAA ATCTCCATTG AACCCAATAG 540
CCCCTATCAA AGCTACTTAG CCTCTTGGAC AAAATTTTAT TAATAGCACT CACATGCCTA 600
CCATATGTAG TGTGAAAGGG AGACCCAAGC AATGACATTG ATTCGTCATT GAGATAAATT 660
CGTACCAAAT TCAGAAAGAG GTTTTTTTCT GTAGGTCCTA AAGCCTCTCA AAATCCAAGA 720
GCCTCCTCTA CCAAATCCAT GGCCATTAAC CTCCCTGTTC CACAACTGGC CTTGTCACTA 780
AATCCCCCTG CGTGACTGAT AAATCTGGGA CTCCTACCCA CCTAAGACCT GAATAACCTG 840
GAGCTGGAGC TGTAACCAAT CAGAGCATCC CTATGGGCAA GTAAGTGTCA GCCAATGTTT 900
TTGTTGTTGT TGTTGTTTTA GATCATGTCT CATTCTGTCA CCCAGACTGG AGTGCAATGG 960
CATGATCAGG GCTCACTGCA GCCTCAACCT TCTGCATTCA AGTGATCCTC CCACCTCAGC 1020
CTCCCAAGTA ACAGGGACCA TGGGCATGCA CTGCCATGCC CAGCTAATTC TTTAAAAATT 1080
TTTTTGTAGA GAGTCTCACT ATGTTGCCAA GGCTATTCTC AAACTCCTGG CCTCAAGCAC 1140
TCCTCCCACC TCAGCCTTCC AAAGGGCTGG GATTACAGGT GTAAGCCACC ACACCCAGCT 1200
GGGCCAGTGT TTCTTTACTT CTTCCCTGGT GACTCATGGG CTAGCCAGGA AACAGAAACA 1260
GAGGATGCCT CTGAGACAGG TAGTTTTTCA ATACATGGCA AAGAAATGAA GTTAGAAAGC 1320
AGGACAGGAA AGAGTCTATA ATAGAAGCAG AAGACCGAGC AAGAAAGATA AAGTCTCACT 1380
|
