| Tag | Content |
|---|
EnhancerAtlas ID | HS012-26571 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chrX:69439730-69440740 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chrX:69439983-69439995 | AAGTAAACAGAC | + | 6.52 | | FOXP2 | MA0593.1 | chrX:69439983-69439994 | AAGTAAACAGA | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chrX:69440689-69440704 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | 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 |
| GH0XI070219 | chrX | 69439598 | 69440570 |
|
Enhancer Sequence | GGTGCTTTCT AGGCAGAAGC AAGACTCCAA CCCAATGGCA CAACACTACC TCATGTGCAG 60
CAAAATCAGT GGTCAAGGTC CCTTAGCATT TGTTGAGCTG AAAAGAAATG AATGGGGCCT 120
CTGCTCAGGC ATCCCTCAGG TGCCTCAGGC CCAAGCTCAC TTCTATTCTG TCGCTGCATA 180
ACAAGAAAGT ACCAAGAGGG ACAAGGGAGA GGTTGGATGT AATGTAGATA GGGGAACAAT 240
TCCTTGTTGA GGGAAGTAAA CAGACCTTCA GACTCACTGC TGCTGCCAGG TCCACAACTG 300
TCACAGGGAA CTCACTCTTT TCAGGCCTCC ACAACATAAA CCACCACAGT CTCAAGGCAC 360
GATGTCTGAG GAAGAATTAA AAACATTGAG AGCCTACATG CTGGCTCCCA AGACCTGGTG 420
GCGCTTTTTC TCAACAACCA GTTTTCCTGT TTTCCCCAGT AACTGGAAGA AAACAGAGCT 480
TAGGGATGGC CTTGGACAGG GAACTGGTGA ATCAGAAAAC ACAGCAGTCA TGCTGATAGC 540
TAGAGGAGGG CTCCACCCGC TTTACAAACC AACTGCCTGG AGGTGAGCCA GGTAACACAG 600
CCCCAAAGCA TCTGTGCAAA CAAGTCCTCC CTGAAGACAA GCAGAGTCTG GGAGATGCCT 660
CACTCTTTAT CTCCGAGATC TGTCACACCA TATGACATAT ACAGGTCATT ATAGCACATG 720
GTGTTTGTAG AGGATTAGCA GTTCAGCAAA TGTGTCAACC TGACAAATCA CTCAGTGCTT 780
TCAAGTGATC ACTACCCTGT TCTTTGGTTA TTTTAACAAA TGCTTATGGA GTTCCTACTA 840
TGTGGCAACC ACTGTTCTAT TAGGTTGGTG CAACCTAATA GAACTACTTT TGCACTAAGG 900
CTGGGTGCAG TGGCTCATGC CTGTACCAGC GCTTTGGGAG GCCGAGGTGG GCAGATCACG 960
AGGTCAGGAG TTCAAGACCA GCCTGGCCAA TATGGTGAAA ACCTGTCTCT 1010
|
