| Tag | Content |
|---|
EnhancerAtlas ID | HS048-00695 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:26221320-26222580 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:26222064-26222083 | CCGCCTCAAGGGGGCAGCA | + | 6.12 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_03348 | chr1:26222021-26223614 | Brain_Angular_Gyrus | | SE_04754 | chr1:26221685-26228407 | Brain_Anterior_Caudate | | SE_05300 | chr1:26221344-26235071 | Brain_Cingulate_Gyrus | | SE_06612 | chr1:26221152-26230525 | Brain_Hippocampus_Middle | | SE_07163 | chr1:26221197-26235018 | Brain_Hippocampus_Middle_150 |
|
| | 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 |
| GH01I025888 | chr1 | 26215117 | 26223131 |
|
Enhancer Sequence | CCAAAGTGCT GGGATTACAG GTGTGTACCA CCACACCCAG CAACAGGCTG GCTCCAATTT 60
TAGAAATTCT ACCTCCAAAG GTCTGAGGGT CCTGAGTCTC ATATTTTGAA AAAGTACCAT 120
GTGATCCTGA TACCCAGCTG GTGTCTGGCC CATAGAGGTG CCAGCAAGTG TTTGGTGACT 180
GGGCTTAGAG GTACAGTACA TCTCTGGAAG GAGACACGGG AGACAGCTAG GTGACCTGGG 240
AGGGAGGGAG ATTCACTTTT ATTATACGTC TTTTTTTTTT TTTTTTTTTT TGAGACACAG 300
TATCGCTCTG TTGCCCAGAC TGGAGTGCGG TGGCGTGATC TATGCTCACT GCAACCTCTA 360
CCTCCCGGGT TCATACCATT CTCCTGCCTC AGCCTCCCGA GTAGCTGGGA CTACAGGCAC 420
CCGCCACCAC GCCCGGCTAA TCTTGTTTTT GTATTTTTAG TAGAGACGGG GTTTCACCGT 480
GTTAGCCAGG ATGGTCTCAA TTTCCTGACC TCGTGATCTG CCCGCCTCGG TCTCCCAAAG 540
TGCTGGGATT ACAGGCTATT ACACGTCCTT TTATACTGAC TGGACTTTTG ATCTAAAAAA 600
CAGTTTGGCT GACTTGGAGT GATGGAGTTA CTAGTCTCTG TGTCAGGGAC TGCAAATGCT 660
GGGCCTCCAG CAGGGGCAGG GCGGATCCAG CGAAAGACAG AAGTGGGTGG GCCCAAGGGG 720
ATGGAGAGCT GCAGAACACA AGTCCCGCCT CAAGGGGGCA GCAACTGCCC AGAGTCCGCT 780
GACGGCCGCT GGGTGGGACT GCAAGCCCAG GGTTGCCAGA TCTGTCAGCT TTTTTCAAGA 840
TAAGCTTGAA ATCAGATTTT CACATGGAAT TGTCAGCTAA TTCAACAATT TAAAACACAG 900
CATGGGCTGA ATGCAACATG CCTATGGTTC AACATTGGCT GCAGGCCACC AGTTTGTGCG 960
TTCGGATCCA GGAGGATTCC ATTAAGGATT GTGCACCTCA GAGCCATCTG CAAAGCTGGT 1020
GCAGACCCTT CATTTGCTTC TAGAAAATCG GGTTTACTCC ACATGGGGTC CGCAAAGGAT 1080
GAGGACAAAG CCAGTGCCCT GAGGTAGACC GTGGGAGTCA CCCACCCACT CATCATTATT 1140
TAATCCAGCA CATTAACCTC CCACCACGAG CCAGGAGATC CAGTGGTGAA TGTGACAGGA 1200
GGAGTCCCTG TTTTCAGGGA CCCTGTGTTC TAGCTGGGGA GACACTTGAA TTAATGAGTA 1260
|
