| Tag | Content |
|---|
EnhancerAtlas ID | HS012-12037 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr12:120890880-120891600 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr12:120891346-120891361 | AGTCAATCATTAATT | - | 6.72 | | HNF1B | MA0153.2 | chr12:120891347-120891360 | GTCAATCATTAAT | + | 6.34 |
|
| | 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 |
| GH12I120452 | chr12 | 120890670 | 120891614 |
|
Enhancer Sequence | TAGATGGAAG TAGAGGGGTC CACAAGAAGC TATTCCTTCC AGCCAGATAG CAGAAAAGAA 60
GCTCAAAGAA AGAAAAGCAG TGGGAGAACG GTCCCATCAG TGAGTCCAAG GGCTGACAGA 120
ATCACAAATG GAGCCACTTT GTCCTCCCTG TTGCCACAGC ACTTTCCAAT GCCACCGTAG 180
CAGCATTTCT CACAGTTACT TAAGTTATTG TTCCTGAGTT TTAACCAGCA GGGACTTCTA 240
GTTTACAACT GAAGTCTTTC TCAACCAGGG TTCCTCAGCC AAACCAGAAC ACAGAAAGAT 300
TCAAGTGACT TTTTTTCAGT TCTCCCAAGG ACAGTATATG ACAAATGTTA GCTTAAACAC 360
ACAGGAGATA AGTTAACTTA TCATCAGAAT GGGTGTCTTG GGGTATGTAG GCTAACTTAT 420
CTTACAGAAC CCTGATTGGG AAAGACAGGT GGTGAGGTAG AAGTTTAGTC AATCATTAAT 480
TGATCTGAAA AGCTCATCTG GTCCTGTTCA GTGTTTTATA TAATTCTGAG GTCCAAGAAA 540
GTGAAGCAAC TCACCAAGTG AGAGGTATGC TTGCTGTACC ACTGTCACAG AGACCGTGGG 600
TTCAGGAGCC TGTAATTAAT AAAGCTAGGT ATGGTGGTGC ACACCTGTAA TCCCAGCTGC 660
TTGGGAAGCT AAGGTGGGAG GATCACTTGA GCCCAGAAGT TTGAGACCAG CCTAGGCAAC 720
|
