| Tag | Content |
|---|
EnhancerAtlas ID | HS177-05078 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr12:26392250-26393420 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LMX1B | MA0703.2 | chr12:26393315-26393326 | GATTTAATTAA | + | 6.02 | | NFYB | MA0502.1 | chr12:26392297-26392312 | ATGTCAGCCAATCAG | + | 6.03 | | RARA(var.2) | MA0730.1 | chr12:26392894-26392911 | AGTTCATCTATAGGTCA | + | 6.14 | | TFAP4 | MA0691.1 | chr12:26393015-26393025 | AACAGCTGAT | + | 6.02 |
|
| | 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 |
| GH12I026238 | chr12 | 26391098 | 26393585 |
|
Enhancer Sequence | CACCCTCAGA TACTGGCTGG GCTTCACAGT GCTGCCCAGA GGAGGACATG TCAGCCAATC 60
AGCAGGAAAG ATGCTCATTT CTTGTTGAAA AAGTCCCAAA TTGTAACTTA ACAGGGTGAT 120
CTCTCTCTCA CTCTCTCTCT CTCTTTTTTT TTTTAATTTC CAGAATGTGT TTTTCCCCTA 180
GAGTCCTTGA GCACAGACCT GCGGTTTTCT CTCTCCTGGT TTTACAGTCT ATCTGCCTCA 240
AGCCAAGAGA CTTGGCTCTG CTCCCCCCTG ACTCAGAGTC TCGGCTGGTA GCTGAACCCA 300
GGAAGCCCTG GCCCCACGTC TCTCCCTGGA ACCACCAGAC CACACAGCCT CCTGTGCTCA 360
ACCCTTTGGC TGGGTGTCCT GCCTCCTCTT TGTTTGGAAA GAGATGTCTT ACGTAACTCC 420
ACAACCTTCT AAAGGCTCCA TTGTCTTCCA CTTGGGAGAG CTCAAAACAA CCCATTAGTG 480
ACTTATGACT TATCACAAAG AGAATCTATT GCCCACATAT CCACAGCCCC CATGGAGCTA 540
GCCTCACCTA TCTTACTTAG ATCAATAATC AACAATGAGA CTTAATGACT TGTGGTCTTT 600
GGGAAATTAT AAGTTCAGTA CAAGGTGCAG GAAATACAAA GGCTAGTTCA TCTATAGGTC 660
ACGGTACTTC GCCCAGGCAG CACATGAAAG TCATTTGTAA TTCAAGATTG AGACAGGCAT 720
AAACAATTCT GATCTGATTA TTCTTTTACT AATCTGATTT TGATAAACAG CTGATGAAAA 780
TGGAAGGTGT CTGGTCATCA GAGGAGAGAT ACTCAGGCAG TGAAATAAGT TTTCCTTATC 840
TCACTGGATA GGGATTTATT TCAAGGCTCC TATTAATAGC CCCTAATGCC AAGAACTGTG 900
ATCGCTGCCC TGGACTGCAA GAGCCTTCTG AGCAAAATGA CAGAAACCCA TTGGGTAGGG 960
CATTCTCCTT CATTTTTATT TTCTATAAGT CTCTGATTAG CCCTGTTGGG AATTCTAGTA 1020
ATTATTTTAA GCTGGCACCT TTAGGAAAAA AAATATATCT CTTAGGATTT AATTAAAAAT 1080
GAAAAGAACC TCTGCATGAT GTTGCCAAGG AGCTTTCACT GTTTAAGGTG GGGTGTAGAC 1140
CAGGAAGAAT AAAACACTCT GCACTAGGTG 1170
|
