| Tag | Content |
|---|
EnhancerAtlas ID | HS175-11989 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr17:79937990-79939280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr17:79938135-79938146 | GATGAGTCACC | - | 6.32 | | IRF1 | MA0050.2 | chr17:79939230-79939251 | TTAGGGTTTCATTTTTATTTC | + | 6.05 | | JUND | MA0491.1 | chr17:79938135-79938146 | GATGAGTCACC | - | 6.62 | | NR2C2 | MA0504.1 | chr17:79938193-79938208 | TGGGGGCAGAGGGCA | + | 6.14 |
|
| | 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 |
| GH17I081980 | chr17 | 79938119 | 79939461 |
|
Enhancer Sequence | TGAGATTAGA GGTGCTCACC AACACACCCA GCTAATTTTT ATATTTTTAG TAGAGATGGG 60
GTTTCACCAC ATTGGCCAGG ACGGTCTAGA ACTCCTGACC TTGTGATCCG CCTGCCTTGG 120
CCTCCCAAAG TACTGGGATT ACAGAGATGA GTCACCATGC CTGCCCTTGA AGACCTGTTT 180
TTACAGTACT GTTGTCCTAA CACTGGGGGC AGAGGGCAGG AGCTTGCCCT CCTGGCATTG 240
CCCACCCTGC CTTACGAGGC TCTCCTGGGA GGAGTTTCTT AGGGGTGATA CCTGCCAAGT 300
CATTCCAGTC TTCTACCTTG TGTCTGGACC ACGTGAGAAT CCCAGGACCT GTGCTCTGAA 360
TGCCAGGTGG TCTTGGGCTT TCTGCCCCAG ACCTTCACAC CATCCTTCTC CAGTCTCTCT 420
TGTCAACTGA AGAATGCGGT TCATATGTTT GGAAAGGAGG GCTTTATTTC TCATAACCGG 480
TTGCAGCTTG CAGGGTGGCC ATTCTAACAG GCTGGGAAGT GTAGCCTCCA GCCAGAAGCT 540
GGAAACAGAC ACTTCAAGAG AGGGAAGAAT AAGACAGGGA TTTACACCGA ATGGGGTGGC 600
TGATACAGAC GTACTTAATA CGCTGTAGGA GGATCATGAG TATTCATGAA AGGAGAACTG 660
TGCACACAGT TGAGCTTCCT GCCTCTTCAC GGGTCCTATG TGCAAAAAAT GGCAGTGCCA 720
GCATGACCTG AGGGTGGAAT TTTTGGCCTC TGAAGTCAGA GGTGAAGCAG GCTGGGTGAA 780
GTGGCTCATG CCTGTAATCC TAGCACTTTG GGTGCCCGAG GCGGAGGATT GCCTGAGCCC 840
AGGAATTCGA GATCAGCCTG GGGAACATAG TGAGACCCTG TCTCTACAAA AAAAGTAAAT 900
AAGTAAATAA ATAAATAAAT GGCAAATCAG AGGACATGAA GACTGTGCCA CGAAAACCCT 960
GACTGTGCCA GAACCACTCC ATGGTTGGTG GTTTCTTATC AGGAAATACC TGTGGGTTGT 1020
TTTGAAGAAA CCGCAAGAGA GAAGGGCCTG GCGGGAGGTT GGCTGATGTC AGATACCAGC 1080
CCAGGGGTCT TTGGAAAGGG CTGCTTTCTG TTTATCCCTT AGGGAAGAGA GCCTGCAGAT 1140
GTGTCTGATC TCCCACCCAG CCATGGCCAG GAACTCAGCT TTCAAGGTTT CTGGGGTCCC 1200
CTGGGCCAAG AGGAGGCTGG TTCAGTTGGT TGGGGGGGGC TTAGGGTTTC ATTTTTATTT 1260
CTTTTTTATT TTATTATTTT TTGAGGTGGA 1290
|
