| Tag | Content |
|---|
EnhancerAtlas ID | HS098-57383 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr9:75665060-75666470 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr9:75666418-75666428 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr9:75666418-75666428 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr9:75666418-75666428 | AATGGAAAAT | - | 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 |
| GH09I073050 | chr9 | 75665057 | 75666434 |
|
Enhancer Sequence | AGATGGAAAC ATTGGGCTGA GACCACCCAG ATTTGAAGAC AGGAAAATTT TACCATACAC 60
AGAAGCTTTC GTAAGTGAAG TATTCAGACA TGCCTCTTTT CTTCCATTTA CTATTCCACA 120
TTGGCAAGCA TGTAATTCTC CTTTAAAACA GCCACTAGTG GTGGGGTGGA GGCATTGAAG 180
AATCTTAGAC ATTGGAATAC CTTAAGTTCT TTAAAATGTA CATTGTATTA TGGTTTTAAT 240
ATTACTTTAA ATCTTATTTT ATTTTTAAAC ACTGTAATAA AATTTTTGTG GTCAGTGAAA 300
GCACATTTCA TGAGCATTTT TCATTACTAA ACTATGTTGT CATTAACTTT TATTTTATGT 360
GTACTAATCA CAGGGTCAGA AAGTTATGGA ATGTCCAAGC AACAGATAAT CCAACCGTAA 420
TATGTATTTG GCTATGAAAA GTCATGCAAG CTTGCTTAAT TTAAGCTAAG GAGCCGACTT 480
AGCTTCCTTC TTATATGGAT TTGTTTTTAG TAGCCTAGAA TTTTGCTAAA CAGTAAACTA 540
AGGAAGCTAA TGTTGTCACA ATGAGATTAA ACAGAGTATT CATTTGCAGA TACTTGAAAC 600
TTTACTGAAT CTTACTCCAG AATCTCTAGC ACGCAAATGC ATGCCAGCAT AAATTAGGTA 660
GATAGCTTCA TTAAATGCAT CTGTGGGGAA CCAAAGTTCT AGTAGTTTGT TCTGTTTTTA 720
TTCCACACAA TTAAAAATTA TTAAAAAAAA AAAACCACCT GGAATTCTCA GTGTTCGTTC 780
TTCCCCCTCC CTTTAAATAG TGAAGGAGTG GGAATATCTC TCTTCCCAGG AAACTGATGT 840
AATCATTTAG TAATTGGTGT GACAGCATGC AGTGTCCTTA GGTAAGTGTC CCAAAGGGCA 900
AGACCGCCAG CTGAGCAGAG GCAAGGCCAG ACAGCAAGTG ACATAGTTCC CTGTATTTTG 960
CCCTTTGTTT GCTCTCTTTA TTCACACACA GTGGCTATTT TTTTCACAGC GATCCATTTT 1020
TTTTTTCTAG CTGCTATGTC AGATCCTCTC TCAGTTAAAG CAAATTTCGT TTTATTGTAA 1080
GTTTTAAAAA AATTAAAAAG TTCTACCTAT TTAAAAGCAA CTCTTCTGTC CCAATAACTT 1140
TTAAAGGTGA CTTTGGGTGC TTCATACGAG TATTATCTAC ACTTTTGCTA AGTACCCAGG 1200
AACAGAGAGG CTCTGCCAAG TTTATAGGCA TCATTTGGAA CGAAAGTGAT CATCTAATTA 1260
GGGCCCTGTA AACTCATCTG AGGGTCTAAG TGATAGGGAG AAATATGTAT TAGGACATAG 1320
ATATTCATTG TATTATTAAA AGTAACGGAA TACATTAAAA TGGAAAATTG AAAGAACTAC 1380
TGCATTGGCT AATGAAAGCA GCATGATATG 1410
|
