| Tag | Content |
|---|
EnhancerAtlas ID | HS092-15363 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:113927920-113929080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr13:113928733-113928744 | AATGAGTCACA | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 113928164 | 113928348 | | chr13 | 113928610 | 113928824 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I113272 | chr13 | 113926846 | 113930190 |
|
Enhancer Sequence | ACTGAGGAGT GAATGAAGCA GGGCCAGTGG AAGGAACAAA GACCAGCAAG ATAAGAATGG 60
GGAGAAGTAC GAGTGTGACA GAACAAAAGA AGGGAGTTTT AAGGTATGGT GAGAATCAGA 120
AACAGACCAT CACGGTGGCA TCTCGGGCCA TTCAGTTTGT GTGCTGGGCC CGACGGGTAG 180
TGGGTGCGGC GAGATGTAGC TGGAGGCAAG GCAGAGGCCA GGGAGAGCTG CTCTCGGGTA 240
ATGAGAATTG AGCAAGCATC AAACTGAGCA AGCAAGAGAG AAAAGGGGAG AATCTGAGCA 300
TACGGAAAGG AGAAATAACT GCGGGCAGGT TTCCCAAACA GCAGGGGAAA CCACATCCCC 360
GCGCAGCGTG CTCCTCCCAG GGAACAGAAC AGGGAAACCA CATCCCCGCG CAGTGTGCTC 420
CCCCGGCAGA GGTCCTAAGG AAGCCGAGGG GCGGACAGCC GAGCAGAGGT AAGGCTTTCT 480
GTGGTCCGTG ATGGAGGAAC CAAGGCCAAC TGCAGCACAA GTTGAGGGAG CATTGTACTG 540
AGAAGTGGAC GCCTGCCAGG AGTCCACTCT TCACAGAATG AACAGCACCT TCAAGGCACT 600
GGGATCAGCA GAGAAGCTTT AACACTGGCC AGGTCCCCCC TCTGCCAGGT CCTCCATCTG 660
TCACTCTCCA GGTGCCCCTG AGCAAATTCC TGCAATTCTT TAAACCTTGG TTTTCTTATA 720
AGTGGAGATA ATAATCCTAC TTACCTCATG GGGTGGTTCC AAGTGAACAC ACACAAAGCT 780
GCTTAGGACA CGTACTACAC ACCAGCAAAG AGGAATGAGT CACAGTCACG CACAAGCACA 840
GTGCCTCTTC ATCAGGAAAA CCCAGTTCCA TACAAATCTA AGTGGCTTAT CTTCAGAAAC 900
ATTAGTGAAG AGCTGAAGCA AACACTGTCA GCTGGGAAGT CTGTATTCAG TGAACATACA 960
TTTCTGAATG GAGGCAAAGT ATGCCTTTTC AGACAGAGAC CTCTAGTAGG AGAAGTGCAG 1020
GAGGAAGGAG CTTCAGCTGC TGGAAAGCAA AGCCAGATAG AAGCCAGGGT CTGCCGAAGG 1080
CCTGGGGAGC GCCCGCACTT GCAAGCATTT GGGTAGACAC TCACACAAAT TAGCTACACA 1140
ATCATTATTT TCTTTAAAAA 1160
|
