| Tag | Content |
|---|
EnhancerAtlas ID | HS092-14180 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:31151150-31152340 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2B | MA0660.1 | chr13:31151854-31151866 | GCTAATAATAGC | + | 6.07 |
|
| | 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 |
| GH13I030577 | chr13 | 31151476 | 31151750 |
|
Enhancer Sequence | TGGAGCCCTG ATCTGATAGG ATCAGTGTCC TTATAAGAAG AGACTAGAGC TGGGCACAGG 60
GGCTCACACC TGTAATCCCA GTATTTTGGG AGGCTGAGGT GGGAAGATCA CTCAAGGAGA 120
GGAGTCTGAG ACCAGCCTGG GCAACAGAGT GAGACTCCAT CTCTACAAGA AAATAAAATA 180
GTCAGACACA GTGGTACACA CCTGTGGTCC CAGCTCCTCA GGAGGCTGAG GCAGGAGGAT 240
GGCTTGAGCC CAGGAATTTG AGGCTGCAGC AAGCTATGAT CACACCTCTG CACTCCAGCC 300
TGGGTGACAG CATGAGACCC AGTCTCTTTA AAAAAAAAAA AAAAAAAGGC CATATATAGC 360
CCAGAAGAGC GTCCTCACCA AAACCCAATC CTGATAGCAC CTGGAGGACT TCCAGCCTCC 420
AGAGCTGTGA GAAAATTTCT GTTGCTTGCA CCGCCCAGTC TGTGGTATTT TGCTGTGGCA 480
GCCCAAGCTG ACTCATCAGT GACCTTCTCT CTGTTACCGC AGAGTAGCTC ATCATCCTCT 540
CTTCCCTAGA GTCCAGCCAC TCTCTCACAT CTACCTACCT AGCAGTATCA CTGTGGGTTA 600
GAGTCAGATC ACTGCGGATT AAGTCCTCAT TCTGCCACTG CCTGTGTAAA TCTGAGCAAG 660
TTACTTAATC TCTCTGTGTG TCAGTAACCT CCCTGTGAAA TGAGGCTAAT AATAGCAGGG 720
TTGTTTCAAC AAGGCGATAC ATGCATAATG CTTACAACAC AGCTTGGCAC ATTATAAGCA 780
TTCAACGAAA AGTGAGCTAC TATTATCTCA TCCGTTATCA GAATAAACCA CCTAAGCCAC 840
AAGGCTGCCC ACATCATCCT CATGTTTTAA AACACTTCAG TGGGCTCCCC ACCATCAACA 900
GGATAAAGTC CAAGCTTCCT TAGCATTTCT TAGAGGCTCC ATATGAATCC CCAAGTTCCA 960
CTACAGGAAC ACAGGTGAAC TTTCCACTCC AACCTCAGGC TCCTTCGTGT CACTCCTCAT 1020
CCACATGGAG GTAAGCAGCA AGAGACTCCG TGCAGTTCCT GGTGGTTCCC TGACCCTCAG 1080
GCAGACTCTC CCCAGCCCTC TGCCTGCAAC GTCCTTGCCC TTTGCTTCCC TTGGCCAGCT 1140
CCCATTCATT CTCCTTGATT CTGCTTGGAA GTTTCCCTCT CAGGAAGGCT 1190
|
