| Tag | Content |
|---|
EnhancerAtlas ID | HS092-15321 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:111451110-111453780 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP2 | MA0516.2 | chr13:111451172-111451189 | AGGGAGGCGGGGCTAAC | - | 6.04 |
|
| | 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 |
| GH13I110798 | chr13 | 111450483 | 111453216 |
|
Enhancer Sequence | ACCCTTGTTG GATAGTGTTT GTCGATTTCA AGCTGCCAAA CGGCTGGCAC TGAACTTGGA 60
GTAGGGAGGC GGGGCTAACA GCTCTGGCCA TCCTGGGAAC TGTGGTTGGC GTGCCCTGGC 120
GGAGTCTGGG TTCTCAGGCC TGTGGGTATC ACCAAGTCCA CCTCTCACTT CCCTGGGAAC 180
ACTCTGCACC CACCAAAGTG CAGTGGACAA GTCAGCCCTG GCACGGGGAG AAGGCGGGAA 240
GGAGGAAGCA AGTGCAGGAG CTGGTGGGGC AGAGTAAAGA GCCACAGACC TGGGTAAAGT 300
CAGAATCCAT CACGCACTAG CTGCACGGCC TGGCAACGAG AAATAACCAG TGTCCACCTG 360
GGGGGCTGCT ATAAAGATTA GAGCCCTCGG TGCGGTTTCC GGTGCATAGA GACACTCAGT 420
AAGTGACAGC TGGTGGCATT TTTCTAGGCA GCTCTGGCAG GGGTCACCTG GAGGTCTATT 480
GGGCAGTTTC CCTAGCCTCA CAAGTCCCCT ACACCACAGG CTGCCTGGAA GGTCCATAGA 540
GAGGCCAGAT GCAAAACGTT GCGTAGGAAG AATGGATTCT TCTGGGAATC GCAATTGCGT 600
TGCCTCAATC CCTGGGTGGA TGGGTCATGG GCTGGGGAGA TGCATGAGAG GAAACTCTTG 660
GCCCTGGGCA TGTCCTGGGT CTGGACCTGA GGCACACATG GGAAGGTCAC AGAGCTGTGC 720
GCTTAAGATT CGCGCACTTC CTCTACTGTG TGGTATGTGT GCTGGCCCTC CGTTTAGAAA 780
AACTAACTTA GCGCACTTTT CTCTCCCTGT TGGATGGACA AAGACCTCTT TCAGCTTGGG 840
CACCGAGGAA GGGAAGCGTA GCGTCAGAAC AGAGAGTGGA TCACACTGTC GGGCTCAGCA 900
CGAAAGACTG ACAGTCTGGG CACAGCACCC GGTCCTCCCT CCCAGCGCTG ACTGCAATCC 960
CGGCCAGGGC TGAGGAAACC GCAGGACCAT GCGTGGATGG AAGGGTAGAA GCCTTCCTGT 1020
TTCCTGGCAG GTCAGGAGAA AGGGCAAGTT AGGAAAAAGG GCTGAGCTTC CAGTGTATGA 1080
GGCGCCACAC TGGGTTTTCC AGTAAAAGGA AACCTAGTTG CTCAGCTCAG ACTTTGAAAA 1140
ATATTATTTG GTCCCTGAGT AGAAACAGAT GTTGTTTCCT GTTACAGAAA TGAGCTGTAG 1200
CTCTTCCACA CACACACACT GGCAGCCCAC GCATTTCGTT CTCCCTCCAG GATCCGATCC 1260
ATGAGGCAAA AGCAAATGGA AAGAATTCCA ACTTCATCTT CTCTGTCATT CGTCTTGTGA 1320
GAAGTGGGCA GAAAAGATGT TTTTCCTACT GAACTATATT TCATCATCGT TTCCCTTCCC 1380
TTCACCACAG CAGCTGGAAA TGTAATGTCA GTGCCCTCCC AGACTCCTCT CCACCGAGCG 1440
TTCAGAGAGC GCAGCGGCTG TTCACGGAAG GACTTTCTTT TTCTTTTCTT TTTCTTTTTT 1500
GATATGGAGT CTGGCTCTGT CACCCAGGCT GGAGTGCAGT GGCACGATCT CAGCTCACTG 1560
CAACCTCTGC CTCCCGGGTT CAAGTGATTC TCCTGCCTCA GCCTCCTGAG TAGCTGGGAT 1620
CACAGGCGTG CGCCACCACA CCCGGCTAAT TTTTGTGTTT TGTTTTAGTA GAGACAAGGT 1680
TTCACCATAT TGATCAGGCT GGTCTCAAAC TTCTGACCTC GTGATCCACC CGCCTCAGCC 1740
TCCGAAAGTG CTGGGATTAT AGGCTTAAGC CACCGCGCCC AACCTCATGG AAGGACTTTC 1800
TTTGTCATTA GGTGTGAGGG GGTCAGGGCT GCTGGCTGAT TGATTGACTG ATTGTATCTC 1860
AGCTCCCACC CATCTAATTT GTCCAGTGTT GGAAAGTGGC ATTTGCTTCT TTGCCCAGGC 1920
TAACAAGAGT TGCTGCTGGA AATACAGATG TGCAGATGCC AAGGCGATGC TTTCAGGCAC 1980
CCGGGCGGCT CCCTGTGCAG TGGGCAGTGT CTGTCTGCAG TGCTTTGCTC ACTCCTCGCC 2040
TCTCGGTCCC CTGCAATGGC AGCCCTCCTC CCACCTGCCA GGATGCCCCT CCCCTCTCCT 2100
TCAAGGTGTT CACGCACTCT CTCTCTCTCC CATTTTGTGG ACATAGTTAC ACCTTCTAAA 2160
GGATTTTCAC CCAGAATTGT ATTTCTTTGA CATTCTTATA AGCTGCCCCA GAAGACAACA 2220
CAGGGCAAAT AATAATGCTC TATCTGTTTT GACAGTTTGA GCTATTATTT GCCTTGATTT 2280
ATGGGGAATT AGACCTGAGG TAATGGTTTT CTCAGATGTT GCTAAGCACA GCAGAGGGTG 2340
ACAAGAGCAT CCTAGGGTCT GTCTGGGTTC TCCAGCAGCT GGGAGAAGCA AAGTCGTGAA 2400
AAACCCTGCC CAGGGAGGCT GACAGGAGTG CCTCCGCCAT GGCAGACTCC CCAGCCCGGG 2460
GCTTTTGGGT ATAGCCTGTG CACTAGCGCT TGGCAGTCAC TAGCTCACCC CAGTGTTCGA 2520
CTGAGGGGAT GCTACTCTGA AGTCACCAGC TACAGAGGGC AATGCACGGG ACAAGCTTTG 2580
GAGCTTCAGT TTCCAGCAGG ATCTTCTGCA GCGATGGAGA GGTTCTGCAT CTGCTCTGTG 2640
CAACATGGTG GTCCTCAGGT TGGGACTGTG 2670
|
