| Tag | Content |
|---|
EnhancerAtlas ID | HS092-13588 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:120378170-120379300 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr12:120378897-120378913 | CCCAAAGTAAACAATG | + | 6.81 | | FOXF2 | MA0030.1 | chr12:120378898-120378912 | CCAAAGTAAACAAT | + | 6.29 | | Foxa2 | MA0047.2 | chr12:120378898-120378910 | CCAAAGTAAACA | - | 6.74 | | MEF2A | MA0052.3 | chr12:120379137-120379149 | ACTAAAAATAGA | + | 6.27 | | MEF2B | MA0660.1 | chr12:120379137-120379149 | ACTAAAAATAGA | + | 6.32 | | MEF2C | MA0497.1 | chr12:120379135-120379150 | CTACTAAAAATAGAA | + | 6.57 | | Nr2f6(var.2) | MA0728.1 | chr12:120379086-120379101 | GAGGTCAGGAGTTCA | + | 6.22 | | TFAP4 | MA0691.1 | chr12:120378572-120378582 | ATCAGCTGTT | - | 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 |
| GH12I119941 | chr12 | 120378821 | 120378970 |
|
Enhancer Sequence | GTGAGCCACT GCGCTCGGCC GCTGACTAAC ACATCTTGAC AAAGATGTAG AGAATTTATG 60
TAATGACCAG GAGCACTGGT AAAATTTTGA CTTGTAAATG TCTTGAGGAG AGAATCCCTG 120
TGCAAACTAG ATGGATCCAA TTCCCCTGCG AGCCTACTGT GTAAATCCTG GTGTGACGCT 180
TGCAAACTCA GTAGATGCAG CTGCCTCGTG GCCACCACAC CGCCTCCATT CCTTTAAGGT 240
TTTATACTTC CCCAGGCTTT CACAATCATT ATCTCATTTG CCTTCTGCCA CATCCCAACC 300
AGACAGAGAA GGAGATTTTA CCATCCCCAT TTCCAGGTGA GAAAATGAAG ACACCATGAG 360
GCTAGACGAT TTTTTTCATG TAATTCAAGG ATTTGAGAAG AGATCAGCTG TTCTCAAATT 420
CGATCGGTCA TGACCTGTGC CATGAGTGAT CTGATGGTAA TGGTTAAAGT ACCATTAGCT 480
GGAGGATGAT TCATATATTT TTAAATAATA CATTATCCCT ATACCAACCT AATTCTTGCC 540
AGCATTTAAT ATGCTTTCCC TACCGGGAGA AAAAGGAGCA GAGTTACAGC TGGCATATTA 600
AGACTTCCCC TGGGAGTGTT ATGCATATGA ATGCCTGACC ATGTGCAGCG TAACAGAAAA 660
CAAGGTGGAG AGTCCATGGA ATAGCCAGTT CCAAAAGCTG CTTCCAGCTC TACAATGGGA 720
TGATTCACCC AAAGTAAACA ATGAGTTGAT GGCATTCAAA TCAAAACTAA CCACTTTTCC 780
TTGTCCATGT ATCTGACCAA GGATCACTCA CTTCAAACAG TTGTAGGATG ATTATAAAAT 840
GTGTCATCGG GGCCGGACTC AGTGGCTCAC GCCTGTAATC CCACCACTTT GGGAGGCTGA 900
GGCAGATGGA TCACCTGAGG TCAGGAGTTC AAGACCAGCC TGGCCAACAT GGTGAAACCC 960
CGTCTCTACT AAAAATAGAA AAATTAGCCA GGAGTGGTGG CAGGTCCCTG TAATCCCAAC 1020
TACTTGGGAG GCTGAGGCAG GAGAATTGCT TGAACCCAGG AGGCAGAGGT TGCCGTCAGC 1080
CGAGATTGCC CCACTGCACT CCAGGCTGGG CAACAAGAGC AAAAACTCTG 1130
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