| Tag | Content |
|---|
EnhancerAtlas ID | HS095-07980 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:123293200-123294190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr12:123293590-123293602 | TCTATTTATAGC | - | 6.62 | | MEF2B | MA0660.1 | chr12:123293590-123293602 | TCTATTTATAGC | - | 6.52 | | Nkx2-5(var.2) | MA0503.1 | chr12:123293921-123293932 | AGCCACTCAAG | + | 6.62 | | Nr2f6(var.2) | MA0728.1 | chr12:123294116-123294131 | GAGGTCAGAAGTTCA | + | 6.38 | | RARA | MA0729.1 | chr12:123294116-123294134 | GAGGTCAGAAGTTCAAGA | + | 6.88 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TTAGCTGGGA CTGTAGGCAT GAACCATTAT GCCCAGCTCA TTTTTACATT TGTTGTGGAG 60
ATGTGGTCTT GTTATGTTGC CCAGGGTGGT CTCAAACTCC TTACCTCAAG CAATCCTCCT 120
GCCTCAGCCT CCCAAAGTGC TGGGGTATAT TTAACATTTT AAGGAACTGC AAGATGTTTT 180
CCAAAGTGGT TATACCAGTT ACATTCCCAC CATCAGTGTG GTGCTGATGC TCCGGTCCCA 240
GCTGCTCCAG ATTCCAGTCA ATACTTGCAA TGGTCAATTT TTAAATTCCA GACATTCTAA 300
TAGGTATGAA GAGGTATCTC AGTGTGGTTT TAACTTTCAT TCCCCTAATG ACTAACAATG 360
TTGTGCACCT TTTCACACGC TAAACCACCA TCTATTTATA GCTTCGATTT CAACTGATAG 420
AGAAGTTCTA GCCAGTTATT CAATCCCAAA GAGACGCTAT TCTTTATGTC TGTGTAGAAT 480
ATCCCTTCTT TAATTACTTC TCCAGATTTA CCTCCTCTCT GCACTATGCG AACAAAACAC 540
TTATCAGGCC ATCAGGCCGG GCGTGGTGGC TCATGCCTGT AATCCCAGCA CTTTGGGAGG 600
CTGAGGTGGG CAGATCACCT GAGGTCAGGA GTTGAAGACC AGCCTGGCCA ACATGGTGAA 660
ACCCCATCTC TACTAAAAAT ACAAAAATTA GCCAGGTGTT GTAGCTCGTG CCTGTGGTCC 720
CAGCCACTCA AGAGGTTGAC GTGGAAGAAT CACTTGAGCC CGGGAGGCGG AGGCTGCAGC 780
AAGCTGAGAT TGTGCCATTG CACTTCAGCC TGGGCGACAG AGCCAGACCC TGTCTTAAAA 840
AATAATAATA GGCTGGGCGT GGTGGCTCAT GCCTGTAATC CCAGCACTTT GGGAGGCTGA 900
GGCGGGTGGA TCACCTGAGG TCAGAAGTTC AAGACCAGCC TGGTCAACAT GGTGAAACAC 960
CATCTGGCTA TGGCGAGGTG CCAATGACTT 990
|
