| Tag | Content |
|---|
EnhancerAtlas ID | HS102-06484 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr12:123293000-123294310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EN2 | MA0642.1 | chr12:123293195-123293205 | CCCAATTAGC | + | 6.02 | | 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: 2 | Chromosome | Start | End |
| chr12 | 123293332 | 123293781 | | chr12 | 123293365 | 123294229 |
|
Enhancer Sequence | ATAGACACAT TTTTTTTTCG TTTATCTAGG AATGGAATGC TAGCTAGCTC ATATGGTAGG 60
TGTATATTTA ACCTTTTTTT TTCTTTTTTT AGAGACAGGG TCTCACTCTG TCGCCCAAGC 120
TGGAGTGCAG TGATGCCATC CTGGCTTACT GCAATCTCAA ACTCCTGGGC TCAAGTAATC 180
CTCCCACTGC AGCCTCCCAA TTAGCTGGGA CTGTAGGCAT GAACCATTAT GCCCAGCTCA 240
TTTTTACATT TGTTGTGGAG ATGTGGTCTT GTTATGTTGC CCAGGGTGGT CTCAAACTCC 300
TTACCTCAAG CAATCCTCCT GCCTCAGCCT CCCAAAGTGC TGGGGTATAT TTAACATTTT 360
AAGGAACTGC AAGATGTTTT CCAAAGTGGT TATACCAGTT ACATTCCCAC CATCAGTGTG 420
GTGCTGATGC TCCGGTCCCA GCTGCTCCAG ATTCCAGTCA ATACTTGCAA TGGTCAATTT 480
TTAAATTCCA GACATTCTAA TAGGTATGAA GAGGTATCTC AGTGTGGTTT TAACTTTCAT 540
TCCCCTAATG ACTAACAATG TTGTGCACCT TTTCACACGC TAAACCACCA TCTATTTATA 600
GCTTCGATTT CAACTGATAG AGAAGTTCTA GCCAGTTATT CAATCCCAAA GAGACGCTAT 660
TCTTTATGTC TGTGTAGAAT ATCCCTTCTT TAATTACTTC TCCAGATTTA CCTCCTCTCT 720
GCACTATGCG AACAAAACAC TTATCAGGCC ATCAGGCCGG GCGTGGTGGC TCATGCCTGT 780
AATCCCAGCA CTTTGGGAGG CTGAGGTGGG CAGATCACCT GAGGTCAGGA GTTGAAGACC 840
AGCCTGGCCA ACATGGTGAA ACCCCATCTC TACTAAAAAT ACAAAAATTA GCCAGGTGTT 900
GTAGCTCGTG CCTGTGGTCC CAGCCACTCA AGAGGTTGAC GTGGAAGAAT CACTTGAGCC 960
CGGGAGGCGG AGGCTGCAGC AAGCTGAGAT TGTGCCATTG CACTTCAGCC TGGGCGACAG 1020
AGCCAGACCC TGTCTTAAAA AATAATAATA GGCTGGGCGT GGTGGCTCAT GCCTGTAATC 1080
CCAGCACTTT GGGAGGCTGA GGCGGGTGGA TCACCTGAGG TCAGAAGTTC AAGACCAGCC 1140
TGGTCAACAT GGTGAAACAC CATCTGGCTA TGGCGAGGTG CCAATGACTT TCTTCACAGA 1200
ATTGGAAAAA AATACTTTAA AGTTCATATA GAACCAAAAA AGAGCTCGCA TTGTCAAGTC 1260
AATCCTAAGC CAAAAGAACA AAGCTAGAGG CATCACGCTA CCTGACTTCA 1310
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