| Tag | Content |
|---|
EnhancerAtlas ID | HS147-12250 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr12:123292940-123294210 |
Target genes | |
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: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTGGTGTGCT AGATAATACA AATAAAGCTG CTTGCATATT CATGTATCAT AAGTCTTTGT 60
ATAGACACAT TTTTTTTTCG TTTATCTAGG AATGGAATGC TAGCTAGCTC ATATGGTAGG 120
TGTATATTTA ACCTTTTTTT TTCTTTTTTT AGAGACAGGG TCTCACTCTG TCGCCCAAGC 180
TGGAGTGCAG TGATGCCATC CTGGCTTACT GCAATCTCAA ACTCCTGGGC TCAAGTAATC 240
CTCCCACTGC AGCCTCCCAA TTAGCTGGGA CTGTAGGCAT GAACCATTAT GCCCAGCTCA 300
TTTTTACATT TGTTGTGGAG ATGTGGTCTT GTTATGTTGC CCAGGGTGGT CTCAAACTCC 360
TTACCTCAAG CAATCCTCCT GCCTCAGCCT CCCAAAGTGC TGGGGTATAT TTAACATTTT 420
AAGGAACTGC AAGATGTTTT CCAAAGTGGT TATACCAGTT ACATTCCCAC CATCAGTGTG 480
GTGCTGATGC TCCGGTCCCA GCTGCTCCAG ATTCCAGTCA ATACTTGCAA TGGTCAATTT 540
TTAAATTCCA GACATTCTAA TAGGTATGAA GAGGTATCTC AGTGTGGTTT TAACTTTCAT 600
TCCCCTAATG ACTAACAATG TTGTGCACCT TTTCACACGC TAAACCACCA TCTATTTATA 660
GCTTCGATTT CAACTGATAG AGAAGTTCTA GCCAGTTATT CAATCCCAAA GAGACGCTAT 720
TCTTTATGTC TGTGTAGAAT ATCCCTTCTT TAATTACTTC TCCAGATTTA CCTCCTCTCT 780
GCACTATGCG AACAAAACAC TTATCAGGCC ATCAGGCCGG GCGTGGTGGC TCATGCCTGT 840
AATCCCAGCA CTTTGGGAGG CTGAGGTGGG CAGATCACCT GAGGTCAGGA GTTGAAGACC 900
AGCCTGGCCA ACATGGTGAA ACCCCATCTC TACTAAAAAT ACAAAAATTA GCCAGGTGTT 960
GTAGCTCGTG CCTGTGGTCC CAGCCACTCA AGAGGTTGAC GTGGAAGAAT CACTTGAGCC 1020
CGGGAGGCGG AGGCTGCAGC AAGCTGAGAT TGTGCCATTG CACTTCAGCC TGGGCGACAG 1080
AGCCAGACCC TGTCTTAAAA AATAATAATA GGCTGGGCGT GGTGGCTCAT GCCTGTAATC 1140
CCAGCACTTT GGGAGGCTGA GGCGGGTGGA TCACCTGAGG TCAGAAGTTC AAGACCAGCC 1200
TGGTCAACAT GGTGAAACAC CATCTGGCTA TGGCGAGGTG CCAATGACTT TCTTCACAGA 1260
ATTGGAAAAA 1270
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