| Tag | Content |
|---|
EnhancerAtlas ID | HS076-13296 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr12:43665500-43666730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr12:43665957-43665978 | AAAGTAAAACTCAAAGTGAAA | - | 6.02 | | IRF1 | MA0050.2 | chr12:43665963-43665984 | AAACTCAAAGTGAAACTGACT | - | 6.76 | | NKX2-3 | MA0672.1 | chr12:43665515-43665525 | ACCACTTGAA | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 43665590 | 43665736 | | chr12 | 43665965 | 43666597 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I043271 | chr12 | 43665573 | 43666903 |
|
Enhancer Sequence | TATTCTTAAT GTGGTACCAC TTGAAAACCT CAATTTGATG GGTACCTATT TTACAAAGAA 60
GAGCATTTTT AGGGAAGCGA GAAGTGTTCT AGTCTAAGCA CTAATAAGGT GATTAAATCA 120
CAATGGACAT GTGTAGGCAG CCTTGGGGGC ACATGTATAC TCCTAGCTAG AAGAGACTTT 180
GGCAAGGGGA GGAAGTATTG GGCAATATGT TTATAGAACT CGTGATGGAG CCTCCAGGAA 240
AATACCAACA ACAATATTTT GCCCAACATT ACTGTGAATC CTTTAATTTT TCTTTCTTCT 300
AAGAACAGAT TTAAAAGGGC ATTTGGCATT TATTTTGTTT TGTTTTCAAG TAATAGCTAC 360
CTCATTAAAC CTCAGGTTTG ACAGTGTGGG CTCATATGCC AGGTTGTATT AATTCATCTT 420
TGCCCTGTTA AACGGGAATA ATTCAAAGAA ACTCCCCAAA GTAAAACTCA AAGTGAAACT 480
GACTTCCCAA AGTACTAAGA AATATTGTTC AGAAAAAATA AAACTTCAAC ATTTGGTACA 540
ATTTATTTCG CCCATCTTCT TGAAGCATAT TCGTTTTATT AGCATTAAAA ATTATAGTTG 600
TGTCAGTTCT GCAGCTGACA GTGGTTTGGT TCAAACCAGA GTCAGTGGCA GCTGCAAAAA 660
TAAGGAAACA TCTTGTCTGT TGCCATGAGA GGATTACAGT ATAACTCACA GCAAGCCAGC 720
TTTATGCAAA CTATCTCAGG TTTGTCATGT AAAAATCAAA GTCACATGTC TCTACATGAG 780
CGGCATTAGC TGAAAAACTT CCAGCCTACT AAGCAGAGAT AGTAACCACA AAGACATGAG 840
ACTTTCTGCA TTTAAAGGAC AAACCAGTAG GGCATTCTTT TCTTGTACAA ACCAGTAGGG 900
CATTCCATCC CAAAAGCCTG TCCCATTCCT GCAGCTCTAA TTGACTCTTC ACCCCACATC 960
AAGGACACTC TGAGGAGAAA CTAGTTGGAG AATCGCTTCC AGCAGTGTGA GGCTCTCCCC 1020
TAACAACAGT GCAGTCTGCC CTTCTCAGGC CCCTACTGTT AATTCCTAAC CCCTAGAAGA 1080
AGGATTTTGT TTTTGTTTTG TTTTGTTTTT GAGACATAGT CTCGCTCTGT TGCCAGGCTG 1140
GAGTGCAGTG GTGCTATCTC GGCTCACTGC AACCTCCACT TCCTGGGTTC AAGCGATTCT 1200
CCTGCCTCAG CCTCCCAAGC AGCTGGGACT 1230
|
