Tag | Content |
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EnhancerAtlas ID | HS030-01402 | Organism | Homo sapiens | Tissue/cell | CyT49 | Coordinate | chr1:112394140-112395290 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr1:112394255-112394266 | TTTGTTTACTT | - | 6.62 | IRF1 | MA0050.2 | chr1:112395170-112395191 | AGAGTGAAACTGAAATCGAAT | - | 6.21 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AATCTCAACA ATCTCATCAC AACTCCTCCT GGCAAATTTA GTCACTCCCT TCTCTGTGTT 60 CAAACCTCTG TAAACATGCC TGCATTACAG TCTTTACCCC ATTGTATTGC AAACATTTGT 120 TTACTTATCT GTCTTCCTCA CTAGACGTGA GCTCCTCAGG GACCAAGCCT GTTCCTCATT 180 CTTCTTGTAT TCCCCAACGC AGCACCTAGC AGGGAATCTG GCACAATGCG AACACTCAGT 240 GCCTGTGTGT GGGGTGAATC ACCACCATGA GGCGGCCGTG GCTATGGAAC AAAGAGTGGC 300 TCACAGCTCA ACAGGGACCC TGGATTCTCC AGGAGAGACT CCTCAGAGCC ACTGCCCACT 360 TGCTGAGGGC AGTAAGGTGC AAAGGATGTT TACCACGACA GCCAGCAACT TGGTTTGGCT 420 CCCTATAGCC TCCTCTTGTC TCTGCCTCTA AGCTCCCAGG AGTACCTGAC CCATCAATCT 480 CTACAGCTGC CACTGTCTGG ATAATCAACT ATTTGTGGAG GTCACAAAAT ACGTGGGTCA 540 CAGGCTCAGG TTTCTCCCCT GGAGGATGGA TGGAGCTTTT CTTTGTCCTC TTCTCATCCT 600 AGTCACCTGC GTTGCCCAAT ATTAATCAGG TGCCTACTAT GTCTAAGTCC CTATTCCAGG 660 TGCTGAAAGC ACTTTTCTGG AAAGTCTGAG TGGTCAGTGG TTGTCATGAC TTGGAGGAAG 720 GTTGGCAGGG AGAAGATGGA GTGGGGGCTG GAAAAGCAAA GCAAGCCCAG GAACAAGAAA 780 TTACAAATGC CTTCAAGGCA GCCTGCAGCC CTCAGCCCTC TGTGGGGCCT GCTCAGCAAC 840 ATGCCTAGCA GGTGGGGAGT CCTTTTTGTG GGCCGGCAGG GACTAAGCCT GAGCTGTGCA 900 TGCTGGCAAC AGGCGTCATC TACATAAGCC TGGCCCAGAC AGCTTCCAGC CTGGTGCTGG 960 GCTCTGTCTC CGGCACCTTC TTTTAAGGGG TAATCATTTT AATAAATAGG GATTGTGGGC 1020 CTCTTGCCTG AGAGTGAAAC TGAAATCGAA TCCATAATCC AGACAGAGGG GAGTGCAGCT 1080 GCACTGGGTT AATTACGCAC ACACCAAGCA TATGGCAGCG CACCTCCAGA CCAACAGGCG 1140 GAGAGCATTC 1150
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