| Tag | Content |
|---|
EnhancerAtlas ID | HS187-17774 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr3:148921090-148922500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPIC | MA0687.1 | chr3:148921744-148921758 | CTAAAGGGGAAGTA | + | 6.26 | | TBXT | MA0009.2 | chr3:148922333-148922349 | TCACATGTAGGTGTCA | + | 6.48 | | TBXT | MA0009.2 | chr3:148922333-148922349 | TCACATGTAGGTGTCA | - | 6.7 | | TCF3 | MA0522.2 | chr3:148921510-148921520 | AACACCTGCT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I149203 | chr3 | 148921681 | 148921830 |
|
Enhancer Sequence | CCCAAGCTGG AGTGCCGTGG TGTGATCTTG GCTCACTGCA AACTCTGCCT CTCTGGTTCA 60
AGTGATTCTC ATACCTCAGC CTCCTGAATA ACTGGGATTA CAGGCATATG CCACCATGCT 120
CAGCTAATTT TTTGGTTTTT AATAGAGACG GGGCTTTGGT ATGTTGGCCA GGCTGGTCTC 180
GCACTCCTGG CCTCAAGTGA TCCACCCGCT TTGGCCTCCC AAAGTGCTGG GATTACAGGC 240
ATGAGCCACG GCGCTTGGCC AGGAGCTTTT GTTTATTAGC TGAAACTCAC ATGACATCGC 300
AACAAAGTTG GTATTATTCT CCCTATTTTG CAAACGAAGA AATTAAATTT CAGAAAGGTA 360
ATTATTTGAC TTGCGCAAAG CCACCTCATT CATCATTTCT TTCACTTGAC AAATGCATCA 420
AACACCTGCT CTTTGCTGGG AATCCTGCTA TGTGTTGATG ACTTAACCAT AAGCAAGGTG 480
GACTCTTCCT TGTCCACGTG GACCTTACAT CTGGCAGAGA AGACAGGCCA TGAACCCATC 540
AATATAATAC AGTGTAATAA GCACAGGGTA TTATGGAGCA TTTCTTTGAG GTTGGGGAAA 600
GTGCAGTGAA GAGGCCACAA AGACATTCCA GAGGAAGTGA TTACTCAAAA CTACCTAAAG 660
GGGAAGTAGA GTTAGCAAGA TGAAGTGTGT GTGTAGCGCA GAGACTAGGG CAGGTGTATA 720
CAAAGAGGAA ACTGCTTATG AGCAGGCTTA GAGAAAAGAG CGAGCATGCC ATGTTCTAGA 780
AAATATGGCA GAAGCATAGC ATGCAAGACA GGGCAGAGGA GTGAAGAATG AGGCTTAGAT 840
AGATGGGAGA TAAGCAGTAG GACCTAGTTA AGGTTTCAGC CTTCCATCCC AGGGCAGTGA 900
GAAGCATTTG AAAGATTTAA GCATTCAGGA TTAGCATTTT AGGAGGATCC CTCTGGCAGA 960
TGTTTGGAGA ATGTGTTGGA AAATACAAGA CTGCAGTAGG GAGACCAGTC AGGAGCCTGC 1020
TTTTCTAATC TCAGTGAGAG GCAGAGATGA GTTCATAGGT ATTGGCAAAG AAGATGGAGA 1080
GAAGTAGACA GCCTTCAGAG ATAGTTTCTA TAAAACAAGG CAGTACTTGA TGAGGAGAGG 1140
AGTTTGAATA GCCTCATCCA TGTGGGGGTG TCACTAAGAA GTTTGAAATG CAATCTGAAA 1200
TTCACTAGAT CCTCCTGAGT TGGAGACGCA GCGTTGGGAG TAATCACATG TAGGTGTCAG 1260
TGTAGCATGG GACTTAAATC TCTGCTTCAG GAGTCACAGG TCTGGGCTGA GCAAGTCCTA 1320
GCTATCCATT TATTGTGTGA TGTTGGATGA ATTACTTAAC CTTTCCAAGG AGGGTATTTT 1380
TAATATGGAT GGCAAACAGG GCTTCTCTGA 1410
|
