| Tag | Content |
|---|
EnhancerAtlas ID | HS042-23822 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr2:10023630-10024780 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr2:10023644-10023658 | ACCCTTTGATGTTC | - | 6.36 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 10024085 | 10024324 | | chr2 | 10024309 | 10024600 |
| Enhancer Sequence | ACCTCTATTC AGATACCCTT TGATGTTCAA CTTAATGTTG AGGTTTATCC CTTTCCAGCC 60
TGTCAGTGTT AATAAATGCA GACATAAAGT GAATTTGCAA ATTTTATGGA AGTTTCAGCA 120
TTTCATGTTA TCTTTGAAAT TAATGTAGGA GAACTGCTTG CAAATCCATT GACAAACACA 180
GAGCTGGCAG AGAATTTAAA GTTGAAGAAG AGAAAACCAA TAATGAGGAT GGCACAATAG 240
GTGCTTCCAA AGGGAAAATT TGAATGTCAA AGGATTAAGA GTACTCCCTG GCAAAGCTGA 300
TAGAGCCCCT GAATATTTTG TAAAATAATT CTCTTTGTAG TTATGCTATA ATATCAAAGG 360
CAATAGGAAG GATGTCATAT TGTTGCGGGA TCTTTGGGGT GCCGTTTTTC TGGCTGGAAA 420
ACCTTTGTGG CCGGTGGCAT CTTTGCCCAA GTTTTGCACT AGGCTCATTT CGCCCACTCC 480
GCCTGGCAGG CTGTGCTTGG CTCACGCTAC CGGCCTGGGT CTCATGCCTG CCAAGGGCAA 540
GTCAGGCATG GAATGGTGAT GGATGTGTGA GCAAGCATGG GGTCTGGCCA GTCAGATATG 600
CCACCTGCTG CAGCGGGGCA GGCAGTTCCA GGTGCCAGCA TGATTGCCAG CGATCCGCGA 660
GGCTGCGACC GGACCAGTCG CGCTGCAAGC AGTTTCCGCA GCTGGCATTG GGGAACACGG 720
TGGTACCTGG GAGCTTGGAG ATGCCAGGAA CCACAGGGCC TCAAAGAGGG AGTCACAGCC 780
CTGGCTCGAG GAGCTCCCAG GTCTGGACTC CCCAAAGGAC CGCAGCTCTT CTTTCCTTCT 840
CTTTGCCCAC AACATGGCGA GCAAGGGGCA TGTTTCAGAC CTGTTTGTGT TACAACTGTT 900
TTAGCCTTGC CATTCTGTGC GTCCTGAGTT CGTGTCCTGC AACCAGGAAG AATGAGGTAC 960
ACAGATAAGT GGAGGGTGAG CGAGATGAAG AGGAGCTTTA TTGAGCGACA GAACAGCTCA 1020
GTCTCCCACA GCGGGCAGCT CCTTTCTGCA GCCAGGGTAT CCTGATGAGC GTTCAGCTCC 1080
TAGCAGAAAG GAGACTCTGG AATGGGAAGC TCCTGTCTGC AGGCAGGTCG TCCTATTGTC 1140
TTTGCAGCTC 1150
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