| Tag | Content |
|---|
EnhancerAtlas ID | HS098-42833 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr4:110841980-110843380 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr4:110843203-110843215 | TTCTGTTTACTG | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr4 | 110842471 | 110842980 | | chr4 | 110842589 | 110842871 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH04I109920 | chr4 | 110841814 | 110843400 |
| Enhancer Sequence | ATATTGTTCA CCATGAAGGA AGTATTGCCT AGATATTAGG TGAACTAAGA ACTAGATTCA 60
CTTTGTAGAG ATTCTTTATT ACCACTGAGG TGGTTGTGCA CACGGCCATC CCAGGCCCTT 120
CCCAGATGTC CTGTTTGCTG GGGCTCATGA CAAGATGACT GAGAGTCAGG TCTGGAAGGA 180
TGAATACTAT TATTGCCAGG TGTAGACGAA GAAAAAATTT CACTGAACAG AAGGGATCTT 240
TACACTTCTT GAAAGATCTT ACTATCTCTG AAAATGTTTT ACTCTCTTGT TTTATATGGC 300
CAAAGTTAAT AACTTCCAAA GGCAATTGTG GAATAATGCT TGTCAATATG TCTTTCTTTA 360
GGAGATGTTC TATTTCTTAA GAGCATCTTC CAGAGCTTTC TTCTCAATTC TGGGAATTAG 420
CAAATGTATA GAAACTTCAG TTGTTTTAGC CAAATACAAG GCAGAAACTT CTACTCTCAT 480
CACCTGTTGA CCTCCTTGCT AAGTCTGGAA TCTGAATTGG TGTGAGCATC TGTTTTTTTT 540
TTTATTCTGA CTTGATTTTC TGATTCTCCC AAGTTGACCA AACATACTAA TGCCTCTCAC 600
TGTCTGGGTT TCCCAAGTAT TTCCCAGGAC ATTCAGTACA CTGGAATTTG TGTGTGTGTG 660
TGAAGGTATT TGAGAGCCAG CCAACTGCTG TGACAGTGAT TCATGGTAGG CACTAATTTA 720
TTTGCAAAGC TTCTTCCCAG TGATGTAAGA GTCCTTTTGG AGAAAAGCAC TGCCTCCTTC 780
CTCCATTCAG ACTAACTTCC CAGGGTGCTA TGGACCAGCT TTGTGTGCAG TAAGGGAATT 840
ACATCCATGA GGTGGTTCTT TCTGTGGGTA GGTGGTTGCT AGGATACAGA TAGTCACAAC 900
AGCATCACGG CAGCTGCCTT GTTCTTCAGC ACATGGTGTA TCAGTTGAGA AATAGTGTTT 960
TATTTCATTC ACTCCAACAC TTTTCTGGTT AAAATTTTAA AAGCTTGAAG GAGGATCTTT 1020
CTTTTTCACA CACACCATTC TTGTATAAAC AGGTCAAAAA CAGATTAGTC AAACTGAACA 1080
TTGTCATAAT ACATGCCGGT TGACACCAAT CCTCTGCTCT TCCAGCCCAG GCCTTCCCTT 1140
ACGAGGTTTA AAAACATGCT GAAGGGTTGA AGCTACCAAG GGTCTTCTGG TGTTTTTCTC 1200
CCTTCCTCTG AAGTGCATAA TTATTCTGTT TACTGGAAGA TTTTCAACAC AAAGGAAATT 1260
AACTTCTCCT TGGTGTGCAA GGAAATTGCA AAGGTTATTG TCATTAATGT TAATTTACCC 1320
ACTATATCTT TTAGATTCAA GCAACATTGT TTAGAATGGT CAATGCTCTA AGTGGATCAA 1380
AAGGCTTATT ATTTTTTGGA 1400
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