Tag | Content |
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EnhancerAtlas ID | HS129-20795 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr2:170676150-170677200 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr2:170677013-170677029 | CTTTGTTTACTTAATA | - | 7.62 | FOXP2 | MA0593.1 | chr2:170677014-170677025 | TTTGTTTACTT | - | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I169818 | chr2 | 170675257 | 170676197 |
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Enhancer Sequence | TCCCTGTGAA GAGTAGAAAA AAAGCTCCTA TTTACCTCTT CTCAAAACAG AAGATTAAGT 60 TAGTAGGATT TAGAAATATT TTCTTCCAAA CTTCAAAATA GCCACCTTGA AATCTTTTAG 120 CAATAAGGGT ACAAATAAAC TATCAAAATA TTATTTTAAG GCTGGTAGAA TAAAACCAGA 180 ATTATACTGT CTTGGTTAAA TAAGGATAAA GTAAAAATTT TAATATTATA TTCCAACATT 240 AATGACTTCA AAAAGGGGAG AAGGAAATGC ATAGAGTACT ATTCAGAATC ATCTTGGTGG 300 GGGCAGGGTA CTTTTTAAAC TATGCATGTC TTTTTTTTTT TTGTTTCGCT CTTGTTGCCC 360 AGGCTGGAGT GCAATAGCAT GATCTCAGCT CACCGCAACC TCCGCCTCCC GGATTCAAGT 420 GATTCTCCTG CCTCAGCCTC CCTAGTGGCT GGGATTACAG GCATGTGCCA CCATGCCTGG 480 CTCATTTTGT ATTTTTAGTA GAGACGGGGT TTCTCCATGT TGGTCAGGCT GGTCTCAAAC 540 TCCCGACCTC AGGTAATCCA CCCACCTCAG CCTCCAAAGT GCTGGGATTA TAGGCGTGAG 600 CCACCACGCC CGGCCAAACT ATGCATGTCT TTTCCTACCC TCACTGACTT CCTAACCTCC 660 TTGCCCACAG TACACACAAA ATTAACAGCC ACGGTGAGTC ACTGTTACTG ATGGGCACAT 720 GTAGAAACCC TTGGGTCTGT TAAGACATTA AAAAACAGAT TCTGAAAGTA TAAAATTCTT 780 TCTATGTTTC GTATTCATTC ATAAGGGTTA GGCAAATTAT TCCTGAAAGC AAATGGGAGA 840 TATACAATAA ATGACATGAC TATCTTTGTT TACTTAATAC AAATTTGTAA AAATGAAAGT 900 TGAAAAACTC AGTTTCTTAG CCATGCATTA AACAAATTGA AATGTAAATT ATAAGAACTA 960 TACAAATAAG AGATTGGTTT ACTTAATGAA GAGTAATAAC ATCACTTAGC CTTGGTTTAT 1020 TTAATGAAGA GTGATAAAAT CACTTAGCCC 1050
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