Tag | Content |
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EnhancerAtlas ID | HS047-18561 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:25706420-25707460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROD2 | MA0668.1 | chr2:25706979-25706989 | ACCATATGGC | - | 6.02 | SPI1 | MA0080.4 | chr2:25706673-25706687 | CACTTCCTCTTTTA | - | 6.65 |
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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: 2 | ID | Chromosome | Start | End |
GH02I025485 | chr2 | 25706601 | 25706750 | GH02I025483 | chr2 | 25706763 | 25707096 |
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Enhancer Sequence | CAAATTTAAA CTTCAAGGTT AGCATTTTTG GTAACTTGTC TTTAGCTGCA GGTTTTCTAG 60 ACTCAGGTCC ATTTCTCCTT CTTGTGAAAG TCCTGAAGGA ATGAATTCAA GCTTCTCAAA 120 AAGGTGCCAG GTATCTTGCC TTCCAGCCAT TCTTCAACCC CTCTCCCTCC CTACCAGGTT 180 CAGCTACAAA AGGGTTCTGT CTTGCATCTG GAACCACATG ACTATTGCTA AATACTTAAA 240 CTGGAAAATT TCTCACTTCC TCTTTTAAAC TGGAAGAAGT ACAGTCATGT GCCACACAAT 300 GATGTTTAGG TCAATGACAA ACCACATACA TTATAACAGA TTATAATACT GTATTTTTAC 360 TGTACCTTTT CTATGTTTAG ATACATAAAT ACCCTTGTGT AACAGTTGCC TCCAGTATTT 420 AGTACAGTCC CATGTTGTAC AGGTTTGTAG CTTGGAGGCT ACATACATAG AGTGTACTTA 480 CACATACTTG GATGGTTTTG CCTGCTGCAA ACCTAGGCTA CACCATATAG CCTAGGCTAC 540 ACCATACGGC CTAGGCTACA CCATATGGCC TAGGTATGAA GCAGGCGAAA CCACCTAGGT 600 TTGTGTAAGT ACACTCTCTG ATGTTAACAC AACACAAAAT TGTCTAACAA AGCATTTCTC 660 AGAATGCATC CCCCATTGTT AAGTTATGCA TGATTATACT TCTCATATTT GTCTATCAAA 720 AGCATAAAAC TGAAGCTGAA AGTCCTTCTC TCATATTTAG GTGCTTGGGA ACTAACTACC 780 TTCTGGTTTC TCCTTCCGTT TAAGGACAGA GTTAATTATG TAAAATGTTT CTGGAGAGGT 840 TATACTTAGC AATTCTTTGT GAATATTAAG GGATCACAGG CTTTATTGTT TTGCAGGTTT 900 CATAGTACAC TCAAATAAAA GCTCAAGGGG AAATATTTCA GGGAGGGCCA AGGAACCCAG 960 ATGTTAAAGA AGGATCTCTT TCTCCATCTA TCTATGCACT TTTTTTTCTT CTTAAACCAA 1020 CTGCATTTCT GTATAGGGAT 1040
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