| Tag | Content |
|---|
EnhancerAtlas ID | HS047-07264 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr12:2733740-2734860 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:2733856-2733875 | CAGCGCCCCGTGGTGGCCA | - | 6.4 |
| | | 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 |
| GH12I002624 | chr12 | 2733321 | 2734829 |
| Enhancer Sequence | TACGGAAACC TAGACATTCT CTTGGGCTAG GTCTTCAATC CTTTCTGGAC CCAGTGCTCT 60
TCTTTTTGGA ATAGTCTCCG CACCCACTGT ATACTCCATG TCCCTACAGA GCTCCACAGC 120
GCCCCGTGGT GGCCAGTGTC ACCCCCTCTC TAAGAACCCA CACATAGCCT CAGGCTGGCT 180
GACTCAGCGT CTTAGTGACT TTTAGATGAA ACCTGTTTAT CCAATCTATT GAGAAACTGC 240
AGTGTCTGCC ACCGTCCACA GAAATCCCTA GGTAGAGAAA TGCATTAAAA GGAGTAGAAA 300
AGGGACCGGG AAAGAAGGGC AGCAGCTGCG GATGAAATGC GGCAACTCTT GCCCCAGCCT 360
TCGCCATCGG CACAGAATTC AGAGGCCAAA GCTGTGTGGG CCAAGCTCCC GCATTCCCCT 420
GATTATTATT TATTTGCAGA GTGCCCACGG GGCACCGGGT GCCACGCAGT GCTCCTTAGA 480
CAGGCAGGCC CCAGCTTTGC CAGGAGGACC TTCCCCCGCT CCCCCCGCCC CCCATGGCTC 540
TGCACTCAGG GATTTGCATT TTGTTACAAC ACTGTGACAG GTTTCTTTCC GGCCTTGTGC 600
TGGAGAGCTT AAAAGTCACT ATGAAGCATA AAAAATAATT ATATGACTTG CATAAAGCCT 660
TCATGTGGGA AGGCTAGTAT TAGCTATTAC ATTTAATTAT TTAATGTAGA AAATTATTCA 720
CACGGTGTAA AAAAGCCCGG TGGGAAAGTA CACTGTGGTT TCCGTCTCTG GCCCTGCCAC 780
AGGGAAGGAA ACTGGAACAC ACCGGTCTGG TAGGAAGAAG AGGGATTCCC AGACCTACAG 840
GGTGCGTCGG CGATAACCCG ACCCACCAAA GCCCGAGGTG CTGCCAGTGC TTCCGGCCCT 900
GCGCTGGGTC AGCCTGCCTT AGGGGCAGGA AGGACCTTCT GTGACACAGG CTGCGGGCAG 960
TACAGGAAGG TAGCCTCTCA GCAAGAACCC CACCAACAAC AGCAATAGTA GCAACTGTAG 1020
CAATCAGTGA GCACGTTCTC GGTGCCAGAC AGGGCAGGTG TGAACTTATA TCATTCTCAC 1080
AAAGCCCTAT AAGGGGCCAG GCACAGTGGC TCACACCTGT 1120
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