| Tag | Content |
|---|
EnhancerAtlas ID | HS191-10595 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr13:42066430-42067720 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr13:42067326-42067347 | GAAGGGAAAGGGAAAGGGAAA | - | 6.31 | | IRF2 | MA0051.1 | chr13:42067330-42067348 | GGAAAGGGAAAGGGAAAC | + | 6.58 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_31340 | chr13:42065457-42068154 | Fetal_Thymus | | SE_58470 | chr13:42061587-42087475 | Ly1 | | SE_59875 | chr13:42063524-42078940 | Ly4 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 42066566 | 42066810 | | chr13 | 42066974 | 42067300 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I041491 | chr13 | 42065582 | 42068100 |
|
Enhancer Sequence | CCACATGTGA GAGGCATGTC TGAAATGAGG AGCAGTAGAA GGGCGGCCAT TGGCAATTAG 60
TCAAGGTTGG GAATCCTGAG GAGGCTTCTC CATGGGAACA TCCCCCTGGG TCTGGGCTGA 120
GGAAAGGAGG AGAAAGTATG AGCTTTCAGG CTAGACAGGG TTCAAATCCC AGCTCTGCCT 180
TGTAGTAGCT GGGTGACCTT GAGCAAGCTC TTTAACCTCT CAGAGGCTCT GTTTCCTCAT 240
TTGTAAAGTG TAGGTGTGAG TCACTGTCTC CTAGGGTCAT TGCAATGATC AAATATAGAA 300
AAGAAAAAGT GTCTGGCACT CCTCCTCCTC CTTTTCATAC CACAAGGACA TTGGGCTCCT 360
GTACCCAAGG TAAAATTAAG CTTTGCCTAC AGTGGCTGCA GAGGGCAGTT CTAGCCCCAT 420
TATTCCTTGT CTGATAGAAG AAAGTGGCAA ATCTGGCCTA ATGCAATCAC AGCGAGGAAG 480
GCAGAGAAAA AACACTGGGC AAAGGGGCAG GAGAGAGGGT GAAAGCCCCA GTCCTGCTGT 540
GAACTGGATC CCTTCCCCTC TCTGGGCCTC AGATTCCTCC AAGTTAATCG GACTAAATGG 600
CCTGGGGTCT GTTCAGTTCA TACAGTTGGT GGGCTCTGGC CTTATCCTCA GACTGCCAGC 660
TCTTCTCTGA AAAATAGATG GAATTTTTCT TGAATTTTCA GTATGTGCAA GAAGCACGTA 720
CTTCTCCAAA ATGCCTTCCT GTGTTAATTT ATTTGACTAA GAAGGTTTGC AGTGACAGAC 780
ACCAAACAGG AAACGGCTGT CATAGCTGCT GTCTGCAAGT TTTGTTTTTT TTTAAGGCTT 840
TCTCCTGCAC AACTCACCTT CTCTTCATGG CTTGGTATCA AGTGCTGGGG TGAATGGAAG 900
GGAAAGGGAA AGGGAAACAC ATTTTTAGAA GGGAACATTT TCCTTCAAGT TCAGGGTCTA 960
CTGAAGGTTA AGGAGTATGA CTATCCACAA TGGCAGCGTT AGGTGGCTCC ATTGCAGGGC 1020
CTTTGCACAC TCAGTTCCCT CTGCCTGGAA TGTCCACTCT GCTCGGTTTT TCTAGTTAAT 1080
TCTACTTCTT TAGGATCAGC TCAAGCATCA CTTTCTCAGA GTCTTCCAGA TCCGTCTAGA 1140
TTGTTTGTTG GTGCTGTGTT CTTGTAGAAC CTTCCTTCAG TGCACTCATC TTGGTTTGCA 1200
ATGGCATGTT CAGTAGTGTG ATGTTTTGGT TAATGTCTCC CTACCCTCCT GTAACTGGAC 1260
CATAAGCCCC ACAAAGACAG GAGCCTTGTG 1290
|
