| Tag | Content |
|---|
EnhancerAtlas ID | HS191-06501 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr11:13961220-13962690 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ONECUT1 | MA0679.1 | chr11:13962109-13962123 | GGTATTGATTTTCT | - | 6.15 | | ONECUT3 | MA0757.1 | chr11:13962109-13962123 | GGTATTGATTTTCT | - | 6.15 |
|
| | 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 |
| GH11I013939 | chr11 | 13961272 | 13962643 |
|
Enhancer Sequence | CCCGAGTCCA CAGGGAAGGG GGTTCTTTTT CCTGTGACAA GGTAAGTTGG TGCAGCCCTT 60
TTGGCAGGGA ACTTGCACTG TGTAATAACA GCTGCAAAAG GCAATTCCAT TTAACAGTCA 120
TTTAATTCAT TTAACACACA GCCATAGAGC TGCTTGAGAA TTTTTCATAA CGCCATGATG 180
GAAATTACCT TCTTCTCATG GGAATTCCAT TTAAGAAGGG GTCACATGGT ACTATTTACT 240
ATTCTCCCAA CTACCTGTCA ATCTGGTATC TCTCCCATGG GGCTCACTGG GAGAAGCCAG 300
CTTCTGCTAC AGGGTCACAT TAATTACCGT AGCCCTTAGG ATCCTGTCTC CAGAGGACCC 360
AGGTAGAGCT GGAGCCCAAG AACAGTCCCT TCCTGATGTG GGCAGGAAAC TCTAGCTTCC 420
TTATTAAGGA CACCTCCCAG CTCTCCAAAG TTGAACAGCC TGACTTTGTC ACTGTGATTC 480
ACATTCCTCT CATCTCTTCT TGATGACCTG GCTGCCCCGT CACTCTGGCC CCAGGGGATA 540
CTGTTTTTCC TTTAACATCC TTACTTCATT CTGAGTGCTG CTTCAGAAGG AAGGGGCCCA 600
CAGCTCTCTG CCAATGATTT AATTCCAAAT ACTCTTTTTT TCATCGCCCC AACCCAGACC 660
CCATCCCCTT CCCAGCAGCC TGGAGGTCCT GAGCAAATGA ATTCCTGGTC ATGACCTTTC 720
CCTATAGTCT TCCTGGACAT GGTCACCTCC ACTCTTGATG CCCTCCGGGT CTTGGACAGC 780
ACACTTTTAA ATCTAAGTAC TGTTAGCTCC GCCTGGGCCC AGGGCAGCGG GTGGGGCAGG 840
GGGTCAGAGA GCACAGGCAG GAAGCATGCT CCTGTGCCCT TCATTGCCTG GTATTGATTT 900
TCTCCCATCC CTCACTCTTC CACTGCCCCA TAAAGAAGTC AGAGTTGTAA AGCTGTCAGG 960
ACATTTTCTA TGAGACAGGT ATGCAGAATG GAAGTGTTGT TAGTGGCTCT TAAAGAAAGA 1020
AACCGGGTGG CTCTGTGGTA GTCTCTGGCA TTGTTGTGGG CTGTGCATAG AGAATGGGGT 1080
TTGGAGAGAG ACCTGCACTG TCAAGGATGT GGTTGCTGAT GTTTCTAGAG ATGAGGGAAC 1140
ACCATGGCTA ATTCCTTCCC TCAGTAAGTA GCACGACACA CAAAGGAGCT GCTGCACTGC 1200
TTCAGTTTCC CAAGATGAGG GTGAAAGCTC AGTGTAACTT AAAGTTTCTG CACCTCCATG 1260
GATGCATCTG TAGTCCAAGA GAGAGAGAAG GACGGAAGAG CTGAAGGTAT TTATACCTTA 1320
CAGAATCCAT GCATCAAGGG AAACACATTG TCCACCTTGC AGGATGTTGC AAAGGTGTTT 1380
TGTTTGCTGT AACACTCTCT AATCAAAATC CACCTCTGCC ATTTACTAGC TCTATGGCAT 1440
CAGGCAAGGT ACACAAGCTT TCTGAGCCTC 1470
|
