| Tag | Content |
|---|
EnhancerAtlas ID | HS095-04998 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:13961180-13962620 |
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 | AAATGGTATT AATTTAGGCA ACAATTTTTA CATGAGCAAA CCCGAGTCCA CAGGGAAGGG 60
GGTTCTTTTT CCTGTGACAA GGTAAGTTGG TGCAGCCCTT TTGGCAGGGA ACTTGCACTG 120
TGTAATAACA GCTGCAAAAG GCAATTCCAT TTAACAGTCA TTTAATTCAT TTAACACACA 180
GCCATAGAGC TGCTTGAGAA TTTTTCATAA CGCCATGATG GAAATTACCT TCTTCTCATG 240
GGAATTCCAT TTAAGAAGGG GTCACATGGT ACTATTTACT ATTCTCCCAA CTACCTGTCA 300
ATCTGGTATC TCTCCCATGG GGCTCACTGG GAGAAGCCAG CTTCTGCTAC AGGGTCACAT 360
TAATTACCGT AGCCCTTAGG ATCCTGTCTC CAGAGGACCC AGGTAGAGCT GGAGCCCAAG 420
AACAGTCCCT TCCTGATGTG GGCAGGAAAC TCTAGCTTCC TTATTAAGGA CACCTCCCAG 480
CTCTCCAAAG TTGAACAGCC TGACTTTGTC ACTGTGATTC ACATTCCTCT CATCTCTTCT 540
TGATGACCTG GCTGCCCCGT CACTCTGGCC CCAGGGGATA CTGTTTTTCC TTTAACATCC 600
TTACTTCATT CTGAGTGCTG CTTCAGAAGG AAGGGGCCCA CAGCTCTCTG CCAATGATTT 660
AATTCCAAAT ACTCTTTTTT TCATCGCCCC AACCCAGACC CCATCCCCTT CCCAGCAGCC 720
TGGAGGTCCT GAGCAAATGA ATTCCTGGTC ATGACCTTTC CCTATAGTCT TCCTGGACAT 780
GGTCACCTCC ACTCTTGATG CCCTCCGGGT CTTGGACAGC ACACTTTTAA ATCTAAGTAC 840
TGTTAGCTCC GCCTGGGCCC AGGGCAGCGG GTGGGGCAGG GGGTCAGAGA GCACAGGCAG 900
GAAGCATGCT CCTGTGCCCT TCATTGCCTG GTATTGATTT TCTCCCATCC CTCACTCTTC 960
CACTGCCCCA TAAAGAAGTC AGAGTTGTAA AGCTGTCAGG ACATTTTCTA TGAGACAGGT 1020
ATGCAGAATG GAAGTGTTGT TAGTGGCTCT TAAAGAAAGA AACCGGGTGG CTCTGTGGTA 1080
GTCTCTGGCA TTGTTGTGGG CTGTGCATAG AGAATGGGGT TTGGAGAGAG ACCTGCACTG 1140
TCAAGGATGT GGTTGCTGAT GTTTCTAGAG ATGAGGGAAC ACCATGGCTA ATTCCTTCCC 1200
TCAGTAAGTA GCACGACACA CAAAGGAGCT GCTGCACTGC TTCAGTTTCC CAAGATGAGG 1260
GTGAAAGCTC AGTGTAACTT AAAGTTTCTG CACCTCCATG GATGCATCTG TAGTCCAAGA 1320
GAGAGAGAAG GACGGAAGAG CTGAAGGTAT TTATACCTTA CAGAATCCAT GCATCAAGGG 1380
AAACACATTG TCCACCTTGC AGGATGTTGC AAAGGTGTTT TGTTTGCTGT AACACTCTCT 1440
|
