| Tag | Content |
|---|
EnhancerAtlas ID | HS102-04215 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr11:34182630-34184120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr11:34183077-34183088 | AGGCACTCAAG | + | 6.14 | | TFAP2C | MA0524.2 | chr11:34183997-34184009 | TGCCCTGGGGCT | - | 6.11 |
|
| | 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 |
| GH11I034160 | chr11 | 34182544 | 34185939 |
|
Enhancer Sequence | GGTCCAGGCA GGGAAGGGCA GGCAGTCACG CACCACAGCT GAGCGCTCCC GGCACAGACC 60
ACAGCCTTTT CTGGGCAGAC TCTCTCGGGA TGCCCCCGCT GTCTGCAGAG CACCCCGCCC 120
GCCCCCTCCC GCCTGCCCCC TTCCTGGGCA TGGAGTGGCC CTCTCAGGAT GGCCATAGAA 180
TGAAAGCTTT AATTCATTCT AATAGGTCTT GCTGGCAGGT CAGAGTGGAG TTTCAGGTTC 240
TCATGAGATG AGGTGGAGGA ATGGCTTCGG CCCAAATGCA GGGAACTCAA GCTCTGAAAG 300
TTGACCGCCC AGCCTGGGGA TTTGGAAGTA TGGGCCCAGC ACCCAAAGTA GCCTTGTTGC 360
TTAGTGGGCT CAAGAATTAC TTGCTAGAGA GGTCTCATTA GTTGTGGAGG GGTGGCCAGG 420
AGGGCTTGGA TGGCCAGAGA ATATGCCAGG CACTCAAGGA CACACAGGCC TCCTTGTCTG 480
CACGGAAGCT TGAAACGAAC CCGGTCCTAT CACGAGGGGC TCTCCAGCAC ACAGAGCACT 540
GGAAAGCCGC TGCACATCCC CAGGCACATA ATGACTGTTT TACAGTTCCC CAGCATGTGT 600
CAGTGGGGCT GTAACTTAAC ATTGCTGTGG GAAGTTCATG ACATAAACTA GTCCTGTCCC 660
TGGTAATTAG AGAGACAGCT TCTTACCCCA ACCTCACTGT GGATCAAAGA ACTGACGGCA 720
TTCCCCAGCG ACACATTGAC AGTAGTGTGG TGTGTTAGTA TCCTTGGGTT ATTGACTGCA 780
GGTGGGAGTG ACGTCTCTGT TTTACGGTGA AGAACACTGA GGCTGACTCA CTGCTGTCTT 840
GGCCCGGCCC TGGGGGTTTG TGGCCTTGTG ATGACAGTGA CGGTGCTGTC ATCCACCAAG 900
TGCTCACGGT GGCCACTACG CCTTGTACTT CAGGTGATGT CACCTCATTC TTAGATAAGG 960
ATCATTAGCA CCAAAGCCAC AGAGGTGGGA GTTGAGGCTT GGAGAGAGGA CGTGGTATGC 1020
AGCTAACACA GGACCTGACC TAAGTCTGTC TGACTAGCCT CCCTGGAGGA CACCAAAAGT 1080
CCACAGACTC GCAGACCCAA GGAGTGCAAG GTCAGCCGAG TGACAGGACT GCCGCCTCAC 1140
AGCGTGGAGT CCCGGGGCTT CAGAGGCTCC CAGTGCTCGA CATCCCTGGG CTGTGACTGG 1200
GGAGGGGGCA GCGAAGCTCC AGCCAGGCAG GGTGGAGGGC CCGAGGGCAG GGGACTGGGC 1260
CATGACCCCA AGACGTGGCA CTGTTGAGCA CTGTCTGAGG CCCAGGGCCC CTCCTGAACT 1320
GGCCGTGTAG CAGGGGGGTC CCAGCCTCCA CCCAGTCTGT GCTCAGCTGC CCTGGGGCTT 1380
GTCTGTCCCT GCAGGCCCTG GCCCTCTCAG GCCTGCTGAA GAGCAGCAGG GAGTGACCGT 1440
GTGTGTCCAT ATGCATGCAT GGACATGGGT GTGCATGCCC GTGAGGCCTC 1490
|
