| Tag | Content |
|---|
EnhancerAtlas ID | HS092-18961 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr16:3898810-3900290 |
Target genes | | Number: 23 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYCN | MA0104.4 | chr16:3900212-3900224 | GGCCACGTGGTC | + | 6.52 | | MYCN | MA0104.4 | chr16:3900212-3900224 | GGCCACGTGGTC | - | 6.52 |
|
| | 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 |
| GH16I003848 | chr16 | 3898951 | 3900980 |
|
Enhancer Sequence | CACACTCATA CAGACTCTTC TTAAAATGCC AGGTACAAGT AAAACTTAAG TTCACGTTCC 60
TCTCTACTAA CATTTCAAAA AAGACAAATG CAATTTAAAC ATTGAGCATT ACTTCATCTT 120
CATTTCTTAA GTTAAAAAAA AATCCTCTCG TTTCCGACAT TCACAGGGTT TTGCATCCGT 180
CACCCAACGC TCTCATCAAC CTTCTGGGGA AACTGTGTTC TACTCTTATT CTCCCTCACC 240
CCTACTTGGG ACTAAACAAA TCCAAAGAAC AGCCCAAACT GATTTTCTGT TCTGGGATGT 300
GCTGAATTCC ACTGCCTGAA GACGTGCCTG GTGGCTGCTG TTGAGAAGCC TCTGGCCGCA 360
GAGCATCCAC AGTGTTTGTC ACTTCAGTGG GAATAGGCTG CCCTTCCTTC TCTGTGCTCC 420
TGTCAGTCCT GGGCTTTTCC AGCTGTCTCA CATCTATCCA GGCATCTGCC TTCCCCCTTC 480
TCCAAGTCCA GTTCCTACTC TAGAAGGCAG CTGCAAGGCT GGTGGCTGCA AATCCCAGTC 540
CAGGCCTTTC CCTAGCAGAG CTCTTGGCCG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 600
TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 660
TGTGTGTGTG TGTGTGTGTG ATGTGCGTGA CCTTGGAGCC ACCTGGAGGC TGCTGCTTTT 720
TTTTTTTTTT TTTTTTTTTT TCCAAGAGAC AGGGTTTCGC CACATTGCCC AGGCTGGTCT 780
CAAACTCCTA GAGTTGAGCT ATCCACCCAC CTTGGCCTCC CAAAGTGCTG GGATCACAGG 840
CGTGAGTCAC TGTGTCCAGC ACCCATCTGG AGGCTTCTTA AAGCCCAGGC CCCACGCCGA 900
GCTTCTGAGT CAATAAAGAA GTCTGCATTT CTAACAAGCT TCTAGGGGAT GCTGCTGCTG 960
CTGCTGGTCC AGGGGACCCC ACTTGAAGAA CCACTGCACT GGTGTTTCCT CTGGGACCCG 1020
AATGCCTGTG CTTCTCCCCG GCTCTGCCAC CTCTTCCTTG TTAACATAGC AGGGAGTGAG 1080
CTGACAACCC TGGAACACAG CTTTCTCATT CAGTGAAATG GATACTGTGC CAACAGATAC 1140
TTCACTGGAT GGCCACAGAG GAGCATACAG ACCAGTGATC ACCTCCTCAG TGGGCAGTAC 1200
ACAGGCAGAA AGCAACCTCT ACCAGGTTCA CGGACACATT AGGCCCTGTA CTTTCCAACT 1260
GCCTGACCTG CAAGCTGTCC TACTTCTTTA AGAATTCTCA TTTTAAAGAC AGAAATGGGG 1320
CAGAGATCTT TATCCTAGAA AGAAATCTGT CTCTTCCAAG CATGAGTGGC ACGTGGAGAG 1380
CCCAAGAGGA AAAACAGGAG TGGGCCACGT GGTCCCATTT TACGCATTAC TCGGAGGGAA 1440
AGCCCGCGGT TAGGTAGGAA GTATTGAAAG TGCTTCAGTT 1480
|
