| Tag | Content |
|---|
EnhancerAtlas ID | HS076-27656 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr19:3665470-3667310 |
Target genes | | Number: 19 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:3666016-3666035 | TGGCCGCCAGGGGGCAGGC | + | 6.27 | | Klf1 | MA0493.1 | chr19:3667087-3667098 | AGGGTGTGGCC | - | 6.32 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_02226 | chr19:3666968-3672957 | Aorta | | SE_54699 | chr19:3666824-3676511 | Stomach_Smooth_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH19I003665 | chr19 | 3665481 | 3666317 | | GH19I003667 | chr19 | 3667232 | 3674163 |
|
Enhancer Sequence | AGGTGGGGGT GGGAACAGAG CGGGGGTCAG GCTTCCTGCC AACACGGTGT GAGCCAGGCC 60
AGCCTCAGAG CATCTCACCC ACCGCCTGAG GTGGTGGTGG GAGTCGTAAC TCCTCTCCCT 120
CACCAGGGCC CCTAACTGTG AGACCGCTGG GATGGAAGGA TTGAAAAGAC CACCTTGTCC 180
CTGAGGGAGA TGGTCTCACT GGCCAGGGTC AGGCCCGGCT CCTGCAAGCT GTCGGGCAGC 240
GCGGGTGTCC CAGCAGATGG GACCGCCGAC CCCAGGGGGC CTCAGCTTGT TGCCCTCGAG 300
GGAGGATGTG AGGAGGGGCC TTGGGAGCCT GAAGGGACAC AGAGGCCAAC CAAGGAGAAC 360
AGCCCCGCCT GGCACCGTCA TTTAAGGAGC GCCACTGCGT TTGCTAGGAG ACCCCATGGA 420
CCCTCCACTG GCCAGACCCC ATCCCACCGC TATCAGCCCC AGGGACACGC CTGCAGCCCT 480
GACCCCTGCC CCTGCCCTCC CTCCACAGCC GACGCTGCTC AGCCATGTTC CCTGCATTCT 540
CCCAGGTGGC CGCCAGGGGG CAGGCTCTCC CCAGGAATTC ACCCCGCCAC CCGGGCCACC 600
CTCCACCCGC GCCACCCTCC ACACTGCCCC CACGCCGGGG GACTCTGAGG AAGGATCCCA 660
GGGTCCCAGG CCTGGTGGAC AAAGCCCTCC AAGCTCTGGC TACGGACGCA GGGCCAAGGG 720
TGGCCCAGGT GGGACAGGTG CCTTGGGGAC TGCTCCTGTG AATGGGGCTC ATGGACAGGT 780
GCCCTGAGGA CTGCATGCGG GAAGACGGGA GATGCAGCAG CTCGGGTGCC CTCAGAGGAC 840
GGCCCACCCC ACTGCGCCCA CTGGGGCTGG GAAGAAGGCC ACTCGGCGCC ACGGGGCTGG 900
CAGAAGCTGC AAAGGCAGGG CCAACGTGCA GAGAAAGCTC TCGGGAGGAG ACGGGCAGCA 960
ATGACAGGAC CCATGTACAT GCAGATGTGC ACACACACAG ACAAATATGC ACACAGGCAA 1020
ACACACGTGC AGACGTGCAC ACAGGCAAAC GTGTACATAC GCACGCAGGC AAACAGGCAC 1080
ACAGGCAAAC ACACATGCAC TCAGGCAAAC ATGAACACAG GCAAACACGT GCACACACGC 1140
ACGTAGGCAA ATGAACACAG GCAAACACGT GCACACATGC ACGCAAACAT GCACACACAC 1200
AAACGTGCAC ACACACAGGC AAACATCCAC ACAAGCAAAA ATAGATGCAC ACACGCACGC 1260
AGGCAAACAT GCACACACAC AAACGTGCAC ACACGCACGC AGGCAAACAT GCACACACAC 1320
AAACGTGCAC ACACGCACGC AGGCAAACAT GCACACATAG GCTGCACACA GCCTCACTGT 1380
GCACTACGCC TGTGTGGCTC ACAGACACTG AGGGCGTGGG TGCAGCTGGT AGCCTCGGGC 1440
ATCGCCCTCT GGGCAGCGTC TAACCCTCCA GCCAGGTCTT CCATTCCTGC CCCCAGTCCC 1500
CCGGCGAGAG CTGCTCTCTC CCCACCGCCC ACCCCCCAGA ATCCAGGCTC CACGTGGCCT 1560
GGAACCCAGA GAAGCCCTTC CTGCCCCTGC AGCCCTGACC AGGCACCCCT GCCACTGAGG 1620
GTGTGGCCCC TCAGATGCAG GGCCCCCTCC TCCATCACGG AATTTCACCC CGACCTCTCA 1680
AGACGCAGTT GGTGTAGACC TCACGTTCAT CCTGCTTGTG GACACTGGAC GGCATTTGGG 1740
GCCCAGAGAG GTGTAGTGAG CTGCCCCAGG CCACACAGCT TCTCCGCGAG TAGGGAGGCA 1800
GCAGGTCAGG GTGGGGACCC CAGGCCCTTC GTCCGCTCCA 1840
|
