Tag | Content |
---|
EnhancerAtlas ID | HS076-28600 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr19:17371520-17372280 |
Target genes | Number: 29 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr19:17371841-17371860 | CCGCCACCAGAGGGCGCCT | + | 7.05 | IRF1 | MA0050.2 | chr19:17372114-17372135 | GTTTTCTTTCTTTTTCTTTCT | + | 6.21 | IRF1 | MA0050.2 | chr19:17372136-17372157 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 |
|
| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_47714 | chr19:17371376-17371785 | Pancreas | SE_47714 | chr19:17371795-17372144 | Pancreas | SE_57118 | chr19:17371817-17372146 | VACO_400 | SE_68828 | chr19:17371559-17372228 | H9 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 17371801 | 17372164 | chr19 | 17371829 | 17372200 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH19I017261 | chr19 | 17371281 | 17372175 |
|
Enhancer Sequence | ACTCAGACAT ATAGCTGCTC CCTTGAGGAC CCCACGTGGA TGTCTCATGG ACACTTGAGC 60 TTATCAAGGG CTAAAGAGAT CTGGTCACCC CCAGCCAAAC CTGCCTACCC TGTAGCTCCT 120 CCATCTCTCC CTTCTAGTCC AGCAGGTCCC AAAGCCTGAA GTTGTCCTTG ACTTCTCTCT 180 AGCCTTCACG CTCACACGTC AGTTCCATCT GCCACATCAC CCAGAATCCG TCCGCATCTC 240 TCCACTTCTA CAACCTCCAC CATCGTGCAT GTCTGGACCA ATGAAGTCGC CTCCTGGCTC 300 TCCAGGAGTC CACCCTCACC TCCGCCACCA GAGGGCGCCT GTGAACACCT GCGTCGAGCA 360 TGCCCCTCCT CTGCTCAAAA CCCTCCAGGG CTCTCACCTT AATCCAAGCA AAGCCCAAGC 420 GTCTCCTTGC AGCCCACGAG GCCCTACGCG ATCTGCATTT GTTCTCCCTC TGTTCTGTTC 480 TGGCTCCCCA CACTCTCCCT GTTGCCCCCT GTGTTCCAGC CACACTGGCC TCCTTCGGGT 540 TTCTTGAACA GGCCAGTCAT GCTGCCACTC CAGGGCCTAC TCCCACCACC CTCAGTTTTC 600 TTTCTTTTTC TTTCTTTCTT TCTTTCTTTT TTTTTTTTTT TTGAGAAAGA GTTTTCTTCT 660 GTCGCCCAGG CTGGAGTGCA ATGGCGGGAT CTCGGCTCAC TGCAAGCTCC GCCTCCCGGG 720 TTCACGCCAT TCTCCTGCCT CAGCCTCCGG AGTAGCTGGG 760
|