| Tag | Content |
|---|
EnhancerAtlas ID | HS105-38261 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:1015070-1016520 |
Target genes | | Number: 42 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP1 | MA0079.4 | chr19:1016160-1016175 | CAGGCCCCGCCCACA | + | 6.57 | | SP4 | MA0685.1 | chr19:1016160-1016177 | CAGGCCCCGCCCACAGA | + | 6.24 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_45457 | chr19:1016208-1017706 | NHLF | | SE_49748 | chr19:1016260-1017811 | Right_Ventricle | | SE_69051 | chr19:1015077-1018754 | H9 |
|
| | 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 |
| GH19I001014 | chr19 | 1014913 | 1018775 |
|
Enhancer Sequence | GATCTCACCA CCTGAAAATA GCTTCTCTCA CCTGGCGGGG CGCCCTGTGC AACCCTCCCA 60
GGCCTGGCGG GGCCAGCCGC AGCTGCTGGG GACACAGTGG ACCTCCGTGG CTGGGCAGAG 120
CGCCCCACGG CAGGGCGAGG CTGCCGTGCC CGAGGCACAA CCTATGAACT GGGGTGCCAG 180
CAGCTCTCAC CTGGGGGCTC CTGCCCAGGG GATGCTTGGG ACATCTGTGG TTGTCACAAT 240
TGGGGGAGCT CCTGGCATGG AGTGGGTGAG GCCAGGGATG CTGCTCGGCA CCCCGCAGTG 300
CCCAGGACGG CCCCACCCCG ACGTCCACAG GGCTTGGGGA GCCCACGCCC CAGCGTGCTG 360
CAGGCACAAC TCAGAGTGGG GCCCCTCTAG GGGCAGTTCA GGGCAGCCCC TCTTCCAGGG 420
AGCCCGCCTC ACCGTCTGGC GGTTTGGCTG CCCACTGTAC CTCCCAACCT GAGGTCCAGG 480
CATCACCCCC GAGCCTGGTG AGGGTCACGT CTACCTGCTG CCCCGATCCG CAAAACTGAG 540
GACCCAGCTG GGCCAAGGGG GCGCCCACGG CCACATGGAA CCCCAGACTC TCAGGGAAGA 600
ATTGATCAGA CTCAAAATCA CAAGCCAGAG AGCCTGGAGC ACAGGGCCCC TCCGTGACCC 660
GTGACCTGCT GGCAGGTGCA CCAATGCCCG GGGTGCAGTG AGCCACCTGT GGCCGCACAG 720
CCATAGGCAA GACCACCAGG AGCCTCAACT CTTCCACGCC CACAGTGAGC TGGGGCCTCC 780
TCTCCAGAAC CCTCTGTAGA CTGAGCAAAG GGCCGAGTCA GCAAAGCAAC CCACTTCCAG 840
CCCGGCCGCA GTGCTGTGAC CTGTGGGAGG CCCTGAGTCT GAGCACGGAT AAAGCCCTGG 900
GTCTAGCCGC ACGTGCACCT GGGGCGAGCC CCATCACACT CCCCAGCCCC AGGAGCTGGA 960
GAATCCCTTG GGCTGATCTG AACTGCATTT CTAGTCCTTA CAGCCAAAAG AGCCGCAGGG 1020
GATGAAGGCT GGCCCGGCGC TGAGATTTAA GCAGAAACAG GCAAGAGCAG AACCCTGACC 1080
GCCAGGCATT CAGGCCCCGC CCACAGACGC CGGAGCTACA AATGAGGGGT GGGCGGGGGG 1140
AGGGGGCAGG GCCCTCTGCT GGGGAGGGTT CCCCTGTGTC CTGGGGAAGA CAGGGAGGGC 1200
AGTGTGGAAG GGGGGCAGCC CCGGAGCCTG AGATGCTTTC AAAGCCTAGC GTTTCCCCAT 1260
ATGGCATCTG GGGACAGGAG CCACGGAGGC TGGGCCCAGT GGTGGGTCAC GGTCAGAGAC 1320
ACTGACCCCA CAGCCCCTCG GCTCAGCACT CTCAGGAGAG AGGGGCCCGC GAGGCCCATG 1380
GTGGATGCTG CTGGTGGCCA CGCTCTGCCT TCCAGGCCCA CACATCCAGC AGGAGCTGTG 1440
CCCAGGACAG 1450
|
