| Tag | Content |
|---|
EnhancerAtlas ID | HS064-07768 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr19:47689510-47691080 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxa2 | MA0047.2 | chr19:47689646-47689658 | CCTGTGTAAACA | - | 6.14 | | TBX20 | MA0689.1 | chr19:47690520-47690531 | CTTCACACCTA | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_34491 | chr19:47689593-47695832 | HCT-116 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 47689758 | 47690163 | | chr19 | 47689614 | 47690884 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I047185 | chr19 | 47688934 | 47694994 |
|
Enhancer Sequence | AAAAAAAATA ATAAAAGCTC ATTGGAGCAT TTTGGATTTG GGATTCTTAG ATTTGGGGTG 60
CTCTATTGGT AAGTACAATG CAAATATTTC AAAATCTGAA AATACCCAAA ATTCAAACAC 120
TTCTGCTCCC TGACATCCTG TGTAAACAAC ACTGCAGTGA ACATTTATAG GTAATTCATT 180
CAGCGGGTAA GGGTCAGGAC CTTTTATAGG GATCCTTAAT ACCACATTTT TACATGGTTC 240
ATTGAGCATT CGTGCTCCCC TCTGCTGTGG GTGAGGGTGC AGGTCCCTCA GCCTTCTTGC 300
TTGGGTTGAG TCATCCTGGT CTTTAATTTG GTAAGCAAAA AATGGCATCT TGTTTTTGAG 360
CTCGTTTCTG AGAAAGTGCA TGCTCCTTTT CCCCATCAAC AACTTTCATC CGGCGCCTCG 420
GAACCTCTTC AGTAGAGAGT GAGATGCAAA TAGCGAGGCA CAGCTTCTTT CCCTCTTCTG 480
AGCTGATGCC TGGTGAGGTC ATAGACTGGG TTTCATTGCA AAGACGAAAG CGTGGGCAGG 540
ACTTTTGGAG CACAAAAAGG GGCATTTCAG AGTAGTCTTC ATGGGCGGCC ACTCCAGAGG 600
TGAAGTTTTC TAGAGAAAGA CATGAAAGTA CTGTGTGGCT GTGGCGACAG ACAGAGGCTT 660
ACGAGCCTGC CCTCTAGAGA CTGTGAGCTC CGCGTGTGAG GGCAAGGCCT GGGGCTGTCT 720
GGGTCGCTTC TGGGTCCCCA CCACAGCTAG CATAGGGTAG GGGTGGAGGG GGGGTGCTCA 780
GGAAGTGATT TTTGAAGAGT GGATGACTGA ATACATGCAC ACACATACTT TTAAGTTTCT 840
GGGTTAAAGA GGAAAACAGA ATGAGGTAAA CAAAGGAAAG TAATGTGGAG GTGAACTGAG 900
CAGATGGCAA GATGCCGTGA ATGGTTAGAG GCCAGGAGAG CCAGAATCAG AGTGGCTTCC 960
GTGAAGTGTC CCTACCTCCT CCCCCAGCCC AGCTATGTCA CTCCTCTGAG CTTCACACCT 1020
ATGGACTGTT CTGCACCCTA GCCCTCAGAT GCAACGGTGA AAGTGGGACT CCTATTGGGT 1080
TTCCCTGTTG AGGACAGACA TGGTGCCCTG TGTATCTGCT GCTGCTTTTT TCTTTTTTTC 1140
TTGCTGAGTA TTCCATGTGT AGCATGTTTG TAACACTTGA TAAGAAACAG AACCATCCCA 1200
GATAGCTTGA ACACTTTTCA ATTCAGTCAG TAACAGACCA GGTCTGCTTT GGATTTCCAG 1260
GAGCTTGTGT CACTTTATTT TTTTTCTGAG CCAGGGTCTC GCTTTGTCAC CCAGCTGGAG 1320
TGCAGTGGTG CAATGTCAGC TCACCACAGC CTCTGCCTCC TGGGTTCAAG CAATTCTCGT 1380
ACCTCAGCCT CCCAAGTAGC TGGGACTACA GGTGCCTGCC ACAACACCCG GCTCATTTTT 1440
GTGTTTTTAG CAGAGACGGG GTTTCACCAT GTTGGCCAGG CTGGTCTCAA ACTCCTGACC 1500
TCAGTTGATC TGCTTGCCTT GGCCTCTCAA AGTGCTGGGA TTACAGGCGT GAGCCACTGC 1560
ACCCGGCCTC 1570
|
