| Tag | Content |
|---|
EnhancerAtlas ID | HS180-24721 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr19:47689600-47690960 |
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 | AAAATCTGAA AATACCCAAA ATTCAAACAC TTCTGCTCCC TGACATCCTG TGTAAACAAC 60
ACTGCAGTGA ACATTTATAG GTAATTCATT CAGCGGGTAA GGGTCAGGAC CTTTTATAGG 120
GATCCTTAAT ACCACATTTT TACATGGTTC ATTGAGCATT CGTGCTCCCC TCTGCTGTGG 180
GTGAGGGTGC AGGTCCCTCA GCCTTCTTGC TTGGGTTGAG TCATCCTGGT CTTTAATTTG 240
GTAAGCAAAA AATGGCATCT TGTTTTTGAG CTCGTTTCTG AGAAAGTGCA TGCTCCTTTT 300
CCCCATCAAC AACTTTCATC CGGCGCCTCG GAACCTCTTC AGTAGAGAGT GAGATGCAAA 360
TAGCGAGGCA CAGCTTCTTT CCCTCTTCTG AGCTGATGCC TGGTGAGGTC ATAGACTGGG 420
TTTCATTGCA AAGACGAAAG CGTGGGCAGG ACTTTTGGAG CACAAAAAGG GGCATTTCAG 480
AGTAGTCTTC ATGGGCGGCC ACTCCAGAGG TGAAGTTTTC TAGAGAAAGA CATGAAAGTA 540
CTGTGTGGCT GTGGCGACAG ACAGAGGCTT ACGAGCCTGC CCTCTAGAGA CTGTGAGCTC 600
CGCGTGTGAG GGCAAGGCCT GGGGCTGTCT GGGTCGCTTC TGGGTCCCCA CCACAGCTAG 660
CATAGGGTAG GGGTGGAGGG GGGGTGCTCA GGAAGTGATT TTTGAAGAGT GGATGACTGA 720
ATACATGCAC ACACATACTT TTAAGTTTCT GGGTTAAAGA GGAAAACAGA ATGAGGTAAA 780
CAAAGGAAAG TAATGTGGAG GTGAACTGAG CAGATGGCAA GATGCCGTGA ATGGTTAGAG 840
GCCAGGAGAG CCAGAATCAG AGTGGCTTCC GTGAAGTGTC CCTACCTCCT CCCCCAGCCC 900
AGCTATGTCA CTCCTCTGAG CTTCACACCT ATGGACTGTT CTGCACCCTA GCCCTCAGAT 960
GCAACGGTGA AAGTGGGACT CCTATTGGGT TTCCCTGTTG AGGACAGACA TGGTGCCCTG 1020
TGTATCTGCT GCTGCTTTTT TCTTTTTTTC TTGCTGAGTA TTCCATGTGT AGCATGTTTG 1080
TAACACTTGA TAAGAAACAG AACCATCCCA GATAGCTTGA ACACTTTTCA ATTCAGTCAG 1140
TAACAGACCA GGTCTGCTTT GGATTTCCAG GAGCTTGTGT CACTTTATTT TTTTTCTGAG 1200
CCAGGGTCTC GCTTTGTCAC CCAGCTGGAG TGCAGTGGTG CAATGTCAGC TCACCACAGC 1260
CTCTGCCTCC TGGGTTCAAG CAATTCTCGT ACCTCAGCCT CCCAAGTAGC TGGGACTACA 1320
GGTGCCTGCC ACAACACCCG GCTCATTTTT GTGTTTTTAG 1360
|
