| Tag | Content |
|---|
EnhancerAtlas ID | HS048-31523 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr6:33455380-33456650 |
Target genes | | Number: 17 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr6:33455850-33455868 | AGAAAGAAAGAAGGAAGG | + | 6.56 | | EWSR1-FLI1 | MA0149.1 | chr6:33455858-33455876 | AGAAGGAAGGAAAGAAAG | + | 6.94 | | EWSR1-FLI1 | MA0149.1 | chr6:33455854-33455872 | AGAAAGAAGGAAGGAAAG | + | 7.22 | | HNF4G | MA0484.1 | chr6:33456369-33456384 | TGGGAACAAAGTCCA | + | 6.05 | | IRF1 | MA0050.2 | chr6:33455976-33455997 | CTTCACTTTCTGTTTCTTCTG | + | 6.26 |
|
| | 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 |
| GH06I033487 | chr6 | 33455514 | 33456607 |
|
Enhancer Sequence | GCCATGACAC CTGGCTAATT TTGCATTTTT AGTAGAGACA GGGTTTCACC GTGTTGCCCA 60
GGCTGGTCTC TAACTCCTGA CCTCTGGTGA TCCACCTGCC TTGGCCTCCC AAAGTGCTGG 120
GATTACAGGT GTGAACCACT GTGCCTGGCC GACACCTTTA ATATTATGAT ATGACTAAAA 180
AGGAAGGAAA GGGCGCCAGG TGTGGTGGCT CACACCTGTA ATCTCAGCAC TTTGGGAGGC 240
CAAGGCGGGC AGACCACCTG ATGTCAGGAG TTCGAGACCA GCCTGGACAA CATGGTGAAA 300
CCCTGCCTCT ACTAAAAATT AAAAAATTAC CTGGGCATGG TGGTGGGTGC CTGTAACCCC 360
AGCTACTTGG AAGGCTGAGG CAGGAGAATC GCTTGAACCC GGGAGGTAGA GAAAGAAAGA 420
AAGAAAGAGA GGGAAAAAGA AAGAGAGAGA GAGAAAGAAA GAAGAGAGAG AGAAAGAAAG 480
AAGGAAGGAA AGAAAGGCAG GCAAAGCAAA ATTACTCTCT AGGTGTTTGC AGATTGGCTC 540
TGTGTTGGGA GAACTTTTTC AATGCCTAAC CTGGCCATTT ACAACTCTTT CTTAGCCTTC 600
ACTTTCTGTT TCTTCTGAGC CTAAAGACCA TTTGGAGGTG AATGCTTGTG CTCTTCTCAG 660
GTCTTTTCTG GGCATGCATC CTGCCTTGGG CATGTGTGTG GATTTCTAGG TTCCCCAGTA 720
TACAGAGGAG ATTTTCCAGA CCTCCTATTT CCCCAAAATC TCACTCTCCA GCTTTTCCCC 780
CCAGGCTTTC TTCATGTCTT CTTTGCCCCA ATGTTACGTT TTGCCCTGGG TGGCAGCAGC 840
TAGTTCATTT ATCTTTCAGT TTTCAAAGAA TGCCCTCTGC ACAGCTGCTC CACCCTGATA 900
GATTTCTGAG TTAGGCAAAA CAAAGAGAAG CCTCTTATAT CAATCCTTCA GGGAAACCCA 960
TCAGGTGAAA ACAGATAAAC ACAACTTCTT GGGAACAAAG TCCACTCTGT TCCCTCTGGA 1020
ACCAGTTATC AGGAACGCCA GCCGCCATCT TCCATGCCAA GGAGGGGTGT GGGGAAAGGC 1080
TCGTTTAAAA CATCTCGAGG GGCCGGGCAC AGTGGCTCAC GCCTGTAATC CCAGCATTCT 1140
GGGAAGCCGA GGTGGGAGGA TCACGAGGTT AGGAGATCGA GACCATCCTG GCTAACATGG 1200
TGAAACCCCA TCTCTACTAA AAATACAAAA AGTTAGCCAG GCGTGGTGGC ACGCACCTGT 1260
AGGCCACGCT 1270
|
