| Tag | Content |
|---|
EnhancerAtlas ID | HS101-10807 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr12:69417440-69418910 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:69417689-69417707 | GGAAAGAAGACAGGAAGC | + | 6.28 |
|
| | 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 |
| GH12I069023 | chr12 | 69417570 | 69419526 |
|
Enhancer Sequence | AGAGAGAACG AGGCCAGCTC CCTAAAGGAG GCAGCCCCAT GAGATGGAGG AAAGAAAGGG 60
AATCCTACTA AGAGCTCCCC GTTTTCCTGT CATTTTGTTT TGTTTTGTTT TGTTTGACAG 120
AGGCTAATGT GGCTTTCTGA CACCAGAGAC AGAAATATGC TCAGGAAAAT AAAGGATGAA 180
AAAGACATGG ATGTTTCCTT CCAATAGCTC ACAGGACAGT GGGGGAGACA GACAGACAAA 240
CAAGCAAACG GAAAGAAGAC AGGAAGCACT AAGGGCTAAA GTAAAGCCAC CTTTTAAATG 300
CTGCGGGAGC ACAAGGAAGG GGACTCAACA CAGCATCAAT TAGAGACATG TGTGTCTTCC 360
ACGTGTTGGG CACTGTGCTG GGTGCCCTGC GGTTGACTCT GTTAATATTT CAAGTAGAAT 420
GAAATAATTT GCGTCCTTTG CTTTTTGGGC CTTTATTGGT GCCTCTTCTG CAATGAATAC 480
AGGGTACCCT ACAGTCTGCT AGGATTCAGT GTTGGTTCAT CTGTGATGTG GCATTTCTTA 540
CTTATAGTTT AATTATGATT GTTCTATGCC AACAATGCTG CAGTGAGGTC TGCAAATGGG 600
CTAGGGAAAG CATTTGTTAA AATATAAAAA TGTAATTAAA AAAAGTCAGG GTTGTCTTTC 660
CACTAGCCAA ATTATATACT TGCTTACATT TTAGGTACTA ACTTATTAAA GGGGGGTCCC 720
AATTATGTCT CCCTTTCACA ATGCAAGCAT GCCTTTAGCC ACAATTATTT GTTGTTGGAA 780
AACTGCACAC ACAATTGCAG CCACAGTTGT CTAATTGTAG GCTGAAAATG AAGGGCAGGC 840
AGTTAATTAT TTCTCAGATG CCTGATGCTG CATGTCATTA GCTGGCTGTG GCACAGGTCA 900
TTGCACAAGG CGTTCTTCAG CTACGAAAGG TAAGAGCCTG GGTGACGCAC TCCACTGGGT 960
GTGGACTTGG AGAGTTAAAC GCCCGCTCAT CTCTGCCAGG GTGTGCTTTG CTCCGAAGAG 1020
AACTGACTTC CCTGTCAACC TTTCACTTAA TACTAGCTTA CCTATTCTCT CTGTCTTGCT 1080
TCTTTGTCTG TTCTGATTTC TTCAGGAATC ATCTTGTCAG CTGAAGTGGA TGTGCGCTTT 1140
TAAAAAAAAC AAAAATCTTT ATTCCAATTT AAATTGTTTT TTTCATTTCT GTCTTCCAGC 1200
TTTTCTCATA TTAGAAAGAT TGGAGAGAAT TGTTTCTATG GAAGTGGTGA ACATGGGACA 1260
GAAGTACTTC TCTCTTGATA AGACCAGCAT GTGCAAACCA GGAAGAAAAA GTAAAATCTC 1320
CAATAATAGA GAGATAAATC AAACAGGAAA AAAAAAAGTC TGGGTCCGAA AAACACGTGC 1380
ATTCCTGTAG CAGAGTTTAT GCGAGTTTTT TTTTCTTTTT TTCTTTTTTG TGATGAGGTC 1440
ACTATTACTC ACATGGCTGT GTGGGATAGA 1470
|
