| Tag | Content |
|---|
EnhancerAtlas ID | HS101-28792 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr22:30957560-30958940 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arid3b | MA0601.1 | chr22:30958501-30958512 | ATATTAATTAT | + | 6.02 | | EWSR1-FLI1 | MA0149.1 | chr22:30957624-30957642 | GGAAGGAAGGAGGGAAAG | + | 8.46 | | FOSL1 | MA0477.1 | chr22:30958600-30958611 | AGTGACTCATC | + | 6.02 | | JUND | MA0491.1 | chr22:30958600-30958611 | AGTGACTCATC | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr22:30958885-30958900 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | 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 |
| GH22I030560 | chr22 | 30956935 | 30957988 |
|
Enhancer Sequence | TGCTTCCTGC TTTGTCCATG GCAGCCCCTG CCTGGTGTGT CCTAAGCCCT GTCCCAAGCC 60
CAGGGGAAGG AAGGAGGGAA AGTTGCATTG CAGGAAGTGG GGGATGTGGG GTTGGACAGG 120
AAGCTCTATC CTGGGAGCAC AGCAGGGTCC CGTCTCTGTG GGCTGAGCCT GCGGCCAGGA 180
TAAGGGGAGG GAAAGCAGAG GGGGCCCTGG TGTCCGTCCC TCCCGTGCCA GCCACCTGAG 240
GGGTCCAAGG CTGGTTGTGC CTTTCCTGCC TAGCTACTGT AAACTTAGGC ATGAAGCTAT 300
GAACCTCACC CTCCCTAAGC CTCAGTCTCC TCGTGTGTGC AATGGACACA CAACAGCAAG 360
ATCAAGGCAC ACAGAGCGCT CTGTAATCAC AGGCAGAGCC CCTGGGCAGA CTGAGGTCGG 420
GAGAGGAGCT AGCTGGCAGC CAGGAGCCTG GCTTGAGGGA GAACAGTCAC TAGGCTATGA 480
GATAATTTTT TTAAAAAGAC AGGATCTTGC TCCATCACCC AGGCTGAAGT GAAGTGGCAC 540
GATCATAGCT CATTGCAGCC TTGAAATCCT GGGCTCAGTG GATCTTCTTG CCTCGGCCTC 600
CTGAGTAGCT AGGACTAACA GGCATGCACC ACCATGCCTG GCTACTTTTT AAAAAAAATT 660
TTGTAGAGAT GGGGGTCTCA CTCTACTGCC CAGGCTGGTC TCGAACACCT GGCCTCAAGT 720
GAATTTCCCA CCTCGGCCGC TCAAGTGCAT ACCACCCATG CCCAGCTAAG TTTTTAATTT 780
TTTGTAGAGA TGGGGGCTCT CACTATGTTG CAGGCTGATC TTGAGTTCCT GGCCTCAAGT 840
GATCCTCCCA CCTCCACCTC CCAAAGTGCT GGGTGTAAGC CACCATGCCA TGCCCTAAGG 900
CTGTGAGACT GAGATAATGC ACGTACCCAG GAGATCAACT CATATTAATT ATTATCATAC 960
CATTGACTCT GACCCAGCCT TGGTTCACCG GCGTGCCAGA GGTGAGGTCC CTTCCATGCC 1020
CCGCTGCAGG CAAGCCTACC AGTGACTCAT CCCTGAGCTC CCCGAGCCTG GCACCTGGTG 1080
AATGTGTGAT GAATGACTTC CCATGACCCT CAGGGCAGAA GGTGTCCAGG GCTATAGAGC 1140
CCGTGCAGAG AATGTGGATG AGGACATGGT CCAGGCAGAC AACACCTCAC TGAGACACAG 1200
GAGAGATCCT GTGTAGGAGA CCTACAGACG AAAGTAATAC ATGTGAGGCA CATGCATGTA 1260
AAAGCTCCCA TGGGCCAGGC CCGGTGTAAT CCCAGCACTT TGGGAGGCCG AGACAGGCAG 1320
ATCACGAGGT CAGGAGTTCA AGACCAGCCT GGCCAACATG CTGAAACACC GTCTCTACTA 1380
|
