| Tag | Content |
|---|
EnhancerAtlas ID | HS101-12342 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr13:42294070-42295500 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arid3b | MA0601.1 | chr13:42294634-42294645 | CTAATTAATAT | - | 6.02 | | FOS | MA0476.1 | chr13:42295393-42295404 | TCTGACTCATT | + | 6.32 | | NR2F1 | MA0017.2 | chr13:42294896-42294909 | CAGAGGTCAAGAG | + | 7.04 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TCCTTTTTAA ATAAATGCCA GAATTTGAGG GGAAAGAGTT CCTCCTCTCA AATGTTAGAG 60
CAGTGCCTAG ATCCTGGTGT CAGTGATTGC CACTGCTTTC TGAAATCTCC TGCCTTTAAT 120
ATGAGTACCA GATCGAACAG TTTAAAAATG CTAGTTATGT AAAGGAGCGT GTTAAATATC 180
TATACTGAAG TTTTCAGAAA AGTCAGTCTA TGAATAAATG AAGAAGAAAA GATAAAGCAA 240
CAAGAAAAGA AGGAAAGAAC ATAAAAAGTG CAAACAACAG AGAAACAGGG AGCAGTAGAG 300
GGCAAGAAAA CAAGTATGAC TACAACTGAA TTTACACTGC TCATGTCCTC TGAGTCCTTT 360
CCTGGGTCTG CTTTGATTTT CTTTAGGTGA TGGGTTCTGA GCTGGCTGAA TTGGACTTAC 420
GGTTTTATAG GCAGAACAAA GCTGTTATTT TTAATCTTGA TTTCTTTCCA TATATTTTTA 480
ATTGACAAAT AATAACTGTA TATATTTATG GGGTACAATG TGATATTCCA ATGTATGTAT 540
GCCTTACAGA ATGGTTAAAT CACACTAATT AATATATCTA TCATTTAACA CACCTTTATT 600
TATGGTACAA CCATTACTTA AAATCTACTT TCTCAGCAAT TTCAAAATAT ACATTACATT 660
GATATTAACT ATAGTTACCA GGCTGTGCAA TAGATCTCAA AAACTTATTT CTCCTGTCTA 720
ACTGGAACTT TGTATCCTTG GATCAACATC TTCCCCTGTG TGTATTCTCC CTGCCCCACC 780
TTTCTACTTT TCTTTCTAGG GTTTTCTTGG AGGGTTGGGG ATAAGGCAGA GGTCAAGAGT 840
TGTTGGGTTG TGACTGTTAG CTTGGAGACC CTTATTTGTT CTGTAAGTAA GATTTATATT 900
ATTTTTTATT TGTTTGTTTT CTTTACTAAG GTGGAGTACA CATTGTACAT GGTCGCAGGA 960
AATTTCATTC TCCTGCCTAC TCTATCTTGT GAAACTTCCT TGCGGTATTT ACAGGTATTT 1020
AATCAGTACG GTTAGTTCCT ACTCTGTTTA CTGTTGTCTC CATGTGATTT GCTTCAAAAT 1080
GAAAATATTT TTTACCTGCA TACCACATGC TTGTTGTAAA AAGCCAAAGA ACAGAACAGG 1140
AAGGTTTCCC CACTGACTCA CTCTCTTGCT TCACCTGCCC TCTAACAGCC TCCCACCAAA 1200
TTTCCTAACT CCTTGGTAAT GATTACAGAC TTTGCCAAAG TTAATTCAAA AGCTGAACAG 1260
ATAATAATGT TCATTGGCCT ACCATATTTA TAACTTAGAT TATACACATT TCAAATCATG 1320
TAATCTGACT CATTATTGTA TTTATGGAAA TTAAAAACTC TGGTACAAAC TGTACAGTCT 1380
GAAAAAATAA AAAAGAGAGT GATGGCTCTT AGGTACAGGT GTGTGCCATA 1430
|
