| Tag | Content |
|---|
EnhancerAtlas ID | HS040-08295 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr12:50968170-50969150 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr12:50968796-50968817 | CATCTCTTTCATTTTTAGTTT | + | 6.68 | | RREB1 | MA0073.1 | chr12:50969050-50969070 | CCCCACAACAACAACTCAGA | + | 6.5 | | Sox3 | MA0514.1 | chr12:50968592-50968602 | CCTTTGTTTT | + | 6.02 |
|
| | 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 |
| GH12I050571 | chr12 | 50965140 | 50970313 |
|
Enhancer Sequence | TAAAGGAAGC AGCTTAAGGT TAGAGCCAAA TTGGTTTGCT AAGTGAATTC CATCATTATT 60
CAGACCTACC CCGTGGGCAC AGTGGTGCTG GATTGGAGAG GTCATATGCA GTATGCAGAC 120
CCTCCACTCA ACGCAGCTTC AGCAGACAGC TTATGCGTAT GAGGAAGAAG AGCATGAACA 180
GACTATTTAT CCCAAATTTA CCAGTCAGTC AGTTGCTTCC CTCTCCAGGA TAGAATGATC 240
TAAGTGGCAA AGACATGCTA AAGATGTTAC AACTGGTGGA CCTCGATTCA TGCAAGGAAC 300
CCTCAGAAGT GAGGAATGAA TGTTCCCATC TGGTACTTCG TTCCCTCTTC CATGCATGGC 360
TTTTATGAAG AATGGGTTGG TGCCAGGGTA GGAGAAGTAG CCTGACTAGG CCAATGAGCA 420
AACCTTTGTT TTAGGGAAGA GACCTTGTAA CAATTGGCCT CTTGGAAATT GCAGCCAAGG 480
TTTGTTTATC GGAACGATGG GAATTTGTCC TTAGGCAGTC CTCTTTGCCT TTCTGAAACA 540
TCTGTGATTT AGTATTATTT CTGGGCAATA AGTCAAGGTC CACAACTTAG TTTTCTGTTG 600
TCCTTTAACA TTTTAAAATA TGCCTACATC TCTTTCATTT TTAGTTTTCT TCACAGACTC 660
CTTTTGTTTA CCTCCCTCTC TGGTGTTTTG CATGATTATA GCTAACTTTC TTTTCTTTCG 720
ACATTCTCCC CTTGGACACA GTTTTAACTC TTTCATATCT TGGTGGTTAC CAGATCTCTG 780
TCTCCAACCC TGACCTCTGT TCTGAGCTCC ATATTTGTAT CCAGCTCTCT ATTTAGCAGT 840
TCCATCTGGG CTGTCTAAAA CTAAACTCTC TTCTAGCCAC CCCCACAACA ACAACTCAGA 900
AACCCTTGCC TTTTATTTTG TGATACCACA GCCTTTTCAT TAGTTTAAGC TAGAAAGGGA 960
AAGCTGGGGG TCACCACAGG 980
|
