| Tag | Content |
|---|
EnhancerAtlas ID | HS040-19705 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr2:46361310-46362680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr2:46361894-46361904 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr2:46361894-46361904 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr2:46361894-46361904 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr2:46361894-46361904 | AACAGCTGTT | - | 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 |
| GH02I046134 | chr2 | 46361268 | 46364764 |
|
Enhancer Sequence | TTCACTTTTC TGCTCTTATT CCTTCATCCA TTTGACCAGT AGGTATTGAG ACACTGGGAT 60
GCATCAGACA CTGTGGGAAC TTGGAGACCC TGCCCTCATG GAATGGTCCC TTGTGGAGGA 120
TAGACACTCA TAGTGGAACA GGAGACAGGG ACCATCTGAA GGTTCCTCTG GCCTTCTAGC 180
CTTTTCCATC ATCATACACT CTCCTGATCC AAACTGGATG GATGAGGCTA GAAGGCCATG 240
GGGGACCACA AAGGGCCTCT CACACCATGC TAACAACCCT GCTTCTGGGG TGCCATTGAA 300
GAATGCAAGC AGCAGGGGAG CATCATCTGA TTTACATTTC GTGTAAAAAT GCCTGCTGGC 360
AAAGGTTTGC TCCAAAGTGG AAAGGGAAAA CATTTGGTGT GCAACAGCCA GGACTGCAAG 420
TTCAAGCAAG TTCTTTCACG GGCTCCAGCT GCCTTCGCTT CCTGGATCTT AGACTGGAAA 480
GGCCCTTGGG GATTAACTCA TCCAGCCGTC TTATCTCATA TTTGAGGACA GTAATGCTCA 540
GAAAAGTGAC TTGCTTGTGG TCACTCTGTC CTGGGCTTTG CCCAAACAGC TGTTTTGATG 600
ACCAAGTTGA TTGGCCTGGA GAGAGATAGG GGAACTAGGT GTAAGTGTCA CGACGGATCG 660
TCAGGCTAGC TCACCCACAT GCTGGAAACA CAAGGCAATG CCTGCTTCCC CTCAGCAGGG 720
ATCAGGATTT TATCCATGAA TATTAAGGAT AAGAATGTAC TTTCATTATT GTGGGTTAAA 780
AAAAGTAATT GGATGATCAT GCAATCAGAT AAGCAATTCT GTAGTGATTC CAAGGCTTAA 840
TGCCCAGGTA CAGCCACAGG CTGTTTATTA TTATTTTTTC TATTGGCGGG ATCAACCAGG 900
TACCAGGCTA TTTATTTTGG CTTCAAACCG AGATGTTGTT TGACACCTCA GGCTTCCAGC 960
TGTCAGTGTA GTGTCTAAAA GTCTTCTCTC TCCAGTTGAG AGGACATCTA TTTGATCAAA 1020
ATAGCATTGT CTGGCTTATC TGTTACATCT TATAAGCATG TTTCCATGAG TTAGAAACAA 1080
CCACCACCCC AACAACTACA ACTGTGTTCT CTATCCCATG AAAGGGCGGG CGTGTGGACA 1140
CGATGTATAT TTTTTTCTCC TCAAACAACA CAGTGAAGTG ATTCAGAGCA TGGAAGTGGG 1200
GTCAGGCAGG GTGGACTCTG TTGCTCACTC ACCACCTGTG TGTCCTGGGC CAGTCAAGTA 1260
ACCCCTCAAA CTCTTTTTCC TCATCTAGCA GGTAGGGATA ATAACAGTCT TACCAGATTC 1320
ACAGAGCACT TGTGGGATTA AATGAAGTAA GAGATAGAAA AGATTTAACA 1370
|
