| Tag | Content |
|---|
EnhancerAtlas ID | HS040-00899 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:22466960-22468230 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:22467766-22467778 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr1:22467770-22467782 | GTTTGTTTGTTT | + | 6.32 | | PROP1 | MA0715.1 | chr1:22468041-22468052 | TAATCAAATTA | + | 6.02 | | SOX10 | MA0442.2 | chr1:22467753-22467764 | TTCTTTGTTTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65544 | chr1:22465140-22469318 | Pancreatic_islets |
|
| | 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 |
| GH01I022140 | chr1 | 22467332 | 22467678 |
|
Enhancer Sequence | GGCTCACACT CAGCTCTTTC CTCTGACAGC CATAGAGCAT GTGCCCTGTT CCACCCAGTC 60
GTGGTTTTAT CATGTCTTTC TACCTAGACT CCAGGCTTGT GGGAGGCCAG GCTGTGACAT 120
CCATTTCCCC CAGAGCTGCC ATTCCTGGCC AGCTGATTGT TCGACAGAGG TTGATAAATA 180
TTGGACCAAC CTTGGTATGT GCCCAGTGTC TTCTCCTTCA TAGCCTCTCT GGTTTGGGAG 240
GGTCCTGGGA AGCCTCTTGT TCCTCTTGCC TTGGGTGGAG CAGAGAGACC CTTGGCTTGA 300
AGCCGGGGGT GGAGCAGGAG TGAGCTGGGT CATCCAGAGA CCTGCTTCGT GGCAACCTGA 360
ACCATCACCG TTGCAGAGAA CAGGTTTGCC AACCTCTCTT CTCCTAGGCT GCCCCTCCTC 420
ACCCCACCCC CAACAGCACA GGCAGGAGAA CTGAGTTGTT GGAATTCCCC ACAGTTTGCA 480
TGATCCAAAG CCGAGGCTGC CTTCCTGGCT GGGATTCTGG GGGTGGACAT GGGTGAAGGT 540
GAGTGGTGAT GCCACCGGGC CATGCTGGCT CCACTTTGGG ACAGCTTCAG GGAAGGGGGT 600
ATAGGGTCAC TGCCTGGGAG TCAGAACACC TGGGTTCAGT TCTCAGCTCT GAGTTTGGGC 660
AAGTAGCTTC CACTCCCTAG GCCTCAGTTT CCTCATCTGA GTCAAAGATG AGATGTTCCT 720
GAAGGACTTT CCACTGCAGA TGTCGCTGTC TTCCATGTAG GCCTGGGCCA GACGCTTGGA 780
CTGCCACTTT TTTTTCTTTG TTTTTTGTTT GTTTGTTTGT TTTTTGTGGC TTTGGCGGTG 840
CTGGGCAGGT GAGACACAGT TCTTGCTCCT TCTGATGCTC AGATCTGTTT TGGAGGCCCC 900
CGCTCTGAAC CCATGCATTC AAGAACCAGC TCCAGGGACA CCCAGGGTCC TCCAAGTCCA 960
AATCAGCTCC CTCCCCAGCT CTGTGACCCA GGCTCCATTC AGGGGGTGGC CTGCAGGGGG 1020
GCAGTGGGAG AAGGTGGTGG TGCCTTGCTT TCTGTACACT CTGCCACTGC TCCTGAAGTG 1080
TTAATCAAAT TAAGGCTCCA AGAAAAACAA AAGCTCCGCA GCCACTTCGG GCTGCCTTGG 1140
AGTCGTTTGC TCTCGGAACA GCTGGGAGAA TTCCACATCA CCTCCGTCCC CCAAGCCCTG 1200
GGTGGCTCTG ACCCCAACGA ACACACTCCT TCCAGCCTGG AGGGCTCTGG CTGGCCACAA 1260
TGACCTCATA 1270
|
