| Tag | Content |
|---|
EnhancerAtlas ID | HS040-07714 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr11:130272950-130274290 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr11:130273217-130273228 | CTGCAGCTGTT | - | 6.02 | | Tcf12 | MA0521.1 | chr11:130273217-130273228 | CTGCAGCTGTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_08530 | chr11:130270251-130275391 | Brain_Inferior_Temporal_Lobe | | SE_39023 | chr11:130269984-130274795 | IMR90 | | SE_69174 | chr11:130272967-130276303 | H9 |
|
| | 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 |
| GH11I130400 | chr11 | 130270005 | 130274950 |
|
Enhancer Sequence | ATTAACTTTA TGCTACTGTA CCACCTTCGA AGTATTTCTG GCAGGTGCCT GGAGGATTCA 60
GATTAATGAC CAAATTACCT GCCAAGTCAG GGCCTCCCAT TAGAAGAGAG TACCAGTTTC 120
CATTAGGAGC ACTAGCTGGA AAACACAATC TTTCAGCAGA GGAAATACAG TCTTCTCTCC 180
TTCTCTGGGT GCACAGAGTG GTCGTGGTTG GCTGGGGCAG ATAATGGTGT GGTCTTCCTC 240
TGCAGATCTG GTTTCTGAGT CCCTGGGCTG CAGCTGTTGA ATTTCCAGAC ACAAACAAGT 300
ATGCGTTCTG AGAGCCTCGC CGAGCCCACA CAACCGGGAG AGCCAAGCTG GATTCCATTC 360
TGCTTTGCAC ATCAGCAGCT CTGCTGCCAG CTGAACTCCA GGGCAAAAGC TGTGCCTGGT 420
AATGATGCAG GCAGCAGGGA TGGCACAGCT GGCCTGGCTT AGGCCGTTAA GGGGGACACG 480
CTTGGCCTTA TTTGGGGGAG AGCGAGAAAT GGAAGGCGAT GAAGAGTTGC GGAAGCATAC 540
ATCAGCCTCC ACAAAACTGG TGCACAGCAG GGAAACAATC TGGTTTTGCT AGTCATCAAC 600
AACATGCCTG TGTGTGTGCC TGTTTATGCT TAGGTAAGCC CAGCCTCCCA CTCGCTGAAA 660
AGAGTAGGCA GACAAGAAGG AGTGACCAAC TCTGAGTCAG CTGTCATCGT GTAGAGAGCA 720
GCTAAGGGGA ACAGTGGGGC TGGAATCTCA TGGCCTTGCC TAGTGCCCCT ACAGCATCCT 780
CTCTGCCCAT GGTGCCAGAT ATCTGAATGG GAGGACAAAG GGGGCACAGG TGGTGAAAAA 840
AACCAAGATG CACATTTGGG TATTTTCCTT CTTTTGCTAG AATGTCATTT CTTGATGTCT 900
GTTTCTTGTC ACCCATTTGT GATCAGGGAC TAAGTAAGTT CCCTCTGCAC CAGACCAGGT 960
GGAAGACTGA GCCAGAGTTC CTCTGAGCCA CAGGAGAGAT GAGGAGCTAT GGAGCGGAGT 1020
AGGGGCTGAG GATCTGGTGC CCCCAGCTAA ACTAAAAGGA GGCAGGCAGC ATGTAAGAGG 1080
ATGATGGGGT AGCTCACAGA GAGGAAGGGG ATATTCTTTC TCAAGAATGA TGAGCCCAAA 1140
GGCATCGCAT AACAATTGTG ATCTCCCAGC TGGACGTTTC CTGTAGCACA GGTGTTCACA 1200
GTGTGGCTCC CAAACCAGCA GCCTCCATGT CAGTCACTGG GAACTTGTTA GAAATGCAGA 1260
TTCTCAGGCC ACCCCAACCA TTAGATCAGA AACTCTGGGG ATGGGGCCCC ACAATCTGTG 1320
TTTTCTTTTC TTTCTTTCTT 1340
|
