| Tag | Content |
|---|
EnhancerAtlas ID | HS040-08470 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr12:57380720-57381850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:57381484-57381503 | GCGCGCCCCCTGGTGGTTC | - | 6.28 | | NR2C2 | MA0504.1 | chr12:57380990-57381005 | TGCCCTCTGCCCTCC | - | 6.45 |
|
| | 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 |
| GH12I056987 | chr12 | 57381185 | 57383337 |
|
Enhancer Sequence | CAGGCTCTCT AGGATGAGAA GGAGAAGGCA AAAAAGTGAA CAAGAGCAAG TCCCCTCCTG 60
CTACAGTAGT TTTCTGGGGC AGAAAGATGT GGAACACCCA CAGGGAGAGT CCAACCTCAC 120
AGGTAAAGAA AGGGGAAAGA AGGGAATGGA GCCTTGGAAC CCACAGGAAG GAAGTACCCA 180
GGGCTGCTGG GAAGGGGAAT GGAATGACTT ATGCAGGTGT CACAGGGCTC ACCTGCTCAC 240
CTCCTGATAT GCCCTGGGTG CTGGCTCCAC TGCCCTCTGC CCTCCCCTGT CAGGGCCCAC 300
ATCCAGGATC TGGACCCCTC AGACACTGAG AGGCTAAAAA CATTGCTCAT TTGAACAAGG 360
ACAATGAGGA TGGTGGTCCA AAACCTTGCC CAAGCAGGGA AGGATATGAA CCCTAGTAAC 420
TGTAAAGGTA TTACTTCAGT TTGTATCAGG GTGTTGATGG ACAGGAGGGA TCTCCTTCTC 480
AGGAGACTAC AGAAAGGGGT ACAGACTGGA CCTCTGCTGT CCATGGAGGG TCCCTCGGTG 540
TGAGGTCGAG GAAACTATTT CATAACTGGT GGGCAGGATG TAGAGGGGCA GGGAGCTGGG 600
GGAGTAGGTG TGGGACAGAA TAATCCAGGG TTTATTTGCA CTGGGCCTCT CTCCCACTGT 660
CCATGTTTGC CCAATTTCTG TCCCCTAATT GAAGGAAGAA GTGGAGATGG ACTGGGAGGG 720
GGAAGGAGAG GTTTCCTGCA GAAACCAGAG GCTAGCAAAG AGCCGCGCGC CCCCTGGTGG 780
TTCTTCTCTA GCCCTGCAGT CACGACGTGG GCATCGGCCT GGGATCAGCC AAGGCTCTTC 840
AGCTCATCCC AATGGCCACT CTCTCCAGCA TCGGGGAGCC CCCATATCTC CCTGCACGGA 900
TCCTCCAAGA AGGAGGGAAA CAGCAAGACT GCTGGCTGGT AAGAGACTGG ACTACTGTTA 960
ATTAAGCAAC ATGGATGGTG CCTTGAGTGT GCTGCATACT AGAGGTTTGA CAGACTCGGA 1020
GCCCCTTGAG GGCTCCGAGA CTGAGTCCAG TCATTTTTGT ATTTCCAGCC CCGGCAGTGC 1080
TAGCTTCTAG CAGAGATGAA GGAATGTTGA GGTAGCTGAC ACTGCAACAT 1130
|
