| Tag | Content |
|---|
EnhancerAtlas ID | HS110-00675 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr11:67230350-67231810 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr11:67230936-67230947 | TCCTTATCTGT | + | 6.14 | | NR2C2 | MA0504.1 | chr11:67231356-67231371 | TGCCCTCTGCCCCCA | - | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27544 | chr11:67231042-67233407 | Esophagus | | SE_42089 | chr11:67231301-67232191 | LNCaP |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr11 | 67231285 | 67231800 | | chr11 | 67230800 | 67231000 | | chr11 | 67230654 | 67230827 |
|
Enhancer Sequence | ATGGGGTTTT CCCATGTTTC CCAGGTTGGT CTCGAACTCC TGGGCTCAAG TGATCCTCCC 60
ACCGTGGCCT CTCAAAGTGC TGGGATTACA GGCATGAGGC ACGGCACCCG GCTAGTTCTT 120
CTTATGAAAG TACTGGACCG TGATGGATTA GAAATGAAAA CTGGTCCTTT ACCATAGCTA 180
GTTGGGGGAC CACTGGTTTA GGAGTTCCTG CATCCAATGG GTGCCCCCTA AGTGCCTTGA 240
ATGGGGGATG AGGGTGGGAA GTCTGCGGGG CCTGGAAAGG TGGGAGCGAG AGCAAGAGTC 300
TGGGTGTCCA TTCCTCTAAC TCAGAATCCT GAAGGCCCCG CTGTGTTGGG TGCTGCAGAC 360
AGTGGTTTGT GGGACCCGTG TTTTGGTGGG GGAGATAGAC AGTACGGGCA GGTGCACCAA 420
CAGGGCCTCC CAACCCTTGC TCACTCAGCC AGCCTCTTGG TTGGCCGGTA GGGGAGACCA 480
GCTCAGTGCC GGTTTCCTTC TCCCTCCCCG ACAGTGTCAT GGGAAGAGCC CTGGGCTACG 540
TTCCTAATTC TACCTACCAC CTGCTGGCTG TCCTTGGGTG AGTCAGTCCT TATCTGTAAA 600
ATGGGACGGA GGTAGTGAAG ATTACAAGAT ATAACCCGTG TTCAGTGCTT AGCGCAGGGC 660
CTAGTATATT TTCTTTTCTT TTTTTTTTTT TAAATAGAGA TGGGTTCTCG CCATGTTGTC 720
CAGGTTGGTC GCGAACTCCT GGGCTCAAGC GATCCTCCCA CCTTGGCCTC TCAAAGTGCT 780
AGGATTACAG GCTTGAGCCA CCGTGCCCGG CCATCCTGGG GTCTTTCAAC AAATTGATAA 840
CTGGTAGCTA CTATGATCTC AGATTTCAGG TTTCTCAAAG ATTCTGTTTC TTGTTTCGTA 900
AGATTCTGAA ATGCTGATGT TCCAAAATTC TGAGATGGTT TGTTTCTAAC GTTCTGCATT 960
TCTAAGTCTT TGACCACTGA GGGTGTCTGT CAGGCGCGGC TTCCTATGCC CTCTGCCCCC 1020
AGGTTCTCCC AACCTCTGGG ACTGGGAAGG AGGGCAGTGG GTGGAGGGGG CTGGGCCATT 1080
GCCTTGACAT GGCCCACATT CAGGGCTGGC TGTGGCAGCC CAGGGCCCCA GAGCCAGGCT 1140
GGAACTAGGA TACCAGCCTC CAGGTCCCAG GCCTGCGTCA TCTCTGCGTG CCCTCGGCCA 1200
GGGCCACCAG ACAGAGACGG GCTGGTTGAG TCATCCAAGG GCTGGGGGTG GGGCAGGCTG 1260
TTCCGGCCGG CTCCTGGCTG GCAAGGCAGG AGTCCTACGC CCAGCTCTGC CCCTAACATG 1320
CCCCGTGCCC TTGGGCAAGC CTCAGCATCA GGGCTGCCAC GCGTTCGGTG GTGCTCGAAG 1380
CCCTTCAGCG TCAGGGTCAG TCCTTGGGAG GGGGGCTGTG GTCAGGCTGG TGGGCTGGGC 1440
TAGCAGTGGC AGGACAGGAG 1460
|
