| Tag | Content |
|---|
EnhancerAtlas ID | HS091-08064 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:67230220-67231810 |
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 | AGTGCAGTGG TGCAATCATG ACTCCACTGC AGCCTCCCAG GCTCCGTGAT CCTCCCACTC 60
CAGCCTCGCA AGTGGGTGGG ACTACAGGCG CCCCACCATG CCTGGCTAAG TTTTTGTATT 120
TTTTGTAGAG ATGGGGTTTT CCCATGTTTC CCAGGTTGGT CTCGAACTCC TGGGCTCAAG 180
TGATCCTCCC ACCGTGGCCT CTCAAAGTGC TGGGATTACA GGCATGAGGC ACGGCACCCG 240
GCTAGTTCTT CTTATGAAAG TACTGGACCG TGATGGATTA GAAATGAAAA CTGGTCCTTT 300
ACCATAGCTA GTTGGGGGAC CACTGGTTTA GGAGTTCCTG CATCCAATGG GTGCCCCCTA 360
AGTGCCTTGA ATGGGGGATG AGGGTGGGAA GTCTGCGGGG CCTGGAAAGG TGGGAGCGAG 420
AGCAAGAGTC TGGGTGTCCA TTCCTCTAAC TCAGAATCCT GAAGGCCCCG CTGTGTTGGG 480
TGCTGCAGAC AGTGGTTTGT GGGACCCGTG TTTTGGTGGG GGAGATAGAC AGTACGGGCA 540
GGTGCACCAA CAGGGCCTCC CAACCCTTGC TCACTCAGCC AGCCTCTTGG TTGGCCGGTA 600
GGGGAGACCA GCTCAGTGCC GGTTTCCTTC TCCCTCCCCG ACAGTGTCAT GGGAAGAGCC 660
CTGGGCTACG TTCCTAATTC TACCTACCAC CTGCTGGCTG TCCTTGGGTG AGTCAGTCCT 720
TATCTGTAAA ATGGGACGGA GGTAGTGAAG ATTACAAGAT ATAACCCGTG TTCAGTGCTT 780
AGCGCAGGGC CTAGTATATT TTCTTTTCTT TTTTTTTTTT TAAATAGAGA TGGGTTCTCG 840
CCATGTTGTC CAGGTTGGTC GCGAACTCCT GGGCTCAAGC GATCCTCCCA CCTTGGCCTC 900
TCAAAGTGCT AGGATTACAG GCTTGAGCCA CCGTGCCCGG CCATCCTGGG GTCTTTCAAC 960
AAATTGATAA CTGGTAGCTA CTATGATCTC AGATTTCAGG TTTCTCAAAG ATTCTGTTTC 1020
TTGTTTCGTA AGATTCTGAA ATGCTGATGT TCCAAAATTC TGAGATGGTT TGTTTCTAAC 1080
GTTCTGCATT TCTAAGTCTT TGACCACTGA GGGTGTCTGT CAGGCGCGGC TTCCTATGCC 1140
CTCTGCCCCC AGGTTCTCCC AACCTCTGGG ACTGGGAAGG AGGGCAGTGG GTGGAGGGGG 1200
CTGGGCCATT GCCTTGACAT GGCCCACATT CAGGGCTGGC TGTGGCAGCC CAGGGCCCCA 1260
GAGCCAGGCT GGAACTAGGA TACCAGCCTC CAGGTCCCAG GCCTGCGTCA TCTCTGCGTG 1320
CCCTCGGCCA GGGCCACCAG ACAGAGACGG GCTGGTTGAG TCATCCAAGG GCTGGGGGTG 1380
GGGCAGGCTG TTCCGGCCGG CTCCTGGCTG GCAAGGCAGG AGTCCTACGC CCAGCTCTGC 1440
CCCTAACATG CCCCGTGCCC TTGGGCAAGC CTCAGCATCA GGGCTGCCAC GCGTTCGGTG 1500
GTGCTCGAAG CCCTTCAGCG TCAGGGTCAG TCCTTGGGAG GGGGGCTGTG GTCAGGCTGG 1560
TGGGCTGGGC TAGCAGTGGC AGGACAGGAG 1590
|
