| Tag | Content |
|---|
EnhancerAtlas ID | HS081-00162 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr1:17541120-17542590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr1:17541286-17541297 | AGAGATAAGGA | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27475 | chr1:17540193-17543189 | Esophagus | | SE_33802 | chr1:17540690-17542938 | HCC1954 |
|
| | 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 |
| GH01I017215 | chr1 | 17541633 | 17542151 |
|
Enhancer Sequence | AGAGGATTAT TAGATTTGGA GGAAGCCGGG AGCAGCTCCA GAAAGCTGGC GCAATACAGC 60
CCACTGCAGG GTGGCCTGGG GCTCCCCACA AGCTCCCACT CCTGCCTGTC ACACCTCCCA 120
AGGGCAGCCC TTCATCCATG ACCAGGCCCA CAGATCTGGG CACCTGAGAG ATAAGGAAAG 180
GCAGTATAAG CCCCGTCTCC CAGCCCCGGG GCAAGGGTTG GGGTAGGATG CCAAGGGAAT 240
GAGAATCAAA GGCAGCGCAG GGCTCACCCG GCATAACCTG CCTTGCTTGG GTGCCAGAGA 300
GAATAAGCAG ACCCCTCCTC CTGCCTCTTC CTGGTGGTTT TCAAAGCTCC TGCTGGGGTA 360
CCTGCCGCTC TTCTGTAGCT GAAGCTGACC TGGATGGGGG TGATGGGAAC CAAGTCTTGA 420
AGGCAGTGGG GCTGGGAACT AGAATAGGCC CCTCCCCATG CCTGTGGGAG TGGCCCTGGG 480
CCTCAGACCT GCATAGCAGG TGTCTCCTGC AGGAAGCCAC ATTTCCCCCA AGGCCTGACC 540
CCTCTAGGCA CTGCCCACTC ATCTGTTACT CACAGGGGAG GGAGACACTG AGACCAGGAG 600
CCCAGCACCC CAGAGAGAGG TGAACAGAGG TGTGAGCTAT TGAGCAAGTT TGGGGTGGGG 660
AGGGAGCAGA TCTAGACTAC AGGAAGCTAG GCTGGGCTTG GAGGGTCTTG ATAGCCCCAG 720
AGAAATTGTA CCTGTCATTT CTTCCCCCTT CTTTCATCAT CATCATCATC GTCATCATCA 780
TCATCATCAT CATTTTCTAC CAAGACTCCA AATAGGGGGC TGTGACTTAG AGATGTCAAC 840
TTTTGCCCAA AGCTAGGGAT TGGCTCCACA GAGTCCTGCT TCCCTTGAAA GGGCTGTGTC 900
TGGCACCGGT GGTCCCTGAG TGGGGTGGAG CAGGAGTCAC CCATGAGCTA GAAACCCTTC 960
TGCTGCCAGC TGGGTGCCCT GGGCTTGTGG CTACTTGCTC TTGGAACTCA TGGGCCAGGC 1020
CGACTGGATT CAATCATGAC TCAGCCACCT CCCCGCTGGG CAGTCCTGAG AAAGCCACTC 1080
CACCATCCTG AGTCGCTGTG TCCTTGTCCA GAACGCGTTG ATTGTGCCCC TGGTTCATGC 1140
CAGGCACTAA GCTGGATGCA GAGATGACAG CAGCGATGCA GACAGCATAA AACAGAAAAA 1200
AAATCTCTGC ATTTTAGAGG GAGAGACTGC AATGAGCAGA TATGTGCTCT GTCAGGTGGC 1260
TGGGAGGTGG CCGGTGCCAT GGGCTGGAAT GAAGCTGGGG TTGGGGAACC AGACTCATGG 1320
TGTCATTTGT GTCACGCCAT TTGCAACAGG CAAGAAGGGT ACATCAGAAA GGCCTCGTAT 1380
GCTACCCTGA GAGAAGGAAG TGAGGGGCTG GGCGGACCGC AGGGATTGGT GACAGGAACA 1440
TTCCGGACAG ACAGAGCTGC AGCCCTGGCA 1470
|
