| Tag | Content |
|---|
EnhancerAtlas ID | HS147-04765 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:224391840-224393000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:224392357-224392378 | CTTTACTTTCTGTTTCTATAA | + | 6.29 | | IRF1 | MA0050.2 | chr1:224392233-224392254 | AATAAAAAAATGAAAGAAAAA | - | 6.5 | | IRF1 | MA0050.2 | chr1:224392239-224392260 | AAAATGAAAGAAAAAGAAAAA | - | 6.89 | | SRF | MA0083.3 | chr1:224392016-224392032 | TCACCATATATGGTCA | + | 8.04 | | SRF | MA0083.3 | chr1:224392016-224392032 | TCACCATATATGGTCA | - | 8.08 | | Zfx | MA0146.2 | chr1:224392066-224392080 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65181 | chr1:224391966-224393881 | NHEK |
|
| | 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 |
| GH01I224202 | chr1 | 224390586 | 224394441 |
|
Enhancer Sequence | AGAGTCTCAC TCTGTTGCCC AGGCTGGAGT GCAATGGTGC AATCTCAGCT CACTGCAACC 60
TCTGCCTCCC GGGTTCAAGC AATTCTCCTG CCTCAGCCTC CCAAGTAGAT GGGATTACAG 120
GCGCCCACCA CTGCACCTGG CTAATTTTTT TTTGTATTTT TAGTAGAGAT GGGGTTTCAC 180
CATATATGGT CAGGCTGGTC TCAAACTCCT GACCTCAGGT GATCCACCCG CCTCGGCCTC 240
CCAAAGTGCT GGGATTACAG GCATTAGCCA ACGCACCCAG CCCATTGTTA CCATTTTCAC 300
GTGTCCAGTT CAGGAGTATT ACATACATTC ACATTGTTAT GCAACCTATC TCCAGAACTT 360
TTCATCTTGA AAATCTGAGA TTCAAAAAAT AAAAATAAAA AAATGAAAGA AAAAGAAAAA 420
AAAAATAAAA AGAAGAAGAA GGAAAAAAGA AAAACCGAAA TTCCATGCTC ATTAAACAGC 480
TCCCTATTTT CCCTCCCCCA GCCCCTGGCA ACTAGCACTT TACTTTCTGT TTCTATAAAT 540
TTGACTTGAG TATTTTTTTT TTAATCAACA AAACTCTTAA CTTGCACTGT CAATATATTC 600
CAAATATTCC AATATATTCC AAAATATTCC ACAGCAGGCC TGGGTCATGC TGGATTAGCA 660
AAGACAAGGA CTGGCCTAGA TGGAGTCACA CCCTCCCCAG CCTTGGGTTT GGGTAATTCT 720
CAACACCCTA ATTCATTCTC CCCTGGCAGC TGGAGAGACC CGTGGGACAG CCACTCACTG 780
CAGAAGGGGC TGGTGAGAGA CATGCTCGTC ATCTCCGAGG GCCTGGCTCT GCGCCAGCCA 840
CACACTTATC TGCCTGCTCC ATCTCCGGAG TTTCTGTCTC TGAGCTTTGG CAATGGAAGT 900
TGTGCTTCCA CTATTAGCCA ACACCGAGCT GGACTCTGGT AACTGACACA GCCGTGCATC 960
TAGTGTAGCT CGGGTTGAGA TGACTTGGCT TTTTTTTTTT TTTTTTTTTT TTTGAGACGG 1020
AGTCTCGCTC CGTCACCCAG GCTGGAGTGC AGTGGCGGGA TCTCGGCTCA CTGCAAGCTC 1080
CGCCTCCCGG GTTCACGCCA TTCTCCTGCC TCAGCCTCCC GAGTAGCTGG GACTACAGGC 1140
GCCCGCCACC ACGCCCGGCT 1160
|
