| Tag | Content |
|---|
EnhancerAtlas ID | HS098-36963 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr22:37373220-37374560 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr22:37374272-37374291 | TGCTGCCACCTACAGGTCA | - | 6.73 | | IRF1 | MA0050.2 | chr22:37374058-37374079 | AAATTAAAAAAGAAAGAAAGA | - | 6.18 | | ZNF263 | MA0528.1 | chr22:37374217-37374238 | CCTCCCAGCCCCGCCTCCTTC | - | 6.32 |
|
| | 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 |
| GH22I036976 | chr22 | 37373021 | 37374830 |
|
Enhancer Sequence | ACATTTTGTT CCCCAGTGAG AACAACCCAT CGTGCCTGCC GGACCTTGCT GTGCTCTCTG 60
CCTTCTGATA GGGAGGAGAG GGTTGGAGGG AGACCACGGG GGATGGAGGC TAGTGGGGCT 120
GCCACACTTC CACCCCATGA CGCCACAGGA TGAAGGAGCT TCCAAAATGC ACGTGGACCC 180
CAAGGAAGGG AGTGAGGCGT GAGTGGCCAC GCAGAGCCCA TCCAAGGGGG CAGACAACTG 240
GGTGAGAACA CCCCAGCAGG CCAAGGCTGT GGGGTGTGCC CTAGAGGAGG GCAGGACCCG 300
AGGCAGTATG GGGAGCTGCT GAGCCAGTGC ATCTCCCTCA CGGGGGCGCT GTGCAGTGTA 360
GGTGCCCCTA TGGGACACGC ACACCTCCTC CAAGAGCGGC CCCCGCAGCG GAGCAGAGCT 420
GGCCAGAGGA GCACTAAGTA AGCCAGGCTG ACAGAGGTGC TGGAAAAGAG GTCCAAGGGG 480
GAGCTGGAAC TGTTACAGGC ATTCAAACCA GAGTGACTCC ATTTTGAACA GGGGCTGGGC 540
TACTGGGCTG CGTTCCCAGG AAGTCAGGCA TTGTTAGCCA CGGGATGAAA TAGAAAAAAA 600
AAAGTTAGCC AGGTCTGGTG GCGCACACCT GTAGTCCCCG GAAGGATCGC TTGAGCCCAG 660
GAGTTCGAGG CAGCATTGAG CTAAGATCTC GCCATTGCAC TCGGCCTGGG TGACCGAGTG 720
AGACCCTGAC TCTAAAATAA GTAAATAAAA AGAACCAAAA AGTATCTAAT TATGGATGAT 780
TTTTACTTTC GTTTAGACGC TATTCTCTAT AATAAAAAAT GTTGCATTTG TAATCAGAAA 840
ATTAAAAAAG AAAGAAAGAA AGAAAGAAAG AAAACTGTTA AAACTGAATT GGTAGAAGAA 900
TGGGTTAGTG AGACAATCCC TCGCAGAATC TTGTGCTTTG GGAAATCTCC GTGCCGTTTG 960
TAGAAGGATT GCACCAGTGA CGCGGTGACA CCCATCTCCT CCCAGCCCCG CCTCCTTCCT 1020
TCCGGTCCGC TGCTGAGGCT TGGCTCGGCT TGTGCTGCCA CCTACAGGTC AGCGACAGAC 1080
ATTACTTCAA CCCCCCTTCC GCAGGGGCAG CCGCTCCCAG CTGCAGTTTT CCCTTTTCAT 1140
TTTAAGCCCT TGGATTTCAG AGTTGAGGAT GGAGATGTGT GGGAACTTCC AATGTGAAGT 1200
CAAGATAGGG GAGAGGGCAA GACAGAATGA GATAGAGAAC ACCTGTGTGT GCATCTGTAC 1260
ATGCAGGGCC CAGTGCAAAA TGAAGATGTG GGGGCCCCTT GTTCAAAAAT TATTAAGAAT 1320
CTCAATATTG TAACAGTAGG 1340
|
