| Tag | Content |
|---|
EnhancerAtlas ID | HS042-30534 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr22:43559250-43560660 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr22:43560091-43560105 | TGCTTCCTCTTTTC | - | 6 | | SPIC | MA0687.1 | chr22:43560091-43560105 | TGCTTCCTCTTTTC | - | 6.1 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_23668 | chr22:43559512-43560072 | Colon_Crypt_1 | | SE_24969 | chr22:43558628-43560231 | Colon_Crypt_3 | | SE_26727 | chr22:43558596-43561245 | Esophagus | | SE_32000 | chr22:43558390-43560967 | Gastric |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr22 | 43560000 | 43560338 | | chr22 | 43559294 | 43559513 | | chr22 | 43559631 | 43560203 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I043163 | chr22 | 43559100 | 43560546 |
|
Enhancer Sequence | ATGGCCTTTT TGCTTGGGTG GGACCCCTGG CCACAGGGAA GAGGGGGAGC TGGGGCTGCA 60
CTGGAGCTCG TCTCTGCAGG ATCTGCCTGG GCTGCCTTCT CCAGACAGGG CTGGATCCAG 120
CTGGGGCTGC CCCACGCTTC CTGGGACGCT CCCGAAGCCC TGCAGGAGAT GAACAGAGCA 180
GCCCTGGGTG CCACCCTGGG GCCCACACTG GCGCAGACCC AGCTGGGGCC GTGGGCTTCA 240
GCAGAGGGAG GGGGTCCTGT CCGCTTCCCA TGGCTTCCGG GATGCTCAGC CCGGGCCCTT 300
TAATGGCCGG GCCCACAACC ACTGTTCGAC GCCTGGTCCT GCCCAGTGCG TGGCCCTCAG 360
CTGCTTTTAC CCAGGACAGA GTTGGGGGTG CTGACTGCCC TGTCCCCCGG GGGCCCAGGC 420
TTATGGCAGC CTCACTGCAC CAGGGATAGC CCCGCAAACA CCCAGTTGGC TCGAGGGGGA 480
GTCAGAGGCA GGAAAGGTTA GGTCCCGACT CCAGCAGACA GGGCCTCCTT GCTGGCCCAG 540
AGCGGCCAGG ATTGGAGGTG TCACAGCCAC TCACTCCCTC ACCCCGGCTT CGAACTGGGT 600
GACCCATGGC CTCTCCAGGC AGCTGTTTGG AGTAAATGAG CCGAGTCCCA TACGCAGCAC 660
TCCTCCGTCT TGCTCTCGGT CACCACACCC ATGCAGCACT CAGCAACACA GCCCGCGGCT 720
CCCTCCCCTC GGCCAGGCCT GACCTGCCGG GCTTTTTGTT TTTTGTTTTT GGCAGCTAAG 780
TTCATTCAAA TTGGCAAAAT GTTCATAGAC AGCTCGTCAT CACTCAACAG CCCGCGGCTG 840
CTGCTTCCTC TTTTCTCCCC CGGCTCCTGT GTCCTCTCCC GACCTGTACG CTCAGACACA 900
ACCTGACGTT CACAAAAGCT TGGACACAGT GGCTCACACC TGTAATCCCA GCACTTTGGG 960
AGGCTGAGGC GGGAGGATTG CTTGAGGCCA GGTGTTTGAG ACCAGCCTGG GCAACATAGG 1020
GAGACTCTTG TCTATACCAT CCACTCTGGT GCACGCACAA CACACACACA CACACACACA 1080
CACACACACA CACACACGAA AGAACGAACA GCTCAGGGAA ATGGGTAGAC AGTCGACTGC 1140
ATTCTTCTGA CAGAAGGGAT GGCTCCCGCC CAGGGGCTGC GCTACTCCAC CCTGACCCTC 1200
AGCCTCCCGC TCCCTTGACT CTGGCAGAGT TTGATGCCCA ACAGATCACG CTCTGCAGGA 1260
TCCAAAAACT CTGCGGCCAC GGGCACTCAG CTGAGCCCTC AGCCCTCATG GCTTTCCCGA 1320
TGCTCACCGG TGCAGAGGAG CCAGCTGGGG AGCCTCTGTG TATCCTTTTT ATTAACTTAT 1380
TTCTGAAGTT CTCCAAGACG CCCAGAGTTG 1410
|
