| Tag | Content |
|---|
EnhancerAtlas ID | HS105-73583 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr7:50602220-50603590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr7:50602374-50602395 | AAACTAAAAGAAAAAGTAAGT | - | 6.33 | | IRF1 | MA0050.2 | chr7:50602848-50602869 | CTTTTCTTTCTTTTTTTTTTT | + | 6.41 | | NFE2L1 | MA0089.2 | chr7:50602762-50602777 | ATTGCTGAGTCATTG | - | 8.33 | | Nfe2l2 | MA0150.2 | chr7:50602764-50602779 | TGCTGAGTCATTGTT | - | 7.8 | | ZNF263 | MA0528.1 | chr7:50603213-50603234 | GAAGGAGGAGCACGTGGAGGG | + | 6.26 |
|
| | 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 |
| GH07I050533 | chr7 | 50600846 | 50604128 |
|
Enhancer Sequence | GGAGGCAGTG GTTGCAGTGA GCTGAGATCG TGCCACTGCA CTCCAGCCTG GGCGACAAGA 60
ATGAGACTTC GTCTAAAAAC AAGACAAAAT AAAAAAAAAA AATGAGAGGA ACAAATGGAA 120
AAGAAATGGA AAAGTAGACC TTGTCCCGTG TATAAAACTA AAAGAAAAAG TAAGTCGGCC 180
ACCAACATCG AGGCCTCTTG TAAAGGGTTA GACCATGCAT GCCCTTGCCT GGAATCAAAA 240
CCACGCCCTC TGCAGGCACG CAGCTGTCCC ACTGGGTCGC TGAGTGCTGC TGCCCTCTGT 300
CCCCTGGAGA ATCAGGACTG ATGTTCCAGA GGCCAGAAAG CCATCTGGCC CTCACCAAGG 360
CAAAGTGCAG CTGACAGAGC ACTGGCTGCG GACAGTGTGC AGTAGCTCCC TCCCCTCGCT 420
GGAAGGGCAC CTGTGACAGC CTATCCTTGC TGTGATCTTG GCCAAGGAGG CTTCTCCAGC 480
TGCATACTCA CTGACCAGAA GAAAATTGTG CTGGGACTGA AGCATGATTC ATTTGCTGAA 540
TCATTGCTGA GTCATTGTTG CTGCTACGTA GAATGGTATG GTTCACAGCA ACGTATTGAA 600
GCTTTGCTTA CAACATAGCT GACGTTTTCT TTTCTTTCTT TTTTTTTTTT CTTGATGGAG 660
TTTCCCTCTC GTCAACCAGG CTGGAGTGCA ATGGCAAGGT CTTGGCTCAC GGCAACCTCT 720
GCCTCCCAGG TTCAAGCAAT TCTCCTCCCA AGTAGCTGGG ATTATAGGTG CCCGCCACCA 780
CACCTGGATA ATTTTTGTAT TTTTAGTAGA GACAGGGTTT CACCATGTTG GCCAGGCTGG 840
TCTCAGACTC CTGACCTCAG GTGATCTGCC TGCCTTGGCC TCACAAAGTG CTGGGATTAC 900
AGGCGTGAGC CACTATGCCT GACATTTCAT TTTCCTCAGC TCCCCATTTA ATATCACTTA 960
TGTCTGATGG AAAAAGAGAT AACCAAAGAA TGCGAAGGAG GAGCACGTGG AGGGATGACT 1020
CTGAGCCTGG CCACAGGGCC TGTGGGTCAT GGAGAAGGCA GTCATCAGTC CCGGCATGTG 1080
GCCTATTCAG GAATCTGGGT GTCATCCGGA TGAATTAGCG TTCACATTTT TTGGCCCAGA 1140
GTCTAGGAAT AGGCATTACA AGCAAGTTCC CTCCATGACT CTGAAGCACA CTGGATGTGG 1200
TAGGCACATT AATGCACCCT CATTCCCAGA GATTTCAGGT CTTGGTCCCC AGAATCTGTG 1260
ACTGTTTCCC TTCCAGGGAA AAGGTGACTT TGCTGATGTG ATTAAGTTAA GAAACTTGAC 1320
TTGAGAGATT ATCTCAGATT GCCTGGATGG ACCCAATCCA ATCATATGTG 1370
|
