| Tag | Content |
|---|
EnhancerAtlas ID | HS098-52069 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr7:50602240-50603660 |
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 | GCTGAGATCG TGCCACTGCA CTCCAGCCTG GGCGACAAGA ATGAGACTTC GTCTAAAAAC 60
AAGACAAAAT AAAAAAAAAA AATGAGAGGA ACAAATGGAA AAGAAATGGA AAAGTAGACC 120
TTGTCCCGTG TATAAAACTA AAAGAAAAAG TAAGTCGGCC ACCAACATCG AGGCCTCTTG 180
TAAAGGGTTA GACCATGCAT GCCCTTGCCT GGAATCAAAA CCACGCCCTC TGCAGGCACG 240
CAGCTGTCCC ACTGGGTCGC TGAGTGCTGC TGCCCTCTGT CCCCTGGAGA ATCAGGACTG 300
ATGTTCCAGA GGCCAGAAAG CCATCTGGCC CTCACCAAGG CAAAGTGCAG CTGACAGAGC 360
ACTGGCTGCG GACAGTGTGC AGTAGCTCCC TCCCCTCGCT GGAAGGGCAC CTGTGACAGC 420
CTATCCTTGC TGTGATCTTG GCCAAGGAGG CTTCTCCAGC TGCATACTCA CTGACCAGAA 480
GAAAATTGTG CTGGGACTGA AGCATGATTC ATTTGCTGAA TCATTGCTGA GTCATTGTTG 540
CTGCTACGTA GAATGGTATG GTTCACAGCA ACGTATTGAA GCTTTGCTTA CAACATAGCT 600
GACGTTTTCT TTTCTTTCTT TTTTTTTTTT CTTGATGGAG TTTCCCTCTC GTCAACCAGG 660
CTGGAGTGCA ATGGCAAGGT CTTGGCTCAC GGCAACCTCT GCCTCCCAGG TTCAAGCAAT 720
TCTCCTCCCA AGTAGCTGGG ATTATAGGTG CCCGCCACCA CACCTGGATA ATTTTTGTAT 780
TTTTAGTAGA GACAGGGTTT CACCATGTTG GCCAGGCTGG TCTCAGACTC CTGACCTCAG 840
GTGATCTGCC TGCCTTGGCC TCACAAAGTG CTGGGATTAC AGGCGTGAGC CACTATGCCT 900
GACATTTCAT TTTCCTCAGC TCCCCATTTA ATATCACTTA TGTCTGATGG AAAAAGAGAT 960
AACCAAAGAA TGCGAAGGAG GAGCACGTGG AGGGATGACT CTGAGCCTGG CCACAGGGCC 1020
TGTGGGTCAT GGAGAAGGCA GTCATCAGTC CCGGCATGTG GCCTATTCAG GAATCTGGGT 1080
GTCATCCGGA TGAATTAGCG TTCACATTTT TTGGCCCAGA GTCTAGGAAT AGGCATTACA 1140
AGCAAGTTCC CTCCATGACT CTGAAGCACA CTGGATGTGG TAGGCACATT AATGCACCCT 1200
CATTCCCAGA GATTTCAGGT CTTGGTCCCC AGAATCTGTG ACTGTTTCCC TTCCAGGGAA 1260
AAGGTGACTT TGCTGATGTG ATTAAGTTAA GAAACTTGAC TTGAGAGATT ATCTCAGATT 1320
GCCTGGATGG ACCCAATCCA ATCATATGTG TCCTTAAAAG TGGAGACCCA CTTTCCGATC 1380
TTATATGTGG TCACAAGGAG ATGCGACCAG GAAAGTGTGA 1420
|
