| Tag | Content |
|---|
EnhancerAtlas ID | HS073-11103 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr4:89303020-89304370 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mafb | MA0117.2 | chr4:89303973-89303985 | AGTCAGCAGTTT | - | 6.22 | | Mecom | MA0029.1 | chr4:89303308-89303322 | AAGATAAGATTACA | + | 6.45 | | NFYA | MA0060.3 | chr4:89304025-89304036 | TCTGATTGGTT | - | 6.62 | | RORA(var.2) | MA0072.1 | chr4:89303056-89303070 | ATGACCTACTTTTA | - | 6.35 | | RREB1 | MA0073.1 | chr4:89304340-89304360 | GGTTGGGGGGTGTTTTGTTT | - | 6.94 |
|
| | 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 |
| GH04I088381 | chr4 | 89302260 | 89304530 |
|
Enhancer Sequence | GTGCCAGAGA TGGGAGCTTC TCACAAAAGG ATATTTATGA CCTACTTTTA GGTAGATAAG 60
AAGAGAGCAG AGACCTCTTC CTGCATCTGT TGATTCTCAA TTGCCTTCAG CTCAAATTCT 120
TAAAGTAGCA TGTTTTCAGG TCTTATCACC CTCATTTGGA AATGAAGGGC AACATGATAC 180
TTAACCCCAA ATTGTTCTCT AGAAAAATGG TACCAATTTC TATCTTTGTG AGTGCATGAA 240
TCTTTGGGAA ATTTTAACCT TGCATAAATT GACAGTAAAT AGTTGAAAAA GATAAGATTA 300
CAAAGATAAA AGGAAAAACA AAATCTTAAA TGTTGCAAAA ACTTTACTGG TATGATGTTC 360
TCAACTCCAA ACCTCTAATA ATTCAGAGAC AGACACCTTG GGAAAGCAGT TTAGGTTGGC 420
TTGTAGGGAA ATGTGATCCG GTTTTCATTT GTGGGCATAT TTAGGGCCTC CATAGGGGCA 480
TATTTTTCAC TTTTCATTGT AAGAGGATCC AGCATCTGCC TCTCACACTC ATGAGGTAGG 540
CTCCCTTCCA ATTTCCTTCT GAGCAAGGGA TTCACTGCTT TCAGTGTTTA GGGTGGGAAG 600
ACAGAATAGC AAAATGGAGG AGATCCCAAC TTTTTTCTGG GTCTCTTTAT TTTGCTAGGT 660
TTTGCTAGAG AAACATTTGG TCATGTGTCA TAGTCCCTAG AAGTTACCCC CTCCGTGATG 720
CCTACTCCTT TAAATAACAG CCATTAAAAG ATAGACTTGG GTAATTGAAT GTTTTTAAGA 780
GTCAATTTGA ACATTCAGCA GTTCATGAAT TGAGCAGCAC CAGACCTCAA GCAGTTGGGC 840
TCCACTAAGG GAGGTGCAAG GAGATGCCAG GGGGAACCTT TGATAACGTG TTCCAGGAAG 900
CAAGACAAAG AAAATACTTG ATTGGTTAAA GTGGAAAGTC CCTTGTTTGA AGTAGTCAGC 960
AGTTTCTGGT TGGTAAAGTC TCTAGTTAGA TGTTAGTTGG TGGTTTCTGA TTGGTTAACC 1020
TTAAGTTTCA TTTTCCTAGG CTATGATCAA TCACTCTGAG TTGGGTTTTG GTTTGCTTAG 1080
GTAGGAACCC AAGGTGCTGG AGCCATCTCA ACCTGATAGT CTCCCTGTTG ATTATTTTAA 1140
CAGAGCTGTA TCCTATAAAG ACAGGGTAAC ATACATTGAA TTTACTTCCT TCAGACATTT 1200
AGAATGGACT TAAGGTCTTG ATTCAAAAGA CCATTGGAGG AGACAAGAAA TCTGGATGAT 1260
CCTTCTTTTT GAAGAAAAGT GCTGTCTTAA ACTTGTGTTA AATTAATAAT CTGCAGTGGT 1320
GGTTGGGGGG TGTTTTGTTT TGTTTCCCAA 1350
|
