| Tag | Content |
|---|
EnhancerAtlas ID | HS060-26496 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr4:89303030-89304370 |
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 | TGGGAGCTTC TCACAAAAGG ATATTTATGA CCTACTTTTA GGTAGATAAG AAGAGAGCAG 60
AGACCTCTTC CTGCATCTGT TGATTCTCAA TTGCCTTCAG CTCAAATTCT TAAAGTAGCA 120
TGTTTTCAGG TCTTATCACC CTCATTTGGA AATGAAGGGC AACATGATAC TTAACCCCAA 180
ATTGTTCTCT AGAAAAATGG TACCAATTTC TATCTTTGTG AGTGCATGAA TCTTTGGGAA 240
ATTTTAACCT TGCATAAATT GACAGTAAAT AGTTGAAAAA GATAAGATTA CAAAGATAAA 300
AGGAAAAACA AAATCTTAAA TGTTGCAAAA ACTTTACTGG TATGATGTTC TCAACTCCAA 360
ACCTCTAATA ATTCAGAGAC AGACACCTTG GGAAAGCAGT TTAGGTTGGC TTGTAGGGAA 420
ATGTGATCCG GTTTTCATTT GTGGGCATAT TTAGGGCCTC CATAGGGGCA TATTTTTCAC 480
TTTTCATTGT AAGAGGATCC AGCATCTGCC TCTCACACTC ATGAGGTAGG CTCCCTTCCA 540
ATTTCCTTCT GAGCAAGGGA TTCACTGCTT TCAGTGTTTA GGGTGGGAAG ACAGAATAGC 600
AAAATGGAGG AGATCCCAAC TTTTTTCTGG GTCTCTTTAT TTTGCTAGGT TTTGCTAGAG 660
AAACATTTGG TCATGTGTCA TAGTCCCTAG AAGTTACCCC CTCCGTGATG CCTACTCCTT 720
TAAATAACAG CCATTAAAAG ATAGACTTGG GTAATTGAAT GTTTTTAAGA GTCAATTTGA 780
ACATTCAGCA GTTCATGAAT TGAGCAGCAC CAGACCTCAA GCAGTTGGGC TCCACTAAGG 840
GAGGTGCAAG GAGATGCCAG GGGGAACCTT TGATAACGTG TTCCAGGAAG CAAGACAAAG 900
AAAATACTTG ATTGGTTAAA GTGGAAAGTC CCTTGTTTGA AGTAGTCAGC AGTTTCTGGT 960
TGGTAAAGTC TCTAGTTAGA TGTTAGTTGG TGGTTTCTGA TTGGTTAACC TTAAGTTTCA 1020
TTTTCCTAGG CTATGATCAA TCACTCTGAG TTGGGTTTTG GTTTGCTTAG GTAGGAACCC 1080
AAGGTGCTGG AGCCATCTCA ACCTGATAGT CTCCCTGTTG ATTATTTTAA CAGAGCTGTA 1140
TCCTATAAAG ACAGGGTAAC ATACATTGAA TTTACTTCCT TCAGACATTT AGAATGGACT 1200
TAAGGTCTTG ATTCAAAAGA CCATTGGAGG AGACAAGAAA TCTGGATGAT CCTTCTTTTT 1260
GAAGAAAAGT GCTGTCTTAA ACTTGTGTTA AATTAATAAT CTGCAGTGGT GGTTGGGGGG 1320
TGTTTTGTTT TGTTTCCCAA 1340
|
