| Tag | Content |
|---|
EnhancerAtlas ID | HS138-25213 | Organism | Homo sapiens | Tissue/cell | MSC_BM | Coordinate | chr22:19053950-19054860 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr22:19054255-19054269 | CTGACTCATCTTCT | - | 6.12 |
| | | 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 |
| GH22I019066 | chr22 | 19053851 | 19054878 |
| Enhancer Sequence | AAAAACAAAA CAACAATAAA AAATGTCAAG GCATCAGCTC TCGAGAAGGT GTGTTGCACA 60
TTCATTGCGT GTTTCCTGGG TGCCACACCA ATGCATGCAG CCTGACCACA TGCCCCGCAG 120
GTGGCTCTGC ACCGTCTCCA TGAAGAGGTG AGGACACTGA GGCAGGCAGA GGCCAGGCCC 180
CTATCTCAGG CAAGGTGAGA GGAAGCCCTG TAGGGAGGGA AGCTGGCTGA GGCATGGAGG 240
GAAGGAGACA TCCCAGGATG GGAGCCAGCT GGCTGGGGCA TGGAGGGAGG AAGCACTCCT 300
GTGCACTGAC TCATCTTCTT TATGTTCTGA ACTTGGTGGA GTTGCTTACT ACCCAGGCAG 360
AAGTGCTGCC TGTTCAAAAC TGAACAGACA GGCAAGGGGA AGGAAGAACA TGGAGCTGAG 420
CATCAGGACC CCCTGGGGCT GCACTGTGAA CTGCCCCTTC CCTACAGGTG GCCTCTCAGC 480
CTCAGTGTCT TCACACACCA AGCCTGTGCA CCACACTTGC ACTGTGGGGA CCCGTTCGGG 540
CTGTGGGCAC AGGCCGGAGA CAAAGTGCAT CACCAGGACA TGTCCAGCCC TGCTTCAGCC 600
GCACCAACAT GCGTGACCAC CTGGAAACAC CTGGCCCCAC TCTGGCCACC CAGGGTTGGT 660
GGGGGTTCTG CCAGAAGCAG ACCTGGTCAC CTCTGAGGTG CTCCCCAGTG CTGAAAGTCT 720
GGGGGCTGAG GAGTAACACA AGCAGACAGG CCCAAGGCAG GGCAGCAGGC CCATCCAGTA 780
TCAGTCCTGC CTGGTCCACA GCCGCTGCTC AGCGTACTTG GGTACCTCGC GCCTGAGAGG 840
GTCTGCTCAG GGCCATTTCA GTGGTGGCTT TTCCTCCCCT CAACCTTCCT TGATGATCTC 900
ATGCCCCTTT 910
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