| Tag | Content |
|---|
EnhancerAtlas ID | HS138-02427 | Organism | Homo sapiens | Tissue/cell | MSC_BM | Coordinate | chr1:155675710-155676360 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESX1 | MA0644.1 | chr1:155676214-155676224 | GTTAATTGGT | - | 6.02 | | FOSL1 | MA0477.1 | chr1:155676075-155676086 | CATGAGTCACC | - | 6.62 | | JUND | MA0491.1 | chr1:155676075-155676086 | CATGAGTCACC | - | 6.02 | | Lhx3 | MA0135.1 | chr1:155675951-155675964 | AACTAATTAATTT | - | 6.29 | | Nr2f6(var.2) | MA0728.1 | chr1:155676341-155676356 | GAGGTCAGGAGTTCA | + | 6.22 | | mix-a | MA0621.1 | chr1:155675952-155675963 | ACTAATTAATT | - | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGAACTCCTG AGCTCAGGCA GTCCATCCAT CTCGGCCTCC CAAAATACTA GGATCACAGG 60
TATGAACCAC TGCACCTGGC CTCTTTTCAT TTATTTATCT ATTTATTTAG ACCAGATCTG 120
AGTGTATCAT GCAGGCTGGA GTACAGTGGC ATGATCATAG CTCTTTAACA CCTGGCCTCA 180
AGTGAGCCTT TTGCCTCAGC CTCCTAAGTA GCTACGACTA CAGTCCTGCA CCACCCTGGC 240
AAACTAATTA ATTTTTTTCT TTTGTTTGTG GAATTGGCGG TCTTACTATG TACCCAAGCT 300
GGTCTCAAAC TCCTGGGCTC AAGCAGTCTT CTCATCCCCG CCTCCCAAAG GGCCGATATT 360
ACAGGCATGA GTCACCATGC CCAGCCTATG TGATTCTCTT GACTGTACTA TAAATTCCTT 420
GACTATAAGA TCAGGGACTA TAATAGTTTG TTCACCATTC CATTCACAGA GCCTGACACA 480
CAGTAGGTGC TCAGTAACTG TTGGGTTAAT TGGTTGCAAC TCTATGGTTG TTATTATTGT 540
TGCTTTAAAG ATTTGGGTTG TGAAAGGTGT GTCTGGGTGC GGTGGCTCAC GCCTGTAATC 600
CCTTTGGGAG GCTGAGGTGG GAGGATCACC TGAGGTCAGG AGTTCAAGAC 650
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