| Tag | Content |
|---|
EnhancerAtlas ID | HS052-02520 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:155675620-155676450 | 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 | AGCTGGGAAA ACAGACATGC ACCACCATGC CAGGCTTATT TTTTATATTT TAGTAGAGAT 60
AGGGTTTCAC CATATTGTCC AGGCTGGTCT TGAACTCCTG AGCTCAGGCA GTCCATCCAT 120
CTCGGCCTCC CAAAATACTA GGATCACAGG TATGAACCAC TGCACCTGGC CTCTTTTCAT 180
TTATTTATCT ATTTATTTAG ACCAGATCTG AGTGTATCAT GCAGGCTGGA GTACAGTGGC 240
ATGATCATAG CTCTTTAACA CCTGGCCTCA AGTGAGCCTT TTGCCTCAGC CTCCTAAGTA 300
GCTACGACTA CAGTCCTGCA CCACCCTGGC AAACTAATTA ATTTTTTTCT TTTGTTTGTG 360
GAATTGGCGG TCTTACTATG TACCCAAGCT GGTCTCAAAC TCCTGGGCTC AAGCAGTCTT 420
CTCATCCCCG CCTCCCAAAG GGCCGATATT ACAGGCATGA GTCACCATGC CCAGCCTATG 480
TGATTCTCTT GACTGTACTA TAAATTCCTT GACTATAAGA TCAGGGACTA TAATAGTTTG 540
TTCACCATTC CATTCACAGA GCCTGACACA CAGTAGGTGC TCAGTAACTG TTGGGTTAAT 600
TGGTTGCAAC TCTATGGTTG TTATTATTGT TGCTTTAAAG ATTTGGGTTG TGAAAGGTGT 660
GTCTGGGTGC GGTGGCTCAC GCCTGTAATC CCTTTGGGAG GCTGAGGTGG GAGGATCACC 720
TGAGGTCAGG AGTTCAAGAC CAGCCTGGCC AACATGGTGA AACCCCGTTT CTACTACAAG 780
TACAAAAATT AGCTGGACAT GGTGGTGTAT GCCTGTAGTC CCAGCTATTT 830
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