| Tag | Content |
|---|
EnhancerAtlas ID | HS052-29534 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr4:175319280-175320650 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PBX1 | MA0070.1 | chr4:175320365-175320377 | ACATCAATCAAT | + | 6.44 |
| | | 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 |
| GH04I174398 | chr4 | 175319200 | 175320689 |
| Enhancer Sequence | TAGAAAATCC AGGATAGTCT CCCCATCTGA TATGGTTTGC CTATGTCCCC AACCAAATCT 60
CATCTTTAAT TGTAGCTCCC ATAATTCCCA CATGTTGTGG GAGGGACCTG GTGGGAGATA 120
ACTGAATCAT GGGGGTGATT CCTCCATACT GCTCTCATGG TAGTGAATAA GTCTCACAAG 180
ATCTATTGGT TTTATAAGGG GAAATCCCTT TCACTTGGTT CTCAGTTGCT CTCTTGCCTG 240
CTGCCATGTG AGACGTGCCT TTGCCTTCTG CCATGAGTGT GAGGCCTCCC AGCCATGTGG 300
AACTGTGAGT TCATTAAACC TCTTTTACTT CATAAGTTAC CCAGTCTCGG GTATGTCTTT 360
ATCAGCAGCA TGAAAATGAA CTAATACACC TTCTCAACAT TAATTTATTA ACAATTTTAA 420
TTCCATCTGC AGCCTTAATT CCTTCTTGTC ATGTAACATA GCATATTCAC AGTTTCCAGG 480
AATTAGGATG TAGACATCCT TAGGAAGCTA TTATTCTGCC TACCACATTG ATGGGACTAT 540
AAATCTTGGG TTTTCATGTA GCTTTCATGA CCAATTCCAG TTAATCTTAC TCATGCAATG 600
GTCATTTAAA AACATGCAAT TAGTTCCATG AATTTGAAGT CCTCACCAAT CTGATATGAG 660
CCTTTAAAAA TTCATCCAGA ACAGAAAGGA CAACTGGATT AGAACATTGC TGGCATGGCT 720
TTTATGAGAA CTGCGTGCCT ATAGTCCCAG TCTGTATGTT CAATTCTGGT TCATTCTGAC 780
CGTGTGTTGC TTCAGTATGT ACAACTCCAA GGAACTGATG TTTTCTTAGC ACCATCTGTT 840
TATTACAGAT TATGAGTCAT CAGTTGGCTC CCAGAACCTT AAGGCCTTAG ACACTTTAAT 900
ATTAATTCAT AAGTCTTTGT GAGTATGAAC CCTGAAAATC TGAGACAGGT CTCAGTTAAC 960
TTAGAAAGTT TATTTTCCCA AGGTTGAGGA TGCATGCCCA TGACACAGAC TCAGGAGGTC 1020
CTGATGGCAT ATGTCCAAGG CGGTCAGGGC TCAGCTTGGT TTTATACATT TTAGGGAGGC 1080
ATGAGACATC AATCAATATG TATAGGATGT ACATTGGTTC AGTCTGGAAA AGTGGGACGA 1140
CTTGAGGCAA AGATGGGACA ACTCAAAGTG GGGAGGGGGC TCCCAGATCA AAGGTAGATA 1200
AGAGACAAAT GGTTGCATTC TTTTGAGTTT CTGATTTCTG TCACTCAGGC TGGAGTGCAT 1260
GGCCTGACCC CAGCTCACTG CAATTTCTCC CTCCTGGGTT CAAGCAATTC TCATGCTTCA 1320
GCCTCCCAAT AAGCCGGAAT TACAGGTATG CGCCACCGTG CTAGGCTAGT 1370
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