| Tag | Content |
|---|
EnhancerAtlas ID | HS052-28547 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr4:54938910-54940770 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PRDM1 | MA0508.2 | chr4:54939550-54939560 | GTGAAAGTGA | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCTACTTCTT CTATATGATG GTCCTTCAAA TATGTTAAGA TGTGCGCGTC TGGGCGTGGT 60
GGCTCATGCC GGTAATCCCA GCACTTTGGG AGGCCAAGGC GGATGGATCA CAAAGTCAGG 120
AGATCAAGAC CACCCTGGCT AACACAGTGA AACCCCGTGT CTACTAAAAC TACAAAAAAT 180
CAGCCAGGCA TGGTGGCGGG CGCCTATAGT CCTACTTGGG AAGCTGAGAC AGGAGAATGG 240
CATGAACCCA GGAGGCCGAG CTTGCAGTGA GCCGAGATCG TGCCACTGCA CTCCAGCCTG 300
GGTGACAGAG CGAGACTCCG TCTAAAAAAA AAAAAAGATG TTCACATCCC AAATCTTTTT 360
TGTTTGTGAG CTAAACATGC CCATTTACTT CAACCATATT TCCTCCTGGA AGGGAGTTTC 420
TAGTCCCTGC CTCTTTGCAG AGGCAGTCTC TCACTCCCAT CAGCCTTGGT TTGGTCAACA 480
GCCTTCTTAA CATTTGGGGC TCTGACTAGA TGGTGTGACT TAACTATTGT GATAGCCAGC 540
CTTCAGGATG GTCCCTGAGA GACTCATCAA CTTGTGTGCA AGCCATTCTA TAGTTCCCTC 600
CCACACTGAA TAGAGGTGAC CTGTGTGACC AATAGGATTT GTGAAAGTGA CAGTATATGA 660
CTTCCAAAGC TAAGTTATAA AAGACATGAC ACATTTTATC TTATTCCCTT AAATAACTCA 720
TTCTGGAGGA AGCCACTCAC CATGTCATGA GGACACTCAA ACAGACCTAT GGAGAGACTC 780
ACATGAACAG GAACTGAGGC TTTCTGCCAC TCATGGGAGT GAGCCACCCT AAAATTGGAT 840
CCTCCAGCTC CAGCCAAGCA GCCCCAACTA ACATCTTGAC TGCAACCCCA GACCACCCAG 900
CCATTCACCA ATTCCTAACC TCCAGAAACT GTCAGAAATG ACAAATGTTT ATTGTTGTTT 960
TAAGCTACCA AGTTTTGGGG CAATTGGTTA TGTAGCAATA GATGACTAAT ACAGCAAGGC 1020
TAGAAGAAAG AGGGACTTAG CCCTTTCTTC CTGACCCTGG ATATCATAAG AAACAGTAGA 1080
AAGACAAAGA AAAATAGATC AAACTATTAA TTTTTAAAGT CGTAGGTTTT AGACCGGGCG 1140
CAGTGGCTCA TGTCTGTAAT CCCAGCACTT TGGGAGGCTG AGATGGGCAG ATCACAAGGT 1200
CAAGAGATGG AGACCATCCT GGCCAACTTG GTGAAACCCT GTCTCTACTA AAAAAAATTC 1260
AAAAATTAGC CGGGCATGGT GGTGCACACC TGTAGTCCCA GTTACTCAGG AGGCTGAGGC 1320
AGGAGAATCG CTTGAACCCG GGAGGCGGAG GTTGCAGTGA GCCTAGATGG CACCACTGCA 1380
CTCCAGTCCG GGTGACAGTG AGAGATTCCA TCTCAAAAAA AAAAAGTCAT AGGTTTTTTT 1440
CTCTTCTGTG TCTGTGTGTA AAATTTAAGG GATATTTTTA ATTAAGTTGT GTTATGTCTC 1500
TGTTAAGTGC CATACTTAAC TTAGACACTT AAAACATGGC TTTTAAGACA CTGGTTTTCA 1560
CTTTTAAGAT CTGAGAGGCA CAAGCACTTT CTTTTGGCCC CTGAATGCAT GCTGAGAAAA 1620
TCTACTCTTT ATCCTTTGGA ACTCTCACTT GAAGTCAATG GCCTTCTTAC ACACCAGTGT 1680
TAAGATTTTC TGTAGTTCTT TGCACATGGT ACAGGGAAAA GTTGGATTTA ATAGTTATAA 1740
TCATGTTGGC CTTCTCACTT AATTGAGATT AGGAAGTACC CAGCTTCATC TGGGAACTCA 1800
AAAGAGAAGT TGTTTCTATG TTCTCCCACT GCCATCTCCA CCTACAACAC ACAAACACAC 1860
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