| Tag | Content |
|---|
EnhancerAtlas ID | HS138-02092 | Organism | Homo sapiens | Tissue/cell | MSC_BM | Coordinate | chr1:112490320-112491750 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:112491131-112491152 | TTCTACTTTCTCTTTCTTCTT | + | 7.57 |
| | | 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 |
| GH01I111947 | chr1 | 112490499 | 112492188 |
| Enhancer Sequence | CTGGGGCTTC CAAGAGGGAT GCTGAGGTTT GGAAGAACTC CAGGTATTCT CATAATGGCT 60
AAAAAATAAC CTATATCGGT AGACCAGCTG TTTAAGAATT GTCAGAGGGA CCTGTGAAAT 120
CCTGGGCTGG GATGATAATT GTTGTTCGAT TAGTTTTTTG TTTATTTGCT TGTATTACTG 180
TGTTTGGCTT TCTAACCCTT GTCTTGGGTA CGATGACACT TCTCCAGTGG GGACTATGTG 240
TGTATATATG TGAGGAGGGT CAGGTAAGCA GTCAGGGGGA AGTGAGGAGG GACAGGTTGT 300
ACAGGCCTCA CCTCCGAGGA GCCCTGTTCA GCCACCACTC ATTCCTTCCA TGAATACCTA 360
GTGAGTTCCT AGTGTACCCT GGGGTACAAG GATGGCCAAG GAAAGTCCTA TCTGTGTGCT 420
TTGGGGAGGC TGCCCCATCA TGCCCACAGG GCAAATGGGC CCCACCATGC CCCTATCCTG 480
TGCGTGGCCT CCCTCTCTGC TCTGCCTCTA CAGAAAGATC TATTTCAAGC CACGGGGCTG 540
GTGCTGGCCA TGGGCTCCCC TGCCAGAGAT GAGTGCTGTT CCCATCTGTA AATGACTCCA 600
GCTCCTGGAA AAGCAGCCAC AGACAAGTGC TTAGCAGCAA ATAGATCACT CCCCACAGAG 660
CCTGTGATTC ACAGGGCAGA AAGCCAGCCT CCTGAGGTGG CGTAGGGAGG CGGCAGCCCT 720
GGGAGGTGCC AGGGAGGTGC TCAGGACTCT GGCCCACACT TAAGGATAGA ATTTATCTCT 780
TCCCTTCCCC ACAGCATAGG GCTGTTCTGC CTTCTACTTT CTCTTTCTTC TTTCTTCTGT 840
TCTCCCACTT TTTTCCCCCT GGGTTGGAGA GAGTTCCTAT CCCATCTGCA CAGGTCACTT 900
CCCCAGAGAG GCTTAAAAAC CCTCGGACCA ATTAGCTGGA AGCCTGTGGC CAGGGTCTTT 960
TCCCTCTGCT GCAAGCAGAC CTGCTGCTCC CCTCTGGGGA GCTGGCCCAG TCTAGCCCTC 1020
CTCACTGCCA GGAGGGCTGG GCAAGATCCT CTTATCACAG CTGTGAGCAG ACAACCATGC 1080
ACAGCAGGAG AGGGAGGGAC AGGGAAGTGG GGAAGATGAG GGAGGGATAG GCGAGAAGGG 1140
AAGGGCTTCT GGAAGGTGAG AGAAGGAGGA GCAGCAAGCA GCAGGCAGAG AAGAGAGGGC 1200
AAGTCCAAAC AAAGAAGAAC ACAAACAATA GAAGGGCTGG CTATCAAGAA GATCTTTTCT 1260
TTGGGGGCCA ATGCCATATT CCAGCATGGG CAGGAAACCA CAACAAGCCT TTCTGAGCCT 1320
CACTCTGAGT GTCTAGGCTT GTGGGAGGTG TAGAAGCATG ACACGCAGCC TTTGTCCCAC 1380
AGGGGCTTGC AACTGGGCTG AAGGGCTGGT GTGAGTATCA CATGTGCAAG 1430
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