| Tag | Content |
|---|
EnhancerAtlas ID | HS056-00225 | Organism | Homo sapiens | Tissue/cell | GC_B_cell | Coordinate | chr1:21004890-21006060 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:21005984-21006005 | AAAATAAAAATAAAAGCAACA | - | 6.4 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 21005121 | 21005454 | | chr1 | 21005012 | 21005636 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I020678 | chr1 | 21005094 | 21005693 |
| Enhancer Sequence | TCCTTATACA AAAAAAATTT AAAAATAAAA TAAAATAAAC AGCATCCTAG GTACCTGAGG 60
ATGAAAACAT CCATCTAAGC CTGAATCTCT CCAACAAGAC CTCCAAAAAA ACATGCAGAA 120
GAACCAGGAG AGAAAAATAA AGCCACCCTT AACCAGCCTA CAGCATGACC TGAAGACAGA 180
GAACGCTGGA ACCTTTGAAT TACATGGAAG TACAGAGATA AACCCCCAAG TGCAGCAGAC 240
AGCCCCGGAG CCACCCCATG GGGAGGTAAG CAGAGAGCAT CCAGGACAGC ATGGGGCGAG 300
GAGGAATGAG GTGATGGAAG GCAGGGTGCA GTCCCTCCAC AAGGAGCAAG ACAATCCTAA 360
AAACGGATCT GAAACCTGAA AATGAGAAAC TGATGGAAGA GACCAGTACG TGTGCAGGAC 420
CAGAGGAGTT AGTCTCCGGA AGGTGCTGCA TTTAGAAGTG GGAAGCGCCC TTGAGGTGGA 480
AACTGAAAGT CCTGCAGAAA CAAGAGAAAA CCACAAAAGA CAACCACCAC CAAAAAAATA 540
AGCTTTCACC CCCAAGATTT TTGCCCCCTG TTTTTGTGCC TGTGAATATG GTATCTTCCT 600
TGGCAAAAAA AAAAAAAAAA AAAGGACTTT GCAGCCAGGT GCAGTGGCTG ATGCCTGTAA 660
TCCCGGCACT TTGGGAGGCT GAGGCCGGCA GATCATTTGA ACTCAGGAGT TCGAGACCAG 720
CCTGGGCAAC ATGGCAAAAC CCCTTCTCTA CAAAACAATT AGCTGGGTGC AGTGGCATGC 780
GCCTGCAGTC CCAGCTACCT GGGAGGCTGA GGCAAGAGAA TCGTTTGAGC CTGGGACAGC 840
CAGCGTAACA CAGCAAGACC CCCAGGAGTT TGAGACCAGC CTGGGTAACA TAGCAAGACC 900
CCTCCGCTAC AAAAAATAAT AATAATAAAA AAATTAGCCA GGCGTGGTGG TGCATACCTG 960
TAGTCCCAGC TACTCAGGAG GCTGAGGCAG GAGGATTTCT TGAGCCCAGG AGGTCAAGGC 1020
TGCAGTGAGC TATGATTGTG CCACTGCACT CCAGCCTGGG CGACAGAGTG AGACCCTATC 1080
TCAAAATAAA ATGAAAAATA AAAATAAAAG CAACAGAGAA GGCAGAGAGG CAGGCAGGAG 1140
AGATGTGGTA GAAGAGATGC TTCTGAAAGA 1170
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