| Tag | Content |
|---|
EnhancerAtlas ID | HS056-16335 | Organism | Homo sapiens | Tissue/cell | GC_B_cell | Coordinate | chrX:101914130-101915590 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chrX:101914564-101914576 | GAATGTTTGTTT | + | 7.22 | | GCM1 | MA0646.1 | chrX:101915247-101915258 | GATGCGGGTAC | + | 6.14 | | MITF | MA0620.2 | chrX:101914857-101914875 | GTGGGTCATGTGACCAGG | + | 6.09 | | MITF | MA0620.2 | chrX:101914857-101914875 | GTGGGTCATGTGACCAGG | - | 6.09 | | Myod1 | MA0499.1 | chrX:101915173-101915186 | AGCAGCTGTTGCT | + | 6.59 | | Stat6 | MA0520.1 | chrX:101914311-101914326 | TTTTCTCAGGAAAAA | - | 6.37 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGAAAAATTA AAAATTATTT AAAGGACCAA ACTGTAAAAT TACCAAAGTT CCTGAGTTCA 60
TCCCACATGT ATTTTTACAT TTAAAAAGGT TGGAACATAT ATGTTCAGAC AGTAGCAAGA 120
GACAGGGATA AAGTCGGTTT GGGGAGAGAG TCCAGGATAA CAGGAAATAT GCAAAGTTTT 180
ATTTTCTCAG GAAAAAAAAA TAGATACAGT GACCCTTTTA CATTTGGTTT GCCTCAGGAT 240
GCAAAGGCTT TTTCCCACCT GATCTTATTT CTCATTACTT CCTATTTCTG GTTCATTATA 300
AATGATATAA ATTAAATTCC AATATGATGT TAGTTTGCTA AGGTTTACGA AAGCAGGGCA 360
AAGTGGCAGT TTTGCCTCCC TTCACAAATC AAAAATTTTA ACAGGGATCA TCCTGGTGGT 420
GCAAATTGGA GTTTGAATGT TTGTTTTGCT TACCAGCATT TTTCAAGACA GATCTTGCGT 480
GTGTTTTAGT ATGTCGCTCT AGTCGTATAC AAAATATCAC AAATCACTTC ATCTCCCCAA 540
TCCTCATCGA ATGTTCCTCG CCAGCCCAGT GGTCCTCCAG AGCAAAGCCC GGCCTTCCTT 600
CCAGCTGTCT GGGCCAGGAG CTTGAGGGTC TTCTAGCAAG CACCCCGGAG GCTGTCTTCT 660
GACTGTCATG CAGGGCTGTG GCAAACTAGC TGACTGCGCA GTCACGTGGA GGGGGGAGGG 720
GCTGACGGTG GGTCATGTGA CCAGGCTCTG GGTTGAGCCG GCCTAGAGGA GTGTTTTCTT 780
ACACCCAGAA AGTACAGGAA AGGCAGACGA CAACTGTGCT CCGCAGAGCG GGAGGTGGGG 840
GGAACGGCGG AATATTAAGG TGGGTAGGTG TCTCTCCATG CTTCATCAGC CTGAAAACTA 900
ATTTCTCAGG CGACCGGAAT TACAGCATTT CTTGGTAGAG GAAACTATCC CTCAGCCAAC 960
CGCTAGCGGT CTTAGACGGT CTGTCTTTTG TCCAGGAGCT CAAGAAGCAG AGACTCTACC 1020
TGCCCTAGGC GTTCGTGAAG AGAAGCAGCT GTTGCTATTG GAGGAGGTGG GTGCAAGGAC 1080
GGCAGATGCC ATCCCTGAGA GGCGGTGACT GAGACTAGAT GCGGGTACAG GTAGTGCCTC 1140
GGATCCCCGG GCTGCCTCCT GCCTTTTGAA CATCCCAGGG GTCCCAACCC AGCGCCCTGT 1200
GTTTCTATGT GTGGGTGGGA GAGGTGGGCA TATGGATGGA GTTGGCTTCA GGGGAGCCCA 1260
GAGAGGGGAA ATGGTGAAGT GACAATTCGT GAACACGTGT GGTGCTGGAT CAGGAAAGGT 1320
AAGGGTGGGG ATGGGAACCA TGGACTATGC TACTGCTGTC TTCCTCCCAC CAAGTAGGCA 1380
CTCACTCTGC TCTCTGTCTG TCTGTTTACT GGCAGTATTC AGGCAGTGGG GATGGCTGAT 1440
ACCAGCTCAA AACTGGCGGA 1460
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