Tag | Content |
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EnhancerAtlas ID | HS010-04063 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr6:169989330-169990460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr6:169989918-169989928 | TTTAATTAGA | - | 6.02 | IRF1 | MA0050.2 | chr6:169990263-169990284 | AGTTTCTTTCATTTTTCCTTT | + | 6.74 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I169588 | chr6 | 169989009 | 169991118 |
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Enhancer Sequence | TGATAAAATA CAGAGGTTAA CAGCAGCAAG TACTTTCTGG ACACTGACCT TTTGCCAGGC 60 ACTGATAAGA ATTTTACATA AATTTTCTCG TGTAACCCTC TCAACAGCAC TATGAAGAAA 120 ACACTTATTG CCCCAATTCT ATAGACAAGG AAGCCAGGCT GAGGGCAGGC AGCCTTCCAA 180 GGCCACTCAC CTCTTGAAAA GCGCTTCCTG AGATCAGCTG GCTCCCATTT GCATGAAACC 240 TCAAAACACA CACTGAATGA CATAATACAG TGGCAGGAGG TGAGGTAAAA CGTATCCAGG 300 AAAGGCCTTT TGTTTCCTCA GTGAGAATGA AATTAAATGA AACATCTTTT GGTCCAGGGG 360 ATTCTTGGGG TACATGAATT TTCTGATCAT GACAACTTTA CATGTGACAC AGCAATTGGA 420 AGCCCAAATA TCAATATTTT AGTAGATAGG CAGGTTTCTT ATGCTGTGAT CCTACACAGT 480 GTCATAAATA CAGAAGGACA ATAAGCCTCT TGTATGACAC AGAGCGATGG TAATGAACAG 540 CTCTGCAAAT GATTCAATGT AACCACAATC CATGTGTGAA AGAAACATTT TAATTAGAGG 600 TACTCACTGG ATTCATGAAG CACTTCACCC ACCACAGAGA AACGAGCTGT GGCTAAGACA 660 TACTCAGAAA ACAAACAGAG TTGGAAATAA AACCTATGCG GGTAAATCTT ATGCCAGAAC 720 CAAATCAAGG GAAGCAATAT TTTTCAGGCA AAAGATGAGG ATGTGGCATA AATCTGTGGG 780 TGCTGGAATA ACGCTTGACT GCTCAAAAAT GTTTTTACAA AAATTGTAAG GGACTGAATG 840 TACTACTGAA GAAGAGAAGT GTTTTGGAAA CAGGACTACA CCGATTCATT ACAACTATTT 900 TGTAACTCTG TTGAGCCACA TCTGTGAGAA TGAAGTTTCT TTCATTTTTC CTTTCACAGA 960 GTACCTAACG TGACCTTCAT TTCCCTTTAC CCAAATTAAC CCCACAGCAG AAAGGAGACA 1020 AAGAATTACA AACAGAAGTG AGTGTTGCAC TCCTGAAACT TGACAATGGT AGTGATATTT 1080 TCCACAGGGG AATCAACTAT CATATTATGC TCACTTATTT TGCTTTTGAA 1130
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