Tag | Content |
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EnhancerAtlas ID | HS010-00833 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr11:57192100-57193010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Tcf12 | MA0521.1 | chr11:57192872-57192883 | AACAGCTGCTG | + | 6.32 | ZNF263 | MA0528.1 | chr11:57192583-57192604 | TGAGGAGGATGAGGATGAAGC | + | 6.08 | ZNF263 | MA0528.1 | chr11:57192132-57192153 | AAAGGAAGGGGAGGAAAGGGG | + | 6.25 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_09866 | chr11:57186394-57195934 | CD14 | SE_40224 | chr11:57191266-57195506 | K562 | SE_56335 | chr11:57191056-57196539 | u87 | SE_58962 | chr11:57170849-57195646 | Ly3 | SE_67811 | chr11:57191056-57196539 | u87 |
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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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Enhancer Sequence | AATATCCTAA GGCTGGAGAA GAGGGAGGGG ACAAAGGAAG GGGAGGAAAG GGGAGGTAGC 60 AGGGAGCCAA GGACCAAGAA GGACTGAGGT ACAGTCATTC TGCATCCAAA GGCTTAAATT 120 GTAAGGGACT GGCTTTACTC TGGCTGTTTC CGGAAAGGCA GGCCCAGCCA GCCCTCCCGT 180 CTCTCTCTCT GACAGCCAAT CTCACATGTG CCTCCCTGGG AGCACCTGCT CTGAGCTGTA 240 TCAGCCCCCA GCAGGCCGCT GATTACCACT GAGCCTGGCC ACAGAGCACG AGATTAGGAT 300 GCAGCAACAC ACTGTGTGTG AGATCACGTC CCGAACCTTC TGACTCATCT GCACAGGAAA 360 CCCCCCCAGT CTCCCCTCCA GTCAGAAGGG ACCTGAAATT CCACCAGTGG CAATACCAAA 420 GAAACTTCCT ATTAGCTAAG CCCCTAGGGA GTGATTGGCT GTTGGGGCGG GGAGGGGGGG 480 CGGTGAGGAG GATGAGGATG AAGCCTGGGC AACCTGGATG TGAGGCTGTG CAGGGGATGA 540 GGACAAGGAT CCTTGGGGTG AAGGAAGAGA AGAGCAATTT TAGGTTTTGC TAATTTTGTA 600 ACCCTGGCTC CAAGCCAGCC CTTACAGGAA GTCACCCTGG CCTCCGGCTC AATTCAGCAC 660 GTGATAGGGA AGCCACATTT ATGCAGAGCA GGGAACGAGG TAAGGAAATG GAAGTGGGGC 720 TGTGGTGAAG TGGGCAAGTC TAGAGAGAGT CCCGCTGCCT GGGGCTGTTC CTAACAGCTG 780 CTGGGAGCGA GCTGCAGGTG TGGTGCCTGG CAGGGTGGCC GGGCTGTCTG ACTCTGGATT 840 TCACTCCAAG CTAGGCTGCT GCCTGAAGGA TTCCTCTTAC CCACCTTTGC CTGGGCTGGC 900 CTTTGGGACT 910
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