Tag | Content |
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EnhancerAtlas ID | HS010-03927 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr6:106439680-106441060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BHLHE41 | MA0636.1 | chr6:106440481-106440491 | GTCACGTGAC | + | 6.02 | BHLHE41 | MA0636.1 | chr6:106440481-106440491 | GTCACGTGAC | - | 6.02 | IRF1 | MA0050.2 | chr6:106440390-106440411 | GTGCAGAAAGTGAAAGTGGGA | - | 6.48 | KLF5 | MA0599.1 | chr6:106440453-106440463 | GGGGCGGGGC | - | 6.02 | TCF3 | MA0522.2 | chr6:106440185-106440195 | AACACCTGCT | + | 6.02 | USF1 | MA0093.2 | chr6:106440480-106440491 | GGTCACGTGAC | - | 6.14 | USF2 | MA0526.2 | chr6:106440477-106440493 | CCCGGTCACGTGACGC | + | 6.4 |
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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 |
GH06I105991 | chr6 | 106439475 | 106446468 |
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Enhancer Sequence | CCAAGCTCAT GTTAGTGATC TGGAATGGTT TCTTTCTATA GGTGAACTTA TTTAGGACTA 60 TGGAAGAATG TTTTAGTCAG TGACCAGCCG CGATAATGAC TGATAAGGGC GGTTAGTGAT 120 AAGCGATAAG GACAGGTACA GACATAGGAC CGCTGGCTGG GCTCATCCAG AGCTGGCGCG 180 CAGCCCTCTC CCTGCACTCG TACTGAACTG AGTCCAGTCC AGTCCCCCAC AGGTTAGAGG 240 TGAGACGGAA GCCATCGTGA GTTTGTTTTT TCAGCGAGTG CCGTTTCCTA GGTTGGATGA 300 CAAGCCAGCT TTGGTGGCCC TTCGCTCTCG CTACCCTAAT AAACTACCTG GAGCAAGTCC 360 TTCTTCAGAA ACAAATCACC ACGTCAGCGC TCGGAGGGTG AAGCCCCTAC TACTTTCTAC 420 TTTTGGTTGT GATGCTGGAG GCCCTTACAA TTTCGCAGAA CGTTTTGTGG ACGCGCGAGC 480 TCAGTGTTGC CCTTGCAATG GGGAAAACAC CTGCTTTCCG GGTCCTCGTC CTCCCGGGAG 540 CGCGGACCCT GAACAGCCCC CGTCCGACCT CCCCGGCTCA TCACCCCCTT CCAGAAACGC 600 ATGGAGCTCT TTTTCTTTGG ACTGCCTCTT TTTTGTACTG GCCATCTCAA AATCAAACAA 660 AACAAAAAAC AAAAGAAAAC AAAACAATAT CACTCAGGTG TGAAGCCCCA GTGCAGAAAG 720 TGAAAGTGGG ACTAATCCCG GCTGCTGCAG CACCGCCGAG TGAGCGCCAG GGAGGGGCGG 780 GGCTCCAGGG CACGGCGCCC GGTCACGTGA CGCGCGTCCG CCCAATCCCA GCGGGCCCTC 840 GCCGCGCGCA GAGCTGGGCC TGGGTAGCTC TTCTCTCTCA ATGAAAGCTA TATTTTGGGC 900 TGTTACCACC TAAACGCCAT GTGGAAACAA TGCACCTCCC TCCACTTCAG GTCCCCCTTG 960 CCTGTAAACC TCGAGAGCTG GACGTCCCTT AGCCTGGGAG TTCCTGGACA CTGTGCACAA 1020 TCACTCGTCA ACCGCTACCT ACTAGGTAGG CGGGAAAGAG CTTTGCTTTC TAGGCGTGTG 1080 TCTCCAGATG GGCCCAGGAA AGATAGGGCC TCAGTTCTCT CTGGTTTGTT TGCTGGGGAG 1140 GGAGTTAGAG CTGTAAGCCT CCTTCCTCCA AAAGGATGGT TGGAGGGAGT CCGAAACCTT 1200 TGGGTCCCAA GACATGACCT AAGGAGTCCC GCTGTCGCCA CTCTTCCCGG TTTGGTAGAG 1260 GGGGCCCGTG AGTGGCATTT AGCTCTCGCA AAACTGGGCA GATAGACGCA CATGTCGACC 1320 CTCCTTTTAC AATATTTCAA AATAATTCTG CATTGTTTCT CTACTGGAAT CGTTAATTAT 1380
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