Tag | Content |
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EnhancerAtlas ID | HS060-06698 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr11:93262770-93264070 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr11:93263616-93263629 | AGAAACAGCTGCT | - | 6.28 | RREB1 | MA0073.1 | chr11:93263524-93263544 | TGTGGGTGGGTGGGTAGGTG | - | 6.18 | RUNX1 | MA0002.2 | chr11:93263510-93263521 | GTTTGTGGTTT | + | 6.02 | Tcf12 | MA0521.1 | chr11:93263619-93263630 | AACAGCTGCTG | + | 6.32 | ZNF263 | MA0528.1 | chr11:93263936-93263957 | CTCCCTCTCTCCCCCTTCTCC | - | 6.73 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_09940 | chr11:93261258-93264560 | CD14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 93262915 | 93263000 | chr11 | 93263836 | 93264058 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I093527 | chr11 | 93261041 | 93266723 |
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Enhancer Sequence | CCCGAGCCCT CATTACACAA GGGCCAGGCC CCTTCCTTTG GAGGCAAAAA GGAAATTAAA 60 TGTCAACCAA ATAAGGATAT TTCCCTTTAA CTCCAAGGCC AAGGAATCTG AAGTAGTGAT 120 TCCCCCAGTA ACTGGGCAAA CTGAACCGAC GACACAGGCC ACAGACCAGC AGGCCAGGCC 180 CGCTGAGGGC CAGCCTCCGC CTGGAGTTCC TTCTTCTTTT TAATGACCAA TACTCAGATT 240 GCAGGCTGAA GTGTTTTTAT GACAAATAAG AACAACAATG TGTGAACACT TTGTAGGCCA 300 GTAACAAGGC TGGCAGCAGA GGGCCCTGGG CCCACGTACC AAGACCACAC AGCCATCTAC 360 TCACTGTCTC CAAAGGTCCT CTTGGATGTT CCTCCCTGTC CCACATTTTC AAGGCCAAAT 420 GTGGCCTGCT GACCAGGAGA GCTGACTCAA CTCTTTTCAC AGCATAGTGA TTTTATACAC 480 AGAAGAATCC TGGAAGCCCA GAAGAATCCA CATAGCTTGC ACACTGACCT TGGCATTTTC 540 TAAATCTACC CAGGTTAAAG ACCACCTGAA TGGCAGGCAT GGCGTTCACC AGGCAGGCCC 600 AAGGCTGAAG GGGTCGTGGG GGGAAGAGCC CACCAGTTCA CACGTGTGAG GCCCTGCAGC 660 TCACAGCAGG GCAGCTAAGC ACACAGTTTC CTAGCAATTC CTGCCACCAC AGCCTTGTCT 720 GTTTGCTCTC TCTTCTTCGT GTTTGTGGTT TATGTGTGGG TGGGTGGGTA GGTGAAAAGC 780 ATACAGAAAG GAAAGGGTGG TGGATCAAGG GTCAGTACAG CACTAACATT TTTTAAAAAC 840 CTGCCTAGAA ACAGCTGCTG CAAAATATCT AGGCACACAC ACAGCTCAGC TACATCCATC 900 TGAACTTAGA AAAGTCCTCA ATGAGCTGGC CCACACTACC TGCTTTCATT CATGCTCACA 960 GGCACAACAG TGGCTCCCAT CTTACTAGAA CAAAGGCCAC AGTCCACGCA AAGAAGGACC 1020 TCTTGATCCT CATCCTCTTC TTTACTCCCA ACCTCTCCCT TTCCTCCCCT GACACAATGG 1080 ACTCAAATTG TACTGTCCCT ACACTTCAGG GCCTCTGCCT GTGCTGTCCC CTTCACACAG 1140 AATCCTCTTC CTCCACACAG CAGCTCCTCC CTCTCTCCCC CTTCTCCAGC CCCAAGTGCA 1200 CACATTCCTT CTCAGCAAAG CCCTCCTTGA CCACCTCACC TTCCCCTCTG CTGCGGGACT 1260 CTTCCACTTT TTCAGCAGTC ACCAATATCT CACATACCAC 1300
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