Tag | Content |
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EnhancerAtlas ID | HS054-03900 |
Organism | Homo sapiens |
Tissue/cell | FT246 |
Coordinate | chr22:50730460-50733140 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EGR3 | MA0732.1 | chr22:50732060-50732075 | AGCGCGGGGGCGGGG | - | 6.01 | KLF16 | MA0741.1 | chr22:50732065-50732076 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr22:50732066-50732076 | GGGGCGGGGC | - | 6.02 | REL | MA0101.1 | chr22:50732640-50732650 | GGGGATTTCC | + | 6.02 | RREB1 | MA0073.1 | chr22:50732812-50732832 | CCCCCCACCACACCCCCAAC | + | 6.34 | RREB1 | MA0073.1 | chr22:50732814-50732834 | CCCCACCACACCCCCAACGC | + | 7.53 | Zfx | MA0146.2 | chr22:50730526-50730540 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_00972 | chr22:50731311-50733306 | Adrenal_Gland | SE_02167 | chr22:50730831-50733572 | Aorta | SE_03045 | chr22:50732003-50733002 | Bladder | SE_09673 | chr22:50730603-50731690 | CD14 | SE_23215 | chr22:50730780-50733494 | Colon_Crypt_1 | SE_23860 | chr22:50731140-50733524 | Colon_Crypt_2 | SE_24775 | chr22:50730869-50733547 | Colon_Crypt_3 | SE_26638 | chr22:50730763-50733572 | Esophagus | SE_30794 | chr22:50731094-50733450 | Fetal_Muscle | SE_31387 | chr22:50715749-50746188 | Gastric | SE_42291 | chr22:50728269-50733599 | Lung | SE_46883 | chr22:50730820-50731141 | Ovary | SE_46883 | chr22:50731155-50733168 | Ovary | SE_47582 | chr22:50730832-50733525 | Pancreas | SE_49007 | chr22:50730624-50733589 | Right_Atrium | SE_49760 | chr22:50731177-50733068 | Right_Ventricle | SE_50366 | chr22:50730820-50733593 | Sigmoid_Colon | SE_52737 | chr22:50730808-50733581 | Small_Intestine | SE_53473 | chr22:50730616-50734116 | Spleen | SE_57403 | chr22:50731159-50733141 | VACO_503 | SE_58063 | chr22:50731209-50733347 | VACO_9m | SE_65363 | chr22:50726286-50745784 | Pancreatic_islets | SE_69052 | chr22:50730682-50733434 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 50732000 | 50733000 | chr22 | 50730793 | 50733104 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I050290 | chr22 | 50728635 | 50730614 |
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Enhancer Sequence | TTCTCACCAC ATATTTGAAA GTTTTGCCAG GCCCGGTGGC TCACGCCTGT AATCCCAGCA 60 CCTTGGGAGG CCGAGGCGGG CGGATCACGA GGTCAGGAGT TTGAGACCAG CCTGGCCAAC 120 ATGGTGAAAC CCCGTCTCTA CTAAAAACAC AAAAAAATTA GCCAAGCGTG CTGGCACCCG 180 CCTGTAGTCT CAGCTACTCC AGAGGCTGAG GCAGGAGAAT CGCGTGAACC TGGGAGGCGG 240 AGGTTGCAGC GAGCCAAGAT TGCACCACTG CACTCCAGCC TGGGTGACAG AGCGAGACTC 300 TGTCTCAAAA AAAAAAAAAA AAAAAAAAAG TTTTAAGTGT ACAAAGAACA AGCCACAAAA 360 TGCAAATGTT TCCACATCCC TGTGTCTCTG ACGGCCAGGC TGACCACGAC AGCCTGTGAC 420 CCATTTCTCA GGTGAAGAAA CTGAGGCACG GAGCAGAATT TACCCAAGGC CACACCGCGG 480 GCATGGGTGG GGCTGGGATT CTGACATGCA GTGGGAGCAG CTTGGCCTCT GACCACTGTG 540 TTTCTCCACC CTTTTGACAA CCCCCCAAAC CCCCTGGCCT CTGTCCTCCC AGGAGGGCAG 600 GGGAGCCCGC TCTGCTGCTC CGTAGCCAGG GGAAGTGTTT CTCCCGAGCC TCGGCTTTGG 660 GTGAAGCTGC ATTTACTGGC ACAGCCGCCC TCCACCTGCC CGTGGCAACC CCCCGTTCTG 720 ATTGCCCGCA CGCTTCCTGA AATCTCTTGA GGTGTAACCA AGACGCAACC GACCGACAAC 780 ATCTGAGCCA CCCCAGGGCC CGCATGAGTG AGACAGCGCT GCACTGGCCT TCCTGCTCCC 840 TGGGAGTGCA CCCATTAGAC AGGCAGCTCC TGCCCGGCAC AGAACTCCCT CCCTGCACTG 900 GGGGTTCAGT GCTCAGCTGC TGCCCAACCC CTGGAGCCCC CCAGGTGCCC ACGAGCACAG 960 CAGCCGCTGG GAGAGGTGAC CACCCACAGG CTAGGGAGTT CCTGGCCGAC TGGTGGCAGA 1020 GAGGCTGGGT AGGGCCATGG GACCCCAGGC TTCACCAGGA TAGGGGTGAT CAGCCAGGAA 1080 AAGATGCTGG CTTTAGTGAG AGACAGGAAG ATTCTACAAG CCCACGGGAA CCTCTGGGCA 1140 TGATCCTGGT GGAGGGGGTT CTATGCCCAG CTCAGCCAGG GTCCCCCGCT GTGGCTCAGT 1200 GGCCTGTCCA GGGGAGAGGA GAGGAGGGCA CAGGAGTCCC AGGCCTCCAG GAGAGGCCCG 1260 TAGGCTACAG CCACAGCCCA TGGCCCTACC AGGGAGGAGC AGCGCCTGCC CGAAGGCTCC 1320 CCAACCCCCG CCGCGCCCCT CCCCTACCCA CAGCCACCCG GGGGCAGGTC CCGCAGGCCC 1380 CCGCCTTCTA AGTGCACCCA GTGGCGCCAG CGGGGGCAGG CAACGTCCAG GCCCCTCGGC 1440 CCTGCGCCCA GGCCTGCTGC CCTCCCCTCC CAGCCCCGCT CACCCGGCCC AGCTCGCTCA 1500 CCCGGCCCAG CTCGGTGGCA GTGGCAGAGG CAGCCTCAGC CAGGCGCAGC TCCCGGGAAT 1560 GAATGGAATG CGCCCGCAGC TGGGAGGGGA ATGCGGGGGC AGCGCGGGGG CGGGGCCCAC 1620 GGTCCCCTCG GATCTGGCCC GGACCGTGGT GGGGCAGCCT GGGGAACCCT GCGGCGCCCC 1680 TAGCCCCAGG AAAAGCAATG GCTCTGGGCC CCCACAAGCC ACCCCTCAGC CGTCCCCCAG 1740 CTTCCACCCA GGGAAGACAC TCACCCACCC GCCAGGGCTG TAGGGGCCCC GGTACAGGAA 1800 GAAGGCTCTC CTGTCCCTGC CGGGGGCTGG CACACCCTAA GTGCTCAATA AACACCACCG 1860 TGTGCCACCA GGGAAAGCCT GACTCCCAGG GTCCTACAGG CCCAGGCTTT TCAGGGTGGC 1920 AGGCGCGGCT GGGGTGACAC CCTACAGGTG GCAGCTGCCT TCTGGTTCCT GGACAAACAA 1980 GGCCTCAGGT GACCTGCCTG CCCAGGCCCA GGAGCAAAGG GCAACCCACC GGACCAGCAG 2040 CAAAGCTCCG GCGGCGCAGG AGGCGCCAGG CACAGCCAGC TACGCTTCCT GCTGCCTGTG 2100 TTCCTGGAAC AGGAGGGAGG GCGGGCAGCA GGCACTTCCT GTTTTGAAGC CCTCCTGGGA 2160 CCCCCACTTA CGGGGCTGGC GGGGATTTCC TCGGGCCCTC TGGTGCCTTC CTCCTGGCTG 2220 AAGCTCGGAG GGGCACTTTC AAGAGGCCAC AGCAACTCCG GCTGCTGCTG GGCAGGGAAG 2280 CTCCCCACTT CCATCCAGAC CAGGCCACAG CAACTCCAGC TGCTGCTGCC CACAAAGCGT 2340 CTGCACAGGC ACCCCCCCAC CACACCCCCA ACGCTCCAAT TCCCAGCCCT GATGTCCCAG 2400 AACCCGGTGC CACAGTCTCA CTGCAGACCA CTCCACCTGA GCAAAAGCTT GGCCTGAGCA 2460 ACAGCTTGGC CTCAGAGAAC CATGGGAGCC TCACAGCGGC TCCATGGGCA GGGAAGCTCC 2520 CCACTTCCAT CCAGGCCAGG CCATGGGAAG GGTGGCAGAG TGACAGGTAC GGTTGAAACC 2580 TGGCTGGACA GAGCCTTGCA GACACCACAT GGCAGTTCTA GATACCTCCG GCCTCCCTGT 2640 CCACATAGCC CCAGCCACCC ACTGCCTTTC CCAGGTGGGG 2680
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