Tag | Content |
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EnhancerAtlas ID | HS052-25218 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr22:43281150-43282570 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REL | MA0101.1 | chr22:43282221-43282231 | GGAAATCCCC | - | 6.02 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_00993 | chr22:43281302-43282103 | Adrenal_Gland | SE_31403 | chr22:43279940-43282350 | Gastric | SE_31403 | chr22:43282397-43285902 | Gastric | SE_47465 | chr22:43281144-43282360 | Pancreas | SE_65321 | chr22:43279870-43284940 | Pancreatic_islets |
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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 |
GH22I042884 | chr22 | 43280151 | 43282054 |
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Enhancer Sequence | AATGTTAAAA AGCAGGTGTG GCCTATCTCA AGAATATCCA GGGGCAGCTA GAAAACGTGT 60 GAAATTCCTA AGACATGGCT AAAGTGGGCA CATTCATCTG GTGGGGATGT GCCTCGAGGT 120 CAATGACCTC ACACTGGTAC ACACTTCCCC GCACCCCCTC ATCTCAGCAT GCAGGGCCAC 180 CAGTTTGGTG GCCAGGTGGT TTTGTTAGTT GGTGGGATCA TGGTCGTGTT GTCCCCCTGG 240 GGTGGGTGAG AGATAGCAGG GCTGGGGCCA CCTATTTATT GCAATTCTTT CTACTATGGG 300 GGTAGTCACG GGCTCCACTC AGGTCTAAGC TTTGCTGTCC CTAACAACAT GTGCAGGGCC 360 TTCTGAGGAA GGATGGAGCG CTTCCCGAGA CACTGCAGGC CTATCGGGCA CCCTCTCTGC 420 CCCCAGCTGG GACTGAGTCT ACCCTGCCCA TGCGGCTCCC CTCCCAGATG CTCTCCTCTG 480 ACTCACGTGG CTCAGAGCCC TGGGAGACTC TGCTTCAGGC TCCAAAGCAA CTCCTCTTCT 540 TGAAGCCTTC CCCAGCCTCG TGAGACCAGG TTCCACCCCG CCCTCTAGGG CCCTGACTCC 600 TGCCCCTTTC TCCTCTCCTG GTATCCGGGT CCTTGCTCTG CTTCTCAGCC TCCTAAGATG 660 GCTGGGCTTG GGTCCTCTGT GCCAGGAAAA GGCCACCCCT GCCAGGGCTG GGGCATGCCC 720 AGCAGAGAAA GAGCTCCACA GCGCTGTGGC TATTCCCCTA TTCCCCACAG CCATCCACAC 780 TGCCCGTGCC CACTACCTGG CAGCCCTGCA TGGGAGCCTA GCTCAGAAGC CCAAGACACA 840 TAGCTGTGGG TTCAGCGCCC AGCATCTGGA GGATACTGCT GAAGTGACAC AGAGCAGCCC 900 CATCTCAGGA GCCTTCAAGA CACAATAGCC TCCCGGGAGC TCTCAGGGTA CTCAGTGGCA 960 ACAAGATGCT CCACCTCTGG GCTGCCCCTG CCCTCAGCCT GTGCCGACCC TGCTAGCCCC 1020 AAGTCCTGCC CCCAGCACAG GCCAGGTACT CAGCAGGGTC ATCACTGTTC TGGAAATCCC 1080 CTTGCAGGGC ATAGAAAGTT CTCAGCGAAC ACCCATGGAG TAAAACAAGA GGCGGCCTTC 1140 ACCCTTAGGT GGATTGTAAT ATTTTAGCAC TAAATGCAAA AAGTTCTTTT ATGATGGATG 1200 CTACAAGATG TAGTTGATGG CTGATAAGAA ACATGAAAGT ACATGTGCAA CCAGTCAGCA 1260 ATGGTATGTA TGTAGGTAGG TAGGTAGGTA GGTAGGTAGG TAGGTAGGTA TGTATGTACC 1320 TACCTACTTA CCTACTTTAG AGATGAGGTC TCACTCTGTC ACCCAGGCTG GAGTGCAGTG 1380 GTGTGACCAC AGCTTGCAGC AGCCTTGAAC TCCTGGGCTC 1420
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