Tag | Content |
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EnhancerAtlas ID | HS052-16204 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr17:45019690-45022000 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6 | MA0463.2 | chr17:45021739-45021755 | CAGCTTTCTAAGAATG | + | 6.1 | CTCF | MA0139.1 | chr17:45020063-45020082 | TTGCCCCTAGGGGGCGGCA | + | 6.35 | Nr5a2 | MA0505.1 | chr17:45021083-45021098 | AGGTTCAAGGCCACT | + | 6.06 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28004 | chr17:45020996-45022067 | Fetal_Intestine | SE_29222 | chr17:45020100-45021954 | Fetal_Intestine_Large |
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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 |
GH17I046942 | chr17 | 45019521 | 45021942 |
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Enhancer Sequence | TCCTGGCTCC ATCCCTGCCA ATCTGAAACC CTCTCACTTA TGTTCTCCAT CATTTATCCT 60 CATTATGCAG ACAAGGGGCT GAGCTGTGGT GACTGTGAAG GCCTCACAGG AGTCCGAGAG 120 GAGCTGGCCC CTCATCCAGC TTGGAACCAT GGGCCCACTT AATCTCCCAC ACTTCTCGTG 180 GGGTGCTCTG CTGGGGTCTG GGGGGATTGA GAGGTGTGCA GGGGACTGAG ATGGTGCAGC 240 CTGCTGGCAT GGACTATAGA GCTATAAGGT GTTTGCTGCA GACCCTTCAG ATAGTATAGG 300 GCAAGTTCCC TGTTGGGAAA TAATTTCCTA ACTGGAAGGG GAGGGAATCT GAAGTGAAAG 360 CTGTCCTCAG GCCTTGCCCC TAGGGGGCGG CATAGCCCTA TCTGTGGCTA GTGGGCCCTG 420 AACACACTGC CTTAGGCCTG CTGTACTTAG AAGCTGAGAA AGGAAAGTGT CATTCCTTCC 480 CCATTTTCTG TGTCCTTTTC ATTTCATATG GAAGGCACAT GGGAGAGGAG TGTTCAGGGG 540 TGCTGGGCCC CCAAGTGCTG TTGGTAAGTT CCCCACCATG GAGCCTCTGT GAGCCATCCC 600 TCCCCGCCTC ATCCCCATGT CCCTCTAGTA CAGGGTTCCC AACCTTGGCT CTGCATTGGA 660 ATTCCCTCGG GAGCTTTAAA AACCCATGTG TGGGTCTTCC ATTCACCCTC TTATTAATTG 720 GCCTGGAGTG CAGCCGGGGC ATTGGGAGTT GCCCAAGGCG ATTGTAATGC CCAGGGGTAG 780 GGAGCCGATG GCTCTAATAC AAGAACATCA ACCCAAGGCT AGCCCGTCCC CCATGCACTT 840 CCCCTGGCCG CACCGTGGGA ACCACTTGCA GAGACCAACT AGGGGCAGGG ATGGAAGCCT 900 GATTCTCCCT CTGGATCAGA AGGAGCCAGA TCCCTTGTGG CCATTGGGTG CCCCTCATTA 960 ACTGACACCT CTCTGCTGAG TAAAGCACCT TGATGTGACA GGCCAGCTCT TCGCTGCCCC 1020 TGCAGTGCAG CCCCCAGCCC TCCCCACCAC CCCTGCCTGG TGTTCCGTCC TCCCTGGACT 1080 GCTTGGTCTT CTCAGAACAT GCCACACACT CAGTACAGCT GCACCTTTGC ACAAGATGTT 1140 TCCTCTCAGA TGTGCCACAA ACACCCCCAC AATCCCATGA AACCTCCAAG AAGCCTGCCC 1200 CTCCCCTCCA AACAACCTCA TACTGCACGC TTCCTGCGGA ATGGGAGTTG CTCCTCACCG 1260 CAGGGGCCTT TGTGCATCCC GGGCACGTAG TAGGCGCAGG CGCCATCGGG TAAGCGGCTG 1320 CAGGAGAGCA CTTGAGCCCA TCCCCCATGC AGGGCCAGCA AAGCTGTTGC AGCCAGGCCA 1380 GGAGGAAGCC AGAAGGTTCA AGGCCACTGA TGCTACGAGC CATGTGCTCA CAGGGCCTCA 1440 ACAACAGCAA TGACTGCAGT AAAAGAGGAG AGGCATGGGG CCCCGTGAGG GAAACTGTCA 1500 CTCAGGACTG GGGAGAGAGA AGTAGAGTGA CCAACTTGTC TGGGTTTTAA AGCTGAAAGT 1560 CCTGAATCCT GGCGATCCCT CGGTCTGATG GTCACCCTAG ATAAGCTAAA GGCTAGGACA 1620 GGCGTGACTA ATGCAGGGTA TCTAGGAAGA GGGGGCTCTC GGAGGCTGAC TCCTGGCTTA 1680 GCAATTCCAT TAGTGTGGTT CCACTGGCCC TTCCTTCCAG GCATCTGTGA CATGGTGGCT 1740 CCTGGAGAGC TGGCAGAGGC TGGGCCAGGC CCAGGAGGGA AGTATTCCAA CCTCCTCAGA 1800 AGACAGTGGC TGACAGTACA AGAGGGGACA TTCATCTTTA TTCCGTCTTC CAGAGCCCTG 1860 GCATGTGTCC AGTGCCAGTG TTAGCTGTTT CAGGGCAGAG GGAAGGAGTT GGAGACAAGC 1920 AGCCCTCCGC AGTTTGCACT GGTTACAGCG GCCGGAGGCT GTGGTAAGAG CGCTGAGCCC 1980 AGGATGCAGA GCCTGGCTTC AAGTCCCAGC CCTGCTGGCA GCAACCACGG GCCACACACC 2040 TCTCAGCCTC AGCTTTCTAA GAATGGGGGT AACACCTGTC CCACGTCCCT TTCTGGGGTG 2100 GACATGAGGC CCGAGTCACG TAGTGCTTTT GGCAGATTCC AGAGGTCTGA GGCAGTGACC 2160 CTCAGCCTGG GCTGCTTCCT GGAGTCCCCC AGAGAGTTTG GAAGTCCCGA TTCTGGGCCT 2220 CGCTCCCCAG AGATGCCGAG CTACCTGGTC TACAGTGGGG CCTGGGCTTC AGAATTTTTA 2280 ATTTTCTTTT TTTTTTTTTT CCTCTCATTC 2310
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