Tag | Content |
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EnhancerAtlas ID | HS095-15415 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr19:46945900-46947330 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HLTF | MA0109.1 | chr19:46946758-46946768 | AACCTTATAT | + | 6.02 | IRF1 | MA0050.2 | chr19:46946287-46946308 | GTGTACTTTCACTTTTGATAA | + | 6.14 | Nr5a2 | MA0505.1 | chr19:46945921-46945936 | GAGGCCAAGGCCAGC | + | 6.4 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_29984 | chr19:46946044-46946921 | Fetal_Muscle |
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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 |
GH19I046442 | chr19 | 46945535 | 46946865 |
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Enhancer Sequence | CCTGTAATCC CAGCACTTTA GGAGGCCAAG GCCAGCAGAT CACCTGAGGT CAGGAGTTTG 60 AGACCAGTCT GGCCAACATG GTGAAACCCC GTCTCTACTA AAAAATATAC AAAAATTAGC 120 CAGGCATGGT GACAGACACC TGTAATCCCA GCTACTCAGG AGGCTGAGGC AGGAGAATCT 180 CTTGAACCCA GGATGCGGAG GTTGCAGTGA GCCAAGATCG CACCATTGCA CTCCAGCCTG 240 GGTGACAAGA GTGAGACTCC ATCTCAAAAT AAATAAATAA ATAAAAATAA GTGACCAATG 300 GGAAACCTAT AGGAGGTATT TGGACCTAAG AAGATCCTGT ATCCGGGGCC CTTGAGCAGC 360 TGCTGGGGCC TGCTCCCACA CTGTGGTGTG TACTTTCACT TTTGATAAAT CTCTGCTTTC 420 CTTGCTTTGC TGTGCGTTTT GTCCAATTCT TTGTTCAAAA CACCAAGAAC CTAGACAACT 480 TGCAGTCAAG ACCCTCTATC GGTAACAACA TCATCTCTGA AGAATAGACA TGCTTCCTTC 540 TTTCTAAGGT TCATACTCTT CTTCCTTTTC CCTATATAAT TACATGAGTC ATGTTCCTTG 600 AATCTGAGCC CAGCACTCAA GGTTTTTGCT TCCTGGCACA GGGCCTGGGG CCTCTGTCCA 660 TCCTTGAAAT TCTTTGCCTA TCATTTTCTG CTCCAAAACG GTTATACCCA AAGGTGCTTT 720 ACCATGACTT CTCAGGCACG GAGGCATCAC TCCATTGGGA GCCATTTCGG CAGGAAGCTT 780 CTCTGACTGT CCCAAGTCCT CATTCCAATA AACATAAAAA CAACAATCAT ATTATAGGCA 840 TTGACATGCA TTCTGAAGAA CCTTATATTT TGCTCAATAG CATGTTTGTT TTTTGTTGTT 900 CTTTTGTTTT TTTTTTTTTT TTTTGAGACG AAGTCTCGCT CTGTCGCCCA GGCTGGAATG 960 CAGTGGCAAG ATCTCGGCTC ACTGCAAGCT CCGCCTCCTG GGTTCTGGCC ATTCTCCTGC 1020 CTCAGCCTCC CAAATAGCTG AGACTACAGG CACCCACCAC CATGCCCAGC TAATTTTTTG 1080 TATTTTTAGT AGAGACAGGG TTTCACTGTG TTAGCCAGGA TGGTCTCAAT CTCCTGACCT 1140 CGTGATCTGC CCACCTCGGC CTCCCAAAGT GCTGGGATTA CAGGTGAGAG CCACCGCGCC 1200 CAGCCTGTTT TTTGTTTTTG AGACGGAGCC TCGCTCTATT GCACAGGCTG GAGTGCAGCG 1260 GCGTGATCTC AGCTCACTGC AACCTCTGCC TCCCAGGTTC AAGCGATTCT TCTGCCTCAG 1320 CCTCCCCAGT AGCTGGGATT ACAGGTGTGT GCCACCACAC CTGGCTAATT TTTGTATTTG 1380 TAGTAGACAC GGGGTTTCAC CATGCTGGCC AGGCTGGTCT CAAAACTCTT 1430
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