Tag | Content |
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EnhancerAtlas ID | HS060-26258 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr4:40724020-40725170 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELF5 | MA0136.2 | chr4:40724954-40724965 | TACTTCCTGGT | - | 6.02 | FOXP1 | MA0481.2 | chr4:40724923-40724935 | TACTGTTTACTT | - | 6.18 | Foxa2 | MA0047.2 | chr4:40724926-40724938 | TGTTTACTTTGC | + | 6.27 | Sox3 | MA0514.1 | chr4:40724791-40724801 | CCTTTGTTTT | + | 6.02 | ZNF263 | MA0528.1 | chr4:40724822-40724843 | TCATCTGCCTCTTCCTGCTCC | - | 6.17 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33946 | chr4:40723041-40726224 | HCC1954 |
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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 |
GH04I040721 | chr4 | 40723301 | 40726255 |
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Enhancer Sequence | TCCACTGAAA TCTCCTAAGT TACTAACAAC TTCCTTGTTA CTAAATTCAA TAGCAAATTT 60 CAGTCCTTGC TCTACTGACC TCTCTTTAGC AGCTGACACA TTTGACCACT TCTTTCCTTG 120 GCCTCTGTGA CTCGATGATC CTACGATTCT CCTCATTCCT CTTGGCCTCA CCTCTGTTTC 180 CTTTTCTGGC TCCTCCCTTC TGTCTTTCTC TGACTTGTTA GTGTTTCCCC ATGGTTCTAC 240 CAAAAGATAA GAGATCCCTT CTCTTTTCAT TCTACTTTCC CTGGATCTGA TCTCCTCCCA 300 TGGCTACAAT TACCATCCCC AGGTGGATGA CTAGTGATGG TTCCAGGCCA AGTCTTTGCA 360 TCTAGTAGGC ATATTTGTTT GAATATCTTT GGAAGTATCA TGATCGTAAC ATTTCTAAAC 420 TGAAAGCTCC CCAAATCGCC TCCCTTTCTG TGCTCCTGGA ACAGTGAAGG GCCCCAAGTT 480 GCCCATGCCA GAACCTTGAT TCCTTTTCTC TGATACCTCA TTCCAATTAA TCACTAAGTC 540 CTGCTGATTC AACTTCACAT CTCTTACTCC TGTCTACCTC TCATCATCCT CAGGGTTACC 600 ACCCTGGTTC AGGCACACTA CCTCTCACCA AGGTTATCCT TCCTGGTCTC CTAACCGGTC 660 TTTCCACTTC CAGCCTTGCC TCACCCCAAT CCATCCTACA TTCTGCAGTG ATGTCTCAAA 720 AACGCAAATG TGATCATGTC ATTTGCCTCT TCAACAGCTT CTGATGGTTC CCCTTTGTTT 780 TGTCACATGA GTGGTCTGAC CCTCATCTGC CTCTTCCTGC TCCCCACCGC ATTTCCACTG 840 ATCTAAACTT TTTTCAGTTC CCTAAGCATA CCATGTGCTG TTTCATCTGT GGGCCTTTAA 900 CTATACTGTT TACTTTGCCA AGAACACCAT AATTTACTTC CTGGTGAATA GAGACAGGAA 960 GTAAATTATA TTCATAATCT CTCTTACCGT AACTTACTGC TTCTTAGACA TTACTTACTG 1020 CTTCTTAGAA ATTACTTCCT GCATAAGTGC CGCTGACCCA GCCCCCTCCA CCTCCTGCAA 1080 TGTTTGTTTA ACTTGTCTGT CTCCCTGATA AACACTAACC TCCATAAGGA CTGGGACCTT 1140 GTCTATTCTC 1150
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