Tag | Content |
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EnhancerAtlas ID | HS134-00193 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:9919210-9920380 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr1:9920070-9920085 | GGGACAAGCTGACCT | - | 6.58 | MAFK | MA0496.2 | chr1:9919733-9919752 | TATAGCTGGGTCAGCAATA | + | 6.26 | MAFK | MA0496.2 | chr1:9919733-9919752 | TATAGCTGGGTCAGCAATA | - | 6 | SPI1 | MA0080.4 | chr1:9920302-9920316 | AAAAAGGGGAACTT | + | 6.2 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_03800 | chr1:9919178-9919654 | Brain_Angular_Gyrus | SE_08037 | chr1:9918751-9920367 | Brain_Inferior_Temporal_Lobe | SE_33608 | chr1:9919644-9924262 | H2171 | SE_58597 | chr1:9839934-9924553 | Ly1 | SE_60796 | chr1:9907685-9935747 | DHL6 |
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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 |
GH01I009859 | chr1 | 9919251 | 9920306 |
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Enhancer Sequence | CCCTATCTCT GCCTACTGCC CTACCAGACA CCTCACTAGT CCCCTGGCTC ACCTGCCCTG 60 GAAACCAGGG CCAGGACACT GGCAAAGGCG CAGCTTTCTA AACCAGGACA GGGTATCCAG 120 CAGGCCCTCC CATCCTATGC CCAATGCCAG CTTTGCCCCT TTAGTGGAGT CCAGTCAATT 180 GACTGGGGAG AAAAAATGAC AAATATGCAG GAGCTTAGAA AAGGGAAGCT GGCCCCTAGC 240 CGGGGGCGGG AGAGAGACAA TGGGAGCTCA GGATGAACTC CCACCAGCAT GCTGGAACCA 300 GCTCTGCTCC CGCCAACACT CACCCTAGGC CTGGCCTGGC TTACTCAGGC TTTTGGAGAA 360 AGCCTCCTGG GGGCCTCTGA CAACTCCCAA AGTCTGCTGA GAATCCCTCT TGCTATTTGA 420 GACTCTTAAG CTGAAGTCTT TCAAAGGTCC TTTCCTGAAT ATACTGGGCA GCTCGATGCA 480 TTTCCTGAAC TGCCAGGGCA GGCTGCTATT GGCCCTGCAG GATTATAGCT GGGTCAGCAA 540 TAGTGGATGA AAGAGAGGAG CATGGAGATT CTAAAGCCCC AAGGCCAATC CACAGAGCAA 600 GGGCATTTCA CAGACCTGGC TGGGGAAATC CTGGCGGAGC CTAGTGCTGC ACTAGCTCCT 660 AATTTGCAAA CTTGGAAACA GGCTGGTCCC AGGCCACATG GGTGAAATGT AGCAGACAAA 720 GGCCTGTGAC CCTGATCTGT AGACCCTGTT CCCACCTCCA GGGTGCCTCC CTGGACTATC 780 CAACATGGTG GGGTCTGCTT TCACAGCAAA GAGGAGGGCT TGGTCCTGGC TTCATTTCAC 840 CAAAGCATCT GGGTGTGGGA GGGACAAGCT GACCTCTTAC CCCAGGGAAC TTCTCCAGAT 900 CCAGGATCCT GCAAAGTCCA ACTCAGCACA GGTGCTCAGA GGTGGCCAGG GAGAAAGAAA 960 ACAGACCTGA GCACAAGTCC TTCCTCCAAA ATTGATGAGG GTACAAAAAA GCCTGGCTAA 1020 ACTCCCAAAG GCCGCAGGCC CTGCAGGCTC CACAGACCAG GCAGGGCACA GCCCTGTACA 1080 ATGTCACTGG AGAAAAAGGG GAACTTCAGT CACAGATGGA CACTCCCGCA TCACCCAATT 1140 CAGAACCAGG ATTCTAGGCC GGGTGTGGTG 1170
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