Tag | Content |
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EnhancerAtlas ID | HS187-17511 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr3:108524630-108525780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DUX4 | MA0468.1 | chr3:108525535-108525546 | TAATCTAATCA | + | 6.32 | LMX1B | MA0703.2 | chr3:108524990-108525001 | TTAATTAAATT | - | 6.32 | Nr2f6(var.2) | MA0728.1 | chr3:108524645-108524660 | GAGGTCAGGAGTTCA | + | 6.22 | PHOX2A | MA0713.1 | chr3:108524991-108525002 | TAATTAAATTA | - | 6.62 | PROP1 | MA0715.1 | chr3:108524991-108525002 | TAATTAAATTA | + | 6.32 | PROP1 | MA0715.1 | chr3:108524991-108525002 | TAATTAAATTA | - | 6.62 | Phox2b | MA0681.1 | chr3:108524991-108525002 | TAATTAAATTA | - | 6.62 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_18523 | chr3:108523318-108526457 | CD4p_CD25-_Il17-_PMAstim_Th | SE_63170 | chr3:108524249-108557426 | Tonsil |
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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 |
GH03I108805 | chr3 | 108524741 | 108526281 |
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Enhancer Sequence | GCGGGCGGAT CACTTGAGGT CAGGAGTTCA AGACCAGCCT GGACAACAGG GTAAAAACCT 60 CACCTCTACT AAAAGTACAC AAATTAACAG GACTTGGTGT TGGGCACCTG TCCAACACCA 120 ATTCCAGCTA CTGGGGAGGC TAAGGCACGA GAATCATTTG AACCCAGGAG GCAGAGGTTG 180 CAGTGAGCCA AGATTACACC ATTGCACTCC AGCCTGGGCA ACAGAGAGAG TATGCCAAGG 240 TAGCAAGAAT GAGTTCCAGA TTTCTGGCTG GAACTAGATT TCTGGGTGAT GATAGTGCTA 300 TTATCAAGAT GTGGAAGATG GAGGAAGAAA AAAAGTTAGG TTTCAGCGAG TTTTAATTTC 360 TTAATTAAAT TAAGATCTAC AAGACATCCT GTGTCACTCT TCAGAATGCC TGAATCACTA 420 CAAATAAAAA TAAAGCATTT TTAAAGAAGC AGGTGAAAGA GCAAAGCAAG CCTCATATCC 480 AGTCATTCAC ACAAGAATGG CTGGGAGGGA GTGTACTTAA GCCCCTCTCA GCAGATCACG 540 ATATAATATA TAGAGATACC AGGCCGTGAA GCTACACAAT CAAATGCAAC TCAGGACTTT 600 TGTTAAGGTG GCCACAACTA TCACTTCCTT TGTCAAAATA GAAGAACTCC TTCCGCATAG 660 GAAGCTGCAT ACTCTACCTC TTATCTCTGT TTCTGCACTG TCAGTAAGCA AAATGGTAGA 720 GCAGTGAAAG GGGACTGATT GCAGGCAGAT AAAAATAACT GGTGTAGAAA GACACAGGAT 780 GTTAGTTGTG ACCAGCAAAT GATGCTGCAA ATGTGCTGCT ACACATATTT CTCTGTTGGG 840 CTTTGACCAC ATCCTAAAAC ACAACTCAAC ATGTCAATAC GTCAGAGCTA GTTTGCTTGG 900 TGGAGTAATC TAATCATAGG CATAAGAAAA AAAGTAACTA TATTTTACTG TTTTGACTTA 960 ATTCAACTTA AACCGGATAC TCCTAGGAAC ACTACTTCAG AAAGCAATCA CAGAAATAGG 1020 GAATGAGTTA GTGGACTGTG AGTTAGAACA CAAGCGAAAT AATGTTTCCC AATCTATTCT 1080 GTATTAGTAG GTAAAGTTTT AACAGGTGAT TTTTGGTCAA ATATATTTAA GATAAAATTT 1140 AAGAAGCATA 1150
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