Tag | Content |
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EnhancerAtlas ID | HS089-12607 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr9:22103200-22104480 |
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) |
NEUROD2 | MA0668.1 | chr9:22104186-22104196 | ACCATATGGC | - | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_02690 | chr9:22102223-22105910 | Astrocytes | SE_36500 | chr9:22101717-22105229 | HMEC | SE_37282 | chr9:22101630-22106155 | HSMMtube |
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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 |
GH09I022101 | chr9 | 22101774 | 22106087 |
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Enhancer Sequence | TGCCCAGAAA ACCATACCCA CTTTCCCACA TATCCCAACT ATGACTGGGC AATTATGTCA 60 TTATCACCAC TGATATATAG CTGGAAGAGT TTAGTGTTGC CCTGCTAAGA TCTGGATTTT 120 CTTTTCTGGA GCTTGGCTAT TGGGGCATTG AGAAGTCCAG CCAGGAGGTT GGTCAGAGGC 180 TAACCCAAAA AGCTTTGCTT AACTCTGGGC TACAGCTGGG GGTTGCCAGA GAGAAGTGCC 240 TGGCATTCCT GCATGCTGAC ATCAAGCTTC GAAGTTGCTG CCCTCTGGTG AGTCAGCAGC 300 AAAGGCCCAC ATCGTTCGAG AATGCTGCCC AATCAGAAGA TGTGATGCCA CACCTCAGAA 360 ATCTTTCTAA ACCTCAGCAT TCTGTAGACT TCAAACAACT CCTCCTGAGA AAGAATGTAG 420 AAATAATTAA ATTTATAAGA TTAAAGTTAT AAAAAGCATA GAGCCTATAA TAATAACAGC 480 AATAAGATAA ACTCCACATT TGCTTTTAAA ACAATTTATT TGAGTAGACA GCCAACCCCC 540 TGTATTGTAC TCCTTTAAAA AATATTTTAG GCTTTTTAAA TGCTGAGGCA AGGGGACATA 600 CCAAACACTA ACAGGCACAT TGGGGTTTTC TGGCTATTGA AATAAAAATG TCCTTACATA 660 ACACTGATGT ACTGGAATAG CACTGCGTTC CAGTGACGGT TATTGCAACT CAGCCAGCAT 720 ATCTGTAGCT TGTGAGCTTT TCTTATCAGA ATTTTATCTA TAAATATACA TATACGTAAA 780 TTCTATTGTG AAATAAAAAT AAAATGTAGA ATCTTCTCAT CTTTCTTATT AGTCAATATT 840 GTGCTACTCT TTAATAATTT CTCTCAATTT TTTCATTAAG CAGATATTAC TAGGGAAATA 900 TACATGAGGC AGAAGGCAAA TTATTTGCTT AGTGCAATGC AAACTTGCTT AACAGGTAAG 960 AGCAGAGTCC CTTCCATAGC ATTGCCACCA TATGGCATTG CCATATCGTG GAGGCCATAA 1020 AGAGGAATGA CATTGTAAAG ATTAACTGGA TTTTACTTGG CAAGGTCAGG CACCTAGATG 1080 GCATGCTATA AAATGGTTAG AAGTGCAAAG GAAACCTGTA GCTAGAGGCC ATGTGAGATT 1140 ATGGAAGTGA CTTTTCTTAC AATCCTGCCA TCTGGTTTGG ATTGTCAGGA TCAAAACATT 1200 TCACTTGCCC AAGTGAGGAT GCTCTCTACA TGGTTTTGGG GATGAGGGAG ACTCAGAAAT 1260 AATGTTTGTG GTACTGTAGC 1280
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