Tag | Content |
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EnhancerAtlas ID | HS182-14423 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr21:38616540-38617850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr21:38617472-38617490 | GAAAGGAAGGAGGGGAAG | + | 6.05 | EWSR1-FLI1 | MA0149.1 | chr21:38617485-38617503 | GGAAGTGAGGAAGGAGAG | + | 6.42 | Klf1 | MA0493.1 | chr21:38617182-38617193 | GGCCACACCCA | + | 6.62 | RUNX1 | MA0002.2 | chr21:38617003-38617014 | AAACCACAAAC | - | 6.02 |
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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: 2 | ID | Chromosome | Start | End |
GH21I037244 | chr21 | 38617121 | 38617270 | GH21I037245 | chr21 | 38617349 | 38617928 |
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Enhancer Sequence | CACATTTTCT AACTTTGTAT TCTCTTTTTT TTCCTCATTC ACTCTGTCAC CCAGGCTGGA 60 GTGCAGCGGC ACGCTGCAAC CTCCGCCTCC TGGGTTCAAG CAATTCTCCT GCCTCAGCCT 120 CCCAAGTAGC TGGGACTACA GGCATGCACC ACCACACCCA GCTAATTTTT TGTATTGTTA 180 GTAGGGTTTC ACCAATGTTG GTCAGGCTGG TCTCGAACTC CTGACCTCAA GTGATCCACC 240 CATCTCAGCC TCCCAAAGTG CTGGGATTAC AGGTGTGAGC ACCCAGCCTA ACTTTGTATT 300 CTCTAAATGT AAAAGGCCAC TACCAAACTA TACAACTCTT TTTCTTATTT GTTCTCTGTA 360 ATAAAATGCC AAAACCATAA TTGGAACTCT GGATTTGAAA ATAGTGGCAT CAAGTCCGCG 420 ACCCCTCTTG GCTTCCTGGA AATCACCCAA AGAATGAGAA CCAAAACCAC AAACTGCATT 480 TTCGGCGAGG CAAGGAGATA GCTAAATACC ATGAAATAGG TGGAAGAGCT GTTAAAAGAA 540 GTGAAGACTG AGCAGGGGGA CGTGATGAAA AACGGAAAGA AGGCCCCCAG CTCTGCAAAC 600 GTGCTTCTTC TGGAAAGTGA GGGTACACCT GGGAACAGCT GAGGCCACAC CCAGAGAGGC 660 ATCCTGTCAA CCCGCCCCAT GCTGGAAGCA GTCGGTCTCT GCAGTGGTGG AGACAATGAG 720 CCCCTCTGCA AGGTGCAAAC GCCCTGCAGC TGGTTACTGC ATGGGCTCAT GCAAAGTCAA 780 GATGAAAGAA ACTCTCACGT AAATCCTCCG GCTATTAGAA CACTCCAGCC AGCCTGGTCT 840 AGGAATAAAT TCATCTCCTG CAAGGAGAGG TTAAAAGGAA CCAGCAGAGG AGCACATGAC 900 ATCTAATGGA TTAAAAAATG AGAGTGGGAA GGGAAAGGAA GGAGGGGAAG TGAGGAAGGA 960 GAGAAATACG AGTGGCAGAT GAATGCGAAA GCCAGGTCAG GTCACTGTTC CACTTAGATT 1020 TTTCAGCAGC TCACCATCTC AAGCACACAG TAAGAGCCAC AGCAGCCTAC AAAGGGGGAC 1080 CCGCCCTCTC CTTACCTGAC GGCCCTCATA TGGGGCCCTC TGCTCCCTCG CTCCTGCCCT 1140 GGCCCCCTTG CCATTCCTTT CAGAGGCCTG CACATTCCAG CCTTAGGCAA CTGCCCACGT 1200 TCCTTGCTCC ACCTGCTTGT TCTTCTCAGA TACCTGCAGG ACTCGGTTCC GTGAGCCCAC 1260 ATTTGAAACT GTACTACTCC CTCCCTAGCA CTCATTATCC CCCCTCCCTG 1310
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