Tag | Content |
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EnhancerAtlas ID | HS187-00846 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:57772880-57773760 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr1:57773221-57773232 | CCACACCCTCT | + | 6.02 | Klf12 | MA0742.1 | chr1:57773219-57773234 | GGCCACACCCTCTTT | + | 6.05 | Klf1 | MA0493.1 | chr1:57773219-57773230 | GGCCACACCCT | + | 6.32 | PHOX2A | MA0713.1 | chr1:57773024-57773035 | TAATTAGATTA | - | 6.32 | PROP1 | MA0715.1 | chr1:57773024-57773035 | TAATTAGATTA | - | 6.14 | Phox2b | MA0681.1 | chr1:57773024-57773035 | TAATTAGATTA | - | 6.32 | SP4 | MA0685.1 | chr1:57773443-57773460 | TAGGCCACACCCCCTTT | + | 6.01 |
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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 |
GH01I057306 | chr1 | 57772500 | 57778001 |
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Enhancer Sequence | CTGTCCTCAT TTTACCATGG TTGGAGATGA TATAAGCCAC AGATTTTCCA GCTAAATAGG 60 ACTGGACTCC ATGCCTTTTG AGTCCAAGAT CTCTTCTGTA CCTTGTAAAT ACCACCTGAC 120 TTCTGGCTCT ATATTATGCT ACCTTAATTA GATTATCAGC CCTAGTACAG GTACTGCCAC 180 CCTGAATGAT AGTGAAAGAG CAGGACCTCT TGCTAGTAGG TGAGTTGCCC ACAATCTTCC 240 CCACTCCTCC CCAGCTGGTG AGACCACACC TCCTTCACCA TCTGTTGAAT CTAGACCGCA 300 CCTCCCAGAC CACACCTCCT TCTCCATCCG CTGAGTCTAG GCCACACCCT CTTTCCCTTT 360 CTGTTGAATC TAGGCCACAC TCCCTTTCCT GTCTGTTGAA TCTGGACCAC ACCCCGTTTC 420 CTGTCTGCTG AACCTAGGCC ACACCTTCTT TGCCTGTCTG TTGAATCCAG ACCACATCCC 480 CTTCCCTGTC TGTTGAATCT AGACTACACC CCCTTTCGTA TCTGTTGAAT CTAGGCCACA 540 CCTCCTTTCC TGTTTGTTGA ATTTAGGCCA CACCCCCTTT CCTGTATGTT GAATATAGAC 600 CATACTCTCT TCCCTGTCAA TTCAATCTAG ACCACACCTC CTAGACCACC TTCTTTCCCT 660 AGCTATGGAA TCTAGATCAC ACCTCCCAGA CCAGGTCTCC TTCTCCATCT GCTGAATCTA 720 GACTACACCT CCTGTCCAAT CTGTTGAATC TCTGCACCTT TGCCCAGCCA CCTGATGAGA 780 GCTGTGGGGT CACTAACCTG AATAATAGTG CTTTTTCCCT CTCTGGAGGG AACTTTAACC 840 TTAGCTCATT AAAATTTACA GTCTAAATTA AAAGTATTCT 880
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