Tag | Content |
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EnhancerAtlas ID | HS170-00102 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr1:57772760-57774060 |
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 | TTTTAGGAGG GTCCCCTCGG GTCCCTCTTT GTGCACTCAT TTGACATTTC CTTTCTAACA 60 ACGACTGTCA TGGTTTGCCA AATACCTTCT CTTTTGTGCT TTCATTTCAT CTTCATGGTG 120 CTGTCCTCAT TTTACCATGG TTGGAGATGA TATAAGCCAC AGATTTTCCA GCTAAATAGG 180 ACTGGACTCC ATGCCTTTTG AGTCCAAGAT CTCTTCTGTA CCTTGTAAAT ACCACCTGAC 240 TTCTGGCTCT ATATTATGCT ACCTTAATTA GATTATCAGC CCTAGTACAG GTACTGCCAC 300 CCTGAATGAT AGTGAAAGAG CAGGACCTCT TGCTAGTAGG TGAGTTGCCC ACAATCTTCC 360 CCACTCCTCC CCAGCTGGTG AGACCACACC TCCTTCACCA TCTGTTGAAT CTAGACCGCA 420 CCTCCCAGAC CACACCTCCT TCTCCATCCG CTGAGTCTAG GCCACACCCT CTTTCCCTTT 480 CTGTTGAATC TAGGCCACAC TCCCTTTCCT GTCTGTTGAA TCTGGACCAC ACCCCGTTTC 540 CTGTCTGCTG AACCTAGGCC ACACCTTCTT TGCCTGTCTG TTGAATCCAG ACCACATCCC 600 CTTCCCTGTC TGTTGAATCT AGACTACACC CCCTTTCGTA TCTGTTGAAT CTAGGCCACA 660 CCTCCTTTCC TGTTTGTTGA ATTTAGGCCA CACCCCCTTT CCTGTATGTT GAATATAGAC 720 CATACTCTCT TCCCTGTCAA TTCAATCTAG ACCACACCTC CTAGACCACC TTCTTTCCCT 780 AGCTATGGAA TCTAGATCAC ACCTCCCAGA CCAGGTCTCC TTCTCCATCT GCTGAATCTA 840 GACTACACCT CCTGTCCAAT CTGTTGAATC TCTGCACCTT TGCCCAGCCA CCTGATGAGA 900 GCTGTGGGGT CACTAACCTG AATAATAGTG CTTTTTCCCT CTCTGGAGGG AACTTTAACC 960 TTAGCTCATT AAAATTTACA GTCTAAATTA AAAGTATTCT TTAGAGATAA AAAGACCAAA 1020 ATAAAGATAA CAGAATACTA AATGGCTTCC AAGAGCCAAA CTAGTAGGTC AGTTCATCCA 1080 GATTTGTAAT TGAGTTATCC CTAAAAAATG AGCCAGCCTT GATTAGGTGC CCATTAGCTT 1140 TCAGCTTCCA GAGAGCAGCA AGCTAGTCCT GCAAACAGTC ATTCTCTTGA CATCTGTGAT 1200 TCTCTAGATA TTACCAGTTA ACGTCCATGC AAGGAGGAAT GGATATATGA TCAGAAGAAG 1260 CATGAAAAGA TCTCCTCCTC TCAGGAATTC CAGGGGGAAA 1300
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