Tag | Content |
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EnhancerAtlas ID | HS141-00238 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:21290990-21292000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:21291565-21291586 | TTTTGGTTTCACTTCCTCATT | + | 6.51 | ZNF263 | MA0528.1 | chr1:21291049-21291070 | TTCTCCTCTCCATTCTCCTCA | - | 6.42 |
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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 |
GH01I020964 | chr1 | 21290694 | 21292130 |
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Enhancer Sequence | ACAGTTTCAA ATTCTGTCTA CTTCTCATTA GGGTAAAAAC AGCAGCAGCA AAAATTTGTT 60 TCTCCTCTCC ATTCTCCTCA CAGAAACCCA ATGCAGTTTC CCTCAATTAA CTCATAGCTT 120 GTGTCACAAA TTTAATATAA TTGCTCCCTC GGCATCCACT TTTAGGGCTA GCATATGTTT 180 TTGAAACCCT TTCACATTTG GCCTAGTTCA AATATTTCCT TCCTGTGTAG TTGCTTGTGA 240 AAGAGGCCGT TTGTTCCTCA TCTCACTGAC CCAAAACACA ACATATCCCA TAGCTGCTGA 300 CCATGATAAA ACCTAATGGT TAACACCAGA GTCCTGTAAG TAAGTTCACC CTTTGAAAGT 360 GTTTTCTTCA AACTAGCAAA TCCATAACTC CAGTGGGGAA GCCTAAGGGA GGACATGGAC 420 CTTAATAAAG GGACAGTCCC ACGAGTCGTC TTTCTCTCTC TCTCCACCTG CTGGGTGAGT 480 TCCCTGCTGT CTTCAGAGCT CCCCTATCAG CCTCCCATCA GCACTGCTAA CCTCTCTGGG 540 ATTAGGAAGT AGTAAATTTT TTTCTGTTTC ATGCATTTTG GTTTCACTTC CTCATTATGT 600 CTCACCTGAC AAACACACCC AAACATAACT TTTCCCTGGT CAGGGCTCTC TTAGAGAGTG 660 GCTATCCTGG TTTATGGCCA CTCTTGACAG AGAAACCTCA AGACCAAATT AGATAAAAAT 720 CACAATGGCT TGACCACCTG CCAAAAGCAA ACTCATTATA TCCCGCTCTT TAAACTTCCC 780 CATGTATACT CAATATTATG TTTCACTACA AAAGACGTAT TTTTAAACAT GAAGAGGCAT 840 CCCTGACTCT CTCTCTCCCT TACATCTGGA GAAAACTTGC ATCCCCATTT ACATGTGCAG 900 TACTGATTAC GCCTGCTGTG CTGGCATTAA CAATAGCATT GCCATTCATT TCCACAATCA 960 CCCCAATTTA GATGGTAAAT TATATGGTCA TCCTTTTTAG AGTCCTTATC 1010
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