Tag | Content |
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EnhancerAtlas ID | HS018-01152 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr1:117129200-117129720 |
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) |
NEUROG1 | MA0623.2 | chr1:117129519-117129529 | GACATATGTC | + | 6.02 | NEUROG1 | MA0623.2 | chr1:117129519-117129529 | GACATATGTC | - | 6.02 | NFKB1 | MA0105.4 | chr1:117129278-117129291 | AGGGAAATCCCCT | - | 6.15 | NFKB1 | MA0105.4 | chr1:117129278-117129291 | AGGGAAATCCCCT | + | 6.1 | REL | MA0101.1 | chr1:117129280-117129290 | GGAAATCCCC | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_59077 | chr1:117079459-117152311 | Ly3 |
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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 |
GH01I116586 | chr1 | 117129425 | 117129730 |
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Enhancer Sequence | AGACTTCACT AAATGTGTTG AGGGGGGTCC TTCTAGTCCT TCCGCACTGT CCCACTTAGC 60 TTGATTGTAG TCTCAGAGAG GGAAATCCCC TCAATAAATT TAGGATCCTC CAAGAATCTC 120 TTGGTTTCAG TACAAATGAG GAAAGGAAAA AATGGTGATG ACTAGAGTGG AAATGCAGAG 180 TGGTGGGGGT GATCATGTTC TTTCAGTAGA GAAAATAATC AGAACTGAAA ACAGATGAAA 240 AATAGGAACC AAAAGAACAC TGGTGGGCCT AATGACAACC TTCAATGTTC AAAAGCCCCA 300 GGGACTGGCC TGAAGTCAGG ACATATGTCA CCGAAAATGC CAATGGGAAT CACTTCAGAC 360 CAGAGCTTCC TGTTTAATGC ACCAGCAGAG GTTAGCAGAA AATGCCACCG AGAGGCCAGT 420 GAGAATCTCT GGAAATATAA TAACCTCAGG CAAAGGAGGG GAACAGACTC ACTGCATTCA 480 GCAGGGCACA GGCCACATGT GGAGTTTGGT ATCGGGTTCC 520
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