Tag | Content |
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EnhancerAtlas ID | HS176-22884 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:210506910-210507710 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr2:210507381-210507392 | ATGAGTCATCC | - | 6.62 | Foxq1 | MA0040.1 | chr2:210507346-210507357 | AATTGTTTATT | + | 6.02 | GSC | MA0648.1 | chr2:210507003-210507013 | GGGGATTAGC | - | 6.02 | IRF1 | MA0050.2 | chr2:210507161-210507182 | AAAAAGAAAGAAAAAGAAGAA | - | 6.34 | IRF1 | MA0050.2 | chr2:210507155-210507176 | AAAAAAAAAAAGAAAGAAAAA | - | 6.59 | JUN(var.2) | MA0489.1 | chr2:210507381-210507395 | ATGAGTCATCCTTA | - | 6.02 | JUNB | MA0490.1 | chr2:210507381-210507392 | ATGAGTCATCC | - | 6.62 | NFE2L1 | MA0089.2 | chr2:210507377-210507392 | AATGATGAGTCATCC | - | 6.33 |
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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 |
GH02I209639 | chr2 | 210504655 | 210507806 |
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Enhancer Sequence | AATCCCAGTG TTTTGGAAGG CTGAGGCAGA GGAATTGCTT GAGGCCAGGA TTCCAGGCAA 60 CATAACAAGA CCCATCTCTT GGTGGTGGAT GGGGGGGATT AGCTGGCTAT AGTGATGTGC 120 ACTTATAATC TTAGCTACTC AGGAGGCTGA GGCTTGCTTG AGCCCAGGTG TTTGAGACTG 180 CAGCGAGCTA TGATTGTGTC TCCGCATTCC AGCCTGAGTG ACAGTGTGAG ACCCTGTCTT 240 TGAAAAAAAA AAAAAAGAAA GAAAAAGAAG AAAACACAAA ATAATAACAA GTAGTAGGTA 300 ACATTTCTTA AGCCCTTCCA ACTTGTCTGA ACTTATACTT TATTTGTACT ATCTATTTCT 360 AGCAATAACC TAATGTTATC TGTGCCTATG ATCATTTGAA ATTACGTGTT ATGCACCCAC 420 CAGCTCTCTT CTTTCTAATT GTTTATTAGT CATGGTATGT GATGAAGAAT GATGAGTCAT 480 CCTTATAGGT ATTTTACAAT CAGCCTGAAA TAAAGCAGGG AAGATATGAA ACAAATATCT 540 GGATTTTCAG CATATCTTTT TCATGTTATC AAGAACCTTT TCCTCTGTTT TTCTTAGAAG 600 ACAAAGAGGG AGAATATAGA GTTGCAGGCA GCTTATTAAC AAATGTTTAA GCTTAGAACT 660 TCTCAGCATT TATAAGCAAA AATATGGATT CTGCATAAAC TTCTAATACC ATTAAGGACC 720 AAAACAAAAG TTTCTATTTT GTGATACTGA TATGCATAGT AACAGTATAA AGCATAATTG 780 AGCCTACATG GAAAAGAGAA 800
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