| Tag | Content |
|---|
EnhancerAtlas ID | HS052-01929 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:92389320-92390550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:92389724-92389745 | ACCATCTTTTACTTTCATTTT | + | 6.1 | | MYCN | MA0104.4 | chr1:92389851-92389863 | GACCACGTGGCC | + | 6.52 | | MYCN | MA0104.4 | chr1:92389851-92389863 | GACCACGTGGCC | - | 6.52 | | RREB1 | MA0073.1 | chr1:92390180-92390200 | CCCCCACCCACCCACACACA | + | 8.61 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I091923 | chr1 | 92389391 | 92390469 |
|
Enhancer Sequence | CGGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCG CGCCCGGCCA GGAATAACTT 60
CCTATGTGTC TGTGGGTCCT GCATCACCCC AAACATGTCC TTCCACTCTG CATTCTTCCC 120
CTGAATTAGT CACTCTCATA ATCCATTTTA GTAAAGCATC CTCAGGAAGC CAATGACACC 180
AGTCTACAAA ATGGAACGAT TCCTTCACAC TCTCCTTCTG GTTTCAATAG TTACTTGGTT 240
TTGCCCTTCC TTCACATTGA CTACCTTCTT GGTAACCACA GATCTCAGAG GCACATTCTG 300
TTGTCCCTGT ATAATTTTCT CCTTTGTGGG TGACTTTGAG GCTAGTGGCC TGAGCTCAGA 360
CAGACCCACA TCTGAGGTTG GTCAGCCTCA AGTCCTGACC CAGCACCATC TTTTACTTTC 420
ATTTTAGCCA TTGCAGATAA CAATAACCAA TGAATTAAAT ATCTTAACTC CACTTGTAAC 480
TTTTACCTTT AGTAACTGAT CTCAACACAG CTGTGGCTTC ATACCGTGGG TGACCACGTG 540
GCCACCCAGA AATCAAAGAT TTCTCATCCC CACCCTTTTA TTGTTTCTCT TCCCAAACCA 600
CATGTTTCCA TGAGTCAGAG CCATTCCAGC AAATCCTGCT TCACTGACAT CAGTTGTGTA 660
GGGAAAACTC TAACTGTGTT TTTCCTCTAC TCTCACACCA CAACAATCAT CAACACAAAA 720
GGAGACTTCT GTGACCATAT GTATGGGTTT ATTTTCCCCT GGACACCAAG CAGTGGACAC 780
CATCTGGGTG TCTTCTAATT CAGTTCCAAC ACTGTCTACC GGAATAGTGT CAGATCCCAC 840
AGGTTGAGAC CAAGACTGGC CCCCCACCCA CCCACACACA CCAGTCTCAC GTCCAGGCCT 900
CCAGAACTTC TAACCAACTG GCTTCAAGTT GGGGTTCCTA TGTCCCCCTC TTTGAGTTTG 960
ATTAATTCGC TGGAGTGGCT CACAGAACTC AGGGAAACAC TTACTTGTGT TTACCGGTTT 1020
ATTATAAAGC ATATTGCAAA GGATACAGAT GAAGAAACAC GTAGGGCAAA GTATGGGTGA 1080
AGGGTGTGGA GTTTCCATGC CCTCCCTGGG TGCGCCACCC TCCAGGAACC TCTGTGTGTT 1140
CAGCTGTCTG GAATCTCTGT ATCATCAATT TCTGCCTCCA TTTTCACATG GTCTTCTCCA 1200
CTTTTGTCTG TGTTTGTCCT CTGAGTGTCT 1230
|
