| Tag | Content |
|---|
EnhancerAtlas ID | HS053-02457 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr1:146763360-146764940 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUND(var.2) | MA0492.1 | chr1:146764771-146764786 | TGTGGTGATGTCATC | + | 6.03 |
| | | 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 |
| GH01I147291 | chr1 | 146762954 | 146765694 |
| Enhancer Sequence | CACAGACTAG GTAGCTTAAA CAACAGAAAT GTATTTCCTT ATAGTTCTGG AGGCTGAAAG 60
TCCAAGATCA AGGTATCAGC AGGTTTGGTT TCTCCCGAGG ATTCTCTCCT TGGCTTGCAG 120
ATGGCGGTCA TCTTGCTGTG CATGCACAAC CCTGGTGTCT GTGTGTCCAG GTTTCCTTTC 180
TTGTAAGGAT AGCACTCAGA ATGGATCAGG CCCCACCCTA AACCCTTGTT TTAACTTCAT 240
TGCCCCTTTA AAGACTCTGT CTCTAAATAC AGTAAACATG AGGTACGGGG GGTTGGGGCT 300
TCAATATATG AATTTGGGGG GACACAGTTC AGCCTATAAC AAGCAGATTG GGCCATAGTC 360
TCCACTGTAC TTCCCCTGTC CCCAGGCTTC CATCCATCTG TCCCCGGAGC ACCGTCCAGA 420
TAGCAGATCC CATCTTAAGT ACGAGGATTT CTATTTGTCT TTTTATCCTC AGTACCCTAC 480
ATAGTACTAG CTCATAAGAA ATGCTCCATA AACATTTACT GCATGAGTAA GAAAGCATGA 540
CTCAGAACTC TGACGGTTTC ATTTCTTACC ATGTGAAAAT TTCTATGAAA GATTGTGTTT 600
TCTAGTCAGC CATAATAAAG CAGGAGAGAG GAACTAACAC ATATGTCCTC TGCCCACATC 660
AGAATCCTTT TGCATCTTAG GCATCTTGGG ATGCCTGCAG TGAGTTTGAT TAACCCCACC 720
TACCTGGCTT TCTCCAAGGC CTGGGTTCAT GTTCAGATTT TAAGCCAGAA TTAAGAAATT 780
TCAAAATCAG GCCAAAAGAG AGGTTCATCC TTTTGAGGTT GCTGTCTATG TGACTGTGTT 840
AGGCTGTTTT TGCACTGTGA TAAAAGAATT CCCTGAGACT GGGTAATTTA CAAAGAAAAG 900
AGATTTATTT GCTCATGGTT CTGCATGCTG TACAGGAAGC CTGATACTGA CATCTGCTCC 960
TGCTGGGGGC TTCAGGAAGC TCACAGTCAT GGTGGAAGGC AAAGGGGAAG CTAGTTTATC 1020
ACACATGGCA AGAGCAGGAA CAAGAGAGAG TGGGGGAAGG TGCCACACTG CTTTAAATAA 1080
CGAGATGTCA TGTGAACTAC CAGAGCAAGA ACTCATCACC AAGGGTATGG CATTAAGCCA 1140
TCCATGAGGG ATCCACCCCA TGATCCAATA CCTCCCACTA GGCCCCACCT CCAACACTGG 1200
GGATTACATC CTAACATGAG ATTTGGAGGG GGACACACAT CCAAACTACA CAGTGACTAA 1260
CAGCAAAGTG GTTTCTGTTG AGTCATTCCT TCAGTAATTT CTAAAATGCT AAAAAAGGAG 1320
AAAAGTAAAG TGTCTGTGCA TGAGAAACTC AGAATCCAGT GATTCAGGAA AACTGTTTAC 1380
AGGGAGTAGA GCACCATGTC TATGATATGA CTGTGGTGAT GTCATCCCGG AAGCTCCCTT 1440
GACACTCTCC AGCTCTGCCC ACTTAGGTTA GGATGGTTGA GAGATACTTG GCATTTTGTC 1500
CTCATGGGAA TTGTTCGAAC AGAGATGGAA TGACTGCTTG TCCTGGGGGT TGTGGAGCTG 1560
ACTCAGGCAT CAAAGGGCTG 1580
|
| |
|
|
|
