| Tag | Content |
|---|
EnhancerAtlas ID | HS104-39184 | Organism | Homo sapiens | Tissue/cell | HUVEC | Coordinate | chr22:44758390-44760230 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr22:44758743-44758754 | GGCCACACCCT | + | 6.32 |
| | | 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 |
| GH22I044357 | chr22 | 44753579 | 44761199 |
| Enhancer Sequence | GAGGAACAAG CAGTTGAGTG AGCCCTGGTG GGTCCATTCA ATGGAGTCCA AAGTAGCTTA 60
CACCAGTTGG TCTGAAAGTT ACACCCAGGG AAATGCAGAA GGTGACCGAT GCCTATTGAA 120
TGACCCTCCA AGCAGCGCCT GGCTCCAAGA AATGCTTTCT GTAAGTTATC TTGTTTATTT 180
TTCTTCCTAA GGAAGCTAGA TATTTTTGTC CCTATTTTAC ACACAAGACT AAAGAACATC 240
TCAAAGGCAG GGATTTGGTC TCCCTCACTT CCCTTCCCAG CACCCAGGAC CCAGCACAAG 300
GCTCCATCCA GTTGACCATA GCAGCAAACA TGGGCACCCA CTGGCTGTGT GCTGGCCACA 360
CCCTGAGCCC TTGACATGGG CTGGCTTATA CCATGCTCAA TGCCCATGGC AAATACTGTG 420
TCAGACCCAT TTCACAGATA AAGAATCTGA AGCCCAGAGG GGCTGTGACT TGTCCAAGGT 480
AAACGCCTAG AACGTGGGGG TGCCAGGAGT CACCCCTGGC ACTGCTGGGC TCCTAGCCCA 540
AGTGTGCAGA CGCTGGCTAT CCTGCCTCTC AGCCCACGGT AGTTGAAGGA CTGAATGAGC 600
GAGTGGCCCT GCTACGTCCT GGCTGCGGGG TCTGCAGTAA GTCCCCTAGA CCTGCTAAGC 660
CCCAGTGTCC TCATCTGTAA AATGGGCTTC CCCCGCTCCC CACCAGGAGC TGCCTTGTGT 720
TGCTGAGAGA GATGTGGCCT GATTCCAGAG ACTCGGCCTC GTTGGGTGGA CTGCCGGCTT 780
TGTGGGGGCA GGGAGGGCGG GGAGCATGGG GCCATCTGCA GCCCCTGGTG CCTGACTATG 840
AGTGTCTGAT GAAGGACCTC ACCCTAGGAC TTGGGGCCCT CAAGGCATGG TGACTCACCC 900
CGGCTCCTTC CTTCCTCCAT GGCCCTGTGT CACTGGCTTA GGAGCCCCCA GCTCAGCAGC 960
CTGCGTGAGC GAGCCCCAAG TGCTCTCAGA CCAGCCCAGG CTCACACCCA GGACATGAGG 1020
CCACGACGAC CACCTGGCAC ATCCCTCTGC TCGCCACAGC CCCGGCCCTG ATGGCTCCCA 1080
GCCCTCTGGA AGGGCCAGCC CGGCTGGATC AGGAACGCCA GTCCGGAGAG TAATGAGGGT 1140
TCCCTGTGGA ATGAGAGAGA CTCCACATGG TTGGCGGCGG CGCCTGGACG GTAGCCAGCA 1200
CTTTTCCAGG GCATTCCGGG AATCCCGCTC TGGCCCCTTG TCTGACGCAC TTTGAGTCAG 1260
CACTTGAGCC AGACGGCCGC TCTGGGCTGG CCAAGAGACA GGCCAAGCGT CCCCACAGGA 1320
GCGCTAGTTG TGTGAGGGAG CCCAGAGTCC CCTGACTTAA ACGGGCCTGG CTCACTGCCC 1380
CCATTTCACA GATGAGAACA CCAAGGTCCA GAGGCAGGGC AACCTGTCCA CCCTGGATAC 1440
TCCCTGTCAA TCATCAGAGT GGCTCCCCTC AGCCCCTGCT CACCCCATCC TCCATCCTGC 1500
CGCATTTATA ATTGCAGTGG TGGGATCATC CTGACCCCAC CTCCCCCTGG GGGGGCTCGC 1560
CCTGACCTGA GGAAGGAGGG GCTGGGCCTC AGGCACAGGG AAGAGGCCCT GGGACTGCCA 1620
CATCCCAGGT CACACACCCC CATCCCCGGG GGACAGAGGC TTCATCTGGT TATTTATGGA 1680
ACTGCCACTC TGTGCCAGAG CCTGCCCAGG ACACGGTTTC TGCCTTTGAA GACATGCATG 1740
GAAGGAGTGA CCTCCAGGCC AGAGCGATAA ATGCCGAAAT GAGGGGAGCA CAGTGGGAGG 1800
ACGGAGCACA GGGATGGAGG CGCTGGGGAC AGCCTCCTGA 1840
|
| |
|
|
|
