| Tag | Content |
|---|
EnhancerAtlas ID | HS104-00684 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:20436640-20438100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr1:20437456-20437467 | AATGAGTCACA | - | 6.62 | | Foxd3 | MA0041.1 | chr1:20437173-20437185 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:20437177-20437189 | AAACAAACAAAC | - | 6.32 | | RREB1 | MA0073.1 | chr1:20436841-20436861 | CGGTGGGTGGTGCTGGGGGG | - | 6.28 |
|
| | 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 |
| GH01I020109 | chr1 | 20436265 | 20438010 |
|
Enhancer Sequence | CAGCCAAAGT GAGAGCGGGT TGCAGTCCCT GGCTCTGGGC TTGCTCGCCC AACACAAATT 60
CCATCAGCTA CCCAACCCCT CAGGGACATT GATCCTGTTC CGTCTTGGGG GTAAATAAAT 120
CCTAATGAAT CTAAACCAAC CAGGCTCATC CCATTGTCTT GGGTAACCTC TGGGTTAGGG 180
CGGCCTGTCC TGAAGAGAAG TCGGTGGGTG GTGCTGGGGG GCTTATTAAA AAGACAGAGG 240
AGGCCGGGTG GGGTGGCTCA CACCTGTAAT CCCAGCACTT TGGGAGGCCC AGGCAGGCGG 300
ATCATGAGGT CAGGAGATCG AGACCATCCT GGCTAACATG GTGAAACCCT GTCTCTACTA 360
AAAATACAAA AAATTAGCCG GGCATGGTGG CGGGCGCCTG TAGTCCCAGC TACTCGGGAG 420
GCTGAGGCAG AAGAATGGCT GGGAGGCAGA GCTTGCAGTG AGCTGAGATT GCGCCACTGC 480
ACTCCAGCCT GGGCAACAGA ACGAGACTCC GTCTCAAAAA CAAACAAAAA AGCAAACAAA 540
CAAACAAACA AAAAGACACA GGAAGAGAGG AAGACACAGC GTCTCCTTGG CTGGATGCTG 600
TCACGTCCTG GCCTGCGGGC TGGCATCATG GTTGCCAGCT TGGAGCTGTG AGGGGAGTCA 660
CCTAGAGGGC AAAGCCAACA CACAGAGGTG GCTTGCCAGG AGCAGGAAGG AAACCAGGCC 720
CTGATGATAT CAAGCTCCGA AGAGCCAGAC TTGGAACCAC CTCCTCTCCG AACGTCTCAT 780
CATGTGAGAT CATAAACGCC TGCATTGTTT CAGCCCAATG AGTCACAGTT TTTAGCTGGA 840
AGCTTCTTAA CCAATACAAA CGTGATGCGG CGAGGGAGCG GAGCAAGAAG AGGCTGGGGC 900
GAAGCTGTGG CTCTGCCTTT CTTGGGTTGT GGGACCTCAG GAGGGTCCTC AATTATAAAA 960
TGGGGATCGT AATGGCTAAG TCAGCCAACA TGAATATTAA GAGAGATGTT GCTGCAAAGC 1020
CATAGGGAGC TATTGGGCCA AATTTGGTAG ACAAATAAGA GTCATCAGCT CCCGATGGTG 1080
TCTCTTGAGT AAATGCATCC AGTGTCACTG AGAGAAGACT TGGCGGGAAA GGAGGAGGAC 1140
ACTTTCTCCT CCTGATTTCT CTTGGGGGTG ACTTTAGATC TGGTCACTAC GAAACAACAA 1200
CATTAACCAT GCCGTTAACA TTTAAAGTTA ATACCCTGTG CCAGGTGCCT GCTGTGCTAA 1260
GAATTTAATC TACGCTAATC TTATTTAATA CAAACATGAA CACCTTCTTA TTCTCTTCTT 1320
TTTAAAAAAT TTTCAGTCCA GTGCAGTGGC TCACGACTGT AATCCCAACA TGTTGGGAGG 1380
CCAAGGCAGG AGGATCACTT GAGCCCAGGA GTTTGAGGCC AGCCTAGACA GCATAGTGAG 1440
GCCCCATCTC TACAAAAAAT 1460
|
