| Tag | Content |
|---|
EnhancerAtlas ID | HS086-01263 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr1:223306600-223307970 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:223307176-223307195 | AGACCAGCAGAGGGCGCAA | + | 6.93 | | Gfi1b | MA0483.1 | chr1:223307445-223307456 | AAATCACAGCA | + | 6.62 | | ZNF263 | MA0528.1 | chr1:223306991-223307012 | TTCACTTCCCCTTCCTCCCCA | - | 6.21 | | ZNF263 | MA0528.1 | chr1:223307075-223307096 | TGAGGAGGAGGGGATGGATGG | + | 6.55 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATTACACTGT GGAGCTCGGA TTTGAATCCC GCTGCAAACT TAGTTGTCAC TGTGACCTTT 60
GAACAAAACA AAATTGAATA TGCTGCAAAA CATCCACAGA GCCTCAAAGC GAGCTCGGAA 120
CCTGAAACGG CCCGCCTGAG ACCTCCTTGA AACGGTGATT CTGATTCATC AGGGCTGTGG 180
CTGAAGGACC TGAGAGTCTG CATTTCTAAC GGGCTCCCAC GTGATGCTGC TGCTGGTCCA 240
CTGACCACAC TGTTAGCGGT GAGAACCTAA GAGTCTGTAA TTGCCTCCCT GCTCATTACC 300
CCCATGCCCA CGTGAGCTGC CTCGTTCTTC CAGGATAAGG CATGGCTAAG ATGCTGCACG 360
ATTGGTTTTG AGAAGGGGCT ATACTAATAC ATTCACTTCC CCTTCCTCCC CATTTTTCTC 420
AGCGCTGAAG AGTGAAGCAT CAGAGAGTAC CTCAAAGAAG ATTCATGTGA GGCTTTGAGG 480
AGGAGGGGAT GGATGGGTCA TATCGCTTTA CTAGGAGCTA AGGAAACGGG ACAGCTTGGG 540
TGCGACTTCT GATTTCAGGA GATGCGCTTT CCCTAGAGAC CAGCAGAGGG CGCAAAAGGG 600
GCAGGGACCG AGGGGGAGGA GCCCGCGGAG CCGCGGCCGG AGAGTCGAGC GGGGCGCGGG 660
GAGCTGCAAG CGTCCCTGAG CTGAGCTCCG CTGGGAAGTT CCTATCGCTT GCGCAGTAGA 720
GTGCATTTAG ACATTTCAAT GACAACTAAA TTTGTAGCTG GATTCAAATC CTAGCTCCAC 780
AGTTTAGTAG GTGTGTGAGC TTGGGCGAGT GCTGAACCTC TCTAAGCATC AGTTTACTGC 840
CTATAAAATC ACAGCAATAA GTTTCTACCT CCCACCCCCG CCGCCCCTAC CCCGGCAGCA 900
ACAGCCTGCT TCCGGCTTCC AGGGATCCTC CAGTGCCCAA ACCAGAATAT CCAGTTACCC 960
ATGCTTAATA CTCCAACAGT TCTTGCTTGC TGAAGTAGGC AGCCATCATT TACGCAACTA 1020
CACCTTACCA GAAACGCCTT CCCTTTAGAA CACTGAAGGG GAAAGTTAGA GAGGGAAAGG 1080
AAATTTCTCA AGGCACTGGG GTGATTTTGT GTTTCTTTAG CATGAGTTAC CGGAAAGCTT 1140
CCTGTGTTTT CTTTACTATC TTTAGGTGGT GGTTCCCAGC ATCAAAAAAC AGCAAAAACA 1200
GCAGCAAGCA AAGGCGCTGA TACTCTGAAA AGTTATGTTG AAAACACATG GTTTAGGTAC 1260
AGAATGGCTT CCCCGTTGTT TGCACATTAT AACTCTTTAG CACACAATTT TAAAGCATCT 1320
GATTGAAAGA AATAATTTTT AGTGATTATT AAAAACGAAC AACTAGCACA 1370
|
