| Tag | Content |
|---|
EnhancerAtlas ID | HS044-08205 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr20:55683630-55684790 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr20:55683719-55683731 | GGGCACGTGGCT | - | 6.18 | | ZNF263 | MA0528.1 | chr20:55683873-55683894 | CCTCCTTCTTCATCCTGCTCT | - | 6.11 | | ZNF263 | MA0528.1 | chr20:55683860-55683881 | CTCCCTGCCTCTGCCTCCTTC | - | 6.13 |
|
| | 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 |
| GH20I057108 | chr20 | 55683721 | 55685130 |
|
Enhancer Sequence | CAGGTCCCAG GAGGGCAGGA TGGACCCCAC CTGTCGATGA GTGCAACAGC ATAGTCACAC 60
TACCAACAGT AAGGTCAGAG GGAGTGGTGG GGCACGTGGC TGTTTAAAAA CTCTACCACT 120
AGGAAGATGA CAGCAGAAAG CTGCCCAGGT ATTTTTTTTT TTCTCTCTCT CTCTGCACCT 180
GCACCACTCA CATTCCACAT CTGACCATTG GGAAATTCTT CCTCTGACAC CTCCCTGCCT 240
CTGCCTCCTT CTTCATCCTG CTCTGATTTC AGCCTAGGAC ACCTTTGCTG GGTAAATCTG 300
CCACCGTGGA GCTGAGAAAA GACCCACGAG GCCCCCGGCA GGCCATCCCC AGCACTGAAG 360
GTTCCTGGCG CCTGATGCCA GCACGCTGGA CCTCAAGGGG GCCACAGGAC TTCTCAGCTC 420
AGCTCTTGAT TTTTCAACCA CCAAGTCATA AAAGCTTCCA CGGAAATGGC CAGGAAAGCC 480
CCTGTAGCCC TTTTGTAGTG CTGGTTTCTG GGTTGGCCTG ACCAGCAAGG ATCTTTCCAG 540
ATCTGCAGTA AAATCTGACC TTCGATTCAA CCCGGCTTAA TGAGTACGTA CGGCTCACAA 600
AGGCCCGGCA CAGTCCCCAG AGCTGCTTTG GGGTGAGGCC TCCAGCCACG GGGCCAGCCC 660
TTCCCTGTGA TCTCAGTGCC CCCTCCCAGT CCCCACAGAG CCAGCAGTGG CAGCTGCGGG 720
GCTGCAGTTT GGGAAACGAA CTGAGGCAAG AGGAGGAAAC ACTGAGAGCT GGAGCAAACC 780
CAGCTGCTGG GAAGTCCCCG CAGGGCCAGC CAGACCTCCA GAAGGCCTGG AGGGTCCCAG 840
CCTCTTTGCT TGCACAATGT AATGAGGCCG TTACCAGGGT GGACCTAGCA TCAGACTGCC 900
TGAGTTCAAA GTCCTGCCCT GCCGCTCACC AGCTTGTGAT CTGAACACGA GGCTCACCCT 960
CTCTGAATGC ATATTAGCCA TCCTCAAGGT GGGGTTAAGA GCATCCACCG CCCAGGCTCA 1020
CTGTATGGAC GAAAGAAGAG CCACGAGGAA AGCTCAATAA ATATTAGCTC TAATTGTTAT 1080
TGCAGGCTTG GAGCACACCT CACTAATTTG GAAGGCCCAG CGCAGAGGAA CCACGCCCAG 1140
CCCAGCAATG AGAAAGCTTG 1160
|
