| Tag | Content |
|---|
EnhancerAtlas ID | HS078-11740 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr22:44657560-44659080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr22:44657727-44657744 | CAGGTCACCTTGCCCCT | - | 6.45 | | ESR2 | MA0258.2 | chr22:44657728-44657743 | AGGTCACCTTGCCCC | + | 7.16 | | IRF1 | MA0050.2 | chr22:44658949-44658970 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 |
|
| | 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 |
| GH22I044262 | chr22 | 44658661 | 44658810 |
|
Enhancer Sequence | GAAGGAATCT TTGGCAAATG TCAACTCTTG TTCTGCTCTC ACGGCAAACA CGCCTTGGTC 60
ACATACCCGT GAGTGCAGGA AACTGTTCCT GTGTGGCCAC TGACTCCTGC CACGGAGAGC 120
ACTCGCCTGC CCTGATGCGG GGGTCATGTG TCCTCCTAGG CACTCTGCAG GTCACCTTGC 180
CCCTCATGGC CAGTTCTGTG GACCCCAGGC TCAGGCCCAC CAGTGCTCCC CTCACTCAGT 240
GGCAACTTGT GGCCCCTCAC ACTAGGCCTT CCATAAGCTG GAACTATAGC ACCTTCGGCC 300
AGGGCCTGGG CTGGGGGCTC AGAACTGAGT CAGGTGTGGG CCCTGCCCTT GAGGGCTCGA 360
AGCGGGTAGG GGAGCCACAC CAGGACCCTG AAACAAGAGC AGCAGACCCA CACTGTGTCA 420
GCGGCGAGTG TCTGGCAGTC TTGGGGTCCT GGCCAGGGTG GGAATTGGGG GAAAAGTTCT 480
TGGGAGCAGC CACAGAGCTG GGCCCTGGAC AAGGCTTGTT GGGACGACAG GGAGGGCACT 540
CCAGGCGGAC GGAACAGCCT CAGCCAAGGT CATTCAGAGG ATCACAAGGA GCATGGCTGT 600
CATGGCACAA GATGCTCCTG GCAGGGGTGA GTCTGCAGAG GCGGCAGCCA CAAAGCCTTC 660
ATCTGCCAGG AGAAGGTGTC TGGACCTGAT CCCAAAGTTG TGGGGAGCCG ACATGGAAGA 720
TCATGCCTAA TTCTCATAGC AGCAAGATTA GGGCTGCAGG GTACTGATTA TCTCTTCTGT 780
GCCGGGCACT GTGCCAAGCA CCTCCCATGC GTGTGGAGCC TCAGTTCTCT CAGCAGCCTC 840
AGGGGTGGGG ACCACTAGTC CCTGCAACTT GCTGATGAGG AAAATGAGGC TCAGAGAGAC 900
AATGTCACTA GCCCAGAACT GCATATCTAG CTAGCAGTGG AGCTTGGCCT GTGCTGCTGA 960
CCGCAGGGCC ACACGGCCAG CCCCTCTCGT CTGGGGCAGT GGCCTGGGCA GGCTGGGGAG 1020
TAGCAGGCTG CCCTGCTGGC CCTAGTGGCC CTGGCGAGAG AGGAGCTGAG CCTGGAACCA 1080
GGAGCAGGGC CCACGGGGTG AGGAGGGTCT GCAGCTGGCA GGCCTGGTGG GCTGGTGCCT 1140
GCAACCTAAG TGGGAAGATA ACAGAGCACC TGGTAATTTG AATAACAATG AAAGCTTCCA 1200
GAATGTGGAA CATCTGTGAC AATAACCCTT CCCGCAGACG AAAGCAGAGG AGTCATGAGG 1260
CACAACACGC CTCATTCCAG GTGAACTGGA GACAATGTGT TCCCCAGCAG CAGCAACAGC 1320
TTCTGTTAGT TAGTTGGTGC TGACGGTATG CATGTGGGGT GTGGGGCTGG GAGCCTTCAC 1380
GTATTTTTTT CTTTCTTTCT TTTTTTTTTT TTTTTTTTTG GAGATGGAGT CTGTGTCGCC 1440
CAGGCAATAG CGCAATCTTG GCTCACTGCA ACCTCCGCCA CCCGGGTTCC AGCGATTCTC 1500
CTGCCTCAGC CTCCCGAGTA 1520
|
