| Tag | Content |
|---|
EnhancerAtlas ID | HS098-35858 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr21:38432300-38433740 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX5 | MA0510.2 | chr21:38432711-38432727 | GGTTGCCTTAGAAACC | + | 6.08 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr21 | 38432359 | 38433260 | | chr21 | 38433494 | 38433599 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH21I037059 | chr21 | 38431865 | 38434432 |
| Enhancer Sequence | TACAGGTGTG AGCCACCGCG CCCAACCCCC CATATTCTTT ATACCCCTGG GAAGAGCTGT 60
GACTTAGCCG ATGGGTGAAA ACGAGCCAAG AGTGACTGCA TGGAGTTGTC TGCTATCCAC 120
CTGGCCCTGC CACCTCCTGA GCATGCAGCT GGTCAGGCCA TGTCTCCAGG TCTGCAGGCC 180
CAGTCCTCCT CACATCAGTC CCCAAGTCTA GATTTAGGGA AGAAAGCATG ATTTTGGCTT 240
CAGGCTTATG CAGCACTTGA AAATCGGGCT CCATCAGCAA TAAGGTAGAC ACTGCATTTT 300
AATTCTTGCC AGGTGCGTAA GTCCTTCACA GAATGGTGGT GAGGAGTGAG TGACTGAACT 360
TTCCCCAGGA TGTGCCCACC CATGGTGCAT TCACTGAGAA CATTCAAAAG AGGTTGCCTT 420
AGAAACCAAA GTATCACAGG GAGAGATGGG CCTCTTGGGG CAGCAGCAGC AGCTGAAGCA 480
GGCTGACTCA CAGCTGCTTC TAATATGCTA GGCTTTGTGT AAACAGGCTT TATGACACAA 540
GTGGGCTGAC TACAGTGCAA TTGGAGTGTG GCATCTGAGT CACTGTGAGG CTCTAGCTGG 600
CTTCTTCCAG CCCTGGCCAT AGGGTCCCCT GTGACTGTAA CCTATACAAG CAGAGCTTGG 660
GCATGCTGGA TTTGCAGAAA TAACCTTAGG CAGGTATTGA ATTATTGGAC ATTAACTTCC 720
CCTGCATTGT GTGAAAATAT AAATCTTGGT CCACAAATGC CCTTGTTCAA GACTGTATTT 780
TCCACAATGC CATCATTTCT CACTCTGTGA GTCCTTTGGT CCCTAATTGA GATTTCCATT 840
GCATTTCTGA CCTCTGAGAC TTAAGTGGTG ATGAGGCACA GAGAGGAAAA GAATATCTGG 900
TCCTCAGTCA TAGGTCCAGA TAGGTAATCA CTGAAACATC CACTGTGCTT GTCCATGTGG 960
CCCTGTTCAG ATTTGGTGGC TACCTCAAAG TGCAGTTCTT TGAAAACTAA ACTGTTATGT 1020
TAAGCCATTG ACAATTTAGG ATTATTATTT ATTTATTTAT TTTACCATGG AATGACAAAC 1080
TCTCCTGACT AGAAAAGGTG GGATAAGTAC ATTTCCTCCC AACCCAAAAT AGTAAATAGT 1140
GCCACCATGA ACCTAATTGT GTTAAACTGA GTGACTGAGA CCCATGAAAA CTGCCATAGC 1200
CTGACCTGCA CCCCAGCACG ATGAATCAAG AAGAATCTCT CTTTCCTCTT CCGTTTTCTG 1260
TCTTCCTTTC CCCATGTCCC ATCAAGTCTG TTCTAGTTAC TGGCTGGTGG GTCTGTACTA 1320
TACAATGTAC TGGGTTCCAT CACTATTGCT GTAGGAGTTG ATTTATTTGG ATTTTCAAAG 1380
TTCCATGGGC ATGGGACTGT TAATATGACA TTTTCATATA GCCTACTGAA TCTTTAAAAA 1440
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