| Tag | Content |
|---|
EnhancerAtlas ID | HS099-14532 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr22:24500630-24501740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arid3b | MA0601.1 | chr22:24501376-24501387 | ATATTAATTAG | + | 6.02 | | MEOX2 | MA0706.1 | chr22:24501333-24501343 | AGTAATTAAC | + | 6.02 |
|
| | 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 |
| GH22I024104 | chr22 | 24500256 | 24502221 |
|
Enhancer Sequence | CTTCTCAGCC TGACAATGGG CACCCCGATT TCCCGGGCCA GCCTTGCTTC TGGTGGACGT 60
GTTCTTTTCC TGTGGTTGGC CAGGATTGAC TGAGGCAGCT TTTATCTAGT CAGAAAATTT 120
CTCAAAATAC TAATTCCACC CAAGTTTACG GTTCTTAGAA ACCTGTTGTT TCCTGGTCGG 180
CAGGACATTT GTGGTCTTTT CTGGGGCACT AGTCAGAGCT GTTGCAGTAG CACAAGCATA 240
CATCTTCTTC CTCAGGCTTT CACTGCCCCA GGCTGATGGA ACAAATGGCC GTGAGCTGTT 300
TCTGGTCTTA CTGCTGGAGC AAATGGAGGA AACACACTTA AAGAGACACT GGAAAGTTGC 360
ATCTTGTAAC TAAAGAGCTC TTTTAGGCTG GCCTGAGAAT CCTGGGATTG TCCAAGGGAT 420
CTGAGCTGAG TCAGACCTGA ACAAGGAGGA CTCAGAACAC AGAGTCTTTT CTCACACTGA 480
GTGGGGACAG GCAGCCTTTC TGTCACTGAG CCAGGTCTCT TTCCCTCTGC GTTGCCAGCT 540
GTCATTCCTT TACAGTTGAT CCTGCAAATC CCACCCTGGA AGTAGAAGGT TCTGGAGCTT 600
AGAGGGAGGC AGTTTAATAA GCACTTGGCT GGCAGACGCA CATCCCCCTA AGGATTCAGA 660
GGGAAGGCTG GCGTGGCCCA GATGCATAGA CACGAAACAT TCCAGTAATT AACAGTAACA 720
ATAAAATATT TATAATCTTG CCACAAATAT TAATTAGTAT GAGCAGGTTT TGTGTGGGCA 780
GATTTTTAAA AGAACATTCT GAAAAAAAGA GCAAGGCCAA CCTATAGCCT GCTTGCTAGT 840
GCCATTCTTC TTTCCTGTTG GCCTCCAAGT AGCTCCCTAA AGAAATCAGC TCTCAGCTCC 900
TGAGTCTCAA GGCTAGATAC CTGGACTGTG GACAGTCCCT GGAGGTTCCA TCCAGGGTGC 960
CTGTTTCCCT GGAAGGCTCT CTCCACCCAG CCCCATAGGA AGTTTAGGCT AAGTCTGGCT 1020
CTCCTACATC AAAGAGGCTT TCCATCTGTC TCTTGCTCTG CCTCAGAACC AGGGGGCCCA 1080
GAACCCCCTC CTCACCCAAA AGCCCCTCCA 1110
|
