| Tag | Content |
|---|
EnhancerAtlas ID | HS069-04652 | Organism | Homo sapiens | Tissue/cell | GM18951 | Coordinate | chr2:39454710-39456390 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:39455413-39455432 | GCGCGCCCTCTGCTGGCTG | - | 6.67 |
| | | 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 |
| GH02I039227 | chr2 | 39454785 | 39456341 |
| Enhancer Sequence | AAAAAAAAGA GAGAAGCCCA AAGCACCAAA CCAATTTGTT TTCTATGTGC TCCACTGCCT 60
AAAAGAGCAG AAAGGCAAAG AGTGGAAGAG ACTAGGTCAT CTAAAAAGCC AGTGGCTTTG 120
TGCCGCTGCA AAACCACAGT ATGGAAGCAA AGCAGGATCT CTACTAGGGG AGTAAAAGAT 180
TTACAGATAC TACAGTTTGA TGCAATGTCA AGGTTAAACC TGGTCCAATC TCCTGTCTTT 240
GGGTAGGTCA GCAATTTATA CCGCCTTTGC AAATGAAGTT AACCTAGCCC AGGAAAACAG 300
TAACTTGCCT AAAGAAAAAC AGGTGGTAAG GACAGAGAGG CAAGCAATTT AAATAACAAG 360
ACTATGTGAG GAAAGGAAGG TCGACTGATC ACAGAAGGAG CTGTTCAGGA CCTACATGGA 420
CACAACATAC CAAAAGCAGA AAGATGGACG TTCTGACATT CTGAGGGCCT TCATCAGAGA 480
CCAAGCTGAG TCATAATCAG GCTAGTTTTT ACCTTACAGC CTCATTCTCC AGTTGGGCAC 540
TTGTAATGCA GAAGGTACTA CCTGAGCATT AACTTTATCT GAAGACTTGG GACGGAGAGG 600
CTGACAGGTA AAAGCATTAT TTTTATTAGA AAGCCACACT GCTTGGTTCA GACCCGCCCT 660
GCAGCTTAGC TCAGTGAGGG TGCCAGAGCT GGCTAGCTGA CCGGCGCGCC CTCTGCTGGC 720
TGAGAGGTAA GAGTGAACTT TTTTTTATCA TGATGGATGT GTTCCTGAAG ACTGTATCAA 780
GTTATATTTC AAACAAAACC CTAGTGTGTA TTAGTTGAGG AAACCTGTGG GAAATAATAT 840
TTGAAAATGA GAGAAAACAT GATAATTATT AGTGATAATT ATTATCCTCC CTTACAAACT 900
GAATTTCTGG GGATTTTCTA AAAACAGACG ACGTGTCAAA AATGAAGGTT GCCTGTGTGT 960
CCTTGAAATC ACAGGGTCTT GTCACATAAT GTGTAGCCCA CAAACCAGCA GCTTCCGCAC 1020
TTCCTGCGTA CTCAGAAATG CAGAATCTCG GGCCCACCCC AGACCTCCCA ACTCAGAATC 1080
TGCATTTCAA CAAGGTCCCC GGGGATTCCA ATGCATATTA ACATTTGAGA AGTGCTGCCC 1140
CAGACCTCCG TTTCCTCTGC GGAAAATATG GTTGTTAGAT AAGAAGCATC TCTACGGTCG 1200
CTTATAGATC TAAAACTGTA AGATATTTAG CGTAAGAAAA AATTTACATT GAGAACTTAG 1260
GAATCTTACA TGTCAAATCT TATCAGAGTG AAAACAATTA TAACAAAAAC CTTTATGTAA 1320
AAAATGTGTA CGTTACCGGG GGTGCTATTC AGTATGTCTA AGAACCTGGG GTGCAGTGCA 1380
GGCAGGAACC AACGCATGTC GATGCCTACC AGGGCATTGG TGCGGTCCTG TGGGACTGAC 1440
TCTCTGTGCC AGGAGGTGCT CTTTTAGTTG CTGGTTGGTA GGGGAAGTAT TTGGAGGGAT 1500
ATCCAGAGGA GGGCCAGGGT TGGGGGCGAG CGTAAACACT GGGGTGAGTG GACTTAGGAT 1560
ATTTACTAAC AAGAATAAAA GTTCTTTTCA GTATAACAAT CTATAGCTGT ATTCATACAC 1620
AGACAAAATC AGAGTGGCCG AAGTCCAAAG TGATAATCAA CTTATTACCC AAAGGTGCTG 1680
|
| |
|
|
|
