| Tag | Content |
|---|
EnhancerAtlas ID | HS037-10217 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr13:47224850-47226350 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr13:47225428-47225449 | TTTTAGTTTTGTTTTTAGTTT | + | 6.15 | | IRF9 | MA0653.1 | chr13:47225774-47225789 | AACAAAAGCGAAACT | + | 6.52 | | Stat6 | MA0520.1 | chr13:47225822-47225837 | ATTTCTGTAGAAGTG | - | 6.05 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 47224954 | 47225004 | | chr13 | 47225277 | 47225344 |
|
Enhancer Sequence | AAGGAGCAAA AAAAAAAAAA AAAAAAAGAG AAAGCCTGGG TGATCTTTGG CAATTATTGG 60
TAACATTGGG CTTTGCTACC TAGTACTAAT TGAGCCCATT CACTTTAAGC CTTCTTAAGA 120
AAGTTGAGGA GCACTGAACA ACTCTAGCCA GATACAAAGT TTGCTATCTA TCTTTACATC 180
CCGCTAACTT AGGTCAGTGT TTGCTGAGCA TGGTTTAGTA ATGTGCATTG ATTGATTATG 240
CACAACATAA TATCATATAT TAATGCCCCT GAGTAGCTCT GATATTAAGA AAATCAGTTA 300
TTTTAAGGCC TTGGTTTTAG ACTTTGCAGC TAGGTTCTCT GGTCAAATTC TAAATCCTTT 360
CCCCATATCT GGGATGTCAG GAGAGAAAGG GAAGCTGTTT CATCAAATAT ATCTTTACGG 420
TGAATACAAG ATCCCCAATT GCAAGCCTGA ATGTAGCCTT TACTCATGTC ATTGCGTCAT 480
GTTAGTGTGC AAAGGGGAGC AAGACTTGTG TTGAATAACA GATATACCCA ACATCAAAGT 540
TCAGAAAGTT CAATGAACCA GGTATAATGT CAGTGGTTTT TTAGTTTTGT TTTTAGTTTT 600
GATTTAGTTG GCTACTGAAA ATTACTGGTT TTGTCTTGTT TTCCTTGCAG TCAAAAATGA 660
GTTTCTGGCC GGGTGTGGTG GCTCAGGCCT GTAATCCCAG CACTTTGGGA GGCCGAGGCG 720
GAGGGATCGC CTGTCAGGAG TTCGAGACCA GCCTGGCCAA CACGGTGGAA CCCCGTCTCT 780
ACTAAAAATA CAAAATTAGC TGGGCGTGGT GGCGCATGCC TATAATCCCA GCTACTCAAC 840
GAAGCTGAGG CAGGAGAATC GCTTGAACCC GGGAGGCAGA GGTTGCGGTG AGCCAAGATA 900
GCGCCATTGC ACTCCGGCCT GGGTAACAAA AGCGAAACTC CATGTCAAAA AAAAAAAAAG 960
AGTTTAAGTT GCATTTCTGT AGAAGTGCTT TTTTTTTTTT TTTGATATGC AGTCTCACTC 1020
TGTCACCCAG GCTGGAGTGC AGTGGCGCCA TCTCAGCTCA CTGCAAGCTC CGCCTCCCGG 1080
GTTCACACCA TTCTCCTGCC TCAGCCTCCC AAGTAGCTGG GACTACAGGC GCCGGCCACC 1140
AGGCCTGCTG ATGTTTTGTT TTTTTTGTTT TGTTTTGTTT TGTTTGTTTT GAGACGGAGT 1200
CTTGCTCTGT CGCCCAGGCT GGAGTGCAGT GGCGCGATCT CGGCTCACTG CAAGCTCCGC 1260
CTCCCGGGTT CACGCCATTC TCCTGCCTCA GCCTCCCAAG TAGCTGGGAC TACAGGCGCC 1320
GGCCACCAGG CCTGCTGATG TTTTTTTTTT TTTTTTTTTT GTTTTGTTTT GTTTGTTTTG 1380
AGACGGAGTC TTGCTCTGTC GCCCAGGCTG GAGTGCAGTG GCGCGATCTC GGCTCACTGC 1440
AAGCTCCGCC TCCCGGGTTC ACGCCGTTCT ACTGCCTCAG CCTACTGAGT AGCTGGGACT 1500
|
