| Tag | Content |
|---|
EnhancerAtlas ID | HS058-03204 |
Organism | Homo sapiens |
Tissue/cell | GM10847 |
Coordinate | chr17:3992590-3994010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat6 | MA0520.1 | chr17:3993769-3993784 | CCCTTCCTGAGAAGC | + | 6.05 | | TFAP2A | MA0003.3 | chr17:3992957-3992968 | AGCCTGAGGCG | - | 6.14 | | TFAP2A | MA0003.3 | chr17:3993023-3993034 | AGCCTGAGGCG | - | 6.14 | | TFAP2A | MA0003.3 | chr17:3993558-3993569 | AGCCTGAGGCG | - | 6.14 |
|
| | 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 |
| GH17I004090 | chr17 | 3993941 | 3994842 |
|
Enhancer Sequence | AGGAAAACAG TCCTGTCTAC TCAAATCTAG GGCCATTTTC CAAACCCAAC TTTCATGCAA 60
ACTACCTGCT TCTTATGGTG AGCGCTCTTT GTTAAGGGCC TTTCAGAATA CACTACTCAA 120
CTGCGTAAAT ATTTACCGAG CACCTACTAT TACGTGCCCT TAAGAGAGTT CCTAATTACT 180
TATTTAAGCC TGAGATTTAC ATCCAAGGTT TAGCAAAAAA TTAAGCAGCC AAATAATGAT 240
TGGTCCTTTC TATGGAAAGA CACCTCTCTT GAGTTGATGC CTGTGTTCTC ACTATTCTCT 300
CAGCCTGAGG TGCCCTCCTC CACACACTGT AGCATGGCTA AGGATGCTGT GTTCTCACTA 360
TTCTCTCAGC CTGAGGCGCC CTCCTCCACA CACTGTAGCC TGGCTAAGGA TGCTGTGTTC 420
TCACTATTCT CTCAGCCTGA GGCGCCCTCC TCCACACACT GTAGCCTGGC TAAGGATGCT 480
GTGTTCTCAA CTATTCTCTC AGCCTGAGAC GCCCTCCTCC ACACACTGCA GCCTGGCTAA 540
GGATGCTGTG TTCTCAACTA TTCTCTCAGC CTGAGACGCC CTCCTCCACA CACTGCAGCC 600
TGGCTAAGGA TGCTGTGTTC TCAACTATTC TCTCAGCCTG AGACGCCCTC CTCCACACAC 660
TGCAGCCTGG CTAAGGATGC TGTGTTCTCA ACTATTCTCT CAGCCTGAGA CGCCCTCCTC 720
CACACACTGC AGCCTGGCTA AGGATGCTGT GTTCTCAACT ATTCTCTCAG CCTGAGACGC 780
CCTCCTCCAC ACACTGCAGC CTGGCTAAGG ATGCTGTGTT CTCAACTATT CTGTCAGCCT 840
GAGACGCCCT CCTCCACACA CTGTAGCCTG GCTAAGGATG CTGTGTTCTC AACTATTCTC 900
TCAGCCTGAG ACGCCCTCCT CCACACACTG CAGCCTGGCT AAGGATGCTG TGTTCTCACT 960
ATTCTCTCAG CCTGAGGCGC CCTCCTCCAC ACACTGTAGC CTGGCTAAGG ATGCTGTGTT 1020
CTCACTATTC TCTCAGCCTG AGGTGCCCTC CTCCACACAC TGTAGCCTGG CTAAGGATGC 1080
TGTGTTCTCA ACTATTCTCT CAGCCTGAGA CGCCCTCCTC CACACACTGT AGCCTGGCTA 1140
AGGATGACAA CTTAATCTTC AACATTTGAC ATCACACCAC CCTTCCTGAG AAGCTTTCGA 1200
GTTACATATT TTTCCCCTGG TTGCCAACAG CTCTCTGTCT CTCCTTTTAT CACAGCTCGT 1260
ATCACACTGT CTTACACATC TGTCTCTCCC ACAGAGTATG AACTCCCTGA AGGTAGATTC 1320
GCCTCTGGGG TTGTAGCATT GGCACAGGGC TGATACACAA TCACTACTCA AAAAACACAG 1380
AATAAAAGGA GGGGAGTGGG CAAACGACGC ACTAATGCTT 1420
|
