| Tag | Content |
|---|
EnhancerAtlas ID | HS108-17290 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:48681740-48683250 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr17:48682741-48682752 | TTCTTATCTGT | + | 6.14 | | Gata1 | MA0035.3 | chr17:48682741-48682752 | TTCTTATCTGT | + | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 48681743 | 48682422 | | chr17 | 48682432 | 48682991 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I050604 | chr17 | 48681409 | 48682797 |
|
Enhancer Sequence | CATTCCAGAA AGGAATAAGC AGGGACGCTT CCCTCCAGGC TCTAGGCCCT TTTACCTCCT 60
GGGCATTTCA AAGAAAAGTG GGAGCCTAGA GGAAGGCCCC AAGGAGGACC GGGGCTGCCG 120
AGAGGCTTCA GGCCATGGGA GCCGCAGGCT GCTGTTCCTG CCCTCTGCAC GCACTCCCTG 180
AGCACAGACG CTGGCCCGCG GTCTACTCCG GGATCCCCTC CCTTCCTTCC CGGCTCGAGC 240
ACAGTGGGCT GCAGGCCAGG TCTGGGGATC CAGGGCCCAG ACAGCTGGGC CAGGTTAGCA 300
GCGTGCTGGC AGGCAGGCGG GTGCAGACCC CAGACGAGGC AGGAAGTGGG GGCTGCTGGG 360
GAAACTTGGC CTTGGGCCCA GGGAGGAGAC TTGGCTTTGG AAGAGAAAGA GCCAGAGCTG 420
CCTGCAGGAT TCAGCAGACG CCTCAGGGGG CCGGGGAGCC CCTCCATCAT AGTCTTCCAG 480
GGCCCTTGGC TCCAGCTGTT TCAGCTGCAG GGTAGACAGC TGGCTGTTCA GGCAGCGTGG 540
GAGCCCCTGG GTGGCTACAC CCTCCCCTCC CCGCCCCTCG TTCCCTTGGC TTCCTGGGAT 600
GTCCACTCTG CCCTGGGTTG GGGGCTGTTC CCTGACTTCC TAGAAATTCT CTAGCCCTAG 660
GGAACAGGCT GGGGTGCATT TACCAAAGCT GTGTGGTGCC TCTCTGTACA CCCTCCCCAC 720
TCCCACCCAG TGCCCTTCCC CTTCCTCACT TCCCAGCCTC CTTGGGTCAG TAGAGTGAAG 780
CATTGTTGAG CCCAGTCCTT CCGGTGGATT TAGGTCTGTT TTGAGCAGTT TGCTCAGGCC 840
CCCTGGTCCT GCCTTCCGTT TTTCACTAGT GGTCATAGCC TGGTTTATAA TGGAATGAGG 900
GTGAGCTTTC CAATCAGACA GACCTGGGTT CGAGCTCCCT TTCTGCTACC TGCTGGCTAT 960
GGGACCTTAG TGAGTGGATT AACTTCTCTG AGCCTCCGTT GTTCTTATCT GTAAAGTGGG 1020
GTTGATGATA CCCACTCCCC CACCCAGAGC TGCTGTGAGA ATTAAATGCC CAGCTCAGTG 1080
GTTCTCAAAC TTGAGTTTGC GTCAGAATCA CCAGAACGGC TTGTTAAAAG ATCGCTGCTC 1140
CCCCACCTCA GAGTGTATGA TTCAGCAGAT CTGGGCTGGA CCTGAGAAGA TGTGTTTCTA 1200
GCATGTTCCC AGATGATGCT GGGGACTCCC ACTTGGCACA CGCCTGGCCT AACCGTTGGT 1260
GGAAGATGAA TGACTGTTAC CCGCCTCCAC CCTTTCCCAC TGCCCGCCCC GATTACCTTT 1320
CCTCCCCACT CTTGGAAAGG AAGGGGGTGT CGGCAGGGGA GACTCTTGTC AGTGTTTCCC 1380
TGACTTGACT GGCCCCAGAG CAGAGCACCC CACACTCACT CAAAATGTGC CCAGGCTGGC 1440
GTGGGGGTGG GGCTCAGGAG TCCTGGGCTT CCTGTGGTCA CAGCTCACTT TTCTCTGTCT 1500
CTGGGAATGT 1510
|
