| Tag | Content |
|---|
EnhancerAtlas ID | HS108-22961 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr2:102857130-102857860 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:102857456-102857475 | TTGCGCCCTCTAGTGGCTG | - | 7.46 | | RUNX1 | MA0002.2 | chr2:102857249-102857260 | GTTTGTGGTTT | + | 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 |
| GH02I102238 | chr2 | 102854507 | 102858977 |
|
Enhancer Sequence | AGGCTGCTGG TCCCCCTGTC AATCACGATA CTTTGGCTAC TTTGCTTTCT TCAATCAACA 60
AGGCTTTATC AAGAACTTAT GGCTCTTTTA ATTATCTGAC TTCCTGGTCA ATCAGCTTTG 120
TTTGTGGTTT TAAATGACCA CAGGATAGTA GAAGTGAACA TAATTTCCTG CCTGTGTAAA 180
AGGATGACAT CAAGAGGAAA AGAAAGCAGC TCACTGGGTG AAGGACCTTG AGAAAGAGAT 240
GAACATTTCC TCTCTTGAGA CACAGGACAA ACAAGGTCAC GCCTGAGCTC GGCAAACAAG 300
GACTTCGGTG CCTGCCTACG GCGCCATTGC GCCCTCTAGT GGCTGCTGAG GAACCGCTGT 360
CCAGCCCGAA GCTCACAGAG CCCCGTTCAG GCTGCCGCAA CCTACCTAGG CGGCCAGAAT 420
GGAGACTTAC AGGTGGGCGG GCATCCCGGG GTGCACACAT TACCTTCTCG GGGCTCTCCA 480
ACTTAAGGCC AAGGATATCT TTCTTCTTTT TCGGCTGCTG AGAAGGTGGA GATAGTGCCA 540
TTTTCGAATG TGTTCCTAAC TCTTGGGCTT CTGAGACTGT CGCAGTCTGT CCAAGGGTGG 600
TGAGTGGGGA TCAGCAGGCC CTGTTTACTA TGTGCTCGCA AGAGGGGACT GCGGTCATAG 660
GGATTTCAGA GAGGTGGCCC TGGCGTCGGG CCCCTGGACT CCAGTCACAA CTCAACCACT 720
TGCTGAGGGA 730
|
