| Tag | Content |
|---|
EnhancerAtlas ID | HS108-07075 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:16617500-16618490 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr11:16617955-16617972 | GCCTTTCTAGGAATCAC | + | 6 | | HNF4G | MA0484.1 | chr11:16618100-16618115 | ACAGATCAAAGGCCA | + | 6.07 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCACTCTGAG GATTAATTTA TTTTCATATT ATCCCTCAAT AAAAAAGAAG TTATGATATA 60
CACCAACTTT GCCATTGGAA AAACTTAATT ATAAATATGA GGCACCTAAA GAGCTGCAAC 120
ACATAAGGGA AACAGAAATA ACACCTAGAT CTAAAAGCTT TCAGACACAG CTTTTTCTCT 180
AAGATCATGC TTGTCCATTT TCTAAAAGTG TATTACAGTG TAAGATACAA GATTTTATTA 240
ACTCACAGCC CTGATCATCA GTTCATATAT TAATAAGCCA CTTACTGTAA TTTTCATACC 300
TAGTTGACAT ATTTGAAGGA AAGTAATAAT TTGAAAGATT CCTCTGTACC TTAAAATGCA 360
CTCACAATGT TCCTGACCAC AAAACTGAGC TAAGAAAGAG AAGTGCAGTG GCTAAGCTGC 420
TGGCTTATGT CCATATCACA TTCATGACAG ACACAGCCTT TCTAGGAATC ACAAAGAAAC 480
ATGTACGAGA CATTTCAGTG TCAGATCTAC AGAAAAGCTA GTTATACTGT CAAATGTTCC 540
CCCATGTTCA GTGCTCTTTA GGATGTTACC TAAAGCCAGT TCCTCATCAT CCTTTAAATC 600
ACAGATCAAA GGCCATCTCC TACTAGAAGC TTTCCCTGAC ATAGGTACTT CTGCTGTTAT 660
ACATAACGCC ATGACAGTAA TTAGCACACT GTACAGAATC ACCTATATCC ATACCTCTTC 720
ACTAGTACAA TGCATTTTCA TCTTTGAAAT TATGTAATCA AGTTCTTCTC AGCCTTTTCA 780
CCATCAAGGA TTCTTTTATT AATGAACCTC ATGTTTTGAA AGATTGTTTT CTATCAAACT 840
TGCCACACTT ATTATTACAT AATTTTCTAA TTTGTATTAA TCAAAGACAT ATAGAACTGA 900
TGTTTAATGC TTCTGATCAG CATGGTATTA TTCTTTTACA TTGGTGTACG GGAAATGCAG 960
CAATAATTTG GCTCTGGAAG TAAGTATGAA 990
|
