| Tag | Content |
|---|
EnhancerAtlas ID | HS098-12448 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:13277660-13278700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr12:13278328-13278344 | CTGCTTTCTAGGAATG | + | 8.15 | | BCL6B | MA0731.1 | chr12:13278329-13278346 | TGCTTTCTAGGAATGCT | + | 7.09 |
|
| | 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 |
| GH12I013124 | chr12 | 13277619 | 13279095 |
|
Enhancer Sequence | ACAACAAGAT CTGTTTTATA TGGTTGTTGG AAGGATTAAA TGAGCTCATG CAGCAGAAGG 60
CTCAGCAGAG TGGCAGGGCT TCATAAATGC TGCCTGTGTT GATCATTGAT GGTTCCAGGA 120
AGCCCTGGAA TGTCTTATGG ACAGAGAACT CACCCGCTGT TTCCTGTTTC CTCCTCCTCA 180
CCTTATTGCC CTGTCCGAAC AGGTGACTCC CTTCATGTCC CCACCATCTC ATTTACTAAA 240
ACCAGAAACC AAGACATCAC CCTAGACAGC TCTCTCTCCT CCTCCCTCAC TTCAACATCT 300
AAGCAGTCTC TAAAGTCTAT GAGTTCTACC AGCTCACCCT CCTTCCCCCG ACCTTAGCCC 360
AGCTACTTGG TCCAGAGCAG CCTCATTCCT ATTTTGGACA ATGGCAGCAC CCTCAGACTG 420
GCCCCTGCCC CAGTTGTTCA GAAATGCAAA TCTGAGCTGA TTGCTTCCTT GCTTAAGACT 480
ATCCACTGGT GCCCTCTTTA TCTACAGGAT AAAGCCTGCA TTTCTTTGGG ATTAATCATG 540
GTTTTGAAAG ACCTAGCCTG TCTCCTTACT GCTGCTATCA CAATCCCTGT GTCCATCAAC 600
AGGGCATTCT CGGTGCACTT TCAACAGCTT CATGGCATTT CCTGTCTCTG TGCCTTTGAC 660
ATGTTGTTCT GCTTTCTAGG AATGCTGTTG ATGATGACGA TGAAGAGGAA GAGGCTGAGA 720
GTAACAGTAA CAGCTGCCAT GCATTGGCGA TTTACAACAA TAACCGTTTT CTGTGCTCAG 780
TGCTTTGCAT TCATAATCTG TCTTTCCCCA ACCTTGGTTA CCTGGTGAAC TCCTCAAATA 840
GAATTATGAT TTTTCTTTTT TGAGATGGAA TCTTGCTCTG TCACCCAGGC TGGAGTGCAG 900
TGGTGCGATC TTGGCTCACT GCAACCTCCG CCTCCCAGGT TCAAGCAATT CTCCTGCCTC 960
AGCCTCCTGA GGCGTGTGCC ACCCCACCCA GCTAATTTTT GTAATTTTAG TAGAGATGGG 1020
GTTTCACCAT ATTGTTCAGG 1040
|
