| Tag | Content |
|---|
EnhancerAtlas ID | HS150-02723 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr12:13277300-13278490 |
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 | | GATA2 | MA0036.3 | chr12:13277625-13277636 | TTCTTATCTGT | + | 6.14 | | Gata1 | MA0035.3 | chr12:13277625-13277636 | TTCTTATCTGT | + | 6.62 |
|
| | 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 | GGTGGCTTAT TTAGTTCCCA GGTCAGTTCA CACTGTCCAG TGTACAGTGG TGCAGGTTGC 60
ACCCTGCCAA GTGTCCCCAG CTGAGGGAAG AGTGAGCTCC GTCTCCAAAC TGTGTACCCA 120
AGTGGGGTCT GGGTCTGTTA GGGAGACAAG GCCACATGTT TCTAGTTCAC ACAAAGGAGA 180
AAGGGCAGGA GGTGATGGCC GTCCAAAGAG TCAATAGAGT GGATTAATTT GGAGCATGTG 240
GGCTTTGCAG GAAGATGTGC ATAGGTTTAG ATCTTTGCCC CCACCACTGT CCGTGTGACT 300
TTTGGCAAGT TTGTAAGCCT CAGTTTTCTT ATCTGTAAAA CAAGAATAAA AGCAACAGCA 360
ACAACAAGAT CTGTTTTATA TGGTTGTTGG AAGGATTAAA TGAGCTCATG CAGCAGAAGG 420
CTCAGCAGAG TGGCAGGGCT TCATAAATGC TGCCTGTGTT GATCATTGAT GGTTCCAGGA 480
AGCCCTGGAA TGTCTTATGG ACAGAGAACT CACCCGCTGT TTCCTGTTTC CTCCTCCTCA 540
CCTTATTGCC CTGTCCGAAC AGGTGACTCC CTTCATGTCC CCACCATCTC ATTTACTAAA 600
ACCAGAAACC AAGACATCAC CCTAGACAGC TCTCTCTCCT CCTCCCTCAC TTCAACATCT 660
AAGCAGTCTC TAAAGTCTAT GAGTTCTACC AGCTCACCCT CCTTCCCCCG ACCTTAGCCC 720
AGCTACTTGG TCCAGAGCAG CCTCATTCCT ATTTTGGACA ATGGCAGCAC CCTCAGACTG 780
GCCCCTGCCC CAGTTGTTCA GAAATGCAAA TCTGAGCTGA TTGCTTCCTT GCTTAAGACT 840
ATCCACTGGT GCCCTCTTTA TCTACAGGAT AAAGCCTGCA TTTCTTTGGG ATTAATCATG 900
GTTTTGAAAG ACCTAGCCTG TCTCCTTACT GCTGCTATCA CAATCCCTGT GTCCATCAAC 960
AGGGCATTCT CGGTGCACTT TCAACAGCTT CATGGCATTT CCTGTCTCTG TGCCTTTGAC 1020
ATGTTGTTCT GCTTTCTAGG AATGCTGTTG ATGATGACGA TGAAGAGGAA GAGGCTGAGA 1080
GTAACAGTAA CAGCTGCCAT GCATTGGCGA TTTACAACAA TAACCGTTTT CTGTGCTCAG 1140
TGCTTTGCAT TCATAATCTG TCTTTCCCCA ACCTTGGTTA CCTGGTGAAC 1190
|
