| Tag | Content |
|---|
EnhancerAtlas ID | HS116-08044 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr12:29793540-29794590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr12:29793925-29793940 | GCATGACTCAGCAGA | + | 7.23 | | Nfe2l2 | MA0150.2 | chr12:29793923-29793938 | CTGCATGACTCAGCA | + | 7.41 |
|
| | 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 |
| GH12I029639 | chr12 | 29792844 | 29794549 |
|
Enhancer Sequence | AAGCAGCAGA AAGGCCCTGG GAGCTCGCGG GCTCCCCTGG CAGGCCGTTC CTGCCTGGAA 60
CCACAGGGAT CCAATGGGAG AGAAGCAGGG GATAAAACTA CACAGAGAGA AGGAAATCTC 120
TAGCTGAACT TTGTAACAGT TTGAACGGGG TGAGAAGCCT CCTGGCCAGA ACTCGGGGGA 180
GGGTGCAAAT CTGATGTGCA GACTCCACAG GCTAGGGAAG AACCAAGCCC TTTTCTTATG 240
CAGCTGGGAG GCAGACAGCC TCATATCGCT TACGGTCTGG GGGTTGTTGA GGGGGGCATG 300
GTGGGAGTGA GACCAGCCCT TCGGTTTGTG TGGGAGCTGG GTGAGGCCTG TGACTGCCGG 360
CTTTCCCCGG CTTCCCTGAC AACCTGCATG ACTCAGCAGA GGCAGCCGTA ATCCTCCTAC 420
ATACACAATT CCAGTGACCT AGGAATCTCA CTCCCAGCCC CCACAGCAGC CACAGCAAGA 480
CCCGCCCAAG GAGGGTCTGA GCTCAGATAT GCCCAGCCCT ACCCCCACCT GATGGTCCTT 540
CCCTACCCAT CCTGGTAGCA AAAGACAAAG GGCATATACT CTTGGGAGTT CTAGGGCCCT 600
GCCCACCATC GGTCCCTCCC TATACTAGCA CAGATGAAGC TCTCTGGAAA GCACCACCTC 660
CTGGTAGGAG GCCAACCAGC ACAAAAATAG AGCATTAAAC CACCAAAGCT AAGAACCCTC 720
ATGGAGTCCA TTGCACACCC CAGCCACCTC CACTGGAACA GACACTAGTA TCCATGGCTG 780
AGAGACCCAT AGACGGTTCA TATCACAGGA CTCTGTAGAC AACCCCTGGT ACTAGCCCAG 840
AGCCCAGTAG ATTCAATGGG TGGCTAGATC CAGAAGAGAG ACAATAATCA CTGCAGTTTG 900
GCTCACAGGA AGCCACATCC ATAGGAAATG GGGGAGAGTA CTTCATCAAG GGAACACACC 960
GTGGGACAAA AGAATCTGAA CAACAGCCTT CAGCCCTAGA CCTTCCCTCT GACAGCACCT 1020
ACCCAAATGA GAAGGAACCA GAAAACCGAC 1050
|
