| Tag | Content |
|---|
EnhancerAtlas ID | HS095-06889 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:29793410-29794520 |
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: 2 | Chromosome | Start | End |
| chr12 | 29793538 | 29794216 | | chr12 | 29794264 | 29794398 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I029639 | chr12 | 29792844 | 29794549 |
|
Enhancer Sequence | AGGGAGACCC TCCTCTCCCA AACACGTCCC CCACAACTGG AGAAGCTGAA GGTCTGTTTG 60
TGGGAGAAGT TTCTGACTTT ACCTGGAGCT GAGTCAATTT GGAGAGCCAA GTGAAATACT 120
GGGGTAGAGG AAGCAGCAGA AAGGCCCTGG GAGCTCGCGG GCTCCCCTGG CAGGCCGTTC 180
CTGCCTGGAA CCACAGGGAT CCAATGGGAG AGAAGCAGGG GATAAAACTA CACAGAGAGA 240
AGGAAATCTC TAGCTGAACT TTGTAACAGT TTGAACGGGG TGAGAAGCCT CCTGGCCAGA 300
ACTCGGGGGA GGGTGCAAAT CTGATGTGCA GACTCCACAG GCTAGGGAAG AACCAAGCCC 360
TTTTCTTATG CAGCTGGGAG GCAGACAGCC TCATATCGCT TACGGTCTGG GGGTTGTTGA 420
GGGGGGCATG GTGGGAGTGA GACCAGCCCT TCGGTTTGTG TGGGAGCTGG GTGAGGCCTG 480
TGACTGCCGG CTTTCCCCGG CTTCCCTGAC AACCTGCATG ACTCAGCAGA GGCAGCCGTA 540
ATCCTCCTAC ATACACAATT CCAGTGACCT AGGAATCTCA CTCCCAGCCC CCACAGCAGC 600
CACAGCAAGA CCCGCCCAAG GAGGGTCTGA GCTCAGATAT GCCCAGCCCT ACCCCCACCT 660
GATGGTCCTT CCCTACCCAT CCTGGTAGCA AAAGACAAAG GGCATATACT CTTGGGAGTT 720
CTAGGGCCCT GCCCACCATC GGTCCCTCCC TATACTAGCA CAGATGAAGC TCTCTGGAAA 780
GCACCACCTC CTGGTAGGAG GCCAACCAGC ACAAAAATAG AGCATTAAAC CACCAAAGCT 840
AAGAACCCTC ATGGAGTCCA TTGCACACCC CAGCCACCTC CACTGGAACA GACACTAGTA 900
TCCATGGCTG AGAGACCCAT AGACGGTTCA TATCACAGGA CTCTGTAGAC AACCCCTGGT 960
ACTAGCCCAG AGCCCAGTAG ATTCAATGGG TGGCTAGATC CAGAAGAGAG ACAATAATCA 1020
CTGCAGTTTG GCTCACAGGA AGCCACATCC ATAGGAAATG GGGGAGAGTA CTTCATCAAG 1080
GGAACACACC GTGGGACAAA AGAATCTGAA 1110
|
