| Tag | Content |
|---|
EnhancerAtlas ID | HS091-12184 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr13:100764320-100765550 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr13:100765048-100765063 | TGAACTCCTGACCTT | - | 6.04 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TATATTTTTG CTTTGTTTAA ATCAGGACTT AATTTTGGGT CAAGCAGAAA AAGTGAGACA 60
TACAGGCTTT TTTTCTTGGC CTGCACAAGA TACATTCAAG TTTAAAAACT GTTTACTTGT 120
TCACTGTTGT GTTAAGCAAA ACGACAGTAT CACAGTATCT TCTATATGTG CCGTAAGTAT 180
TTTCTTTTCA TAGCTTTAAA AACTTAGACA GAAAAATTGC CAGGCTGATT GCTGGTCACC 240
AAGTAGATTT AAGCAAAGCA TGAGAAAATT TGAGTCAAAG ATTAATGAAA TGTTTACACA 300
GTGCTCCCTT ATGAGAGCAC TTTCCCCCAG CATAGCTTCA GTATCACTAA GGGAATGCTA 360
CAATTGTTTA ACCTTTCCTA AATGCTTCAA CGTGTTCAGC TGAAAGTTTG ACAAAAATGA 420
AAGGTAGGCT AATGCTAATT GGATACAAAC AAAAGAAGGT TTAGCATAAA GCAGATATAC 480
TTTTATTTGG TACTTTTAAC ACAGCAGGCC TTTTTTTTTT TTTTTTTTGG GACAGAGTCT 540
TGCTTTGTTG TCCAGGCTGG AGTGCAGTGG TGTGATCTCA CCTCACTACA ACCTCTGCCT 600
CCTGGGTTCA AGCGATTCTC CCGCCTCAGC CTCCGGAGTA GCTGGGATTA CAAGCACCTG 660
CCATCATGCC TGGCTGATTT TTGTATTTTT GTAGAGACAG GGTTTCACCA AGTTGGCCAG 720
GCTGGTGTTG AACTCCTGAC CTTAGGTGAT CTGCCTGCCC CGGCCTCCCA AAGTGCTGGG 780
ATTACAGGCT TGAGCCACCA CACCCGGCCC ACAGCAGGGA TTTTTTTTAG TAGTAATGTT 840
ATGAATGAGT AGAAAAAAAT CCCATGGGGA AAGAATGTAA ATTATTAAAT CTTTATGGCA 900
TGAAATATAA GTAGTTGAAT ACTAATGCAA GCATTGTTTC TCATTGTCTC ATACTACTTT 960
TGATAATGGG ACCCTTTGGT AGGGTCCATC AGTTAATGAC AGGGATATGT TCTGAGAAAT 1020
GCATCGTTAG GTGAATTCAA TATTGTGTGA CCATCACAGA ATGTACTTAC ACAAACCTTG 1080
ATGATACAGC CTAGTACACA CCTATATAGT ATAGCCTATT CCTCCTGTGC TACAAACCTG 1140
TGCAGCACGT GACTGTACTA AATACTGTAG GCAATTGTAA CACAATGGTA AGTATTTGTG 1200
TATATAAGTG TATCTAAACA CAGAAAAGGT 1230
|
