| Tag | Content |
|---|
EnhancerAtlas ID | HS101-03414 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:185381090-185382530 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LBX2 | MA0699.1 | chr1:185381474-185381484 | GCTAATTGGC | - | 6.02 | | MEF2A | MA0052.3 | chr1:185381415-185381427 | TCTAAAAATAGT | + | 6.02 | | SOX10 | MA0442.2 | chr1:185381093-185381104 | TTCTTTGTTTT | - | 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 |
| GH01I185412 | chr1 | 185381188 | 185382583 |
|
Enhancer Sequence | TGTTTCTTTG TTTTAGAACC AGCCATGTAT GTGTTGTCTT GATACCTTGT GTATATCACC 60
TCCCAGGCCA CTTTCAAAAC AGGAACCAGT GGAATTTTTG ATGAACAGCT AAGTTCGGGT 120
TATTTCTGAG AGGCATGTGG AGATAGACAC GAAGCTTTCT TGATGCTGCA GGAGGAACTT 180
AAAACAAAAG TCTTGGATGC CTCGCAGAAG GCTGTGCCCT AAGCAGAGAA AGGAAATCTT 240
TCTTCTAAAT TGCACCAATT GTTTTCAATC TTCTTTTACT TTTACCTTCC CACACACTAA 300
GTCTATCAGT TCTGCCAGTC TGATGTCTAA AAATAGTTGC TATAGGGATA TTTGCGTTTG 360
ATAAAATGCC ACGGGGTCCT TGAGGCTAAT TGGCAGGTTG AATTATTTCA TGATCAATCC 420
TTTAGATATT TGTTCTCAAT TAAATTGACC ATCTTAAAGT TTTTTTAAGG GAGCATGAGC 480
AAATGTCAAG TTCAAAGTGC CGTATAAAAG CAAGAAGCAG ATCTGAGGTG AAGAATCTGT 540
AGGGTTAGTG TGGTCAGAGG GACACATTCA TCACCTGCCT GTGGCTATGT CTACAGACAA 600
AGAGAGGAGA ATAGCAAGGT TGCTTGGGCA GAAATGAGAG CACTGAGGGA GCTGGGGTTA 660
ACCCAGGTTC ACAGAGAGCC CACGGTCAGT AGTGGAGTTG GCGTGGAACC CAGCCCCACG 720
GGCTTAACAC GGTTATGTTA TTTCTGTCTC CACTAAACTC CAGGAACTTA CTAGAAGAAC 780
ACAAGACATG CATACGTTAA GAACCAGAAA GCACAGTCAG TGGGTGTCAC TGTGCTGCAT 840
GTGGGACACG GAAATGCAAA ACAAGGCATT GAAGAGCATG GGAGTGGCAG GGCTCATCCC 900
AGCCAGACAA GGAAGAAGTC AGGATTGTTC TGGCCTGTCA TGCTGGCACT TGTCCTGGTG 960
TCTTTCTTGA TCCACCCTTC AGGCCCCAGG TGTCCCTATA CTCTTTCCCT CCCATCCAAA 1020
CCTGCTCTCA GAGAAAAGTC AGGAAGCCTT CAGTTGTTGC ACAACCAAGG TGTGGCCTGG 1080
CTGGTTTCCA CACAGCAGAG GTACTCTGTT CTGGGAATTT AGATGGGGAA AGATTCTTAA 1140
AAGTTTCTTC TTGCAAATAT TTTCAAAATT AAGTCTTAAT ATTTTAAAAA GAAGCAATTA 1200
ACAAGCAAAC AAGAAGTCCC CAAATCCTCA AATGTTTACT CCATGAAATT TCCTCGGACC 1260
ACTCCCCTGA GCTGTCAACC TTCTCTCTTT TTGTTGCCAG AGCTTTTTGT GTATACAGCT 1320
TTTGATATAC ATTATCATGT AATGACAGGG ATATGTTCGG GACATGCATT ATTAGGCAAT 1380
TTTGTTGTTG TGAGAACAAC ATAGAGTGTC CTTACACTCT ATGGTAAGGA CACTCTCTGG 1440
|
