| Tag | Content |
|---|
EnhancerAtlas ID | HS098-05492 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:231630300-231631600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr1:231630302-231630318 | CACTAAGTAAATAAGA | + | 6.04 | | Nr2f6(var.2) | MA0728.1 | chr1:231631480-231631495 | TGAACTCTTGACCTC | - | 7.64 | | RARA | MA0729.1 | chr1:231631477-231631495 | TCTTGAACTCTTGACCTC | - | 6.45 |
|
| | 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 |
| GH01I231494 | chr1 | 231630305 | 231630490 |
|
Enhancer Sequence | ATCACTAAGT AAATAAGAGA TGCACATCAC TGTTTTCAAA GTCTATCAGA GGCTGTTCCT 60
ATCAGTTCCT GTGCATCTTC TATTCAGTTC ACACTCAGAC AACAAAGCAT GTAGTCATGT 120
TGTCTCCTTG TCTTATGATA GACCCACGTG ATATGTTACA AAATTGGATA ATTGAAAGAG 180
GACATAGCTA AAGATAAAAG TGCAAGAAAG TTTTCTGAGA AGATAGACTC TGGGGGGAAA 240
AAAAGAAAGA AAAAAAGTGC TACAAAGAAA GAAAAGTGAT AACATTGGAA GTGAAATTCA 300
AATTACACAT AAACAGAGTT ACAGAAGAAA AAATTAACCA TGGGAATGTT GACACTACCA 360
CCATTTGAGA GACTTAAGAT ATGCTGCCAT AGCCAGTTAG TGAATGCAAA CTTCACTAAC 420
TAAATGAAGA AAGTGATTGT GACTGAAAGG ATGAAGATAT CCCAGAAGAC AGGACACCAT 480
TTAAAAAAAC CTTCACACTA AAGGAACTCT CAAAGGGCAG TGTGGTGGCT CACTCCTGTA 540
AACCCAGTGC TTTGGGAGGC CGAGGAGGGA GGATTACTTG AAGCCAGGAG TTAGAGACCA 600
GCCTGGGCAA CATAGCAAGA CTCTGTCTCT ACAAAATGAT TTAAAAATTA GCTGGGGATA 660
GTGGTATGCA CCTGTAGTCT CAGCTACCCA GGAGGCTGAG GCAGGAGGAT TGCTTGAGCC 720
TAGGAGTTAA AAGGCTGCAG TGAACTAGGA TCATGCCACT GGACTCCAGC CTGGACGACA 780
GAGCAAAGGC CCTAAGGGAC TCTCAGACAT AATCCACCAT GTTGAAAGTT CAGATGATAA 840
AATATTGAAG CTGATCCAAA CTTAGAAAGG AATATGACAA TTTGCCAAGG CATAGAAACA 900
TGCTCATTTC ATATAAAAGT TACACAATGA GAAGGCAAGC ACTGTTCCAA CCACTCGATT 960
TTTTCTTTTC TTTTTTTTTT TTTTTTTGAT GGAGTCTCGC TCTGTCACCC AGGCTGGAGT 1020
GCAGTGGTAC GATCACTGCA ACCTCTGTCT CCTGGGTTCA AGAAATTCCC ATACCTTAGC 1080
CTCCCGAGTA GCTGGGATTA CAGGCATGCA TCACCATGCC TGGCTAATTT TTTGTATTTT 1140
TAGTAGAGAT GGGGTTTCAC TGTGTTGGCC AGGCTGGTCT TGAACTCTTG ACCTCAAGTG 1200
ATGTGCCTGC CTTGGCCTCC CAAAGTGCTG GGATTACAGG CGTGAGCCAC TGTGCCTAGT 1260
CCACTTGATA CTTTTTTTTT TTTTTTTGAG ACGGAGTCTG 1300
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