| Tag | Content |
|---|
EnhancerAtlas ID | HS068-03436 |
Organism | Homo sapiens |
Tissue/cell | GM18526 |
Coordinate | chr2:242224620-242226020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr2:242225171-242225182 | GGTGACTCATG | + | 6.62 | | JUND | MA0491.1 | chr2:242225171-242225182 | GGTGACTCATG | + | 6.02 | | Sox6 | MA0515.1 | chr2:242224623-242224633 | CCATTGTTTT | + | 6.02 |
|
| | 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 |
| GH02I241285 | chr2 | 242224781 | 242224930 |
|
Enhancer Sequence | ATACCATTGT TTTTCTAAAC ATGTTACAGC TTTTATATGC ACTGGGAAAC GTAAAACTCA 60
TGTGATGTGC TTTATTGGGA TGTCAGGCTT TCTTGTGGTG GTATCACAAA CCTGCAGTGT 120
CTCTGCAGTG TGCCTGATGT GCACTGTAGC ATTTTTGTAG AGTCAGAAGA TTAAACATTT 180
GCATTGGTTC AGTCCGGGAC TGGGTAAACA AAGGGTGGCA GAACACAAAG CACTATCACT 240
GACCTCCATA AACGACCTGA TGAATGACCA AGTCTCCACC CCCACAGTAA AATATTAATT 300
GATGTCATGA GCAGAGTGCC TTCTAGTGTG CCCTGAACAC CGATCCCCAC CAGTGATGAT 360
GTGTGCTTAG TAAGACTCAG TTTTACTTGC TCTCAAACCT GTTTATGCCA GTTTCACTAG 420
TTAATGTAAC TACATTTAGA AATAATTCAA AATAATGAAG GAGTGAAGAG AAATTTATCT 480
ATGGATATTA AATTTACCAC ACTGAAATTT CAAGAAAAAC AAGTTGCCTT AAAAAAATTA 540
TGGCTGGACA TGGTGACTCA TGCCTATAAT CCTAGCACTT TGGGAGGCCA AGGCAGAAGG 600
ATCACTTGAG GCCAAAAGTT TGAGACCAGC CTGGGCAACA AAGTGAGACC TCATTTCTTA 660
AAAAAATAAA AAATAAAAAC AATTAGCCTG TGCCTGTAAT CCTAGTTACT CAGGAGACTG 720
AGGCAGAAGG ATCATTTGAA CCCAATTTGA AGCTGCAGTG AGTTACAATC GTGCCACAGC 780
ACTCCAGCCT GGGAAAAAGA GCAAGACCTG TTTGTTTAAA AGAAAAAGTC AAATGGAGGA 840
AAACCTTTAA AATCTCAGAG AATCTACACT GATTATGAGT TTCTTAAATT TTTGTTCCAC 900
TTAAATGAAT GCTGAAAATC CTAGACGACA TATTATCAAT TTCATTTACA TAAGAAGAGA 960
GTATGTGGCC AGGCATGGTG GCTCATGCCT GTAATCCCAG CACTTTGGGA GGTTGAGGTG 1020
GGTAGATCGC TTGAGCCCAG GAGTTCAAAA CCAACACAGG CAACATAGTC TGAAAGGAAA 1080
ATAAATCTTG GGGCCCCCAA ATCACTAAGT TAAAAGGAAA AGTCTAGCTG GGAACTGCTT 1140
AGGGCCAACG TGCTTCCCAT TCTCTTCAAA GTCTCCCCTC TGTTCACTGA GATAAATGCG 1200
TATCTGACTG CCTCCTTTGG AGAGGCTCAT CAGAAACTCC AAAGAATGCA ACCATTTGTC 1260
TCTTACCTGC CTGTGACTTG GAAGTCCCCT CCCCACTTGG AGTCTTCCTG CCTTTGCTTC 1320
GAGCCATCCT GCCTCTCCAG ACCGAACCAA TGTTCGTCCT GTATATGCTG ACTGATGTCT 1380
CATGTCTCCC TACAATGTAT 1400
|
