| Tag | Content |
|---|
EnhancerAtlas ID | HS037-19136 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr2:37050950-37052450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP3 | MA0746.2 | chr2:37051162-37051175 | CACCACGCCCACC | + | 6.48 | | SP8 | MA0747.1 | chr2:37051163-37051175 | ACCACGCCCACC | + | 6.32 | | Zfx | MA0146.2 | chr2:37051120-37051134 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | 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 |
| GH02I036824 | chr2 | 37051541 | 37051650 |
|
Enhancer Sequence | CACTGCAACC TCTGCCTCCC AGATTTCAGC AATTCTCCTG CCTCAGCCTC CTGAGTAGCT 60
GGGAGTACAG GCACATGCCG CCATGCCCGG CTAATTTTTG TATTTTAGTA GAGACGTGGT 120
TTTACTCTGT TGCCCAGGCT GGTCTCGAAC TCCTGAGCTC AGGCAGTCGG CCCGCCTCGG 180
CCTCTGCAAG TGTTAGGATT ACAGGCATAA GCCACCACGC CCACCCCAGC TGCAGGCTTT 240
AAAATGTGTT CATTGATCAC GCCACTGCAC TCCAGCCTGA GCCACAGAGC AAGACCATCT 300
CTCAAAAAAA AAAAAAAAAA AAATCATTCA TTGCCTTCTA GAATTGGTAT CCCACCACAC 360
ATGACGTCCA TCACCTGGCT CCTTGTTTTT GTGCTGTCCT GTGGGATGAG GGAGCTAGCA 420
TCATGCTGAT CTTGCTTTTG CTGACTACAT AAGTAATACA CCGTCTGAAT CCATTTGGGT 480
CTATCATGTC TTTACCTGCC AAACCTGTGG CAGCGTGGCA AGCCCACTGC AGCAGTAATC 540
ACTGTTTATT AGGGGCTGCT TGACAGCAAC TGTTTCCTGA GATGCCCTAG GAAGATGCCC 600
TCCATACCAC ATTGTCTCCC AGGAGGCTTC TGAACACCCC TCCCCCTACA CATCCATAAC 660
AATGCCGAAT CCTACCCCAG CTGCAGATCA TCTGCCAGTG ACCAGGGAAC TGTTTCTCAC 720
TAAGAAGCAA AGAGCAGAAC GAAGAATTCT TCCTTCAGAT CTGTGAATGT TTGCAATTAC 780
ACTGCCTTCA CCACACTCGG GATGGTTCCC TAAAAGCCCA CGGGCTGGGA TAATATGCAG 840
GTTTTGCCTT GGCGGGTCGA GATGTCATGA TTGCCTGAAT AACCATAGGA AGAAAGATTC 900
TGAATCTTTA GGATTCTCTT AAAGAAAGAG ATGCTAAAAT CAATTATCCA TGTCTGTCAT 960
GGGAGACTGA TAGGGCAGGG TCGGTTCTCA CAGTTGGCAT TTACCCAACT TTTTTTTTTT 1020
TTTTTGAGAC AGGGTCTCGC TATGTTGCCC AGGCTGGAGT GCAATGGCAC AATCATGGCT 1080
CACTGCAGCC TTGACCTCCT GGGCTCAGGT GATCCTCCCA CCTCAGCCTA GCAAGTGGCT 1140
GGGTGGGACC ACAGTCATGT GCCACCATGC CAAGCTTTTT TTTTAAACTT TTTTGTGGAG 1200
ACATGGTCTC ACTTTGTTGC CTAAGCTGGT CTTGAACTAC TGGGCTCAAG TGATCCTCCC 1260
ACCTCAGCCT CCCAAAGTGC TGGAATTACA GGCATGAGCC ACCATACCTG GCTGATTTAC 1320
TCATCTTTGT TTTTTGTTTT TGTTTTTGTT TTTGTTTTTG AGACAGCGTC TCACTCTGCC 1380
ACACAGGCTG GAATGCAGGG GCATGATCTC GGCTCACTGC AACCTCCGCC TCCCGGGTTC 1440
AAGCGATTCT CCTGCCTCAG CCTCCTGAGT AGCTGGGACT ACAGGTGTGC ACCACCACGC 1500
|
