| Tag | Content |
|---|
EnhancerAtlas ID | HS037-02004 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr1:118250350-118251600 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GSC | MA0648.1 | chr1:118251056-118251066 | GCTAATCCCC | + | 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 |
| GH01I117708 | chr1 | 118250679 | 118251611 |
|
Enhancer Sequence | TTATACACTG GGAGTCCATG GAGCACCTAA CAGTTTTGAG GAGGTCTGAG ATGCTGCTGG 60
AGGAGTTTGT ATTCTAGTTC CTGGCAGGAG ATCTGAAGCA TATTTAAGAA TTAAGTGAAT 120
GGGGGGTGGG AGGTGGAAGA GGAAACTGGA GAGAGTAGGA GGCTCCAGGC AGAAGGATCA 180
GCTTCGTCAA AGACTAAGAA GTGAGACTGC ATGGTCCTCA AATCCCTTCT CTTACTCTTC 240
TGCCTTCTTT CCAATTCCCG TTTGTCCCAG GCTAAGGCCT TGCTTAAGTG ATCTCTGTCA 300
GAAGGATGGA GTGAAAGCAG GAAGAGAGTC CCTTCTGGCT CACAAGCAGG GTGGCCAACC 360
ATCACAGTTT GCCTGGGACT GTCCTGGCTT TAGCACTGAA GGGTTCATGT CCTGGAAAAC 420
CTTTGGTCCC TGGATAAACA GGAAAAGTTG GTCACCCTGC TCAGAGGGTT TGTTCTGGTC 480
ACCCAAGTCA CCTGGAAGGA GAAACAGGGC ATCTGAGTGT CTTGGAATGA TCCCTGGGCT 540
GGGGCCAGGA CACCCGGGTT TAAGTCCCAG CTCTGTCCCA CACCAGCCTT GTAATTCTGA 600
GGAAGTTGTG TCTCTAGCCT CCCTATATTG ACAACATTTG CTTAGTTTCT ATATTCTGTA 660
TGCTCTGGAA ATTGGGGCTT CGATCCTAGA GAGATTTCTA GGGCTAGCTA ATCCCCAGAG 720
TAAGCAAATG GCTCCCCGTG GAGCATGCTT TTGATATGCA AACCAGCCAA TCCAGAGCCT 780
GCACCCCCAA CCCTCTCCTT TATCAAACGC TCACACACCA ATGCAATATC TCCCCTGCCC 840
TAAACCACCC CAGGGCCAAG TCCTGGACAA CTAGGGATCA CGCCTATAGC CCAGAACCTA 900
CTGAAATTAT CCAAACTACC CAAAGCTGAA CTTACTCAGC ATAGTTGCAG TACCTTGCCC 960
ATTCCTTCCC ACAGGAACCC CAGTAAAGGC CCTGAGCCAT GCATACTCTC CTCTCCCCTC 1020
CCCACTTCTG CCTCCTGACC GACCCAGCGC TTCCTGGGGT GGCCTGCGTG GCACGCCGTA 1080
CCTCCTGTTC TAGAGGCCTG TGAGTATAAA CTTTTTCCTC CCTGACAATC ATTTCCATTT 1140
CTTACCATGC CTGATTAAAA CAAACTCCAG GTCCATTTTA TCACACTCCT CCCTGCCGTT 1200
ATTGGCCCTC CTGCCTCACG GGGTTGTTGC GAGGGCCTAA TAAGATAATG 1250
|
