| Tag | Content |
|---|
EnhancerAtlas ID | HS187-16788 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr3:23481530-23482920 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mecom | MA0029.1 | chr3:23481894-23481908 | GGCTATCTTATCTT | - | 6.27 | | Nr2f6(var.2) | MA0728.1 | chr3:23481548-23481563 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 23481600 | 23482600 | | chr3 | 23481986 | 23482151 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH03I023441 | chr3 | 23481892 | 23482091 | | GH03I023440 | chr3 | 23482292 | 23482491 |
|
Enhancer Sequence | GGTGGGTGGA TCACGAACGA GGTCAGGAGT TCAAGACCAG CCTGGCCAAG ATGGTGAAAC 60
CCCATCTCTA CTAAAAATAC AAAAATTAGC CAGGTGCAGT GGCAGGTGCC TGTAATCCCA 120
GCTACTCGGA GGGCTGACGC AGGAGAATCG CTTGAACTCA GGGGTCGGAG GTTGCAGTGA 180
GCCAAGATCA CGCCACTGCA CTCTAGCCTG AGTGACAGAG TGAGACTCTG TCTCAAAAGA 240
AAAAAAGGAA AAATAATGGG GTCTCACTAT GTTGCCCAGG CTGGTCTCAA ACTCCTGGAC 300
TCAAGCAATC CTTGCATCTC GTCCTCCCAA AGTGCTGAGA TTACAGGCAT GGGCCATTGT 360
ACCCGGCTAT CTTATCTTCT TTATATAGAT ATCTAATAAG ATGTAAAATA CTGACCTGCA 420
TTATCTCCAT GTTAACATTT ACACTTCAAA ATCTGTAAAC GGACCCACGT TCATACGCGT 480
GAACAGAAAT CTTTCAGCAA CAAAAGAGAA AATTGTATTT CTCGATAGAA AGGAAGTGGT 540
CAGATCATGC CAGCCAAACA AATCTGTCAG GCTTTGAAAT ATAGAACCGT TAGGTAAGAT 600
ACTGAGAAAA AGGATAAAGT AAGATCAGCC TAAATGTTTC AGTCTAGTTA AGTTGATTTG 660
TATATTACTT AGAAATTTCA TTTTCAGGGA AATAGTTTTC AGATTTAAAT AACTGTAAAG 720
AGCTGAGTTA TTCTTTGACT TGGATTTAAA AAAAAAGAAA AAAAGTGTCC TGAAGTCATT 780
TCCTGCCAGT TTGTCCCCCC AACTTTTTTT CCTGCTCTTC CTGTAACTGG TTCTTGTTAC 840
GGCAATGTAG CTGTATATTT AAATCCTAAG AGACTCGCTT ATTGTGAGTA GGCAGGGTCA 900
GTAGTCTGCT GAAACAAGCA CAGGAAACTT GAAACACCTA GGGGCTATTT TAAAAATCCC 960
TTGCCACTGA CATTTTAGTT AGAATTCTAA AGAGAGAATG GGCTGTTTGG ATACTGAGCT 1020
CCAGTACAAA AGAGCTGGGG TTTTTACACC GACTTGCAAA CCACTAAAAT CATTTGACCT 1080
GGTGTTGTGT CACTTGGGTA TTCTGAAGCA TCAGATGAAA ACTAATATCC ACCCTGCAAG 1140
GTTGGCAGGC AACAATTGTA CCTGTGAAGT GAGCATCTAT CAAAGAATTG GGGAAGGAAG 1200
GCCGGGCGCA GTGGCTCACG CCTGTAATCC CAGCCAGTAC TTTGGGAGGC CAAGGCGGGC 1260
AGATCACGAC GTCATGAGAT CGAGACCGTC CTGGCTAACA CAGTGAAACC ACGTCTCTAC 1320
TAAAAATCCA AAAAAAAAAA AAAAAAAAAA TTAGCTGGGC ATGGTGGCGG GCGCCTGTAG 1380
TCCCAGCTAC 1390
|
