| Tag | Content |
|---|
EnhancerAtlas ID | HS051-19532 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr3:48934840-48936120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DMRT3 | MA0610.1 | chr3:48935688-48935699 | AATGTATCAAA | + | 6.02 | | HINFP | MA0131.2 | chr3:48936038-48936050 | CAGCGTCCGCGC | + | 6.22 | | HNF4G | MA0484.1 | chr3:48935336-48935351 | TGGACTTTGGTCCCC | - | 6.39 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr3 | 48935999 | 48936096 | | chr3 | 48934891 | 48935000 | | chr3 | 48935000 | 48935200 |
|
Enhancer Sequence | AGAACTAATA AGATATCTGC CTATATGGAC CAAGAGCAGG AAGAAAGGCC AGACAATCGT 60
CCCTCAGTAG ACAGTGCCGC TTGGAATGAC CACAGTCTGG GAAGCACTAA CACATGGCAT 120
TTACCACCAG CTAAATAAAC ATTTGATTTC ATGTTGCACA ATGACCTAGC CAGTCCAGCT 180
ACTTTAACCC TGGTCTTCCT ATAGAATGAC CCCAGTATGA GCTCTACTTC AGGGCAGCTC 240
CTCTCTTGGA TGAAAGGCAG CAAAGAGCTT GCTGCCCAAG CTGGCCAAGA GGAAGTGCCC 300
ACAAAACTAT TTCGCTGTGG AAGAAATCTG ACCCAACATC CTAACAAACC CCCTCACATG 360
GGCTTCCAAT CTTTTAAAAC TCATGTCTGC TCCCCACAGG CCCACCCTGG CAATGACTTG 420
TCAATTTCCT TCACGTCTAC GTCTAGAAAA AAAGTGAGAA AACTGGATGC AGCTTCGAGT 480
GCTAAGCCAT GGGGGATGGA CTTTGGTCCC CAAGCAAAGC ATTAATGAAG GTGTTGCAAG 540
GGGAATAGTT GAGATATGAT ATGAGGAAGA CCAGAGAACA ATTCCTGATG AACGTCCTCC 600
CTCCCAAGCC TCAGTCTGAC CATAGCTTCC TCATCTGGGA GTTGTGAGAA TGAGGCTGGC 660
CTTGTGCAAA GCTGATCACC TTGCTTTCCG TGGAAGGGGC TCGGTCACTG AGGTCATCAT 720
TGCTTCTCAC AGGGATGCCT CTGCCCAGGA GGCTGAGCAG GCCACCGTTG GGTGACAGGC 780
CGAAGAGTGT CAAGTATCTC CCCGGGCCGG GAAAGGTGCG AAAGAGATGG GTACTCTTGC 840
CCCAGGGGAA TGTATCAAAG GACACCTCCA GAACAACCGT ACCGCTCTGT CTTTAGTTGT 900
CTTCCTGGGG CAGGCTTTAC AGGGGACCTG TTTCAACCTT AACGATAATA TTAGTGTTGG 960
CTGAAACCAA AACTATGGAG AGACGTTTAT TCCTTCCCAT CCCTAAAGAA GTGGCGCAGG 1020
GTCAGAAGAG ACTGCGGGAC AGGGAACTTT ACATCAGAGC TCTTGACAGG CAGTTAGAGG 1080
CTGCTCACTT TGCGCCGCCG CCTGGCTCTT TGGGGCGCAA GGTACAGCTT CCTGCCCACC 1140
CCTGAAAGAG AGATTCCCTA GACTTCTCAC GGAAGCTCAC ACATGCCCCT CTTCTGCCCA 1200
GCGTCCGCGC CTCGCGGGGG ACCATGCTTT CCGCGCCCCG CCCGGGCCTC CTCCCCAAAG 1260
CCTGCGACCC AGCCTCCCGC 1280
|
