| Tag | Content |
|---|
EnhancerAtlas ID | HS190-09051 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr3:48934940-48936120 |
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: 2 | Chromosome | Start | End |
| chr3 | 48935999 | 48936096 | | chr3 | 48935000 | 48935200 |
|
Enhancer Sequence | GAAGCACTAA CACATGGCAT TTACCACCAG CTAAATAAAC ATTTGATTTC ATGTTGCACA 60
ATGACCTAGC CAGTCCAGCT ACTTTAACCC TGGTCTTCCT ATAGAATGAC CCCAGTATGA 120
GCTCTACTTC AGGGCAGCTC CTCTCTTGGA TGAAAGGCAG CAAAGAGCTT GCTGCCCAAG 180
CTGGCCAAGA GGAAGTGCCC ACAAAACTAT TTCGCTGTGG AAGAAATCTG ACCCAACATC 240
CTAACAAACC CCCTCACATG GGCTTCCAAT CTTTTAAAAC TCATGTCTGC TCCCCACAGG 300
CCCACCCTGG CAATGACTTG TCAATTTCCT TCACGTCTAC GTCTAGAAAA AAAGTGAGAA 360
AACTGGATGC AGCTTCGAGT GCTAAGCCAT GGGGGATGGA CTTTGGTCCC CAAGCAAAGC 420
ATTAATGAAG GTGTTGCAAG GGGAATAGTT GAGATATGAT ATGAGGAAGA CCAGAGAACA 480
ATTCCTGATG AACGTCCTCC CTCCCAAGCC TCAGTCTGAC CATAGCTTCC TCATCTGGGA 540
GTTGTGAGAA TGAGGCTGGC CTTGTGCAAA GCTGATCACC TTGCTTTCCG TGGAAGGGGC 600
TCGGTCACTG AGGTCATCAT TGCTTCTCAC AGGGATGCCT CTGCCCAGGA GGCTGAGCAG 660
GCCACCGTTG GGTGACAGGC CGAAGAGTGT CAAGTATCTC CCCGGGCCGG GAAAGGTGCG 720
AAAGAGATGG GTACTCTTGC CCCAGGGGAA TGTATCAAAG GACACCTCCA GAACAACCGT 780
ACCGCTCTGT CTTTAGTTGT CTTCCTGGGG CAGGCTTTAC AGGGGACCTG TTTCAACCTT 840
AACGATAATA TTAGTGTTGG CTGAAACCAA AACTATGGAG AGACGTTTAT TCCTTCCCAT 900
CCCTAAAGAA GTGGCGCAGG GTCAGAAGAG ACTGCGGGAC AGGGAACTTT ACATCAGAGC 960
TCTTGACAGG CAGTTAGAGG CTGCTCACTT TGCGCCGCCG CCTGGCTCTT TGGGGCGCAA 1020
GGTACAGCTT CCTGCCCACC CCTGAAAGAG AGATTCCCTA GACTTCTCAC GGAAGCTCAC 1080
ACATGCCCCT CTTCTGCCCA GCGTCCGCGC CTCGCGGGGG ACCATGCTTT CCGCGCCCCG 1140
CCCGGGCCTC CTCCCCAAAG CCTGCGACCC AGCCTCCCGC 1180
|
