| Tag | Content |
|---|
EnhancerAtlas ID | HS087-14530 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr3:48934830-48936120 |
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 | CCAGAGGCCT AGAACTAATA AGATATCTGC CTATATGGAC CAAGAGCAGG AAGAAAGGCC 60
AGACAATCGT CCCTCAGTAG ACAGTGCCGC TTGGAATGAC CACAGTCTGG GAAGCACTAA 120
CACATGGCAT TTACCACCAG CTAAATAAAC ATTTGATTTC ATGTTGCACA ATGACCTAGC 180
CAGTCCAGCT ACTTTAACCC TGGTCTTCCT ATAGAATGAC CCCAGTATGA GCTCTACTTC 240
AGGGCAGCTC CTCTCTTGGA TGAAAGGCAG CAAAGAGCTT GCTGCCCAAG CTGGCCAAGA 300
GGAAGTGCCC ACAAAACTAT TTCGCTGTGG AAGAAATCTG ACCCAACATC CTAACAAACC 360
CCCTCACATG GGCTTCCAAT CTTTTAAAAC TCATGTCTGC TCCCCACAGG CCCACCCTGG 420
CAATGACTTG TCAATTTCCT TCACGTCTAC GTCTAGAAAA AAAGTGAGAA AACTGGATGC 480
AGCTTCGAGT GCTAAGCCAT GGGGGATGGA CTTTGGTCCC CAAGCAAAGC ATTAATGAAG 540
GTGTTGCAAG GGGAATAGTT GAGATATGAT ATGAGGAAGA CCAGAGAACA ATTCCTGATG 600
AACGTCCTCC CTCCCAAGCC TCAGTCTGAC CATAGCTTCC TCATCTGGGA GTTGTGAGAA 660
TGAGGCTGGC CTTGTGCAAA GCTGATCACC TTGCTTTCCG TGGAAGGGGC TCGGTCACTG 720
AGGTCATCAT TGCTTCTCAC AGGGATGCCT CTGCCCAGGA GGCTGAGCAG GCCACCGTTG 780
GGTGACAGGC CGAAGAGTGT CAAGTATCTC CCCGGGCCGG GAAAGGTGCG AAAGAGATGG 840
GTACTCTTGC CCCAGGGGAA TGTATCAAAG GACACCTCCA GAACAACCGT ACCGCTCTGT 900
CTTTAGTTGT CTTCCTGGGG CAGGCTTTAC AGGGGACCTG TTTCAACCTT AACGATAATA 960
TTAGTGTTGG CTGAAACCAA AACTATGGAG AGACGTTTAT TCCTTCCCAT CCCTAAAGAA 1020
GTGGCGCAGG GTCAGAAGAG ACTGCGGGAC AGGGAACTTT ACATCAGAGC TCTTGACAGG 1080
CAGTTAGAGG CTGCTCACTT TGCGCCGCCG CCTGGCTCTT TGGGGCGCAA GGTACAGCTT 1140
CCTGCCCACC CCTGAAAGAG AGATTCCCTA GACTTCTCAC GGAAGCTCAC ACATGCCCCT 1200
CTTCTGCCCA GCGTCCGCGC CTCGCGGGGG ACCATGCTTT CCGCGCCCCG CCCGGGCCTC 1260
CTCCCCAAAG CCTGCGACCC AGCCTCCCGC 1290
|
