| Tag | Content |
|---|
EnhancerAtlas ID | HS190-08876 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr3:16890840-16891770 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata4 | MA0482.1 | chr3:16891344-16891355 | AGGAGATAAGA | - | 6.14 | | Myog | MA0500.1 | chr3:16891571-16891582 | AACAGCTGCAG | + | 6.02 | | NFAT5 | MA0606.1 | chr3:16891024-16891034 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr3:16891024-16891034 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr3:16891024-16891034 | AATGGAAAAT | - | 6.02 | | Tcf12 | MA0521.1 | chr3:16891571-16891582 | AACAGCTGCAG | + | 6.62 |
|
| | 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 |
| GH03I016848 | chr3 | 16890321 | 16892180 |
|
Enhancer Sequence | CTGGGGAGTG TTCTCCGCAA TGTAATTTGG TTGCTAGGAA ACCTGTGGGC GGGCGTTAGC 60
AAGAGGAAGA GAAAGCTCCT CCGCCAGCAA TTCAATAGCA GTATTGGCTT TCATTTCAAA 120
CGTGCTAAAT AATAGGGCCC TGCAATTTGC CTCCGTTAGC CCAAGTTGCT TACGTTTCTT 180
CCTGAATGGA AAATTAATCT GGTTTAGTGC CGGGTAACAT TTGCAACCAT ACTTCCTCTG 240
CCAGGCATTA AAAAAAGAAG TTTCCCACTT TGGGAAATAA GAAAGTTCTG TGTCTTTCTT 300
CATGTTTTAT CATGTTTTTT TTTTTTTTTC CTTTCTTTTC CTTTTCTCTC TCTCTCTCTG 360
TCAAGAAAAT GCATCATGTT AACAGCCTTT AAGCCCAAGA TCAAGCCAAG AGGTAGCAGA 420
GCTCAGGAAA AAGAGATCAG GACAGCCCTT TATTTCTAGG GTGTAGGTAG GGTTGGGTAT 480
AAAGAGTTCT GCTAGGGTCT GAGGAGGAGA TAAGAGAATT GACCTAGGCA TAGAGAGTGC 540
TTGGGGAAAT TGGCAAGAGG TAAAAGGAAA CCACATTTCT ATGTCAGCTC AGGTCCAGCA 600
TATCCTCTAC TTGACCCCTG TCCACACATA AAGCAGAACA TAACATCTTG CATAGAGTAG 660
GTGCTCAAGA AACATGTGTT GGCAACACAC AAATCCTAAT GTAATGAGCC TGGATACAGG 720
AATTCTATCA GAACAGCTGC AGTCAGTCAT AGCGTTGTTG GGGTGCATGT TTTAGGCCTT 780
ATGTAATTTC CTGTCTCGGG ATGAAAAAAA ATGGACTAAC AGCCAAGGCT GGCAAGCTGT 840
TCCTGGCTGA ATGTGAACCA GGCTCCAGTT CCACATCCCC AAAAACCCTC CTATGCTTTC 900
CCCCTTTTGA GTAAATTAAT TTTTATCTGC 930
|
