| Tag | Content |
|---|
EnhancerAtlas ID | HS044-06472 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr19:11734130-11735960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DUX4 | MA0468.1 | chr19:11734699-11734710 | TGATTGAATTA | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 11734591 | 11734663 | | chr19 | 11734236 | 11734387 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I011623 | chr19 | 11734483 | 11736248 |
|
Enhancer Sequence | ATTGTAGAAA TTTCCCTAAA CCTTTTTCAC TCTGATATCC CATGTTCTTC AACATTTTAA 60
ATCCTGGATT ATCAAAGTTT TCATTTGTAA GTCTCCTATC CCATGCTGTA AGTCTCGACC 120
CCATAAATTG ATGGCTATAT TTGCAACATA AGGCTGCAAA GTCCAGAGCA AGCTTAAAGT 180
TGTAAAAGTT CTTTAATAAA TAAACAGAGT AACCTGATAG GACGGGCGCG GTGGCCCACG 240
CCTGTAATCC CAGCACTTTG GGAGGCCGAG GCGAGCGGAT CACGAGGTCA GGAGATCCAG 300
ACCATCCTGG CTAACACAGC GAAACCCCGT CTCTACTAAA AATACAAAAA ATTAGCCGGG 360
CGCGGTGGCA GGTGCCTGTA GTCCCAGCTA CTCGGGAGGC TGAGGCAGGA GAATGGCGTG 420
AACCCGGGAG GCGGAGCTTG CAGTGAGTGG AGATCGCACC ACTGCACTCC AGACTGAGCG 480
ACAGAGCGAG CCTCCGTCTC AAAAATAAAT AAATAAATAA ATAAACAGAG TAACCTTAGC 540
TCTCTGAGTG CTAGTAAACT CAGATCGAGT GATTGAATTA TGTGGTCTCT ACTAGCCTGC 600
TGCTTTTCCA TGTTTACCAG ACCCATCAGT AAACCGTGTT AAAGCCTTAG GTATGGGGGA 660
GTGAAATACC GCTTCGAATT GCCTTTTACT TAAACGAATC CTGATGATAT GAGGGTCATA 720
ACTTAGCATT TGGACTGCAT TAATCATTAA GATTGCTAGC TGAAATAGTA ATAAGTTTAA 780
AAAGAAAATC TGAACGCGTC TCTAGAAGCA GAGACTTAAA TGATATACTT TAACCATGTG 840
CTTAAAACCA CGGGCGGAAT AGCTTAAATC TTGTAATTGA GTTTTTGGGC TGACCAAGTT 900
TATGGACTTT AATCTGGCAA ACAGTCTTGA AAACAGTGAC TCACTGGCTG GGGAACTCAA 960
TTTAGGACTC TTTTAGCAAG TACAAATCAC ACTATCTGTA ATCAGTGGGT AAGACAGTCA 1020
TTCATGCATA AGTTTTCACT ACACTTACAA CTTTTCTTCA CTTTCTGAGA AGGACACAAC 1080
ATTTTTACCT TCTAATTTGA CAAATATCAT TTAATTAGGT TTAAAGTTCT CCTTTAAAGG 1140
GTAATGTGTG GTTTTACATG CCTAGCTTTT AATTACTCAT TAATGAATTC GTGGGCCCTC 1200
TGTAATCTCT TTCCCTTCAG AGGTTACTGT TTTACTTAAA TTGAATTTGG AAAGCTACCT 1260
TAGGGGTAGG AGAGAGATAA CAGTGGCCAT TATTAGAAAA GAGGTTTTTC AAATTCTTAC 1320
ATTTTACTTA AATCTTAGCA GAGAATCATA GTCTGGGACG TACGTAACAC ATGAACTTTT 1380
GCTATGGGCT GCTCACAGAG CCAGAGGGCT GCGGTGCAGG TCCTTGGCGG CGGCCGCATT 1440
GTACTTGCTC AGGTTTTGCC TGTGTCTGCG CCGCTCCCTC CCTCCTTTGC CGGGGGTGGG 1500
GCATGCTGCC AGCCTGGGCG GACCTTGTGG GCTTGGTCGC TGCCAGCTTT TCTGCTGCTG 1560
AACCTTCTAT TCCGCCCACC GCTTGCTTGG TCGCGCGGTT TCGGCTTCTA ATGCCTTTTT 1620
TCTTTCTTTT TTTTTGAGAC GGAGTTTTTG CTCTTGTTGC CCAGGCTGGA GTGCAATGGC 1680
GCGATCTCGG CTCACCGCAA CCTCCGCCTT CCAAGTTCAA GCGATTCTCC TGCCTCAGCC 1740
TCCCGAGTAG CTGGGATTAC AGGCACTTGC CACCACGCCC GGCTAATTTT GTATTTTTAG 1800
TAGAGACAGG GTTTCTCCAT GTTGCTCAGG 1830
|
