| Tag | Content |
|---|
EnhancerAtlas ID | HS044-10112 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr4:170359410-170360880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr4:170359476-170359491 | TGGGGGCAAAGTTCA | + | 6.54 | | Hnf4a | MA0114.3 | chr4:170359477-170359493 | GGGGGCAAAGTTCAAA | + | 6.9 | | Rxra | MA0512.2 | chr4:170359477-170359491 | GGGGGCAAAGTTCA | + | 6.03 | | ZNF143 | MA0088.2 | chr4:170360186-170360202 | TACCTACAATGCACTG | + | 6.55 |
|
| | 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 |
| GH04I169437 | chr4 | 170358624 | 170360736 |
|
Enhancer Sequence | CTGTGAAAAC AAAAAATAAA AAATCATGCT AGTTCTCAAA ATGATGCATT TTATCTGTAA 60
TGGCATTGGG GGCAAAGTTC AAAAAGCTGC ATTACTGCAA CAGGCAATTA CTAGTTAAGC 120
TCTGTTACAT ATTAGAAGTT AATAAGTGAC TACAGTATAT GAAAGTCAAA TTTCATTTCA 180
ATTGTACATA ATAATTTCTA TGGTGGTCAA AATGGTTTAC CTTCTTTCTG CTTTTGGTAA 240
AATTAATATG TGTATTAGAA TACTATTTTT TAAATTATTA ACTAGTTGAT TCTGTTTATA 300
TGAAGTAACT CCTAGTTACT TCTAATTGCT CTGAAATTCT CCACACTAAG GAGAGAGGAG 360
GTTTACCTCA GAACATCCTG AGACAGGTTC AAAAAAGAAT AAAAAGAAAA AAAAACTACC 420
TCAGAATAGC TTAATGCAGT TATTTACCAC CTTCTCACTC CTATTAATCC GTTGAAGATT 480
TTACTTTCCA GGTTACAAGC TCCCCAACAC TAACTCTGTC ATAACTAATT TAGGTGATTT 540
CTATATTTGT ATCAATAATC CTTCCAAAAG GTAGGCCTCT TGGTTTGTTG CACTTCACTC 600
TACCTCAGTC TTCATCCTAT CTCCAGCACT CCAATGGTCA TATCTTAGAG AACTTGTCAT 660
TAATTATAGC CTCTTTAAAT TTCCAGTGTT AAGTATTCCA CCCTCTAATC TCTAACACTC 720
ATTTTCCACT TCTCCGCCTC TACAACTCCA ACTCTAAAAA AATTTTACCC TGAAAGTACC 780
TACAATGCAC TGATTCTGCT ACATTTTCTG TCATCTCCAT TAAAATTCAC AGAAATTCCA 840
TAATATAGTC ATTCTCTTGT GCATCCTCAA CTTATTGTAT TCAAGTGGCA AAACCCCAAT 900
TTTGCATAAA TTCAATTCTC TGCCTACTAT ATCTGCATAC ACAGGGTTAA AATGGTTGAA 960
GAAAAACAGA AATCCTTGCT CATTGGTCTC AATTTAAATT CATTGTTTCT AAAGCCAAGT 1020
AGGCCCTTTG TGTTGGCTGC AGTCCTTTTA TAACACTGGG CTAGCAGGAA CTGTCCTTAG 1080
CTCAGTTAAT TTCCAGAGCA AAAAAGTTGT TCATCAAGTA TTTATAAGTT GTTTTACTCT 1140
TTACTTCTTT CTAGTCAACA GAGAACAAAA CTATAGTGTT GCAAATGTTT CAGAATCATT 1200
TCCCTGCACT GTACTTCAAC AAACTGCTTG CCAAAACAAA CTGACTGTAG CAGAGATCAC 1260
ATCTGTGTTT TTCCTCCTTC AGCCCTACCA TTCTGCAATA AAATCATGTC TATTAACACC 1320
AGGAATCAGG ATACCATATC GCATTATTAT TATTATTAAA GATTGCTTTA GTGGGTTCTA 1380
ACAGAAGAAT AGGAAATAAT CAAAATATAG GATAAAAATC TATTTCTTGT CACTGATGAT 1440
AAATCTGCAC ATTTGGAACA TCTAATATCT 1470
|
