| Tag | Content |
|---|
EnhancerAtlas ID | HS044-08473 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr22:24840920-24842230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr22:24841475-24841496 | TCCTCCCCACACCCATCCCCC | - | 6.12 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_53996 | chr22:24840286-24842367 | Spleen | | SE_56257 | chr22:24841437-24842758 | u87 | | SE_59734 | chr22:24819560-24869580 | Ly4 | | SE_65698 | chr22:24840241-24842416 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH22I024447 | chr22 | 24841280 | 24841490 | | GH22I024446 | chr22 | 24841513 | 24841670 | | GH22I024445 | chr22 | 24841691 | 24842210 |
|
Enhancer Sequence | ACCCGGGGGC TCAGGGAGCT GAGTAGGGCC ACAGTTCAGT GCGCTGACCA GGGGACAGCA 60
AACCACAGCA GGGCAGGAAG AGGGGCCACC TGGGTGCTGT GAGGAAATGA GCTGCTGATG 120
CTCCCTGCAT CTTCTGGGAC TTGGTATCCC AGAAATGGGA AACTGGTCTT TTCAACTGTG 180
GTGGGGAAAC AAGAACCCGG GGGAATCCAA CTGCTCAGCA TGTGGGAAGG GCTCTGCGCA 240
GCCCGCCCCT GCTCCTGGGG CCGCAGGGAA AAGTGGGTGA GGCCAGCACT CTGTGCCTGG 300
GATGCCACTG CTGTCCTGCG ATGTTGTGCT GCTCCCCCGC ATGGCTGCTG CTACGGGCTC 360
TTGCCACAGC TGGACACCCT CCCCTGAGCT CCAGTGCCGG ACAACTGTTT TCTGAGCATG 420
CTAAGCAATG ACCCTCTGCT GACGGGAGAA GTTACTTTAG AGGGGACAGA ACTTAGGAAG 480
ACCCAGGTGT GCTGTGAGGC AAGTGGCTCC CTCCCTGACC CTTACTGCTC AGTGTGCAAG 540
GTTACCACCT TCTCCTCCTC CCCACACCCA TCCCCCCTCT CTCCCAAGGT GCCCCTCATT 600
GCTGCTGTCA CTCATCATTA GCAGTCACTG TCATTGTTAG GACAGCCCCT GTCAGGCTGC 660
AGAGCCAAGG GAGGGGGCAG GAGAATGTCA GATGACTCAC ACAACCTCAA AAGAGGGGGA 720
TGGACACACA ACACAGAACC TAGCTACAAG AAGCACCTCG TGAGACTCTG GTTCAACCCT 780
TTCTTTTTCC AGAGAAGAAA GAGCAGCTTA GCAGAGTTTC CTGACAAGTC CCTCTGCTTC 840
CCACTAGTCA GGCTTGGAGG GAGGCTGGCC TAGGAGAAAG GCCAGGCCAG GAAGTCAGCA 900
TGAGGCTGGG CAGGTGACAG GTGTAGCCAA CCCAGGGTCC TCTGAGGGAG GTGGGGAAGG 960
CTTTGCATGG ACCCATCCAC ACTTCTTTGC CTTGTCCAAG GAAGTGTTTC CGTTTGGGGG 1020
AGGAGAGGAG TGACTCTTTG TCAAATCAGC CATCTGGACT GTCACCTAAC GACCAGCTAA 1080
GCCCTCGGAT CAAGCTGGTT AGGACCTGAG CCCTGTCTCC TGGCTCTCTG TCCCTCTCCC 1140
AACCACTTAA TGAGCCCTTG CTGATGCACA CTGAGCCGGG GGCAGGACGC AGGGAGCCAA 1200
CAACTGACTG AGGGGAATAA GCCCGACGGG GAGAATAAGC CCGACGGAGG GAATAAGCCT 1260
GTGAGGGACA CACAGGCTCT CAGAGGAGGT GAAAACCACA CGCCAGCGGG 1310
|
