| Tag | Content |
|---|
EnhancerAtlas ID | HS044-11303 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr6:41906710-41908100 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr6:41907002-41907014 | CCAATCACAGCA | + | 6.02 | | STAT1 | MA0137.3 | chr6:41908050-41908061 | TTTCCTGGAAA | - | 6.62 | | Stat4 | MA0518.1 | chr6:41908047-41908061 | CCTTTTCCTGGAAA | - | 6.91 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_25452 | chr6:41898485-41910935 | DND41 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 41906927 | 41907077 | | chr6 | 41907242 | 41907431 |
|
Enhancer Sequence | AAAACCCTCA TACGTGGGCA CACAAACCAC CTCCATCTTT TCACAAAAAG GAAGTTCCCC 60
TTCTACCTTC CAGCCCCAAC CCCTCCAAAA ACATCTTGCT CTCTGGCCCT GGAAACTAGC 120
TCCACCTTCA GACTTGCCAA AAACTACCAG ATTCATCACA AAGAGCTGTG GCGCCTCCTG 180
GATTCCCAAC TCTGGCCTCC TACTCCCATC TCTGAGCTAC TTGGCAGGAA GAGGAATCCT 240
GTTCCTCGAC TCACAGCAGT CGGGGGCCCC AGTACCCTGG CTTCCCTGCC AGCCAATCAC 300
AGCAGCCTGC TTGCTGCCCT CCTCCCTGGG AGATGGGGCC CAGAGACTCC TCTCAGGGTC 360
AGCAGAAGAC TTGGCCCGCC ACAGAGCAAG GTGGAGGAAG GTGCCAGCTC ACCCACCCTC 420
TCCCCCAGCC TCCCTAGGAG ACAATCTGCA TGTCCTAAAT AACCTCTTCC AGATCCAGCA 480
GCTCCCCCGC CTCCTCCCCA GGCTCCTTCT GAGGCGGGAC AGAACCGGTG ACTTTCCTGC 540
CCGGCCTGAG CCCAGCCCAA GTTTCCAGCA AGAGGCCCAG GGAGCCACTT CCCAAACCAC 600
AGGAGTGACA GCAGCTCCCC ACAGGGTTAT GAAAGACCTT GGTCAGAGAG GGCGGGCCAG 660
GGGAGGGGGC ACCATTATCA CATCGGAAGC AGATGCAGCT CACCTCCCTG TCTGTCCCTC 720
AGCTTGGGCC TTGGGCTAAG GGGGGAAGAG GGAGCTGTTT CCACCAGGCC CAAAGCAGCT 780
GCTCCAGTTC CTCAGAATGA GGACGAGGAA GGATTAGGAA GAAGCTGTTT CTTCCGGGAT 840
ATAAGAGGAA GCAAAGAAGG TGGGATGAAA TACATCAGCC CTTCCTTAAA GCAATCAGGG 900
CCTGGCTTTA ATTGGCTCTG GGAGGCTTTT CTATCACAAA GTCCACATGA GGATAAAGAC 960
TCAACCAAGG CAAAACCCCC TCCCCCACAT GAAGCACATT CCACTCCCCT ACTCCAGTGG 1020
GGGTGTGCAG GCATGCCCTT CTGCTGCCAA TAAATAACTC ATGGTGGCTG CGTAAACCCA 1080
GAGGCAAAGT ACTAGTGAGT GTAGACATGC AATTTGACTT GTTGCTATCT GGGGGAAAGA 1140
CCAGGAAGGA GTGGCATCCC CTGGAGGTCA GGAGGAGGGG GTTTAATGCC TGCCTGCAGC 1200
TCAAGCCTGG GCGGGAGTGA TACTAACCAT CACACCACAA TGCCCCATCG TTTGTTCCAC 1260
CCCAATTCCT TTCCCAAAGG TCCTGATCCC CTTGCTTCCT CTCCAGGGGG CAGAAAGCCT 1320
CTGATATCTC AAGCTTTCCT TTTCCTGGAA AGTGGGGAGA CAATACGTGT CGGGGGTGGG 1380
GGGAGTTACA 1390
|
