| Tag | Content |
|---|
EnhancerAtlas ID | HS044-06875 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr2:24658210-24659540 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MIXL1 | MA0662.1 | chr2:24658558-24658568 | TCTAATTAAC | + | 6.02 | | Myog | MA0500.1 | chr2:24659041-24659052 | GACAGCTGCAG | + | 6.62 | | Tcf12 | MA0521.1 | chr2:24659041-24659052 | GACAGCTGCAG | + | 6.14 |
|
| | 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 |
| GH02I024433 | chr2 | 24656789 | 24659939 |
|
Enhancer Sequence | AACATAAAGG GAGTAGCTGA AGCCCTCCGA AGTAGGCCAC GCCTGCGCCA TTGCACAGTT 60
CGGAGCTCTC CCATCAGCCC TTCCGAGTGC ACTGCCTCAA GTCGCACATC CAAAGTGAAA 120
TGTGGGTGTT TTAATCACTG AAGAGAATCC TTAATGCTGC TCCTTCAGCA CATAGCTGTC 180
TCTCCTGTGC CAGGAACCGC AGGGAGCCTA TTGCTTTCCA TCCTGAACTG GATCCAGAAG 240
CGTTAGGTGA GGCTCAATAC AATTTTCAGT TGTTATCATG GGAGGCCCTT AGAGACGCTT 300
CTCAGTTCTA GCAATTAGCC ACACAGGGGT CAACCAAGTG TTCTCAGCTC TAATTAACAG 360
CTGTGTTGAA TCTGGGACAC ATAGAATTCC TTTGGGGACG CACTCTTCAA ACAGAAACAA 420
AGCCAGAATA GCAAGCTCTT TCCTCCTTAT CAGAGGCTAT GAAGTATGAA AATGACTGCT 480
GAGGGGATTC TTAATGAAAA TACCGGGAAG CTGAGTGGCC TCCGGGCTGC ATGTATGAAT 540
TTAAAGGCAA AAAGACAATC TCAGCTTGAC TATGAAGTTA TCTGCTGGGG CTCAGGAGGC 600
TCTGGGGAGC GCTGGGGGAA TTAGGTGCCT CTTAGCTCCA CTCCCAGAGC CCGGTACACC 660
CAGCAGGCTA CATGATAATC ATCACCACAC AAATCAAAGG CTTGATCTCT GGCTTCAAAA 720
GGAAAAGGAA CAGGAACAGG ATACTCTCTG TTGGGACTCC TGCTCTGAGC GGGAACTATG 780
CTGATGCCTG TTCAAGTTGT TCCCTGGGTA TTTTGGCTTC TTGCCCTGCC TGACAGCTGC 840
AGGAGTTCTG TAAGAAATCT GAGGGAGAAT TTCCTTTGCA ACCATGACTG AGAACCCAGG 900
ATCAAGAGCT TTGCAGACAG AAAAGACATT ACCCTTCGAA TATCCCAAGC CATCTATTAG 960
GGTCAGCAAG CAGCCGGCAA AAAGCGGGGC AGCTGGTGGT CCAGCCCTGG GTGGAGAAAG 1020
TGGATTCCAT CGGGAAACAG CCAGTTGAAG TTTTCTTTAC TAACTGAGAG CAAATGCACC 1080
GAGGCATTTA AAAATAAGCA TATGTTCATA CTGGAATATT TCAAATGAAC AGAAACAACA 1140
CCTAAGGCCC AGATCGATAA ATATTAACTT TGTGACACAT TTACTTCACA ACTTTTTCTA 1200
AACAATTTGG TATACATTAA AACCTACCCC TTCTTCCCCT GGCTCCACTC CCCACTCCCA 1260
TCCTGAAGTT AGTAGGTATT TTTCTATGTA AACCACAACC AGGGGTTTAT ATTCTTCTTC 1320
TTCTTTTTTT 1330
|
