| Tag | Content |
|---|
EnhancerAtlas ID | HS044-11241 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr6:34548350-34549520 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr6:34548885-34548906 | CTCCCCGCCTCCCCCTCACCC | - | 6.04 |
| | | 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 |
| GH06I034581 | chr6 | 34548941 | 34549090 |
| Enhancer Sequence | GAGAGAAGTC ATCAAGCTGA GCCTGTAAGT TCTGTGTTCT TTACTGTATG TAAATTATAC 60
CTCAGTAACA AGGAAAAATT AATTCTTACT TCTGGAGGTT GTGAAGATGG AATAGAAAGA 120
ACGTAAACTA TGCCTTACGG AAAAAGTTTT AAAATGACTA TACAGTGTGA ATGTGTCCAT 180
GTATGAATGT ATGAGCTTCT GTGTGGTTGG TGTGAGATTA TGTGACCCTG TGGGTGTGAT 240
GTGTCTGCGT ATGAACTAAG GTAACGGTAA TGAGTGTGCA CCTGGGTGTC AGTATGTGGA 300
TGCACATGTA TTGCATGTGC CTATGTCCCC ATGTGAGGAG TGCACAGAAC TGCACAGGTA 360
TGCTGGATTA CATGCTTGTG AATGGCTGTG TGCATGTGCA GGTATGTGGA GGCTTCTGTG 420
CTCTGAAACC ACACGTTCTA CACAAGACAG AGCCTGAATC TCAAGCCAGT GGTTCTGGGA 480
CCCAGCTGTG CTCCTCACAT GAAGTAAAGT AGGGGCTGGC TAGCAGCAGG GTGTGCTCCC 540
CGCCTCCCCC TCACCCAGAA GGAAGCAGGA GACTGAAGGC CTGGATAAAG GTTCCCAGCT 600
CCCTCTCCCT TCCCACAGCT GCAACTTCTC AAAGATGCAA ATTACCCTCT GCTCCATGGA 660
AACCAGTCCT GAGAGCCAAG GTTGCTTCCC CTCAGGCCCA ACCACTACCA CTATGATTGG 720
ACCCCACTGG ACCCTAGCTG CCCAGCCTAG GGATGGGAGC CAGCTGGAGT CAGTTCCTGT 780
TTCCCAACCA GTCACTGATG TTTTTCCCCC TGGGGTGCCT TGGCTCTCCC TGCTGGCTCA 840
GGTGTTGTGG AGAAAGCCTG GGCTAGGAGT GGTCCACATA GACTGTGGGA CTCTGGGGAA 900
GGTAATGCTG TCTCATCTTT GGGGATGCTC TGAATAGCGA CTGTACTATC CCAAAACACT 960
GGAGCAAGGC CTGGCTCTCC CAGACCCTCC TGCCTGGCAT ATTTGCTGTG GGGCTCACTC 1020
ACAGGACCCT TAGCCTACCT GGATTCCCTA TTGGTGCTCA CTTTTCCCAT CTCCTAGGTC 1080
CTGTCTCCCC ATCAGGGACA TGTGTCTTCA TCAGCCCTGG ATGACGTACA TCACGGGGCC 1140
CAGCAGCGGT TCAGCACACA TAGAGATTCC 1170
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