| Tag | Content |
|---|
EnhancerAtlas ID | HS044-05080 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr16:14050520-14052040 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TBX20 | MA0689.1 | chr16:14050679-14050690 | TTTCACACCTA | - | 6.14 | | TBX2 | MA0688.1 | chr16:14050679-14050690 | TTTCACACCTA | - | 6.32 |
|
| | 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 |
| GH16I013955 | chr16 | 14049334 | 14053154 |
|
Enhancer Sequence | GGGGCGATTT TGCTTGTTGG TGATCAGGAT GAGGGAGCAG AGCAAAGTGG GAGAAGGAAG 60
GCACTAGAGA GAGAACAGAG AATTAGGCAG AACCAAAATT TAGTATTGTG GGGGATGGGG 120
GTGGAGGGAA AAAAACGAAC GTGGTTTTGC TTTTCTTCCT TTCACACCTA CAGAAAACCT 180
GTTTTTGTAT TGAATTGCTT CTTCTTAAAG ACCAGCATCA ACCTGATCAT GCTCCCCACC 240
ATGTGAAACG GAATGGGCAC GCCACGATAA GTAGTAATGA GCCTTTTCGG CAGCCTTCTG 300
TTTTAACAAA AAAACGCTGC TGTTTGGCAT TGAAGTTTGC TTGTGTTTAA GCTCGCGGTG 360
GAACAGCCTA GGACCCCTCT CTGTTTGTAA CCTGGCTTTA TAATTTTGTT ATTATTTAAA 420
GCCTCCCTTT CAGCGATTTT TTAAAACCAA AATATATGCT GGCTAATGTC ATCTGGAAAC 480
TGAAAGTCGA TGTTCAGCAA CTCTCACTCG CCAATCCTAC AACTTGGTAA GGATTTTTAT 540
TTTGGTCGTA CTGAGCTTAC TGTAACTGGG GCGGCTGAGT TGCTATGGTA ATTTGTTCTC 600
AGAACAGAGC ACTTTGCTGC AATGCATGGA AACAGCAGAT AAATCTACTT TATGTTGACT 660
TGATTGTGAC ATTAATTCTA GTTGAAACAT CCTCCATGCT CCCATCAGGA CTCATGTATA 720
AGAATTTTAA ATTGGAGCCA AGAAGGCATT GGCTAAAAGA ATTGCAACTT CGGCTGTTTA 780
AACCCAGGCC TTCACAATTC ATGCAACTGA AGGCTGTTGG CTCACAGCCT AGAGCGCTGC 840
CCCGGGGGCG GCTTGCAGCT GGGGGAAGGT TCATCACTGA GGCAATTATG TGGTTAATTG 900
CTCCAGTGTG GGCTTGGGCT GAGAGTTGTG ACTCATGCCG CCCTCTGTCA CTAATAGATG 960
GGGGTAGGGG GTAGAGTGGA CAGGACTCAA GGACTTACTG AAAACTCAGC TGCCTTTTCC 1020
CTTTCCTCTT GCAAATAAAT CTGTAACTCA CTAACATCTG CCCTGGAGAT GTGGGAGGAA 1080
GGTAGACCTC AACTCCAAGA CTTGGTGCTC CCGGCCTCCA TTGGTAGGGG TCCCCATTAA 1140
GTCCCACGTC CTGAACTACA CTGGAGCCCT CGGACACTTT AAGGATCACT GCACTCCGAA 1200
TTGGGGTGTA TCTTCCTCCA ATTCTTGCCT AACCATGACA GAGGAGAGAC AAAAACTAGA 1260
TGCCTGACTT CGAGCATGAC TCATTATAAA CAAATAGAGG ACAGATTGAC TTCCTCTTAT 1320
CAGAGCCCGA GTCTGCGCCC CAGGACACAG CATGAGTCAG ACTTGAAGTC CCAAGTCTTG 1380
TTGGGAATTT TCCCCCTGAG AAAGAGGTAG ATTTTTGAGT AGAGTTCTGT TGATTTCTTG 1440
AATATTATCA GTGACCCCAT GTTAAGCCCT GGGCTTCTGC ATCAGGTCAC ATCCCTTCGA 1500
AACCAATAGA GCTTCCAGAG 1520
|
