| Tag | Content |
|---|
EnhancerAtlas ID | HS044-13372 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr9:80121660-80123140 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr9:80122877-80122891 | CCCGCCTCGGCCTC | + | 6.01 |
| | | 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 |
| GH09I077506 | chr9 | 80121661 | 80122850 |
| Enhancer Sequence | ACACTCACAG CACATCTTGA TTCAAACCAT CCACATTTCA AAGACTGAAC AGCCACATGG 60
GGCTAGTCAC TACCATATTG GACAGCAAAG AGTTAGAAAA CAAATTAGTG CTCATTTGCA 120
GCAACTACCT TTCATTTGGG TTTCTGATAC CATTAATTTC CTCCACCTAT CCCAGGACTC 180
TTAATCACTT ATCCTCACAT TATCAGAATG GTTTGAGATA TCTTGCCTCT TATAAGTCAC 240
TGGAAATCTT ATTTGGAAGT GTACAGGATA AAAATTCTAA AGGGATAAAG AACATAGCAG 300
ATTTTATCCA CATTTCCCAG TTGAAAGTAA GTTCAGAGCC ACAAGATATC TCTAGTCACA 360
CAGCTAGTAA GTCTTCAGGC CACAACTACA GCCTAGGTTT TAGGACACTA ATTTCAACAT 420
GCCTTTGCCT CCATCTCACC ATCTCTTTTA AAAGTCAGAA CACTTCAGAG CAGGAAAATA 480
CTCAGCTTGT TTGGGAGTTA AATAATGAAG AGAAAGAATC TCTTGCTTCA ATATGCTTAC 540
CCAATTCCTA CATAAAAGTC CAAATGGCTC GTTGGGGTGA GGAAGAGGTC AGGTCTCAAA 600
AGGAAGTTAT TTCCCCAACT TGAAAGATAC TTGGTTCCCT TCCAAAGGCA GGAAAACCTT 660
TTAAAAATAA ATCAATCAAT CCTCATTTTT AAGAACAAAC ATGTAGAGCA TGGATGCTGG 720
ATCCAATGCC ATGGCTGAGA AAATGTCACC GTCAAAGCCA AGAACAGCAA CTGAACCCCC 780
GAGCATCACA AATCTTATTG GAATTCATAA AAAAACAGCT GTATTTCCCT CTGTTTTCAT 840
TGAGTCTAAC CTTGTATGCT ATTTCTTAAA TAAACACACA AAGCATTACT CCAATAATCA 900
GAAAAACAGC CGTTTGTTTT TAACGGCTCC TCTTTTCCTA ATTTCTACCT CTTGTCCAGC 960
TCACTCTTTT TTTCAAGATG TAGTCTTGCT CTGTCACCCA ACTGACAGAG TCCACTGGAG 1020
TCCAGTGGTG CAATCTTGGC TCACTGCAAT CTCCACCTCC TAAGCAATTC TCTTACCTCA 1080
GCCTCCCGAG TAGCTGGGAT TACAGGCACT CATCACTGCG CCCACCACCA TGCCCAGCTA 1140
ACTTTTTATA TTTTCAGTAG AGAAAGTGTT ATCATATTGG CCAGGCTGGT CTCAAACTCC 1200
TGACCTCAGG TGATCCACCC GCCTCGGCCT CCCAAAGTGC TGGGATTACA GGCGTGAGCC 1260
ACTGTGCCTG GCCTCAGCTC ACTCTTATTA GTGGGTTTAG TCATGTGAAA GTTTTCAATG 1320
TTGAAGAAAC TCTCCACTAC TCTGTCCGCT TCCCTGCTCT CTCTCATTCT CTATCATCCC 1380
CTCTGTATTT CTTAATTCTC TACTGCAGTC ACTACTTCCA CCATTGCCTC AATCCCACCC 1440
TTTCTACCCA CTAAGAAAGA AAATACATCT AGAAAATGCA 1480
|
| |
|
|
|
