| Tag | Content |
|---|
EnhancerAtlas ID | HS044-07727 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr2:210360530-210361680 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr2:210360681-210360699 | GAAATAGTTTCAATTTCC | - | 6.19 |
| | | 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 |
| GH02I209494 | chr2 | 210359621 | 210362354 |
| Enhancer Sequence | TTGTTGTTTT GTATTAGAAT GGTACTCTAG CCTTCATAAA ACAAATTCCA TGATTTAGAC 60
ATTTGAAAGT TCTTCATTTT CAACTGACAT TTATTTCTAG TTACTGCATC ACCTAGTCAT 120
TTTATGTTCA GTGTTGTGAC AGCAAATGGG TGAAATAGTT TCAATTTCCC AGCATGTAAC 180
TGGCCTTTTT AGCCTTAACT TTCTTTTCCA GCATTGTTAC GGCAGCTACA GCAAACATGT 240
CAGAGTACAG AACATTCCAT TAAGAGCCTT ATCTCATGCC TCGCTTCCTA TGATGTTTTG 300
TATGAATAAT ACAATGTCTA GAGGTGAAAT TAGTTGGAGT GCTCATGACT CAGCCTCTTT 360
TTCTGGGGAG TGAGTCATTC CACATTTATA GATTCCTGAC TTTGTGCCGT ATACCACACT 420
AAGTGCTTGG AATACAAACA TAGATTTGCT GGGTCATTGA CCCAGAGCAG CCCACAGTCT 480
GGGCAGGCAG GGTATGGCAT TCATTAAGAA CAATATGGGC TTACACATAG CCAGCACTCT 540
ATTAATGTTA TATCTACCTG TCAAGGCAAA GTGTGATTAA ATATACAATA ATATGAGCTG 600
TCTAGACAAC TTAATTCTAT GTTTTGGAAC ATGTACCTCT GACCCTATAG CCCTATATTG 660
GTATATTTTG CCTAATTATA TCACCACAAA TTTAACTCCT TTATTGTTTT GTTTGGATAC 720
TGAGTTTTTA TTCCTTTGCA TATCACGTAA AATCATACCC TCCATGAATA GGTCAGTTGC 780
CTGATGAATA CCTTTCCTTT ATTATCCTGC CAGAAACTCA CACTTAATGT GTCTAATAAA 840
GCCCATTATC CTCTACTTTT ACCCAGCAAC CTGATCTCCC TTCAGGCTTT CCTGTTTCTA 900
AGAATGTACT GGGAGTCTGT TTTTCTTACA CTCTCAAAAT TCTCTTGGCT CCTTTCTTCA 960
TCCTGTGCCT TTCCTGGCCA ATGAATCCTT AAATTCTTTT TTTGTGTGTG TGAGACAGGG 1020
ACTCTGTTGC CAAGGGTGGA TTTCAGTGGT GCAATCATAG CTCACTGTAA CCTCATATGC 1080
CTCTGGCTTC AGCCTCCCCA GTAGCTAGGA CTACAGGTGT GCACTACCAT GCCTGGCTAA 1140
TTTAAAAAAA 1150
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