| Tag | Content |
|---|
EnhancerAtlas ID | HS044-11544 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr6:118989340-118991090 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr6:118990287-118990299 | CAGTAAACAGAA | + | 6.02 | | FOXP2 | MA0593.1 | chr6:118990147-118990158 | AAGTAAACAAA | + | 6.62 | | MSC | MA0665.1 | chr6:118990381-118990391 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr6:118990381-118990391 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr6:118990381-118990391 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr6:118990381-118990391 | AACAGCTGTT | - | 6.02 |
|
| | 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 |
| GH06I118668 | chr6 | 118989358 | 118991379 |
|
Enhancer Sequence | GAATATGCAG TGCTTGTGCA GGCAGGAGAG CAATGATGTA ATTAAATAGG ACAGCTCCCA 60
AAGTTGACAG GCATAAATGA TGAAAGGCAA AGTTTAGATA TCAACCTATG AGCCATGGAC 120
ACCTGCAGAG TTTTAAAATT ATTACAAAGG GACCTGAAGT CCCATAAGGT ATGCTTACCT 180
GAATAAGGTG GGTTGCACTG ATATATACAC CCAGACTTCA AATGGATAGA GATGCTCTTT 240
TGTTTAATAA AGTATGCCTT CAATTAAAAG CATTACTGAA GCCAGATGTG GTACTGTGTG 300
CCTACAGTCC CCACTACTTG CTACTCGGAA GGCTGAGGTG GGAGGATCAC TTGAGCCCAG 360
GGGTTCAAGT CCAGCCTGGG CAAAAAGCAT TACTGAATTC CTAGCAATGT GTTTATCCTT 420
ATGTACTTTC AGTCAACTTT TACTAAAAGT ACAAACACTA TTATGTGCAA CTCTGTGAAA 480
TTTTGTTGTT AAAAATGAAA TCATAGTTGA AAATGTGGGG ACTGTCTGTT CAAGGCTAAA 540
ATAAAGGGAA CAGAACAAAA TTAAGATGGG AAATAATTAT TTTAAAACAT ATTTTGTATG 600
TTTTCCTGTG TTTCTATTTT AAAGCTATAT ATCTAAATTA TTGCTCTTTG TTTTCATGTT 660
GAATGGCTGC TTCTTATCTG GCTTTGTTTA TTAAGTGTGG TCAGATCATT TATTCTCAGA 720
AAAGCTACCC TGTAGCCTGG CCCTACATTC CTCCAAGATA ATATCATCTG CAGGACTCAA 780
GTTTCTTGCC AGAGAGCTGA TTTGCAGAAG TAAACAAACT GGGAGTAAAA CCAAGAAATG 840
TTAAAGAAAC TTTCTGACTT AAGACATTGA TAACAAAAAC TATGTTAGCA ATAAGTGTCT 900
CTAAAAATAT ATAGAATATC CAGTCAAGCT GACCTACAGA ATTGGAACAG TAAACAGAAC 960
ACAAAAAGGG CTGTAAGCAA TACCATCTAG GAACACAGAG GTAACAGATA GGGCTCCATG 1020
TCTGTCAGGG ACTCCAGGAG GAACAGCTGT TCCCTTCTCT CAAAACAAAC CATCCTCTGA 1080
TGCGTTTCAG TTGCTTACCA ACTCAGATCT GCTTTTGAGG AGTAAGCCAA ACACACAGCC 1140
TCTGGTGATT TACCTTATAG AGGGCATTAG GGAAACTTAA AAAACAAATG TCAACTTGAA 1200
AAGGCCACAT TTTATATCTT TCCTTCATCT CTGGCAGTAT TCCGTTGTTG TTCCAACTAC 1260
CCACCCCCTT GCCCTTCCTT ACATTTGATT CTTTGTTAGA TGAAGCATGG AGACAATGGA 1320
AAGCAACTGG GAAACAAACT AAACATTTCC TTCTGGAAAT ATTACCTACT TTTAAATAAC 1380
CACTAGGGTC TATAAATATT TTCATTAGAA ATTTGCCCTC CCTCCACACA CACCAGTCAC 1440
TTTGTGAAAA ACCAATTTCT CCAAGTCAGA ACCTAGAATT TATGGTCTCC TCTCATTGCA 1500
CTACTAAAAC CTTTCATATC CACAGTGAAT CTAGGCTATT ACCTCTGGAG ACTGGAGTTC 1560
AGGGCCTCAC TCATATATTT ATCTCATGAA CTAAACCCCT GTAATTCCCT GTGGAGTTGG 1620
GGTTTGGAGG CAGATGATAG AGAGGAAAGT TAGAGTTACA ACCATTTGGT TCAATGTGGT 1680
AGAGCGCTGA ATTGACTGTG TGATCTTAGG CAAGTCCCAT AAGCTCTCTG GGCCCCAGAT 1740
AACTCATGTG 1750
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