| Tag | Content |
|---|
EnhancerAtlas ID | HS066-02843 |
Organism | Homo sapiens |
Tissue/cell | GM18516 |
Coordinate | chr19:36488950-36490280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:36490093-36490112 | CAGCCTGTAGGGGGCAGCA | + | 6.48 | | Foxq1 | MA0040.1 | chr19:36489049-36489060 | TATTGTTTATT | + | 6.62 | | Nr2f6(var.2) | MA0728.1 | chr19:36489666-36489681 | GAGGTCAGGAGTTCA | + | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr19:36489281-36489296 | TGAACTCCTGACCTC | - | 6.22 |
|
| | 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 |
| GH19I035998 | chr19 | 36489853 | 36490896 |
|
Enhancer Sequence | ACTGCAGCCT CGACTTCCCG GGCTCAAGTG ATCCTTCCAC TTCAGCCTTC TGAGTAGCTG 60
GGACTACAGG CGTGCACCAC CACACCCAGA TAATATTTTT ATTGTTTATT TTATTTTATT 120
TATTTATTTT TGAGACAGAG TTTTGCTCTT GTTGCCCAGG CTGGAGTGCA ATGGTGCGCT 180
CAGCTCACCA CAACCTCCGC TTCCCAGGTT CAAGCCATTC TCCTGCCTCA GCCTCCTGAT 240
TACCTGGGAT TACAGGCATA TGCCACCATG CCTGGCTAAT TTTTGTATTT TTAGTTAAGA 300
TGGGGTTTCA CCATGTTGAC CAGGCTGGTC TTGAACTCCT GACCTCAGGT GATCTGTCCA 360
CCTCGGCTTC CCAGAGTGCT GGGATTACAG GTGTGAGCCA GCGTGCCTGG CCTATTCTTT 420
ATTTTTCGGA GACAGGGTCT CACTGTGTTG CCCAGGCTGG TCTCAAACTC TTGAGCTGAA 480
GCGGTCCTCC CACCTCAGCC TCCCAAAGTG CTGAGATCAC AGTCATGAGC CACCATGCCC 540
AGCCTGATTT AACCTTTTTG CCTGAATGCC CTTATCAGTG AAATGGGCTT AATAAGAGCC 600
TCCCTGATGT GGCCATTATG ATGGTACAGT GAATTAAATG CCTGTTGTGA GGCCAGGCGC 660
AGTGGCTCAC GCCTATAATC CCAGCACTTT GGGAGGCTGA GGTGGGCAGA TCACCTGAGG 720
TCAGGAGTTC AAGACCAGCC TGACCAGCAT GGAGAAACCC TGTCTCTACT AAAAAATATA 780
AAATTAGCCA GGCATAGTGG TACATGCCTG TAAGCCCAGC TACTCAGGAG GCTGAGGCAG 840
GAGAATTGCT TGAACCCGGG AGGCAGAGGT TGCGGTGAGC CAAGATCGTG CCATTGTACT 900
CCAGTCTGGG CAACGAGAGT GAGACTCCAT CTCAAAAAAA AAAACAAACC CTGTTGTGAC 960
AGCAGATGAT GAGGCCTGAC CCCCACCCAT GGCCCTCCTG CCCTCTTGGG TTGACTTGCA 1020
ACTGTAGAAG CAGGTTCTCA GGAGGCTGCA GCCTCCTCCC CTGAGCCCCT GCATCTCTGT 1080
TGCTCTGCCT GAGGGCTTCC TGGGAGTCCT GGAAGGTGGG TTAATGTGCT CAGAGGCAAC 1140
CCTCAGCCTG TAGGGGGCAG CAGTCACTGG ATGAGCGCCC TGGCCCACCT CTCATCTGGT 1200
GGGACAACAT GTGTTCTGCA GGGTTCCTCA GGGGCACCCA TGGAATGGAG CCCCAGTTGC 1260
CCACAGTGGT GTCCACTCCA TGAGCACCTT TTTTGGCTTT TCCCCTGCCC TGTCTCTTCC 1320
CCACTCCCGC 1330
|
