| Tag | Content |
|---|
EnhancerAtlas ID | HS165-05918 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr17:9107770-9109170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6 | MA0677.1 | chr17:9108982-9108996 | GAGGTTAAGGGTCA | + | 6 | | Rxra | MA0512.2 | chr17:9108982-9108996 | GAGGTTAAGGGTCA | + | 6.13 | | SNAI2 | MA0745.2 | chr17:9108405-9108415 | AACAGGTGCA | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26708 | chr17:9108846-9110585 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 9108132 | 9108562 | | chr17 | 9108309 | 9108608 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I009204 | chr17 | 9107861 | 9108800 |
|
Enhancer Sequence | CTGCTAAGTT TTGTATTTTT TAGTAGAGAC AGGGTTTCGC CACACTGGCC AGGCTGGTCT 60
CGAACTCCTG GCCTCATGTG ATCTGCCTGC CTCGGCCTCC CAAAGTGTCG GGATTACAGG 120
CGTGAGCCAA GCAACCCTTT CAGTTCCAAG GGGGTGGATT CTGTGGCCTG CGTCCAGTCT 180
ATCAGTCGGT GGCAAATGGC AGTGAATCGG GGATAGCAAG GATGCATCAG CTTCCCCACT 240
AAGCAACTCC CTACCCTTCA CATACCAGGC AGAGACACAG CTACCCTCCC AAATAGCCAC 300
TGTAGGATGC AGAGCTTGGA AGTTGAAGGA CGTCAATGAG GAATACCTTA CTGAGTTCTG 360
GGCCCCATTA GGGTGCTGTG GTTGATTAGT GATGCCTGCC ATGAGGTTGG GTAGAGTAAC 420
CGGTGGTCTG TGTGCTGCCT GTTCACTTGC TTTCCATCAG TGCTGTCAAC CCTCATTTTT 480
TTTTTTTTCT GAAGATATGT TGCTCATTAT CAGGCCTTTC AAAATAGGAA CTCCAGGTTT 540
CACACTTTCT TCTTTTCTTT CTCTTCTTCC CTGCCTGGGC TTTCATTACC ATTAAGAGCC 600
AGAACTTATC TGCCATTTGG ATGAGGAACT TCAGAAACAG GTGCAGGAAG AGAAACTTGC 660
TCTCTCAAGT GCAGCAACTT CTTGAATGTG GCCCACTTCC CCTGGAAGGC TGTGAACACC 720
ACTTTATCTC CTAAAGGCTT GGCTGGTGGG AGGAGGGGCA GGAAGCCTCA TGGACATGAG 780
GGCACTATTT GGGGAAGGGT ATGGTGGCAA GAATAGATGG GGGTAGAGGA AGCTACACGG 840
AGGTTCTGCC TGAGGGCTGG GAAGCCAAAA GGATGGTCCC TTGAAAAGGG GCAGCCAGGT 900
GCAGTGGCTC ATGCCTGTAA TCCTAACACT TTGGGAGGCC AGAGCAGGAG GATCACTTGA 960
GCCTGAGACT TCGAGACCAG CCTGGGCAAC ATAGTGAGAC CTCATCTCTA CAAAAAATAA 1020
TAAATTAGCT ATGTTTGGTT GTGTGCACCT GTAGTCCTAG CTACGTGGGA GGCTAAGTAG 1080
GATCATTGGA GCCCACGGGT TCGAGGCTGC AGTGAGCTGT GATTGCGCCT CTGCGCTCCA 1140
GCTGGGGTGA CAAAGGGAGA CCCTGTCTCA GAGAGAGAGA GAGAAGGGGC AGCTCCTGCA 1200
TTGCGATGGG GGGAGGTTAA GGGTCAGTAC TCACTAGTCA ACAGGTTGCC ATGGCTCTGT 1260
GTATGGAAAG AGACCCCTCT GTCCTGTGCT GGAGTGGAAG GCAGCTGTGT TAGGGAATGG 1320
GCCCCCACCG GCCAGTGACT TTGGATGCTG AACACTTGTA CCTCTGTTTT CTCCTGTGTG 1380
TAATGGCCAT GGCCGTCCTA 1400
|
